Variant #0001039301 (NC_000012.11:g.49689404G>T, NM_006262.3:c.421G>T (PRPH))

Chromosome 12
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.49689404G>T
DNA change (hg38) -
Published as PRPH(NM_006262.4):c.421G>T (p.(Asp141Tyr))
ISCN -
DB-ID PRPH_000022
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) 0.00318 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TROAP NM_005480.3 ?/. - c.-27734G>T r.(?) p.(=)
PRPH NM_006262.3 ?/. - c.421G>T r.(?) p.(Asp141Tyr)


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