Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGTATTTTCTTCTCTAAAGAAAAGG[A/G]TTGTTGTTACCAACTTGAATGGTCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 616054 MIM: 608731 | ||||||||||||||||||||
Literature Links: |
ELP2 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
ELP2 - elongator acetyltransferase complex subunit 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001242875.2 | 205 | Missense Mutation | ATT,GTT | I,V 49 | NP_001229804.1 | |
NM_001242876.2 | 205 | Missense Mutation | ATT,GTT | I,V 49 | NP_001229805.1 | |
NM_001242877.2 | 205 | Missense Mutation | ATT,GTT | I,V 49 | NP_001229806.1 | |
NM_001242878.2 | 205 | Missense Mutation | ATT,GTT | I,V 49 | NP_001229807.1 | |
NM_001242879.2 | 205 | Missense Mutation | ATT,GTT | I,V 49 | NP_001229808.1 | |
NM_001324465.1 | 205 | Missense Mutation | ATT,GTT | I,V 49 | NP_001311394.1 | |
NM_001324466.1 | 205 | Missense Mutation | ATT,GTT | I,V 49 | NP_001311395.1 | |
NM_001324467.1 | 205 | Missense Mutation | ATT,GTT | I,V 49 | NP_001311396.1 | |
NM_001324468.1 | 205 | Intron | NP_001311397.1 | |||
NM_018255.3 | 205 | Missense Mutation | ATT,GTT | I,V 49 | NP_060725.1 |
SLC39A6 - solute carrier family 39 member 6 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |