Product Details

SNP ID
rs4974988
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:39182479 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTGCTCGCGCGGTCTCCTGGGTGA[C/T]GGGAACGCGGTAGCCTGCTTGGTGG
Phenotype
MIM: 608151
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
WDR19 PubMed Links

Gene Details

Gene
WDR19
Gene Name
WD repeat domain 19
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001317924.1 7 UTR 5 NP_001304853.1
NM_025132.3 7 UTR 5 NP_079408.3
XM_011513724.1 7 Intron XP_011512026.1
XM_011513725.2 7 UTR 5 XP_011512027.1
XM_011513726.2 7 Intron XP_011512028.1
XM_011513727.1 7 Intron XP_011512029.1
XM_017008501.1 7 Intron XP_016863990.1

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