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TCTTTCCCTGCAGTGATGGTTCATT[C/T]GCATATGAGTCTGTGCCTTGGCAAC
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
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
ZMIZ2 - zinc finger MIZ-type containing 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001300959.1 | 1230 | Silent Mutation | TTC,TTT | F,F 21 | NP_001287888.1 | |
NM_031449.3 | 1230 | Silent Mutation | TTC,TTT | F,F 21 | NP_113637.3 | |
NM_174929.2 | 1230 | Silent Mutation | TTC,TTT | F,F 21 | NP_777589.2 | |
XM_005249866.2 | 1230 | Silent Mutation | TTC,TTT | F,F 21 | XP_005249923.1 | |
XM_005249867.4 | 1230 | Silent Mutation | TTC,TTT | F,F 21 | XP_005249924.1 | |
XM_005249868.4 | 1230 | Silent Mutation | TTC,TTT | F,F 21 | XP_005249925.1 | |
XM_005249869.2 | 1230 | Silent Mutation | TTC,TTT | F,F 21 | XP_005249926.1 | |
XM_005249870.2 | 1230 | Silent Mutation | TTC,TTT | F,F 21 | XP_005249927.1 | |
XM_005249871.2 | 1230 | Silent Mutation | TTC,TTT | F,F 21 | XP_005249928.1 | |
XM_005249872.2 | 1230 | Silent Mutation | TTC,TTT | F,F 21 | XP_005249929.1 | |
XM_005249873.2 | 1230 | Silent Mutation | TTC,TTT | F,F 21 | XP_005249930.1 | |
XM_011515566.1 | 1230 | Intron | XP_011513868.1 | |||
XM_017012674.1 | 1230 | Silent Mutation | TTC,TTT | F,F 21 | XP_016868163.1 |