Variant #0001055028 (NC_000015.9:g.31358419G>A, NM_002420.5:c.584C>T (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.31358419G>A
DNA change (hg38) -
Published as TRPM1(NM_001252024.2):c.650C>T (p.(Pro217Leu))
ISCN -
DB-ID TRPM1_000237
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 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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRPM1 NM_001252020.1 ?/. - c.701C>T r.(?) p.(Pro234Leu)
TRPM1 NM_001252024.1 ?/. - c.650C>T r.(?) p.(Pro217Leu)
TRPM1 NM_002420.5 ?/. - c.584C>T r.(?) p.(Pro195Leu)


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