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TGTCTGGTTTCCATACAGTTGATGA[C/T]TTTCTGCCTTTCTGTGGCCAACCGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616520 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
AHCYL2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
AHCYL2 - adenosylhomocysteinase like 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130720.2 | Intron | NP_001124192.1 | ||||
NM_001130722.2 | Intron | NP_001124194.2 | ||||
NM_001130723.2 | Intron | NP_001124195.1 | ||||
NM_015328.3 | Intron | NP_056143.1 | ||||
XM_005250237.1 | Intron | XP_005250294.1 | ||||
XM_011515987.2 | Intron | XP_011514289.1 | ||||
XM_011515988.2 | Intron | XP_011514290.1 | ||||
XM_017011904.1 | Intron | XP_016867393.1 | ||||
XM_017011905.1 | Intron | XP_016867394.1 | ||||
XM_017011906.1 | Intron | XP_016867395.1 | ||||
XM_017011907.1 | Intron | XP_016867396.1 |