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TTAAAATTGGATGATCCACCTTGAT[A/T]GAAACAGCTGGAGTTTCAAGCACTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 609691 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FHOD3 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
FHOD3 - formin homology 2 domain containing 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001281739.2 | Intron | NP_001268668.1 | ||||
NM_001281740.2 | Intron | NP_001268669.1 | ||||
NM_025135.4 | Intron | NP_079411.2 | ||||
XM_005258349.1 | Intron | XP_005258406.1 | ||||
XM_005258354.1 | Intron | XP_005258411.1 | ||||
XM_005258355.1 | Intron | XP_005258412.1 | ||||
XM_011526189.1 | Intron | XP_011524491.1 | ||||
XM_011526190.1 | Intron | XP_011524492.1 | ||||
XM_011526192.1 | Intron | XP_011524494.1 | ||||
XM_011526193.2 | Intron | XP_011524495.1 | ||||
XM_011526195.1 | Intron | XP_011524497.1 | ||||
XM_011526196.1 | Intron | XP_011524498.1 | ||||
XM_011526197.1 | Intron | XP_011524499.1 | ||||
XM_017026006.1 | Intron | XP_016881495.1 | ||||
XM_017026007.1 | Intron | XP_016881496.1 | ||||
XM_017026008.1 | Intron | XP_016881497.1 | ||||
XM_017026009.1 | Intron | XP_016881498.1 | ||||
XM_017026010.1 | Intron | XP_016881499.1 |