Variant #0000553930 (NC_000015.9:g.31355369C>T, NM_002420.5:c.851G>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.31355369C>T
DNA change (hg38) g.31063166C>T
Published as TRPM1(NM_001252020.1):c.968G>A (p.R323H)
ISCN -
DB-ID TRPM1_000086
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) 3.0E-5 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 2019-07-18 18:22:55 +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.968G>A r.(?) p.(Arg323His)
TRPM1 NM_001252024.1 ?/. - c.917G>A r.(?) p.(Arg306His)
TRPM1 NM_002420.5 ?/. - c.851G>A r.(?) p.(Arg284His)


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