Product Details

SNP ID

rs201952309

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:56463585 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTACCTTGGGTGTGGTGGTGGCAG[A/G]GACCTGTGGGGAGGCCGCCTGCGCA

Phenotype

MIM: 113810

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

DST PubMed Links

Gene Details

Gene

DST

Gene Name

dystonin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001144769.2	16723	Missense Mutation	CCT,TCT	P5504S	NP_001138241.1
NM_001144770.1	16723	Missense Mutation	CCT,TCT	P5366S	NP_001138242.1
NM_001723.5	16723	Intron			NP_001714.1
NM_015548.4	16723	Missense Mutation	CCT,TCT	P5000S	NP_056363.2
NM_183380.3	16723	Missense Mutation	CCT,TCT	P5326S	NP_899236.1
XM_005249310.3	16723	Missense Mutation	CCT,TCT	P7647S	XP_005249367.1
XM_005249315.3	16723	Missense Mutation	CCT,TCT	P7614S	XP_005249372.1
XM_005249316.2	16723	Missense Mutation	CCT,TCT	P7552S	XP_005249373.1
XM_005249318.2	16723	Missense Mutation	CCT,TCT	P7509S	XP_005249375.1
XM_005249319.2	16723	Missense Mutation	CCT,TCT	P7476S	XP_005249376.1
XM_005249320.4	16723	Missense Mutation	CCT,TCT	P7469S	XP_005249377.1
XM_005249322.4	16723	Missense Mutation	CCT,TCT	P7462S	XP_005249379.1
XM_005249323.3	16723	Missense Mutation	CCT,TCT	P7436S	XP_005249380.1
XM_005249324.2	16723	Missense Mutation	CCT,TCT	P7110S	XP_005249381.1
XM_011514824.2	16723	Missense Mutation	CCT,TCT	P7623S	XP_011513126.1
XM_011514825.2	16723	Missense Mutation	CCT,TCT	P5513S	XP_011513127.1
XM_011514826.2	16723	Missense Mutation	CCT,TCT	P7327S	XP_011513128.1
XM_017011205.1	16723	Missense Mutation	CCT,TCT	P7656S	XP_016866694.1
XM_017011206.1	16723	Missense Mutation	CCT,TCT	P7650S	XP_016866695.1
XM_017011207.1	16723	Missense Mutation	CCT,TCT	P7635S	XP_016866696.1
XM_017011208.1	16723	Missense Mutation	CCT,TCT	P7632S	XP_016866697.1
XM_017011209.1	16723	Missense Mutation	CCT,TCT	P7626S	XP_016866698.1
XM_017011210.1	16723	Missense Mutation	CCT,TCT	P7656S	XP_016866699.1
XM_017011211.1	16723	Missense Mutation	CCT,TCT	P7632S	XP_016866700.1
XM_017011212.1	16723	Missense Mutation	CCT,TCT	P7578S	XP_016866701.1
XM_017011213.1	16723	Missense Mutation	CCT,TCT	P7547S	XP_016866702.1
XM_017011214.1	16723	Missense Mutation	CCT,TCT	P7523S	XP_016866703.1
XM_017011215.1	16723	Missense Mutation	CCT,TCT	P7547S	XP_016866704.1
XM_017011216.1	16723	Missense Mutation	CCT,TCT	P7523S	XP_016866705.1
XM_017011217.1	16723	Missense Mutation	CCT,TCT	P7448S	XP_016866706.1
XM_017011218.1	16723	Missense Mutation	CCT,TCT	P5845S	XP_016866707.1
XM_017011219.1	16723	Missense Mutation	CCT,TCT	P5570S	XP_016866708.1
XM_017011220.1	16723	Missense Mutation	CCT,TCT	P5528S	XP_016866709.1
XM_017011221.1	16723	Missense Mutation	CCT,TCT	P5492S	XP_016866710.1
XM_017011222.1	16723	Missense Mutation	CCT,TCT	P5466S	XP_016866711.1
XM_017011223.1	16723	Missense Mutation	CCT,TCT	P5461S	XP_016866712.1
XM_017011224.1	16723	Missense Mutation	CCT,TCT	P5241S	XP_016866713.1
XM_017011225.1	16723	Intron			XP_016866714.1

View Full Product Details