Variant #0000329127 (NC_000022.10:g.50962837G>C, NM_001257988.1:c.*1362C>G (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.50962837G>C
DNA change (hg38) g.50524408G>C
Published as SCO2(NM_001169109.1):c.4C>G (p.(Leu2Val))
ISCN -
DB-ID NCAPH2_000013
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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TYMP NM_001257988.1 ?/. - c.*1362C>G r.(=) p.(=)
SCO2 NM_005138.2 ?/. - c.4C>G r.(?) p.(Leu2Val)
NCAPH2 NM_152299.3 ?/. - c.*1033G>C r.(=) p.(=)


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