Product Details

SNP ID

rs138483093

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:43556994 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGTGTGGATGCACCGGTGAATGTG[A/C]AGGTTCGAGCTCTGACTGAAGCCCT

Phenotype

MIM: 601069

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

ZNF239 PubMed Links

Gene Details

Gene

ZNF239

Gene Name

zinc finger protein 239

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001099282.1	1257	Silent Mutation	CTG,CTT	L362L	NP_001092752.1
NM_001099283.1	1257	Silent Mutation	CTG,CTT	L362L	NP_001092753.1
NM_001099284.1	1257	Silent Mutation	CTG,CTT	L362L	NP_001092754.1
NM_001324347.1	1257	Silent Mutation	CTG,CTT	L362L	NP_001311276.1
NM_001324348.1	1257	Silent Mutation	CTG,CTT	L362L	NP_001311277.1
NM_001324349.1	1257	Silent Mutation	CTG,CTT	L362L	NP_001311278.1
NM_001324350.1	1257	Silent Mutation	CTG,CTT	L362L	NP_001311279.1
NM_001324351.1	1257	Silent Mutation	CTG,CTT	L362L	NP_001311280.1
NM_001324352.1	1257	Silent Mutation	CTG,CTT	L404L	NP_001311281.1
NM_001324353.1	1257	Silent Mutation	CTG,CTT	L475L	NP_001311282.1
NM_005674.2	1257	Silent Mutation	CTG,CTT	L362L	NP_005665.2
XM_005271832.2	1257	Silent Mutation	CTG,CTT	L362L	XP_005271889.1
XM_006718001.2	1257	Silent Mutation	CTG,CTT	L404L	XP_006718064.1
XM_006718003.3	1257	Silent Mutation	CTG,CTT	L362L	XP_006718066.1
XM_011540232.2	1257	Silent Mutation	CTG,CTT	L506L	XP_011538534.1
XM_011540234.2	1257	Silent Mutation	CTG,CTT	L404L	XP_011538536.1
XM_011540235.2	1257	Silent Mutation	CTG,CTT	L404L	XP_011538537.1
XM_011540236.2	1257	Silent Mutation	CTG,CTT	L404L	XP_011538538.1
XM_011540237.2	1257	Silent Mutation	CTG,CTT	L404L	XP_011538539.1
XM_011540238.2	1257	Silent Mutation	CTG,CTT	L362L	XP_011538540.1
XM_017016740.1	1257	Silent Mutation	CTG,CTT	L404L	XP_016872229.1

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