Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGTTTTCTGAGGTGAGTTTTTCACA[G/T]TCTTTAATTTTTGTTTGCCCTTTTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 604875 MIM: 604485 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MYO9A PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
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
|
|||||
AMR
|
MYO9A - myosin IXA | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_006901.3 | 7958 | Missense Mutation | AAT,ACT | N,T 2504 | NP_008832.2 | |
XM_006720539.2 | 7958 | Missense Mutation | AAT,ACT | N,T 2575 | XP_006720602.1 | |
XM_011521613.2 | 7958 | Missense Mutation | AAT,ACT | N,T 2594 | XP_011519915.1 | |
XM_011521614.2 | 7958 | Missense Mutation | AAT,ACT | N,T 2594 | XP_011519916.1 | |
XM_011521615.2 | 7958 | Missense Mutation | AAT,ACT | N,T 2594 | XP_011519917.1 | |
XM_011521616.2 | 7958 | Missense Mutation | AAT,ACT | N,T 2594 | XP_011519918.1 | |
XM_011521617.2 | 7958 | Missense Mutation | AAT,ACT | N,T 2593 | XP_011519919.1 | |
XM_011521618.2 | 7958 | Missense Mutation | AAT,ACT | N,T 2576 | XP_011519920.1 | |
XM_011521619.2 | 7958 | Missense Mutation | AAT,ACT | N,T 2575 | XP_011519921.1 | |
XM_011521620.2 | 7958 | Missense Mutation | AAT,ACT | N,T 2574 | XP_011519922.1 | |
XM_011521621.2 | 7958 | Missense Mutation | AAT,ACT | N,T 2554 | XP_011519923.1 | |
XM_011521622.2 | 7958 | Missense Mutation | AAT,ACT | N,T 2522 | XP_011519924.1 | |
XM_011521623.2 | 7958 | Missense Mutation | AAT,ACT | N,T 1693 | XP_011519925.1 | |
XM_017022228.1 | 7958 | Missense Mutation | AAT,ACT | N,T 2575 | XP_016877717.1 | |
XM_017022229.1 | 7958 | Missense Mutation | AAT,ACT | N,T 2522 | XP_016877718.1 | |
XM_017022230.1 | 7958 | Missense Mutation | AAT,ACT | N,T 2503 | XP_016877719.1 |
NR2E3 - nuclear receptor subfamily 2 group E member 3 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |