Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTGGGGCCCAAGTTCATGTAGGTTG[C/G]TGGCAGCTGCACATAATGGTCCCCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600168 | ||||||||||||||||||||
Literature Links: |
MST1R 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 |
MST1R - macrophage stimulating 1 receptor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001244937.2 | 4098 | Missense Mutation | CCA,GCA | P,A 1309 | NP_001231866.1 | |
NM_001318913.1 | 4098 | Missense Mutation | CCA,GCA | P,A 1252 | NP_001305842.1 | |
NM_002447.3 | 4098 | Missense Mutation | CCA,GCA | P,A 1358 | NP_002438.2 | |
XM_005265170.4 | 4098 | Missense Mutation | CCA,GCA | P,A 1359 | XP_005265227.2 | |
XM_011533739.2 | 4098 | Missense Mutation | CCA,GCA | P,A 1319 | XP_011532041.1 | |
XM_011533740.2 | 4098 | Missense Mutation | CCA,GCA | P,A 1310 | XP_011532042.1 | |
XM_011533741.2 | 4098 | Missense Mutation | CCA,GCA | P,A 1290 | XP_011532043.1 | |
XM_011533742.2 | 4098 | Missense Mutation | ACC,AGC | T,S 1313 | XP_011532044.1 | |
XM_011533743.2 | 4098 | Missense Mutation | CCA,GCA | P,A 1258 | XP_011532045.1 | |
XM_011533744.2 | 4098 | Missense Mutation | CCA,GCA | P,A 1253 | XP_011532046.1 |