Product Details

SNP ID

rs514974

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:47857609 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CAGTGCTAACTCAATTTCATACCAC[C/T]GCAAAACTATGGTAAACCATAGTGT

Phenotype

MIM: 616908

Polymorphism

C/T, 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		Intron			NP_001013754.3
NM_207499.2		Intron			NP_997382.2
XM_011514639.2		Intron			XP_011512941.1
XM_017010891.1		Intron			XP_016866380.1
XM_017010892.1		Intron			XP_016866381.1
XM_017010893.1		Intron			XP_016866382.1
XM_017010894.1		Intron			XP_016866383.1
XM_017010895.1		Intron			XP_016866384.1
XM_017010896.1		Intron			XP_016866385.1

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