ClinVar Miner

List of variants in gene KANSL1 reported by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 81
Download table as spreadsheet
HGVS dbSNP
NM_001193466.1(KANSL1):c.*1022C>G rs748062988
NM_001193466.1(KANSL1):c.*1103dupT rs142756815
NM_001193466.1(KANSL1):c.*1234_*1235dupAA rs140510364
NM_001193466.1(KANSL1):c.*1287G>T rs886053064
NM_001193466.1(KANSL1):c.*1306C>G rs886053063
NM_001193466.1(KANSL1):c.*1350A>C rs886053062
NM_001193466.1(KANSL1):c.*1354dupA rs67641084
NM_001193466.1(KANSL1):c.*1433A>G rs886053060
NM_001193466.1(KANSL1):c.*1434T>C rs886053059
NM_001193466.1(KANSL1):c.*1520dupA rs67801660
NM_001193466.1(KANSL1):c.*1551delA rs767830420
NM_001193466.1(KANSL1):c.*32_*35delACTA rs767896466
NM_001193466.1(KANSL1):c.*608C>G rs886053067
NM_001193466.1(KANSL1):c.*637T>G rs886053066
NM_001193466.1(KANSL1):c.*816C>T rs886053065
NM_001193466.1(KANSL1):c.*954C>G rs150500194
NM_001193466.1(KANSL1):c.-146_-142delCTCTT rs141752007
NM_001193466.1(KANSL1):c.-210G>A rs180814097
NM_001193466.1(KANSL1):c.-227A>G rs62060947
NM_001193466.1(KANSL1):c.-269A>T rs11079733
NM_001193466.1(KANSL1):c.-279G>A rs886053071
NM_001193466.1(KANSL1):c.-35C>T rs200079769
NM_001193466.1(KANSL1):c.-364T>A rs2696633
NM_001193466.1(KANSL1):c.-407T>C rs144753624
NM_001193466.1(KANSL1):c.-439_-437delCTC rs534448299
NM_001193466.1(KANSL1):c.-461_-459delCCT rs143625699
NM_001193466.1(KANSL1):c.-475C>G rs1057516026
NM_001193466.1(KANSL1):c.-486C>T rs72836333
NM_001193466.1(KANSL1):c.-54C>T rs548814710
NM_001193466.1(KANSL1):c.-61C>T rs568889635
NM_001193466.1(KANSL1):c.1011C>G (p.Ser337=) rs2240758
NM_001193466.1(KANSL1):c.1124C>T (p.Ser375Leu) rs142696045
NM_001193466.1(KANSL1):c.1162A>G (p.Ile388Val) rs767398590
NM_001193466.1(KANSL1):c.1166C>T (p.Ala389Val) rs368394693
NM_001193466.1(KANSL1):c.1423G>A (p.Ala475Thr) rs547462953
NM_001193466.1(KANSL1):c.1432-4G>A rs749329088
NM_001193466.1(KANSL1):c.1491A>G (p.Pro497=) rs17576165
NM_001193466.1(KANSL1):c.1653-6G>A rs369261388
NM_001193466.1(KANSL1):c.1676A>G (p.His559Arg) rs886053069
NM_001193466.1(KANSL1):c.1831G>A (p.Val611Ile) rs202150313
NM_001193466.1(KANSL1):c.1857G>T (p.Arg619=) rs191986791
NM_001193466.1(KANSL1):c.1940A>G (p.Glu647Gly) rs886053068
NM_001193466.1(KANSL1):c.1945C>G (p.His649Asp) rs759914921
NM_001193466.1(KANSL1):c.2109A>G (p.Leu703=) rs34101027
NM_001193466.1(KANSL1):c.2128C>A (p.Pro710Thr) rs550137256
NM_001193466.1(KANSL1):c.2136G>A (p.Pro712=) rs2277613
NM_001193466.1(KANSL1):c.2152T>C (p.Ser718Pro) rs34043286
NM_001193466.1(KANSL1):c.2256C>T (p.Asp752=) rs760224197
NM_001193466.1(KANSL1):c.2287G>T (p.Val763Leu) rs781594360
NM_001193466.1(KANSL1):c.2294C>T (p.Ala765Val) rs151099014
NM_001193466.1(KANSL1):c.2441C>G (p.Thr814Ser) rs757031050
NM_001193466.1(KANSL1):c.2481C>T (p.Ser827=) rs143653891
NM_001193466.1(KANSL1):c.2490A>G (p.Ser830=) rs200903355
NM_001193466.1(KANSL1):c.2547G>A (p.Gln849=) rs763362339
NM_001193466.1(KANSL1):c.2580T>C (p.Phe860=) rs17574604
NM_001193466.1(KANSL1):c.2628C>T (p.Arg876=) rs149756887
NM_001193466.1(KANSL1):c.2683C>G (p.Leu895Val) rs555819683
NM_001193466.1(KANSL1):c.2698G>A (p.Gly900Arg) rs74867664
NM_001193466.1(KANSL1):c.286T>C (p.Leu96=) rs140268765
NM_001193466.1(KANSL1):c.296A>G (p.Gln99Arg) rs754727332
NM_001193466.1(KANSL1):c.3091-15C>A rs565665710
NM_001193466.1(KANSL1):c.30C>T (p.Asp10=) rs200649587
NM_001193466.1(KANSL1):c.311A>C (p.Lys104Thr) rs17585974
NM_001193466.1(KANSL1):c.414T>G (p.Leu138=) rs17662889
NM_001193466.1(KANSL1):c.431G>A (p.Ser144Asn) rs886053070
NM_001193466.1(KANSL1):c.571G>T (p.Gly191Cys) rs149566146
NM_001193466.1(KANSL1):c.607G>C (p.Gly203Arg) rs138175526
NM_001193466.1(KANSL1):c.608G>A (p.Gly203Glu) rs759522694
NM_001193466.1(KANSL1):c.611G>T (p.Gly204Val) rs766643723
NM_001193466.1(KANSL1):c.635A>G (p.His212Arg) rs141110759
NM_001193466.1(KANSL1):c.662C>T (p.Thr221Ile) rs17662853
NM_001193466.1(KANSL1):c.673A>G (p.Asn225Asp) rs35643216
NM_001193466.1(KANSL1):c.680G>A (p.Ser227Asn) rs150345690
NM_001193466.1(KANSL1):c.688A>G (p.Asn230Asp) rs34756740
NM_001193466.1(KANSL1):c.696C>T (p.Ser232=) rs1881194
NM_001193466.1(KANSL1):c.701T>C (p.Val234Ala) rs199948200
NM_001193466.1(KANSL1):c.727C>A (p.Gln243Lys) rs142096969
NM_001193466.1(KANSL1):c.741A>G (p.Arg247=) rs1881193
NM_001193466.1(KANSL1):c.773T>C (p.Leu258Ser) rs145714368
NM_001193466.1(KANSL1):c.800A>G (p.Lys267Arg) rs140181991
NM_001193466.1(KANSL1):c.910C>T (p.Arg304Cys) rs756749550

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.