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TGCATTTCAAGACTACCTATTTGAA[A/G]TGATGCAGGCCGTTGAACAGGTTAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610304 MIM: 609178 | ||||||||||||||||||||
Literature Links: |
DERL2 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 |
DERL2 - derlin 2 | ||||||
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There are no transcripts associated with this gene. |
MIS12 - MIS12, kinetochore complex component | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001258217.1 | 584 | Missense Mutation | ATG,GTG | M,V 35 | NP_001245146.1 | |
NM_001258218.1 | 584 | Missense Mutation | ATG,GTG | M,V 35 | NP_001245147.1 | |
NM_001258219.1 | 584 | Missense Mutation | ATG,GTG | M,V 35 | NP_001245148.1 | |
NM_001258220.1 | 584 | Missense Mutation | ATG,GTG | M,V 35 | NP_001245149.1 | |
NM_024039.2 | 584 | Missense Mutation | ATG,GTG | M,V 35 | NP_076944.1 | |
XM_005256797.2 | 584 | Missense Mutation | ATG,GTG | M,V 35 | XP_005256854.1 | |
XM_017025033.1 | 584 | Missense Mutation | ATG,GTG | M,V 35 | XP_016880522.1 | |
XM_017025034.1 | 584 | Missense Mutation | ATG,GTG | M,V 35 | XP_016880523.1 | |
XM_017025035.1 | 584 | Missense Mutation | ATG,GTG | M,V 35 | XP_016880524.1 |