Variant #0000930591 (NC_000016.9:g.30748664C>T, NM_006662.2:c.7303C>T (SRCAP))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.30748664C>T
DNA change (hg38) -
Published as SRCAP(NM_006662.2):c.7303C>T (p.R2435*), SRCAP(NM_006662.3):c.7303C>T (p.R2435*)
ISCN -
DB-ID SRCAP_000002 See all 28 reported entries
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2023-07-07 10:10:56 +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     
SRCAP NM_006662.2 +/. - c.7303C>T r.(?) p.(Arg2435Ter)


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