dbSNP Short Genetic Variations
Welcome to the Reference SNP (rs) Report
All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.
Reference SNP (rs) Report
This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.
rs199731115
Current Build 156
Released September 21, 2022
- Organism
- Homo sapiens
- Position
-
chr9:14819441 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
- Alleles
- G>A
- Variation Type
- SNV Single Nucleotide Variation
- Frequency
-
A=0.000110 (29/264690, TOPMED)A=0.000078 (19/244500, GnomAD_exome)A=0.000047 (8/168564, ALFA) (+ 7 more)
- Clinical Significance
- Not Reported in ClinVar
- Gene : Consequence
- FREM1 : Missense Variant
- Publications
- 0 citations
- Genomic View
- See rs on genome
ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.
Release Version: 20230706150541
| Population | Group | Sample Size | Ref Allele | Alt Allele |
|---|---|---|---|---|
| Total | Global | 184882 | G=0.999946 | A=0.000054 |
| European | Sub | 156924 | G=0.999943 | A=0.000057 |
| African | Sub | 9126 | G=1.0000 | A=0.0000 |
| African Others | Sub | 352 | G=1.000 | A=0.000 |
| African American | Sub | 8774 | G=1.0000 | A=0.0000 |
| Asian | Sub | 6294 | G=0.9998 | A=0.0002 |
| East Asian | Sub | 4476 | G=0.9998 | A=0.0002 |
| Other Asian | Sub | 1818 | G=1.0000 | A=0.0000 |
| Latin American 1 | Sub | 442 | G=1.000 | A=0.000 |
| Latin American 2 | Sub | 950 | G=1.000 | A=0.000 |
| South Asian | Sub | 280 | G=1.000 | A=0.000 |
| Other | Sub | 10866 | G=1.00000 | A=0.00000 |
Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").
Download| Study | Population | Group | Sample Size | Ref Allele | Alt Allele |
|---|---|---|---|---|---|
| TopMed | Global | Study-wide | 264690 | G=0.999890 | A=0.000110 |
| gnomAD - Exomes | Global | Study-wide | 244500 | G=0.999922 | A=0.000078 |
| gnomAD - Exomes | European | Sub | 131818 | G=0.999977 | A=0.000023 |
| gnomAD - Exomes | Asian | Sub | 47624 | G=0.99977 | A=0.00023 |
| gnomAD - Exomes | American | Sub | 33958 | G=0.99988 | A=0.00012 |
| gnomAD - Exomes | African | Sub | 15202 | G=1.00000 | A=0.00000 |
| gnomAD - Exomes | Ashkenazi Jewish | Sub | 9948 | G=1.0000 | A=0.0000 |
| gnomAD - Exomes | Other | Sub | 5950 | G=0.9998 | A=0.0002 |
| Allele Frequency Aggregator | Total | Global | 168564 | G=0.999953 | A=0.000047 |
| Allele Frequency Aggregator | European | Sub | 146868 | G=0.999952 | A=0.000048 |
| Allele Frequency Aggregator | Other | Sub | 9438 | G=1.0000 | A=0.0000 |
| Allele Frequency Aggregator | Asian | Sub | 6294 | G=0.9998 | A=0.0002 |
| Allele Frequency Aggregator | African | Sub | 4292 | G=1.0000 | A=0.0000 |
| Allele Frequency Aggregator | Latin American 2 | Sub | 950 | G=1.000 | A=0.000 |
| Allele Frequency Aggregator | Latin American 1 | Sub | 442 | G=1.000 | A=0.000 |
| Allele Frequency Aggregator | South Asian | Sub | 280 | G=1.000 | A=0.000 |
| gnomAD - Genomes | Global | Study-wide | 140218 | G=0.999943 | A=0.000057 |
| gnomAD - Genomes | European | Sub | 75946 | G=0.99993 | A=0.00007 |
| gnomAD - Genomes | African | Sub | 42020 | G=0.99998 | A=0.00002 |
| gnomAD - Genomes | American | Sub | 13644 | G=0.99993 | A=0.00007 |
| gnomAD - Genomes | Ashkenazi Jewish | Sub | 3322 | G=1.0000 | A=0.0000 |
| gnomAD - Genomes | East Asian | Sub | 3134 | G=0.9997 | A=0.0003 |
| gnomAD - Genomes | Other | Sub | 2152 | G=1.0000 | A=0.0000 |
| ExAC | Global | Study-wide | 95308 | G=0.99990 | A=0.00010 |
| ExAC | Europe | Sub | 58050 | G=0.99997 | A=0.00003 |
| ExAC | Asian | Sub | 20254 | G=0.99965 | A=0.00035 |
