Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCAAGCTCCAAAAATCATGGCTTTC[A/C]TCTTCACATCCAGGTCTAGTGGGAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607612 | ||||||||||||||||||||
Literature Links: |
PLSCR4 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 |
PLSCR4 - phospholipid scramblase 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001128304.1 | 1152 | Missense Mutation | NP_001121776.1 | |||
NM_001128305.1 | 1152 | Missense Mutation | NP_001121777.1 | |||
NM_001128306.1 | 1152 | Missense Mutation | NP_001121778.1 | |||
NM_001177304.1 | 1152 | Missense Mutation | NP_001170775.1 | |||
NM_020353.2 | 1152 | Missense Mutation | NP_065086.2 | |||
XM_005247654.2 | 1152 | Missense Mutation | XP_005247711.1 | |||
XM_005247655.2 | 1152 | Missense Mutation | XP_005247712.1 | |||
XM_011513031.2 | 1152 | Missense Mutation | XP_011511333.1 | |||
XM_017006921.1 | 1152 | Missense Mutation | XP_016862410.1 |