Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTGATGAGACAGGCATCATGGTGGC[A/C]AAAATGAGAGCCAGGCAATCAGCCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611122 | ||||||||||||||||||||
Literature Links: |
ANKRD28 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 |
ANKRD28 - ankyrin repeat domain 28 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001195098.1 | 3267 | Missense Mutation | TTG,TTT | L,F 826 | NP_001182027.1 | |
NM_001195099.1 | 3267 | Missense Mutation | TTG,TTT | L,F 826 | NP_001182028.1 | |
NM_015199.3 | 3267 | Missense Mutation | TTG,TTT | L,F 980 | NP_056014.2 | |
XM_005264996.3 | 3267 | Missense Mutation | TTG,TTT | L,F 1010 | XP_005265053.1 | |
XM_011533540.2 | 3267 | Missense Mutation | TTG,TTT | L,F 1013 | XP_011531842.1 | |
XM_011533541.2 | 3267 | Intron | XP_011531843.1 | |||
XM_011533542.2 | 3267 | Missense Mutation | TTG,TTT | L,F 952 | XP_011531844.1 | |
XM_011533543.2 | 3267 | Missense Mutation | TTG,TTT | L,F 946 | XP_011531845.1 | |
XM_011533545.2 | 3267 | Missense Mutation | TTG,TTT | L,F 924 | XP_011531847.1 | |
XM_011533546.2 | 3267 | Missense Mutation | TTG,TTT | L,F 924 | XP_011531848.1 | |
XM_011533547.2 | 3267 | Missense Mutation | TTG,TTT | L,F 924 | XP_011531849.1 | |
XM_017006026.1 | 3267 | Missense Mutation | TTG,TTT | L,F 826 | XP_016861515.1 | |
XM_017006027.1 | 3267 | Missense Mutation | TTG,TTT | L,F 826 | XP_016861516.1 | |
XM_017006028.1 | 3267 | Intron | XP_016861517.1 | |||
XM_017006029.1 | 3267 | Missense Mutation | TTG,TTT | L,F 608 | XP_016861518.1 |