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TTGTGACTCCTGTTTCCAAGAGTCA[C/T]AGTTTCCAGCTTGGGGGTGAGCTTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606750 | ||||||||||||||||||||
Literature Links: |
ZBP1 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 |
ZBP1 - Z-DNA binding protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001160417.1 | 1251 | Missense Mutation | ATG,GTG | M,V 398 | NP_001153889.1 | |
NM_001160418.1 | 1251 | Missense Mutation | ATG,GTG | M,V 324 | NP_001153890.1 | |
NM_001160419.2 | 1251 | Intron | NP_001153891.1 | |||
NM_001323966.1 | 1251 | Intron | NP_001310895.1 | |||
NM_030776.2 | 1251 | Missense Mutation | ATG,GTG | M,V 399 | NP_110403.2 | |
XM_011529057.2 | 1251 | Intron | XP_011527359.1 | |||
XM_011529058.2 | 1251 | Intron | XP_011527360.1 | |||
XM_017028086.1 | 1251 | Intron | XP_016883575.1 |