ClinVar Miner

List of variants in gene NSD1 reported by PreventionGenetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 46
Download table as spreadsheet
HGVS dbSNP
NM_022455.4(NSD1):c.-8G>A rs199639292
NM_022455.4(NSD1):c.1236+17G>A rs886038671
NM_022455.4(NSD1):c.1237-37delT rs886038672
NM_022455.4(NSD1):c.1317C>T (p.Asn439=) rs150421873
NM_022455.4(NSD1):c.1482C>T (p.Cys494=) rs1363405
NM_022455.4(NSD1):c.1690G>T (p.Ala564Ser) rs116520623
NM_022455.4(NSD1):c.1749G>A (p.Glu583=) rs3733874
NM_022455.4(NSD1):c.1792T>C (p.Leu598=) rs28932176
NM_022455.4(NSD1):c.1840G>T (p.Val614Leu) rs3733875
NM_022455.4(NSD1):c.2071G>A (p.Ala691Thr) rs28932177
NM_022455.4(NSD1):c.2169C>T (p.Thr723=) rs11948062
NM_022455.4(NSD1):c.2176T>C (p.Ser726Pro) rs28932178
NM_022455.4(NSD1):c.2295C>T (p.Asn765=) rs146767413
NM_022455.4(NSD1):c.2450C>T (p.Ser817Phe) rs115722008
NM_022455.4(NSD1):c.2731C>T (p.Leu911=) rs886038673
NM_022455.4(NSD1):c.2776C>A (p.Arg926=) rs886038674
NM_022455.4(NSD1):c.3088T>C (p.Leu1030=) rs61756006
NM_022455.4(NSD1):c.3106G>C (p.Ala1036Pro) rs28932179
NM_022455.4(NSD1):c.3330C>T (p.Phe1110=) rs541077303
NM_022455.4(NSD1):c.3389A>G (p.Glu1130Gly) rs113856002
NM_022455.4(NSD1):c.339C>T (p.Cys113=) rs77093936
NM_022455.4(NSD1):c.3705T>C (p.Asn1235=) rs28932181
NM_022455.4(NSD1):c.3796+22A>T rs111663030
NM_022455.4(NSD1):c.4192+16G>T rs886038675
NM_022455.4(NSD1):c.4378+26C>T rs139601377
NM_022455.4(NSD1):c.4473G>T (p.Ser1491=) rs150920473
NM_022455.4(NSD1):c.4498-10del rs200890017
NM_022455.4(NSD1):c.4520C>T (p.Thr1507Met) rs144900277
NM_022455.4(NSD1):c.480C>T (p.Asp160=) rs79427433
NM_022455.4(NSD1):c.4966+43G>A rs184344717
NM_022455.4(NSD1):c.5147-49A>C rs74436451
NM_022455.4(NSD1):c.5303+37C>A rs115164783
NM_022455.4(NSD1):c.5623-22G>A rs79098301
NM_022455.4(NSD1):c.5712C>T (p.Pro1904=) rs756321444
NM_022455.4(NSD1):c.6750G>A (p.Met2250Ile) rs35848863
NM_022455.4(NSD1):c.6782T>C (p.Met2261Thr) rs34165241
NM_022455.4(NSD1):c.6829T>C (p.Leu2277=) rs28580074
NM_022455.4(NSD1):c.6903G>C (p.Gly2301=) rs11740250
NM_022455.4(NSD1):c.7161G>A (p.Pro2387=) rs369778799
NM_022455.4(NSD1):c.7275A>G (p.Leu2425=) rs139879749
NM_022455.4(NSD1):c.7421A>C (p.Gln2474Pro) rs202220730
NM_022455.4(NSD1):c.7636G>A (p.Ala2546Thr) rs78247455
NM_022455.4(NSD1):c.7850T>C (p.Leu2617Ser) rs77618751
NM_022455.4(NSD1):c.7955C>T (p.Ala2652Val) rs886038676
NM_022455.4(NSD1):c.8022G>A (p.Glu2674=) rs149632999
NM_022455.4(NSD1):c.927+48A>G rs79928962

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.