Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGCATCTTCTCCAGCACGCCGCTGC[A/G]GCCCCAGATGTCAAACACCGTGCGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608137 MIM: 612122 | ||||||||||||||||||||
Literature Links: |
NSMF PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
NSMF - NMDA receptor synaptonuclear signaling and neuronal migration factor | ||||||
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There are no transcripts associated with this gene. |
PNPLA7 - patatin like phospholipase domain containing 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001098537.2 | 4063 | Missense Mutation | CGC,TGC | R,C 1231 | NP_001092007.2 | |
NM_152286.4 | 4063 | Missense Mutation | CGC,TGC | R,C 1206 | NP_689499.4 | |
XM_006717102.1 | 4063 | Missense Mutation | CGC,TGC | R,C 1232 | XP_006717165.1 | |
XM_006717104.3 | 4063 | Missense Mutation | CGC,TGC | R,C 1198 | XP_006717167.1 | |
XM_011518664.2 | 4063 | Intron | XP_011516966.1 | |||
XM_017014709.1 | 4063 | Missense Mutation | CGC,TGC | R,C 1198 | XP_016870198.1 |