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GCACCCACGCTCCCGCCGCTCTGCT[C/T]GTGCTTCTCTTTGAGCTGTGAAAAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602255 | ||||||||||||||||||||
Literature Links: |
FARP2 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 |
FARP2 - FERM, ARH/RhoGEF and pleckstrin domain protein 2 | ||||||
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There are no transcripts associated with this gene. |
STK25 - serine/threonine kinase 25 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271977.1 | 1179 | Missense Mutation | AAG,GAG | K,E 374 | NP_001258906.1 | |
NM_001271978.1 | 1179 | Missense Mutation | AAG,GAG | K,E 374 | NP_001258907.1 | |
NM_001271979.1 | 1179 | Missense Mutation | AAG,GAG | K,E 297 | NP_001258908.1 | |
NM_001271980.1 | 1179 | Missense Mutation | AAG,GAG | K,E 297 | NP_001258909.1 | |
NM_001282305.1 | 1179 | Missense Mutation | AAG,GAG | K,E 280 | NP_001269234.1 | |
NM_001282306.1 | 1179 | Missense Mutation | AAG,GAG | K,E 300 | NP_001269235.1 | |
NM_001282307.1 | 1179 | Missense Mutation | AAG,GAG | K,E 280 | NP_001269236.1 | |
NM_001282308.1 | 1179 | Missense Mutation | AAG,GAG | K,E 280 | NP_001269237.1 | |
NM_006374.4 | 1179 | Missense Mutation | AAG,GAG | K,E 374 | NP_006365.2 | |
XM_011510493.2 | 1179 | Intron | XP_011508795.1 | |||
XM_011510494.2 | 1179 | Missense Mutation | AAG,GAG | K,E 300 | XP_011508796.1 | |
XM_011510495.2 | 1179 | Missense Mutation | AAG,GAG | K,E 300 | XP_011508797.1 | |
XM_011510496.2 | 1179 | Intron | XP_011508798.1 | |||
XM_017003168.1 | 1179 | Silent Mutation | ACA,ACG | T,T 335 | XP_016858657.1 | |
XM_017003169.1 | 1179 | Silent Mutation | ACA,ACG | T,T 335 | XP_016858658.1 | |
XM_017003170.1 | 1179 | Missense Mutation | AAG,GAG | K,E 300 | XP_016858659.1 | |
XM_017003171.1 | 1179 | Silent Mutation | ACA,ACG | T,T 241 | XP_016858660.1 |