Product Details

SNP ID

rs61731888

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.18:35253802 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTCATAAGGCTTCTCTCCAGTGTGG[A/C]TTCTCCGATGCCTGATGAGCTCTGA

Phenotype

MIM: 609601

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

ZNF397 PubMed Links

Gene Details

Gene

ZNF397

Gene Name

zinc finger protein 397

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001135178.2	1550	Intron			NP_001128650.1
NM_032347.2	1550	Intron			NP_115723.1
XM_006722558.2	1550	UTR 3			XP_006722621.1
XM_011526229.2	1550	UTR 3			XP_011524531.1
XM_011526230.2	1550	UTR 3			XP_011524532.1
XM_011526231.2	1550	UTR 3			XP_011524533.1
XM_017026042.1	1550	UTR 3			XP_016881531.1

Gene

ZSCAN30

Gene Name

zinc finger and SCAN domain containing 30

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001112734.3	1550	Missense Mutation	AGC,ATC	S378I	NP_001106205.1
NM_001166012.2	1550	Missense Mutation	AGC,ATC	S378I	NP_001159484.1
NM_001288711.1	1550	Missense Mutation	AGC,ATC	S191I	NP_001275640.1
XM_005258183.4	1550	Missense Mutation	AGC,ATC	S378I	XP_005258240.1
XM_006722371.3	1550	Missense Mutation	AGC,ATC	S378I	XP_006722434.1
XM_011525789.2	1550	Missense Mutation	AGC,ATC	S191I	XP_011524091.1
XM_017025515.1	1550	Missense Mutation	AGC,ATC	S378I	XP_016881004.1
XM_017025516.1	1550	Missense Mutation	AGC,ATC	S235I	XP_016881005.1
XM_017025517.1	1550	Missense Mutation	AGC,ATC	S235I	XP_016881006.1
XM_017025518.1	1550	Missense Mutation	AGC,ATC	S235I	XP_016881007.1
XM_017025519.1	1550	Missense Mutation	AGC,ATC	S191I	XP_016881008.1
XM_017025520.1	1550	Missense Mutation	AGC,ATC	S191I	XP_016881009.1
XM_017025521.1	1550	Missense Mutation	AGC,ATC	S191I	XP_016881010.1
XM_017025522.1	1550	Missense Mutation	AGC,ATC	S191I	XP_016881011.1

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