Variant #0000681937 (NC_000022.10:g.50962434_50962445dup, NM_001257988.1:c.*1760_*1771dup (TYMP))

Chromosome 22
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.50962434_50962445dup
DNA change (hg38) -
Published as SCO2(NM_001169109.1):c.402_413dupTGACATCTGCCC (p.I136_D139dup)
ISCN -
DB-ID NCAPH2_000026
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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TYMP NM_001257988.1 ?/. - c.*1760_*1771dup r.(=) p.(=)
SCO2 NM_005138.2 ?/. - c.402_413dup r.(?) p.(Ile136_Asp139dup)
NCAPH2 NM_152299.3 ?/. - c.*630_*641dup r.(=) p.(=)


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