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dbSNP Short Genetic Variations

Reference SNP (rs) Report

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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.

rs587779018

Current Build 151

Released July 17, 2018

Organism
Homo sapiens
Position
chr3:37008855-37008857 (GRCh38.p7) 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
delT
Variation Type
Indel Insertion and Deletion
Frequency
None
Clinical Significance
Reported in ClinVar
Gene : Consequence
MLH1 : Stop Gained
Publications
0 citations
Genomic View
See rs on genome
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.p7 chr 3 NC_000003.12:g.37008857delT
GRCh37.p13 chr 3 NC_000003.11:g.37050348delT
MLH1 RefSeqGene (LRG_216) NG_007109.2:g.20508delT
Gene: MLH1, mutL homolog 1 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
MLH1 transcript variant 4 NM_001167619.1:c. N/A Intron Variant
MLH1 transcript variant 3 NM_001167618.1:c. N/A 5 Prime UTR Variant
MLH1 transcript variant 6 NM_001258273.1:c. N/A 5 Prime UTR Variant
MLH1 transcript variant 7 NM_001258274.1:c. N/A 5 Prime UTR Variant
MLH1 transcript variant 1 NM_000249.3:c.497...

NM_000249.3:c.497delT

L [TTA] > * [TA] Coding Sequence Variant
DNA mismatch repair protein Mlh1 isoform 1 NP_000240.1:p.Ala...

NP_000240.1:p.Ala165_Leu166insTer

L (Leu) > * (Ter) Stop Gained
MLH1 transcript variant 2 NM_001167617.1:c....

NM_001167617.1:c.203delT

L [TTA] > * [TA] Coding Sequence Variant
DNA mismatch repair protein Mlh1 isoform 2 NP_001161089.1:p....

NP_001161089.1:p.Ala67_Leu68insTer

L (Leu) > * (Ter) Stop Gained
MLH1 transcript variant 5 NM_001258271.1:c....

NM_001258271.1:c.497delT

L [TTA] > * [TA] Coding Sequence Variant
DNA mismatch repair protein Mlh1 isoform 4 NP_001245200.1:p....

NP_001245200.1:p.Ala165_Leu166insTer

L (Leu) > * (Ter) Stop Gained
MLH1 transcript variant X2 XM_005265163.1:c. N/A 5 Prime UTR Variant
MLH1 transcript variant X3 XM_005265164.1:c. N/A 5 Prime UTR Variant
MLH1 transcript variant X4 XM_005265166.1:c. N/A 5 Prime UTR Variant
MLH1 transcript variant X7 XM_011533727.1:c. N/A 5 Prime UTR Variant
MLH1 transcript variant X5 XM_017006449.1:c. N/A 5 Prime UTR Variant
MLH1 transcript variant X6 XM_017006450.1:c. N/A 5 Prime UTR Variant
MLH1 transcript variant X8 XM_017006451.1:c. N/A 5 Prime UTR Variant
MLH1 transcript variant X1 XM_005265161.1:c....

XM_005265161.1:c.497delT

L [TTA] > * [TA] Coding Sequence Variant
DNA mismatch repair protein Mlh1 isoform X1 XP_005265218.1:p....

XP_005265218.1:p.Ala165_Leu166insTer

L (Leu) > * (Ter) Stop Gained
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.

Allele: delT (allele ID: 95721 )
ClinVar Accession Disease Names Clinical Significance
RCV000075736.2 Lynch syndrome Pathogenic
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").

None
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 TTT= delT Note
GRCh38.p7 chr 3 NC_000003.12:g.37008855...

NC_000003.12:g.37008855_37008857TTT=

NC_000003.12:g.37008857...

NC_000003.12:g.37008857delT

GRCh37.p13 chr 3 NC_000003.11:g.37050346...

NC_000003.11:g.37050346_37050348TTT=

NC_000003.11:g.37050348...

