Variant #0000981146 (NC_000015.9:g.31373644A>T, NC_000015.9(NM_002420.5):c.-63-4457T>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.31373644A>T
DNA change (hg38) -
Published as TRPM1(NM_001252024.2):c.-83-3T>A
ISCN -
DB-ID TRPM1_000229
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
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.55-4457T>A r.(=) p.(=)
TRPM1 NM_001252024.1 -?/. - c.-83-3T>A r.spl? p.?
TRPM1 NM_002420.5 -?/. - c.-63-4457T>A r.(=) p.(=)


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