Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTCTGATGAAGAATCACTGGCAGAA[C/T]TGTCACTGCTACTGCTACTGGAACT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZCCHC10 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 |
ZCCHC10 - zinc finger CCHC-type containing 10 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001300816.2 | 495 | Intron | NP_001287745.1 | |||
NM_001300817.2 | 495 | Intron | NP_001287746.1 | |||
NM_001300818.2 | 495 | Intron | NP_001287747.1 | |||
NM_001300819.2 | 495 | Intron | NP_001287748.1 | |||
NM_001300822.2 | 495 | Intron | NP_001287751.1 | |||
NM_001308127.1 | 495 | Intron | NP_001295056.1 | |||
NM_001308128.1 | 495 | Intron | NP_001295057.1 | |||
NM_001308129.1 | 495 | Intron | NP_001295058.1 | |||
NM_001308130.1 | 495 | Intron | NP_001295059.1 | |||
NM_017665.3 | 495 | Missense Mutation | AAT,AGT | N,S 96 | NP_060135.1 | |
XM_011543502.1 | 495 | Missense Mutation | AAT,AGT | N,S 114 | XP_011541804.1 | |
XM_011543503.2 | 495 | UTR 3 | XP_011541805.1 |