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TCATACTTGCAGAGCTCGCAGCAGC[A/G]CGTGTCGGAGCTCTTGATCCACTGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613335 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC102724323 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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LOC102724323 - uncharacterized LOC102724323 | ||||||
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There are no transcripts associated with this gene. |
MARCH8 - membrane associated ring-CH-type finger 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001002266.2 | 1958 | Missense Mutation | CGC,TGC | R,C 121 | NP_001002266.1 | |
NM_001282866.1 | 1958 | Missense Mutation | CGC,TGC | R,C 403 | NP_001269795.1 | |
NM_145021.5 | 1958 | Missense Mutation | CGC,TGC | R,C 121 | NP_659458.2 | |
XM_005271804.2 | 1958 | Missense Mutation | CGC,TGC | R,C 403 | XP_005271861.1 | |
XM_006717704.2 | 1958 | Missense Mutation | CGC,TGC | R,C 403 | XP_006717767.1 | |
XM_011539492.2 | 1958 | Missense Mutation | CGC,TGC | R,C 403 | XP_011537794.1 | |
XM_011539493.2 | 1958 | Missense Mutation | CGC,TGC | R,C 403 | XP_011537795.1 | |
XM_011539494.2 | 1958 | Missense Mutation | CGC,TGC | R,C 403 | XP_011537796.1 | |
XM_011539495.1 | 1958 | Missense Mutation | CGC,TGC | R,C 121 | XP_011537797.1 | |
XM_017015894.1 | 1958 | Missense Mutation | CGC,TGC | R,C 121 | XP_016871383.1 |