Variant #0000557935 (NC_000016.9:g.30997778C>T, NM_014712.1:c.*2434C>T (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.30997778C>T
DNA change (hg38) g.30986457C>T
Published as HSD3B7(NM_001142777.1):c.357C>T (p.T119=), HSD3B7(NM_001142777.2):c.357C>T (p.T119=)
ISCN -
DB-ID HSD3B7_000010 See all 2 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) 0.00261 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 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.357C>T r.(?) p.(Thr119=)
SETD1A NM_014712.1 -?/. - c.*2434C>T r.(=) p.(=)
HSD3B7 NM_025193.3 -?/. - c.357C>T r.(?) p.(Thr119=)
STX1B NM_052874.3 -?/. - c.*6364G>A r.(=) p.(=)


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