Product Details

SNP ID

rs200561399

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:74843450 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCGTTCTGTCCACTGGTGCAGGACA[A/G]CACCTGCAGGAAAAGAAGCCAGGAG

Phenotype

MIM: 609788

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

RNF169 PubMed Links

Gene Details

Gene

RNF169

Gene Name

ring finger protein 169

There are no transcripts associated with this gene.

Gene

XRRA1

Gene Name

X-ray radiation resistance associated 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001270380.1	2199	Silent Mutation	CTG,TTG	L588L	NP_001257309.1
NM_001270381.1	2199	Missense Mutation	GCT,GTT	A435V	NP_001257310.1
NM_182969.2	2199	Missense Mutation	GCT,GTT	A710V	NP_892014.1
XM_005273765.2	2199	Missense Mutation	GCT,GTT	A718V	XP_005273822.1
XM_005273770.2	2199	Missense Mutation	GCT,GTT	A477V	XP_005273827.1
XM_011544755.1	2199	Missense Mutation	GCT,GTT	A703V	XP_011543057.1
XM_011544756.1	2199	Missense Mutation	GCT,GTT	A676V	XP_011543058.1
XM_011544757.1	2199	Missense Mutation	GCT,GTT	A661V	XP_011543059.1
XM_011544758.1	2199	Missense Mutation	GCT,GTT	A661V	XP_011543060.1
XM_011544759.1	2199	Missense Mutation	GCT,GTT	A653V	XP_011543061.1
XM_011544760.2	2199	Intron			XP_011543062.1
XM_011544761.1	2199	Missense Mutation	GCT,GTT	A637V	XP_011543063.1
XM_011544762.1	2199	Missense Mutation	GCT,GTT	A631V	XP_011543064.1
XM_011544763.1	2199	Silent Mutation	CTG,TTG	L683L	XP_011543065.1
XM_011544764.1	2199	Missense Mutation	GCT,GTT	A606V	XP_011543066.1
XM_011544765.1	2199	Missense Mutation	GCT,GTT	A477V	XP_011543067.1
XM_011544766.2	2199	Missense Mutation	GCT,GTT	A555V	XP_011543068.1
XM_011544767.1	2199	Missense Mutation	GCT,GTT	A555V	XP_011543069.1
XM_011544768.1	2199	Missense Mutation	GCT,GTT	A555V	XP_011543070.1
XM_017017221.1	2199	Missense Mutation	GCT,GTT	A648V	XP_016872710.1
XM_017017222.1	2199	Silent Mutation	CTG,TTG	L641L	XP_016872711.1
XM_017017223.1	2199	Silent Mutation	CTG,TTG	L626L	XP_016872712.1
XM_017017224.1	2199	Silent Mutation	CTG,TTG	L596L	XP_016872713.1
XM_017017225.1	2199	Silent Mutation	CTG,TTG	L571L	XP_016872714.1
XM_017017226.1	2199	Missense Mutation	GCT,GTT	A477V	XP_016872715.1
XM_017017227.1	2199	Missense Mutation	GCT,GTT	A477V	XP_016872716.1
XM_017017228.1	2199	Silent Mutation	CTG,TTG	L442L	XP_016872717.1
XM_017017229.1	2199	Missense Mutation	GCT,GTT	A420V	XP_016872718.1
XM_017017230.1	2199	Missense Mutation	GCT,GTT	A398V	XP_016872719.1
XM_017017231.1	2199	Missense Mutation	GCT,GTT	A390V	XP_016872720.1
XM_017017232.1	2199	Silent Mutation	CTG,TTG	L330L	XP_016872721.1
XM_017017233.1	2199	Missense Mutation	GCT,GTT	A333V	XP_016872722.1
XM_017017234.1	2199	Missense Mutation	GCT,GTT	A333V	XP_016872723.1

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