Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGCCTTCTTCCCAGGGCACCGGGGG[C/T]GTGGGTGCTGCGGGCGTGCGCCGAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605453 MIM: 607668 MIM: 608920 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ABCB9 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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ABCB9 - ATP binding cassette subfamily B member 9 | ||||||
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There are no transcripts associated with this gene. |
ARL6IP4 - ADP ribosylation factor like GTPase 6 interacting protein 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001002251.2 | 402 | Missense Mutation | GCG,GTG | A,V 86 | NP_001002251.2 | |
NM_001002252.2 | 402 | Missense Mutation | GCG,GTG | A,V 86 | NP_001002252.2 | |
NM_001278378.1 | 402 | Missense Mutation | GCG,GTG | A,V 86 | NP_001265307.1 | |
NM_001278379.1 | 402 | Intron | NP_001265308.1 | |||
NM_001278380.1 | 402 | UTR 5 | NP_001265309.1 | |||
NM_016638.3 | 402 | Missense Mutation | GCG,GTG | A,V 86 | NP_057722.3 | |
NM_018694.3 | 402 | Missense Mutation | GCG,GTG | A,V 86 | NP_061164.3 |
OGFOD2 - 2-oxoglutarate and iron dependent oxygenase domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001304833.1 | 402 | Intron | NP_001291762.1 | |||
NM_001304834.1 | 402 | Intron | NP_001291763.1 | |||
NM_001304835.1 | 402 | Intron | NP_001291764.1 | |||
NM_001304836.1 | 402 | Intron | NP_001291765.1 | |||
NM_001304837.1 | 402 | Intron | NP_001291766.1 | |||
NM_001304838.1 | 402 | Intron | NP_001291767.1 | |||
NM_024623.2 | 402 | Intron | NP_078899.1 |
PITPNM2 - phosphatidylinositol transfer protein membrane associated 2 | ||||||
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There are no transcripts associated with this gene. |