Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CACACTGAGCGGCGGCATTGACGTG[C/T]TGGTGGTGAAGCAGGTGGACGGCTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 605520 | ||||||||||||||||||||
Literature Links: |
LPIN3 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 |
LPIN3 - lipin 3 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001301860.1 | 256 | Silent Mutation | CTG,TTG | L,L 34 | NP_001288789.1 | |
XM_005260516.2 | 256 | Missense Mutation | CTG,TTG | L,L 34 | XP_005260573.1 | |
XM_006723863.2 | 256 | Missense Mutation | CTG,TTG | L,L 34 | XP_006723926.1 | |
XM_011528996.1 | 256 | Missense Mutation | CTG,TTG | L,L 34 | XP_011527298.1 | |
XM_011528997.2 | 256 | Missense Mutation | CTG,TTG | L,L 34 | XP_011527299.1 | |
XM_011528998.2 | 256 | Missense Mutation | CTG,TTG | L,L 34 | XP_011527300.1 | |
XM_011528999.2 | 256 | Missense Mutation | CTG,TTG | L,L 34 | XP_011527301.1 | |
XM_011529000.1 | 256 | Missense Mutation | CTG,TTG | L,L 34 | XP_011527302.1 | |
XM_011529001.1 | 256 | Missense Mutation | CTG,TTG | L,L 34 | XP_011527303.1 | |
XM_011529002.2 | 256 | Intron | XP_011527304.1 | |||
XM_011529003.1 | 256 | Missense Mutation | CTG,TTG | L,L 34 | XP_011527305.1 | |
XM_011529004.1 | 256 | Missense Mutation | CTG,TTG | L,L 34 | XP_011527306.1 | |
XM_011529005.2 | 256 | Missense Mutation | CTG,TTG | L,L 34 | XP_011527307.1 | |
XM_011529006.2 | 256 | Missense Mutation | CTG,TTG | L,L 34 | XP_011527308.1 | |
XM_017028020.1 | 256 | Missense Mutation | CTG,TTG | L,L 34 | XP_016883509.1 |