Product Details

SNP ID

rs201880764

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.21:44012513 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACGCCCATGGACGCCTCTGAGGAGC[C/T]GCTGCCGCCGGTGATCTACACCATG

Phenotype

MIM: 602103

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

TRAPPC10 PubMed Links

Gene Details

Gene

TRAPPC10

Gene Name

trafficking protein particle complex 10

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003274.4	182	Missense Mutation	CCG,CTG	P7L	NP_003265.3
XM_005261168.4	182	Missense Mutation	CCG,CTG	P7L	XP_005261225.1
XM_011529714.2	182	Missense Mutation	CCG,CTG	P7L	XP_011528016.1
XM_011529715.2	182	Missense Mutation	CCG,CTG	P7L	XP_011528017.1
XM_011529716.2	182	Missense Mutation	CCG,CTG	P7L	XP_011528018.1
XM_011529717.2	182	Missense Mutation	CCG,CTG	P7L	XP_011528019.1
XM_011529718.2	182	Missense Mutation	CCG,CTG	P7L	XP_011528020.1
XM_011529719.2	182	Missense Mutation	CCG,CTG	P7L	XP_011528021.1
XM_011529720.2	182	Missense Mutation	CCG,CTG	P7L	XP_011528022.1
XM_011529721.2	182	Intron			XP_011528023.1
XM_011529722.2	182	Intron			XP_011528024.1
XM_011529723.2	182	Intron			XP_011528025.1
XM_011529725.2	182	Missense Mutation	CCG,CTG	P7L	XP_011528027.1
XM_011529726.2	182	Missense Mutation	CCG,CTG	P7L	XP_011528028.1
XM_011529727.2	182	Intron			XP_011528029.1
XM_011529728.2	182	Intron			XP_011528030.1
XM_011529729.2	182	Intron			XP_011528031.1
XM_011529730.2	182	Missense Mutation	CCG,CTG	P7L	XP_011528032.1
XM_017028454.1	182	Missense Mutation	CCG,CTG	P7L	XP_016883943.1
XM_017028455.1	182	Intron			XP_016883944.1

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