Product Details

SNP ID

rs201359857

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:207081240 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGATATGTCTCTTCATGTGGAGGGC[A/G]AGATGGTCAGACCTGGAAAAACACC

Phenotype

MIM: 604865

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

KLF7 PubMed Links

Gene Details

Gene

KLF7

Gene Name

Kruppel like factor 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001270942.1	1116	Missense Mutation	TCG,TTG	S227L	NP_001257871.1
NM_001270943.1	1116	Silent Mutation	CTC,CTT	L261L	NP_001257872.1
NM_001270944.1	1116	Silent Mutation	CTC,CTT	L266L	NP_001257873.1
NM_003709.3	1116	Silent Mutation	CTC,CTT	L294L	NP_003700.1
XM_005246926.3	1116	Silent Mutation	CTC,CTT	L295L	XP_005246983.1
XM_006712815.3	1116	Silent Mutation	CTC,CTT	L295L	XP_006712878.1
XM_011512072.2	1116	Silent Mutation	CTC,CTT	L295L	XP_011510374.1
XM_011512073.2	1116	Silent Mutation	CTC,CTT	L264L	XP_011510375.1
XM_011512074.2	1116	Silent Mutation	CTC,CTT	L262L	XP_011510376.1
XM_011512075.1	1116	Intron			XP_011510377.1
XM_017005161.1	1116	Silent Mutation	CTC,CTT	L294L	XP_016860650.1
XM_017005162.1	1116	Silent Mutation	CTC,CTT	L267L	XP_016860651.1
XM_017005163.1	1116	Intron			XP_016860652.1
XM_017005164.1	1116	Missense Mutation	TCG,TTG	S227L	XP_016860653.1

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