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CCACAGGTAGAGCCTGCTGCCTCCC[A/G]TGCAGATGGCCAGCCGCGGCTGCTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
3 submissions
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Phenotype: |
MIM: 604266 MIM: 611460 MIM: 606040 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MEGF6 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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MEGF6 - multiple EGF like domains 6 | ||||||
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There are no transcripts associated with this gene. |
TPRG1L - tumor protein p63 regulated 1-like | ||||||
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There are no transcripts associated with this gene. |
WRAP73 - WD repeat containing, antisense to TP73 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_017818.3 | 1257 | Missense Mutation | ACG,ATG | T,M 392 | NP_060288.3 | |
XM_005244754.1 | 1257 | Missense Mutation | ACG,ATG | T,M 347 | XP_005244811.1 | |
XM_017001387.1 | 1257 | Missense Mutation | ACG,ATG | T,M 385 | XP_016856876.1 |