Variant #0000981147 (NC_000015.9:g.31373646G>C, NC_000015.9(NM_002420.5):c.-63-4459C>G (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.31373646G>C
DNA change (hg38) -
Published as TRPM1(NM_001252024.2):c.-83-5C>G
ISCN -
DB-ID TRPM1_000230
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.55-4459C>G r.(=) p.(=)
TRPM1 NM_001252024.1 -?/. - c.-83-5C>G r.spl? p.?
TRPM1 NM_002420.5 -?/. - c.-63-4459C>G r.(=) p.(=)


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