Product Details

SNP ID

rs140142659

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:31394330 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTTTGGGCAGAGCGTGGTGCAGTT[C/T]GGTGGATCTCGGTAGGCCCCACTCA

Phenotype

MIM: 602453

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

ITGAD PubMed Links

Gene Details

Gene

ITGAD

Gene Name

integrin subunit alpha D

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001318185.1	253	Silent Mutation	TTC,TTT	F42F	NP_001305114.1
NM_005353.2	253	Silent Mutation	TTC,TTT	F42F	NP_005344.2
XM_011545835.2	253	Missense Mutation	TTC,TTT	F42F	XP_011544137.1
XM_011545836.2	253	Missense Mutation	TTC,TTT	F42F	XP_011544138.1
XM_011545837.2	253	Missense Mutation	TTC,TTT	F42F	XP_011544139.1
XM_011545838.2	253	Missense Mutation	TTC,TTT	F42F	XP_011544140.1
XM_011545839.2	253	Silent Mutation	TTC,TTT	F42F	XP_011544141.1
XM_011545841.2	253	Missense Mutation	TTC,TTT	F42F	XP_011544143.1
XM_011545842.2	253	Missense Mutation	TTC,TTT	F42F	XP_011544144.1
XM_011545843.2	253	Missense Mutation	TTC,TTT	F42F	XP_011544145.1
XM_011545844.2	253	Missense Mutation	TTC,TTT	F42F	XP_011544146.1
XM_011545845.2	253	Missense Mutation	TTC,TTT	F42F	XP_011544147.1
XM_011545846.2	253	Missense Mutation	TTC,TTT	F42F	XP_011544148.1
XM_011545847.2	253	Missense Mutation	TTC,TTT	F42F	XP_011544149.1
XM_011545848.2	253	Missense Mutation	TTC,TTT	F42F	XP_011544150.1
XM_017023215.1	253	Missense Mutation	TTC,TTT	F42F	XP_016878704.1

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