Variant #0000997730 (NC_000009.11:g.140099602dup, NM_001128228.2:c.-4439dup (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.140099602dup
DNA change (hg38) -
Published as TMEM203(NM_053045.1):c.265dupA (p.(Thr89fs))
ISCN -
DB-ID NDOR1_000003
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TPRN NM_001128228.2 ?/. - c.-4439dup r.(?) p.(=)
NDOR1 NM_014434.2 ?/. - c.-628dup r.(?) p.(=)
TMEM203 NM_053045.1 ?/. - c.265dup r.(?) p.(Thr89Asnfs*65)


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