Product Details

SNP ID

rs1127066

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.14:22901846 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

GGGGGGTAAAGAGGCTGGAGAGCTG[C/G]AAACACTGGGAGGCAAGGTTCAGGG

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

RBM23 PubMed Links

Gene Details

Gene

RBM23

Gene Name

RNA binding motif protein 23

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001077351.1	1563	Missense Mutation	TTC,TTG	F428L	NP_001070819.1
NM_001077352.1	1563	Missense Mutation	TTC,TTG	F394L	NP_001070820.1
NM_001308044.1	1563	Missense Mutation	TTC,TTG	F258L	NP_001294973.1
NM_018107.4	1563	Missense Mutation	TTC,TTG	F412L	NP_060577.3
XM_011536890.2	1563	Missense Mutation	TTC,TTG	F472L	XP_011535192.1
XM_011536892.2	1563	Missense Mutation	TTC,TTG	F456L	XP_011535194.1
XM_011536893.2	1563	Missense Mutation	TTC,TTG	F456L	XP_011535195.1
XM_011536894.2	1563	Missense Mutation	TTC,TTG	F454L	XP_011535196.1
XM_011536895.2	1563	Missense Mutation	TTC,TTG	F438L	XP_011535197.1
XM_011536896.2	1563	Missense Mutation	TTC,TTG	F438L	XP_011535198.1
XM_011536897.2	1563	Missense Mutation	TTC,TTG	F430L	XP_011535199.1
XM_011536900.1	1563	Missense Mutation	TTC,TTG	F410L	XP_011535202.1
XM_011536902.1	1563	Missense Mutation	TTC,TTG	F258L	XP_011535204.1
XM_011536903.1	1563	Missense Mutation	TTC,TTG	F258L	XP_011535205.1
XM_011536904.1	1563	Missense Mutation	TTC,TTG	F258L	XP_011535206.1
XM_011536905.1	1563	Missense Mutation	TTC,TTG	F258L	XP_011535207.1
XM_011536906.1	1563	Missense Mutation	TTC,TTG	F258L	XP_011535208.1
XM_017021398.1	1563	Missense Mutation	TTC,TTG	F488L	XP_016876887.1
XM_017021399.1	1563	Missense Mutation	TTC,TTG	F470L	XP_016876888.1
XM_017021400.1	1563	Missense Mutation	TTC,TTG	F462L	XP_016876889.1
XM_017021401.1	1563	Missense Mutation	TTC,TTG	F460L	XP_016876890.1
XM_017021402.1	1563	Missense Mutation	TTC,TTG	F460L	XP_016876891.1
XM_017021403.1	1563	Missense Mutation	TTC,TTG	F444L	XP_016876892.1
XM_017021404.1	1563	Missense Mutation	TTC,TTG	F444L	XP_016876893.1
XM_017021405.1	1563	Missense Mutation	TTC,TTG	F442L	XP_016876894.1
XM_017021406.1	1563	Missense Mutation	TTC,TTG	F446L	XP_016876895.1
XM_017021407.1	1563	Missense Mutation	TTC,TTG	F428L	XP_016876896.1
XM_017021408.1	1563	Missense Mutation	TTC,TTG	F426L	XP_016876897.1
XM_017021409.1	1563	Missense Mutation	TTC,TTG	F428L	XP_016876898.1
XM_017021410.1	1563	Missense Mutation	TTC,TTG	F394L	XP_016876899.1
XM_017021411.1	1563	Missense Mutation	TTC,TTG	F412L	XP_016876900.1
XM_017021412.1	1563	Intron			XP_016876901.1
XM_017021413.1	1563	Intron			XP_016876902.1
XM_017021414.1	1563	Missense Mutation	TTC,TTG	F290L	XP_016876903.1
XM_017021415.1	1563	Missense Mutation	TTC,TTG	F290L	XP_016876904.1
XM_017021416.1	1563	Missense Mutation	TTC,TTG	F290L	XP_016876905.1
XM_017021417.1	1563	Missense Mutation	TTC,TTG	F290L	XP_016876906.1
XM_017021418.1	1563	Missense Mutation	TTC,TTG	F290L	XP_016876907.1
XM_017021419.1	1563	Missense Mutation	TTC,TTG	F290L	XP_016876908.1
XM_017021420.1	1563	Missense Mutation	TTC,TTG	F258L	XP_016876909.1

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