ClinVar

NM_000179.3(MSH6):c.2701C>T (p.Arg901Cys)

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

2p16.3

Genomic location:

• Chr2: 47800684 (on Assembly GRCh38)
• Chr2: 48027823 (on Assembly GRCh37)

Preferred name:

NM_000179.3(MSH6):c.2701C>T (p.Arg901Cys)

HGVS:

• NC_000002.12:g.47800684C>T
• NG_007111.1:g.22538C>T
• NM_000179.3:c.2701C>TMANE SELECT
• NM_001281492.2:c.2311C>T
• NM_001281493.2:c.1795C>T
• NM_001281494.2:c.1795C>T
• NP_000170.1:p.Arg901Cys
• NP_000170.1:p.Arg901Cys
• NP_001268421.1:p.Arg771Cys
• NP_001268422.1:p.Arg599Cys
• NP_001268423.1:p.Arg599Cys
• LRG_219t1:c.2701C>T
• LRG_219:g.22538C>T
• LRG_219p1:p.Arg901Cys
• NC_000002.11:g.48027823C>T
• NM_000179.2:c.2701C>T
• p.R901C

This HGVS expression did not pass validation

Protein change:

R599C

Links:

dbSNP: rs772514245

NCBI 1000 Genomes Browser:

rs772514245

Molecular consequence:

• NM_000179.3:c.2701C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001281492.2:c.2311C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001281493.2:c.1795C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001281494.2:c.1795C>T - missense variant - [Sequence Ontology: SO:0001583]