Product Details

SNP ID

rs191862325

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:58515545 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAAACGCGCTCTTAGACCATGGCGA[C/T]CCAGGCGAAGCGTCCACGGGTGAGT

Phenotype

MIM: 604917 MIM: 614463 MIM: 616424

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CNOT1 PubMed Links

Gene Details

Gene

CNOT1

Gene Name

CCR4-NOT transcription complex subunit 1

There are no transcripts associated with this gene.

Gene

NDRG4

Gene Name

NDRG family member 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001130487.1	67	Intron			NP_001123959.1
NM_001242833.1	67	Intron			NP_001229762.1
NM_001242834.1	67	Intron			NP_001229763.1
NM_001242835.1	67	Intron			NP_001229764.1
NM_001242836.1	67	Intron			NP_001229765.1
NM_020465.3	67	Intron			NP_065198.1
NM_022910.3	67	Intron			NP_075061.1
XM_006721252.3	67	Intron			XP_006721315.1
XM_006721253.3	67	Intron			XP_006721316.1
XM_006721254.3	67	Intron			XP_006721317.1
XM_006721256.3	67	Intron			XP_006721319.1
XM_006721257.3	67	Intron			XP_006721320.1
XM_006721258.3	67	Intron			XP_006721321.1
XM_006721259.3	67	Intron			XP_006721322.1
XM_006721260.3	67	Intron			XP_006721323.1
XM_006721261.3	67	Intron			XP_006721324.1
XM_006721262.3	67	Intron			XP_006721325.1
XM_011523290.2	67	Intron			XP_011521592.1
XM_011523291.2	67	Intron			XP_011521593.1
XM_011523292.2	67	Intron			XP_011521594.1
XM_011523293.2	67	Intron			XP_011521595.1
XM_011523294.2	67	Intron			XP_011521596.1
XM_017023582.1	67	Intron			XP_016879071.1
XM_017023583.1	67	Intron			XP_016879072.1
XM_017023584.1	67	Intron			XP_016879073.1
XM_017023585.1	67	Intron			XP_016879074.1
XM_017023586.1	67	Intron			XP_016879075.1
XM_017023587.1	67	Intron			XP_016879076.1
XM_017023588.1	67	Intron			XP_016879077.1
XM_017023589.1	67	Intron			XP_016879078.1
XM_017023590.1	67	Intron			XP_016879079.1

Gene

SETD6

Gene Name

SET domain containing 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001160305.2	67	Missense Mutation	ACC,ATC	T3I	NP_001153777.1
NM_024860.3	67	Missense Mutation	ACC,ATC	T3I	NP_079136.2
XM_011523336.1	67	Missense Mutation	ACC,ATC	T3I	XP_011521638.1

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