Product Details

SNP ID

rs2732705

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:46274563 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACGTACAGGAATCATTGATAAGATA[G/T]GGATGGATTATATGTAACCGTGGCT

Phenotype

MIM: 616555

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

ARL17B PubMed Links

Gene Details

Gene

ARL17B

Gene Name

ADP ribosylation factor like GTPase 17B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001039083.3	1732	Intron			NP_001034172.3
NM_001103154.1	1732	Intron			NP_001096624.1
XM_005256918.4	1732	UTR 3			XP_005256975.1
XM_011524160.2	1732	Intron			XP_011522462.1
XM_011524161.2	1732	Intron			XP_011522463.1
XM_011524162.2	1732	UTR 3			XP_011522464.1
XM_011524163.2	1732	Intron			XP_011522465.1
XM_011524164.2	1732	Intron			XP_011522466.1
XM_011524165.2	1732	Intron			XP_011522467.1
XM_011524166.2	1732	Intron			XP_011522468.1
XM_011524167.2	1732	Intron			XP_011522469.1

Gene

LRRC37A

Gene Name

leucine rich repeat containing 37A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014834.4	1732	Intron			NP_055649.4
XM_005257879.4	1732	Intron			XP_005257936.1
XM_005257880.4	1732	Intron			XP_005257937.1
XM_005257882.4	1732	Intron			XP_005257939.1
XM_005257883.4	1732	Intron			XP_005257940.1
XM_005257884.4	1732	Intron			XP_005257941.1
XM_006722210.3	1732	Intron			XP_006722273.1
XM_006722211.3	1732	Intron			XP_006722274.1
XM_011525539.2	1732	Intron			XP_011523841.1
XM_017025472.1	1732	Intron			XP_016880961.1
XM_017025473.1	1732	Intron			XP_016880962.1

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