Variant #0000623780 (NC_000017.10:g.78155448G>A, NM_000199.3:c.*28803C>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.78155448G>A
DNA change (hg38) g.80181649G>A
Published as CARD14(NM_024110.4):c.211G>A (p.G71R)
ISCN -
DB-ID SGSH_000083
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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SGSH NM_000199.3 ?/. - c.*28803C>T r.(=) p.(=)
CARD14 NM_024110.4 ?/. - c.211G>A r.(?) p.(Gly71Arg)


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