Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTTGGCTTGGGCAACTGCCACGTTG[A/G]TGCACTGGAGCCATTCTTCTGCATT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609594 | ||||||||||||||||||||
Literature Links: |
VEPH1 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 |
VEPH1 - ventricular zone expressed PH domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001167911.1 | 2499 | Missense Mutation | ACC,ATC | T,I 769 | NP_001161383.1 | |
NM_001167912.1 | 2499 | Missense Mutation | ACC,ATC | T,I 814 | NP_001161384.1 | |
NM_001167915.1 | 2499 | Intron | NP_001161387.1 | |||
NM_001167916.1 | 2499 | Intron | NP_001161388.1 | |||
NM_001167917.1 | 2499 | Intron | NP_001161389.1 | |||
NM_024621.2 | 2499 | Missense Mutation | ACC,ATC | T,I 814 | NP_078897.2 | |
XM_011513134.2 | 2499 | Missense Mutation | ACC,ATC | T,I 825 | XP_011511436.1 | |
XM_011513135.1 | 2499 | Missense Mutation | ACC,ATC | T,I 769 | XP_011511437.1 |