chr1:94466625:G>T Detail (hg19) (ABCA4)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr1:94,466,625-94,466,625 |
| hg38 | chr1:94,001,069-94,001,069 View the variant detail on this assembly version. |
HGVS
| Type | Transcript | Protein |
|---|---|---|
| RefSeq | NM_000350.2:c.6319C>A | NP_000341.2:p.Arg2107Ser |
| Ensemble | ENST00000370225.4:c.6319C>A | ENST00000370225.4:p.Arg2107Ser |
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Frequency
[No Data.]
Prediction
ClinVar
| Clinical Significance | Conflicting classifications of pathogenicity |
| Review star |  |
| Show details | |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
| Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
|---|---|---|---|---|---|
Conflicting interpretations of pathogenicity
|
2023-10-08 | criteria provided, conflicting interpretations | not provided |
germline
|
Detail |
CIViC
[No Data.]
DisGeNET
| Score | Disease name | Description | Source | Pubmed | Links |
|---|---|---|---|---|---|
| 0.442 | STARGARDT DISEASE 1 (disorder) | Mutations in ABCR (ABCA4) in patients with Stargardt macular degeneration or con... | UNIPROT | 11527935 | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| NM_000350.3(ABCA4):c.6319C>A (p.Arg2107Ser) AND not provided | ClinVar | Detail |
| Mutations in ABCR (ABCA4) in patients with Stargardt macular degeneration or cone-rod degeneration. | 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
- rs2297669 dbSNP
- Genome
- hg19
- Position
- chr1:94,466,625-94,466,625
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- T
Genome browser