Variant #0000546465 (NC_000012.11:g.110246277G>A, NC_000012.11(NM_021625.4):c.387-4C>T (TRPV4))

Chromosome 12
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.110246277G>A
DNA change (hg38) g.109808472G>A
Published as TRPV4(NM_001177428.1):c.387-4C>T (p.?), TRPV4(NM_021625.5):c.387-4C>T
ISCN -
DB-ID TRPV4_000010 See all 3 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) 0.00368 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-10-29 21:08:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRPV4 NM_021625.4 -/. - c.387-4C>T r.spl? p.?


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