| ExAC | African | Sub | 8172 | G=1.0000 | A=0.0000 |
| ExAC | American | Sub | 8106 | G=0.9999 | A=0.0001 |
| ExAC | Other | Sub | 726 | G=1.000 | A=0.000 |
| The PAGE Study | Global | Study-wide | 78696 | G=0.99990 | A=0.00010 |
| The PAGE Study | AfricanAmerican | Sub | 32516 | G=0.99997 | A=0.00003 |
| The PAGE Study | Mexican | Sub | 10810 | G=1.00000 | A=0.00000 |
| The PAGE Study | Asian | Sub | 8314 | G=1.0000 | A=0.0000 |
| The PAGE Study | PuertoRican | Sub | 7918 | G=0.9999 | A=0.0001 |
| The PAGE Study | NativeHawaiian | Sub | 4532 | G=1.0000 | A=0.0000 |
| The PAGE Study | Cuban | Sub | 4230 | G=0.9998 | A=0.0002 |
| The PAGE Study | Dominican | Sub | 3828 | G=0.9987 | A=0.0013 |
| The PAGE Study | CentralAmerican | Sub | 2450 | G=1.0000 | A=0.0000 |
| The PAGE Study | SouthAmerican | Sub | 1982 | G=1.0000 | A=0.0000 |
| The PAGE Study | NativeAmerican | Sub | 1260 | G=1.0000 | A=0.0000 |
| The PAGE Study | SouthAsian | Sub | 856 | G=1.000 | A=0.000 |
| GO Exome Sequencing Project | Global | Study-wide | 12124 | G=0.99992 | A=0.00008 |
| GO Exome Sequencing Project | European American | Sub | 8280 | G=0.9999 | A=0.0001 |
| GO Exome Sequencing Project | African American | Sub | 3844 | G=1.0000 | A=0.0000 |
| 1000Genomes_30x | Global | Study-wide | 6404 | G=0.9995 | A=0.0005 |
| 1000Genomes_30x | African | Sub | 1786 | G=1.0000 | A=0.0000 |
| 1000Genomes_30x | Europe | Sub | 1266 | G=1.0000 | A=0.0000 |
| 1000Genomes_30x | South Asian | Sub | 1202 | G=0.9992 | A=0.0008 |
| 1000Genomes_30x | East Asian | Sub | 1170 | G=0.9983 | A=0.0017 |
| 1000Genomes_30x | American | Sub | 980 | G=1.000 | A=0.000 |
| 1000Genomes | Global | Study-wide | 5008 | G=0.9996 | A=0.0004 |
| 1000Genomes | African | Sub | 1322 | G=1.0000 | A=0.0000 |
| 1000Genomes | East Asian | Sub | 1008 | G=0.9990 | A=0.0010 |
| 1000Genomes | Europe | Sub | 1006 | G=1.0000 | A=0.0000 |
| 1000Genomes | South Asian | Sub | 978 | G=0.999 | A=0.001 |
| 1000Genomes | American | Sub | 694 | G=1.000 | A=0.000 |
| KOREAN population from KRGDB | KOREAN | Study-wide | 2922 | G=1.0000 | A=0.0000 |
Help
Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.
Genomic Placements
| Sequence name | Change |
|---|---|
| GRCh38.p14 chr 9 | NC_000009.12:g.14819441G>A |
| GRCh37.p13 chr 9 | NC_000009.11:g.14819439G>A |
| FREM1 RefSeqGene | NG_017005.2:g.95796C>T |
Gene: FREM1, FRAS1 related extracellular matrix 1
(minus strand)
| Molecule type | Change | Amino acid[Codon] | SO Term |
|---|---|---|---|
| FREM1 transcript variant 2 | NM_001177704.3:c. | N/A | Genic Upstream Transcript Variant |
| FREM1 transcript variant 3 | NM_001370058.2:c. | N/A | Genic Upstream Transcript Variant |
| FREM1 transcript variant 5 | NM_001370061.2:c. | N/A | Genic Upstream Transcript Variant |
| FREM1 transcript variant 4 | NM_001370060.1:c. | N/A | Genic Downstream Transcript Variant |
| FREM1 transcript variant 6 | NM_001370063.1:c. | N/A | Genic Downstream Transcript Variant |
| FREM1 transcript variant 7 | NM_001370065.1:c. | N/A | Genic Downstream Transcript Variant |
| FREM1 transcript variant 13 | NM_001379081.2:c.2339C>T | A [GCG] > V [GTG] | Coding Sequence Variant |
| FRAS1-related extracellular matrix protein 1 isoform 1 precursor | NP_001366010.1:p.Ala780Val | A (Ala) > V (Val) | Missense Variant |
| FREM1 transcript variant 1 | NM_144966.7:c.2339C>T | A [GCG] > V [GTG] | Coding Sequence Variant |
| FRAS1-related extracellular matrix protein 1 isoform 1 precursor | NP_659403.4:p.Ala780Val | A (Ala) > V (Val) | Missense Variant |
