Variant #0000315798 (NC_000012.11:g.57502001C>T, NM_005967.3:c.*13497C>T (NAB2))

Chromosome 12
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.57502001C>T
DNA change (hg38) g.57108218C>T
Published as STAT6(NM_001178078.1):c.61G>A (p.D21N), STAT6(NM_003153.5):c.61G>A (p.D21N)
ISCN -
DB-ID STAT6_000005 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STAT6 NM_003153.4 ?/. - c.61G>A r.(?) p.(Asp21Asn)
NAB2 NM_005967.3 ?/. - c.*13497C>T r.(=) p.(=)


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