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TGGCCTTGCGTAGGCAGCAGGAGGC[A/G]CAGCTAAAGAAGCACCTGATGAGGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614806 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DMRTC2 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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DMRTC2 - DMRT like family C2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040283.2 | 384 | Silent Mutation | GCA,GCG | A,A 93 | NP_001035373.1 | |
XM_011527214.1 | 384 | UTR 5 | XP_011525516.1 | |||
XM_011527215.1 | 384 | UTR 5 | XP_011525517.1 | |||
XM_011527216.2 | 384 | Silent Mutation | GCA,GCG | A,A 98 | XP_011525518.1 | |
XM_017027123.1 | 384 | Silent Mutation | GCA,GCG | A,A 98 | XP_016882612.1 | |
XM_017027124.1 | 384 | Silent Mutation | GCA,GCG | A,A 96 | XP_016882613.1 | |
XM_017027125.1 | 384 | Silent Mutation | GCA,GCG | A,A 93 | XP_016882614.1 | |
XM_017027126.1 | 384 | Silent Mutation | GCA,GCG | A,A 93 | XP_016882615.1 | |
XM_017027127.1 | 384 | Silent Mutation | GCA,GCG | A,A 93 | XP_016882616.1 | |
XM_017027128.1 | 384 | Silent Mutation | GCA,GCG | A,A 93 | XP_016882617.1 | |
XM_017027129.1 | 384 | Silent Mutation | GCA,GCG | A,A 98 | XP_016882618.1 |
LYPD4 - LY6/PLAUR domain containing 4 | ||||||
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There are no transcripts associated with this gene. |