Variant #0000808971 (NC_000019.9:g.48741730C>T, NM_001184900.1:c.119G>A (CARD8))

Chromosome 19
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.48741730C>T
DNA change (hg38) -
Published as CARD8(NM_001351782.1):c.119G>A (p.R40Q)
ISCN -
DB-ID CARD8_000005
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) 0.00022 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 2021-09-17 14:40:49 +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     
CARD8 NM_001184900.1 ?/. - c.119G>A r.(?) p.(Arg40Gln)
CARD8 NM_014959.3 ?/. - c.59+2489G>A r.(=) p.(=)


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