Product Details

SNP ID

rs75989324

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:1795437 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TAGGGGCTCCGCCCAGGCCCTCATA[C/T]GCCAGGCCTCCTCCGAGGATGGGGC

Phenotype

MIM: 613084

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MYT1L PubMed Links

Gene Details

Gene

MYT1L

Gene Name

myelin transcription factor 1 like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001303052.1		Intron			NP_001289981.1
NM_015025.3		Intron			NP_055840.2
XM_011510318.1		Intron			XP_011508620.1
XM_011510319.1		Intron			XP_011508621.1
XM_011510320.2		Intron			XP_011508622.1
XM_011510321.2		Intron			XP_011508623.1
XM_011510322.2		Intron			XP_011508624.1
XM_011510323.1		Intron			XP_011508625.1
XM_011510324.1		Intron			XP_011508626.1
XM_011510325.1		Intron			XP_011508627.1
XM_011510326.1		Intron			XP_011508628.1
XM_011510327.1		Intron			XP_011508629.1
XM_011510328.2		Intron			XP_011508630.1
XM_011510331.2		Intron			XP_011508633.1
XM_011510332.2		Intron			XP_011508634.1
XM_017003604.1		Intron			XP_016859093.1
XM_017003605.1		Intron			XP_016859094.1
XM_017003606.1		Intron			XP_016859095.1
XM_017003607.1		Intron			XP_016859096.1
XM_017003608.1		Intron			XP_016859097.1
XM_017003609.1		Intron			XP_016859098.1
XM_017003610.1		Intron			XP_016859099.1
XM_017003611.1		Intron			XP_016859100.1
XM_017003612.1		Intron			XP_016859101.1
XM_017003613.1		Intron			XP_016859102.1
XM_017003614.1		Intron			XP_016859103.1
XM_017003615.1		Intron			XP_016859104.1
XM_017003616.1		Intron			XP_016859105.1
XM_017003617.1		Intron			XP_016859106.1
XM_017003618.1		Intron			XP_016859107.1
XM_017003619.1		Intron			XP_016859108.1
XM_017003620.1		Intron			XP_016859109.1
XM_017003621.1		Intron			XP_016859110.1
XM_017003622.1		Intron			XP_016859111.1

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