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TGTCCTCTCCCTGGCCGAAGACCAC[A/G]ACCCCTATGGTAACTCCCTCACCCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611947 MIM: 607146 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CCDC153 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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CCDC153 - coiled-coil domain containing 153 | ||||||
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There are no transcripts associated with this gene. |
NLRX1 - NLR family member X1 | ||||||
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There are no transcripts associated with this gene. |
PDZD3 - PDZ domain containing 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001168468.1 | 147 | Missense Mutation | AAC,GAC | N,D 37 | NP_001161940.1 | |
NM_024791.3 | 147 | Missense Mutation | AAC,GAC | N,D 37 | NP_079067.3 | |
XM_011543000.2 | 147 | UTR 5 | XP_011541302.1 | |||
XM_011543001.2 | 147 | UTR 5 | XP_011541303.1 | |||
XM_011543002.2 | 147 | UTR 5 | XP_011541304.1 | |||
XM_011543005.2 | 147 | Missense Mutation | AAC,GAC | N,D 38 | XP_011541307.1 | |
XM_017018334.1 | 147 | UTR 5 | XP_016873823.1 | |||
XM_017018335.1 | 147 | UTR 5 | XP_016873824.1 | |||
XM_017018336.1 | 147 | UTR 5 | XP_016873825.1 | |||
XM_017018337.1 | 147 | UTR 5 | XP_016873826.1 |