Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCCTCTTGAGCCTCCACTGCCGCTA[C/T]TTGCACTAGCCCAGGAAGGTCCAAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 616447 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KIAA1429 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
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
|
|||||
AMR
|
KIAA1429 - KIAA1429 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015496.4 | 5208 | Missense Mutation | AAT,AGT | N,S 1786 | NP_056311.2 | |
NM_183009.2 | 5208 | Intron | NP_892121.1 | |||
XM_017013306.1 | 5208 | Missense Mutation | AAT,AGT | N,S 1451 | XP_016868795.1 | |
XM_017013307.1 | 5208 | Missense Mutation | AAT,AGT | N,S 1451 | XP_016868796.1 | |
XM_017013308.1 | 5208 | Missense Mutation | AAT,AGT | N,S 1451 | XP_016868797.1 |