Product Details

SNP ID

rs77972416

Assay Type

Functionally tested

NCBI dbSNP Submissions

11

Location

Chr.1:169795747 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTTAAAAGATGTTCAGTAAATAAAA[A/G]TGATTTTCCTCCTTCCCCTCTCAGA

Phenotype

MIM: 615255

Polymorphism

A/G, Transition 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	339	Intron			NP_001306976.1
NM_001320048.1	339	Intron			NP_001306977.1
NM_001320050.1	339	Intron			NP_001306979.1
NM_001320051.1	339	Intron			NP_001306980.1
NM_018186.3	339	UTR 5			NP_060656.2
XM_005245317.4	339	Intron			XP_005245374.1
XM_011509735.2	339	Intron			XP_011508037.1
XM_017001722.1	339	Intron			XP_016857211.1
XM_017001723.1	339	Intron			XP_016857212.1
XM_017001724.1	339	Intron			XP_016857213.1
XM_017001725.1	339	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	339	Intron			NP_001307128.1
NM_001320201.1	339	Intron			NP_001307130.1
NM_033418.3	339	Intron			NP_219486.1
XM_006711627.3	339	Intron			XP_006711690.1

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