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GGGGCCACGAGTTCCGCTCGCACCA[C/T]GATTACTACATCATTGGTACTGCTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603333 MIM: 602297 MIM: 612661 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DNAH2 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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DNAH2 - dynein axonemal heavy chain 2 | ||||||
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There are no transcripts associated with this gene. |
EFNB3 - ephrin B3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001406.3 | 796 | Silent Mutation | CAC,CAT | H,H 133 | NP_001397.1 |
WRAP53 - WD repeat containing antisense to TP53 | ||||||
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There are no transcripts associated with this gene. |