Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAGGCTGCCGAGTACGGGCTGGTGG[C/T]GCTGGAGGAGAAGCTGACCCTCAAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 602204 | ||||||||||||||||||||
Literature Links: |
BICD1 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 |
BICD1 - BICD cargo adaptor 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001003398.1 | 203 | Missense Mutation | GCG,GTG | A,V 41 | NP_001003398.1 | |
NM_001714.2 | 203 | Missense Mutation | GCG,GTG | A,V 41 | NP_001705.2 | |
XM_005253465.3 | 203 | Missense Mutation | GCG,GTG | A,V 41 | XP_005253522.1 | |
XM_005253466.2 | 203 | Missense Mutation | GCG,GTG | A,V 41 | XP_005253523.1 | |
XM_006719134.3 | 203 | Missense Mutation | GCG,GTG | A,V 41 | XP_006719197.1 | |
XM_011520812.2 | 203 | Missense Mutation | GCG,GTG | A,V 41 | XP_011519114.1 | |
XM_011520813.1 | 203 | Missense Mutation | GCG,GTG | A,V 41 | XP_011519115.1 | |
XM_011520814.2 | 203 | Missense Mutation | GCG,GTG | A,V 41 | XP_011519116.1 | |
XM_011520815.2 | 203 | Missense Mutation | GCG,GTG | A,V 41 | XP_011519117.1 | |
XM_011520816.2 | 203 | Missense Mutation | GCG,GTG | A,V 41 | XP_011519118.1 | |
XM_017019797.1 | 203 | Missense Mutation | GCG,GTG | A,V 41 | XP_016875286.1 |