Product Details

SNP ID

rs10119254

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:105698693 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGAAATGAGCCTATTAGGTTATTTT[A/G]TTGTGTGACCCTCAGTTTGGGCCCA

Phenotype

MIM: 611236

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

TMEM38B PubMed Links

Gene Details

Gene

TMEM38B

Gene Name

transmembrane protein 38B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_018112.2		Intron			NP_060582.1
XM_005252075.2		Intron			XP_005252132.1
XM_005252076.2		Intron			XP_005252133.1
XM_005252077.3		Intron			XP_005252134.1
XM_011518829.1		Intron			XP_011517131.1
XM_011518831.2		Intron			XP_011517133.1
XM_011518832.2		Intron			XP_011517134.1
XM_011518833.2		Intron			XP_011517135.1

View Full Product Details