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Search Thermo Fisher Scientific
CGCCAGTCCACAGCCTTGCGGGAGC[A/G]GATCCAGCCCACGGCCACCACCGAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 158378 | ||||||||||||||||||||
Literature Links: |
SLC20A2 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 |
SLC20A2 - solute carrier family 20 member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001257180.1 | 2257 | Missense Mutation | CGC,TGC | R,C 609 | NP_001244109.1 | |
NM_001257181.1 | 2257 | Missense Mutation | CGC,TGC | R,C 609 | NP_001244110.1 | |
NM_006749.4 | 2257 | Missense Mutation | CGC,TGC | R,C 609 | NP_006740.1 | |
XM_005273613.3 | 2257 | Missense Mutation | CGC,TGC | R,C 609 | XP_005273670.1 | |
XM_005273615.3 | 2257 | UTR 3 | XP_005273672.1 | |||
XM_006716390.3 | 2257 | Missense Mutation | CGC,TGC | R,C 562 | XP_006716453.1 | |
XM_006716391.3 | 2257 | Missense Mutation | CGC,TGC | R,C 472 | XP_006716454.1 | |
XM_017013748.1 | 2257 | Missense Mutation | CGC,TGC | R,C 609 | XP_016869237.1 | |
XM_017013749.1 | 2257 | Missense Mutation | CGC,TGC | R,C 562 | XP_016869238.1 | |
XM_017013750.1 | 2257 | Missense Mutation | CGC,TGC | R,C 472 | XP_016869239.1 | |
XM_017013751.1 | 2257 | Missense Mutation | CGC,TGC | R,C 472 | XP_016869240.1 | |
XM_017013752.1 | 2257 | Missense Mutation | CGC,TGC | R,C 472 | XP_016869241.1 |