Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCGGGTCAGGTTCTTCAGACTCGAC[C/T]GCTGGGCCGACGTGCGGTTCCCAGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
2 submissions
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Phenotype: |
MIM: 610742 | ||||||||||||||||||||
Literature Links: |
MOV10 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 |
MOV10 - Mov10 RISC complex RNA helicase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130079.2 | 1488 | Missense Mutation | CGC,TGC | R,C 81 | NP_001123551.1 | |
NM_001286072.1 | 1488 | Missense Mutation | CGC,TGC | R,C 25 | NP_001273001.1 | |
NM_001321324.1 | 1488 | Missense Mutation | CGC,TGC | R,C 81 | NP_001308253.1 | |
NM_020963.4 | 1488 | Missense Mutation | CGC,TGC | R,C 81 | NP_066014.1 | |
XM_005270869.4 | 1488 | Missense Mutation | CGC,TGC | R,C 25 | XP_005270926.1 | |
XM_005270870.4 | 1488 | Missense Mutation | CGC,TGC | R,C 25 | XP_005270927.1 | |
XM_017001318.1 | 1488 | Missense Mutation | CGC,TGC | R,C 25 | XP_016856807.1 | |
XM_017001319.1 | 1488 | Missense Mutation | CGC,TGC | R,C 81 | XP_016856808.1 |