Variant #0000622779 (NC_000012.11:g.110238466C>T, NM_021625.4:c.810G>A (TRPV4))

Chromosome 12
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.110238466C>T
DNA change (hg38) g.109800661C>T
Published as TRPV4(NM_021625.4):c.810G>A (p.G270=), TRPV4(NM_021625.5):c.810G>A (p.G270=)
ISCN -
DB-ID TRPV4_000052 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) 0.00681 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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.810G>A r.(?) p.(Gly270=)


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