Variant #0000853468 (NC_000012.11:g.57493095A>G, NM_005967.3:c.*4591A>G (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.57493095A>G
DNA change (hg38) -
Published as STAT6(NM_003153.5):c.1873T>C (p.F625L)
ISCN -
DB-ID NAB2_000012
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-05-09 15:40:45 +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.1873T>C r.(?) p.(Phe625Leu)
NAB2 NM_005967.3 ?/. - c.*4591A>G r.(=) p.(=)


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