Product Details

SNP ID

rs10814376

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:36343167 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTTATTTTTTCCTGAATATTTTCAA[C/T]CTTTGGTTGGTTGAATACAGAGGGC

Phenotype

MIM: 612488

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

RNF38 PubMed Links

Gene Details

Gene

RNF38

Gene Name

ring finger protein 38

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_022781.4		Intron			NP_073618.3
NM_194328.2		Intron			NP_919309.1
NM_194329.2		Intron			NP_919310.1
NM_194330.2		Intron			NP_919311.1
NM_194332.2		Intron			NP_919313.1
XM_005251366.3		Intron			XP_005251423.1
XM_005251367.3		Intron			XP_005251424.1
XM_005251368.3		Intron			XP_005251425.1
XM_006716721.3		Intron			XP_006716784.1
XM_011517712.2		Intron			XP_011516014.1
XM_011517713.2		Intron			XP_011516015.1
XM_017014294.1		Intron			XP_016869783.1
XM_017014295.1		Intron			XP_016869784.1
XM_017014296.1		Intron			XP_016869785.1
XM_017014297.1		Intron			XP_016869786.1

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