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CATGCCGCTGCTGAAGCTCTGGGTC[A/G]GGCCAGTGCCCATGGTGGCCCTTTA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608614 | ||||||||||||||||||||
Literature Links: |
CYP4V2 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 |
CYP4V2 - cytochrome P450 family 4 subfamily V member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_207352.3 | 372 | Missense Mutation | AGG,GGG | R,G 95 | NP_997235.3 | |
XM_005262935.3 | 372 | Missense Mutation | AGG,GGG | R,G 95 | XP_005262992.1 | |
XM_017008037.1 | 372 | UTR 5 | XP_016863526.1 |
FLJ38576 - uncharacterized LOC651430 | ||||||
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There are no transcripts associated with this gene. |