LYN

LYN proto-oncogene, Src family tyrosine kinase

Summary

This gene encodes a tyrosine protein kinase, which maybe involved in the regulation of mast cell degranulation, and erythroid differentiation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2011]

Known Variants194 total

rsidPosition (GRCh37)AllelesClassClinVar
rs726514548:56,791,446A/Gregulatory region variant—
rs14507418:56,792,159T/Cregulatory region variant—
rs10508558:56,792,586G/T——
rs69831308:56,793,239A/Gregulatory region variant—
rs5584921718:56,823,701T/C——
rs12032208148:56,854,428A/G—uncertain significance
rs13209795708:56,854,441G/A—uncertain significance
rs18066219668:56,854,449A/G—uncertain significance
rs14736994628:56,854,454G/A—likely benign
rs7754487758:56,854,460C/T—likely benign
rs21304739698:56,854,462A/G—uncertain significance
rs24874907008:56,854,490A/G—uncertain significance
rs13417439958:56,854,492G/A—uncertain significance
rs3771534348:56,854,506A/G—uncertain significance
rs14269513188:56,854,527A/G—uncertain significance
rs560946688:56,854,529G/A—likely benign
rs24874908568:56,854,540A/G—uncertain significance
rs3702911268:56,854,563T/A—likely benign
rs7767881428:56,854,567A/G—likely benign
rs14613446738:56,858,993A/T—likely benign
rs7707389908:56,859,002C/T—likely benign
rs7741957588:56,859,003G/A—conflicting classifications of pathogenicity
rs7458150888:56,859,007G/A—uncertain significance
rs1456656348:56,859,015A/C—uncertain significance
rs18067812508:56,859,025T/C—likely benign
rs7620294418:56,859,027A/G—likely benign
rs7699521808:56,859,030T/C—likely benign
rs14560589958:56,859,033A/G—likely benign
rs1999582518:56,859,056T/C—uncertain significance
rs1847921988:56,859,064T/C—likely benign
rs24875031668:56,859,065A/T—likely benign
rs21304840888:56,859,066G/A—likely benign
rs7633444288:56,859,071A/G—likely benign
rs7812847178:56,860,158C/T—likely benign
rs24875057918:56,860,169A/C—likely benign
rs13486628658:56,860,173T/C—likely benign
rs21304863438:56,860,174T/C—uncertain significance
rs7734856098:56,860,182G/A—uncertain significance
rs7631457138:56,860,195A/T—uncertain significance
rs7712126238:56,860,201T/C—uncertain significance
rs7747111168:56,860,206G/A—uncertain significance
rs1809535958:56,860,215C/G—uncertain significance
rs7662923708:56,860,232C/T—likely benign
rs7603013228:56,860,234C/T—uncertain significance
rs3723487138:56,860,235G/A—likely benign
rs7568794238:56,860,238C/T—likely benign
rs24875060998:56,860,241C/T—likely benign
rs13148092248:56,860,246C/G—uncertain significance
rs10082018788:56,860,256A/G—likely benign
rs12720289358:56,860,262G/T—uncertain significance
rs5384670288:56,860,271A/G—likely benign
rs24875062108:56,860,272G/A—uncertain significance
rs8997666988:56,860,289G/T—likely benign
rs7469421598:56,860,291T/C—likely benign
rs7699163078:56,860,294C/G—likely benign
rs3769206958:56,860,300C/T—likely benign
rs18068262748:56,860,301G/T—likely benign
rs11784129778:56,862,999A/T—likely benign
rs5396806438:56,863,002T/G—likely benign
rs13184828578:56,863,003G/A—likely benign
rs7726245388:56,863,015T/C—uncertain significance
rs7759411238:56,863,021T/G—uncertain significance
rs24875126078:56,863,047T/C—uncertain significance
rs21304917038:56,863,053C/G—uncertain significance
rs7762764508:56,863,057A/G—likely benign
rs3753948888:56,863,072C/A—likely benign
rs24875127498:56,863,084T/C—likely benign
rs24875127598:56,863,092A/T—uncertain significance
rs5762538608:56,863,110C/T—uncertain significance
rs21304918608:56,863,126C/G—likely benign
rs11638047538:56,863,251A/G—uncertain significance
rs24875134128:56,863,254A/G—uncertain significance
rs3684839118:56,863,256A/G—uncertain significance
rs7672137668:56,863,270C/T—likely benign
rs7527391118:56,863,271G/A—uncertain significance
rs24875134878:56,863,273A/G—likely benign
rs1436189278:56,863,294A/C—likely benign
rs1475474708:56,863,303C/T—benign
rs1417699188:56,863,304G/A—uncertain significance
rs24875136968:56,863,331G/A—uncertain significance
rs3694842398:56,863,336A/G—likely benign
rs13965378548:56,863,350A/G—likely benign
rs18069197708:56,863,357C/A—likely benign
rs7665497428:56,864,514T/G—likely benign
rs7550871978:56,864,516C/T—likely benign
rs7529535878:56,864,520C/T—likely benign
rs7564776458:56,864,522T/C—uncertain significance
rs8684301248:56,864,525G/T—uncertain significance
rs1459780658:56,864,526A/C—likely benign
rs21304948588:56,864,528G/A—uncertain significance
rs24875168898:56,864,542G/C—uncertain significance
rs5489512628:56,864,556C/T—likely benign
rs14551032918:56,864,593A/C—likely benign
rs1427773248:56,864,607T/C—likely benign
rs18069657268:56,864,616T/C—likely benign
rs12619881468:56,864,636C/G—uncertain significance
rs14506165238:56,864,641C/G—uncertain significance
rs9936320788:56,864,645G/T—uncertain significance
rs5420494048:56,864,649C/T—likely benign
rs21304950758:56,864,650A/G—uncertain significance

Showing 100 of 194 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.