Product Details

SNP ID

rs6624228

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:66595017 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCATTTTATAATTCTACCAGCAATA[C/T]ATGAGGCTTCTCATTTCTCCACATC

Phenotype

MIM: 300276

Polymorphism

C/T, 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	4152	Intron			NP_001186616.1
NM_001242310.1	4152	Intron			NP_001229239.1
NM_001324199.1	4152	Intron			NP_001311128.1
NM_001324201.1	4152	Intron			NP_001311130.1
NM_001324202.1	4152	Intron			NP_001311131.1
NM_001324204.1	4152	Intron			NP_001311133.1
NM_001324205.1	4152	Intron			NP_001311134.1
NM_001324206.1	4152	Intron			NP_001311135.1
NM_021783.4	4152	Intron			NP_068555.1
XM_011531000.1	4152	UTR 3			XP_011529302.1
XM_011531001.1	4152	UTR 3			XP_011529303.1
XM_011531002.1	4152	UTR 3			XP_011529304.1
XM_011531003.2	4152	UTR 3			XP_011529305.1
XM_011531004.1	4152	Intron			XP_011529306.1
XM_011531005.2	4152	UTR 3			XP_011529307.1
XM_011531006.2	4152	UTR 3			XP_011529308.1
XM_011531007.2	4152	Intron			XP_011529309.1
XM_017029703.1	4152	UTR 3			XP_016885192.1
XM_017029704.1	4152	UTR 3			XP_016885193.1
XM_017029705.1	4152	UTR 3			XP_016885194.1
XM_017029706.1	4152	UTR 3			XP_016885195.1
XM_017029707.1	4152	UTR 3			XP_016885196.1
XM_017029708.1	4152	UTR 3			XP_016885197.1

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