Product Details

SNP ID

rs10919246

Assay Type

Functionally tested

NCBI dbSNP Submissions

37

Location

Chr.1:169795911 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGAGGCGCTTAGCGCCTTCTTCGTC[C/G]GGGTGCAGCACATTCTTGATTGGTC

Phenotype

MIM: 615255

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

C1orf112 PubMed Links

Gene Details

Gene

C1orf112

Gene Name

chromosome 1 open reading frame 112

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001320047.1	200	UTR 5			NP_001306976.1
NM_001320048.1	200	Intron			NP_001306977.1
NM_001320050.1	200	Intron			NP_001306979.1
NM_001320051.1	200	Intron			NP_001306980.1
NM_018186.3	200	UTR 5			NP_060656.2
XM_005245317.4	200	Intron			XP_005245374.1
XM_011509735.2	200	Intron			XP_011508037.1
XM_017001722.1	200	Intron			XP_016857211.1
XM_017001723.1	200	Intron			XP_016857212.1
XM_017001724.1	200	Intron			XP_016857213.1
XM_017001725.1	200	Intron			XP_016857214.1

Gene

METTL18

Gene Name

methyltransferase like 18

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001320199.1	200	Intron			NP_001307128.1
NM_001320201.1	200	Intron			NP_001307130.1
NM_033418.3	200	Intron			NP_219486.1
XM_006711627.3	200	Intron			XP_006711690.1

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