Variant #0000308725 (NC_000002.11:g.5833193_5833201del, NM_003108.3:c.340_348del (SOX11))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.5833193_5833201del
DNA change (hg38) g.5693061_5693069del
Published as SOX11(NM_003108.3):c.340_348delCCCGACTAC (p.P114_Y116del)
ISCN -
DB-ID SOX11_000005
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SOX11 NM_003108.3 ?/. - c.340_348del r.(?) p.(Pro114_Tyr116del)


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