| FREM1 transcript variant 8 | NR_163238.2:n.3155C>T | N/A | Non Coding Transcript Variant |
| FREM1 transcript variant 9 | NR_163239.2:n.3099C>T | N/A | Non Coding Transcript Variant |
| FREM1 transcript variant 12 | NR_163242.2:n. | N/A | Genic Upstream Transcript Variant |
| FREM1 transcript variant 10 | NR_163240.1:n. | N/A | Genic Downstream Transcript Variant |
| FREM1 transcript variant 11 | NR_163241.1:n. | N/A | Genic Downstream Transcript Variant |
| FREM1 transcript variant X28 | XM_006716729.4:c. | N/A | Genic Upstream Transcript Variant |
| FREM1 transcript variant X27 | XM_011517758.3:c. | N/A | Genic Upstream Transcript Variant |
| FREM1 transcript variant X29 | XM_047422859.1:c. | N/A | Genic Upstream Transcript Variant |
| FREM1 transcript variant X1 | XM_017014316.3:c.2366C>T | A [GCG] > V [GTG] | Coding Sequence Variant |
| FRAS1-related extracellular matrix protein 1 isoform X1 | XP_016869805.1:p.Ala789Val | A (Ala) > V (Val) | Missense Variant |
| FREM1 transcript variant X2 | XM_047422844.1:c.2366C>T | A [GCG] > V [GTG] | Coding Sequence Variant |
| FRAS1-related extracellular matrix protein 1 isoform X1 | XP_047278800.1:p.Ala789Val | A (Ala) > V (Val) | Missense Variant |
| FREM1 transcript variant X30 | XM_047422845.1:c.2366C>T | A [GCG] > V [GTG] | Coding Sequence Variant |
| FRAS1-related extracellular matrix protein 1 isoform X1 | XP_047278801.1:p.Ala789Val | A (Ala) > V (Val) | Missense Variant |
| FREM1 transcript variant X3 | XM_017014319.3:c.2366C>T | A [GCG] > V [GTG] | Coding Sequence Variant |
| FRAS1-related extracellular matrix protein 1 isoform X1 | XP_016869808.1:p.Ala789Val | A (Ala) > V (Val) | Missense Variant |
| FREM1 transcript variant X4 | XM_017014320.3:c.2366C>T | A [GCG] > V [GTG] | Coding Sequence Variant |
| FRAS1-related extracellular matrix protein 1 isoform X1 | XP_016869809.1:p.Ala789Val | A (Ala) > V (Val) | Missense Variant |
| FREM1 transcript variant X5 | XM_017014321.3:c.2366C>T | A [GCG] > V [GTG] | Coding Sequence Variant |
| FRAS1-related extracellular matrix protein 1 isoform X1 | XP_016869810.1:p.Ala789Val | A (Ala) > V (Val) | Missense Variant |
| FREM1 transcript variant X6 | XM_017014322.2:c.2366C>T | A [GCG] > V [GTG] | Coding Sequence Variant |
| FRAS1-related extracellular matrix protein 1 isoform X1 | XP_016869811.1:p.Ala789Val | A (Ala) > V (Val) | Missense Variant |
| FREM1 transcript variant X7 | XM_047422846.1:c.2339C>T | A [GCG] > V [GTG] | Coding Sequence Variant |
| FRAS1-related extracellular matrix protein 1 isoform X2 | XP_047278802.1:p.Ala780Val | A (Ala) > V (Val) | Missense Variant |
| FREM1 transcript variant X8 | XM_047422847.1:c.2339C>T | A [GCG] > V [GTG] | Coding Sequence Variant |
| FRAS1-related extracellular matrix protein 1 isoform X2 | XP_047278803.1:p.Ala780Val | A (Ala) > V (Val) | Missense Variant |
| FREM1 transcript variant X9 | XM_047422848.1:c.2339C>T | A [GCG] > V [GTG] | Coding Sequence Variant |
| FRAS1-related extracellular matrix protein 1 isoform X2 | XP_047278804.1:p.Ala780Val | A (Ala) > V (Val) | Missense Variant |
| FREM1 transcript variant X10 | XM_017014324.3:c.2366C>T | A [GCG] > V [GTG] | Coding Sequence Variant |
| FRAS1-related extracellular matrix protein 1 isoform X3 | XP_016869813.1:p.Ala789Val | A (Ala) > V (Val) | Missense Variant |
| FREM1 transcript variant X11 | XM_017014325.3:c.2366C>T | A [GCG] > V [GTG] | Coding Sequence Variant |
| FRAS1-related extracellular matrix protein 1 isoform X4 | XP_016869814.1:p.Ala789Val | A (Ala) > V (Val) | Missense Variant |
