Variant #0000272625 (NC_000009.11:g.139266522G>T, NM_003086.2:c.*3738C>A (SNAPC4))

Chromosome 9
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.139266522G>T
DNA change (hg38) g.136372070G>T
Published as CARD9(NM_052813.4):c.9C>A (p.D3E)
ISCN -
DB-ID CARD9_000016
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_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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SNAPC4 NM_003086.2 -?/. - c.*3738C>A r.(=) p.(=)
CARD9 NM_052813.4 -?/. - c.9C>A r.(?) p.(Asp3Glu)


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