chr18:45729946:C>A Detail (hg38) (SLC14A1)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr18:43,309,911-43,309,911 View the variant detail on this assembly version. |
hg38 | chr18:45,729,946-45,729,946 |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_001146036.2:c.-21-354C>A | |
NM_015865.6:c.-21-354C>A | ||
NM_001308278.1:c.-164-1069C>A |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.121 | Malignant neoplasm of urinary bladder | European genome-wide association study identifies SLC14A1 as a new urinary bladd... | GWASCAT | 21750109 | Detail |
0.005 | Bladder Neoplasm | [European genome-wide association study identifies SLC14A1 as a new urinary blad... | GAD | 21750109 | Detail |
0.027 | Carcinoma of bladder | These findings suggest that seven bladder cancer risk-associated variants (rs964... | BeFree | 24740636 | Detail |
0.107 | Malignant neoplasm of urinary bladder | These findings suggest that seven bladder cancer risk-associated variants (rs964... | BeFree | 24740636 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibi... | DisGeNET | Detail |
[European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptib... | DisGeNET | Detail |
These findings suggest that seven bladder cancer risk-associated variants (rs9642880, rs2294008, rs7... | DisGeNET | Detail |
These findings suggest that seven bladder cancer risk-associated variants (rs9642880, rs2294008, rs7... | 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
- rs17674580 dbSNP
- Genome
- hg38
- Position
- chr18:45,729,946-45,729,946
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- A
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