Variant #0000543080 (NC_000011.9:g.16036482A>G, NC_000011.9(NM_033326.3):c.1732+6T>C (SOX6))

Chromosome 11
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.16036482A>G
DNA change (hg38) g.16014936A>G
Published as SOX6(NM_001367873.1):c.1732+6T>C, SOX6(NM_017508.3):c.1651+6T>C
ISCN -
DB-ID SOX6_000004 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) 0.00027 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SOX6 NM_033326.3 -?/. - c.1732+6T>C r.(=) p.(=)


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