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TGCCATTCCCCCCACCCAGTCCCCC[A/G]CCCCCACTCTCTGCCGTTGTTCATT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 276903 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
MYO7A PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
---|---|---|---|---|---|---|---|---|
Global
|
Caucasian
|
CEPH (CEU) - Not Available | ||||||
EAS
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African American
|
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
|
MYO7A - myosin VIIA | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000260.3 | Intron | NP_000251.3 | ||||
NM_001127179.2 | Intron | NP_001120651.2 | ||||
NM_001127180.1 | Intron | NP_001120652.1 | ||||
XM_011545044.2 | Intron | XP_011543346.1 | ||||
XM_011545046.2 | Intron | XP_011543348.2 | ||||
XM_011545050.2 | Intron | XP_011543352.1 | ||||
XM_017017778.1 | Intron | XP_016873267.1 | ||||
XM_017017779.1 | Intron | XP_016873268.1 | ||||
XM_017017780.1 | Intron | XP_016873269.1 | ||||
XM_017017781.1 | Intron | XP_016873270.1 | ||||
XM_017017782.1 | Intron | XP_016873271.1 | ||||
XM_017017783.1 | Intron | XP_016873272.1 | ||||
XM_017017784.1 | Intron | XP_016873273.1 | ||||
XM_017017785.1 | Intron | XP_016873274.1 | ||||
XM_017017786.1 | Intron | XP_016873275.1 | ||||
XM_017017787.1 | Intron | XP_016873276.1 | ||||
XM_017017788.1 | Intron | XP_016873277.1 |
Set Membership: |
Validated |