Product Details

SNP ID

rs202095799

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:14151384 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CACAGGTGGCACAGGGGGCTCAGGC[A/G]GTGGAGGGCCCTTGGCCGCGCTGCT

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	4323	Missense Mutation	CCG,CTG	P1305L	NP_001008701.1
NM_014921.4	4323	Missense Mutation	CCG,CTG	P1300L	NP_055736.2
XM_005259818.3	4323	Missense Mutation	CCG,CTG	P1324L	XP_005259875.1
XM_011527796.2	4323	Missense Mutation	CCG,CTG	P1336L	XP_011526098.1
XM_011527798.2	4323	Missense Mutation	CCG,CTG	P1331L	XP_011526100.1
XM_011527801.2	4323	Missense Mutation	CCG,CTG	P1256L	XP_011526103.1
XM_017026475.1	4323	Missense Mutation	CCG,CTG	P1337L	XP_016881964.1
XM_017026476.1	4323	Missense Mutation	CCG,CTG	P1337L	XP_016881965.1
XM_017026477.1	4323	Missense Mutation	CCG,CTG	P1330L	XP_016881966.1
XM_017026478.1	4323	Missense Mutation	CCG,CTG	P1313L	XP_016881967.1
XM_017026479.1	4323	Missense Mutation	CCG,CTG	P1307L	XP_016881968.1
XM_017026480.1	4323	Missense Mutation	CCG,CTG	P1251L	XP_016881969.1
XM_017026481.1	4323	Intron			XP_016881970.1

Gene

LOC100507373

Gene Name

uncharacterized LOC100507373

There are no transcripts associated with this gene.

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