chr18:657646:C>T Detail (hg38) (TYMS)

Information

Genome

Assembly Position
hg19 chr18:657,646-657,646 View the variant detail on this assembly version.
hg38 chr18:657,646-657,646

HGVS

Type Transcript Protein
RefSeq
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Type Database ID Link
Gene MIM 188350 OMIM
HGNC 12441 HGNC
Ensembl ENSG00000176890 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
Disease Drug EL ET ED CS VO TR Pubmed Links
cancer Methotrexate B Predictive Supports Adverse Response Common Germline 3 23652803 Detail
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
499 children from ALL trials treated with methotrexate were genotyped for 8 SNPs in 5 genes. The TYM... CIViC Evidence Detail
Gene
-
Genome
hg38
Position
chr18:657,646-657,646
Variant Type
snv
Reference Allele
C
Alternative Allele
T
Variant (CIViC) (CIViC Variant)
RS34743033
Transcript 1 (CIViC Variant)
ENST00000323274.10
Variant URL (CIViC Variant)
https://civic.genome.wustl.edu/links/variants/779
Genome browser