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TGAGCAGGACATTGGTTACCGAAGC[C/T]GAATGTCATCTCCCTGCTGGAGCAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604077 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ZNF135 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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ZNF135 - zinc finger protein 135 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001164527.1 | 103 | Intron | NP_001157999.1 | |||
NM_001164529.1 | 103 | Missense Mutation | CCG,CTG | P,L 72 | NP_001158001.1 | |
NM_001164530.1 | 103 | Missense Mutation | CCG,CTG | P,L 72 | NP_001158002.1 | |
NM_001289401.1 | 103 | Missense Mutation | CCG,CTG | P,L 60 | NP_001276330.1 | |
NM_001289402.1 | 103 | Missense Mutation | CCG,CTG | P,L 18 | NP_001276331.1 | |
NM_003436.3 | 103 | Missense Mutation | CCG,CTG | P,L 60 | NP_003427.3 | |
NM_007134.1 | 103 | Missense Mutation | CCG,CTG | P,L 72 | NP_009065.1 | |
XM_005259211.1 | 103 | Missense Mutation | CCG,CTG | P,L 72 | XP_005259268.1 | |
XM_006723362.3 | 103 | Missense Mutation | CCG,CTG | P,L 60 | XP_006723425.1 | |
XM_006723363.3 | 103 | Missense Mutation | CCG,CTG | P,L 60 | XP_006723426.1 | |
XM_017027240.1 | 103 | Missense Mutation | CCG,CTG | P,L 60 | XP_016882729.1 | |
XM_017027241.1 | 103 | Missense Mutation | CCG,CTG | P,L 18 | XP_016882730.1 | |
XM_017027242.1 | 103 | Nonsense Mutation | CGA,TGA | R,* 30 | XP_016882731.1 |
ZSCAN1 - zinc finger and SCAN domain containing 1 | ||||||
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There are no transcripts associated with this gene. |