Product Details

SNP ID
rs79770432
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.6:56462901 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACTCTCACATCTTCCAAGAACTGCT[C/T]GGTTGATACTTATCTTATAGAAGTG
Phenotype
MIM: 113810
Polymorphism
C/T, 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 Intron NP_001138241.1
NM_001144770.1 Intron NP_001138242.1
NM_001723.5 Intron NP_001714.1
NM_015548.4 Intron NP_056363.2
NM_183380.3 Intron NP_899236.1
XM_005249310.3 Intron XP_005249367.1
XM_005249315.3 Intron XP_005249372.1
XM_005249316.2 Intron XP_005249373.1
XM_005249318.2 Intron XP_005249375.1
XM_005249319.2 Intron XP_005249376.1
XM_005249320.4 Intron XP_005249377.1
XM_005249322.4 Intron XP_005249379.1
XM_005249323.3 Intron XP_005249380.1
XM_005249324.2 Intron XP_005249381.1
XM_011514824.2 Intron XP_011513126.1
XM_011514825.2 Intron XP_011513127.1
XM_011514826.2 Intron XP_011513128.1
XM_017011205.1 Intron XP_016866694.1
XM_017011206.1 Intron XP_016866695.1
XM_017011207.1 Intron XP_016866696.1
XM_017011208.1 Intron XP_016866697.1
XM_017011209.1 Intron XP_016866698.1
XM_017011210.1 Intron XP_016866699.1
XM_017011211.1 Intron XP_016866700.1
XM_017011212.1 Intron XP_016866701.1
XM_017011213.1 Intron XP_016866702.1
XM_017011214.1 Intron XP_016866703.1
XM_017011215.1 Intron XP_016866704.1
XM_017011216.1 Intron XP_016866705.1
XM_017011217.1 Intron XP_016866706.1
XM_017011218.1 Intron XP_016866707.1
XM_017011219.1 Intron XP_016866708.1
XM_017011220.1 Intron XP_016866709.1
XM_017011221.1 Intron XP_016866710.1
XM_017011222.1 Intron XP_016866711.1
XM_017011223.1 Intron XP_016866712.1
XM_017011224.1 Intron XP_016866713.1
XM_017011225.1 Intron XP_016866714.1

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