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CCTGTGGGTCTTTATCTTGGGGCAT[C/T]CTTTCCAAGCCACTGAAGGGAGTAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604656 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FMNL1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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FMNL1 - formin like 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005892.3 | Intron | NP_005883.2 | ||||
XM_006722062.3 | Intron | XP_006722125.1 | ||||
XM_006722063.3 | Intron | XP_006722126.1 | ||||
XM_006722064.3 | Intron | XP_006722127.1 | ||||
XM_006722065.3 | Intron | XP_006722128.1 | ||||
XM_006722066.3 | Intron | XP_006722129.1 | ||||
XM_006722069.2 | Intron | XP_006722132.1 | ||||
XM_006722070.3 | Intron | XP_006722133.1 | ||||
XM_011525179.2 | Intron | XP_011523481.1 | ||||
XM_011525180.2 | Intron | XP_011523482.1 | ||||
XM_011525182.2 | Intron | XP_011523484.1 |
LOC339192 - uncharacterized LOC339192 | ||||||
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There are no transcripts associated with this gene. |