Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCCAAGATTATATTTCCACCATTAT[A/T]TAAAGGACAATCCTCCTTAGCAATC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||
Literature Links: |
SLC10A5 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 |
SLC10A5 - solute carrier family 10 member 5 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
ZFAND1 - zinc finger AN1-type containing 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001170796.1 | 729 | Missense Mutation | AAT,TAT | N,Y 236 | NP_001164267.1 | |
NM_001170797.1 | 729 | Intron | NP_001164268.1 | |||
NM_024699.2 | 729 | Missense Mutation | AAT,TAT | N,Y 243 | NP_078975.2 |