Variant #0000926262 (NC_000016.9:g.30992133del, NM_014712.1:c.4655del (SETD1A))

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.30992133del
DNA change (hg38) -
Published as -
ISCN -
DB-ID HSD3B7_000028
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HSD3B7 NM_001142777.1 +/. - c.-4685del r.(?) p.(=)
SETD1A NM_014712.1 +/. - c.4655del r.(?) p.(Ile1552Thrfs*7)
HSD3B7 NM_025193.3 +/. - c.-4492del r.(?) p.(=)


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