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- SNP ID:
- rs202076664
- Gene
-
GALNT7HMGB2LOC105377538 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.4: 173332851 - 173332851 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
CATATTTCTCCTTTAGCTTAGCTGC[C/T]TTCTGTTCATATGGTTGTTTATCTT
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 - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
| EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
| SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
| AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
| EUR - Not Available | ||
| AMR - Not Available |
| 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 | 574 | Silent Mutation | AAA,AAG | K,K 147 | NP_001124160.1 | |
| NM_001130689.1 | 574 | Silent Mutation | AAA,AAG | K,K 147 | NP_001124161.1 | |
| NM_002129.3 | 574 | Silent Mutation | AAA,AAG | K,K 147 | NP_002120.1 | |
| LOC105377538 - uncharacterized LOC105377538 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
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