Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TACCTTAAAGTTAGAAGGTAACTGA[C/T]GATATGCCTGGGTTGAAAGTCCTGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 611524 MIM: 605634 | ||||||||||||||||||||
Literature Links: |
RARS2 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 |
RARS2 - arginyl-tRNA synthetase 2, mitochondrial | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001318785.1 | 1967 | Missense Mutation | ATC,GTC | I,V 347 | NP_001305714.1 | |
NM_020320.4 | 1967 | Missense Mutation | ATC,GTC | I,V 522 | NP_064716.2 | |
XM_011535948.2 | 1967 | Missense Mutation | ATC,GTC | I,V 522 | XP_011534250.1 | |
XM_011535949.2 | 1967 | Intron | XP_011534251.1 | |||
XM_017011072.1 | 1967 | Missense Mutation | ATC,GTC | I,V 347 | XP_016866561.1 | |
XM_017011073.1 | 1967 | Missense Mutation | ATC,GTC | I,V 347 | XP_016866562.1 | |
XM_017011074.1 | 1967 | Missense Mutation | ATC,GTC | I,V 347 | XP_016866563.1 | |
XM_017011075.1 | 1967 | Missense Mutation | ATC,GTC | I,V 347 | XP_016866564.1 | |
XM_017011076.1 | 1967 | Missense Mutation | ATC,GTC | I,V 347 | XP_016866565.1 | |
XM_017011077.1 | 1967 | Missense Mutation | ATC,GTC | I,V 347 | XP_016866566.1 | |
XM_017011078.1 | 1967 | Intron | XP_016866567.1 | |||
XM_017011079.1 | 1967 | Missense Mutation | ATC,GTC | I,V 347 | XP_016866568.1 | |
XM_017011080.1 | 1967 | Missense Mutation | ATC,GTC | I,V 347 | XP_016866569.1 | |
XM_017011081.1 | 1967 | Missense Mutation | ATC,GTC | I,V 347 | XP_016866570.1 |
SLC35A1 - solute carrier family 35 member A1 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |