Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCATCTTCCTGATCAAACTGTCCGT[C/T]GTCTAATTCCCGGAGGACGTTGTCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
RFTN2 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 |
RFTN2 - raftlin family member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_144629.2 | 2075 | Missense Mutation | AAC,GAC | N,D 486 | NP_653230.2 | |
XM_011510595.2 | 2075 | Missense Mutation | AAC,GAC | N,D 496 | XP_011508897.1 | |
XM_011510596.2 | 2075 | Missense Mutation | AAC,GAC | N,D 495 | XP_011508898.1 | |
XM_011510597.2 | 2075 | Missense Mutation | AAC,GAC | N,D 485 | XP_011508899.1 | |
XM_011510598.2 | 2075 | Missense Mutation | AAC,GAC | N,D 479 | XP_011508900.1 | |
XM_017003332.1 | 2075 | Missense Mutation | AAC,GAC | N,D 469 | XP_016858821.1 |