Variant #0000266482 (NC_000009.11:g.139265024_139265026del, NM_003086.2:c.*5236_*5238del (SNAPC4))

Chromosome 9
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.139265024_139265026del
DNA change (hg38) g.136370572_136370574del
Published as CARD9(NM_052813.5):c.757_759delGAG (p.E253del)
ISCN -
DB-ID CARD9_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) 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.*5236_*5238del r.(=) p.(=)
CARD9 NM_052813.4 ?/. - c.757_759del r.(?) p.(Glu253del)


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