Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTGCCAATGAACTCCATGAACCCCA[G/T]GAAACCTGCCCTGCCCCCTGCGCCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611196 | ||||||||||||||||||||
Literature Links: |
ZMIZ2 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 |
ZMIZ2 - zinc finger MIZ-type containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001300959.1 | 1187 | Missense Mutation | AGG,ATG | R,M 7 | NP_001287888.1 | |
NM_031449.3 | 1187 | Missense Mutation | AGG,ATG | R,M 7 | NP_113637.3 | |
NM_174929.2 | 1187 | Missense Mutation | AGG,ATG | R,M 7 | NP_777589.2 | |
XM_005249866.2 | 1187 | Missense Mutation | AGG,ATG | R,M 7 | XP_005249923.1 | |
XM_005249867.4 | 1187 | Missense Mutation | AGG,ATG | R,M 7 | XP_005249924.1 | |
XM_005249868.4 | 1187 | Missense Mutation | AGG,ATG | R,M 7 | XP_005249925.1 | |
XM_005249869.2 | 1187 | Missense Mutation | AGG,ATG | R,M 7 | XP_005249926.1 | |
XM_005249870.2 | 1187 | Missense Mutation | AGG,ATG | R,M 7 | XP_005249927.1 | |
XM_005249871.2 | 1187 | Missense Mutation | AGG,ATG | R,M 7 | XP_005249928.1 | |
XM_005249872.2 | 1187 | Missense Mutation | AGG,ATG | R,M 7 | XP_005249929.1 | |
XM_005249873.2 | 1187 | Missense Mutation | AGG,ATG | R,M 7 | XP_005249930.1 | |
XM_011515566.1 | 1187 | Intron | XP_011513868.1 | |||
XM_017012674.1 | 1187 | Missense Mutation | AGG,ATG | R,M 7 | XP_016868163.1 |