Product Details

SNP ID

rs138770431

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:64805088 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAAGAAAGGTGGCCCAGCCCACATG[C/T]AGCACAGGCGTGGGACTGCCCTCCT

Phenotype

MIM: 603166 MIM: 613733

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MAP4K2 PubMed Links

Gene Details

Gene

MAP4K2

Gene Name

mitogen-activated protein kinase kinase kinase kinase 2

There are no transcripts associated with this gene.

Gene

MEN1

Gene Name

menin 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000244.3	1788	Silent Mutation	CTA,CTG	L437L	NP_000235.2
NM_130799.2	1788	Silent Mutation	CTA,CTG	L432L	NP_570711.1
NM_130800.2	1788	Silent Mutation	CTA,CTG	L437L	NP_570712.1
NM_130801.2	1788	Silent Mutation	CTA,CTG	L437L	NP_570713.1
NM_130802.2	1788	Silent Mutation	CTA,CTG	L437L	NP_570714.1
NM_130803.2	1788	Silent Mutation	CTA,CTG	L437L	NP_570715.1
NM_130804.2	1788	Silent Mutation	CTA,CTG	L437L	NP_570716.1
XM_005274001.4	1788	Silent Mutation	CTA,CTG	L432L	XP_005274058.1
XM_011545040.1	1788	Silent Mutation	CTA,CTG	L474L	XP_011543342.1
XM_011545041.2	1788	Silent Mutation	CTA,CTG	L474L	XP_011543343.1
XM_011545042.2	1788	Silent Mutation	CTA,CTG	L474L	XP_011543344.1
XM_017017765.1	1788	Silent Mutation	CTA,CTG	L479L	XP_016873254.1
XM_017017766.1	1788	Silent Mutation	CTA,CTG	L479L	XP_016873255.1
XM_017017767.1	1788	Silent Mutation	CTA,CTG	L479L	XP_016873256.1
XM_017017768.1	1788	Silent Mutation	CTA,CTG	L479L	XP_016873257.1
XM_017017769.1	1788	Silent Mutation	CTA,CTG	L432L	XP_016873258.1
XM_017017770.1	1788	Silent Mutation	CTA,CTG	L432L	XP_016873259.1

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