Variant #0000263540 (NC_000003.11:g.52439240T>C, NM_015512.4:c.*4778T>C (DNAH1))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.52439240T>C
DNA change (hg38) g.52405224T>C
Published as BAP1(NM_004656.2):c.1002A>G (p.L334=), BAP1(NM_004656.3):c.1002A>G (p.(Leu334=)), BAP1(NM_004656.4):c.1002A>G (p.L334=)
ISCN -
DB-ID BAP1_000011 See all 4 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) 0.00593 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BAP1 NM_004656.2 -/. - c.1002A>G r.(?) p.(Leu334=)
DNAH1 NM_015512.4 -/. - c.*4778T>C r.(=) p.(=)


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