Product Details

SNP ID

rs201413717

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:74843928 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTCATCCAGAAGTTGGGCTCTAGTC[G/T]TCTTTGGGGGTGGAATCGGGATTCT

Phenotype

MIM: 609788

Polymorphism

G/T, Transversion 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	2121	Intron			NP_001257309.1
NM_001270381.1	2121	Missense Mutation	AAG,ACG	K409T	NP_001257310.1
NM_182969.2	2121	Missense Mutation	AAG,ACG	K684T	NP_892014.1
XM_005273765.2	2121	Missense Mutation	AAG,ACG	K692T	XP_005273822.1
XM_005273770.2	2121	Missense Mutation	AAG,ACG	K451T	XP_005273827.1
XM_011544755.1	2121	Missense Mutation	AAG,ACG	K677T	XP_011543057.1
XM_011544756.1	2121	Missense Mutation	AAG,ACG	K650T	XP_011543058.1
XM_011544757.1	2121	Missense Mutation	AAG,ACG	K635T	XP_011543059.1
XM_011544758.1	2121	Missense Mutation	AAG,ACG	K635T	XP_011543060.1
XM_011544759.1	2121	Missense Mutation	AAG,ACG	K627T	XP_011543061.1
XM_011544760.2	2121	Missense Mutation	AAG,ACG	K692T	XP_011543062.1
XM_011544761.1	2121	Missense Mutation	AAG,ACG	K611T	XP_011543063.1
XM_011544762.1	2121	Missense Mutation	AAG,ACG	K605T	XP_011543064.1
XM_011544763.1	2121	Intron			XP_011543065.1
XM_011544764.1	2121	Missense Mutation	AAG,ACG	K580T	XP_011543066.1
XM_011544765.1	2121	Missense Mutation	AAG,ACG	K451T	XP_011543067.1
XM_011544766.2	2121	Missense Mutation	AAG,ACG	K529T	XP_011543068.1
XM_011544767.1	2121	Missense Mutation	AAG,ACG	K529T	XP_011543069.1
XM_011544768.1	2121	Missense Mutation	AAG,ACG	K529T	XP_011543070.1
XM_017017221.1	2121	Missense Mutation	AAG,ACG	K622T	XP_016872710.1
XM_017017222.1	2121	Intron			XP_016872711.1
XM_017017223.1	2121	Intron			XP_016872712.1
XM_017017224.1	2121	Intron			XP_016872713.1
XM_017017225.1	2121	Intron			XP_016872714.1
XM_017017226.1	2121	Missense Mutation	AAG,ACG	K451T	XP_016872715.1
XM_017017227.1	2121	Missense Mutation	AAG,ACG	K451T	XP_016872716.1
XM_017017228.1	2121	Intron			XP_016872717.1
XM_017017229.1	2121	Missense Mutation	AAG,ACG	K394T	XP_016872718.1
XM_017017230.1	2121	Missense Mutation	AAG,ACG	K372T	XP_016872719.1
XM_017017231.1	2121	Missense Mutation	AAG,ACG	K364T	XP_016872720.1
XM_017017232.1	2121	Intron			XP_016872721.1
XM_017017233.1	2121	Missense Mutation	AAG,ACG	K307T	XP_016872722.1
XM_017017234.1	2121	Missense Mutation	AAG,ACG	K307T	XP_016872723.1

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