Product Details

SNP ID

rs723796

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:4030914 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACTTGTGAGGATGTGTTTATACTAT[C/T]ACCATCATCAGTATCAGCTACCAAT

Phenotype

MIM: 602338

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

PRPF4B PubMed Links

Gene Details

Gene

PRPF4B

Gene Name

pre-mRNA processing factor 4B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003913.4		Intron			NP_003904.3
XM_011514970.2		Intron			XP_011513272.1
XM_017011410.1		Intron			XP_016866899.1
XM_017011411.1		Intron			XP_016866900.1
XM_017011412.1		Intron			XP_016866901.1
XM_017011413.1		Intron			XP_016866902.1
XM_017011414.1		Intron			XP_016866903.1
XM_017011415.1		Intron			XP_016866904.1
XM_017011416.1		Intron			XP_016866905.1
XM_017011417.1		Intron			XP_016866906.1
XM_017011418.1		Intron			XP_016866907.1
XM_017011419.1		Intron			XP_016866908.1
XM_017011420.1		Intron			XP_016866909.1
XM_017011421.1		Intron			XP_016866910.1
XM_017011422.1		Intron			XP_016866911.1
XM_017011423.1		Intron			XP_016866912.1
XM_017011424.1		Intron			XP_016866913.1
XM_017011425.1		Intron			XP_016866914.1
XM_017011426.1		Intron			XP_016866915.1
XM_017011427.1		Intron			XP_016866916.1
XM_017011428.1		Intron			XP_016866917.1
XM_017011429.1		Intron			XP_016866918.1
XM_017011430.1		Intron			XP_016866919.1
XM_017011431.1		Intron			XP_016866920.1
XM_017011432.1		Intron			XP_016866921.1
XM_017011433.1		Intron			XP_016866922.1
XM_017011434.1		Intron			XP_016866923.1
XM_017011435.1		Intron			XP_016866924.1

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