Variant #0000692249 (NC_000017.10:g.10599148G>A, NM_004589.2:c.274C>T (SCO1))

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.10599148G>A
DNA change (hg38) -
Published as SCO1(NM_004589.3):c.274C>T (p.P92S)
ISCN -
DB-ID SCO1_000008
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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCO1 NM_004589.2 ?/. - c.274C>T r.(?) p.(Pro92Ser)
ADPRM NM_020233.4 ?/. - c.-1854G>A r.(?) p.(=)


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