Product Details

SNP ID

rs1128868

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:43556737 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATCTTTCTTGTGAACCCGCTGGTGG[A/C]TGTGAAGGTTGGAGCTCTGGCTGAA

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	1514	Missense Mutation	AGC,ATC	S448I	NP_001092752.1
NM_001099283.1	1514	Missense Mutation	AGC,ATC	S448I	NP_001092753.1
NM_001099284.1	1514	Missense Mutation	AGC,ATC	S448I	NP_001092754.1
NM_001324347.1	1514	Missense Mutation	AGC,ATC	S448I	NP_001311276.1
NM_001324348.1	1514	Missense Mutation	AGC,ATC	S448I	NP_001311277.1
NM_001324349.1	1514	Missense Mutation	AGC,ATC	S448I	NP_001311278.1
NM_001324350.1	1514	Missense Mutation	AGC,ATC	S448I	NP_001311279.1
NM_001324351.1	1514	Missense Mutation	AGC,ATC	S448I	NP_001311280.1
NM_001324352.1	1514	Missense Mutation	AGC,ATC	S490I	NP_001311281.1
NM_001324353.1	1514	Missense Mutation	AGC,ATC	S561I	NP_001311282.1
NM_005674.2	1514	Missense Mutation	AGC,ATC	S448I	NP_005665.2
XM_005271832.2	1514	Missense Mutation	AGC,ATC	S448I	XP_005271889.1
XM_006718001.2	1514	Missense Mutation	AGC,ATC	S490I	XP_006718064.1
XM_006718003.3	1514	Missense Mutation	AGC,ATC	S448I	XP_006718066.1
XM_011540232.2	1514	Missense Mutation	AGC,ATC	S592I	XP_011538534.1
XM_011540234.2	1514	Missense Mutation	AGC,ATC	S490I	XP_011538536.1
XM_011540235.2	1514	Missense Mutation	AGC,ATC	S490I	XP_011538537.1
XM_011540236.2	1514	Missense Mutation	AGC,ATC	S490I	XP_011538538.1
XM_011540237.2	1514	Missense Mutation	AGC,ATC	S490I	XP_011538539.1
XM_011540238.2	1514	Missense Mutation	AGC,ATC	S448I	XP_011538540.1
XM_017016740.1	1514	Missense Mutation	AGC,ATC	S490I	XP_016872229.1

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