Variant #0000931511 (NC_000016.9:g.30990813C>T, NM_014712.1:c.3706C>T (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.30990813C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID SETD1A_000046 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs903350409
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-07-20 09:18:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SETD1A NM_014712.1 +?/. - c.3706C>T r.(?) p.(Arg1236Ter)


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