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ACAGGGTTTTAAAAACAGAAAATGA[G/T]AACCAGAAGACAAAGTGTATTTTGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615655 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ZRANB3 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
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
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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ZRANB3 - zinc finger RANBP2-type containing 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286568.1 | 4449 | UTR 3 | NP_001273497.1 | |||
NM_001286569.1 | 4449 | UTR 3 | NP_001273498.1 | |||
NM_032143.3 | 4449 | UTR 3 | NP_115519.2 | |||
XM_005263809.1 | 4449 | Intron | XP_005263866.1 | |||
XM_006712788.1 | 4449 | Intron | XP_006712851.1 | |||
XM_011511958.2 | 4449 | Intron | XP_011510260.1 | |||
XM_011511959.2 | 4449 | Intron | XP_011510261.2 | |||
XM_011511960.1 | 4449 | Intron | XP_011510262.1 | |||
XM_011511961.2 | 4449 | Intron | XP_011510263.2 | |||
XM_011511963.1 | 4449 | Intron | XP_011510265.1 | |||
XM_011511966.2 | 4449 | Intron | XP_011510268.2 | |||
XM_017005065.1 | 4449 | Intron | XP_016860554.1 | |||
XM_017005066.1 | 4449 | Intron | XP_016860555.1 | |||
XM_017005067.1 | 4449 | Intron | XP_016860556.1 | |||
XM_017005068.1 | 4449 | Intron | XP_016860557.1 | |||
XM_017005069.1 | 4449 | Intron | XP_016860558.1 | |||
XM_017005070.1 | 4449 | Intron | XP_016860559.1 | |||
XM_017005071.1 | 4449 | Intron | XP_016860560.1 |