Variant #0000543526 (NC_000011.9:g.22294441C>G, NM_213599.2:c.2141C>G (ANO5))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.22294441C>G
DNA change (hg38) g.22272895C>G
Published as ANO5(NM_001142649.1):c.2138C>G (p.(Thr713Ser)), ANO5(NM_213599.2):c.2141C>G (p.T714S), ANO5(NM_213599.3):c.2141C>G (p.T714S)
ISCN -
DB-ID ANO5_000060 See all 21 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) 0.00087 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +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     
ANO5 NM_213599.2 ?/. - c.2141C>G r.(?) p.(Thr714Ser)


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