Variant #0000519839 (NC_000003.11:g.43474153T>C, NM_018075.3:c.1864A>G (ANO10))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.43474153T>C
DNA change (hg38) g.43432661T>C
Published as ANO10(NM_018075.4):c.1864A>G (p.M622V)
ISCN -
DB-ID ABHD5_000005 See all 2 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) 0.00018 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.-258332T>C r.(?) p.(=)
ANO10 NM_018075.3 +?/. - c.1864A>G r.(?) p.(Met622Val)


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