Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGTGTCTGCTTCTGCTGTCTTGGGC[C/T]TTTTCGAGGCCTAAAAATGGAGGAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612778 | ||||||||||||||||||||
Literature Links: |
NRADDP 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 |
NRADDP - neurotrophin receptor associated death domain, pseudogene | ||||||
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There are no transcripts associated with this gene. |
SETD2 - SET domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014159.6 | 8910 | Missense Mutation | AAG,AGG | K,R 2454 | NP_054878.5 | |
XM_011533631.2 | 8910 | Missense Mutation | AAG,AGG | K,R 2480 | XP_011531933.1 | |
XM_011533632.2 | 8910 | Missense Mutation | AAG,AGG | K,R 2462 | XP_011531934.1 | |
XM_011533633.2 | 8910 | Missense Mutation | AAG,AGG | K,R 2435 | XP_011531935.1 | |
XM_011533634.1 | 8910 | Missense Mutation | AAG,AGG | K,R 2410 | XP_011531936.1 | |
XM_017006270.1 | 8910 | Missense Mutation | AAG,AGG | K,R 2380 | XP_016861759.1 |