Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCCATGGGAGCACCCTCCGAAGCCC[A/G]TGCACTGGTGACACCATATGGCTTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 606110 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LYNX1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
LYNX1 - Ly6/neurotoxin 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_023946.3 | 108 | Missense Mutation | NP_076435.1 | |||
NM_177457.4 | 108 | Intron | NP_803252.1 | |||
NM_177458.1 | 108 | Missense Mutation | NP_803253.1 | |||
NM_177476.3 | 108 | Intron | NP_803429.1 | |||
NM_177477.3 | 108 | Intron | NP_803430.1 |