Variant #0000309141 (NC_000008.10:g.133899124C>T, NM_003235.4:c.1507C>T (TG))

Chromosome 8
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.133899124C>T
DNA change (hg38) g.132886879C>T
Published as TG(NM_003235.5):c.1507C>T (p.Q503*)
ISCN -
DB-ID TG_000014
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLA NM_001045556.2 +/. - c.*151645G>A r.(=) p.(=)
TG NM_003235.4 +/. - c.1507C>T r.(?) p.(Gln503Ter)


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