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AGCTGGGATCTGAGGCCTAAGCAAG[G/T]TTCCTTTCTTCTTCTGTGAAGTGAC
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 |
---|---|---|
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 |
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 | 1331 | UTR 3 | NP_001231888.1 | |||
NM_001244960.1 | 1331 | Intron | NP_001231889.1 | |||
NM_001244961.1 | 1331 | UTR 3 | NP_001231890.1 | |||
NM_001244962.1 | 1331 | UTR 3 | NP_001231891.1 | |||
NM_174938.5 | 1331 | Intron | NP_777598.3 | |||
XM_017014588.1 | 1331 | Intron | XP_016870077.1 | |||
XM_017014589.1 | 1331 | Intron | XP_016870078.1 | |||
XM_017014590.1 | 1331 | Intron | XP_016870079.1 | |||
XM_017014591.1 | 1331 | Intron | XP_016870080.1 |
LOC102723989 - uncharacterized LOC102723989 | ||||||
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There are no transcripts associated with this gene. |