Variant #0000537560 (NC_000009.11:g.140094509G>T, NM_001128228.2:c.655C>A (TPRN))

Chromosome 9
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.140094509G>T
DNA change (hg38) g.137200057G>T
Published as TPRN(NM_001128228.3):c.655C>A (p.R219S)
ISCN -
DB-ID TMEM203_000005 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) 0.00102 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +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.655C>A r.(?) p.(Arg219Ser)
TMEM203 NM_053045.1 ?/. - c.*4947C>A r.(=) p.(=)


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