Variant #0000622234 (NC_000009.11:g.140093767dup, NM_001128228.2:c.1402dup (TPRN))

Chromosome 9
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.140093767dup
DNA change (hg38) g.137199315dup
Published as TPRN(NM_001128228.3):c.1402dupC (p.Q468Pfs*68)
ISCN -
DB-ID TPRN_000016 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-06-26 13:08:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TPRN NM_001128228.2 +/. - c.1402dup r.(?) p.(Gln468ProfsTer68)
TMEM203 NM_053045.1 +/. - c.*5694dup r.(?) p.(=)


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