Variant #0000329130 (NC_000022.10:g.50964599G>C, NC_000022.10(NM_001257988.1):c.1160-29C>G (TYMP))

Chromosome 22
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.50964599G>C
DNA change (hg38) g.50526170G>C
Published as TYMP(NM_001113755.2):c.1160-29C>G (p.(=))
ISCN -
DB-ID SCO2_000006
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) 0.03716 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 2022-05-09 15:51:19 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ODF3B NM_001014440.3 -?/. - c.*4310C>G r.(=) p.(=)
TYMP NM_001257988.1 -?/. - c.1160-29C>G r.(=) p.(=)
SCO2 NM_005138.2 -?/. - c.-712C>G r.(?) p.(=)
NCAPH2 NM_152299.3 -?/. - c.*2795G>C r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.