Variant #0000615954 (NC_000016.9:g.30991513C>T, NM_014712.1:c.4406C>T (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.30991513C>T
DNA change (hg38) g.30980192C>T
Published as SETD1A(NM_014712.2):c.4406C>T (p.T1469I)
ISCN -
DB-ID HSD3B7_000013
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
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.-5305C>T r.(?) p.(=)
SETD1A NM_014712.1 ?/. - c.4406C>T r.(?) p.(Thr1469Ile)
HSD3B7 NM_025193.3 ?/. - c.-5112C>T r.(?) p.(=)


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