Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
SETD4 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
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CEPH (CEU)
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EAS
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African American
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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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SETD4 - SET domain containing 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001007259.2 | 1366 | Intron | NP_001007260.1 | |||
NM_001007261.2 | 1366 | Intron | NP_001007262.1 | |||
NM_001286752.1 | 1366 | Missense Mutation | ATA,GTA | I,V 363 | NP_001273681.1 | |
NM_017438.4 | 1366 | Missense Mutation | ATA,GTA | I,V 387 | NP_059134.1 | |
XM_011529636.1 | 1366 | Missense Mutation | ATA,GTA | I,V 387 | XP_011527938.1 | |
XM_011529637.1 | 1366 | Missense Mutation | ATA,GTA | I,V 387 | XP_011527939.1 | |
XM_011529638.2 | 1366 | Missense Mutation | ATA,GTA | I,V 387 | XP_011527940.1 | |
XM_011529639.1 | 1366 | Missense Mutation | ATA,GTA | I,V 387 | XP_011527941.1 | |
XM_011529640.2 | 1366 | Missense Mutation | ATA,GTA | I,V 387 | XP_011527942.1 | |
XM_011529642.1 | 1366 | Missense Mutation | ATA,GTA | I,V 363 | XP_011527944.1 | |
XM_011529643.1 | 1366 | Missense Mutation | ATA,GTA | I,V 363 | XP_011527945.1 | |
XM_011529644.1 | 1366 | Missense Mutation | ATA,GTA | I,V 363 | XP_011527946.1 | |
XM_017028403.1 | 1366 | Missense Mutation | ATA,GTA | I,V 387 | XP_016883892.1 | |
XM_017028404.1 | 1366 | Missense Mutation | ATA,GTA | I,V 363 | XP_016883893.1 | |
XM_017028405.1 | 1366 | Intron | XP_016883894.1 |
Set Membership: |
HapMap Validated |