ClinVar

NM_024426.6(WT1):c.-110C>T

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: 32435470 (on Assembly GRCh38)
• Chr11: 32457016 (on Assembly GRCh37)

Preferred name:

NM_024426.6(WT1):c.-110C>T

HGVS:

• NC_000011.10:g.32435470G>A
• NG_009272.1:g.5072C>T
• NG_050766.1:g.4723G>A
• NM_000378.6:c.-110C>T
• NM_024424.5:c.-110C>T
• NM_024426.6:c.-110C>TMANE SELECT
• LRG_525:g.5072C>T
• NC_000011.9:g.32457016G>A
• NM_024426.4:c.-125C>T
• NR_160306.1:n.70C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs886048241

NCBI 1000 Genomes Browser:

rs886048241

Molecular consequence:

• NM_000378.6:c.-110C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_024424.5:c.-110C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_024426.6:c.-110C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NR_160306.1:n.70C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Observations:

1