chr12:101764642:TT> Detail (hg38) (GNPTAB)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr12:102,158,420-102,158,421 |
| hg38 | chr12:101,764,642-101,764,643 |
HGVS
| Type | Transcript | Protein |
|---|---|---|
| RefSeq | NM_024312.4:c.2274_2275delAA | NP_077288.2:p.Asn759Ter |
| Ensemble | ENST00000299314.12:c.2274_2275delAA | ENST00000299314.12:p.Asn759Ter |
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Frequency
[No Data.]
Prediction
ClinVar
| Clinical Significance |
Likely pathogenic
|
| Review star |  |
| Show details | |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
| Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
|---|---|---|---|---|---|
not provided
|
no assertion provided | Mucolipidosis type II |
unknown
|
Detail | |
|
Likely pathogenic
|
2017-12-05 | criteria provided, single submitter | Pseudo-Hurler polydystrophy,Mucolipidosis type II |
unknown
|
Detail |
|
Likely pathogenic
|
2017-12-05 | criteria provided, single submitter | Pseudo-Hurler polydystrophy,Mucolipidosis type II |
unknown
|
Detail |
CIViC
[No Data.]
DisGeNET
| Score | Disease name | Description | Source | Pubmed | Links |
|---|---|---|---|---|---|
| 0.441 | MUCOLIPIDOSIS II ALPHA/BETA (disorder) | NA | CLINVAR | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| NM_024312.5(GNPTAB):c.2275_2276del (p.Thr758_Asn759insTer) AND Mucolipidosis type II | ClinVar | Detail |
| NM_024312.5(GNPTAB):c.2275_2276del (p.Thr758_Asn759insTer) AND multiple conditions | ClinVar | Detail |
| NM_024312.5(GNPTAB):c.2275_2276del (p.Thr758_Asn759insTer) AND multiple conditions | ClinVar | Detail |
| NA | 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
- rs281864992 dbSNP
- Genome
- hg38
- Position
- chr12:101,764,642-101,764,643
- Variant Type
- snv
- Reference Allele
- TT
- Alternative Allele
- -
Genome browser