Search Thermo Fisher Scientific
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ACCAAAATCCCAACAGCACCATCAA[C/T]GGAATCTAAAGATAAGGAAAATAAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611128 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MDGA2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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MDGA2 - MAM domain containing glycosylphosphatidylinositol anchor 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001113498.2 | 2290 | Missense Mutation | ATT,GTT | I,V 930 | NP_001106970.3 | |
NM_182830.4 | 2290 | Missense Mutation | ATT,GTT | I,V 701 | NP_878250.2 | |
XM_011536519.2 | 2290 | Missense Mutation | ATT,GTT | I,V 954 | XP_011534821.1 | |
XM_011536522.2 | 2290 | Intron | XP_011534824.1 | |||
XM_011536525.2 | 2290 | Missense Mutation | ATT,GTT | I,V 490 | XP_011534827.1 | |
XM_017021060.1 | 2290 | Missense Mutation | ATT,GTT | I,V 545 | XP_016876549.1 | |
XM_017021061.1 | 2290 | Intron | XP_016876550.1 |