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TCCCTTTTTTGACATCGCGCACTAT[C/G]TAGTGTCAGTGATGGCGGTGAAACG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 611236 | ||||||||||||||||||||
Literature Links: |
TMEM38B 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 |
TMEM38B - transmembrane protein 38B | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_018112.2 | 207 | Missense Mutation | CTA,GTA | L,V 27 | NP_060582.1 | |
XM_005252075.2 | 207 | Intron | XP_005252132.1 | |||
XM_005252076.2 | 207 | Missense Mutation | CTA,GTA | L,V 27 | XP_005252133.1 | |
XM_005252077.3 | 207 | Missense Mutation | CTA,GTA | L,V 27 | XP_005252134.1 | |
XM_011518829.1 | 207 | Missense Mutation | CTA,GTA | L,V 27 | XP_011517131.1 | |
XM_011518831.2 | 207 | Missense Mutation | CTA,GTA | L,V 27 | XP_011517133.1 | |
XM_011518832.2 | 207 | Missense Mutation | CTA,GTA | L,V 27 | XP_011517134.1 | |
XM_011518833.2 | 207 | UTR 5 | XP_011517135.1 |