Product Details

SNP ID
rs41274748
Assay Type
Functionally tested
NCBI dbSNP Submissions
11
Location
Chr.1:217429131 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTCAAACACCAAATTTTGAATAGA[A/C]CCCAGAGCACAATACACTATCACAA
Phenotype
MIM: 616836
Polymorphism
A/C, Transversion 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 3732 Intron NP_001284683.1
NM_018040.3 3732 UTR 3 NP_060510.1
XM_011509689.2 3732 Intron XP_011507991.1
XM_011509690.2 3732 Intron XP_011507992.1
XM_011509691.2 3732 Intron XP_011507993.1
XM_011509693.2 3732 Intron XP_011507995.1
XM_011509694.2 3732 Intron XP_011507996.1
XM_017001592.1 3732 Intron XP_016857081.1
XM_017001593.1 3732 Intron XP_016857082.1

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