Variant #0000329136 (NC_000022.10:g.50969220T>C, NM_001257988.1:c.-933A>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.50969220T>C
DNA change (hg38) g.50530791T>C
Published as ODF3B(NM_001014440.3):c.602A>G (p.(Gln201Arg))
ISCN -
DB-ID ODF3B_000001
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) 5.0E-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     
ODF3B NM_001014440.3 ?/. - c.602A>G r.(?) p.(Gln201Arg)
TYMP NM_001257988.1 ?/. - c.-933A>G r.(?) p.(=)
SCO2 NM_005138.2 ?/. - c.-5333A>G r.(?) p.(=)
NCAPH2 NM_152299.3 ?/. - c.*7416T>C r.(=) p.(=)


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