Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TAGCGTGGTCCACCTCTACAGGGAC[A/G]GGAAGGACCAGCCATTTATGCAGAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 615606 | ||||||||||||||||||||
Literature Links: |
BTNL8 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 |
BTNL8 - butyrophilin like 8 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040462.2 | 247 | Missense Mutation | AGG,GGG | R,G 70 | NP_001035552.1 | |
NM_001159707.1 | 247 | Intron | NP_001153179.1 | |||
NM_001159708.1 | 247 | Missense Mutation | AGG,GGG | R,G 70 | NP_001153180.1 | |
NM_001159709.1 | 247 | Intron | NP_001153181.1 | |||
NM_001159710.1 | 247 | Intron | NP_001153182.1 | |||
NM_024850.2 | 247 | Missense Mutation | AGG,GGG | R,G 70 | NP_079126.1 | |
XM_011534649.1 | 247 | Missense Mutation | AGG,GGG | R,G 70 | XP_011532951.1 | |
XM_011534650.2 | 247 | Missense Mutation | AGG,GGG | R,G 20 | XP_011532952.1 | |
XM_011534651.2 | 247 | Intron | XP_011532953.1 | |||
XM_011534652.2 | 247 | Intron | XP_011532954.1 | |||
XM_011534653.2 | 247 | Intron | XP_011532955.1 |