Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAACTTCTGTGTTCAGGTGGCTCCA[C/T]GAGATCATTTATAGTATGAGGAATA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614014 | ||||||||||||||||||||
Literature Links: |
RNASE9 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 |
RNASE9 - ribonuclease A family member 9 (inactive) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001001673.3 | 716 | Missense Mutation | ATG,GTG | M,V 186 | NP_001001673.2 | |
NM_001110356.1 | 716 | Missense Mutation | ATG,GTG | M,V 186 | NP_001103826.1 | |
NM_001110357.1 | 716 | Missense Mutation | ATG,GTG | M,V 186 | NP_001103827.1 | |
NM_001110358.1 | 716 | Missense Mutation | ATG,GTG | M,V 191 | NP_001103828.1 | |
NM_001110359.1 | 716 | Missense Mutation | ATG,GTG | M,V 191 | NP_001103829.1 | |
NM_001110360.1 | 716 | Missense Mutation | ATG,GTG | M,V 191 | NP_001103830.1 | |
NM_001110361.1 | 716 | Missense Mutation | ATG,GTG | M,V 191 | NP_001103831.1 | |
NM_001289110.1 | 716 | Missense Mutation | ATG,GTG | M,V 186 | NP_001276039.1 |