Product Details

SNP ID

rs113470073

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:145765711 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAGGGAGGATGAAGAGGGGCTATTT[A/G]ATTCGCTGGGGGTCTTCCTGTCTTC

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

C4orf51 PubMed Links

Gene Details

Gene

C4orf51

Gene Name

chromosome 4 open reading frame 51

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001080531.1	3487	Intron			NP_001074000.1
XM_006714289.3	3487	Intron			XP_006714352.1
XM_011532196.2	3487	Intron			XP_011530498.1
XM_011532197.2	3487	Intron			XP_011530499.1
XM_017008547.1	3487	Intron			XP_016864036.1
XM_017008548.1	3487	Intron			XP_016864037.1
XM_017008549.1	3487	Intron			XP_016864038.1
XM_017008550.1	3487	Intron			XP_016864039.1
XM_017008551.1	3487	Intron			XP_016864040.1
XM_017008552.1	3487	Intron			XP_016864041.1
XM_017008553.1	3487	Intron			XP_016864042.1
XM_017008554.1	3487	Intron			XP_016864043.1
XM_017008555.1	3487	Intron			XP_016864044.1
XM_017008556.1	3487	Intron			XP_016864045.1

Gene

ZNF827

Gene Name

zinc finger protein 827

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001306215.1	3487	Missense Mutation	TCA,TTA	S963L	NP_001293144.1
NM_178835.4	3487	Missense Mutation	TCA,TTA	S963L	NP_849157.2
XM_011531634.2	3487	Missense Mutation	TCA,TTA	S963L	XP_011529936.1
XM_011531635.2	3487	Missense Mutation	TCA,TTA	S951L	XP_011529937.1
XM_011531645.2	3487	Missense Mutation	TCA,TTA	S295L	XP_011529947.1
XM_017007768.1	3487	Missense Mutation	TCA,TTA	S961L	XP_016863257.1
XM_017007769.1	3487	Missense Mutation	TCA,TTA	S951L	XP_016863258.1
XM_017007770.1	3487	Missense Mutation	TCA,TTA	S885L	XP_016863259.1
XM_017007771.1	3487	Missense Mutation	TCA,TTA	S963L	XP_016863260.1
XM_017007772.1	3487	Missense Mutation	TCA,TTA	S963L	XP_016863261.1
XM_017007773.1	3487	Missense Mutation	TCA,TTA	S963L	XP_016863262.1
XM_017007774.1	3487	Missense Mutation	TCA,TTA	S963L	XP_016863263.1
XM_017007775.1	3487	Missense Mutation	TCA,TTA	S963L	XP_016863264.1
XM_017007776.1	3487	Intron			XP_016863265.1
XM_017007777.1	3487	Missense Mutation	TCA,TTA	S374L	XP_016863266.1

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