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GTGCTGGTCACCGAACTCATGACCT[C/T]GGGCACGCTCAAGACGTGAGCTCTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610907 MIM: 601844 | ||||||||||||||||||||
Literature Links: |
VPS25 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 |
VPS25 - vacuolar protein sorting 25 homolog | ||||||
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There are no transcripts associated with this gene. |
WNK4 - WNK lysine deficient protein kinase 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001321299.1 | 844 | UTR 5 | NP_001308228.1 | |||
NM_032387.4 | 844 | Missense Mutation | TCG,TTG | S,L 259 | NP_115763.2 | |
XM_011525135.2 | 844 | Missense Mutation | TCG,TTG | S,L 259 | XP_011523437.1 | |
XM_017024962.1 | 844 | Missense Mutation | TCG,TTG | S,L 259 | XP_016880451.1 | |
XM_017024963.1 | 844 | Missense Mutation | TCG,TTG | S,L 259 | XP_016880452.1 | |
XM_017024964.1 | 844 | Missense Mutation | TCG,TTG | S,L 259 | XP_016880453.1 | |
XM_017024965.1 | 844 | Missense Mutation | TCG,TTG | S,L 259 | XP_016880454.1 | |
XM_017024966.1 | 844 | Intron | XP_016880455.1 |