Product Details

SNP ID

rs141990164

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:56223717 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCCCCTGGACGCATCTGGTTCACCG[A/C]GGAGGCCCGTTGGCTGGACACGTCT

Phenotype

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

ZSCAN5A PubMed Links

Gene Details

Gene

ZSCAN5A

Gene Name

zinc finger and SCAN domain containing 5A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001322061.1	851	Missense Mutation	GCG,TCG	A221S	NP_001308990.1
NM_001322062.1	851	Intron			NP_001308991.1
NM_001322064.1	851	Missense Mutation	GCG,TCG	A168S	NP_001308993.1
NM_001322065.1	851	Missense Mutation	GCG,TCG	A168S	NP_001308994.1
NM_001322066.1	851	Missense Mutation	GCG,TCG	A168S	NP_001308995.1
NM_001322067.1	851	Missense Mutation	GCG,TCG	A168S	NP_001308996.1
NM_001322068.1	851	Missense Mutation	GCG,TCG	A168S	NP_001308997.1
NM_001322069.1	851	Missense Mutation	GCG,TCG	A168S	NP_001308998.1
NM_001322070.1	851	Missense Mutation	GCG,TCG	A168S	NP_001308999.1
NM_001322072.1	851	Missense Mutation	GCG,TCG	A168S	NP_001309001.1
NM_001322073.1	851	Missense Mutation	GCG,TCG	A168S	NP_001309002.1
NM_001322074.1	851	Missense Mutation	GCG,TCG	A168S	NP_001309003.1
NM_001322075.1	851	Missense Mutation	GCG,TCG	A168S	NP_001309004.1
NM_001322076.1	851	Missense Mutation	GCG,TCG	A168S	NP_001309005.1
NM_001322077.1	851	Missense Mutation	GCG,TCG	A51S	NP_001309006.1
NM_001322078.1	851	Missense Mutation	GCG,TCG	A38S	NP_001309007.1
NM_024303.2	851	Intron			NP_077279.1
XM_005259254.1	851	Intron			XP_005259311.1
XM_006723377.3	851	Missense Mutation	GCG,TCG	A244S	XP_006723440.1
XM_011527308.1	851	Intron			XP_011525610.1
XM_017027298.1	851	Missense Mutation	GCG,TCG	A244S	XP_016882787.1
XM_017027299.1	851	Missense Mutation	GCG,TCG	A168S	XP_016882788.1

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