Variant #0000802268 (NC_000006.11:g.112382393G>A, NM_003880.3:c.248G>A (WISP3))

Chromosome 6
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.112382393G>A
DNA change (hg38) -
Published as WISP3(NM_003880.3):c.248G>A (p.(Gly83Glu))
ISCN -
DB-ID WISP3_000019 See all 31 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) 0.00247 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 2021-09-17 14:40:49 +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     
WISP3 NM_003880.3 -?/. - c.248G>A r.(?) p.(Gly83Glu)
WISP3 NM_198239.1 -?/. - c.302G>A r.(?) p.(Gly101Glu)


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