Product Details

SNP ID

rs138110009

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:56221587 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCGGATTATGCAATCACTGAGAAGT[A/G]GCTTCTGGATGTGTTTTCTGGTGGC

Phenotype

Polymorphism

A/G, Transition 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	1828	Silent Mutation	GCC,GCT	A545A	NP_001308990.1
NM_001322062.1	1828	Intron			NP_001308991.1
NM_001322064.1	1828	Silent Mutation	GCC,GCT	A493A	NP_001308993.1
NM_001322065.1	1828	Silent Mutation	GCC,GCT	A493A	NP_001308994.1
NM_001322066.1	1828	Silent Mutation	GCC,GCT	A493A	NP_001308995.1
NM_001322067.1	1828	Silent Mutation	GCC,GCT	A493A	NP_001308996.1
NM_001322068.1	1828	Silent Mutation	GCC,GCT	A493A	NP_001308997.1
NM_001322069.1	1828	Silent Mutation	GCC,GCT	A493A	NP_001308998.1
NM_001322070.1	1828	Silent Mutation	GCC,GCT	A493A	NP_001308999.1
NM_001322072.1	1828	Silent Mutation	GCC,GCT	A493A	NP_001309001.1
NM_001322073.1	1828	Silent Mutation	GCC,GCT	A492A	NP_001309002.1
NM_001322074.1	1828	Silent Mutation	GCC,GCT	A492A	NP_001309003.1
NM_001322075.1	1828	Silent Mutation	GCC,GCT	A492A	NP_001309004.1
NM_001322076.1	1828	Silent Mutation	GCC,GCT	A492A	NP_001309005.1
NM_001322077.1	1828	Silent Mutation	GCC,GCT	A376A	NP_001309006.1
NM_001322078.1	1828	Silent Mutation	GCC,GCT	A363A	NP_001309007.1
NM_024303.2	1828	Intron			NP_077279.1
XM_005259254.1	1828	Intron			XP_005259311.1
XM_006723377.3	1828	Silent Mutation	GCC,GCT	A568A	XP_006723440.1
XM_011527308.1	1828	Intron			XP_011525610.1
XM_017027298.1	1828	Silent Mutation	GCC,GCT	A569A	XP_016882787.1
XM_017027299.1	1828	Silent Mutation	GCC,GCT	A492A	XP_016882788.1

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