Variant #0000537160 (NC_000009.11:g.139272339G>A, NM_003086.2:c.3940C>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.139272339G>A
DNA change (hg38) g.136377887G>A
Published as SNAPC4(NM_003086.3):c.3940C>T (p.L1314=)
ISCN -
DB-ID CARD9_000024
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) 0.00063 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-26 11:51:29 +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.3940C>T r.(?) p.(Leu1314=)
CARD9 NM_052813.4 -?/. - c.-4372C>T r.(?) p.(=)


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