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ATACGGCACTCCGAACAGACACTAA[A/G]AACAGCTCTCATCTCAAAGAACCCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 615169 MIM: 610008 | ||||||||||||||||||||
Literature Links: |
AMZ2 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 |
AMZ2 - archaelysin family metallopeptidase 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001033569.1 | 690 | Intron | NP_001028741.1 | |||
NM_001033570.1 | 690 | Intron | NP_001028742.1 | |||
NM_001033571.1 | 690 | Intron | NP_001028743.1 | |||
NM_001033572.1 | 690 | Intron | NP_001028744.1 | |||
NM_001033574.1 | 690 | Intron | NP_001028746.1 | |||
NM_001289054.1 | 690 | Intron | NP_001275983.1 | |||
NM_001289056.1 | 690 | Intron | NP_001275985.1 | |||
NM_016627.4 | 690 | Intron | NP_057711.3 | |||
XM_005257432.4 | 690 | Missense Mutation | AAA,AGA | K,R 76 | XP_005257489.1 | |
XM_005257433.3 | 690 | Intron | XP_005257490.1 | |||
XM_005257435.4 | 690 | Intron | XP_005257492.1 | |||
XM_005257436.3 | 690 | Intron | XP_005257493.1 | |||
XM_006721940.2 | 690 | Intron | XP_006722003.1 | |||
XM_017024723.1 | 690 | Missense Mutation | AAA,AGA | K,R 12 | XP_016880212.1 | |
XM_017024724.1 | 690 | Intron | XP_016880213.1 | |||
XM_017024725.1 | 690 | UTR 5 | XP_016880214.1 | |||
XM_017024726.1 | 690 | Intron | XP_016880215.1 | |||
XM_017024727.1 | 690 | Intron | XP_016880216.1 | |||
XM_017024728.1 | 690 | UTR 5 | XP_016880217.1 |
ARSG - arylsulfatase G | ||||||
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There are no transcripts associated with this gene. |