Variant #0000999767 (NC_000012.11:g.122247951C>T, NM_015048.1:c.1100C>T (SETD1B))

Chromosome 12
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.122247951C>T
DNA change (hg38) -
Published as SETD1B(NM_001353345.2):c.1100C>T (p.P367L), SETD1B(NM_015048.1):c.1100C>T (p.(Pro367Leu))
ISCN -
DB-ID SETD1B_000019 See all 6 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) 0.00374 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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     
SETD1B NM_015048.1 -?/. - c.1100C>T r.(?) p.(Pro367Leu)


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