| FREM1 transcript variant X12 | XM_017014326.2:c.1958C>T | A [GCG] > V [GTG] | Coding Sequence Variant |
| FRAS1-related extracellular matrix protein 1 isoform X5 | XP_016869815.1:p.Ala653Val | A (Ala) > V (Val) | Missense Variant |
| FREM1 transcript variant X13 | XM_017014327.3:c.1442C>T | A [GCG] > V [GTG] | Coding Sequence Variant |
| FRAS1-related extracellular matrix protein 1 isoform X6 | XP_016869816.1:p.Ala481Val | A (Ala) > V (Val) | Missense Variant |
| FREM1 transcript variant X14 | XM_017014328.3:c.2366C>T | A [GCG] > V [GTG] | Coding Sequence Variant |
| FRAS1-related extracellular matrix protein 1 isoform X7 | XP_016869817.1:p.Ala789Val | A (Ala) > V (Val) | Missense Variant |
| FREM1 transcript variant X15 | XM_017014329.3:c.2366C>T | A [GCG] > V [GTG] | Coding Sequence Variant |
| FRAS1-related extracellular matrix protein 1 isoform X8 | XP_016869818.1:p.Ala789Val | A (Ala) > V (Val) | Missense Variant |
| FREM1 transcript variant X16 | XM_047422849.1:c.2366C>T | A [GCG] > V [GTG] | Coding Sequence Variant |
| FRAS1-related extracellular matrix protein 1 isoform X9 | XP_047278805.1:p.Ala789Val | A (Ala) > V (Val) | Missense Variant |
| FREM1 transcript variant X17 | XM_047422850.1:c.2366C>T | A [GCG] > V [GTG] | Coding Sequence Variant |
| FRAS1-related extracellular matrix protein 1 isoform X10 | XP_047278806.1:p.Ala789Val | A (Ala) > V (Val) | Missense Variant |
| FREM1 transcript variant X18 | XM_047422851.1:c.2339C>T | A [GCG] > V [GTG] | Coding Sequence Variant |
| FRAS1-related extracellular matrix protein 1 isoform X11 | XP_047278807.1:p.Ala780Val | A (Ala) > V (Val) | Missense Variant |
| FREM1 transcript variant X19 | XM_047422852.1:c.2339C>T | A [GCG] > V [GTG] | Coding Sequence Variant |
| FRAS1-related extracellular matrix protein 1 isoform X12 | XP_047278808.1:p.Ala780Val | A (Ala) > V (Val) | Missense Variant |
| FREM1 transcript variant X20 | XM_047422853.1:c.2366C>T | A [GCG] > V [GTG] | Coding Sequence Variant |
| FRAS1-related extracellular matrix protein 1 isoform X13 | XP_047278809.1:p.Ala789Val | A (Ala) > V (Val) | Missense Variant |
| FREM1 transcript variant X21 | XM_047422854.1:c.2339C>T | A [GCG] > V [GTG] | Coding Sequence Variant |
| FRAS1-related extracellular matrix protein 1 isoform X14 | XP_047278810.1:p.Ala780Val | A (Ala) > V (Val) | Missense Variant |
| FREM1 transcript variant X22 | XM_047422855.1:c.2366C>T | A [GCG] > V [GTG] | Coding Sequence Variant |
| FRAS1-related extracellular matrix protein 1 isoform X15 | XP_047278811.1:p.Ala789Val | A (Ala) > V (Val) | Missense Variant |
| FREM1 transcript variant X23 | XM_017014330.3:c.2366C>T | A [GCG] > V [GTG] | Coding Sequence Variant |
| FRAS1-related extracellular matrix protein 1 isoform X16 | XP_016869819.1:p.Ala789Val | A (Ala) > V (Val) | Missense Variant |
| FREM1 transcript variant X24 | XM_047422856.1:c.2339C>T | A [GCG] > V [GTG] | Coding Sequence Variant |
| FRAS1-related extracellular matrix protein 1 isoform X17 | XP_047278812.1:p.Ala780Val | A (Ala) > V (Val) | Missense Variant |
| FREM1 transcript variant X25 | XM_047422857.1:c.2339C>T | A [GCG] > V [GTG] | Coding Sequence Variant |
| FRAS1-related extracellular matrix protein 1 isoform X17 | XP_047278813.1:p.Ala780Val | A (Ala) > V (Val) | Missense Variant |
| FREM1 transcript variant X26 | XM_047422858.1:c.2339C>T | A [GCG] > V [GTG] | Coding Sequence Variant |
| FRAS1-related extracellular matrix protein 1 isoform X17 | XP_047278814.1:p.Ala780Val | A (Ala) > V (Val) | Missense Variant |
Help
Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.
