Product Details

SNP ID

rs34187696

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.19:56222056 on Build GRCh38

Set Membership

Validated

Context Sequence [VIC/FAM]

CGGGTGACTGACTGGGCTCGCAGGG[A/C]CTGGGGAATGAATTGAATTCATCCC

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	1359	Missense Mutation			NP_001308990.1
NM_001322062.1	1359	Intron			NP_001308991.1
NM_001322064.1	1359	Missense Mutation			NP_001308993.1
NM_001322065.1	1359	Missense Mutation			NP_001308994.1
NM_001322066.1	1359	Missense Mutation			NP_001308995.1
NM_001322067.1	1359	Missense Mutation			NP_001308996.1
NM_001322068.1	1359	Missense Mutation			NP_001308997.1
NM_001322069.1	1359	Missense Mutation			NP_001308998.1
NM_001322070.1	1359	Missense Mutation			NP_001308999.1
NM_001322072.1	1359	Missense Mutation			NP_001309001.1
NM_001322073.1	1359	Missense Mutation			NP_001309002.1
NM_001322074.1	1359	Missense Mutation			NP_001309003.1
NM_001322075.1	1359	Missense Mutation			NP_001309004.1
NM_001322076.1	1359	Missense Mutation			NP_001309005.1
NM_001322077.1	1359	Missense Mutation			NP_001309006.1
NM_001322078.1	1359	Missense Mutation			NP_001309007.1
NM_024303.2	1359	Intron			NP_077279.1
XM_005259254.1	1359	Intron			XP_005259311.1
XM_006723377.3	1359	Missense Mutation			XP_006723440.1
XM_011527308.1	1359	Intron			XP_011525610.1
XM_017027298.1	1359	Missense Mutation			XP_016882787.1
XM_017027299.1	1359	Missense Mutation			XP_016882788.1

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