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ACGGGCTACTCGGGGTCCGTGACAC[G/T]ACACCTCAGTCACCGGGCCAACAAC
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
2 submissions
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Phenotype: |
MIM: 605763 | |||||||||||||||||||||||
Literature Links: |
SLC45A1 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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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)
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EUR - Not Available | |||||
AMR - Not Available |
SLC45A1 - solute carrier family 45 member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001080397.2 | 236 | Missense Mutation | CGA,CTA | R,L 71 | NP_001073866.2 | |
XM_011541530.1 | 236 | Missense Mutation | CGA,CTA | R,L 71 | XP_011539832.1 | |
XM_011541531.1 | 236 | Missense Mutation | CGA,CTA | R,L 71 | XP_011539833.1 |
Set Membership: |
HapMap |