Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGTTTTCTTGCAGATGGTCCTGGGA[A/G]GTTCTGAGAGGAGTGATTGCGTTCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 609759 | ||||||||||||||||||||
Literature Links: |
PRDM7 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 |
PRDM7 - PR domain 7 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001098173.1 | 1251 | Silent Mutation | ACC,ACT | T,T 445 | NP_001091643.1 | |
XM_005256274.3 | 1251 | Silent Mutation | ACC,ACT | T,T 445 | XP_005256331.1 | |
XM_011522829.1 | 1251 | Missense Mutation | CCT,CTT | P,L 351 | XP_011521131.1 | |
XM_011522831.2 | 1251 | Intron | XP_011521133.1 | |||
XM_017022882.1 | 1251 | Intron | XP_016878371.1 | |||
XM_017022883.1 | 1251 | Intron | XP_016878372.1 | |||
XM_017022884.1 | 1251 | Intron | XP_016878373.1 |