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TATCAGAGCTAGAGCCGCTTTGACT[A/G]TGTTGATCTGCAGAAGCAGCACTAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607534 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
YAF2 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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YAF2 - YY1 associated factor 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001190977.2 | 632 | Silent Mutation | CAC,CAT | H,H 106 | NP_001177906.1 | |
NM_001190979.2 | 632 | Silent Mutation | CAC,CAT | H,H 172 | NP_001177908.1 | |
NM_001190980.2 | 632 | Intron | NP_001177909.1 | |||
NM_001320080.1 | 632 | Silent Mutation | CAC,CAT | H,H 139 | NP_001307009.1 | |
NM_005748.5 | 632 | Silent Mutation | CAC,CAT | H,H 148 | NP_005739.2 | |
XM_006719184.3 | 632 | Silent Mutation | CAC,CAT | H,H 150 | XP_006719247.1 | |
XM_006719185.3 | 632 | Silent Mutation | CAC,CAT | H,H 145 | XP_006719248.1 | |
XM_011537728.2 | 632 | Silent Mutation | CAC,CAT | H,H 206 | XP_011536030.1 | |
XM_011537729.2 | 632 | Silent Mutation | CAC,CAT | H,H 127 | XP_011536031.1 | |
XM_017018669.1 | 632 | Silent Mutation | CAC,CAT | H,H 155 | XP_016874158.1 | |
XM_017018670.1 | 632 | Intron | XP_016874159.1 |