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ACTGCAGTACCGTGGCACCATGATC[A/G]TGGCACGTGAAACCTGAAGAAGAAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612186 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DMXL2 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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DMXL2 - Dmx like 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001174116.1 | 9048 | Silent Mutation | CAC,CAT | H,H 2900 | NP_001167587.1 | |
NM_001174117.1 | 9048 | Silent Mutation | CAC,CAT | H,H 2263 | NP_001167588.1 | |
NM_015263.3 | 9048 | Silent Mutation | CAC,CAT | H,H 2899 | NP_056078.2 | |
XM_005254255.1 | 9048 | Silent Mutation | CAC,CAT | H,H 2921 | XP_005254312.1 | |
XM_005254256.1 | 9048 | Silent Mutation | CAC,CAT | H,H 2920 | XP_005254313.1 | |
XM_011521402.2 | 9048 | Intron | XP_011519704.1 | |||
XM_017022034.1 | 9048 | Silent Mutation | CAC,CAT | H,H 2903 | XP_016877523.1 |