Product Details

SNP ID

rs149044401

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:150876156 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAGAAAAAAACCCTGCCTTCAAGCC[A/G]GTTCTTGCAATTATCCAGGTAAGCC

Phenotype

MIM: 611427

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

MTHFD1L PubMed Links

Gene Details

Gene

MTHFD1L

Gene Name

methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001242767.1	176	Silent Mutation	CCA,CCG	P98P	NP_001229696.1
NM_001242768.1	176	Silent Mutation	CCA,CCG	P32P	NP_001229697.1
NM_001242769.1	176	Silent Mutation	CCA,CCG	P98P	NP_001229698.1
NM_015440.4	176	Silent Mutation	CCA,CCG	P98P	NP_056255.2
XM_005266907.4	176	Silent Mutation	CCA,CCG	P98P	XP_005266964.1
XM_005266910.4	176	Silent Mutation	CCA,CCG	P98P	XP_005266967.1
XM_005266911.4	176	Silent Mutation	CCA,CCG	P98P	XP_005266968.1
XM_011535729.2	176	Silent Mutation	CCA,CCG	P98P	XP_011534031.1
XM_011535730.2	176	Silent Mutation	CCA,CCG	P32P	XP_011534032.1
XM_011535731.2	176	Silent Mutation	CCA,CCG	P32P	XP_011534033.1
XM_011535732.2	176	UTR 5			XP_011534034.1
XM_011535733.2	176	UTR 5			XP_011534035.1
XM_011535734.2	176	UTR 5			XP_011534036.1
XM_011535737.2	176	Silent Mutation	CCA,CCG	P98P	XP_011534039.1
XM_011535738.2	176	Silent Mutation	CCA,CCG	P98P	XP_011534040.1
XM_017010702.1	176	Silent Mutation	CCA,CCG	P98P	XP_016866191.1
XM_017010703.1	176	Silent Mutation	CCA,CCG	P98P	XP_016866192.1
XM_017010704.1	176	Silent Mutation	CCA,CCG	P32P	XP_016866193.1
XM_017010705.1	176	UTR 5			XP_016866194.1
XM_017010706.1	176	UTR 5			XP_016866195.1
XM_017010707.1	176	UTR 5			XP_016866196.1
XM_017010708.1	176	Silent Mutation	CCA,CCG	P98P	XP_016866197.1

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