Variant #0000307927 (NC_000016.9:g.30992058_30992059del, NC_000016.9(NM_014712.1):c.4582-2_4582-1del (SETD1A))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.30992058_30992059del
DNA change (hg38) g.30980737_30980738del
Published as SETD1A(NM_014712.1):c.4582-2_4582-1delAG (p.?), SETD1A(NM_014712.2):c.4582-2_4582-1delAG
ISCN -
DB-ID SETD1A_000006 See all 12 reported entries
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HSD3B7 NM_001142777.1 +?/. - c.-4760_-4759del r.(?) p.(=)
SETD1A NM_014712.1 +?/. - c.4582-2_4582-1del r.spl? p.?
HSD3B7 NM_025193.3 +?/. - c.-4567_-4566del r.(?) p.(=)


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