Product Details

SNP ID
rs4827499
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:66599381 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TGCTGCTGTTCCTCCACTCCTAGTG[A/G]ATAATACTATTCCAAAAGAGAATTC
Phenotype
MIM: 300276
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
EDA2R PubMed Links

Gene Details

Gene
EDA2R
Gene Name
ectodysplasin A2 receptor
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001199687.2 Intron NP_001186616.1
NM_001242310.1 Intron NP_001229239.1
NM_001324199.1 Intron NP_001311128.1
NM_001324201.1 Intron NP_001311130.1
NM_001324202.1 Intron NP_001311131.1
NM_001324204.1 Intron NP_001311133.1
NM_001324205.1 Intron NP_001311134.1
NM_001324206.1 Intron NP_001311135.1
NM_021783.4 Intron NP_068555.1
XM_011531000.1 Intron XP_011529302.1
XM_011531001.1 Intron XP_011529303.1
XM_011531002.1 Intron XP_011529304.1
XM_011531003.2 Intron XP_011529305.1
XM_011531004.1 Intron XP_011529306.1
XM_011531005.2 Intron XP_011529307.1
XM_011531006.2 Intron XP_011529308.1
XM_011531007.2 Intron XP_011529309.1
XM_017029703.1 Intron XP_016885192.1
XM_017029704.1 Intron XP_016885193.1
XM_017029705.1 Intron XP_016885194.1
XM_017029706.1 Intron XP_016885195.1
XM_017029707.1 Intron XP_016885196.1
XM_017029708.1 Intron XP_016885197.1

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