chr11:108121428:G>T Detail (hg19) (ATM)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr11:108,121,428-108,121,428 |
hg38 | chr11:108,250,701-108,250,701 View the variant detail on this assembly version. |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_000051.3:c.1236G>T | NP_000042.3:p.Trp412Cys |
NM_001351834.1:c.1236G>T | NP_001338763.1:p.Trp412Cys | |
Ensemble | ENST00000713844.1:c.1236G>T | ENST00000713844.1:p.Trp412Cys |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
[No Data.]
Prediction
ClinVar
Clinical Significance |
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Review star | ![]() |
Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.002 | cervix carcinoma | Genetic polymorphisms and cervical cancer development: ATM G5557A and p53bp1 C12... | BeFree | 22200742 | Detail |
0.002 | Malignant tumor of cervix | Genetic polymorphisms and cervical cancer development: ATM G5557A and p53bp1 C12... | BeFree | 22200742 | Detail |
<0.001 | cervix carcinoma | Genetic polymorphisms and cervical cancer development: ATM G5557A and p53bp1 C12... | BeFree | 22200742 | Detail |
<0.001 | Malignant tumor of cervix | Genetic polymorphisms and cervical cancer development: ATM G5557A and p53bp1 C12... | BeFree | 22200742 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
NM_000051.4(ATM):c.1236G>T (p.Trp412Cys) AND Ataxia-telangiectasia syndrome | ClinVar | Detail |
NM_000051.4(ATM):c.1236G>T (p.Trp412Cys) AND not provided | ClinVar | Detail |
Genetic polymorphisms and cervical cancer development: ATM G5557A and p53bp1 C1236G. | DisGeNET | Detail |
Genetic polymorphisms and cervical cancer development: ATM G5557A and p53bp1 C1236G. | DisGeNET | Detail |
Genetic polymorphisms and cervical cancer development: ATM G5557A and p53bp1 C1236G. | DisGeNET | Detail |
Genetic polymorphisms and cervical cancer development: ATM G5557A and p53bp1 C1236G. | 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
- rs79220522 dbSNP
- Genome
- hg19
- Position
- chr11:108,121,428-108,121,428
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- T
Genome browser