Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGTTGCCATAGGTGTGCTGGCCACC[A/G]TCTTTCTGGCTTCGTTTGCAGCCTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 615949 | ||||||||||||||||||||
Literature Links: |
TMEM98 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
TMEM98 - transmembrane protein 98 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001033504.1 | 425 | Missense Mutation | ATC,GTC | I,V 15 | NP_001028676.1 | |
NM_001301746.1 | 425 | Missense Mutation | ATC,GTC | I,V 15 | NP_001288675.1 | |
NM_015544.2 | 425 | Missense Mutation | ATC,GTC | I,V 15 | NP_056359.2 |