Variant #0000557932 (NC_000016.9:g.30992438dup, NM_014712.1:c.4749dup (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.30992438dup
DNA change (hg38) g.30981117dup
Published as SETD1A(NM_014712.1):c.4749dup (p.(Ala1584CysfsTer8))
ISCN -
DB-ID HSD3B7_000007
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HSD3B7 NM_001142777.1 ?/. - c.-4380dup r.(?) p.(=)
SETD1A NM_014712.1 ?/. - c.4749dup r.(?) p.(Ala1584CysfsTer8)
HSD3B7 NM_025193.3 ?/. - c.-4187dup r.(?) p.(=)


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