Variant #0000313089 (NC_000006.11:g.112382313G>T, NM_003880.3:c.168G>T (WISP3))

Chromosome 6
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.112382313G>T
DNA change (hg38) g.112061110G>T
Published as CCN6(NM_198239.2):c.168G>T (p.Q56H)
ISCN -
DB-ID WISP3_000003 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) 0.25498 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WISP3 NM_003880.3 -/. - c.168G>T r.(?) p.(Gln56His)
WISP3 NM_198239.1 -/. - c.222G>T r.(?) p.(Gln74His)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.