Variant #0000656288 (NC_000009.11:g.139265514G>A, NM_003086.2:c.*4746C>T (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.139265514G>A
DNA change (hg38) g.136371062G>A
Published as CARD9(NM_052813.4):c.406C>T (p.L136=)
ISCN -
DB-ID CARD9_000028
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) 0.00043 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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-06-26 11:50:29 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SNAPC4 NM_003086.2 -?/. - c.*4746C>T r.(=) p.(=)
CARD9 NM_052813.4 -?/. - c.406C>T r.(?) p.(Leu136=)


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