Search Thermo Fisher Scientific
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CGCAGACCCTTGACTCAGTCCAACC[A/C]GACAGGGAATGTTCACCTTCAAGTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607568 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
MMAB 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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MMAB - methylmalonic aciduria (cobalamin deficiency) cblB type | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_052845.3 | 1547 | UTR 3 | NP_443077.1 | |||
XM_011538267.2 | 1547 | Intron | XP_011536569.1 | |||
XM_011538268.2 | 1547 | Intron | XP_011536570.1 | |||
XM_011538269.2 | 1547 | Intron | XP_011536571.1 |
Set Membership: |
HapMap |