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AGCACAGCATTAGTCTCTTCTATGA[A/T]ATAATAGCATATTTTCTGGGCTATG
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 |
---|---|---|
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 |
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 | 1363 | Intron | NP_001007260.1 | |||
NM_001007261.2 | 1363 | Intron | NP_001007262.1 | |||
NM_001286752.1 | 1363 | Missense Mutation | ATC,TTC | I,F 362 | NP_001273681.1 | |
NM_017438.4 | 1363 | Missense Mutation | ATC,TTC | I,F 386 | NP_059134.1 | |
XM_011529636.1 | 1363 | Missense Mutation | ATC,TTC | I,F 386 | XP_011527938.1 | |
XM_011529637.1 | 1363 | Missense Mutation | ATC,TTC | I,F 386 | XP_011527939.1 | |
XM_011529638.2 | 1363 | Missense Mutation | ATC,TTC | I,F 386 | XP_011527940.1 | |
XM_011529639.1 | 1363 | Missense Mutation | ATC,TTC | I,F 386 | XP_011527941.1 | |
XM_011529640.2 | 1363 | Missense Mutation | ATC,TTC | I,F 386 | XP_011527942.1 | |
XM_011529642.1 | 1363 | Missense Mutation | ATC,TTC | I,F 362 | XP_011527944.1 | |
XM_011529643.1 | 1363 | Missense Mutation | ATC,TTC | I,F 362 | XP_011527945.1 | |
XM_011529644.1 | 1363 | Missense Mutation | ATC,TTC | I,F 362 | XP_011527946.1 | |
XM_017028403.1 | 1363 | Missense Mutation | ATC,TTC | I,F 386 | XP_016883892.1 | |
XM_017028404.1 | 1363 | Missense Mutation | ATC,TTC | I,F 362 | XP_016883893.1 | |
XM_017028405.1 | 1363 | Intron | XP_016883894.1 |