ClinVar

NM_024426.6(WT1):c.1568G>A (p.Ter523=)

Gene:

WT1:WT1 transcription factor [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11p13

Genomic location:

• Chr11: 32389059 (on Assembly GRCh38)
• Chr11: 32410605 (on Assembly GRCh37)

Preferred name:

NM_024426.6(WT1):c.1568G>A (p.Ter523=)

HGVS:

• NC_000011.10:g.32389059C>T
• NG_009272.1:g.51483G>A
• NM_000378.6:c.1508G>A
• NM_001198551.2:c.908G>A
• NM_001198552.2:c.866G>A
• NM_001367854.1:c.380G>A
• NM_001407044.1:c.1553G>A
• NM_001407045.1:c.1517G>A
• NM_001407046.1:c.1475G>A
• NM_001407047.1:c.1436G>A
• NM_001407048.1:c.1427G>A
• NM_001407049.1:c.1424G>A
• NM_001407050.1:c.1394G>A
• NM_001407051.1:c.806G>A
• NM_024424.5:c.1559G>A
• NM_024425.2:c.1502G>A
• NM_024426.6:c.1568G>AMANE SELECT
• NP_000369.4:p.Ter503=
• NP_001185480.1:p.Ter303=
• NP_001185480.1:p.Ter303=
• NP_001185481.1:p.Ter289=
• NP_001354783.1:p.Ter127=
• NP_001393973.1:p.Ter518=
• NP_001393974.1:p.Ter506=
• NP_001393975.1:p.Ter492=
• NP_001393976.1:p.Ter479=
• NP_001393977.1:p.Ter476=
• NP_001393978.1:p.Ter475=
• NP_001393979.1:p.Ter465=
• NP_001393980.1:p.Ter269=
• NP_077742.3:p.Ter520=
• NP_077743.2:p.Ter501=
• NP_077744.3:p.Ter518=
• NP_077744.4:p.Ter523=
• LRG_525t1:c.1553G>A
• LRG_525t2:c.908G>A
• LRG_525:g.51483G>A
• LRG_525p1:p.Ter518=
• LRG_525p2:p.Ter303=
• NC_000011.9:g.32410605C>T
• NM_001198551.1:c.908G>A
• NM_024426.3:c.1553G>A
• NM_024426.4:c.1553G>A
• NR_160306.1:n.1900G>A
• NR_176266.1:n.1840G>A

This HGVS expression did not pass validation

Links:

dbSNP: rs148856160

NCBI 1000 Genomes Browser:

rs148856160

Molecular consequence:

• NR_160306.1:n.1900G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
• NM_000378.6:c.1508G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001198551.2:c.908G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001198552.2:c.866G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001367854.1:c.380G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001407044.1:c.1553G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001407045.1:c.1517G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001407046.1:c.1475G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001407047.1:c.1436G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001407048.1:c.1427G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001407049.1:c.1424G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001407050.1:c.1394G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001407051.1:c.806G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_024424.5:c.1559G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_024425.2:c.1502G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_024426.6:c.1568G>A - synonymous variant - [Sequence Ontology: SO:0001819]