chr22:36387940:G>A Detail (hg38) (MYH9, LOC112695089)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr22:36,783,985-36,783,985 View the variant detail on this assembly version. |
| hg38 | chr22:36,387,940-36,387,940 |
HGVS
| Type | Transcript | Protein |
|---|---|---|
| RefSeq | NM_002473.5:c.-153C>T | |
| Ensemble | ENST00000216181.11:c.-153C>T | |
| ENST00000685801.1:c.-153C>T |
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Frequency
[No Data.]
Prediction
ClinVar
| Clinical Significance |
Uncertain significance
|
| Review star |  |
| Show details | |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
| Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
|---|---|---|---|---|---|
|
Uncertain significance
|
2018-01-12 | criteria provided, single submitter | MYH9-related disorder |
germline
|
Detail |
|
Uncertain significance
|
2018-01-12 | criteria provided, single submitter | Autosomal dominant nonsyndromic hearing loss 17 |
germline
|
Detail |
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| NM_002473.6(MYH9):c.-153C>T AND MYH9-related disorder | ClinVar | Detail |
| NM_002473.6(MYH9):c.-153C>T AND Autosomal dominant nonsyndromic hearing loss 17 | 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
- rs886057485 dbSNP
- Genome
- hg38
- Position
- chr22:36,387,940-36,387,940
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- A
Genome browser