Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTGGGCGGGGAGCTGAAGTACACGC[A/C]ATGCGCAGCGAGGCCTCGGGTTTTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611870 | ||||||||||||||||||||
Literature Links: |
CNTLN 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 |
CNTLN - centlein | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001114395.2 | 174 | Silent Mutation | GCA,GCC | A,A 33 | NP_001107867.1 | |
NM_001286984.1 | 174 | Silent Mutation | GCA,GCC | A,A 33 | NP_001273913.1 | |
NM_001286985.1 | 174 | Silent Mutation | GCA,GCC | A,A 33 | NP_001273914.1 | |
NM_017738.3 | 174 | Silent Mutation | GCA,GCC | A,A 33 | NP_060208.2 | |
XM_005251492.1 | 174 | Silent Mutation | GCA,GCC | A,A 33 | XP_005251549.1 | |
XM_006716793.3 | 174 | Silent Mutation | GCA,GCC | A,A 33 | XP_006716856.1 | |
XM_011517941.2 | 174 | Silent Mutation | GCA,GCC | A,A 33 | XP_011516243.1 | |
XM_017014839.1 | 174 | Silent Mutation | GCA,GCC | A,A 33 | XP_016870328.1 | |
XM_017014840.1 | 174 | Silent Mutation | GCA,GCC | A,A 33 | XP_016870329.1 | |
XM_017014841.1 | 174 | Silent Mutation | GCA,GCC | A,A 33 | XP_016870330.1 | |
XM_017014842.1 | 174 | Silent Mutation | GCA,GCC | A,A 33 | XP_016870331.1 | |
XM_017014843.1 | 174 | Silent Mutation | GCA,GCC | A,A 33 | XP_016870332.1 | |
XM_017014844.1 | 174 | Intron | XP_016870333.1 | |||
XM_017014845.1 | 174 | Intron | XP_016870334.1 | |||
XM_017014846.1 | 174 | Intron | XP_016870335.1 | |||
XM_017014847.1 | 174 | Intron | XP_016870336.1 |