ClinVar

NM_024426.6(WT1):c.54G>A (p.Ala18=)

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: 32435307 (on Assembly GRCh38)
• Chr11: 32456853 (on Assembly GRCh37)

Preferred name:

NM_024426.6(WT1):c.54G>A (p.Ala18=)

HGVS:

• NC_000011.10:g.32435307C>T
• NG_009272.1:g.5235G>A
• NG_050766.1:g.4560C>T
• NM_000378.6:c.54G>A
• NM_024424.5:c.54G>A
• NM_024426.6:c.54G>AMANE SELECT
• NP_000369.4:p.Ala18=
• NP_077742.3:p.Ala18=
• NP_077744.4:p.Ala18=
• LRG_525:g.5235G>A
• NC_000011.9:g.32456853C>T
• NM_024426.4:c.39G>A
• NR_160306.1:n.233G>A

This HGVS expression did not pass validation

Links:

dbSNP: rs1409626312

NCBI 1000 Genomes Browser:

rs1409626312

Molecular consequence:

• NR_160306.1:n.233G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
• NM_000378.6:c.54G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_024424.5:c.54G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_024426.6:c.54G>A - synonymous variant - [Sequence Ontology: SO:0001819]

Observations:

1