Variant #0000677590 (NC_000006.11:g.112389440A>T, NM_003880.3:c.622A>T (WISP3))

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.112389440A>T
DNA change (hg38) -
Published as CCN6(NM_198239.1):c.676A>T (p.K226*)
ISCN -
DB-ID TUBE1_000001
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) 2.0E-5 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM229B NM_001033564.1 +/. - c.-19659A>T r.(?) p.(=)
WISP3 NM_003880.3 +/. - c.622A>T r.(?) p.(Lys208Ter)
TUBE1 NM_016262.4 +/. - c.*3175T>A r.(=) p.(=)
WISP3 NM_198239.1 +/. - c.676A>T r.(?) p.(Lys226Ter)


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