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Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604657 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
GLTPD2 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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GLTPD2 - glycolipid transfer protein domain containing 2 | ||||||
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There are no transcripts associated with this gene. |
TM4SF5 - transmembrane 4 L six family member 5 | ||||||
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There are no transcripts associated with this gene. |
VMO1 - vitelline membrane outer layer 1 homolog | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001144939.1 | 312 | Missense Mutation | ACT,AGT | T,S 77 | NP_001138411.1 | |
NM_001144940.1 | 312 | Missense Mutation | ACT,AGT | T,S 77 | NP_001138412.1 | |
NM_001144941.1 | 312 | Intron | NP_001138413.1 | |||
NM_182566.2 | 312 | Missense Mutation | ACT,AGT | T,S 77 | NP_872372.1 |