Not Reported in ClinVar
Help
Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".
| Placement | G= | A |
|---|---|---|
| GRCh38.p14 chr 9 | NC_000009.12:g.14819441= | NC_000009.12:g.14819441G>A |
| GRCh37.p13 chr 9 | NC_000009.11:g.14819439= | NC_000009.11:g.14819439G>A |
| FREM1 RefSeqGene | NG_017005.2:g.95796= | NG_017005.2:g.95796C>T |
| FREM1 transcript variant 1 | NM_144966.7:c.2339= | NM_144966.7:c.2339C>T |
| FREM1 transcript variant 1 | NM_144966.6:c.2339= | NM_144966.6:c.2339C>T |
| FREM1 transcript variant 1 | NM_144966.5:c.2339= | NM_144966.5:c.2339C>T |
| FREM1 transcript variant 9 | NR_163239.2:n.3099= | NR_163239.2:n.3099C>T |
| FREM1 transcript variant 9 | NR_163239.1:n.3099= | NR_163239.1:n.3099C>T |
| FREM1 transcript variant 13 | NM_001379081.2:c.2339= | NM_001379081.2:c.2339C>T |
| FREM1 transcript variant 13 | NM_001379081.1:c.2339= | NM_001379081.1:c.2339C>T |
| FREM1 transcript variant 8 | NR_163238.2:n.3155= | NR_163238.2:n.3155C>T |
| FREM1 transcript variant 8 | NR_163238.1:n.3155= | NR_163238.1:n.3155C>T |
| FREM1 transcript variant X15 | XM_017014329.3:c.2366= | XM_017014329.3:c.2366C>T |
| FREM1 transcript variant X14 | XM_017014329.2:c.2366= | XM_017014329.2:c.2366C>T |
| FREM1 transcript variant X15 | XM_017014329.1:c.2366= | XM_017014329.1:c.2366C>T |
| FREM1 transcript variant X3 | XM_017014319.3:c.2366= | XM_017014319.3:c.2366C>T |
| FREM1 transcript variant X3 | XM_017014319.2:c.2366= | XM_017014319.2:c.2366C>T |
| FREM1 transcript variant X4 | XM_017014319.1:c.2366= | XM_017014319.1:c.2366C>T |
| FREM1 transcript variant X4 | XM_017014320.3:c.2366= | XM_017014320.3:c.2366C>T |
| FREM1 transcript variant X4 | XM_017014320.2:c.2366= | XM_017014320.2:c.2366C>T |
| FREM1 transcript variant X5 | XM_017014320.1:c.2366= | XM_017014320.1:c.2366C>T |
| FREM1 transcript variant X1 | XM_017014316.3:c.2366= | XM_017014316.3:c.2366C>T |
| FREM1 transcript variant X1 | XM_017014316.2:c.2366= | XM_017014316.2:c.2366C>T |
| FREM1 transcript variant X1 | XM_017014316.1:c.2366= | XM_017014316.1:c.2366C>T |
| FREM1 transcript variant X11 | XM_017014325.3:c.2366= | XM_017014325.3:c.2366C>T |
| FREM1 transcript variant X10 | XM_017014325.2:c.2366= | XM_017014325.2:c.2366C>T |
| FREM1 transcript variant X11 | XM_017014325.1:c.2366= | XM_017014325.1:c.2366C>T |
| FREM1 transcript variant X10 | XM_017014324.3:c.2366= | XM_017014324.3:c.2366C>T |
| FREM1 transcript variant X9 | XM_017014324.2:c.2366= | XM_017014324.2:c.2366C>T |
| FREM1 transcript variant X10 | XM_017014324.1:c.2366= | XM_017014324.1:c.2366C>T |
| FREM1 transcript variant X5 | XM_017014321.3:c.2366= | XM_017014321.3:c.2366C>T |
| FREM1 transcript variant X5 | XM_017014321.2:c.2366= | XM_017014321.2:c.2366C>T |
| FREM1 transcript variant X6 | XM_017014321.1:c.2366= | XM_017014321.1:c.2366C>T |
| FREM1 transcript variant X14 | XM_017014328.3:c.2366= | XM_017014328.3:c.2366C>T |
| FREM1 transcript variant X13 | XM_017014328.2:c.2366= | XM_017014328.2:c.2366C>T |
| FREM1 transcript variant X14 | XM_017014328.1:c.2366= | XM_017014328.1:c.2366C>T |
| FREM1 transcript variant X23 | XM_017014330.3:c.2366= | XM_017014330.3:c.2366C>T |
| FREM1 transcript variant X19 | XM_017014330.2:c.2366= | XM_017014330.2:c.2366C>T |
