Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGCACAAGGACACAGCCTGGGGGAT[G/T]GACTGGGCCCTTCCACTTACCAGAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606208 | ||||||||||||||||||||
Literature Links: |
LOC101928414 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 |
LOC101928414 - uncharacterized LOC101928414 | ||||||
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There are no transcripts associated with this gene. |
SLC28A2 - solute carrier family 28 member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004212.3 | 181 | Nonsense Mutation | GGA,TGA | G,* 49 | NP_004203.2 | |
XM_011522198.2 | 181 | Nonsense Mutation | GGA,TGA | G,* 49 | XP_011520500.1 | |
XM_011522199.1 | 181 | Nonsense Mutation | GGA,TGA | G,* 49 | XP_011520501.1 | |
XM_011522200.2 | 181 | Nonsense Mutation | GGA,TGA | G,* 49 | XP_011520502.1 | |
XM_011522201.2 | 181 | Nonsense Mutation | GGA,TGA | G,* 49 | XP_011520503.1 | |
XM_011522202.2 | 181 | Intron | XP_011520504.1 |