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TCCCCGTTTTCCGCAGGTAAGTCTT[C/T]TTTAGTTTCTTGGTTAGCCACTTCG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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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 | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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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 | 411 | Intron | NP_004956.5 | |||
XM_011529543.1 | 411 | Intron | XP_011527845.1 | |||
XM_011529544.1 | 411 | Intron | XP_011527846.1 | |||
XM_011529545.1 | 411 | Intron | XP_011527847.1 | |||
XM_011529547.1 | 411 | Intron | XP_011527849.1 | |||
XM_011529549.1 | 411 | Intron | XP_011527851.1 | |||
XM_017028332.1 | 411 | Intron | XP_016883821.1 | |||
XM_017028333.1 | 411 | Intron | XP_016883822.1 | |||
XM_017028334.1 | 411 | Intron | XP_016883823.1 | |||
XM_017028335.1 | 411 | Intron | XP_016883824.1 | |||
XM_017028336.1 | 411 | Intron | XP_016883825.1 | |||
XM_017028338.1 | 411 | Missense Mutation | XP_016883827.1 |