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TCCCTTCACCTATCTTGCAAAATGG[A/G]CATTATCTTATTCTTCTTGCTATCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
9 submissions
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Phenotype: |
MIM: 606373 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FMN2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
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
|
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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FMN2 - formin 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001305424.1 | 145 | Intron | NP_001292353.1 | |||
NM_020066.4 | 145 | Intron | NP_064450.3 | |||
XM_011544237.2 | 145 | Intron | XP_011542539.1 | |||
XM_017001837.1 | 145 | Intron | XP_016857326.1 | |||
XM_017001838.1 | 145 | Intron | XP_016857327.1 | |||
XM_017001839.1 | 145 | UTR 5 | XP_016857328.1 | |||
XM_017001840.1 | 145 | Intron | XP_016857329.1 | |||
XM_017001841.1 | 145 | Intron | XP_016857330.1 | |||
XM_017001842.1 | 145 | Intron | XP_016857331.1 | |||
XM_017001843.1 | 145 | Intron | XP_016857332.1 |
RPS7P5 - ribosomal protein S7 pseudogene 5 | ||||||
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There are no transcripts associated with this gene. |