chr7:87550493:C>T Detail (hg38) (ABCB1)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr7:87,179,809-87,179,809 View the variant detail on this assembly version. |
hg38 | chr7:87,550,493-87,550,493 |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_000927.4:c.1199G>A | NP_000918.2:p.Ser400Asn |
Ensemble | ENST00000265724.8:c.1199G>A | ENST00000265724.8:p.Ser400Asn |
ENST00000543898.5:c.1007G>A | ENST00000543898.5:p.Ser336Asn |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:[No Data.] |
ToMMo:[No Data.] | |
NCBN:[No Data.] | |
NCBN(Hondo):[No Data.] | |
NCBN(Ryukyu):[No Data.] | |
East asia | ExAC:<0.001 |
Prediction
ClinVar
Clinical Significance |
![]() ![]() |
Review star | ![]() |
Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.003 | kidney failure | The purpose of this study is to compare the genotype frequency of C3435T and G11... | BeFree | 17376299 | Detail |
0.030 | Malignant neoplasm of ovary | ABCB1 G1199A polymorphism and ovarian cancer response to paclitaxel. | BeFree | 17828752 | Detail |
0.015 | ovarian carcinoma | ABCB1 G1199A polymorphism and ovarian cancer response to paclitaxel. | BeFree | 17828752 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
NM_001348946.2(ABCB1):c.1199G>A (p.Ser400Asn) AND not specified | ClinVar | Detail |
NM_001348946.2(ABCB1):c.1199G>A (p.Ser400Asn) AND ABCB1-related disorder | ClinVar | Detail |
The purpose of this study is to compare the genotype frequency of C3435T and G1199A polymorphisms in... | DisGeNET | Detail |
ABCB1 G1199A polymorphism and ovarian cancer response to paclitaxel. | DisGeNET | Detail |
ABCB1 G1199A polymorphism and ovarian cancer response to paclitaxel. | 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
- rs2229109 dbSNP
- Genome
- hg38
- Position
- chr7:87,550,493-87,550,493
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- T
- East Asian Chromosome Counts (ExAC)
- 8650
- East Asian Allele Counts (ExAC)
- 0
- East Asian Heterozygous Counts (ExAC)
- 0
- East Asian Homozygous Counts (ExAC)
- 0
- East Asian Allele Frequency (ExAC)
- 0.0
- Chromosome Counts in All Race (ExAC)
- 121310
- Allele Counts in All Race (ExAC)
- 3520
- Heterozygous Counts in All Race (ExAC)
- 3384
- Homozygous Counts in All Race (ExAC)
- 68
- Allele Frequency in All Race (ExAC)
- 0.029016569120435248
Genome browser