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Search Thermo Fisher Scientific
TGAGAAAATTTTGTCTGTGGATAGC[A/G]TGGCAGTGGACTGTGCCTACAGGAC
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613362 | |||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CINP 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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CINP - cyclin dependent kinase 2 interacting protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001320046.1 | 2290 | Intron | NP_001306975.1 | |||
NM_032630.2 | 2290 | Intron | NP_116019.1 |
ZNF839 - zinc finger protein 839 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001267827.1 | 2290 | Missense Mutation | ATG,GTG | M,V 693 | NP_001254756.1 | |
NM_001267828.1 | 2290 | Missense Mutation | ATG,GTG | M,V 693 | NP_001254757.1 | |
NM_018335.4 | 2290 | Missense Mutation | ATG,GTG | M,V 809 | NP_060805.3 | |
XM_006720203.3 | 2290 | Missense Mutation | ATG,GTG | M,V 721 | XP_006720266.2 | |
XM_011536945.1 | 2290 | Missense Mutation | ATG,GTG | M,V 843 | XP_011535247.1 | |
XM_011536946.2 | 2290 | Missense Mutation | ATG,GTG | M,V 793 | XP_011535248.1 | |
XM_011536948.2 | 2290 | Missense Mutation | ATG,GTG | M,V 693 | XP_011535250.1 | |
XM_011536949.2 | 2290 | Intron | XP_011535251.1 | |||
XM_011536950.2 | 2290 | Intron | XP_011535252.1 | |||
XM_017021447.1 | 2290 | Missense Mutation | ATG,GTG | M,V 759 | XP_016876936.1 | |
XM_017021448.1 | 2290 | Intron | XP_016876937.1 | |||
XM_017021449.1 | 2290 | Missense Mutation | ATG,GTG | M,V 474 | XP_016876938.1 | |
XM_017021450.1 | 2290 | Intron | XP_016876939.1 | |||
XM_017021451.1 | 2290 | Intron | XP_016876940.1 |