Product Details

SNP ID

rs201971593

Assay Type

Functionally tested

NCBI dbSNP Submissions

4

Location

Chr.1:70221837 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCGACGAACTGCGCCTCTTCCCGCC[A/G]GAGTGAGTATCGTCCACCATCACTG

Phenotype

MIM: 602010

Polymorphism

A/G, Transition 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	322	Silent Mutation	CCA,CCG	P67P	NP_001177916.1
NM_004768.3	322	Silent Mutation	CCA,CCG	P67P	NP_004759.1
XM_005271338.3	322	Silent Mutation	CCA,CCG	P67P	XP_005271395.1
XM_005271339.3	322	Silent Mutation	CCA,CCG	P67P	XP_005271396.1
XM_011542427.2	322	Intron			XP_011540729.1
XM_011542428.2	322	Intron			XP_011540730.1
XM_011542431.2	322	UTR 5			XP_011540733.1
XM_017002811.1	322	Silent Mutation	CCA,CCG	P67P	XP_016858300.1
XM_017002812.1	322	Silent Mutation	CCA,CCG	P67P	XP_016858301.1
XM_017002813.1	322	Silent Mutation	CCA,CCG	P67P	XP_016858302.1
XM_017002814.1	322	Intron			XP_016858303.1
XM_017002815.1	322	Intron			XP_016858304.1
XM_017002816.1	322	UTR 5			XP_016858305.1
XM_017002817.1	322	Intron			XP_016858306.1
XM_017002818.1	322	Intron			XP_016858307.1
XM_017002819.1	322	Intron			XP_016858308.1
XM_017002820.1	322	Intron			XP_016858309.1
XM_017002821.1	322	Intron			XP_016858310.1
XM_017002822.1	322	Intron			XP_016858311.1
XM_017002823.1	322	Intron			XP_016858312.1
XM_017002824.1	322	UTR 5			XP_016858313.1
XM_017002825.1	322	Intron			XP_016858314.1
XM_017002826.1	322	Intron			XP_016858315.1
XM_017002827.1	322	Intron			XP_016858316.1
XM_017002828.1	322	UTR 5			XP_016858317.1
XM_017002829.1	322	UTR 5			XP_016858318.1
XM_017002830.1	322	UTR 5			XP_016858319.1
XM_017002831.1	322	Intron			XP_016858320.1
XM_017002832.1	322	Intron			XP_016858321.1
XM_017002833.1	322	Intron			XP_016858322.1
XM_017002834.1	322	Intron			XP_016858323.1

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