Variant #0000002858 (NC_000017.10:g.78185927A>G, SGSH(NM_000199.3):c.892T>C)

Individual ID 00002858
Chromosome 17
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.78185927A>G
Reference Sleat et al. 2009. Mol Cell Pteomics 8:1708-18
DB-ID SGSH_000001
Frequency -
Average frequency (gnomAD v.2.1.1) 9.0E-5 View details
Owner Y Yang
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Y Yang
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
SGSH NM_000199.3 ./. 7 c.892T>C r.(?) p.(Ser298Pro) VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000002858 ? ? SGSH 1 Y Yang