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Search Thermo Fisher Scientific
TGCTGGTGGGTGCCCTGCTGCACTA[C/T]GCGGCCCTTGTCCAGCACCACAATG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605453 | ||||||||||||||||||||
Literature Links: |
ABCB9 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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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 |
ABCB9 - ATP binding cassette subfamily B member 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001243013.1 | 2462 | Missense Mutation | ATA,GTA | I,V 655 | NP_001229942.1 | |
NM_001243014.1 | 2462 | Intron | NP_001229943.1 | |||
NM_019624.3 | 2462 | Missense Mutation | ATA,GTA | I,V 675 | NP_062570.1 | |
NM_019625.3 | 2462 | Missense Mutation | ATA,GTA | I,V 718 | NP_062571.1 | |
NM_203444.3 | 2462 | Intron | NP_982269.2 | |||
XM_005253558.2 | 2462 | Missense Mutation | ATA,GTA | I,V 500 | XP_005253615.1 | |
XM_011538095.2 | 2462 | Missense Mutation | ATA,GTA | I,V 718 | XP_011536397.1 | |
XM_011538096.2 | 2462 | Missense Mutation | ATA,GTA | I,V 718 | XP_011536398.1 | |
XM_011538098.2 | 2462 | Missense Mutation | ATA,GTA | I,V 500 | XP_011536400.1 | |
XM_011538099.2 | 2462 | Intron | XP_011536401.1 | |||
XM_017019103.1 | 2462 | Missense Mutation | ATA,GTA | I,V 718 | XP_016874592.1 | |
XM_017019104.1 | 2462 | Missense Mutation | ATA,GTA | I,V 437 | XP_016874593.1 |