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ATGTGTTTCCGAGTTAACCAGGAAC[A/G]AATGGCTAAGAGGTTTGCCCAGAAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604500 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MYO19 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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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
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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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MYO19 - myosin XIX | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001033580.2 | 3036 | Intron | NP_001028752.1 | |||
NM_001163735.1 | 3036 | Missense Mutation | CGT,TGT | R,C 795 | NP_001157207.1 | |
NM_025109.5 | 3036 | Missense Mutation | CGT,TGT | R,C 595 | NP_079385.2 | |
XM_011525286.1 | 3036 | Missense Mutation | CGT,TGT | R,C 872 | XP_011523588.1 | |
XM_011525287.1 | 3036 | Missense Mutation | CGT,TGT | R,C 870 | XP_011523589.1 | |
XM_011525290.2 | 3036 | Missense Mutation | CGT,TGT | R,C 826 | XP_011523592.1 | |
XM_017025157.1 | 3036 | Missense Mutation | CGT,TGT | R,C 872 | XP_016880646.1 | |
XM_017025158.1 | 3036 | Missense Mutation | CGT,TGT | R,C 841 | XP_016880647.1 | |
XM_017025159.1 | 3036 | Missense Mutation | CGT,TGT | R,C 828 | XP_016880648.1 | |
XM_017025160.1 | 3036 | Missense Mutation | CGT,TGT | R,C 872 | XP_016880649.1 | |
XM_017025161.1 | 3036 | Missense Mutation | CGT,TGT | R,C 679 | XP_016880650.1 |
ZNHIT3 - zinc finger HIT-type containing 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001281432.1 | 3036 | UTR 3 | NP_001268361.1 | |||
NM_001281433.1 | 3036 | Intron | NP_001268362.1 | |||
NM_001281434.1 | 3036 | Intron | NP_001268363.1 | |||
NM_004773.3 | 3036 | Intron | NP_004764.1 |