Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CATAAATGTTACAGTTCTTATTGGA[A/T]GTAAACAAGTCAGTGAAGGTACAGA
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610089 | |||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
RINT1 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | CHB (Han Chinese)
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AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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RINT1 - RAD50 interactor 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_021930.4 | 349 | Missense Mutation | AGT,TGT | S,C 40 | NP_068749.3 | |
XM_005250524.3 | 349 | Intron | XP_005250581.1 | |||
XM_011516458.2 | 349 | Intron | XP_011514760.1 | |||
XM_017012496.1 | 349 | Missense Mutation | GAA,GAT | E,D 7 | XP_016867985.1 | |
XM_017012497.1 | 349 | UTR 5 | XP_016867986.1 | |||
XM_017012498.1 | 349 | UTR 5 | XP_016867987.1 |