Product Details

SNP ID

rs200193671

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:35889903 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTGCTTACTTACCCCCTCAGGGCCC[A/G]GCCCGGGCCGCAGCAGGTGAACGGG

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

NFKBID PubMed Links

Gene Details

Gene

NFKBID

Gene Name

NFKB inhibitor delta

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001321831.1	1193	Missense Mutation	CCG,CTG	P307L	NP_001308760.1
NM_139239.2	1193	Missense Mutation	CCG,CTG	P292L	NP_640332.1
XM_005259340.3	1193	Missense Mutation	CCG,CTG	P307L	XP_005259397.1
XM_011527419.2	1193	Missense Mutation	CCG,CTG	P444L	XP_011525721.1
XM_011527420.2	1193	Missense Mutation	CCG,CTG	P307L	XP_011525722.1
XM_011527421.2	1193	Missense Mutation	CCG,CTG	P282L	XP_011525723.1
XM_011527424.2	1193	Missense Mutation	CCG,CTG	P307L	XP_011525726.1
XM_017027389.1	1193	Missense Mutation	CCG,CTG	P307L	XP_016882878.1
XM_017027390.1	1193	Missense Mutation	CCG,CTG	P307L	XP_016882879.1
XM_017027391.1	1193	Missense Mutation	CCG,CTG	P292L	XP_016882880.1
XM_017027392.1	1193	Missense Mutation	CCG,CTG	P292L	XP_016882881.1
XM_017027393.1	1193	Missense Mutation	CCG,CTG	P292L	XP_016882882.1
XM_017027394.1	1193	Missense Mutation	CCG,CTG	P282L	XP_016882883.1
XM_017027395.1	1193	Missense Mutation	CCG,CTG	P282L	XP_016882884.1
XM_017027396.1	1193	Intron			XP_016882885.1
XM_017027397.1	1193	Missense Mutation	CCG,CTG	P259L	XP_016882886.1

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