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TGCCTCCACGCGAAGCGAGAAAGCC[A/G]CTAGGTAGGCGCCGCCGCGACACCA
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) - 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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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 | 480 | UTR 3 | NP_001138411.1 | |||
NM_001144940.1 | 480 | UTR 3 | NP_001138412.1 | |||
NM_001144941.1 | 480 | UTR 3 | NP_001138413.1 | |||
NM_182566.2 | 480 | Missense Mutation | GCG,GTG | A,V 121 | NP_872372.1 |