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- SNP ID:
- rs202098277
- Gene
-
KIAA1429 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.8: 94488775 - 94488775 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
CACTAACAAACTTTCCTCTTGAGCC[C/T]CCACTGCCGCTATTTGCACTAGCCC
Genomic Map
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Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616447
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Literature Links: |
KIAA1429 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 |
| KIAA1429 - KIAA1429 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_015496.4 | 5221 | Silent Mutation | GGA,GGG | G,G 1790 | NP_056311.2 | |
| NM_183009.2 | 5221 | Intron | NP_892121.1 | |||
| XM_017013306.1 | 5221 | Silent Mutation | GGA,GGG | G,G 1455 | XP_016868795.1 | |
| XM_017013307.1 | 5221 | Silent Mutation | GGA,GGG | G,G 1455 | XP_016868796.1 | |
| XM_017013308.1 | 5221 | Silent Mutation | GGA,GGG | G,G 1455 | XP_016868797.1 | |
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