Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCTGAGAGCCACCTTGGCGGCCTCC[C/T]GGAAGACGTCCTCCACATTCTCCCG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616551 | ||||||||||||||||||||
Literature Links: |
RHOF 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 |
RHOF - ras homolog family member F, filopodia associated | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_019034.2 | 5019 | Missense Mutation | CAG,CGG | Q,R 186 | NP_061907.2 |
TMEM120B - transmembrane protein 120B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001080825.2 | 5019 | UTR 3 | NP_001074294.2 | |||
XM_005253843.4 | 5019 | Intron | XP_005253900.1 | |||
XM_017018853.1 | 5019 | Intron | XP_016874342.1 | |||
XM_017018854.1 | 5019 | Intron | XP_016874343.1 |