ClinVar Miner

List of variants in gene NSD1 reported as benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 114
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_022455.5(NSD1):c.3796+108C>G rs6556305 0.91525
NM_022455.5(NSD1):c.1064-137T>C rs7721671 0.83210
NM_022455.5(NSD1):c.5622+100G>A rs12660023 0.63274
NM_022455.5(NSD1):c.6464-67A>G rs6872201 0.45885
NM_022455.5(NSD1):c.1482C>T (p.Cys494=) rs1363405 0.36334
NM_022455.5(NSD1):c.-18+160T>C rs3733873 0.33912
NM_022455.5(NSD1):c.6903G>C (p.Gly2301=) rs11740250 0.16701
NM_022455.5(NSD1):c.2176T>C (p.Ser726Pro) rs28932178 0.15259
NM_022455.5(NSD1):c.1749G>A (p.Glu583=) rs3733874 0.12785
NM_022455.5(NSD1):c.1840G>T (p.Val614Leu) rs3733875 0.12636
NM_022455.5(NSD1):c.3705T>C (p.Asn1235=) rs28932181 0.10490
NM_022455.5(NSD1):c.1237-246G>A rs141260503 0.10468
NM_022455.5(NSD1):c.4766-158A>G rs6890368 0.08903
NM_022455.5(NSD1):c.4966+81T>C rs6872392 0.08417
NM_022455.5(NSD1):c.5622+187C>T rs112423577 0.08318
NM_022455.5(NSD1):c.5147-82T>A rs10071491 0.08311
NM_022455.5(NSD1):c.5893-133G>A rs72813176 0.06049
NM_022455.5(NSD1):c.5147-294T>C rs60761205 0.04831
NM_022455.5(NSD1):c.6463+196G>A rs11953271 0.04797
NM_022455.5(NSD1):c.6010-104G>A rs77309295 0.04791
NM_022455.5(NSD1):c.5623-22G>A rs79098301 0.04787
NM_022455.5(NSD1):c.4967-160T>G rs76796411 0.04785
NM_022455.5(NSD1):c.5304-183A>G rs75441502 0.04785
NM_022455.5(NSD1):c.6750G>A (p.Met2250Ile) rs35848863 0.04785
NM_022455.5(NSD1):c.3797-248T>A rs75737978 0.04784
NM_022455.5(NSD1):c.6782T>C (p.Met2261Thr) rs34165241 0.04781
NM_022455.5(NSD1):c.6464-289del rs565213549 0.03943
NM_022455.5(NSD1):c.4966+77C>T rs550169914 0.03820
NM_022455.5(NSD1):c.4765+90G>A rs56991691 0.02827
NM_022455.5(NSD1):c.1064-194T>C rs10475644 0.02825
NM_022455.5(NSD1):c.4766-196C>T rs116835936 0.02822
NM_022455.5(NSD1):c.3106G>C (p.Ala1036Pro) rs28932179 0.02602
NM_022455.5(NSD1):c.3796+292del rs1354272502 0.02302
NM_022455.5(NSD1):c.4641+98A>G rs12055154 0.02194
NM_022455.5(NSD1):c.7636G>A (p.Ala2546Thr) rs78247455 0.02182
NM_022455.5(NSD1):c.6010-162T>G rs78504286 0.02032
NM_022455.5(NSD1):c.2071G>A (p.Ala691Thr) rs28932177 0.01809
NM_022455.5(NSD1):c.927+48A>G rs79928962 0.01809
NM_022455.5(NSD1):c.1792T>C (p.Leu598=) rs28932176 0.00477
NM_022455.5(NSD1):c.2169C>T (p.Thr723=) rs11948062 0.00453
NM_022455.5(NSD1):c.1690G>T (p.Ala564Ser) rs116520623 0.00445
NM_022455.5(NSD1):c.2295C>T (p.Asn765=) rs146767413 0.00196
NM_022455.5(NSD1):c.4378+26C>T rs139601377 0.00189
NM_022455.5(NSD1):c.7850T>C (p.Leu2617Ser) rs77618751 0.00188
NM_022455.5(NSD1):c.7575C>T (p.Asp2525=) rs148891711 0.00173
NM_022455.5(NSD1):c.760C>T (p.Leu254Phe) rs149334244 0.00145
NM_022455.5(NSD1):c.6464-20A>G rs371359117 0.00130
NM_022455.5(NSD1):c.5147-45C>G rs201065957 0.00103
NM_022455.5(NSD1):c.3150C>T (p.Thr1050=) rs144257298 0.00088
NM_022455.5(NSD1):c.1574G>A (p.Arg525Gln) rs138405802 0.00087
NM_022455.5(NSD1):c.2450C>T (p.Ser817Phe) rs115722008 0.00086
NM_022455.5(NSD1):c.3393C>T (p.Asn1131=) rs150296373 0.00077
NM_022455.5(NSD1):c.5520A>G (p.Glu1840=) rs140815139 0.00073
NM_022455.5(NSD1):c.1980C>T (p.Asn660=) rs140072393 0.00069
NM_022455.5(NSD1):c.480C>T (p.Asp160=) rs79427433 0.00061
