chr12:102151036:>G Detail (hg19) (GNPTAB)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr12:102,151,036-102,151,036 |
| hg38 | chr12:101,757,258-101,757,258 |
HGVS
| Type | Transcript | Protein |
|---|---|---|
| RefSeq | NM_024312.4:c.3387_3388insC | NP_077288.2:p.Val1130AlafsTer10 |
| Ensemble | ENST00000299314.12:c.3387_3388insC | ENST00000299314.12:p.Val1130AlafsTer10 |
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Frequency
[No Data.]
Prediction
ClinVar
| Clinical Significance | no classification for the single variant |
| Review star |  |
| Show details | |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
| Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
|---|---|---|---|---|---|
Pathogenic
|
2012-05-10 | no assertion criteria provided | Mucolipidosis type II |
not provided
|
Detail |
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| NM_024312.4(GNPTAB):c.[3388_3389insC;3392C>T] AND Mucolipidosis type II | ClinVar | 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
- rs281865015 dbSNP
- Genome
- hg19
- Position
- chr12:102,151,036-102,151,036
- Variant Type
- snv
- Reference Allele
- -
- Alternative Allele
- G
Genome browser