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CAATGAATAACTCTTCTTCAGAGAC[A/G]CGAGGACACCCCCACAGTGCCTCCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602332 | ||||||||||||||||||||
Literature Links: |
NCAPH PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
NCAPH - non-SMC condensin I complex subunit H | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001281710.1 | 86 | Silent Mutation | ACA,ACG | T,T 8 | NP_001268639.1 | |
NM_001281711.1 | 86 | Intron | NP_001268640.1 | |||
NM_001281712.1 | 86 | Intron | NP_001268641.1 | |||
NM_015341.4 | 86 | Silent Mutation | ACA,ACG | T,T 19 | NP_056156.2 | |
XM_005263908.3 | 86 | Silent Mutation | ACA,ACG | T,T 19 | XP_005263965.1 | |
XM_006712388.3 | 86 | Silent Mutation | ACA,ACG | T,T 19 | XP_006712451.1 |