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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.

rs758148747

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr12:65170722 (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 / G>T
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.000004 (1/251496, GnomAD_exome)
T=0.000007 (1/140236, GnomAD)
T=0.000008 (1/121408, ExAC) (+ 2 more)
A=0.00000 (0/14050, ALFA)
T=0.00000 (0/14050, ALFA)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
LEMD3 : Missense Variant
LOC124902953 : 2KB Upstream 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 30412 G=0.99997 A=0.00000, T=0.00003
European Sub 19780 G=0.99995 A=0.00000, T=0.00005
African Sub 7736 G=1.0000 A=0.0000, T=0.0000
African Others Sub 298 G=1.000 A=0.000, T=0.000
African American Sub 7438 G=1.0000 A=0.0000, T=0.0000
Asian Sub 112 G=1.000 A=0.000, T=0.000
East Asian Sub 86 G=1.00 A=0.00, T=0.00
Other Asian Sub 26 G=1.00 A=0.00, T=0.00
Latin American 1 Sub 146 G=1.000 A=0.000, T=0.000
Latin American 2 Sub 610 G=1.000 A=0.000, T=0.000
South Asian Sub 98 G=1.00 A=0.00, T=0.00
Other Sub 1930 G=1.0000 A=0.0000, T=0.0000


Help

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
gnomAD - Exomes Global Study-wide 251496 G=0.999996 A=0.000004
gnomAD - Exomes European Sub 135418 G=0.999993 A=0.000007
gnomAD - Exomes Asian Sub 49010 G=1.00000 A=0.00000
gnomAD - Exomes American Sub 34592 G=1.00000 A=0.00000
gnomAD - Exomes African Sub 16256 G=1.00000 A=0.00000
gnomAD - Exomes Ashkenazi Jewish Sub 10080 G=1.00000 A=0.00000
gnomAD - Exomes Other Sub 6140 G=1.0000 A=0.0000
gnomAD - Genomes Global Study-wide 140236 G=0.999993 T=0.000007
gnomAD - Genomes European Sub 75948 G=0.99999 T=0.00001
gnomAD - Genomes African Sub 42022 G=1.00000 T=0.00000
gnomAD - Genomes American Sub 13662 G=1.00000 T=0.00000
gnomAD - Genomes Ashkenazi Jewish Sub 3322 G=1.0000 T=0.0000
gnomAD - Genomes East Asian Sub 3132 G=1.0000 T=0.0000
gnomAD - Genomes Other Sub 2150 G=1.0000 T=0.0000
ExAC Global Study-wide 121408 G=0.999992 T=0.000008
ExAC Europe Sub 73350 G=1.00000 T=0.00000
ExAC Asian Sub 25166 G=0.99996 T=0.00004
ExAC American Sub 11578 G=1.00000 T=0.00000
ExAC African Sub 10406 G=1.00000 T=0.00000
ExAC Other Sub 908 G=1.000 T=0.000
Allele Frequency Aggregator Total Global 14050 G=1.00000 A=0.00000, T=0.00000
Allele Frequency Aggregator European Sub 9690 G=1.0000 A=0.0000, T=0.0000
Allele Frequency Aggregator African Sub 2898 G=1.0000 A=0.0000, T=0.0000
Allele Frequency Aggregator Latin American 2 Sub 610 G=1.000 A=0.000, T=0.000
Allele Frequency Aggregator Other Sub 496 G=1.000 A=0.000, T=0.000
Allele Frequency Aggregator Latin American 1 Sub 146 G=1.000 A=0.000, T=0.000
Allele Frequency Aggregator Asian Sub 112 G=1.000 A=0.000, T=0.000
Allele Frequency Aggregator South Asian Sub 98 G=1.00 A=0.00, T=0.00
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 12 NC_000012.12:g.65170722G>A
GRCh38.p14 chr 12 NC_000012.12:g.65170722G>T
GRCh37.p13 chr 12 NC_000012.11:g.65564502G>A
GRCh37.p13 chr 12 NC_000012.11:g.65564502G>T
LEMD3 RefSeqGene NG_016210.2:g.6152G>A
LEMD3 RefSeqGene NG_016210.2:g.6152G>T
Gene: LEMD3, LEM domain containing 3 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
LEMD3 transcript variant 1 NM_014319.5:c.1126G>A D [GAC] > N [AAC] Coding Sequence Variant
inner nuclear membrane protein Man1 isoform 1 NP_055134.2:p.Asp376Asn D (Asp) > N (Asn) Missense Variant
LEMD3 transcript variant 1 NM_014319.5:c.1126G>T D [GAC] > Y [TAC] Coding Sequence Variant
inner nuclear membrane protein Man1 isoform 1 NP_055134.2:p.Asp376Tyr D (Asp) > Y (Tyr) Missense Variant
LEMD3 transcript variant 2 NM_001167614.2:c.1126G>A D [GAC] > N [AAC] Coding Sequence Variant
inner nuclear membrane protein Man1 isoform 2 NP_001161086.1:p.Asp376Asn D (Asp) > N (Asn) Missense Variant
LEMD3 transcript variant 2 NM_001167614.2:c.1126G>T D [GAC] > Y [TAC] Coding Sequence Variant
inner nuclear membrane protein Man1 isoform 2 NP_001161086.1:p.Asp376Tyr D (Asp) > Y (Tyr) Missense Variant
Gene: LOC124902953, uncharacterized LOC124902953 (minus strand) : 2KB Upstream Variant
Molecule type Change Amino acid[Codon] SO Term
LOC124902953 transcript XR_007063349.1:n. N/A Upstream Transcript 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 T
GRCh38.p14 chr 12 NC_000012.12:g.65170722= NC_000012.12:g.65170722G>A NC_000012.12:g.65170722G>T
GRCh37.p13 chr 12 NC_000012.11:g.65564502= NC_000012.11:g.65564502G>A NC_000012.11:g.65564502G>T
LEMD3 RefSeqGene NG_016210.2:g.6152= NG_016210.2:g.6152G>A NG_016210.2:g.6152G>T
LEMD3 transcript variant 1 NM_014319.5:c.1126= NM_014319.5:c.1126G>A NM_014319.5:c.1126G>T
LEMD3 transcript variant 1 NM_014319.4:c.1126= NM_014319.4:c.1126G>A NM_014319.4:c.1126G>T
LEMD3 transcript variant 2 NM_001167614.2:c.1126= NM_001167614.2:c.1126G>A NM_001167614.2:c.1126G>T
LEMD3 transcript variant 2 NM_001167614.1:c.1126= NM_001167614.1:c.1126G>A NM_001167614.1:c.1126G>T
inner nuclear membrane protein Man1 isoform 1 NP_055134.2:p.Asp376= NP_055134.2:p.Asp376Asn NP_055134.2:p.Asp376Tyr
inner nuclear membrane protein Man1 isoform 2 NP_001161086.1:p.Asp376= NP_001161086.1:p.Asp376Asn NP_001161086.1:p.Asp376Tyr
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#.

