Variant #0000557938 (NC_000016.9:g.31004504G>A, NM_014712.1:c.*9160G>A (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.31004504G>A
DNA change (hg38) g.30993183G>A
Published as -
ISCN -
DB-ID HSD3B7_000011
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 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.*5356G>A r.(=) p.(=)
SETD1A NM_014712.1 +?/. - c.*9160G>A r.(=) p.(=)
HSD3B7 NM_025193.3 +?/. - c.*5000G>A r.(=) p.(=)
STX1B NM_052874.3 +?/. - c.733C>T r.(?) p.(Arg245Ter)


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