Product Details

SNP ID
rs4124773
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:63651892 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AATCTGATTGGTGGCCTAGCTGCGG[C/T]TTGCCATGACTCCTTCCTCAAGGCT
Phenotype
MIM: 613893
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
DPY19L2 PubMed Links

Gene Details

Gene
DPY19L2
Gene Name
dpy-19 like 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_173812.4 Intron NP_776173.3
XM_006719352.2 Intron XP_006719415.1
XM_011538215.2 Intron XP_011536517.1
XM_011538218.2 Intron XP_011536520.1
XM_017019188.1 Intron XP_016874677.1
XM_017019189.1 Intron XP_016874678.1
XM_017019190.1 Intron XP_016874679.1
XM_017019191.1 Intron XP_016874680.1
XM_017019192.1 Intron XP_016874681.1
XM_017019193.1 Intron XP_016874682.1
XM_017019194.1 Intron XP_016874683.1
XM_017019195.1 Intron XP_016874684.1
XM_017019196.1 Intron XP_016874685.1
XM_017019197.1 Intron XP_016874686.1
XM_017019198.1 Intron XP_016874687.1
XM_017019199.1 Intron XP_016874688.1
XM_017019200.1 Intron XP_016874689.1
XM_017019201.1 Intron XP_016874690.1
XM_017019202.1 Intron XP_016874691.1
XM_017019203.1 Intron XP_016874692.1
XM_017019204.1 Intron XP_016874693.1
XM_017019205.1 Intron XP_016874694.1

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