| FREM1 transcript variant X20 | XM_017014330.1:c.2366= | XM_017014330.1:c.2366C>T |
| FREM1 transcript variant X13 | XM_017014327.3:c.1442= | XM_017014327.3:c.1442C>T |
| FREM1 transcript variant X12 | XM_017014327.2:c.1442= | XM_017014327.2:c.1442C>T |
| FREM1 transcript variant X13 | XM_017014327.1:c.1442= | XM_017014327.1:c.1442C>T |
| FREM1 transcript variant X6 | XM_017014322.2:c.2366= | XM_017014322.2:c.2366C>T |
| FREM1 transcript variant X6 | XM_017014322.1:c.2366= | XM_017014322.1:c.2366C>T |
| FREM1 transcript variant X12 | XM_017014326.2:c.1958= | XM_017014326.2:c.1958C>T |
| FREM1 transcript variant X11 | XM_017014326.1:c.1958= | XM_017014326.1:c.1958C>T |
| FREM1 transcript variant X30 | XM_047422845.1:c.2366= | XM_047422845.1:c.2366C>T |
| FREM1 transcript variant X9 | XM_047422848.1:c.2339= | XM_047422848.1:c.2339C>T |
| FREM1 transcript variant X2 | XM_047422844.1:c.2366= | XM_047422844.1:c.2366C>T |
| FREM1 transcript variant X7 | XM_047422846.1:c.2339= | XM_047422846.1:c.2339C>T |
| FREM1 transcript variant X8 | XM_047422847.1:c.2339= | XM_047422847.1:c.2339C>T |
| FREM1 transcript variant X16 | XM_047422849.1:c.2366= | XM_047422849.1:c.2366C>T |
| FREM1 transcript variant X17 | XM_047422850.1:c.2366= | XM_047422850.1:c.2366C>T |
| FREM1 transcript variant X19 | XM_047422852.1:c.2339= | XM_047422852.1:c.2339C>T |
| FREM1 transcript variant X18 | XM_047422851.1:c.2339= | XM_047422851.1:c.2339C>T |
| FREM1 transcript variant X20 | XM_047422853.1:c.2366= | XM_047422853.1:c.2366C>T |
| FREM1 transcript variant X24 | XM_047422856.1:c.2339= | XM_047422856.1:c.2339C>T |
| FREM1 transcript variant X22 | XM_047422855.1:c.2366= | XM_047422855.1:c.2366C>T |
| FREM1 transcript variant X21 | XM_047422854.1:c.2339= | XM_047422854.1:c.2339C>T |
| FREM1 transcript variant X25 | XM_047422857.1:c.2339= | XM_047422857.1:c.2339C>T |
| FREM1 transcript variant X26 | XM_047422858.1:c.2339= | XM_047422858.1:c.2339C>T |
| FRAS1-related extracellular matrix protein 1 isoform 1 precursor | NP_659403.4:p.Ala780= | NP_659403.4:p.Ala780Val |
| FRAS1-related extracellular matrix protein 1 isoform 1 precursor | NP_001366010.1:p.Ala780= | NP_001366010.1:p.Ala780Val |
| FRAS1-related extracellular matrix protein 1 isoform X8 | XP_016869818.1:p.Ala789= | XP_016869818.1:p.Ala789Val |
| FRAS1-related extracellular matrix protein 1 isoform X1 | XP_016869808.1:p.Ala789= | XP_016869808.1:p.Ala789Val |
| FRAS1-related extracellular matrix protein 1 isoform X1 | XP_016869809.1:p.Ala789= | XP_016869809.1:p.Ala789Val |
| FRAS1-related extracellular matrix protein 1 isoform X1 | XP_016869805.1:p.Ala789= | XP_016869805.1:p.Ala789Val |
| FRAS1-related extracellular matrix protein 1 isoform X4 | XP_016869814.1:p.Ala789= | XP_016869814.1:p.Ala789Val |
| FRAS1-related extracellular matrix protein 1 isoform X3 | XP_016869813.1:p.Ala789= | XP_016869813.1:p.Ala789Val |
| FRAS1-related extracellular matrix protein 1 isoform X1 | XP_016869810.1:p.Ala789= | XP_016869810.1:p.Ala789Val |
| FRAS1-related extracellular matrix protein 1 isoform X7 | XP_016869817.1:p.Ala789= | XP_016869817.1:p.Ala789Val |
| FRAS1-related extracellular matrix protein 1 isoform X16 | XP_016869819.1:p.Ala789= | XP_016869819.1:p.Ala789Val |
