Product Details

SNP ID

rs138391803

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:56222722 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTCACCTGTTACGTCAATACTCTTG[C/T]GTAGCAGAAAGTCCTCTCCCTGAAG

Phenotype

Polymorphism

C/T, 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	957	Missense Mutation			NP_001308990.1
NM_001322062.1	957	Intron			NP_001308991.1
NM_001322064.1	957	Missense Mutation			NP_001308993.1
NM_001322065.1	957	Missense Mutation			NP_001308994.1
NM_001322066.1	957	Missense Mutation			NP_001308995.1
NM_001322067.1	957	Missense Mutation			NP_001308996.1
NM_001322068.1	957	Missense Mutation			NP_001308997.1
NM_001322069.1	957	Missense Mutation			NP_001308998.1
NM_001322070.1	957	Missense Mutation			NP_001308999.1
NM_001322072.1	957	Missense Mutation			NP_001309001.1
NM_001322073.1	957	Missense Mutation			NP_001309002.1
NM_001322074.1	957	Missense Mutation			NP_001309003.1
NM_001322075.1	957	Missense Mutation			NP_001309004.1
NM_001322076.1	957	Missense Mutation			NP_001309005.1
NM_001322077.1	957	Missense Mutation			NP_001309006.1
NM_001322078.1	957	Missense Mutation			NP_001309007.1
NM_024303.2	957	Intron			NP_077279.1
XM_005259254.1	957	Intron			XP_005259311.1
XM_006723377.3	957	Missense Mutation			XP_006723440.1
XM_011527308.1	957	Intron			XP_011525610.1
XM_017027298.1	957	Missense Mutation			XP_016882787.1
XM_017027299.1	957	Missense Mutation			XP_016882788.1

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