Product Details

SNP ID

rs199767535

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:58084767 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACCGCCCGCCCTAGCCCCCGCCTGG[A/G]CTTCGCGGGTGGACGGTTGGGGGCC

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

ZSCAN18 PubMed Links

Gene Details

Gene

ZSCAN18

Gene Name

zinc finger and SCAN domain containing 18

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145542.1	1649	Missense Mutation	GCC,GTC	A540V	NP_001139014.1
NM_001145543.1	1649	Missense Mutation	GCC,GTC	A484V	NP_001139015.1
NM_001145544.1	1649	Missense Mutation	GCC,GTC	A348V	NP_001139016.1
NM_023926.4	1649	Missense Mutation	GCC,GTC	A484V	NP_076415.3
XM_005259174.4	1649	Missense Mutation	GCC,GTC	A484V	XP_005259231.1
XM_006723335.2	1649	Missense Mutation	GCC,GTC	A484V	XP_006723398.1
XM_011527237.2	1649	Missense Mutation	GCC,GTC	A539V	XP_011525539.1
XM_011527238.1	1649	Missense Mutation	GCC,GTC	A484V	XP_011525540.1
XM_011527239.2	1649	Missense Mutation	GCC,GTC	A484V	XP_011525541.1
XM_017027169.1	1649	Missense Mutation	GCC,GTC	A483V	XP_016882658.1
XM_017027170.1	1649	Missense Mutation	GCC,GTC	A483V	XP_016882659.1
XM_017027171.1	1649	Missense Mutation	GCC,GTC	A483V	XP_016882660.1

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