Variant #0000951060 (NC_000017.10:g.78163589C>T, NM_000199.3:c.*20662G>A (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.78163589C>T
DNA change (hg38) -
Published as CARD14(NM_024110.4):c.881C>T (p.A294V)
ISCN -
DB-ID CARD14_000048 See all 2 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) 0.00017 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-11-27 17:35:39 +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.*20662G>A r.(=) p.(=)
CARD14 NM_024110.4 ?/. - c.881C>T r.(?) p.(Ala294Val)


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