Variant #0000806632 (NC_000015.9:g.31360213A>G, NM_002420.5:c.296T>C (TRPM1))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.31360213A>G
DNA change (hg38) -
Published as TRPM1(NM_001252020.2):c.413T>C (p.L138P)
ISCN -
DB-ID TRPM1_000129 See all 11 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) 0.00011 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRPM1 NM_001252020.1 +?/. - c.413T>C r.(?) p.(Leu138Pro)
TRPM1 NM_001252024.1 +?/. - c.362T>C r.(?) p.(Leu121Pro)
TRPM1 NM_002420.5 +?/. - c.296T>C r.(?) p.(Leu99Pro)


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