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- SNP ID:
- rs73005353
- Gene
-
GALNT7HMGB2LOC105377538 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.4: 173332027 - 173332027 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
ACTTGAATTCACATTCTTAGCAAAA[C/T]AATTGCCTGAGCACACACACACATT
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 605005
MIM: 163906
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Literature Links: |
GALNT7 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
| GALNT7 - polypeptide N-acetylgalactosaminyltransferase 7 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| HMGB2 - high mobility group box 2 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001130688.1 | 816 | UTR 3 | NP_001124160.1 | |||
| NM_001130689.1 | 816 | UTR 3 | NP_001124161.1 | |||
| NM_002129.3 | 816 | UTR 3 | NP_002120.1 | |||
| LOC105377538 - uncharacterized LOC105377538 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
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