Product Details

SNP ID

rs10987522

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:126924638 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TAATATCTGAGATTGTGTTATGAGG[C/T]TTAAGTCAGAACAAAGAGAGCTGGA

Phenotype

MIM: 614444

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

RALGPS1 PubMed Links

Gene Details

Gene

RALGPS1

Gene Name

Ral GEF with PH domain and SH3 binding motif 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001190728.1		Intron			NP_001177657.1
NM_001190729.1		Intron			NP_001177658.1
NM_001190730.1		Intron			NP_001177659.1
NM_001322320.1		Intron			NP_001309249.1
NM_001322321.1		Intron			NP_001309250.1
NM_001322322.1		Intron			NP_001309251.1
NM_001322323.1		Intron			NP_001309252.1
NM_001322324.1		Intron			NP_001309253.1
NM_001322325.1		Intron			NP_001309254.1
NM_014636.2		Intron			NP_055451.1
XM_006717328.3		Intron			XP_006717391.2
XM_011519225.1		Intron			XP_011517527.1
XM_011519226.1		Intron			XP_011517528.1
XM_011519227.1		Intron			XP_011517529.1
XM_011519228.1		Intron			XP_011517530.1
XM_011519229.1		Intron			XP_011517531.1
XM_011519230.2		Intron			XP_011517532.1
XM_011519231.1		Intron			XP_011517533.1
XM_011519232.1		Intron			XP_011517534.1
XM_011519233.1		Intron			XP_011517535.1
XM_011519234.2		Intron			XP_011517536.1
XM_011519235.2		Intron			XP_011517537.1
XM_011519236.1		Intron			XP_011517538.1
XM_011519238.2		Intron			XP_011517540.1
XM_017015342.1		Intron			XP_016870831.1
XM_017015343.1		Intron			XP_016870832.1
XM_017015344.1		Intron			XP_016870833.1
XM_017015345.1		Intron			XP_016870834.1
XM_017015346.1		Intron			XP_016870835.1
XM_017015347.1		Intron			XP_016870836.1
XM_017015348.1		Intron			XP_016870837.1
XM_017015349.1		Intron			XP_016870838.1
XM_017015350.1		Intron			XP_016870839.1

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