Variant #0000262529 (NC_000003.11:g.43591326C>G, NM_018075.3:c.1683G>C (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.43591326C>G
DNA change (hg38) g.43549834C>G
Published as ANO10(NM_018075.4):c.1683G>C (p.T561=)
ISCN -
DB-ID ANO10_000005
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) 0.0034 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 2020-06-12 18:39:48 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABHD5 NM_016006.4 -?/. - c.-141159C>G r.(?) p.(=)
ANO10 NM_018075.3 -?/. - c.1683G>C r.(?) p.(Thr561=)


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