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TCACTCCAAGACCTGAATTTATATT[A/G]TAACAACATTCCTTCATTAGTGGAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
LRRC36 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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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 |
LRRC36 - leucine rich repeat containing 36 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001161575.1 | 261 | Intron | NP_001155047.1 | |||
NM_018296.5 | 261 | Missense Mutation | TAT,TGT | Y,C 81 | NP_060766.5 | |
XM_005256025.2 | 261 | Missense Mutation | TAT,TGT | Y,C 81 | XP_005256082.1 | |
XM_005256026.2 | 261 | Missense Mutation | TAT,TGT | Y,C 81 | XP_005256083.1 | |
XM_005256027.2 | 261 | Missense Mutation | TAT,TGT | Y,C 81 | XP_005256084.1 | |
XM_005256028.1 | 261 | UTR 5 | XP_005256085.1 | |||
XM_011523200.1 | 261 | Missense Mutation | TAT,TGT | Y,C 81 | XP_011521502.1 | |
XM_011523201.1 | 261 | Intron | XP_011521503.1 | |||
XM_011523202.2 | 261 | Intron | XP_011521504.1 | |||
XM_011523203.1 | 261 | Missense Mutation | TAT,TGT | Y,C 81 | XP_011521505.1 | |
XM_011523204.1 | 261 | Intron | XP_011521506.1 | |||
XM_011523205.1 | 261 | UTR 5 | XP_011521507.1 | |||
XM_011523206.2 | 261 | Missense Mutation | TAT,TGT | Y,C 81 | XP_011521508.1 | |
XM_017023400.1 | 261 | Missense Mutation | TAT,TGT | Y,C 81 | XP_016878889.1 | |
XM_017023401.1 | 261 | Missense Mutation | TAT,TGT | Y,C 81 | XP_016878890.1 | |
XM_017023402.1 | 261 | Missense Mutation | TAT,TGT | Y,C 81 | XP_016878891.1 |