Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CACCTCCTGCCTCATATCACCTTGA[A/C]CTGCAGCCTACACAGAGGAGAAAAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 300385 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
HMGN5 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
HMGN5 - high mobility group nucleosome binding domain 5 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_030763.2 | 299 | Missense Mutation | GGT,GTT | G,V 8 | NP_110390.1 | |
XM_006724688.3 | 299 | Missense Mutation | GGT,GTT | G,V 8 | XP_006724751.1 | |
XM_017029839.1 | 299 | Intron | XP_016885328.1 | |||
XM_017029840.1 | 299 | Intron | XP_016885329.1 |