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CTTCCTGTAGAGGGTGAGCGAGAGC[C/T]GGACCCACCGGATGACCGGGATGCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 136425 MIM: 600829 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FOLR2 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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FOLR2 - folate receptor beta | ||||||
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There are no transcripts associated with this gene. |
INPPL1 - inositol polyphosphate phosphatase like 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001567.3 | 673 | Missense Mutation | CCG,CTG | P,L 123 | NP_001558.3 | |
XM_005273978.3 | 673 | Missense Mutation | CCG,CTG | P,L 123 | XP_005274035.1 | |
XM_005273979.4 | 673 | Missense Mutation | CCG,CTG | P,L 123 | XP_005274036.1 | |
XM_011544999.2 | 673 | Missense Mutation | CCG,CTG | P,L 123 | XP_011543301.1 | |
XM_011545000.2 | 673 | Missense Mutation | CCG,CTG | P,L 123 | XP_011543302.1 | |
XM_017017673.1 | 673 | Missense Mutation | CCG,CTG | P,L 113 | XP_016873162.1 |