Product Details

SNP ID

rs189422284

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:99622557 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTTTTGTCCCTGCTCAGCACTACCT[C/G]TTCTGCAGGCGGGTCCTGGCCTCCC

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

ZSCAN25 PubMed Links

Gene Details

Gene

ZSCAN25

Gene Name

zinc finger and SCAN domain containing 25

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_145115.2	1180	Missense Mutation	CTT,GTT	L200V	NP_660090.2
XM_005250194.2	1180	Missense Mutation	CTT,GTT	L200V	XP_005250251.1
XM_011515905.2	1180	Missense Mutation	CTT,GTT	L200V	XP_011514207.1
XM_011515906.2	1180	Missense Mutation	CTT,GTT	L200V	XP_011514208.1
XM_011515907.2	1180	Missense Mutation	CTT,GTT	L200V	XP_011514209.1
XM_011515908.2	1180	Missense Mutation	CTT,GTT	L36V	XP_011514210.1
XM_011515909.2	1180	Missense Mutation	CTT,GTT	L200V	XP_011514211.1
XM_011515910.2	1180	Missense Mutation	CTT,GTT	L200V	XP_011514212.1
XM_017011824.1	1180	Missense Mutation	CTT,GTT	L200V	XP_016867313.1
XM_017011825.1	1180	Missense Mutation	CTT,GTT	L36V	XP_016867314.1
XM_017011826.1	1180	Missense Mutation	CTT,GTT	L36V	XP_016867315.1
XM_017011827.1	1180	Missense Mutation	CTT,GTT	L200V	XP_016867316.1

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