Variant #0000853292 (NC_000012.11:g.122702861G>A, NM_019887.5:c.267C>T (DIABLO))

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.122702861G>A
DNA change (hg38) -
Published as DIABLO(NM_001278304.1):c.108C>T (p.L36=)
ISCN -
DB-ID DIABLO_000004
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 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DIABLO NM_001371333.1 -?/. - c.267C>T r.(?) p.(Leu89=)
DIABLO NM_019887.5 -?/. - c.267C>T r.(?) p.(Leu89=)


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