Variant #0000850332 (NC_000003.11:g.43607241_43607242del, NC_000003.11(NM_018075.3):c.1219-7_1219-6del (ANO10))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.43607241_43607242del
DNA change (hg38) -
Published as ANO10(NM_001204831.3):c.1219-7_1219-6delTT
ISCN -
DB-ID ABHD5_000020 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +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.-125244_-125243del r.(?) p.(=)
ANO10 NM_018075.3 -/. - c.1219-7_1219-6del r.(=) p.(=)


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