Product Details

SNP ID

rs202011663

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.13:41223350 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATTCGCTCTGACTGGGCTCTTGTT[C/G]CCACCTGTGCCATAACAAAAAGCAA

Phenotype

MIM: 604601

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

LOC101929140 PubMed Links

Gene Details

Gene

LOC101929140

Gene Name

uncharacterized LOC101929140

There are no transcripts associated with this gene.

Gene

MTRF1

Gene Name

mitochondrial translational release factor 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004294.2	1670	Missense Mutation	GCA,GGA	A377G	NP_004285.2
XM_005266599.2	1670	Missense Mutation	GCA,GGA	A377G	XP_005266656.1
XM_006719897.2	1670	Missense Mutation	GCA,GGA	A377G	XP_006719960.1
XM_006719898.2	1670	Missense Mutation	GCA,GGA	A377G	XP_006719961.1
XM_006719900.2	1670	Missense Mutation	GCA,GGA	A377G	XP_006719963.1
XM_011535315.2	1670	Missense Mutation	GCA,GGA	A429G	XP_011533617.1
XM_011535317.2	1670	Missense Mutation	GCA,GGA	A390G	XP_011533619.1
XM_011535318.2	1670	Missense Mutation	GCA,GGA	A377G	XP_011533620.1
XM_011535320.2	1670	Missense Mutation	GCA,GGA	A377G	XP_011533622.1
XM_011535321.2	1670	Missense Mutation	GCA,GGA	A377G	XP_011533623.1
XM_011535323.2	1670	Missense Mutation	GCA,GGA	A377G	XP_011533625.1
XM_011535325.2	1670	Missense Mutation	GCA,GGA	A377G	XP_011533627.1
XM_011535326.2	1670	Intron			XP_011533628.1
XM_011535327.2	1670	Intron			XP_011533629.1
XM_017020856.1	1670	Missense Mutation	GCA,GGA	A429G	XP_016876345.1
XM_017020857.1	1670	Missense Mutation	GCA,GGA	A429G	XP_016876346.1
XM_017020858.1	1670	Missense Mutation	GCA,GGA	A429G	XP_016876347.1
XM_017020859.1	1670	Missense Mutation	GCA,GGA	A429G	XP_016876348.1
XM_017020860.1	1670	Missense Mutation	GCA,GGA	A390G	XP_016876349.1
XM_017020861.1	1670	Missense Mutation	GCA,GGA	A390G	XP_016876350.1
XM_017020862.1	1670	Missense Mutation	GCA,GGA	A377G	XP_016876351.1
XM_017020863.1	1670	Missense Mutation	GCA,GGA	A377G	XP_016876352.1
XM_017020864.1	1670	Missense Mutation	GCA,GGA	A377G	XP_016876353.1
XM_017020865.1	1670	Missense Mutation	GCA,GGA	A377G	XP_016876354.1
XM_017020866.1	1670	Missense Mutation	GCA,GGA	A377G	XP_016876355.1
XM_017020867.1	1670	Missense Mutation	GCA,GGA	A377G	XP_016876356.1
XM_017020868.1	1670	Missense Mutation	GCA,GGA	A377G	XP_016876357.1
XM_017020869.1	1670	Missense Mutation	GCA,GGA	A377G	XP_016876358.1
XM_017020870.1	1670	Missense Mutation	GCA,GGA	A377G	XP_016876359.1
XM_017020871.1	1670	Missense Mutation	GCA,GGA	A377G	XP_016876360.1
XM_017020872.1	1670	Intron			XP_016876361.1
XM_017020873.1	1670	Missense Mutation	GCA,GGA	A377G	XP_016876362.1
XM_017020874.1	1670	Missense Mutation	GCA,GGA	A377G	XP_016876363.1
XM_017020875.1	1670	Missense Mutation	GCA,GGA	A377G	XP_016876364.1
XM_017020876.1	1670	Missense Mutation	GCA,GGA	A213G	XP_016876365.1
XM_017020877.1	1670	Missense Mutation	GCA,GGA	A213G	XP_016876366.1
XM_017020878.1	1670	Intron			XP_016876367.1
XM_017020879.1	1670	Intron			XP_016876368.1

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