ClinVar

NM_024426.6(WT1):c.391C>T (p.Pro131Ser)

Genes:

WT1:WT1 transcription factor [Gene - OMIM - HGNC]
LOC107982234:WT1/WT1-AS bi-directional promoter region [Gene]

Variant type:

single nucleotide variant

Cytogenetic location:

11p13

Genomic location:

• Chr11: 32434970 (on Assembly GRCh38)
• Chr11: 32456516 (on Assembly GRCh37)

Preferred name:

NM_024426.6(WT1):c.391C>T (p.Pro131Ser)

HGVS:

• NC_000011.10:g.32434970G>A
• NG_009272.1:g.5572C>T
• NG_050766.1:g.4223G>A
• NM_000378.6:c.391C>T
• NM_024424.5:c.391C>T
• NM_024426.6:c.391C>TMANE SELECT
• NP_000369.4:p.Pro131Ser
• NP_077742.3:p.Pro131Ser
• NP_077744.4:p.Pro131Ser
• LRG_525:g.5572C>T
• NC_000011.9:g.32456516G>A
• NR_160306.1:n.570C>T

This HGVS expression did not pass validation

Protein change:

P131S

Links:

dbSNP: rs564706633

NCBI 1000 Genomes Browser:

rs564706633

Molecular consequence:

• NM_000378.6:c.391C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_024424.5:c.391C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_024426.6:c.391C>T - missense variant - [Sequence Ontology: SO:0001583]
• NR_160306.1:n.570C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]