Variant #0000885841 (NC_000003.11:g.43618213C>T, NM_018075.3:c.1133G>A (ANO10))

Chromosome 3
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.43618213C>T
DNA change (hg38) -
Published as ANO10(NM_018075.5):c.1133G>A (p.R378Q)
ISCN -
DB-ID ABHD5_000022
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) 0.00067 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABHD5 NM_016006.4 -?/. - c.-114272C>T r.(?) p.(=)
ANO10 NM_018075.3 -?/. - c.1133G>A r.(?) p.(Arg378Gln)


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