chr3:189868639:A>G Detail (hg38) (TP63)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr3:189,586,428-189,586,428 View the variant detail on this assembly version. |
hg38 | chr3:189,868,639-189,868,639 |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_001114978.1:c.1052A>G | NP_001108450.1:p.Asp351Gly |
NM_003722.4:c.1052A>G | NP_003713.3:p.Asp351Gly | |
NM_001114980.1:c.770A>G | NP_001108452.1:p.Asp257Gly |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.440 | ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3 | NA | CLINVAR | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
NM_003722.5(TP63):c.1052A>G (p.Asp351Gly) AND Ectrodactyly, ectodermal dysplasia, and cleft lip-pala... | ClinVar | Detail |
NM_003722.5(TP63):c.1052A>G (p.Asp351Gly) 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
- rs121908844 dbSNP
- Genome
- hg38
- Position
- chr3:189,868,639-189,868,639
- Variant Type
- snv
- Reference Allele
- A
- Alternative Allele
- G
Genome browser