NM_022455.5(NSD1):c.3389A>G (p.Glu1130Gly) rs113856002 0.00058
NM_022455.5(NSD1):c.3922-40A>G rs79222656 0.00056
NM_022455.5(NSD1):c.3000C>T (p.Ser1000=) rs150854966 0.00052
NM_022455.5(NSD1):c.1064-32C>G rs368549002 0.00050
NM_022455.5(NSD1):c.3564G>C (p.Arg1188Ser) rs199814669 0.00042
NM_022455.5(NSD1):c.4892A>G (p.Lys1631Arg) rs201857437 0.00038
NM_022455.5(NSD1):c.4379-15A>G rs143520065 0.00036
NM_022455.5(NSD1):c.4949A>G (p.Asn1650Ser) rs148839758 0.00034
NM_022455.5(NSD1):c.639C>T (p.Ser213=) rs755931458 0.00032
NM_022455.5(NSD1):c.3187A>G (p.Thr1063Ala) rs193290006 0.00025
NM_022455.5(NSD1):c.4966+30T>C rs75429143 0.00023
NM_022455.5(NSD1):c.2861A>C (p.Lys954Thr) rs555067830 0.00022
NM_022455.5(NSD1):c.2968G>A (p.Glu990Lys) rs138673583 0.00022
NM_022455.5(NSD1):c.4509G>A (p.Met1503Ile) rs199574095 0.00020
NM_022455.5(NSD1):c.7352G>A (p.Arg2451Lys) rs200115665 0.00018
NM_022455.5(NSD1):c.2339C>T (p.Ser780Leu) rs201327209 0.00014
NM_022455.5(NSD1):c.3021T>C (p.Ala1007=) rs201312975 0.00014
NM_022455.5(NSD1):c.7057C>T (p.Pro2353Ser) rs758794360 0.00013
NM_022455.5(NSD1):c.6276G>A (p.Thr2092=) rs138041618 0.00012
NM_022455.5(NSD1):c.4192+48A>T rs753269790 0.00011
NM_022455.5(NSD1):c.1317C>T (p.Asn439=) rs150421873 0.00010
NM_022455.5(NSD1):c.1364T>C (p.Met455Thr) rs143585233 0.00009
NM_022455.5(NSD1):c.72C>T (p.Ala24=) rs147146776 0.00009
NM_022455.5(NSD1):c.4642-7T>C rs183928380 0.00006
NM_022455.5(NSD1):c.6258+47C>G rs187713824 0.00006
NM_022455.5(NSD1):c.5712C>T (p.Pro1904=) rs756321444 0.00005
NM_022455.5(NSD1):c.1782T>C (p.Pro594=) rs200002555 0.00004
NM_022455.5(NSD1):c.3330C>T (p.Phe1110=) rs541077303 0.00004
NM_022455.5(NSD1):c.708G>C (p.Gln236His) rs28932175 0.00004
NM_022455.5(NSD1):c.7145C>T (p.Thr2382Ile) rs148027433 0.00004
NM_022455.5(NSD1):c.7852G>A (p.Val2618Ile) rs373787813 0.00004
NM_022455.5(NSD1):c.6045T>C (p.Tyr2015=) rs745760201 0.00003
NM_022455.5(NSD1):c.3286C>T (p.His1096Tyr) rs202208033 0.00002
NM_022455.5(NSD1):c.5082C>T (p.Thr1694=) rs587784136 0.00002
NM_022455.5(NSD1):c.5892+26A>G rs760933594 0.00002
NM_022455.5(NSD1):c.4883T>C (p.Met1628Thr) rs530920626 0.00001
NM_022455.5(NSD1):c.8050G>A (p.Ala2684Thr) rs188326949 0.00001
GRCh37/hg19 5q35.2-35.3(chr5:176582117-176600839)x1
GRCh37/hg19 5q35.3(chr5:176639461-176645012)x3
NM_022455.5(NSD1):c.1237-90del rs11322143
NM_022455.5(NSD1):c.1237-92dup rs560987364
NM_022455.5(NSD1):c.3796+282_3796+296del rs369449613
NM_022455.5(NSD1):c.3796+305_3796+306dup rs34930823
NM_022455.5(NSD1):c.3796+306del rs34930823
NM_022455.5(NSD1):c.3796+306dup rs34930823
NM_022455.5(NSD1):c.3796+34dup rs35159794
NM_022455.5(NSD1):c.3922-157del rs34640392
NM_022455.5(NSD1):c.4473G>A (p.Ser1491=) rs150920473
NM_022455.5(NSD1):c.4498-10del rs200890017
NM_022455.5(NSD1):c.4564G>A (p.Asp1522Asn) rs201483724
NM_022455.5(NSD1):c.4641+206G>C rs10056245
NM_022455.5(NSD1):c.4966+96del rs373383515
NM_022455.5(NSD1):c.5303+113T>G rs10071723
NM_022455.5(NSD1):c.5303+252del rs35703730
NM_022455.5(NSD1):c.5510-147G>A rs59992310
NM_022455.5(NSD1):c.6010-241C>G rs28395268
NM_022455.5(NSD1):c.6010-241C>T rs28395268
NM_022455.5(NSD1):c.6464-290dup rs149890561
NM_022455.5(NSD1):c.6464-298G>C rs1386367711

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.