Variant #0000950326 (NC_000015.9:g.31360294T>C, NM_002420.5:c.215A>G (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.31360294T>C
DNA change (hg38) -
Published as TRPM1(NM_001252020.1):c.332A>G (p.Y111C)
ISCN -
DB-ID TRPM1_000134 See all 16 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) 0.00016 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 2023-11-27 17:35:39 +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.332A>G r.(?) p.(Tyr111Cys)
TRPM1 NM_001252024.1 +?/. - c.281A>G r.(?) p.(Tyr94Cys)
TRPM1 NM_002420.5 +?/. - c.215A>G r.(?) p.(Tyr72Cys)


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