Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGCCTACATCACTGAAATGAAACTG[A/G]TGGCACAGAAGGTAAGGGCTGCAGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 608795 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ACBD4 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
ACBD4 - acyl-CoA binding domain containing 4 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001135705.2 | 1122 | Missense Mutation | ATG,GTG | M,V 95 | NP_001129177.1 | |
NM_001135706.2 | 1122 | Missense Mutation | ATG,GTG | M,V 95 | NP_001129178.1 | |
NM_001135707.2 | 1122 | Missense Mutation | ATG,GTG | M,V 95 | NP_001129179.1 | |
NM_001321352.1 | 1122 | Missense Mutation | ATG,GTG | M,V 95 | NP_001308281.1 | |
NM_001321353.1 | 1122 | Missense Mutation | ATG,GTG | M,V 95 | NP_001308282.1 | |
NM_024722.3 | 1122 | Missense Mutation | ATG,GTG | M,V 95 | NP_078998.1 | |
XM_006722085.2 | 1122 | Missense Mutation | ATG,GTG | M,V 95 | XP_006722148.1 | |
XM_011525259.2 | 1122 | Missense Mutation | ATG,GTG | M,V 95 | XP_011523561.1 | |
XM_011525261.2 | 1122 | Missense Mutation | ATG,GTG | M,V 95 | XP_011523563.1 | |
XM_017025084.1 | 1122 | Missense Mutation | ATG,GTG | M,V 95 | XP_016880573.1 | |
XM_017025085.1 | 1122 | Missense Mutation | ATG,GTG | M,V 95 | XP_016880574.1 | |
XM_017025086.1 | 1122 | Missense Mutation | ATG,GTG | M,V 95 | XP_016880575.1 | |
XM_017025087.1 | 1122 | Missense Mutation | ATG,GTG | M,V 95 | XP_016880576.1 | |
XM_017025088.1 | 1122 | Missense Mutation | ATG,GTG | M,V 95 | XP_016880577.1 | |
XM_017025089.1 | 1122 | Missense Mutation | ATG,GTG | M,V 95 | XP_016880578.1 | |
XM_017025090.1 | 1122 | Missense Mutation | ATG,GTG | M,V 95 | XP_016880579.1 | |
XM_017025091.1 | 1122 | Missense Mutation | ATG,GTG | M,V 95 | XP_016880580.1 | |
XM_017025092.1 | 1122 | Missense Mutation | ATG,GTG | M,V 95 | XP_016880581.1 | |
XM_017025093.1 | 1122 | Missense Mutation | ATG,GTG | M,V 95 | XP_016880582.1 | |
XM_017025094.1 | 1122 | Missense Mutation | ATG,GTG | M,V 95 | XP_016880583.1 | |
XM_017025095.1 | 1122 | Missense Mutation | ATG,GTG | M,V 95 | XP_016880584.1 | |
XM_017025096.1 | 1122 | Missense Mutation | ATG,GTG | M,V 95 | XP_016880585.1 | |
XM_017025097.1 | 1122 | Missense Mutation | ATG,GTG | M,V 95 | XP_016880586.1 | |
XM_017025098.1 | 1122 | Missense Mutation | ATG,GTG | M,V 95 | XP_016880587.1 | |
XM_017025099.1 | 1122 | Missense Mutation | ATG,GTG | M,V 95 | XP_016880588.1 | |
XM_017025100.1 | 1122 | Missense Mutation | ATG,GTG | M,V 95 | XP_016880589.1 | |
XM_017025101.1 | 1122 | Missense Mutation | ATG,GTG | M,V 95 | XP_016880590.1 |
PLCD3 - phospholipase C delta 3 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |