Product Details

SNP ID
rs476873
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:47858642 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AGGATAAACTAAGGCATAAAACAAA[A/G]AGCAATAAGAAATCTGAACACAAGT
Phenotype
MIM: 616908
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
PTCHD4 PubMed Links

Gene Details

Gene
PTCHD4
Gene Name
patched domain containing 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001013732.3 23246 Intron NP_001013754.3
NM_207499.2 23246 Intron NP_997382.2
XM_011514639.2 23246 UTR 3 XP_011512941.1
XM_017010891.1 23246 UTR 3 XP_016866380.1
XM_017010892.1 23246 UTR 3 XP_016866381.1
XM_017010893.1 23246 UTR 3 XP_016866382.1
XM_017010894.1 23246 UTR 3 XP_016866383.1
XM_017010895.1 23246 UTR 3 XP_016866384.1
XM_017010896.1 23246 Intron XP_016866385.1

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