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AGGCTTGATCAACTTTACCGTCATG[C/T]ATTGCTCCCATGAGGCTGATTCTGG
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 615634 | |||||||||||||||||||||||
Literature Links: |
CHCHD6 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
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 |
CHCHD6 - coiled-coil-helix-coiled-coil-helix domain containing 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001320610.1 | Intron | NP_001307539.1 | ||||
NM_032343.2 | Intron | NP_115719.1 | ||||
XM_011513234.1 | Intron | XP_011511536.1 | ||||
XM_011513235.2 | Intron | XP_011511537.1 | ||||
XM_017007320.1 | Intron | XP_016862809.1 | ||||
XM_017007321.1 | Intron | XP_016862810.1 | ||||
XM_017007322.1 | Intron | XP_016862811.1 |