Product Details

SNP ID

rs201225377

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:56223726 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGCATCTGGTTCACCGAGGAGGCCC[A/G]TTGGCTGGACACGTCTTTCAGATCA

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	842	Missense Mutation			NP_001308990.1
NM_001322062.1	842	Intron			NP_001308991.1
NM_001322064.1	842	Missense Mutation			NP_001308993.1
NM_001322065.1	842	Missense Mutation			NP_001308994.1
NM_001322066.1	842	Missense Mutation			NP_001308995.1
NM_001322067.1	842	Missense Mutation			NP_001308996.1
NM_001322068.1	842	Missense Mutation			NP_001308997.1
NM_001322069.1	842	Missense Mutation			NP_001308998.1
NM_001322070.1	842	Missense Mutation			NP_001308999.1
NM_001322072.1	842	Missense Mutation			NP_001309001.1
NM_001322073.1	842	Missense Mutation			NP_001309002.1
NM_001322074.1	842	Missense Mutation			NP_001309003.1
NM_001322075.1	842	Missense Mutation			NP_001309004.1
NM_001322076.1	842	Missense Mutation			NP_001309005.1
NM_001322077.1	842	Missense Mutation			NP_001309006.1
NM_001322078.1	842	Missense Mutation			NP_001309007.1
NM_024303.2	842	Intron			NP_077279.1
XM_005259254.1	842	Intron			XP_005259311.1
XM_006723377.3	842	Missense Mutation			XP_006723440.1
XM_011527308.1	842	Intron			XP_011525610.1
XM_017027298.1	842	Missense Mutation			XP_016882787.1
XM_017027299.1	842	Missense Mutation			XP_016882788.1

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