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TTTAACAGTTTCAACGAATAGGACT[C/T]GGGGATAGATGCGCTCTCAAGAGGG
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 | |||
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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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CHD7 - chromodomain helicase DNA binding protein 7 | ||||||
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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 |