Variant #0000615953 (NC_000016.9:g.30991254_30991256dup, NM_014712.1:c.4147_4149dup (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_30991256dup
DNA change (hg38) g.30979933_30979935dup
Published as SETD1A(NM_014712.3):c.4147_4149dupAGC (p.S1383dup)
ISCN -
DB-ID SETD1A_000005
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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.-5564_-5562dup r.(?) p.(=)
SETD1A NM_014712.1 -?/. - c.4147_4149dup r.(?) p.(Ser1383dup)
HSD3B7 NM_025193.3 -?/. - c.-5371_-5369dup r.(?) p.(=)


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