Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTCTGCCTGGGCCTGCCGCACGCCG[C/T]GGACTGCTGCTTCTGCGGTGAGAAA
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 - 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 |
ASPSCR1 - ASPSCR1, UBX domain containing tether for SLC2A4 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001251888.1 | 149 | Intron | NP_001238817.1 | |||
NM_024083.3 | 149 | Intron | NP_076988.1 | |||
XM_011523601.2 | 149 | Intron | XP_011521903.1 | |||
XM_011523602.2 | 149 | Intron | XP_011521904.1 | |||
XM_017025036.1 | 149 | Intron | XP_016880525.1 | |||
XM_017025037.1 | 149 | Intron | XP_016880526.1 | |||
XM_017025038.1 | 149 | Intron | XP_016880527.1 | |||
XM_017025039.1 | 149 | Intron | XP_016880528.1 | |||
XM_017025040.1 | 149 | Intron | XP_016880529.1 | |||
XM_017025041.1 | 149 | Intron | XP_016880530.1 | |||
XM_017025042.1 | 149 | Intron | XP_016880531.1 | |||
XM_017025043.1 | 149 | Intron | XP_016880532.1 | |||
XM_017025044.1 | 149 | 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 | 149 | Missense Mutation | CAC,CGC | H,R 52 | NP_001257935.1 | |
NM_001271007.1 | 149 | Missense Mutation | CAC,CGC | H,R 34 | NP_001257936.1 | |
NM_144998.3 | 149 | Missense Mutation | CAC,CGC | H,R 34 | NP_659435.2 | |
XM_005256339.2 | 149 | Missense Mutation | ACG,GCG | T,A 96 | XP_005256396.1 | |
XM_017024326.1 | 149 | Silent Mutation | CCA,CCG | P,P 138 | XP_016879815.1 | |
XM_017024327.1 | 149 | Missense Mutation | ACG,GCG | T,A 96 | XP_016879816.1 | |
XM_017024328.1 | 149 | Missense Mutation | CAC,CGC | H,R 52 | XP_016879817.1 | |
XM_017024329.1 | 149 | Missense Mutation | CAC,CGC | H,R 34 | XP_016879818.1 |