Variant #0000308324 (NC_000017.10:g.78195427G>A, NM_000199.3:c.-1315C>T (SGSH))

Chromosome 17
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.78195427G>A
DNA change (hg38) g.80221628G>A
Published as SLC26A11(NM_001166347.2):c.68G>A (p.C23Y)
ISCN -
DB-ID SLC26A11_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) 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     
SGSH NM_000199.3 ?/. - c.-1315C>T r.(?) p.(=)
SLC26A11 NM_001166347.1 ?/. - c.68G>A r.(?) p.(Cys23Tyr)
CARD14 NM_024110.4 ?/. - c.*13283G>A r.(=) p.(=)


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