Product Details

SNP ID

rs149797851

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:99486688 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGGGGCTTCCTTCAAAACCTTAAC[C/G]TTATTCAAGATCAGAATGCGCAAAC

Phenotype

Polymorphism

C/G, Transversion 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	1068	Intron			NP_115540.2
XM_017012710.1	1068	UTR 3			XP_016868199.1
XM_017012711.1	1068	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	1068	Intron			NP_001013276.1
NM_213603.2	1068	Missense Mutation	CTT,GTT	L160V	NP_998768.2
XM_011516067.2	1068	Missense Mutation	CTT,GTT	L153V	XP_011514369.1
XM_011516070.2	1068	Missense Mutation	CTT,GTT	L143V	XP_011514372.1
XM_011516073.2	1068	Missense Mutation	CTT,GTT	L65V	XP_011514375.1
XM_017012018.1	1068	Missense Mutation	CTT,GTT	L160V	XP_016867507.1
XM_017012019.1	1068	Missense Mutation	CTT,GTT	L143V	XP_016867508.1
XM_017012020.1	1068	Missense Mutation	CTT,GTT	L143V	XP_016867509.1
XM_017012021.1	1068	Missense Mutation	CTT,GTT	L143V	XP_016867510.1
XM_017012022.1	1068	Missense Mutation	CTT,GTT	L143V	XP_016867511.1
XM_017012023.1	1068	Missense Mutation	CTT,GTT	L122V	XP_016867512.1
XM_017012024.1	1068	Missense Mutation	CTT,GTT	L102V	XP_016867513.1
XM_017012025.1	1068	Missense Mutation	CTT,GTT	L65V	XP_016867514.1
XM_017012026.1	1068	Missense Mutation	CTT,GTT	L65V	XP_016867515.1
XM_017012027.1	1068	Missense Mutation	CTT,GTT	L65V	XP_016867516.1

View Full Product Details