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TCTCTAATACAACCACCATAGCAGC[A/C]AAAATAGAAGAAGTCTGATTGTTAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 616453 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ZC3H13 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
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
|
ZC3H13 - zinc finger CCCH-type containing 13 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_005266301.3 | 6636 | Intron | XP_005266358.1 | |||
XM_005266302.3 | 6636 | Intron | XP_005266359.1 | |||
XM_005266303.3 | 6636 | Intron | XP_005266360.1 | |||
XM_005266304.3 | 6636 | Intron | XP_005266361.1 | |||
XM_005266305.3 | 6636 | Intron | XP_005266362.1 | |||
XM_005266306.3 | 6636 | Intron | XP_005266363.1 | |||
XM_005266307.3 | 6636 | Intron | XP_005266364.1 | |||
XM_005266308.3 | 6636 | Intron | XP_005266365.1 | |||
XM_005266309.3 | 6636 | Intron | XP_005266366.1 | |||
XM_005266310.3 | 6636 | Intron | XP_005266367.1 | |||
XM_005266311.3 | 6636 | Intron | XP_005266368.1 | |||
XM_005266312.1 | 6636 | UTR 3 | XP_005266369.1 | |||
XM_017020475.1 | 6636 | Intron | XP_016875964.1 | |||
XM_017020476.1 | 6636 | Intron | XP_016875965.1 | |||
XM_017020477.1 | 6636 | Intron | XP_016875966.1 | |||
XM_017020478.1 | 6636 | Intron | XP_016875967.1 | |||
XM_017020479.1 | 6636 | Intron | XP_016875968.1 | |||
XM_017020480.1 | 6636 | Intron | XP_016875969.1 | |||
XM_017020481.1 | 6636 | Intron | XP_016875970.1 | |||
XM_017020482.1 | 6636 | Intron | XP_016875971.1 |