| FRAS1-related extracellular matrix protein 1 isoform X6 | XP_016869816.1:p.Ala481= | XP_016869816.1:p.Ala481Val |
| FRAS1-related extracellular matrix protein 1 isoform X1 | XP_016869811.1:p.Ala789= | XP_016869811.1:p.Ala789Val |
| FRAS1-related extracellular matrix protein 1 isoform X5 | XP_016869815.1:p.Ala653= | XP_016869815.1:p.Ala653Val |
| FRAS1-related extracellular matrix protein 1 isoform X1 | XP_047278801.1:p.Ala789= | XP_047278801.1:p.Ala789Val |
| FRAS1-related extracellular matrix protein 1 isoform X2 | XP_047278804.1:p.Ala780= | XP_047278804.1:p.Ala780Val |
| FRAS1-related extracellular matrix protein 1 isoform X1 | XP_047278800.1:p.Ala789= | XP_047278800.1:p.Ala789Val |
| FRAS1-related extracellular matrix protein 1 isoform X2 | XP_047278802.1:p.Ala780= | XP_047278802.1:p.Ala780Val |
| FRAS1-related extracellular matrix protein 1 isoform X2 | XP_047278803.1:p.Ala780= | XP_047278803.1:p.Ala780Val |
| FRAS1-related extracellular matrix protein 1 isoform X9 | XP_047278805.1:p.Ala789= | XP_047278805.1:p.Ala789Val |
| FRAS1-related extracellular matrix protein 1 isoform X10 | XP_047278806.1:p.Ala789= | XP_047278806.1:p.Ala789Val |
| FRAS1-related extracellular matrix protein 1 isoform X12 | XP_047278808.1:p.Ala780= | XP_047278808.1:p.Ala780Val |
| FRAS1-related extracellular matrix protein 1 isoform X11 | XP_047278807.1:p.Ala780= | XP_047278807.1:p.Ala780Val |
| FRAS1-related extracellular matrix protein 1 isoform X13 | XP_047278809.1:p.Ala789= | XP_047278809.1:p.Ala789Val |
| FRAS1-related extracellular matrix protein 1 isoform X17 | XP_047278812.1:p.Ala780= | XP_047278812.1:p.Ala780Val |
| FRAS1-related extracellular matrix protein 1 isoform X15 | XP_047278811.1:p.Ala789= | XP_047278811.1:p.Ala789Val |
| FRAS1-related extracellular matrix protein 1 isoform X14 | XP_047278810.1:p.Ala780= | XP_047278810.1:p.Ala780Val |
| FRAS1-related extracellular matrix protein 1 isoform X17 | XP_047278813.1:p.Ala780= | XP_047278813.1:p.Ala780Val |
| FRAS1-related extracellular matrix protein 1 isoform X17 | XP_047278814.1:p.Ala780= | XP_047278814.1:p.Ala780Val |
Help
Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.
40 SubSNP,
10 Frequency
submissions
| No | Submitter | Submission ID | Date (Build) |
|---|---|---|---|
| 1 | 1000GENOMES | ss488902487 | May 04, 2012 (137) |
| 2 | EXOME_CHIP | ss491420594 | May 04, 2012 (137) |
| 3 | NHLBI-ESP | ss712876384 | Apr 25, 2013 (138) |
| 4 | ILLUMINA | ss780875260 | Sep 08, 2015 (146) |
| 5 | ILLUMINA | ss783560708 | Sep 08, 2015 (146) |
| 6 | 1000GENOMES | ss1333042091 | Aug 21, 2014 (142) |
| 7 | EVA_EXAC | ss1689424613 | Apr 01, 2015 (144) |
| 8 | ILLUMINA | ss1752768126 | Sep 08, 2015 (146) |
| 9 | ILLUMINA | ss1917834700 | Feb 12, 2016 (147) |
| 10 | ILLUMINA | ss1946253884 | Feb 12, 2016 (147) |
| 11 | ILLUMINA | ss1959168241 | Feb 12, 2016 (147) |
| 12 | HUMAN_LONGEVITY | ss2309695719 | Dec 20, 2016 (150) |
| 13 | GNOMAD | ss2737511731 | Nov 08, 2017 (151) |
| 14 | GNOMAD | ss2748157023 | Nov 08, 2017 (151) |
| 15 | GNOMAD | ss2875819904 | Nov 08, 2017 (151) |
| 16 | AFFY | ss2985456935 | Nov 08, 2017 (151) |
| 17 | ILLUMINA | ss3022911546 | Nov 08, 2017 (151) |
