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TCTTTAGTTTCTTGGTTAGCCACTT[C/T]GGCCTGTTTTCCCTTTGCTCCCCTT
Species: |
Human | ||||||||||||||||||||||||||
dbSNP Submissions: |
9 submissions
|
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Phenotype: |
MIM: 163920 | ||||||||||||||||||||||||||
Literature Links: |
HMGN1 PubMed Links | ||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EUR
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
EAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
SAS - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available | |||
AFR - Not Available | |||||
HMGN1 - high mobility group nucleosome binding domain 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004965.6 | 387 | Intron | NP_004956.5 | |||
XM_011529543.1 | 387 | Intron | XP_011527845.1 | |||
XM_011529544.1 | 387 | Intron | XP_011527846.1 | |||
XM_011529545.1 | 387 | Intron | XP_011527847.1 | |||
XM_011529547.1 | 387 | Intron | XP_011527849.1 | |||
XM_011529549.1 | 387 | Intron | XP_011527851.1 | |||
XM_017028332.1 | 387 | Intron | XP_016883821.1 | |||
XM_017028333.1 | 387 | Intron | XP_016883822.1 | |||
XM_017028334.1 | 387 | Intron | XP_016883823.1 | |||
XM_017028335.1 | 387 | Intron | XP_016883824.1 | |||
XM_017028336.1 | 387 | Intron | XP_016883825.1 | |||
XM_017028338.1 | 387 | Missense Mutation | AAA,GAA | K,E 64 | XP_016883827.1 |