Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GAGGCAAACCACAGAGCTGCTCACA[C/G]GGCGAAGAGGGCATCCTCTGACCGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 615519 | ||||||||||||||||||||
Literature Links: |
TOM1L2 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 |
TOM1L2 - target of myb1 like 2 membrane trafficking protein | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001033551.2 | 1405 | Missense Mutation | CTG,GTG | L,V 457 | NP_001028723.1 | |
NM_001082968.1 | 1405 | Missense Mutation | CTG,GTG | L,V 507 | NP_001076437.1 | |
NM_001288786.1 | 1405 | Missense Mutation | CTG,GTG | L,V 483 | NP_001275715.1 | |
NM_001288787.1 | 1405 | Missense Mutation | CTG,GTG | L,V 462 | NP_001275716.1 | |
NM_001288788.1 | 1405 | Missense Mutation | CTG,GTG | L,V 389 | NP_001275717.1 | |
NM_001288789.1 | 1405 | Missense Mutation | CTG,GTG | L,V 388 | NP_001275718.1 | |
XM_005256461.2 | 1405 | Missense Mutation | CTG,GTG | L,V 536 | XP_005256518.1 | |
XM_005256462.1 | 1405 | Missense Mutation | CTG,GTG | L,V 491 | XP_005256519.1 | |
XM_005256463.2 | 1405 | Missense Mutation | CTG,GTG | L,V 487 | XP_005256520.1 | |
XM_005256466.1 | 1405 | Missense Mutation | CTG,GTG | L,V 438 | XP_005256523.1 | |
XM_011523662.1 | 1405 | Missense Mutation | CTG,GTG | L,V 486 | XP_011521964.1 | |
XM_017024201.1 | 1405 | Missense Mutation | CTG,GTG | L,V 442 | XP_016879690.1 |