Variant #0000926668 (NC_000017.10:g.78157961G>T, NM_000199.3:c.*26290C>A (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.78157961G>T
DNA change (hg38) -
Published as CARD14(NM_024110.4):c.599G>T (p.S200I)
ISCN -
DB-ID SGSH_000160
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) 0.00141 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +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.*26290C>A r.(=) p.(=)
CARD14 NM_024110.4 -?/. - c.599G>T r.(?) p.(Ser200Ile)


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