Variant #0000560258 (NC_000017.10:g.10600567del, NM_004589.2:c.261del (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.10600567del
DNA change (hg38) g.10697250del
Published as SCO1(NM_004589.3):c.261delC (p.S88Rfs*11)
ISCN -
DB-ID SCO1_000007
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-13 08:51:20 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCO1 NM_004589.2 ?/. - c.261del r.(?) p.(Ser88ArgfsTer11)
ADPRM NM_020233.4 ?/. - c.-435del r.(?) p.(=)


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