Variant #0000856204 (NC_000022.10:g.50966963T>C, NM_001257988.1:c.494A>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.50966963T>C
DNA change (hg38) -
Published as TYMP(NM_001113756.2):c.494A>G (p.N165S)
ISCN -
DB-ID NCAPH2_000038
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ODF3B NM_001014440.3 -?/. - c.*1946A>G r.(=) p.(=)
TYMP NM_001257988.1 -?/. - c.494A>G r.(?) p.(Asn165Ser)
SCO2 NM_005138.2 -?/. - c.-3076A>G r.(?) p.(=)
NCAPH2 NM_152299.3 -?/. - c.*5159T>C r.(=) p.(=)


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