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GGTCATGATGAACTTGGAGCACCCA[C/T]ACGTGCTGCGTCTGCACGGCCTTGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607611 MIM: 608076 | ||||||||||||||||||||
Literature Links: |
PLSCR3 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 |
PLSCR3 - phospholipid scramblase 3 | ||||||
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There are no transcripts associated with this gene. |
TMEM256-PLSCR3 - TMEM256-PLSCR3 readthrough (NMD candidate) | ||||||
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There are no transcripts associated with this gene. |
TNK1 - tyrosine kinase non receptor 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001251902.1 | 767 | Missense Mutation | CAC,TAC | H,Y 179 | NP_001238831.1 | |
NM_003985.4 | 767 | Missense Mutation | CAC,TAC | H,Y 179 | NP_003976.2 | |
XM_011524045.2 | 767 | Missense Mutation | CAC,TAC | H,Y 179 | XP_011522347.1 | |
XM_011524046.2 | 767 | Missense Mutation | CAC,TAC | H,Y 179 | XP_011522348.1 | |
XM_011524047.2 | 767 | Missense Mutation | CAC,TAC | H,Y 179 | XP_011522349.1 | |
XM_011524048.1 | 767 | Missense Mutation | CAC,TAC | H,Y 22 | XP_011522350.1 |