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CTTCCTTGCCGTGGGGGGGGCCCTG[A/G]GCAACAGGCCCTTCCGTGCCTTCGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300453 MIM: 300022 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FAM50A 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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FAM50A - family with sequence similarity 50 member A | ||||||
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There are no transcripts associated with this gene. |
MIR6858 - microRNA 6858 | ||||||
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There are no transcripts associated with this gene. |
PLXNA3 - plexin A3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_017514.4 | 230 | Missense Mutation | AGC,GGC | S,G 19 | NP_059984.3 | |
XM_005274705.4 | 230 | Missense Mutation | AGC,GGC | S,G 19 | XP_005274762.2 | |
XM_005274706.4 | 230 | Intron | XP_005274763.2 | |||
XM_006724829.3 | 230 | Missense Mutation | AGC,GGC | S,G 19 | XP_006724892.1 | |
XM_011531183.2 | 230 | Intron | XP_011529485.1 |