Product Details

SNP ID

rs151241928

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:56632032 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CATTTTCCTTATCTGAAACTGTTAT[G/T]CTTTCTTCACTTTTTGTTGTTGATG

Phenotype

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

ZNF280D PubMed Links

Gene Details

Gene

ZNF280D

Gene Name

zinc finger protein 280D

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001002843.2	2265	Missense Mutation	AGA,AGC	R789S	NP_001002843.1
NM_001002844.2	2265	Intron			NP_001002844.1
NM_001288588.1	2265	Missense Mutation	AGA,AGC	R802S	NP_001275517.1
NM_001288589.1	2265	Intron			NP_001275518.1
NM_017661.3	2265	Missense Mutation	AGA,AGC	R802S	NP_060131.2
XM_005254481.3	2265	Intron			XP_005254538.2
XM_005254483.3	2265	Intron			XP_005254540.2
XM_005254484.3	2265	Intron			XP_005254541.2
XM_005254485.3	2265	Intron			XP_005254542.2
XM_011521701.1	2265	Missense Mutation	AGA,AGC	R737S	XP_011520003.1
XM_011521702.1	2265	Missense Mutation	AGA,AGC	R802S	XP_011520004.1
XM_011521704.2	2265	Intron			XP_011520006.1
XM_011521707.2	2265	Intron			XP_011520009.1
XM_011521708.1	2265	Missense Mutation	AGA,AGC	R696S	XP_011520010.1
XM_011521709.1	2265	Missense Mutation	AGA,AGC	R696S	XP_011520011.1
XM_011521710.1	2265	Missense Mutation	AGA,AGC	R696S	XP_011520012.1
XM_011521711.1	2265	Intron			XP_011520013.1
XM_017022344.1	2265	Missense Mutation	AGA,AGC	R802S	XP_016877833.1
XM_017022345.1	2265	Missense Mutation	AGA,AGC	R802S	XP_016877834.1
XM_017022346.1	2265	Intron			XP_016877835.1
XM_017022347.1	2265	Intron			XP_016877836.1
XM_017022348.1	2265	Intron			XP_016877837.1
XM_017022349.1	2265	Missense Mutation	AGA,AGC	R314S	XP_016877838.1

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