Product Details

SNP ID
rs150360294
Assay Type
Functionally tested
NCBI dbSNP Submissions
5
Location
Chr.1:217430845 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGCACACATACATGAATTAAGCAAA[A/G]CATCGGAAAGTATTGACACATGAGA
Phenotype
MIM: 616836
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
GPATCH2 PubMed Links

Gene Details

Gene
GPATCH2
Gene Name
G-patch domain containing 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001297754.1 2186 Intron NP_001284683.1
NM_018040.3 2186 UTR 3 NP_060510.1
XM_011509689.2 2186 UTR 3 XP_011507991.1
XM_011509690.2 2186 UTR 3 XP_011507992.1
XM_011509691.2 2186 UTR 3 XP_011507993.1
XM_011509693.2 2186 Intron XP_011507995.1
XM_011509694.2 2186 Intron XP_011507996.1
XM_017001592.1 2186 UTR 3 XP_016857081.1
XM_017001593.1 2186 Intron XP_016857082.1

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