Variant #0000726760 (NC_000017.10:g.78190903G>A, NM_000199.3:c.177C>T (SGSH))

Chromosome 17
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.78190903G>A
DNA change (hg38) -
Published as SGSH(NM_001352921.1):c.177C>T (p.L59=)
ISCN -
DB-ID SGSH_000120
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 2021-02-08 18:36:18 +01:00 (CET)
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.177C>T r.(?) p.(Leu59=)
SLC26A11 NM_001166347.1 -?/. - c.-3606G>A r.(?) p.(=)
CARD14 NM_024110.4 -?/. - c.*8759G>A r.(=) p.(=)


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