Variant #0000262532 (NC_000003.11:g.43621970C>T, NC_000003.11(NM_018075.3):c.473-6G>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.43621970C>T
DNA change (hg38) g.43580478C>T
Published as ANO10(NM_001204831.2):c.473-6G>A
ISCN -
DB-ID ANO10_000024
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) 0.00016 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 2020-03-23 16:13:27 +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.-110515C>T r.(?) p.(=)
ANO10 NM_018075.3 -?/. - c.473-6G>A r.(=) p.(=)


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