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AAAAAGGAATTAATGTAAAAAGTAA[A/C]AAAGAATAAGCTCAAGGATGAAACT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611507 MIM: 611527 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CISD2 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
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CISD2 - CDGSH iron sulfur domain 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001008388.4 | 1676 | Intron | NP_001008389.1 |
SLC9B1 - solute carrier family 9 member B1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001100874.2 | 1676 | UTR 3 | NP_001094344.1 | |||
NM_139173.3 | 1676 | Intron | NP_631912.2 | |||
XM_006714093.3 | 1676 | Intron | XP_006714156.1 | |||
XM_011531622.1 | 1676 | Intron | XP_011529924.1 | |||
XM_011531623.1 | 1676 | Intron | XP_011529925.1 |