Product Details

SNP ID

rs7788200

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:156640549 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACGGGAACGCACCTGCGTCTAGACG[C/G]TGACGCCGTGCGCGGGGCGGGGGCC

Phenotype

MIM: 610242 MIM: 610241

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

C7orf13 PubMed Links

Gene Details

Gene

C7orf13

Gene Name

chromosome 7 open reading frame 13

There are no transcripts associated with this gene.

Gene

RNF32

Gene Name

ring finger protein 32

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001184996.1		Intron			NP_001171925.1
NM_001184997.1		Intron			NP_001171926.1
NM_001308273.1		Intron			NP_001295202.1
NM_001308274.1		Intron			NP_001295203.1
NM_030936.3		Intron			NP_112198.1
XM_005249522.4		Intron			XP_005249579.1
XM_011515804.2		Intron			XP_011514106.1
XM_011515805.2		Intron			XP_011514107.1
XM_011515806.2		Intron			XP_011514108.1
XM_011515807.2		Intron			XP_011514109.1
XM_011515808.2		Intron			XP_011514110.1
XM_011515809.2		Intron			XP_011514111.1
XM_011515810.2		Intron			XP_011514112.1
XM_011515811.2		Intron			XP_011514113.1
XM_011515812.2		Intron			XP_011514114.1
XM_011515813.2		Intron			XP_011514115.1
XM_017011753.1		Intron			XP_016867242.1
XM_017011754.1		Intron			XP_016867243.1
XM_017011755.1		Intron			XP_016867244.1

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