Product Details

SNP ID
rs183801635
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.X:69616368 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGCCTGCAGCAGCGCCGCGGGAGCG[A/C]GGGAGCCAGGGCTGCGGGTGTGGCG
Phenotype
MIM: 300451
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
EDA PubMed Links

Gene Details

Gene
EDA
Gene Name
ectodysplasin A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001005609.1 283 Silent Mutation CGA,CGC R20R NP_001005609.1
NM_001005610.3 283 Silent Mutation CGA,CGC R20R NP_001005610.2
NM_001005612.2 283 Silent Mutation CGA,CGC R20R NP_001005612.2
NM_001005613.3 283 Silent Mutation CGA,CGC R20R NP_001005613.1
NM_001399.4 283 Silent Mutation CGA,CGC R20R NP_001390.1
XM_006724630.2 283 Silent Mutation CGA,CGC R20R XP_006724693.1
XM_011530885.2 283 Silent Mutation CGA,CGC R20R XP_011529187.1
XM_017029336.1 283 Silent Mutation CGA,CGC R20R XP_016884825.1
XM_017029337.1 283 Silent Mutation CGA,CGC R20R XP_016884826.1

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