Variant #0000804018 (NC_000009.11:g.140094341G>T, NM_001128228.2:c.823C>A (TPRN))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.140094341G>T
DNA change (hg38) -
Published as TPRN(NM_001128228.3):c.823C>A (p.P275T)
ISCN -
DB-ID TMEM203_000008
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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TPRN NM_001128228.2 -?/. - c.823C>A r.(?) p.(Pro275Thr)
TMEM203 NM_053045.1 -?/. - c.*5115C>A r.(=) p.(=)


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