Variant #0000693223 (NC_000022.10:g.50962341A>C, NM_001257988.1:c.*1858T>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.50962341A>C
DNA change (hg38) -
Published as SCO2(NM_001169109.1):c.500T>G (p.V167G), SCO2(NM_005138.3):c.500T>G (p.V167G)
ISCN -
DB-ID NCAPH2_000029 See all 3 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 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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +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.*1858T>G r.(=) p.(=)
SCO2 NM_005138.2 ?/. - c.500T>G r.(?) p.(Val167Gly)
NCAPH2 NM_152299.3 ?/. - c.*537A>C r.(=) p.(=)


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