Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGGTCTGACCAGTACCTGGCTAAGC[A/G]CTCCTCTAAGAAATGGTATCGTTCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612803 | ||||||||||||||||||||
Literature Links: |
NARS2 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 |
NARS2 - asparaginyl-tRNA synthetase 2, mitochondrial (putative) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001243251.1 | 1621 | Missense Mutation | CGC,TGC | R,C 191 | NP_001230180.1 | |
NM_024678.5 | 1621 | Missense Mutation | CGC,TGC | R,C 418 | NP_078954.4 | |
XM_011545253.1 | 1621 | Missense Mutation | CGC,TGC | R,C 418 | XP_011543555.1 | |
XM_017018302.1 | 1621 | Intron | XP_016873791.1 | |||
XM_017018303.1 | 1621 | Missense Mutation | CGC,TGC | R,C 191 | XP_016873792.1 | |
XM_017018304.1 | 1621 | Missense Mutation | CGC,TGC | R,C 191 | XP_016873793.1 |