Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGCTTCCTGCTTTTCCTCCTTCTTC[C/T]CTTTAGCACCTCTGCTAATCTTTGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 604502 | ||||||||||||||||||||
Literature Links: |
HMGN3 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 |
HMGN3 - high mobility group nucleosomal binding domain 3 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001201362.1 | 363 | Missense Mutation | GAG,GGG | E,G 62 | NP_001188291.1 | |
NM_001201363.1 | 363 | Missense Mutation | GAG,GGG | E,G 62 | NP_001188292.1 | |
NM_001318884.1 | 363 | Missense Mutation | GAG,GGG | E,G 62 | NP_001305813.1 | |
NM_001318885.1 | 363 | Missense Mutation | GAG,GGG | E,G 45 | NP_001305814.1 | |
NM_001318886.1 | 363 | Missense Mutation | GAG,GGG | E,G 62 | NP_001305815.1 | |
NM_001318887.1 | 363 | Missense Mutation | GAG,GGG | E,G 62 | NP_001305816.1 | |
NM_001318888.1 | 363 | Intron | NP_001305817.1 | |||
NM_004242.3 | 363 | Missense Mutation | GAG,GGG | E,G 62 | NP_004233.1 | |
NM_138730.2 | 363 | Missense Mutation | GAG,GGG | E,G 62 | NP_620058.1 |