Product Details

SNP ID

rs200779855

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:28326248 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAAGAGTTTACTGCACTGACTGCAC[G/T]GATAGGGTTTCTCACCAGTGTGGAC

Phenotype

MIM: 610794

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

ZSCAN31 PubMed Links

Gene Details

Gene

ZSCAN31

Gene Name

zinc finger and SCAN domain containing 31

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001135215.1	1375	Missense Mutation	CAG,CCG	Q380P	NP_001128687.1
NM_001135216.1	1375	Missense Mutation	CAG,CCG	Q380P	NP_001128688.1
NM_001243241.1	1375	Missense Mutation	CAG,CCG	Q380P	NP_001230170.1
NM_001243242.1	1375	Missense Mutation	CAG,CCG	Q221P	NP_001230171.1
NM_001243243.1	1375	Missense Mutation	CAG,CCG	Q221P	NP_001230172.1
NM_001243244.1	1375	Missense Mutation	CAG,CCG	Q221P	NP_001230173.1
NM_030899.4	1375	Missense Mutation	CAG,CCG	Q380P	NP_112161.3
NM_145909.2	1375	Missense Mutation	CAG,CCG	Q380P	NP_665916.1
XM_005249295.1	1375	Missense Mutation	CAG,CCG	Q380P	XP_005249352.1
XM_005249296.4	1375	Missense Mutation	CAG,CCG	Q380P	XP_005249353.1
XM_011514807.2	1375	Missense Mutation	CAG,CCG	Q380P	XP_011513109.1
XM_011514808.2	1375	Missense Mutation	CAG,CCG	Q380P	XP_011513110.1
XM_011514809.1	1375	Missense Mutation	CAG,CCG	Q380P	XP_011513111.1
XM_011514811.2	1375	Missense Mutation	CAG,CCG	Q380P	XP_011513113.1
XM_011514812.2	1375	Missense Mutation	CAG,CCG	Q380P	XP_011513114.1
XM_011514813.2	1375	Missense Mutation	CAG,CCG	Q380P	XP_011513115.1
XM_017011196.1	1375	Missense Mutation	CAG,CCG	Q380P	XP_016866685.1

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