Variant #0000516492 (NC_000002.11:g.5833904_5833915dup, NM_003108.3:c.1051_1062dup (SOX11))

Chromosome 2
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.5833904_5833915dup
DNA change (hg38) g.5693772_5693783dup
Published as SOX11(NM_003108.3):c.1031_1032insCAGCAGCAGCGG (p.(Ser351_Ser354dup)), SOX11(NM_003108.4):c.1051_1062dupAGCGGCAGCAGC (p.S351_S354dup)
ISCN -
DB-ID SOX11_000019 See all 2 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SOX11 NM_003108.3 -?/. - c.1051_1062dup r.(?) p.(Ser351_Ser354dup)


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