chr1:94001068:C>G Detail (hg38) (ABCA4)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr1:94,466,624-94,466,624 View the variant detail on this assembly version. |
| hg38 | chr1:94,001,068-94,001,068 |
HGVS
| Type | Transcript | Protein |
|---|---|---|
| RefSeq | NM_000350.2:c.6320G>C | NP_000341.2:p.Arg2107Pro |
| Ensemble | ENST00000370225.4:c.6320G>C | ENST00000370225.4:p.Arg2107Pro |
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | 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 | not provided |
not provided
|
Detail |
CIViC
[No Data.]
DisGeNET
| Score | Disease name | Description | Source | Pubmed | Links |
|---|---|---|---|---|---|
| 0.442 | STARGARDT DISEASE 1 (disorder) | Twenty-nine patients with Stargardt dystrophy or fundus flavimaculatus from diff... | UNIPROT | 10206579 | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| NM_000350.3(ABCA4):c.6320G>C (p.Arg2107Pro) AND not provided | ClinVar | Detail |
| Twenty-nine patients with Stargardt dystrophy or fundus flavimaculatus from different pedigrees were... | 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
- rs62642564 dbSNP
- Genome
- hg38
- Position
- chr1:94,001,068-94,001,068
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- G
Genome browser