Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATTTTGGGTTCAGGTCGTCTTCTGG[G/T]TGTGTGTTTTTTCTCTTGAACTATG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614930 | ||||||||||||||||||||
Literature Links: |
LRRC6 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 |
LRRC6 - leucine rich repeat containing 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001321961.1 | 2072 | Missense Mutation | ACC,CCC | T,P 419 | NP_001308890.1 | |
NM_001321962.1 | 2072 | Missense Mutation | ACC,CCC | T,P 357 | NP_001308891.1 | |
NM_001321963.1 | 2072 | Missense Mutation | ACC,CCC | T,P 319 | NP_001308892.1 | |
NM_001321964.1 | 2072 | Missense Mutation | ACC,CCC | T,P 319 | NP_001308893.1 | |
NM_001321965.1 | 2072 | Missense Mutation | ACC,CCC | T,P 319 | NP_001308894.1 | |
NM_001321966.1 | 2072 | Missense Mutation | ACC,CCC | T,P 299 | NP_001308895.1 | |
NM_012472.5 | 2072 | Missense Mutation | ACC,CCC | T,P 439 | NP_036604.2 | |
XM_006716538.3 | 2072 | Missense Mutation | ACC,CCC | T,P 445 | XP_006716601.2 | |
XM_011516950.2 | 2072 | Missense Mutation | ACC,CCC | T,P 425 | XP_011515252.1 | |
XM_017013296.1 | 2072 | Missense Mutation | ACC,CCC | T,P 405 | XP_016868785.1 | |
XM_017013297.1 | 2072 | Missense Mutation | ACC,CCC | T,P 319 | XP_016868786.1 | |
XM_017013298.1 | 2072 | Missense Mutation | ACC,CCC | T,P 319 | XP_016868787.1 |