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GGAGATGGTTCAGCTGTGGTTCATA[A/C]TGGTTTGCATGTTGCAATCCATCTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZGRF1 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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ZGRF1 - zinc finger GRF-type containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_018392.4 | 6364 | Missense Mutation | CAG,CAT | Q,H 2068 | NP_060862.3 | |
XM_005263115.3 | 6364 | Missense Mutation | CAG,CAT | Q,H 2068 | XP_005263172.1 | |
XM_011532091.2 | 6364 | Missense Mutation | CAG,CAT | Q,H 2051 | XP_011530393.1 | |
XM_011532092.2 | 6364 | Missense Mutation | CAG,CAT | Q,H 2048 | XP_011530394.1 | |
XM_011532093.2 | 6364 | Missense Mutation | CAG,CAT | Q,H 2010 | XP_011530395.1 | |
XM_011532094.2 | 6364 | Missense Mutation | CAG,CAT | Q,H 1982 | XP_011530396.1 | |
XM_011532096.2 | 6364 | Intron | XP_011530398.1 | |||
XM_011532097.2 | 6364 | Missense Mutation | CAG,CAT | Q,H 1117 | XP_011530399.1 | |
XM_011532098.2 | 6364 | Missense Mutation | CAG,CAT | Q,H 1025 | XP_011530400.1 | |
XM_011532099.2 | 6364 | Missense Mutation | CAG,CAT | Q,H 1025 | XP_011530401.1 | |
XM_017008369.1 | 6364 | Missense Mutation | CAG,CAT | Q,H 2048 | XP_016863858.1 | |
XM_017008370.1 | 6364 | Missense Mutation | CAG,CAT | Q,H 1993 | XP_016863859.1 | |
XM_017008371.1 | 6364 | Missense Mutation | CAG,CAT | Q,H 1973 | XP_016863860.1 | |
XM_017008372.1 | 6364 | Missense Mutation | CAG,CAT | Q,H 818 | XP_016863861.1 | |
XM_017008373.1 | 6364 | Missense Mutation | CAG,CAT | Q,H 818 | XP_016863862.1 |