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TGCTGTGATGCCTGGGAGGCCTGGG[A/C]CTGGGCCTGGGCTTGAGCCTGAGCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608524 MIM: 609951 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ING4 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) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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ING4 - inhibitor of growth family member 4 | ||||||
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There are no transcripts associated with this gene. |
ZNF384 - zinc finger protein 384 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001039920.2 | 1820 | Missense Mutation | GCC,TCC | A,S 378 | NP_001035009.1 | |
NM_001135734.2 | 1820 | Missense Mutation | GCC,TCC | A,S 494 | NP_001129206.1 | |
NM_133476.4 | 1820 | Missense Mutation | GCC,TCC | A,S 433 | NP_597733.2 | |
XM_006718969.3 | 1820 | Missense Mutation | GCC,TCC | A,S 263 | XP_006719032.1 | |
XM_011520917.1 | 1820 | Missense Mutation | GCC,TCC | A,S 525 | XP_011519219.1 | |
XM_011520918.1 | 1820 | Missense Mutation | GCC,TCC | A,S 525 | XP_011519220.1 | |
XM_011520919.1 | 1820 | Missense Mutation | GCC,TCC | A,S 525 | XP_011519221.1 | |
XM_011520920.1 | 1820 | Missense Mutation | GCC,TCC | A,S 525 | XP_011519222.1 | |
XM_011520921.2 | 1820 | Missense Mutation | GCC,TCC | A,S 525 | XP_011519223.1 | |
XM_011520922.1 | 1820 | Missense Mutation | GCC,TCC | A,S 509 | XP_011519224.1 | |
XM_011520923.1 | 1820 | Missense Mutation | GCC,TCC | A,S 509 | XP_011519225.1 | |
XM_017018941.1 | 1820 | Missense Mutation | GCC,TCC | A,S 494 | XP_016874430.1 | |
XM_017018942.1 | 1820 | Missense Mutation | GCC,TCC | A,S 494 | XP_016874431.1 | |
XM_017018943.1 | 1820 | Missense Mutation | GCC,TCC | A,S 494 | XP_016874432.1 | |
XM_017018944.1 | 1820 | Missense Mutation | GCC,TCC | A,S 478 | XP_016874433.1 | |
XM_017018945.1 | 1820 | Missense Mutation | GCC,TCC | A,S 478 | XP_016874434.1 | |
XM_017018946.1 | 1820 | Missense Mutation | GCC,TCC | A,S 464 | XP_016874435.1 | |
XM_017018947.1 | 1820 | Missense Mutation | GCC,TCC | A,S 464 | XP_016874436.1 | |
XM_017018948.1 | 1820 | Missense Mutation | GCC,TCC | A,S 448 | XP_016874437.1 | |
XM_017018949.1 | 1820 | Missense Mutation | GCC,TCC | A,S 433 | XP_016874438.1 | |
XM_017018950.1 | 1820 | Missense Mutation | GCC,TCC | A,S 433 | XP_016874439.1 | |
XM_017018951.1 | 1820 | Missense Mutation | GCC,TCC | A,S 417 | XP_016874440.1 | |
XM_017018952.1 | 1820 | Missense Mutation | GCC,TCC | A,S 417 | XP_016874441.1 | |
XM_017018953.1 | 1820 | Missense Mutation | GCC,TCC | A,S 417 | XP_016874442.1 | |
XM_017018954.1 | 1820 | Missense Mutation | GCC,TCC | A,S 349 | XP_016874443.1 |