Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AACAGCACCAACTTCCCCGAGCCCA[C/G]CCGGCCGCCGCTGTTCACGTTCCGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 609691 | ||||||||||||||||||||
Literature Links: |
FHOD3 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
FHOD3 - formin homology 2 domain containing 3 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001281739.2 | 199 | Missense Mutation | ACC,AGC | T,S 26 | NP_001268668.1 | |
NM_001281740.2 | 199 | Missense Mutation | ACC,AGC | T,S 26 | NP_001268669.1 | |
NM_025135.4 | 199 | Missense Mutation | ACC,AGC | T,S 26 | NP_079411.2 | |
XM_005258349.1 | 199 | Missense Mutation | ACC,AGC | T,S 26 | XP_005258406.1 | |
XM_005258354.1 | 199 | Missense Mutation | ACC,AGC | T,S 26 | XP_005258411.1 | |
XM_005258355.1 | 199 | Missense Mutation | ACC,AGC | T,S 26 | XP_005258412.1 | |
XM_011526189.1 | 199 | Missense Mutation | ACC,AGC | T,S 26 | XP_011524491.1 | |
XM_011526190.1 | 199 | Missense Mutation | ACC,AGC | T,S 26 | XP_011524492.1 | |
XM_011526192.1 | 199 | Missense Mutation | ACC,AGC | T,S 26 | XP_011524494.1 | |
XM_011526193.2 | 199 | Missense Mutation | ACC,AGC | T,S 26 | XP_011524495.1 | |
XM_011526195.1 | 199 | Missense Mutation | ACC,AGC | T,S 26 | XP_011524497.1 | |
XM_011526196.1 | 199 | Missense Mutation | ACC,AGC | T,S 26 | XP_011524498.1 | |
XM_011526197.1 | 199 | Missense Mutation | ACC,AGC | T,S 26 | XP_011524499.1 | |
XM_017026006.1 | 199 | Missense Mutation | ACC,AGC | T,S 26 | XP_016881495.1 | |
XM_017026007.1 | 199 | Intron | XP_016881496.1 | |||
XM_017026008.1 | 199 | Missense Mutation | ACC,AGC | T,S 26 | XP_016881497.1 | |
XM_017026009.1 | 199 | Missense Mutation | ACC,AGC | T,S 26 | XP_016881498.1 | |
XM_017026010.1 | 199 | Intron | XP_016881499.1 |