Variant #0000519841 (NC_000003.11:g.43591299G>A, NM_018075.3:c.1710C>T (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.43591299G>A
DNA change (hg38) g.43549807G>A
Published as ANO10(NM_001204831.2):c.1710C>T (p.N570=)
ISCN -
DB-ID ABHD5_000006
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) 8.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-02-08 18:36:18 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABHD5 NM_016006.4 -?/. - c.-141186G>A r.(?) p.(=)
ANO10 NM_018075.3 -?/. - c.1710C>T r.(?) p.(Asn570=)


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