Variant #0000317142 (NC_000015.9:g.31359269C>T, NM_002420.5:c.549G>A (TRPM1))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.31359269C>T
DNA change (hg38) g.31067066C>T
Published as TRPM1(NM_001252020.1):c.666G>A (p.K222=)
ISCN -
DB-ID TRPM1_000048
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) 0.00071 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.666G>A r.(?) p.(Lys222=)
TRPM1 NM_001252024.1 -?/. - c.615G>A r.(?) p.(Lys205=)
TRPM1 NM_002420.5 -?/. - c.549G>A r.(?) p.(Lys183=)


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