| 18 | ILLUMINA | ss3630222110 | Oct 12, 2018 (152) |
| 19 | ILLUMINA | ss3635204677 | Oct 12, 2018 (152) |
| 20 | ILLUMINA | ss3640911968 | Oct 12, 2018 (152) |
| 21 | ILLUMINA | ss3644987188 | Oct 12, 2018 (152) |
| 22 | ILLUMINA | ss3653462341 | Oct 12, 2018 (152) |
| 23 | ILLUMINA | ss3654220819 | Oct 12, 2018 (152) |
| 24 | ILLUMINA | ss3726596476 | Jul 13, 2019 (153) |
| 25 | ILLUMINA | ss3744586586 | Jul 13, 2019 (153) |
| 26 | ILLUMINA | ss3745504629 | Jul 13, 2019 (153) |
| 27 | EVA | ss3768959074 | Jul 13, 2019 (153) |
| 28 | PAGE_CC | ss3771488614 | Jul 13, 2019 (153) |
| 29 | ILLUMINA | ss3772996706 | Jul 13, 2019 (153) |
| 30 | EVA | ss3824417170 | Apr 26, 2020 (154) |
| 31 | KRGDB | ss3919242480 | Apr 26, 2020 (154) |
| 32 | TOPMED | ss4813827345 | Apr 26, 2021 (155) |
| 33 | 1000G_HIGH_COVERAGE | ss5279915934 | Oct 16, 2022 (156) |
| 34 | EVA | ss5316115487 | Oct 16, 2022 (156) |
| 35 | EVA | ss5386255308 | Oct 16, 2022 (156) |
| 36 | HUGCELL_USP | ss5476185888 | Oct 16, 2022 (156) |
| 37 | 1000G_HIGH_COVERAGE | ss5571748963 | Oct 16, 2022 (156) |
| 38 | EVA | ss5848199854 | Oct 16, 2022 (156) |
| 39 | EVA | ss5915664935 | Oct 16, 2022 (156) |
| 40 | EVA | ss5976250494 | Oct 16, 2022 (156) |
| 41 | 1000Genomes | NC_000009.11 - 14819439 | Oct 12, 2018 (152) |
| 42 | 1000Genomes_30x | NC_000009.12 - 14819441 | Oct 16, 2022 (156) |
| 43 | ExAC | NC_000009.11 - 14819439 | Oct 12, 2018 (152) |
| 44 | gnomAD - Genomes | NC_000009.12 - 14819441 | Apr 26, 2021 (155) |
| 45 | gnomAD - Exomes | NC_000009.11 - 14819439 | Jul 13, 2019 (153) |
| 46 | GO Exome Sequencing Project | NC_000009.11 - 14819439 | Oct 12, 2018 (152) |
| 47 | KOREAN population from KRGDB | NC_000009.11 - 14819439 | Apr 26, 2020 (154) |
| 48 | The PAGE Study | NC_000009.12 - 14819441 | Jul 13, 2019 (153) |
| 49 | TopMed | NC_000009.12 - 14819441 | Apr 26, 2021 (155) |
| 50 | ALFA | NC_000009.12 - 14819441 | Apr 26, 2021 (155) |
Help
History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).
Added to this RefSNP Cluster:
| Submission IDs | Observation SPDI | Canonical SPDI | Source RSIDs |
|---|---|---|---|
| 45274199, 9542534, 6690955, 874976, 26419874, ss488902487, ss491420594, ss712876384, ss780875260, ss783560708, ss1333042091, ss1689424613, ss1752768126, ss1917834700, ss1946253884, ss1959168241, ss2737511731, ss2748157023, ss2875819904, ss2985456935, ss3022911546, ss3630222110, ss3635204677, ss3640911968, ss3644987188, ss3653462341, ss3654220819, ss3744586586, ss3745504629, ss3768959074, ss3772996706, ss3824417170, ss3919242480, ss5316115487, ss5386255308, ss5848199854, ss5976250494 | NC_000009.11:14819438:G:A | NC_000009.12:14819440:G:A | (self) |
| 59274898, 319122415, 710083, 651204906, 10188406416, ss2309695719, ss3726596476, ss3771488614, ss4813827345, ss5279915934, ss5476185888, ss5571748963, ss5915664935 | NC_000009.12:14819440:G:A | NC_000009.12:14819440:G:A | (self) |
Help
Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.
No publications for rs199731115
Help
The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.
Genome context:
Select flank length:
Genomic regions, transcripts, and products
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Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.