Variant #0000317134 (NC_000015.9:g.31362148C>G, NC_000015.9(NM_002420.5):c.213+86G>C (TRPM1))

Chromosome 15
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.31362148C>G
DNA change (hg38) g.31069945C>G
Published as TRPM1(NM_001252030.1):c.299G>C (p.G100A)
ISCN -
DB-ID TRPM1_000052
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) 0.00871 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 2018-01-15 20:58:59 +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.330+86G>C r.(=) p.(=)
TRPM1 NM_001252024.1 -/. - c.279+86G>C r.(=) p.(=)
TRPM1 NM_002420.5 -/. - c.213+86G>C r.(=) p.(=)


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