Variant #0000307926 (NC_000016.9:g.30977133_30977134del, NM_014712.1:c.1931_1932del (SETD1A))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.30977133_30977134del
DNA change (hg38) g.30965812_30965813del
Published as SETD1A(NM_014712.2):c.1931_1932delCT (p.P644Rfs*14)
ISCN -
DB-ID SETD1A_000003
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 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-09 15:33:40 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SETD1A NM_014712.1 +?/. - c.1931_1932del r.(?) p.(Pro644ArgfsTer14)


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