Variant #0001025684 (NC_000009.11:g.73235262C>T, NM_206945.3:c.1370G>A (TRPM3))

Chromosome 9
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.73235262C>T
DNA change (hg38) -
Published as TRPM3(NM_001366147.2):c.1934G>A (p.R645Q), TRPM3(NM_020952.6):c.1364G>A (p.R455Q)
ISCN -
DB-ID TRPM3_000054 See all 2 reported entries
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) 4.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRPM3 NM_206945.3 -?/. - c.1370G>A r.(?) p.(Arg457Gln)


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