Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGATCGCCTAGCAGCAGCATTCACA[A/G]AACTTGAATGAACCTGTTGCTGGAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||
Literature Links: |
KIAA1210 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
KIAA1210 - KIAA1210 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020721.1 | 3725 | Missense Mutation | TCT,TTT | S,F 1379 | NP_065772.1 | |
XM_006724774.3 | 3725 | Missense Mutation | TCT,TTT | S,F 1203 | XP_006724837.1 | |
XM_017029688.1 | 3725 | Missense Mutation | TCT,TTT | S,F 1218 | XP_016885177.1 | |
XM_017029689.1 | 3725 | Missense Mutation | TCT,TTT | S,F 1152 | XP_016885178.1 |