Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAGCTGGTCCACGTCCACACGGAGC[A/G]CGTCTTCTGCCTGGGCCTGCCGCAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 606236 MIM: 615128 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ASPSCR1 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
|
ASPSCR1 - ASPSCR1, UBX domain containing tether for SLC2A4 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001251888.1 | 179 | Intron | NP_001238817.1 | |||
NM_024083.3 | 179 | Intron | NP_076988.1 | |||
XM_011523601.2 | 179 | Intron | XP_011521903.1 | |||
XM_011523602.2 | 179 | Intron | XP_011521904.1 | |||
XM_017025036.1 | 179 | Intron | XP_016880525.1 | |||
XM_017025037.1 | 179 | Intron | XP_016880526.1 | |||
XM_017025038.1 | 179 | Intron | XP_016880527.1 | |||
XM_017025039.1 | 179 | Intron | XP_016880528.1 | |||
XM_017025040.1 | 179 | Intron | XP_016880529.1 | |||
XM_017025041.1 | 179 | Intron | XP_016880530.1 | |||
XM_017025042.1 | 179 | Intron | XP_016880531.1 | |||
XM_017025043.1 | 179 | Intron | XP_016880532.1 | |||
XM_017025044.1 | 179 | Intron | XP_016880533.1 |
LRRC45 - leucine rich repeat containing 45 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
STRA13 - stimulated by retinoic acid 13 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271006.1 | 179 | Missense Mutation | NP_001257935.1 | |||
NM_001271007.1 | 179 | Missense Mutation | NP_001257936.1 | |||
NM_144998.3 | 179 | Missense Mutation | NP_659435.2 | |||
XM_005256339.2 | 179 | Missense Mutation | XP_005256396.1 | |||
XM_017024326.1 | 179 | Silent Mutation | XP_016879815.1 | |||
XM_017024327.1 | 179 | Missense Mutation | XP_016879816.1 | |||
XM_017024328.1 | 179 | Missense Mutation | XP_016879817.1 | |||
XM_017024329.1 | 179 | Missense Mutation | XP_016879818.1 |