Variant #0001002279 (NC_000016.9:g.30991230_30991232del, NM_014712.1:c.4123_4125del (SETD1A))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.30991230_30991232del
DNA change (hg38) -
Published as SETD1A(NM_014712.1):c.4123_4125delGAG (p.(Glu1375del))
ISCN -
DB-ID HSD3B7_000035
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 2024-08-28 13:16:32 +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     
HSD3B7 NM_001142777.1 ?/. - c.-5588_-5586del r.(?) p.(=)
SETD1A NM_014712.1 ?/. - c.4123_4125del r.(?) p.(Glu1375del)
HSD3B7 NM_025193.3 ?/. - c.-5395_-5393del r.(?) p.(=)


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