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GAGCCATCAGCCGCTCTCCAACCTG[C/T]GCCCGCTGCCGCAACCATGGTGTCA
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 |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
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 | 231 | Silent Mutation | TGC,TGT | C,C 42 | NP_001035373.1 | |
XM_011527214.1 | 231 | UTR 5 | XP_011525516.1 | |||
XM_011527215.1 | 231 | UTR 5 | XP_011525517.1 | |||
XM_011527216.2 | 231 | Silent Mutation | TGC,TGT | C,C 47 | XP_011525518.1 | |
XM_017027123.1 | 231 | Silent Mutation | TGC,TGT | C,C 47 | XP_016882612.1 | |
XM_017027124.1 | 231 | Silent Mutation | TGC,TGT | C,C 45 | XP_016882613.1 | |
XM_017027125.1 | 231 | Silent Mutation | TGC,TGT | C,C 42 | XP_016882614.1 | |
XM_017027126.1 | 231 | Silent Mutation | TGC,TGT | C,C 42 | XP_016882615.1 | |
XM_017027127.1 | 231 | Silent Mutation | TGC,TGT | C,C 42 | XP_016882616.1 | |
XM_017027128.1 | 231 | Silent Mutation | TGC,TGT | C,C 42 | XP_016882617.1 | |
XM_017027129.1 | 231 | Silent Mutation | TGC,TGT | C,C 47 | XP_016882618.1 |
LYPD4 - LY6/PLAUR domain containing 4 | ||||||
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There are no transcripts associated with this gene. |