7 SubSNP, 6 Frequency submissions
No Submitter Submission ID Date (Build)
1 EVA_EXAC ss1691001141 Apr 01, 2015 (144)
2 HUMAN_LONGEVITY ss2190549265 Dec 20, 2016 (150)
3 GNOMAD ss2739961061 Nov 08, 2017 (151)
4 GNOMAD ss2748909691 Nov 08, 2017 (151)
5 GNOMAD ss2911592400 Nov 08, 2017 (151)
6 TOPMED ss4921615672 Apr 26, 2021 (155)
7 TOPMED ss4921615673 Apr 26, 2021 (155)
8 ExAC NC_000012.11 - 65564502 Oct 12, 2018 (152)
9 gnomAD - Genomes NC_000012.12 - 65170722 Apr 26, 2021 (155)
10 gnomAD - Exomes NC_000012.11 - 65564502 Jul 13, 2019 (153)
11 TopMed

Submission ignored due to conflicting rows:
Row 137161329 (NC_000012.12:65170721:G:A 1/264690)
Row 137161330 (NC_000012.12:65170721:G:T 4/264690)

- Apr 26, 2021 (155)
12 TopMed

Submission ignored due to conflicting rows:
Row 137161329 (NC_000012.12:65170721:G:A 1/264690)
Row 137161330 (NC_000012.12:65170721:G:T 4/264690)

- Apr 26, 2021 (155)
13 ALFA NC_000012.12 - 65170722 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
9195798, ss2739961061 NC_000012.11:65564501:G:A NC_000012.12:65170721:G:A (self)
13607128018, ss4921615672 NC_000012.12:65170721:G:A NC_000012.12:65170721:G:A (self)
1305296, ss1691001141, ss2748909691, ss2911592400 NC_000012.11:65564501:G:T NC_000012.12:65170721:G:T (self)
410105877, 13607128018, ss2190549265, ss4921615673 NC_000012.12:65170721:G:T NC_000012.12:65170721:G:T (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 rs758148747

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
Top 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.

Software version is: 2.0.1.post761+d5e8e07