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TACTGGTGCTGAGCTTGGCTCTTGC[A/G]GACAGTGGGATCAGCCTGAATGCCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616103 MIM: 600342 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LRIT1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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LRIT1 - leucine rich repeat, Ig-like and transmembrane domains 1 | ||||||
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There are no transcripts associated with this gene. |
RGR - retinal G protein coupled receptor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001012720.1 | 221 | Silent Mutation | GCA,GCG | A,A 61 | NP_001012738.1 | |
NM_001012722.1 | 221 | Silent Mutation | GCA,GCG | A,A 61 | NP_001012740.1 | |
NM_002921.3 | 221 | Silent Mutation | GCA,GCG | A,A 61 | NP_002912.2 |