Variant #0000863077 (NC_000012.11:g.57500533C>T, NM_005967.3:c.*12029C>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.57500533C>T
DNA change (hg38) -
Published as STAT6(NM_001178078.2):c.421G>A (p.V141I)
ISCN -
DB-ID NAB2_000013
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) 0.00013 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STAT6 NM_003153.4 ?/. - c.421G>A r.(?) p.(Val141Ile)
NAB2 NM_005967.3 ?/. - c.*12029C>T r.(=) p.(=)


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