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CGCCGTCCTCGGCCGTGCAGCTCTC[C/T]GACTCGTCCAGATCGCTCTGGTACA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616416 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ADGRL1 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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ADGRL1 - adhesion G protein-coupled receptor L1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001008701.2 | 4492 | Silent Mutation | TCA,TCG | S,S 1361 | NP_001008701.1 | |
NM_014921.4 | 4492 | Silent Mutation | TCA,TCG | S,S 1356 | NP_055736.2 | |
XM_005259818.3 | 4492 | Silent Mutation | TCA,TCG | S,S 1380 | XP_005259875.1 | |
XM_011527796.2 | 4492 | Silent Mutation | TCA,TCG | S,S 1392 | XP_011526098.1 | |
XM_011527798.2 | 4492 | Silent Mutation | TCA,TCG | S,S 1387 | XP_011526100.1 | |
XM_011527801.2 | 4492 | Silent Mutation | TCA,TCG | S,S 1312 | XP_011526103.1 | |
XM_017026475.1 | 4492 | Silent Mutation | TCA,TCG | S,S 1393 | XP_016881964.1 | |
XM_017026476.1 | 4492 | Silent Mutation | TCA,TCG | S,S 1393 | XP_016881965.1 | |
XM_017026477.1 | 4492 | Silent Mutation | TCA,TCG | S,S 1386 | XP_016881966.1 | |
XM_017026478.1 | 4492 | Silent Mutation | TCA,TCG | S,S 1369 | XP_016881967.1 | |
XM_017026479.1 | 4492 | Silent Mutation | TCA,TCG | S,S 1363 | XP_016881968.1 | |
XM_017026480.1 | 4492 | Silent Mutation | TCA,TCG | S,S 1307 | XP_016881969.1 | |
XM_017026481.1 | 4492 | Intron | XP_016881970.1 |
LOC100507373 - uncharacterized LOC100507373 | ||||||
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There are no transcripts associated with this gene. |