Product Details

SNP ID

rs200135927

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:58085268 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCCTCCTCAGTGGTGCCCGACGGG[C/G]GATCGGCAAGGGCGTCCCCAGGGGG

Phenotype

Polymorphism

C/G, Transversion 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	1148	Missense Mutation	CCC,CGC	P373R	NP_001139014.1
NM_001145543.1	1148	Missense Mutation	CCC,CGC	P317R	NP_001139015.1
NM_001145544.1	1148	Missense Mutation	CCC,CGC	P181R	NP_001139016.1
NM_023926.4	1148	Missense Mutation	CCC,CGC	P317R	NP_076415.3
XM_005259174.4	1148	Missense Mutation	CCC,CGC	P317R	XP_005259231.1
XM_006723335.2	1148	Missense Mutation	CCC,CGC	P317R	XP_006723398.1
XM_011527237.2	1148	Missense Mutation	CCC,CGC	P372R	XP_011525539.1
XM_011527238.1	1148	Missense Mutation	CCC,CGC	P317R	XP_011525540.1
XM_011527239.2	1148	Missense Mutation	CCC,CGC	P317R	XP_011525541.1
XM_017027169.1	1148	Missense Mutation	CCC,CGC	P316R	XP_016882658.1
XM_017027170.1	1148	Missense Mutation	CCC,CGC	P316R	XP_016882659.1
XM_017027171.1	1148	Missense Mutation	CCC,CGC	P316R	XP_016882660.1

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