Product Details

SNP ID

rs144919020

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:55369702 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATCATCCCACCTGCACTGCTGCTCG[C/T]GATGGGTGGGGACGCCTGGGTGCTC

Phenotype

MIM: 613515

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

ATG14 PubMed Links

Gene Details

Gene

ATG14

Gene Name

autophagy related 14

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014924.4	1136	Missense Mutation			NP_055739.2
XM_011536563.2	1136	Missense Mutation			XP_011534865.1

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