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TGAGAATTTGTTAATGGTGGCAACA[C/T]TGCTGTCCTATGGTGCAGTCATCGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616565 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ANKRD30B PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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ANKRD30B - ankyrin repeat domain 30B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145029.1 | 557 | Silent Mutation | CTG,TTG | L,L 158 | NP_001138501.1 | |
XM_006722325.3 | 557 | Intron | XP_006722388.1 | |||
XM_011525662.2 | 557 | Silent Mutation | CTG,TTG | L,L 158 | XP_011523964.1 | |
XM_011525664.2 | 557 | Intron | XP_011523966.1 | |||
XM_011525665.2 | 557 | Silent Mutation | CTG,TTG | L,L 158 | XP_011523967.1 | |
XM_011525666.2 | 557 | Silent Mutation | CTG,TTG | L,L 158 | XP_011523968.1 |