Variant #0001055557 (NC_000016.9:g.30991254_30991256del, NM_014712.1:c.4147_4149del (SETD1A))

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.30991254_30991256del
DNA change (hg38) -
Published as SETD1A(NM_014712.3):c.4147_4149del (p.(Ser1383del))
ISCN -
DB-ID HSD3B7_000044
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HSD3B7 NM_001142777.1 -?/. - c.-5564_-5562del r.(?) p.(=)
SETD1A NM_014712.1 -?/. - c.4147_4149del r.(?) p.(Ser1383del)
HSD3B7 NM_025193.3 -?/. - c.-5371_-5369del r.(?) p.(=)


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