Variant #0000317147 (NC_000019.9:g.49691898G>A, NM_017636.3:c.1744G>A (TRPM4))

Chromosome 19
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.49691898G>A
DNA change (hg38) g.49188641G>A
Published as TRPM4(NM_001195227.1):c.1744G>A (p.?), TRPM4(NM_017636.3):c.1744G>A (p.G582S), TRPM4(NM_017636.4):c.1744G>A (p.G582S)
ISCN -
DB-ID TRPM4_000011 See all 7 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) 0.00051 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 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRPM4 NM_017636.3 ?/. - c.1744G>A r.(?) p.(Gly582Ser)


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