Variant #0000691771 (NC_000015.9:g.31359333C>T, NM_002420.5:c.485G>A (TRPM1))

Chromosome 15
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.31359333C>T
DNA change (hg38) -
Published as TRPM1(NM_001252020.1):c.602G>A (p.R201Q)
ISCN -
DB-ID TRPM1_000089 See all 2 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) 0.00077 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2020-09-15 15:50:26 +02:00 (CEST)
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.602G>A r.(?) p.(Arg201Gln)
TRPM1 NM_001252024.1 ?/. - c.551G>A r.(?) p.(Arg184Gln)
TRPM1 NM_002420.5 ?/. - c.485G>A r.(?) p.(Arg162Gln)


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