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TAAAGAGACTTTTGCAATATATTTT[C/T]TCAGAGTCAGCCTTGCATCTGAAAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
1 submissions
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Phenotype: |
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Literature Links: |
ANKRD45 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 |
ANKRD45 - ankyrin repeat domain 45 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_198493.2 | 885 | Missense Mutation | AAA,AGA | K,R 172 | NP_940895.1 | |
XM_011509466.2 | 885 | Missense Mutation | AAA,AGA | K,R 172 | XP_011507768.1 | |
XM_011509467.1 | 885 | Missense Mutation | AAA,AGA | K,R 172 | XP_011507769.1 | |
XM_011509468.1 | 885 | Missense Mutation | AAA,AGA | K,R 172 | XP_011507770.1 | |
XM_011509470.1 | 885 | Missense Mutation | AAA,AGA | K,R 172 | XP_011507772.1 | |
XM_011509471.2 | 885 | Intron | XP_011507773.1 | |||
XM_017001123.1 | 885 | Missense Mutation | AAA,AGA | K,R 192 | XP_016856612.1 | |
XM_017001124.1 | 885 | Intron | XP_016856613.1 |
LOC730159 - uncharacterized LOC730159 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001195190.1 | 885 | Intron | NP_001182119.1 | |||
XM_011509968.2 | 885 | Intron | XP_011508270.1 |