Variant #0000725033 (NC_000015.9:g.31323249G>A, NM_002420.5:c.2998C>T (TRPM1))

Chromosome 15
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.31323249G>A
DNA change (hg38) -
Published as TRPM1(NM_001252020.1):c.3115C>T (p.R1039*, p.(Arg1039Ter))
ISCN -
DB-ID TRPM1_000024 See all 4 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) 5.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRPM1 NM_001252020.1 +/. - c.3115C>T r.(?) p.(Arg1039Ter)
TRPM1 NM_001252024.1 +/. - c.3064C>T r.(?) p.(Arg1022Ter)
TRPM1 NM_002420.5 +/. - c.2998C>T r.(?) p.(Arg1000Ter)


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