Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGGTCACAACAATAAGTCTTCCCAA[A/G]GGGGACCTTCCGGAAAAATAAGCTA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613221 | ||||||||||||||||||||
Literature Links: |
MTCH2 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 |
MTCH2 - mitochondrial carrier 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001317231.1 | 955 | Missense Mutation | CTT,TTT | L,F 291 | NP_001304160.1 | |
NM_001317232.1 | 955 | Missense Mutation | CTT,TTT | L,F 282 | NP_001304161.1 | |
NM_001317233.1 | 955 | Missense Mutation | CTT,TTT | L,F 143 | NP_001304162.1 | |
NM_014342.3 | 955 | Missense Mutation | CTT,TTT | L,F 291 | NP_055157.1 | |
XM_006718172.2 | 955 | UTR 3 | XP_006718235.1 | |||
XM_011519959.2 | 955 | Intron | XP_011518261.1 | |||
XM_011519960.2 | 955 | Intron | XP_011518262.1 | |||
XM_011519961.2 | 955 | Intron | XP_011518263.1 | |||
XM_017017462.1 | 955 | UTR 3 | XP_016872951.1 | |||
XM_017017463.1 | 955 | Missense Mutation | CTT,TTT | L,F 164 | XP_016872952.1 |