chr12:101786143:G> Detail (hg38) (GNPTAB)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr12:102,179,921-102,179,921 |
| hg38 | chr12:101,786,143-101,786,143 |
HGVS
| Type | Transcript | Protein |
|---|---|---|
| RefSeq | NM_024312.4:c.440delC | NP_077288.2:p.Asn148ThrfsTer4 |
| Ensemble | ENST00000299314.12:c.440delC | ENST00000299314.12:p.Asn148ThrfsTer4 |
| ENST00000549940.5:c.440delC | ENST00000549940.5:p.Asn148ThrfsTer4 |
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 |
Pathogenic
Likely pathogenic
|
| Review star |  |
| Show details | |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
| Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
|---|---|---|---|---|---|
|
Pathogenic
|
2020-07-09 | no assertion criteria provided | Mucolipidosis type II |
germline
unknown
|
Detail |
|
Pathogenic
Likely pathogenic
|
2023-12-23 | criteria provided, multiple submitters, no conflicts | Pseudo-Hurler polydystrophy,Mucolipidosis type II |
germline
unknown
|
Detail |
|
Pathogenic
Likely pathogenic
|
2023-12-23 | criteria provided, multiple submitters, no conflicts | Pseudo-Hurler polydystrophy,Mucolipidosis type II |
germline
unknown
|
Detail |
|
Pathogenic
|
2023-06-21 | criteria provided, multiple submitters, no conflicts | not provided |
germline
|
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.441del (p.Asn148fs) AND Mucolipidosis type II | ClinVar | Detail |
| NM_024312.5(GNPTAB):c.441del (p.Asn148fs) AND multiple conditions | ClinVar | Detail |
| NM_024312.5(GNPTAB):c.441del (p.Asn148fs) AND multiple conditions | ClinVar | Detail |
| NM_024312.5(GNPTAB):c.441del (p.Asn148fs) AND not provided | 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
- rs281864955 dbSNP
- Genome
- hg38
- Position
- chr12:101,786,143-101,786,143
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- -
- East Asian Chromosome Counts (ExAC)
- 8582
- 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)
- 120090
- Allele Counts in All Race (ExAC)
- 1
- Heterozygous Counts in All Race (ExAC)
- 1
- Homozygous Counts in All Race (ExAC)
- 0
- Allele Frequency in All Race (ExAC)
- 8.327088017320342E-6
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