Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGCCGCCTTGTACGGCCACTGCGAG[A/C]GCGTCCCACCGTCGGAGCTGCCTGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 610046 | ||||||||||||||||||||
Literature Links: |
LVRN 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 |
LVRN - laeverin | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_173800.4 | 302 | Missense Mutation | AGC,CGC | S,R 42 | NP_776161.3 | |
XM_011543263.2 | 302 | Missense Mutation | AGC,CGC | S,R 42 | XP_011541565.1 | |
XM_011543264.2 | 302 | Missense Mutation | AGC,CGC | S,R 42 | XP_011541566.1 | |
XM_017009215.1 | 302 | Missense Mutation | AGC,CGC | S,R 42 | XP_016864704.1 |