Product Details

SNP ID

rs150205920

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:58883755 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGTCCGCTTGTGTCCCGTCCATGG[C/T]GTTCAACCACATGTCGCTCCTCAGG

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SLTM PubMed Links

Gene Details

Gene

SLTM

Gene Name

SAFB like transcription modulator

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001013843.2	2774	Missense Mutation	CAC,CGC	H938R	NP_001013865.1
NM_024755.3	2774	Missense Mutation	CAC,CGC	H956R	NP_079031.2
XM_006720686.3	2774	Missense Mutation	CAC,CGC	H1009R	XP_006720749.3
XM_006720690.1	2774	Missense Mutation	CAC,CGC	H525R	XP_006720753.1
XM_011522022.1	2774	Missense Mutation	CAC,CGC	H1098R	XP_011520324.1
XM_011522023.1	2774	Missense Mutation	CAC,CGC	H1080R	XP_011520325.1
XM_011522024.1	2774	Missense Mutation	CAC,CGC	H1048R	XP_011520326.1
XM_011522025.1	2774	Missense Mutation	CAC,CGC	H1032R	XP_011520327.1
XM_011522026.2	2774	Missense Mutation	CAC,CGC	H1025R	XP_011520328.2
XM_011522027.1	2774	Missense Mutation	CAC,CGC	H1016R	XP_011520329.1
XM_011522028.1	2774	Missense Mutation	CAC,CGC	H998R	XP_011520330.1
XM_011522029.2	2774	Missense Mutation	CAC,CGC	H910R	XP_011520331.1
XM_011522030.2	2774	Intron			XP_011520332.1
XM_011522031.2	2774	Missense Mutation	CAC,CGC	H728R	XP_011520333.1
XM_017022576.1	2774	Missense Mutation	CAC,CGC	H888R	XP_016878065.1
XM_017022577.1	2774	Missense Mutation	CAC,CGC	H1007R	XP_016878066.1
XM_017022578.1	2774	Missense Mutation	CAC,CGC	H991R	XP_016878067.1
XM_017022579.1	2774	Missense Mutation	CAC,CGC	H903R	XP_016878068.1
XM_017022580.1	2774	Missense Mutation	CAC,CGC	H525R	XP_016878069.1

View Full Product Details