Product Details

SNP ID

rs138426407

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:99487034 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGGCAGCTCGCGTATCTTGTTGAAC[A/G]TAAGAGGATTCACACCAAAGAAAAA

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

ZNF394 PubMed Links

Gene Details

Gene

ZNF394

Gene Name

zinc finger protein 394

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032164.2	1199	Intron			NP_115540.2
XM_017012710.1	1199	Intron			XP_016868199.1
XM_017012711.1	1199	Intron			XP_016868200.1

Gene

ZNF789

Gene Name

zinc finger protein 789

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001013258.1	1199	Intron			NP_001013276.1
NM_213603.2	1199	Missense Mutation	CAT,CGT	H275R	NP_998768.2
XM_011516067.2	1199	Missense Mutation	CAT,CGT	H268R	XP_011514369.1
XM_011516070.2	1199	Missense Mutation	CAT,CGT	H258R	XP_011514372.1
XM_011516073.2	1199	Missense Mutation	CAT,CGT	H180R	XP_011514375.1
XM_017012018.1	1199	Missense Mutation	CAT,CGT	H275R	XP_016867507.1
XM_017012019.1	1199	Missense Mutation	CAT,CGT	H258R	XP_016867508.1
XM_017012020.1	1199	Missense Mutation	CAT,CGT	H258R	XP_016867509.1
XM_017012021.1	1199	Missense Mutation	CAT,CGT	H258R	XP_016867510.1
XM_017012022.1	1199	Missense Mutation	CAT,CGT	H258R	XP_016867511.1
XM_017012023.1	1199	Missense Mutation	CAT,CGT	H237R	XP_016867512.1
XM_017012024.1	1199	Missense Mutation	CAT,CGT	H217R	XP_016867513.1
XM_017012025.1	1199	Missense Mutation	CAT,CGT	H180R	XP_016867514.1
XM_017012026.1	1199	Missense Mutation	CAT,CGT	H180R	XP_016867515.1
XM_017012027.1	1199	Missense Mutation	CAT,CGT	H180R	XP_016867516.1

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