Variant #0000657821 (NC_000016.9:g.30731656C>T, NC_000016.9(NM_006662.2):c.2987+4C>T (SRCAP))

Chromosome 16
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.30731656C>T
DNA change (hg38) g.30720335C>T
Published as SRCAP(NM_006662.2):c.2987+4C>T (p.?)
ISCN -
DB-ID SRCAP_000115
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) 2.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-07-09 15:27:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SRCAP NM_006662.2 -?/. - c.2987+4C>T r.spl? p.?


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