Product Details

SNP ID

rs36089209

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:68158309 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGTCTTTTGTTTTGAAGCTATCTGA[C/T]GTCACAACTGAACAACCGACGGGTG

Phenotype

MIM: 610881

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

KMT5B PubMed Links

Gene Details

Gene

KMT5B

Gene Name

lysine methyltransferase 5B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001300907.1	2389	Silent Mutation	ACA,ACG	T507T	NP_001287836.1
NM_001300908.1	2389	Silent Mutation	ACA,ACG	T439T	NP_001287837.1
NM_001300909.1	2389	Intron			NP_001287838.1
NM_016028.4	2389	Intron			NP_057112.3
NM_017635.4	2389	Silent Mutation	ACA,ACG	T679T	NP_060105.3
XM_005274035.3	2389	Silent Mutation	ACA,ACG	T679T	XP_005274092.2
XM_005274036.3	2389	Silent Mutation	ACA,ACG	T656T	XP_005274093.2
XM_006718581.1	2389	Silent Mutation	ACA,ACG	T656T	XP_006718644.1
XM_011545091.1	2389	Silent Mutation	ACA,ACG	T679T	XP_011543393.1
XM_011545092.2	2389	Silent Mutation	ACA,ACG	T608T	XP_011543394.1
XM_011545093.2	2389	Silent Mutation	ACA,ACG	T265T	XP_011543395.1
XM_011545094.2	2389	Intron			XP_011543396.1
XM_017017876.1	2389	Silent Mutation	ACA,ACG	T507T	XP_016873365.1
XM_017017877.1	2389	Silent Mutation	ACA,ACG	T507T	XP_016873366.1
XM_017017878.1	2389	Silent Mutation	ACA,ACG	T507T	XP_016873367.1
XM_017017879.1	2389	Silent Mutation	ACA,ACG	T507T	XP_016873368.1
XM_017017880.1	2389	Intron			XP_016873369.1

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