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Search Thermo Fisher Scientific
TGTTCCTCCAGGGAGAATGTGCTAC[A/G]AAACCTAGCGGATAAGGCCTTTGAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 154580 MIM: 608844 | ||||||||||||||||||||
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. |
MIR631 - microRNA 631 | ||||||
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There are no transcripts associated with this gene. |
NEIL1 - nei like DNA glycosylase 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256552.1 | 1029 | Missense Mutation | CAA,CGA | Q,R 236 | NP_001243481.1 | |
NM_024608.3 | 1029 | Missense Mutation | CAA,CGA | Q,R 150 | NP_078884.2 | |
XM_005254659.4 | 1029 | Missense Mutation | CAA,CGA | Q,R 150 | XP_005254716.1 | |
XM_006720677.3 | 1029 | Missense Mutation | CAA,CGA | Q,R 227 | XP_006720740.1 | |
XM_006720678.3 | 1029 | Intron | XP_006720741.1 | |||
XM_006720679.3 | 1029 | Missense Mutation | CAA,CGA | Q,R 193 | XP_006720742.1 | |
XM_006720680.1 | 1029 | Missense Mutation | CAA,CGA | Q,R 150 | XP_006720743.1 | |
XM_006720681.1 | 1029 | Missense Mutation | CAA,CGA | Q,R 150 | XP_006720744.1 | |
XM_011522001.2 | 1029 | Missense Mutation | CAA,CGA | Q,R 213 | XP_011520303.2 | |
XM_011522002.1 | 1029 | Missense Mutation | CAA,CGA | Q,R 150 | XP_011520304.1 | |
XM_011522003.2 | 1029 | Missense Mutation | CAA,CGA | Q,R 150 | XP_011520305.1 | |
XM_011522004.2 | 1029 | Missense Mutation | CAA,CGA | Q,R 150 | XP_011520306.1 | |
XM_011522005.1 | 1029 | Missense Mutation | CAA,CGA | Q,R 90 | XP_011520307.1 | |
XM_011522006.1 | 1029 | Missense Mutation | CAA,CGA | Q,R 81 | XP_011520308.1 | |
XM_011522007.1 | 1029 | Missense Mutation | CAA,CGA | Q,R 81 | XP_011520309.1 | |
XM_011522008.1 | 1029 | Missense Mutation | CAA,CGA | Q,R 81 | XP_011520310.1 | |
XM_017022566.1 | 1029 | Intron | XP_016878055.1 | |||
XM_017022567.1 | 1029 | Missense Mutation | CAA,CGA | Q,R 81 | XP_016878056.1 | |
XM_017022568.1 | 1029 | Missense Mutation | CAA,CGA | Q,R 236 | XP_016878057.1 |