Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCTGCCTGCTTCTTGCTCCAGCACC[A/G]TGGAATGCCTGCGCAGTTTACCCTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
MRS2 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 |
MRS2 - MRS2, magnesium transporter | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286264.1 | 140 | Missense Mutation | ATG,GTG | M,V 1 | NP_001273193.1 | |
NM_001286265.1 | 140 | Missense Mutation | ATG,GTG | M,V 1 | NP_001273194.1 | |
NM_001286266.1 | 140 | Missense Mutation | ATG,GTG | M,V 1 | NP_001273195.1 | |
NM_020662.3 | 140 | Missense Mutation | ATG,GTG | M,V 1 | NP_065713.1 | |
XM_005249242.1 | 140 | Missense Mutation | ATG,GTG | M,V 1 | XP_005249299.1 |