Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTTCAAGCACAAGAAAATGCCCATG[A/G]TCTTTCTTCTTCTCTTCAATCTAAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZCCHC7 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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ZCCHC7 - zinc finger CCHC-type containing 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001289119.1 | 526 | Missense Mutation | GAT,GGT | D,G 118 | NP_001276048.1 | |
NM_001289120.1 | 526 | Missense Mutation | GAT,GGT | D,G 118 | NP_001276049.1 | |
NM_001289121.1 | 526 | Missense Mutation | GAT,GGT | D,G 118 | NP_001276050.1 | |
NM_032226.2 | 526 | Missense Mutation | GAT,GGT | D,G 118 | NP_115602.2 | |
XM_005251608.4 | 526 | Missense Mutation | GAT,GGT | D,G 118 | XP_005251665.1 | |
XM_005251612.2 | 526 | Missense Mutation | GAT,GGT | D,G 118 | XP_005251669.1 | |
XM_011518050.1 | 526 | Missense Mutation | GAT,GGT | D,G 118 | XP_011516352.1 | |
XM_011518051.2 | 526 | Intron | XP_011516353.1 | |||
XM_017015197.1 | 526 | Missense Mutation | GAT,GGT | D,G 118 | XP_016870686.1 | |
XM_017015198.1 | 526 | Missense Mutation | GAT,GGT | D,G 118 | XP_016870687.1 | |
XM_017015199.1 | 526 | UTR 5 | XP_016870688.1 | |||
XM_017015200.1 | 526 | UTR 5 | XP_016870689.1 | |||
XM_017015201.1 | 526 | Intron | XP_016870690.1 |