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Search Thermo Fisher Scientific
TGGCAGGGAAATGGAAGAGATGGAG[C/T]ATAGACAATTTTCATTTTATTCTAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 608892 | ||||||||||||||||||||
Literature Links: |
CHD7 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 |
CHD7 - chromodomain helicase DNA binding protein 7 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001316690.1 | Intron | NP_001303619.1 | ||||
NM_017780.3 | Intron | NP_060250.2 | ||||
XM_011517553.2 | Intron | XP_011515855.1 | ||||
XM_011517554.2 | Intron | XP_011515856.1 | ||||
XM_011517555.2 | Intron | XP_011515857.1 | ||||
XM_011517560.2 | Intron | XP_011515862.1 | ||||
XM_017013612.1 | Intron | XP_016869101.1 | ||||
XM_017013613.1 | Intron | XP_016869102.1 |