Product Details

SNP ID

rs199658590

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:14152393 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTGTTGTAGGGACTGGTGCCCCCAC[A/G]GGGCTGCAGCACGGGGTTGGTCAGC

Phenotype

MIM: 616416

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

ADGRL1 PubMed Links

Gene Details

Gene

ADGRL1

Gene Name

adhesion G protein-coupled receptor L1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001008701.2	3917	Missense Mutation	CGT,TGT	R1194C	NP_001008701.1
NM_014921.4	3917	Missense Mutation	CGT,TGT	R1189C	NP_055736.2
XM_005259818.3	3917	Missense Mutation	CGT,TGT	R1189C	XP_005259875.1
XM_011527796.2	3917	Missense Mutation	CGT,TGT	R1201C	XP_011526098.1
XM_011527798.2	3917	Missense Mutation	CGT,TGT	R1196C	XP_011526100.1
XM_011527801.2	3917	Missense Mutation	CGT,TGT	R1121C	XP_011526103.1
XM_017026475.1	3917	Missense Mutation	CGT,TGT	R1202C	XP_016881964.1
XM_017026476.1	3917	Missense Mutation	CGT,TGT	R1202C	XP_016881965.1
XM_017026477.1	3917	Missense Mutation	CGT,TGT	R1195C	XP_016881966.1
XM_017026478.1	3917	Missense Mutation	CGT,TGT	R1202C	XP_016881967.1
XM_017026479.1	3917	Missense Mutation	CGT,TGT	R1202C	XP_016881968.1
XM_017026480.1	3917	Missense Mutation	CGT,TGT	R1116C	XP_016881969.1
XM_017026481.1	3917	Intron			XP_016881970.1

Gene

LOC100507373

Gene Name

uncharacterized LOC100507373

There are no transcripts associated with this gene.

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