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Search Thermo Fisher Scientific
GGTGACTTTACAATGCCCTCCACTG[C/T]GTGGCTGACAGGCTTCTTCAACCCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603330 MIM: 194524 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DNAH9 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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DNAH9 - dynein axonemal heavy chain 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001372.3 | 12991 | Missense Mutation | GCG,GTG | A,V 4344 | NP_001363.2 | |
NM_004662.2 | 12991 | Missense Mutation | GCG,GTG | A,V 656 | NP_004653.2 | |
XM_011523703.1 | 12991 | Missense Mutation | GCG,GTG | A,V 4359 | XP_011522005.1 | |
XM_017024292.1 | 12991 | Missense Mutation | GCG,GTG | A,V 4320 | XP_016879781.1 | |
XM_017024293.1 | 12991 | Missense Mutation | GCG,GTG | A,V 3653 | XP_016879782.1 | |
XM_017024294.1 | 12991 | Intron | XP_016879783.1 | |||
XM_017024295.1 | 12991 | Intron | XP_016879784.1 |
ZNF18 - zinc finger protein 18 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001303281.1 | 12991 | Intron | NP_001290210.1 | |||
NM_001303282.1 | 12991 | Intron | NP_001290211.1 | |||
NM_144680.3 | 12991 | Intron | NP_653281.2 | |||
XM_011524002.2 | 12991 | Intron | XP_011522304.1 | |||
XM_017025006.1 | 12991 | Intron | XP_016880495.1 | |||
XM_017025007.1 | 12991 | Intron | XP_016880496.1 | |||
XM_017025008.1 | 12991 | Intron | XP_016880497.1 | |||
XM_017025009.1 | 12991 | Intron | XP_016880498.1 | |||
XM_017025010.1 | 12991 | Intron | XP_016880499.1 | |||
XM_017025011.1 | 12991 | Intron | XP_016880500.1 |