ClinVar

NM_005633.4(SOS1):c.3763C>A (p.Pro1255Thr)

Gene:

SOS1:SOS Ras/Rac guanine nucleotide exchange factor 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

2p22.1

Genomic location:

• Chr2: 38986063 (on Assembly GRCh38)
• Chr2: 39213204 (on Assembly GRCh37)

Preferred name:

NM_005633.4(SOS1):c.3763C>A (p.Pro1255Thr)

HGVS:

• NC_000002.12:g.38986063G>T
• NG_007530.1:g.139401C>A
• NM_001382394.1:c.3742C>A
• NM_001382395.1:c.3718C>A
• NM_005633.4:c.3763C>AMANE SELECT
• NP_001369323.1:p.Pro1248Thr
• NP_001369324.1:p.Pro1240Thr
• NP_005624.2:p.Pro1255Thr
• NP_005624.2:p.Pro1255Thr
• LRG_754t1:c.3763C>A
• LRG_754:g.139401C>A
• LRG_754p1:p.Pro1255Thr
• NC_000002.11:g.39213204G>T
• NM_005633.3:c.3763C>A

This HGVS expression did not pass validation

Protein change:

P1240T

Links:

dbSNP: rs972166211

NCBI 1000 Genomes Browser:

rs972166211

Molecular consequence:

• NM_001382394.1:c.3742C>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001382395.1:c.3718C>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_005633.4:c.3763C>A - missense variant - [Sequence Ontology: SO:0001583]