Variant #0000865551 (NC_000017.10:g.78190860G>A, NM_000199.3:c.220C>T (SGSH))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.78190860G>A
DNA change (hg38) -
Published as SGSH(NM_000199.4):c.220C>T (p.R74C), SGSH(NM_000199.5):c.220C>T (p.R74C)
ISCN -
DB-ID SGSH_000011 See all 6 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) 0.00015 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SGSH NM_000199.3 +/. - c.220C>T r.(?) p.(Arg74Cys)
SLC26A11 NM_001166347.1 +/. - c.-3649G>A r.(?) p.(=)
CARD14 NM_024110.4 +/. - c.*8716G>A r.(=) p.(=)


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