chr15:74328657:C>T Detail (hg19) (PML)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr15:74,328,657-74,328,657 |
hg38 | chr15:74,036,316-74,036,316 View the variant detail on this assembly version. |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_002675.3:c.1710+1786C>T | |
NM_033240.2:c.*1660C>T | ||
NM_033250.2:c.*365C>T |
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 |
---|---|---|---|---|---|
0.020 | nicotine dependence | One CHRNA5 (rs16969968) and two CHRNA3 (rs1051703, rs6495308) SNPs were examined... | BeFree | 22223462 | Detail |
0.133 | nicotine dependence | One CHRNA5 (rs16969968) and two CHRNA3 (rs1051703, rs6495308) SNPs were examined... | BeFree | 22223462 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
One CHRNA5 (rs16969968) and two CHRNA3 (rs1051703, rs6495308) SNPs were examined for their ability t... | DisGeNET | Detail |
One CHRNA5 (rs16969968) and two CHRNA3 (rs1051703, rs6495308) SNPs were examined for their ability t... | 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
- rs1051703 dbSNP
- Genome
- hg19
- Position
- chr15:74,328,657-74,328,657
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- T
Genome browser