Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCCACAGCCTCTTTCCCGTCCCGAG[C/G]ATGGGCAACTCGGCCTCGAACATCG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 601250 | ||||||||||||||||||||
Literature Links: |
MSRA PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
MSRA - methionine sulfoxide reductase A | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001135670.2 | 314 | Silent Mutation | AGC,AGG | S,R 22 | NP_001129142.1 | |
NM_001135671.2 | 314 | Intron | NP_001129143.1 | |||
NM_001199729.2 | 314 | Intron | NP_001186658.1 | |||
NM_012331.4 | 314 | Silent Mutation | AGC,AGG | S,R 22 | NP_036463.1 | |
XM_011543822.1 | 314 | Missense Mutation | AGC,AGG | S,R 22 | XP_011542124.1 | |
XM_011543823.2 | 314 | Missense Mutation | AGC,AGG | S,R 22 | XP_011542125.1 | |
XM_017013448.1 | 314 | Missense Mutation | AGC,AGG | S,R 22 | XP_016868937.1 | |
XM_017013449.1 | 314 | Intron | XP_016868938.1 | |||
XM_017013450.1 | 314 | Intron | XP_016868939.1 | |||
XM_017013451.1 | 314 | Intron | XP_016868940.1 | |||
XM_017013452.1 | 314 | Intron | XP_016868941.1 | |||
XM_017013453.1 | 314 | Intron | XP_016868942.1 | |||
XM_017013454.1 | 314 | Intron | XP_016868943.1 |