Product Details

SNP ID

rs2304967

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:35478161 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTGGGAGACAGGTGATGATGTACTT[C/G]CTGGAGAGGGCAGTTCCTCACATAC

Phenotype

MIM: 614956

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

SLFN12L PubMed Links

Gene Details

Gene

SLFN12L

Gene Name

schlafen family member 12 like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001195790.1	7869	Missense Mutation	GCA,GGA	A373G	NP_001182719.1
XM_017024005.1	7869	Missense Mutation	GCA,GGA	A402G	XP_016879494.1
XM_017024006.1	7869	Missense Mutation	GCA,GGA	A373G	XP_016879495.1
XM_017024007.1	7869	Missense Mutation	GCA,GGA	A373G	XP_016879496.1
XM_017024008.1	7869	Missense Mutation	GCA,GGA	A355G	XP_016879497.1
XM_017024009.1	7869	Missense Mutation	GCA,GGA	A355G	XP_016879498.1

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