Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGGCGAGCCCCCTCTCCTGCGCTCG[A/G]GGGACCTCCTCTGCTCCAGGAGTCT
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 602625 | |||||||||||||||||||||||
Literature Links: |
MAGI1 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
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 |
MAGI1 - membrane associated guanylate kinase, WW and PDZ domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001033057.1 | 4858 | Missense Mutation | CCC,CTC | P,L 1384 | NP_001028229.1 | |
NM_004742.2 | 4858 | Intron | NP_004733.2 | |||
NM_015520.1 | 4858 | UTR 3 | NP_056335.1 | |||
XM_005265563.1 | 4858 | Missense Mutation | CCC,CTC | P,L 1414 | XP_005265620.1 | |
XM_005265564.1 | 4858 | Missense Mutation | CCC,CTC | P,L 1413 | XP_005265621.1 | |
XM_005265565.1 | 4858 | Missense Mutation | CCC,CTC | P,L 1403 | XP_005265622.1 | |
XM_005265566.1 | 4858 | Missense Mutation | CCC,CTC | P,L 1401 | XP_005265623.1 | |
XM_005265568.1 | 4858 | Missense Mutation | CCC,CTC | P,L 1400 | XP_005265625.1 | |
XM_005265570.1 | 4858 | Missense Mutation | CCC,CTC | P,L 1347 | XP_005265627.1 | |
XM_005265571.1 | 4858 | Missense Mutation | CCC,CTC | P,L 1317 | XP_005265628.1 | |
XM_005265574.3 | 4858 | UTR 3 | XP_005265631.1 | |||
XM_006713407.1 | 4858 | Missense Mutation | CCC,CTC | P,L 1415 | XP_006713470.1 | |
XM_006713408.1 | 4858 | Missense Mutation | CCC,CTC | P,L 1414 | XP_006713471.1 | |
XM_006713409.1 | 4858 | Missense Mutation | CCC,CTC | P,L 1414 | XP_006713472.1 | |
XM_006713410.1 | 4858 | Missense Mutation | CCC,CTC | P,L 1401 | XP_006713473.1 | |
XM_006713411.1 | 4858 | Missense Mutation | CCC,CTC | P,L 1387 | XP_006713474.1 | |
XM_006713412.1 | 4858 | Missense Mutation | CCC,CTC | P,L 1385 | XP_006713475.1 | |
XM_006713414.3 | 4858 | UTR 3 | XP_006713477.1 | |||
XM_011534236.1 | 4858 | Missense Mutation | CCC,CTC | P,L 1402 | XP_011532538.1 | |
XM_011534240.2 | 4858 | Missense Mutation | CCC,CTC | P,L 696 | XP_011532542.1 | |
XM_011534241.2 | 4858 | Missense Mutation | CCC,CTC | P,L 668 | XP_011532543.1 | |
XM_017007497.1 | 4858 | Missense Mutation | CCC,CTC | P,L 1413 | XP_016862986.1 | |
XM_017007498.1 | 4858 | Missense Mutation | CCC,CTC | P,L 1412 | XP_016862987.1 | |
XM_017007499.1 | 4858 | Missense Mutation | CCC,CTC | P,L 1380 | XP_016862988.1 | |
XM_017007500.1 | 4858 | Missense Mutation | CCC,CTC | P,L 1377 | XP_016862989.1 | |
XM_017007501.1 | 4858 | Missense Mutation | CCC,CTC | P,L 1374 | XP_016862990.1 | |
XM_017007502.1 | 4858 | UTR 3 | XP_016862991.1 | |||
XM_017007503.1 | 4858 | UTR 3 | XP_016862992.1 | |||
XM_017007504.1 | 4858 | UTR 3 | XP_016862993.1 | |||
XM_017007505.1 | 4858 | UTR 3 | XP_016862994.1 | |||
XM_017007506.1 | 4858 | UTR 3 | XP_016862995.1 | |||
XM_017007507.1 | 4858 | Missense Mutation | CCC,CTC | P,L 1146 | XP_016862996.1 | |
XM_017007508.1 | 4858 | Missense Mutation | CCC,CTC | P,L 1090 | XP_016862997.1 |