Variant #0000537562 (NC_000009.11:g.140095048G>A, NM_001128228.2:c.116C>T (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.140095048G>A
DNA change (hg38) g.137200596G>A
Published as TPRN(NM_001128228.3):c.116C>T (p.P39L)
ISCN -
DB-ID TMEM203_000006
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TPRN NM_001128228.2 -?/. - c.116C>T r.(?) p.(Pro39Leu)
TMEM203 NM_053045.1 -?/. - c.*4408C>T r.(=) p.(=)


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