Variant #0000259699 (NC_000012.11:g.124197138C>T, NM_024809.4:c.*4878C>T (TCTN2))

Chromosome 12
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.124197138C>T
DNA change (hg38) g.123712591C>T
Published as ATP6V0A2(NM_012463.4):c.26C>T (p.T9I)
ISCN -
DB-ID ATP6V0A2_000001
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP6V0A2 NM_012463.3 ?/. - c.26C>T r.(?) p.(Thr9Ile)
TCTN2 NM_024809.4 ?/. - c.*4878C>T r.(=) p.(=)


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