Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTTATAGAATATTTTGGAAAAATGC[C/T]TACTGAGAGAGGGCACAAATTATCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607481 | ||||||||||||||||||||
Literature Links: |
MMAA 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 |
MMAA - methylmalonic aciduria (cobalamin deficiency) cblA type | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_172250.2 | 663 | Missense Mutation | CCT,CTT | P,L 167 | NP_758454.1 | |
XM_011531684.2 | 663 | Missense Mutation | CCT,CTT | P,L 167 | XP_011529986.1 | |
XM_011531685.2 | 663 | Missense Mutation | CCT,CTT | P,L 167 | XP_011529987.1 | |
XM_011531686.2 | 663 | Missense Mutation | CCT,CTT | P,L 2 | XP_011529988.1 |