NC_000003.11:g.37050348delT

MLH1 RefSeqGene (LRG_216) NG_007109.2:g.20506_205...

NG_007109.2:g.20506_20508TTT=

NG_007109.2:g.20508delT
MLH1 transcript variant 1 NM_000249.3:c.495_497TTT= NM_000249.3:c.497delT
MLH1 transcript variant 6 NM_001258273.1:c.-229_-...

NM_001258273.1:c.-229_-227TTT=

NM_001258273.1:c.-227delT
MLH1 transcript variant 5 NM_001258271.1:c.495_49...

NM_001258271.1:c.495_497TTT=

NM_001258271.1:c.497delT
MLH1 transcript variant 7 NM_001258274.1:c.-229_-...

NM_001258274.1:c.-229_-227TTT=

NM_001258274.1:c.-227delT
MLH1 transcript variant X3 XM_005265164.1:c.-229_-...

XM_005265164.1:c.-229_-227TTT=

XM_005265164.1:c.-227delT
MLH1 transcript variant X2 XM_005265163.1:c.-229_-...

XM_005265163.1:c.-229_-227TTT=

XM_005265163.1:c.-227delT
MLH1 transcript variant 3 NM_001167618.1:c.-229_-...

NM_001167618.1:c.-229_-227TTT=

NM_001167618.1:c.-227delT
MLH1 transcript variant 2 NM_001167617.1:c.201_20...

NM_001167617.1:c.201_203TTT=

NM_001167617.1:c.203delT
MLH1 transcript variant X4 XM_005265166.1:c.-435_-...

XM_005265166.1:c.-435_-433TTT=

XM_005265166.1:c.-433delT
MLH1 transcript variant X1 XM_005265161.1:c.495_49...

XM_005265161.1:c.495_497TTT=

XM_005265161.1:c.497delT
MLH1 transcript variant X6 XM_017006450.1:c.-322_-...

XM_017006450.1:c.-322_-320TTT=

XM_017006450.1:c.-320delT
MLH1 transcript variant X8 XM_017006451.1:c.-332_-...

XM_017006451.1:c.-332_-330TTT=

XM_017006451.1:c.-330delT
MLH1 transcript variant X5 XM_017006449.1:c.-322_-...

XM_017006449.1:c.-322_-320TTT=

XM_017006449.1:c.-320delT
MLH1 transcript variant X7 XM_011533727.1:c.-332_-...

XM_011533727.1:c.-332_-330TTT=

XM_011533727.1:c.-330delT
DNA mismatch repair protein Mlh1 isoform 1 NP_000240.1:p.Ala165_Le...

NP_000240.1:p.Ala165_Leu166=

NP_000240.1:p.Ala165_Le...

NP_000240.1:p.Ala165_Leu166insTer

DNA mismatch repair protein Mlh1 isoform 4 NP_001245200.1:p.Ala165...

NP_001245200.1:p.Ala165_Leu166=

NP_001245200.1:p.Ala165...

NP_001245200.1:p.Ala165_Leu166insTer

DNA mismatch repair protein Mlh1 isoform 2 NP_001161089.1:p.Ala67_...

NP_001161089.1:p.Ala67_Leu68=

NP_001161089.1:p.Ala67_...

NP_001161089.1:p.Ala67_Leu68insTer

DNA mismatch repair protein Mlh1 isoform X1 XP_005265218.1:p.Ala165...

XP_005265218.1:p.Ala165_Leu166=

XP_005265218.1:p.Ala165...

XP_005265218.1:p.Ala165_Leu166insTer

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#.

1 SubSNP, 1 ClinVar submissions
No Submitter Submission ID Date (Build)
1 CLINVAR ss1457611325 Nov 23, 2014 (142)
2 ClinVar RCV000075736.2 Jul 19, 2018 (151)
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
RCV000075736.2, ss1457611325 NC_000003.12:37008856:delT NC_000003.12:37008854:delT (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 rs587779018

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: 0.1.4.post833+d3ba21e