Product Details

SNP ID
rs74433214
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:63162605 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TAAGCAATTACTCTATTAAATAATT[A/G]AGGAAGAATCATTGTTTTAAATATT
Phenotype
MIM: 610792
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC22A25 PubMed Links

Gene Details

Gene
SLC22A25
Gene Name
solute carrier family 22 member 25
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_199352.3 2992 Intron NP_955384.3
XM_017017684.1 2992 UTR 3 XP_016873173.1
XM_017017685.1 2992 UTR 3 XP_016873174.1
XM_017017686.1 2992 UTR 3 XP_016873175.1
XM_017017687.1 2992 Intron XP_016873176.1
XM_017017688.1 2992 UTR 3 XP_016873177.1
XM_017017689.1 2992 UTR 3 XP_016873178.1
XM_017017690.1 2992 UTR 3 XP_016873179.1
XM_017017691.1 2992 UTR 3 XP_016873180.1
XM_017017692.1 2992 UTR 3 XP_016873181.1
XM_017017693.1 2992 UTR 3 XP_016873182.1
XM_017017694.1 2992 UTR 3 XP_016873183.1
XM_017017695.1 2992 Intron XP_016873184.1
XM_017017696.1 2992 UTR 3 XP_016873185.1

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