Product Details

SNP ID

rs10282508

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:93131425 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACGACGCAGGAGGTCTTTGACTTCA[G/T]TTTTTTTCCACACATCCCCACTGTG

Phenotype

MIM: 611170

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

SAMD9L PubMed Links

Gene Details

Gene

SAMD9L

Gene Name

sterile alpha motif domain containing 9 like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001303496.1	4585	Missense Mutation	AAT,ACT	N1516T	NP_001290425.1
NM_001303497.1	4585	Missense Mutation	AAT,ACT	N1516T	NP_001290426.1
NM_001303498.1	4585	Missense Mutation	AAT,ACT	N1516T	NP_001290427.1
NM_001303500.1	4585	Missense Mutation	AAT,ACT	N1516T	NP_001290429.1
NM_152703.3	4585	Missense Mutation	AAT,ACT	N1516T	NP_689916.2
XM_005250193.3	4585	Missense Mutation	AAT,ACT	N1516T	XP_005250250.1
XM_006715890.1	4585	Missense Mutation	AAT,ACT	N1516T	XP_006715953.1
XM_011515903.2	4585	Missense Mutation	AAT,ACT	N1516T	XP_011514205.1
XM_017011822.1	4585	Missense Mutation	AAT,ACT	N1516T	XP_016867311.1
XM_017011823.1	4585	Missense Mutation	AAT,ACT	N1516T	XP_016867312.1

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