Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GACTGCCGCTTCCGCCTCCCCGATT[G/T]TGCGGATCTTCTCAGCCTCTGCCTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 131560 | ||||||||||||||||||||
Literature Links: |
FLOT2 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 |
FLOT2 - flotillin 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004475.2 | 1019 | Missense Mutation | AAA,ACA | K,T 321 | NP_004466.2 | |
XM_005257950.3 | 1019 | Missense Mutation | AAA,ACA | K,T 321 | XP_005258007.1 | |
XM_005257953.2 | 1019 | Missense Mutation | AAA,ACA | K,T 244 | XP_005258010.1 | |
XM_017024394.1 | 1019 | Missense Mutation | AAA,ACA | K,T 272 | XP_016879883.1 | |
XM_017024395.1 | 1019 | Missense Mutation | AAA,ACA | K,T 272 | XP_016879884.1 | |
XM_017024396.1 | 1019 | Missense Mutation | AAA,ACA | K,T 272 | XP_016879885.1 |