Product Details

SNP ID

rs117579945

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:15564102 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTGGAAAACATCATGAATTTGAATA[C/T]TTCAAGTAATACTGGTGATACCCAA

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CCDC171 PubMed Links

Gene Details

Gene

CCDC171

Gene Name

coiled-coil domain containing 171

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_173550.2	329	Missense Mutation	ACT,ATT	T5I	NP_775821.2
XM_005251397.2	329	Missense Mutation	ACT,ATT	T5I	XP_005251454.1
XM_005251398.3	329	Missense Mutation	ACT,ATT	T5I	XP_005251455.1
XM_005251399.4	329	Missense Mutation	ACT,ATT	T5I	XP_005251456.1
XM_011517788.2	329	Missense Mutation	ACT,ATT	T5I	XP_011516090.1
XM_011517791.2	329	Missense Mutation	ACT,ATT	T5I	XP_011516093.1
XM_011517796.2	329	Intron			XP_011516098.1
XM_017014431.1	329	Missense Mutation	ACT,ATT	T5I	XP_016869920.1
XM_017014432.1	329	Missense Mutation	ACT,ATT	T5I	XP_016869921.1
XM_017014433.1	329	Missense Mutation	ACT,ATT	T5I	XP_016869922.1
XM_017014434.1	329	Missense Mutation	ACT,ATT	T5I	XP_016869923.1
XM_017014435.1	329	Missense Mutation	ACT,ATT	T5I	XP_016869924.1
XM_017014436.1	329	Missense Mutation	ACT,ATT	T5I	XP_016869925.1
XM_017014437.1	329	Missense Mutation	ACT,ATT	T5I	XP_016869926.1
XM_017014438.1	329	Missense Mutation	ACT,ATT	T5I	XP_016869927.1
XM_017014439.1	329	UTR 5			XP_016869928.1
XM_017014440.1	329	Intron			XP_016869929.1
XM_017014441.1	329	Missense Mutation	ACT,ATT	T5I	XP_016869930.1
XM_017014442.1	329	Missense Mutation	ACT,ATT	T5I	XP_016869931.1
XM_017014443.1	329	Intron			XP_016869932.1
XM_017014444.1	329	Intron			XP_016869933.1

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