Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCCCAGGGGCAGGCGTTGAACTGGC[G/T]CAGGATGAAGCCGGTGGTGAACTCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 603930 | ||||||||||||||||||||
Literature Links: |
GPHN 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 |
TMEM229B - transmembrane protein 229B | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_182526.2 | 702 | Missense Mutation | NP_872332.1 | |||
XM_005267373.2 | 702 | Missense Mutation | XP_005267430.1 | |||
XM_005267374.3 | 702 | Missense Mutation | XP_005267431.1 | |||
XM_005267375.2 | 702 | Missense Mutation | XP_005267432.1 | |||
XM_006720062.2 | 702 | Missense Mutation | XP_006720125.1 | |||
XM_017021051.1 | 702 | Missense Mutation | XP_016876540.1 | |||
XM_017021052.1 | 702 | Missense Mutation | XP_016876541.1 | |||
XM_017021053.1 | 702 | Missense Mutation | XP_016876542.1 | |||
XM_017021054.1 | 702 | Missense Mutation | XP_016876543.1 | |||
XM_017021055.1 | 702 | Missense Mutation | XP_016876544.1 |