Search Thermo Fisher Scientific
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TCCAATCTTGCTCGTCATACCAAAG[C/T]CGTCAATGTTGTGCGTTTTTCTCCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601245 | ||||||||||||||||||||
Literature Links: |
CHAF1B PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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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 |
CHAF1B - chromatin assembly factor 1 subunit B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005441.2 | 377 | Intron | NP_005432.1 | |||
XM_011529755.2 | 377 | UTR 5 | XP_011528057.1 | |||
XM_017028477.1 | 377 | Missense Mutation | GCC,GTC | A,V 68 | XP_016883966.1 | |
XM_017028478.1 | 377 | Missense Mutation | GCC,GTC | A,V 68 | XP_016883967.1 |