Product Details

SNP ID

rs8110995

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:40357935 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTATTATTAATCTCCACATTGTTCA[A/G]AGAATGAAAGTGTGGCTTAGAGAAG

Phenotype

MIM: 615698

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

C19orf47 PubMed Links

Gene Details

Gene

C19orf47

Gene Name

chromosome 19 open reading frame 47

There are no transcripts associated with this gene.

Gene

PLD3

Gene Name

phospholipase D family member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001031696.3		Intron			NP_001026866.1
NM_001291311.1		Intron			NP_001278240.1
NM_012268.3		Intron			NP_036400.2
XM_005258704.1		Intron			XP_005258761.1
XM_005258707.4		Intron			XP_005258764.1
XM_005258708.3		Intron			XP_005258765.1
XM_005258709.4		Intron			XP_005258766.1
XM_005258710.4		Intron			XP_005258767.1
XM_006723122.1		Intron			XP_006723185.1
XM_011526692.1		Intron			XP_011524994.1
XM_011526693.1		Intron			XP_011524995.1
XM_017026546.1		Intron			XP_016882035.1
XM_017026547.1		Intron			XP_016882036.1
XM_017026548.1		Intron			XP_016882037.1
XM_017026549.1		Intron			XP_016882038.1

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