ClinVar

NM_000179.3(MSH6):c.182C>T (p.Ala61Val)

Gene:

MSH6:mutS homolog 6 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

2p16.3

Genomic location:

• Chr2: 47783415 (on Assembly GRCh38)
• Chr2: 48010554 (on Assembly GRCh37)

Preferred name:

NM_000179.3(MSH6):c.182C>T (p.Ala61Val)

HGVS:

• NC_000002.12:g.47783415C>T
• NG_007111.1:g.5269C>T
• NM_000179.3:c.182C>TMANE SELECT
• NM_001281492.2:c.182C>T
• NM_001281493.2:c.-555C>T
• NP_000170.1:p.Ala61Val
• NP_000170.1:p.Ala61Val
• NP_001268421.1:p.Ala61Val
• LRG_219t1:c.182C>T
• LRG_219:g.5269C>T
• LRG_219p1:p.Ala61Val
• NC_000002.11:g.48010554C>T
• NM_000179.2:c.182C>T

This HGVS expression did not pass validation

Protein change:

A61V

Links:

dbSNP: rs572336612

NCBI 1000 Genomes Browser:

rs572336612

Molecular consequence:

• NM_001281493.2:c.-555C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_000179.3:c.182C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001281492.2:c.182C>T - missense variant - [Sequence Ontology: SO:0001583]