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AACTGCTCAGTGAGTAAGTGGCCAA[C/G]CGCCATTTTGTGTGAGCCTTTTGGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607619 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
FRMD3 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 | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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FRMD3 - FERM domain containing 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001244959.1 | Intron | NP_001231888.1 | ||||
NM_001244960.1 | Intron | NP_001231889.1 | ||||
NM_001244961.1 | Intron | NP_001231890.1 | ||||
NM_001244962.1 | Intron | NP_001231891.1 | ||||
NM_174938.5 | Intron | NP_777598.3 | ||||
XM_017014588.1 | Intron | XP_016870077.1 | ||||
XM_017014589.1 | Intron | XP_016870078.1 | ||||
XM_017014590.1 | Intron | XP_016870079.1 | ||||
XM_017014591.1 | Intron | XP_016870080.1 |
LOC102723989 - uncharacterized LOC102723989 | ||||||
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There are no transcripts associated with this gene. |