Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCGGGTGCTGTTGGCCTCTCCCTCG[G/C]CCGGCTGGTTGGAGATGAAAGCGAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 609791 | ||||||||||||||||||||
Literature Links: |
LINGO1 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 |
LINGO1 - leucine rich repeat and Ig domain containing 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001301186.1 | 1804 | Missense Mutation | GCC,GGC | A,G 531 | NP_001288115.1 | |
NM_001301187.1 | 1804 | Missense Mutation | GCC,GGC | A,G 531 | NP_001288116.1 | |
NM_001301189.1 | 1804 | Missense Mutation | GCC,GGC | A,G 531 | NP_001288118.1 | |
NM_001301191.1 | 1804 | Missense Mutation | GCC,GGC | A,G 531 | NP_001288120.1 | |
NM_001301192.1 | 1804 | Missense Mutation | GCC,GGC | A,G 531 | NP_001288121.1 | |
NM_001301194.1 | 1804 | Missense Mutation | GCC,GGC | A,G 531 | NP_001288123.1 | |
NM_001301195.1 | 1804 | Missense Mutation | GCC,GGC | A,G 531 | NP_001288124.1 | |
NM_001301197.1 | 1804 | Missense Mutation | GCC,GGC | A,G 531 | NP_001288126.1 | |
NM_001301198.1 | 1804 | Missense Mutation | GCC,GGC | A,G 531 | NP_001288127.1 | |
NM_001301199.1 | 1804 | Missense Mutation | GCC,GGC | A,G 531 | NP_001288128.1 | |
NM_001301200.1 | 1804 | Missense Mutation | GCC,GGC | A,G 531 | NP_001288129.1 | |
NM_032808.6 | 1804 | Missense Mutation | GCC,GGC | A,G 537 | NP_116197.4 | |
XM_011522118.2 | 1804 | Missense Mutation | GCC,GGC | A,G 531 | XP_011520420.1 | |
XM_017022682.1 | 1804 | Missense Mutation | GCC,GGC | A,G 531 | XP_016878171.1 |