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SNP ID: rs143102702
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.19:54155897 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TCTGCCCGAGACCTCTCAGCTGCTT[C/T]CCTCCGCAGACGTTCAGCTCGAAGC
Phenotype: MIM: 604910
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: CNOT3 PubMed Links

Gene Details

Gene: CNOT3
Gene Name: CCR4-NOT transcription complex subunit 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014516.3	667	Intron			NP_055331.1
XM_005278279.1	667	Intron			XP_005278336.1
XM_005278280.2	667	Intron			XP_005278337.1
XM_005278281.1	667	Intron			XP_005278338.1
XM_005278282.2	667	Intron			XP_005278339.1
XM_011526992.1	667	Intron			XP_011525294.1
XM_011526993.2	667	Intron			XP_011525295.1

Gene: LENG1
Gene Name: leukocyte receptor cluster member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_024316.2	667	Missense Mutation	AAA,GAA	K207E	NP_077292.2

Gene: TMC4
Gene Name: transmembrane channel like 4

There are no transcripts associated with this gene.

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