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Search Thermo Fisher Scientific
AGCAGCAGGGCTTGCCCGTCGATTT[C/G]CTGGGCACGGAATTCCTCTGCTATC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
1 submissions
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Phenotype: |
MIM: 602979 | ||||||||||||||||||||
Literature Links: |
A3GALT2 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 |
A3GALT2 - alpha 1,3-galactosyltransferase 2 | ||||||
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There are no transcripts associated with this gene. |
MIR3605 - microRNA 3605 | ||||||
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There are no transcripts associated with this gene. |
PHC2 - polyhomeotic homolog 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004427.3 | 2889 | Missense Mutation | CAA,GAA | Q,E 285 | NP_004418.2 | |
NM_198040.2 | 2889 | Missense Mutation | CAA,GAA | Q,E 820 | NP_932157.1 | |
XM_005270570.1 | 2889 | Missense Mutation | CAA,GAA | Q,E 285 | XP_005270627.1 | |
XM_011540876.2 | 2889 | Intron | XP_011539178.1 | |||
XM_011540877.2 | 2889 | Intron | XP_011539179.1 | |||
XM_011540878.2 | 2889 | Intron | XP_011539180.1 | |||
XM_017000513.1 | 2889 | Missense Mutation | CAA,GAA | Q,E 843 | XP_016856002.1 | |
XM_017000514.1 | 2889 | Missense Mutation | CAA,GAA | Q,E 843 | XP_016856003.1 | |
XM_017000515.1 | 2889 | Missense Mutation | CAA,GAA | Q,E 843 | XP_016856004.1 | |
XM_017000516.1 | 2889 | Missense Mutation | CAA,GAA | Q,E 821 | XP_016856005.1 | |
XM_017000517.1 | 2889 | Missense Mutation | CAA,GAA | Q,E 821 | XP_016856006.1 | |
XM_017000518.1 | 2889 | Missense Mutation | CAA,GAA | Q,E 821 | XP_016856007.1 | |
XM_017000519.1 | 2889 | UTR 3 | XP_016856008.1 | |||
XM_017000520.1 | 2889 | Missense Mutation | CAA,GAA | Q,E 792 | XP_016856009.1 | |
XM_017000521.1 | 2889 | Missense Mutation | CAA,GAA | Q,E 792 | XP_016856010.1 | |
XM_017000522.1 | 2889 | Intron | XP_016856011.1 |