Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCACCGAGAACATCTACTCTTTCAA[C/G]TACACCAGCCAGCCCGACCAGGTAA
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 606816 | |||||||||||||||||||||||
Literature Links: |
SIDT1 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
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 |
SIDT1 - SID1 transmembrane family member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001308350.1 | 852 | Missense Mutation | AAC,AAG | N,K 67 | NP_001295279.1 | |
NM_001322294.1 | 852 | Missense Mutation | AAC,AAG | N,K 67 | NP_001309223.1 | |
NM_001322295.1 | 852 | Missense Mutation | AAC,AAG | N,K 67 | NP_001309224.1 | |
NM_001322296.1 | 852 | Missense Mutation | AAC,AAG | N,K 67 | NP_001309225.1 | |
NM_001322297.1 | 852 | UTR 5 | NP_001309226.1 | |||
NM_001322298.1 | 852 | UTR 5 | NP_001309227.1 | |||
NM_001322299.1 | 852 | UTR 5 | NP_001309228.1 | |||
NM_001322300.1 | 852 | UTR 5 | NP_001309229.1 | |||
NM_017699.2 | 852 | Missense Mutation | AAC,AAG | N,K 67 | NP_060169.2 | |
XM_011512939.2 | 852 | Missense Mutation | AAC,AAG | N,K 67 | XP_011511241.1 | |
XM_011512941.2 | 852 | Missense Mutation | AAC,AAG | N,K 67 | XP_011511243.1 | |
XM_017006664.1 | 852 | Missense Mutation | AAC,AAG | N,K 67 | XP_016862153.1 | |
XM_017006665.1 | 852 | UTR 5 | XP_016862154.1 | |||
XM_017006666.1 | 852 | Intron | XP_016862155.1 | |||
XM_017006667.1 | 852 | Intron | XP_016862156.1 | |||
XM_017006668.1 | 852 | Intron | XP_016862157.1 |