Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ACCTTCTACCAGTGCCTGGTGACCA[C/T]GCTGCTGTGCAAAGGCCTCAGCGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 605881 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC35C1 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
|
SLC35C1 - solute carrier family 35 member C1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145265.1 | 966 | Missense Mutation | ACG,ATG | T,M 72 | NP_001138737.1 | |
NM_001145266.1 | 966 | Missense Mutation | ACG,ATG | T,M 72 | NP_001138738.1 | |
NM_018389.4 | 966 | Missense Mutation | ACG,ATG | T,M 85 | NP_060859.4 | |
XM_011520202.2 | 966 | Intron | XP_011518504.1 | |||
XM_011520203.2 | 966 | Missense Mutation | ACG,ATG | T,M 85 | XP_011518505.1 |