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CACGTTGACACTTCCGGATCCGCCG[C/T]AGATTCCTATTGCAGAAAAGCCCCG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 154580 MIM: 607776 | ||||||||||||||||||||
Literature Links: |
MAN2C1 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 |
MAN2C1 - mannosidase alpha class 2C member 1 | ||||||
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There are no transcripts associated with this gene. |
SIN3A - SIN3 transcription regulator family member A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145357.1 | 3572 | Silent Mutation | CTA,CTG | L,L 1130 | NP_001138829.1 | |
NM_001145358.1 | 3572 | Silent Mutation | CTA,CTG | L,L 1130 | NP_001138830.1 | |
NM_015477.2 | 3572 | Silent Mutation | CTA,CTG | L,L 1130 | NP_056292.1 | |
XM_006720465.3 | 3572 | Silent Mutation | CTA,CTG | L,L 1130 | XP_006720528.1 | |
XM_006720466.3 | 3572 | Silent Mutation | CTA,CTG | L,L 1130 | XP_006720529.1 | |
XM_006720467.3 | 3572 | Silent Mutation | CTA,CTG | L,L 1130 | XP_006720530.1 |