Product Details

SNP ID
rs17882269
Assay Type
Validated
NCBI dbSNP Submissions
NA
Location
Chr.22:46581053 on Build GRCh38
Set Membership
Validated
Context Sequence [VIC/FAM]
AGCCCTGTTGTTTTGCCTTTGGTAT[C/T]TCGGCATGTGGCAGAGGCCTGGGCG
Phenotype
MIM: 613691
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
GRAMD4 PubMed Links

Gene Details

Gene
GRAMD4
Gene Name
GRAM domain containing 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_015124.4 Intron NP_055939.1
XM_005261396.3 Intron XP_005261453.1
XM_006724169.1 Intron XP_006724232.1
XM_006724170.3 Intron XP_006724233.1
XM_011530011.1 Intron XP_011528313.1
XM_011530012.1 Intron XP_011528314.1
XM_011530013.2 Intron XP_011528315.2
XM_011530014.2 Intron XP_011528316.1
XM_017028670.1 Intron XP_016884159.1

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