Variant #0000925666 (NC_000012.11:g.57496699C>T, NM_005967.3:c.*8195C>T (NAB2))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.57496699C>T
DNA change (hg38) -
Published as STAT6(NM_003153.5):c.1218G>A (p.L406=)
ISCN -
DB-ID NAB2_000015
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) 0.00028 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STAT6 NM_003153.4 -?/. - c.1218G>A r.(?) p.(Leu406=)
NAB2 NM_005967.3 -?/. - c.*8195C>T r.(=) p.(=)


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