Variant #0000617448 (NC_000019.9:g.17448814C>T, NC_000019.9(NM_032620.3):c.54-3C>T (GTPBP3))

Chromosome 19
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.17448814C>T
DNA change (hg38) g.17338005C>T
Published as GTPBP3(NM_133644.3):c.54-3C>T
ISCN -
DB-ID ANO8_000004
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-15 15:37:27 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANO8 NM_020959.2 ?/. - c.-3335G>A r.(?) p.(=)
DDA1 NM_024050.5 ?/. - c.*18349C>T r.(=) p.(=)
GTPBP3 NM_032620.3 ?/. - c.54-3C>T r.spl? p.?


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