Product Details

SNP ID

rs200093391

Assay Type

Functionally tested

NCBI dbSNP Submissions

3

Location

Chr.1:70221651 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGAGCAGCGCCATGAGCAACACTAC[A/C]GTCGTCCCCAGCACTGCAGGTCCGG

Phenotype

MIM: 602010

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

SRSF11 PubMed Links

Gene Details

Gene

SRSF11

Gene Name

serine and arginine rich splicing factor 11

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001190987.1	136	Silent Mutation	ACA,ACC	T5T	NP_001177916.1
NM_004768.3	136	Silent Mutation	ACA,ACC	T5T	NP_004759.1
XM_005271338.3	136	Silent Mutation	ACA,ACC	T5T	XP_005271395.1
XM_005271339.3	136	Silent Mutation	ACA,ACC	T5T	XP_005271396.1
XM_011542427.2	136	Intron			XP_011540729.1
XM_011542428.2	136	Intron			XP_011540730.1
XM_011542431.2	136	UTR 5			XP_011540733.1
XM_017002811.1	136	Silent Mutation	ACA,ACC	T5T	XP_016858300.1
XM_017002812.1	136	Silent Mutation	ACA,ACC	T5T	XP_016858301.1
XM_017002813.1	136	Silent Mutation	ACA,ACC	T5T	XP_016858302.1
XM_017002814.1	136	Intron			XP_016858303.1
XM_017002815.1	136	Intron			XP_016858304.1
XM_017002816.1	136	UTR 5			XP_016858305.1
XM_017002817.1	136	Intron			XP_016858306.1
XM_017002818.1	136	Intron			XP_016858307.1
XM_017002819.1	136	Intron			XP_016858308.1
XM_017002820.1	136	Intron			XP_016858309.1
XM_017002821.1	136	Intron			XP_016858310.1
XM_017002822.1	136	Intron			XP_016858311.1
XM_017002823.1	136	Intron			XP_016858312.1
XM_017002824.1	136	UTR 5			XP_016858313.1
XM_017002825.1	136	Intron			XP_016858314.1
XM_017002826.1	136	Intron			XP_016858315.1
XM_017002827.1	136	Intron			XP_016858316.1
XM_017002828.1	136	UTR 5			XP_016858317.1
XM_017002829.1	136	UTR 5			XP_016858318.1
XM_017002830.1	136	UTR 5			XP_016858319.1
XM_017002831.1	136	Intron			XP_016858320.1
XM_017002832.1	136	Intron			XP_016858321.1
XM_017002833.1	136	Intron			XP_016858322.1
XM_017002834.1	136	Intron			XP_016858323.1

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