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AGCTAGGGTCCAGAATGTTTGTCAC[G/T]CGGCGCTCTCTCTCTTGCTTCCATA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608858 MIM: 605181 | ||||||||||||||||||||
Literature Links: |
FGFR1OP2 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 |
FGFR1OP2 - FGFR1 oncogene partner 2 | ||||||
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There are no transcripts associated with this gene. |
TM7SF3 - transmembrane 7 superfamily member 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_016551.2 | 1930 | Silent Mutation | CGA,CGC | R,R 527 | NP_057635.1 | |
XM_005253391.3 | 1930 | Silent Mutation | CGA,CGC | R,R 476 | XP_005253448.1 | |
XM_011520690.2 | 1930 | Silent Mutation | CGA,CGC | R,R 405 | XP_011518992.1 | |
XM_011520691.1 | 1930 | Intron | XP_011518993.1 | |||
XM_017019463.1 | 1930 | Silent Mutation | CGA,CGC | R,R 557 | XP_016874952.1 | |
XM_017019464.1 | 1930 | Silent Mutation | CGA,CGC | R,R 425 | XP_016874953.1 | |
XM_017019465.1 | 1930 | Silent Mutation | CGA,CGC | R,R 374 | XP_016874954.1 | |
XM_017019466.1 | 1930 | Silent Mutation | CGA,CGC | R,R 354 | XP_016874955.1 |