Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TACATAGGGACTGATCTTACACAAA[C/G]AATAGAGGCTGAGAAAGCACTCTTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606141 | ||||||||||||||||||||
Literature Links: |
RANBP17 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 |
RANBP17 - RAN binding protein 17 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_022897.4 | 88 | Missense Mutation | ACA,AGA | T,R 27 | NP_075048.1 | |
XM_011534627.1 | 88 | Missense Mutation | ACA,AGA | T,R 27 | XP_011532929.1 | |
XM_011534631.2 | 88 | Missense Mutation | ACA,AGA | T,R 29 | XP_011532933.1 | |
XM_011534636.2 | 88 | Missense Mutation | ACA,AGA | T,R 27 | XP_011532938.1 | |
XM_011534637.2 | 88 | Missense Mutation | ACA,AGA | T,R 27 | XP_011532939.1 | |
XM_017009736.1 | 88 | Missense Mutation | ACA,AGA | T,R 27 | XP_016865225.1 | |
XM_017009737.1 | 88 | Missense Mutation | ACA,AGA | T,R 29 | XP_016865226.1 | |
XM_017009738.1 | 88 | Missense Mutation | ACA,AGA | T,R 27 | XP_016865227.1 | |
XM_017009739.1 | 88 | Missense Mutation | ACA,AGA | T,R 27 | XP_016865228.1 | |
XM_017009740.1 | 88 | Missense Mutation | ACA,AGA | T,R 27 | XP_016865229.1 | |
XM_017009741.1 | 88 | Missense Mutation | ACA,AGA | T,R 27 | XP_016865230.1 | |
XM_017009742.1 | 88 | Missense Mutation | ACA,AGA | T,R 27 | XP_016865231.1 | |
XM_017009743.1 | 88 | UTR 5 | XP_016865232.1 | |||
XM_017009744.1 | 88 | Missense Mutation | ACA,AGA | T,R 27 | XP_016865233.1 | |
XM_017009745.1 | 88 | Intron | XP_016865234.1 | |||
XM_017009746.1 | 88 | Missense Mutation | ACA,AGA | T,R 27 | XP_016865235.1 | |
XM_017009747.1 | 88 | Intron | XP_016865236.1 |