chrX:78272820:G>T Detail (hg38) (CYSLTR1)

Information

Genome

Assembly Position
hg19 chrX:77,528,317-77,528,317 View the variant detail on this assembly version.
hg38 chrX:78,272,820-78,272,820

HGVS

Type Transcript Protein
RefSeq NM_001282187.1:c.927C>A NP_001269116.1:p.Phe309Leu
NM_001282188.1:c.927C>A NP_001269117.1:p.Phe309Leu
NM_006639.3:c.927C>A NP_006630.1:p.Phe309Leu
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 300201 OMIM
HGNC 17451 HGNC
Ensembl ENSG00000173198 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
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
<0.001 asthma In the initial sample, three SNPs, rs320995 in the cysteinyl leukotriene recepto... BeFree 18829683 Detail
0.010 asthma In the initial sample, three SNPs, rs320995 in the cysteinyl leukotriene recepto... BeFree 18829683 Detail
0.055 asthma A TaqMan allelic discrimination assay was used to genotype a 927T/C SNP and olig... BeFree 16776674 Detail
Annotation

Annotations

DescrptionSourceLinks
In the initial sample, three SNPs, rs320995 in the cysteinyl leukotriene receptor 1 gene, rs1047266 ... DisGeNET Detail
In the initial sample, three SNPs, rs320995 in the cysteinyl leukotriene receptor 1 gene, rs1047266 ... DisGeNET Detail
A TaqMan allelic discrimination assay was used to genotype a 927T/C SNP and oligonucleotide ligation... DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs320995 dbSNP
Genome
hg38
Position
chrX:78,272,820-78,272,820
Variant Type
snv
Reference Allele
G
Alternative Allele
T
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