Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CACTGCATCCCCCTGTGGCGGTGCA[A/G]CCGTCATGTGGAGAGCATCGACAAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 608195 | ||||||||||||||||||||
Literature Links: |
LRRC1 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 |
LRRC1 - leucine rich repeat containing 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_018214.4 | 601 | Missense Mutation | AAC,AGC | N,S 11 | NP_060684.4 | |
XM_011514726.2 | 601 | Missense Mutation | AAC,AGC | N,S 11 | XP_011513028.1 | |
XM_011514727.2 | 601 | Intron | XP_011513029.1 | |||
XM_017010997.1 | 601 | Missense Mutation | AAC,AGC | N,S 11 | XP_016866486.1 |