Product Details

SNP ID

rs142000561

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:35498897 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACCGAGGAAGAAGGTGAGACTCCCC[C/G]CTGCAAAAAGATCAAAGGAAAGTGA

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

DMKN PubMed Links

Gene Details

Gene

DMKN

Gene Name

dermokine

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001035516.3	659	Missense Mutation	CGG,GGG	R68G	NP_001030593.1
NM_001126056.2	659	Missense Mutation	CGG,GGG	R443G	NP_001119528.2
NM_001126057.2	659	Intron			NP_001119529.2
NM_001126058.2	659	Intron			NP_001119530.2
NM_001126059.2	659	Missense Mutation	CGG,GGG	R167G	NP_001119531.1
NM_001190347.1	659	Missense Mutation	CGG,GGG	R427G	NP_001177276.1
NM_001190348.1	659	Intron			NP_001177277.1
NM_001190349.1	659	Intron			NP_001177278.1
NM_001308380.1	659	Missense Mutation	CGG,GGG	R181G	NP_001295309.1
NM_001308383.1	659	Missense Mutation	CGG,GGG	R150G	NP_001295312.1
NM_033317.4	659	Missense Mutation	CGG,GGG	R454G	NP_201574.3
XM_006723477.1	659	Missense Mutation	CGG,GGG	R231G	XP_006723540.1
XM_006723484.1	659	Missense Mutation	CGG,GGG	R201G	XP_006723547.1
XM_006723489.1	659	Missense Mutation	CGG,GGG	R162G	XP_006723552.1
XM_006723493.2	659	Missense Mutation	CGG,GGG	R130G	XP_006723556.1
XM_006723494.2	659	Missense Mutation	CGG,GGG	R124G	XP_006723557.1
XM_006723503.2	659	Missense Mutation	CGG,GGG	R162G	XP_006723566.1
XM_011527494.2	659	Missense Mutation	CGG,GGG	R516G	XP_011525796.1
XM_011527495.2	659	Missense Mutation	CGG,GGG	R516G	XP_011525797.1
XM_011527496.2	659	Missense Mutation	CGG,GGG	R504G	XP_011525798.1
XM_011527497.2	659	Missense Mutation	CGG,GGG	R502G	XP_011525799.1
XM_011527498.2	659	Missense Mutation	CGG,GGG	R502G	XP_011525800.1
XM_011527499.2	659	Missense Mutation	CGG,GGG	R501G	XP_011525801.1
XM_011527500.2	659	Missense Mutation	CGG,GGG	R498G	XP_011525802.1
XM_011527501.2	659	Missense Mutation	CGG,GGG	R496G	XP_011525803.1
XM_011527502.2	659	Missense Mutation	CGG,GGG	R486G	XP_011525804.1
XM_011527503.2	659	Missense Mutation	CGG,GGG	R484G	XP_011525805.1
XM_011527504.2	659	Missense Mutation	CGG,GGG	R478G	XP_011525806.1
XM_011527505.2	659	Missense Mutation	CGG,GGG	R469G	XP_011525807.1
XM_011527506.2	659	Missense Mutation	CGG,GGG	R466G	XP_011525808.1
XM_011527507.2	659	Missense Mutation	CGG,GGG	R454G	XP_011525809.1
XM_011527508.2	659	Missense Mutation	CGG,GGG	R449G	XP_011525810.1
XM_011527509.2	659	Missense Mutation	CGG,GGG	R435G	XP_011525811.1
XM_011527510.2	659	Missense Mutation	CGG,GGG	R434G	XP_011525812.1
XM_011527511.2	659	Intron			XP_011525813.1
XM_011527512.2	659	Intron			XP_011525814.1
XM_011527513.1	659	Missense Mutation	CGG,GGG	R184G	XP_011525815.1
XM_011527514.1	659	Missense Mutation	CGG,GGG	R164G	XP_011525816.1
XM_017027475.1	659	Missense Mutation	CGG,GGG	R199G	XP_016882964.1
XM_017027476.1	659	Missense Mutation	CGG,GGG	R162G	XP_016882965.1
XM_017027477.1	659	Missense Mutation	CGG,GGG	R115G	XP_016882966.1

Gene

KRTDAP

Gene Name

keratinocyte differentiation associated protein

There are no transcripts associated with this gene.

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