chr3:33024297:G>T Detail (hg38) (GLB1)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr3:33,065,789-33,065,789 View the variant detail on this assembly version. |
hg38 | chr3:33,024,297-33,024,297 |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_000404.3:c.1097C>A | NP_000395.2:p.Pro366His |
NM_001317040.1:c.1097C>A | NP_001303969.1:p.Pro366His | |
NM_001135602.2:c.704C>A | NP_001129074.1:p.Pro235His |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
[No Data.]
Prediction
ClinVar
Clinical Significance | no classification for the single variant |
Review star | ![]() |
Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
---|---|---|---|---|---|
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2016-05-13 | no assertion criteria provided | Mucopolysaccharidosis, MPS-IV-B |
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Detail |
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.367 | mucopolysaccharidosis type IVB | NA | CLINVAR | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
NM_000404.2(GLB1):c.[1285C>T;1097C>A] AND Mucopolysaccharidosis, MPS-IV-B | 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
- rs797045010 dbSNP
- Genome
- hg38
- Position
- chr3:33,024,297-33,024,297
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- T
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