NT5C 5', 3'-nucleotidase, cytosolic
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 34 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
36 |
 |
0 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | DNT |
| SYNONYM | DNT1 |
| SYNONYM | HEL74 |
| SYNONYM | P5N2 |
| SYNONYM | PN-I |
| SYNONYM | PN-II |
| SYNONYM | UMPH2 |
| SYNONYM | cdN |
| SYNONYM | dNT-1 |
| MIM | 191720 OMIM |
| HGNC | HGNC:17144 HGNC |
| Ensembl | ENSG00000125458 Ensembl |
| AllianceGenome | HGNC:17144 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000245552.7 | hg38 | chr17 | 75,130,228 | 75,131,742 | 1,515 |
| ENST00000578337.1 | hg38 | chr17 | 75,130,568 | 75,131,321 | 754 |
| ENST00000582170.1 | hg38 | chr17 | 75,130,473 | 75,131,744 | 1,272 |
| ENST00000582160.5 | hg38 | chr17 | 75,130,225 | 75,131,446 | 1,222 |
| ENST00000582160.5 | hg19 | chr17 | 73,126,320 | 73,127,541 | 1,222 |
| ENST00000245552.7 | hg19 | chr17 | 73,126,323 | 73,127,837 | 1,515 |
| ENST00000582170.1 | hg19 | chr17 | 73,126,568 | 73,127,839 | 1,272 |
| ENST00000578337.1 | hg19 | chr17 | 73,126,663 | 73,127,416 | 754 |
Genome browser