Product Details

SNP ID

rs144738060

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:67347510 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTGCCTCCAGATGACCGAACTGTAC[A/G]TGAAGGTGAGAGAAAAGCTGCCAAG

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

LRRC36 PubMed Links

Gene Details

Gene

LRRC36

Gene Name

leucine rich repeat containing 36

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001161575.1	426	Missense Mutation	CAT,CGT	H15R	NP_001155047.1
NM_018296.5	426	Missense Mutation	CAT,CGT	H136R	NP_060766.5
XM_005256025.2	426	Missense Mutation	CAT,CGT	H136R	XP_005256082.1
XM_005256026.2	426	Missense Mutation	CAT,CGT	H136R	XP_005256083.1
XM_005256027.2	426	Missense Mutation	CAT,CGT	H136R	XP_005256084.1
XM_005256028.1	426	UTR 5			XP_005256085.1
XM_011523200.1	426	Missense Mutation	CAT,CGT	H136R	XP_011521502.1
XM_011523201.1	426	UTR 5			XP_011521503.1
XM_011523202.2	426	Intron			XP_011521504.1
XM_011523203.1	426	Missense Mutation	CAT,CGT	H136R	XP_011521505.1
XM_011523204.1	426	UTR 5			XP_011521506.1
XM_011523205.1	426	UTR 5			XP_011521507.1
XM_011523206.2	426	Missense Mutation	CAT,CGT	H136R	XP_011521508.1
XM_017023400.1	426	Missense Mutation	CAT,CGT	H136R	XP_016878889.1
XM_017023401.1	426	Missense Mutation	CAT,CGT	H136R	XP_016878890.1
XM_017023402.1	426	Missense Mutation	CAT,CGT	H136R	XP_016878891.1

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