Variant #0000326693 (NC_000019.9:g.49657751_49657753dup, NM_017636.3:c.-3373_-3371dup (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.49657751_49657753dup
DNA change (hg38) g.49154494_49154496dup
Published as HRC(NM_002152.2):c.782_784dup (p.(Asp261dup))
ISCN -
DB-ID HRC_000003
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HRC NM_002152.2 ?/. - c.782_784dup r.(?) p.(Asp261dup)
PPFIA3 NM_003660.2 ?/. - c.*4272_*4274dup r.(=) p.(=)
TRPM4 NM_017636.3 ?/. - c.-3373_-3371dup r.(?) p.(=)


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