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TATTGATCATCATCCAGTTGCTCCA[A/G]AAGGGTTCTTCTGCGCTTTTCCAAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616285 MIM: 612941 | ||||||||||||||||||||
Literature Links: |
FMNL2 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 |
FMNL2 - formin like 2 | ||||||
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There are no transcripts associated with this gene. |
PRPF40A - pre-mRNA processing factor 40 homolog A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_017892.3 | 3006 | Silent Mutation | CTG,TTG | L,L 923 | NP_060362.3 | |
XM_005246676.4 | 3006 | Silent Mutation | CTG,TTG | L,L 1029 | XP_005246733.3 | |
XM_005246677.4 | 3006 | Silent Mutation | CTG,TTG | L,L 927 | XP_005246734.2 | |
XM_011511446.2 | 3006 | Silent Mutation | CTG,TTG | L,L 1015 | XP_011509748.1 | |
XM_011511447.2 | 3006 | Intron | XP_011509749.1 | |||
XM_011511448.2 | 3006 | Silent Mutation | CTG,TTG | L,L 909 | XP_011509750.1 | |
XM_011511449.2 | 3006 | Silent Mutation | CTG,TTG | L,L 871 | XP_011509751.1 | |
XM_017004453.1 | 3006 | Silent Mutation | CTG,TTG | L,L 1033 | XP_016859942.1 | |
XM_017004454.1 | 3006 | Silent Mutation | CTG,TTG | L,L 1011 | XP_016859943.1 | |
XM_017004455.1 | 3006 | Silent Mutation | CTG,TTG | L,L 905 | XP_016859944.1 | |
XM_017004456.1 | 3006 | Silent Mutation | CTG,TTG | L,L 871 | XP_016859945.1 | |
XM_017004457.1 | 3006 | Silent Mutation | CTG,TTG | L,L 867 | XP_016859946.1 | |
XM_017004458.1 | 3006 | Silent Mutation | CTG,TTG | L,L 853 | XP_016859947.1 | |
XM_017004459.1 | 3006 | Silent Mutation | CTG,TTG | L,L 853 | XP_016859948.1 | |
XM_017004460.1 | 3006 | Silent Mutation | CTG,TTG | L,L 849 | XP_016859949.1 | |
XM_017004461.1 | 3006 | Silent Mutation | CTG,TTG | L,L 849 | XP_016859950.1 |