Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GAGGAGGTCTTTAGAATCCCCAGCC[G/T]TCAAGTAAGTGGGGCTGCTCCTCAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||
Literature Links: |
LRRC27 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
LRRC27 - leucine rich repeat containing 27 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001143757.1 | 347 | Missense Mutation | CGT,CTT | R,L 69 | NP_001137229.1 | |
NM_001143758.1 | 347 | Missense Mutation | CGT,CTT | R,L 69 | NP_001137230.1 | |
NM_001143759.1 | 347 | Missense Mutation | CGT,CTT | R,L 69 | NP_001137231.1 | |
NM_001309474.1 | 347 | Intron | NP_001296403.1 | |||
NM_030626.2 | 347 | Missense Mutation | CGT,CTT | R,L 69 | NP_085129.1 | |
XM_006717983.2 | 347 | Missense Mutation | CGT,CTT | R,L 69 | XP_006718046.1 | |
XM_006717984.2 | 347 | Missense Mutation | CGT,CTT | R,L 69 | XP_006718047.1 | |
XM_011540208.1 | 347 | Missense Mutation | CGT,CTT | R,L 69 | XP_011538510.1 | |
XM_011540209.1 | 347 | Missense Mutation | CGT,CTT | R,L 69 | XP_011538511.1 | |
XM_011540210.2 | 347 | Intron | XP_011538512.1 | |||
XM_017016690.1 | 347 | Missense Mutation | CGT,CTT | R,L 69 | XP_016872179.1 | |
XM_017016691.1 | 347 | Missense Mutation | CGT,CTT | R,L 69 | XP_016872180.1 | |
XM_017016692.1 | 347 | Missense Mutation | CGT,CTT | R,L 69 | XP_016872181.1 | |
XM_017016693.1 | 347 | Missense Mutation | CGT,CTT | R,L 69 | XP_016872182.1 | |
XM_017016694.1 | 347 | UTR 5 | XP_016872183.1 |
STK32C - serine/threonine kinase 32C | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |