ClinVar

NM_024426.6(WT1):c.27G>A (p.Pro9=)

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: 32435334 (on Assembly GRCh38)
• Chr11: 32456880 (on Assembly GRCh37)

Preferred name:

NM_024426.6(WT1):c.27G>A (p.Pro9=)

HGVS:

• NC_000011.10:g.32435334C>T
• NG_009272.1:g.5208G>A
• NG_050766.1:g.4587C>T
• NM_000378.6:c.27G>A
• NM_024424.5:c.27G>A
• NM_024426.6:c.27G>AMANE SELECT
• NP_000369.4:p.Pro9=
• NP_077742.3:p.Pro9=
• NP_077744.4:p.Pro9=
• LRG_525t1:c.12G>A
• LRG_525:g.5208G>A
• NC_000011.9:g.32456880C>T
• NM_024426.3:c.12G>A
• NM_024426.4:c.12G>A
• NR_160306.1:n.206G>A

This HGVS expression did not pass validation

Links:

dbSNP: rs556835183

NCBI 1000 Genomes Browser:

rs556835183

Molecular consequence:

• NR_160306.1:n.206G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
• NM_000378.6:c.27G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_024424.5:c.27G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_024426.6:c.27G>A - synonymous variant - [Sequence Ontology: SO:0001819]