ClinVar Miner

List of variants in gene NSD1 studied for History of neurodevelopmental disorder

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Total variants: 62
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HGVS dbSNP
NM_022455.4(NSD1):c.1064-5C>A
NM_022455.4(NSD1):c.1149C>T (p.Ile383=) rs34921128
NM_022455.4(NSD1):c.1176C>T (p.Phe392=)
NM_022455.4(NSD1):c.1364T>C (p.Met455Thr) rs143585233
NM_022455.4(NSD1):c.140C>G (p.Thr47Ser) rs1562097679
NM_022455.4(NSD1):c.1482C>T (p.Cys494=) rs1363405
NM_022455.4(NSD1):c.1500A>G (p.Arg500=) rs1469000222
NM_022455.4(NSD1):c.1515T>C (p.Asn505=) rs114747882
NM_022455.4(NSD1):c.1558G>A (p.Ala520Thr) rs559617787
NM_022455.4(NSD1):c.1574G>A (p.Arg525Gln) rs138405802
NM_022455.4(NSD1):c.1578G>A (p.Arg526=) rs1562205567
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.1811G>T (p.Arg604Leu) rs61744451
NM_022455.4(NSD1):c.1840G>T (p.Val614Leu) rs3733875
NM_022455.4(NSD1):c.1980C>T (p.Asn660=) rs140072393
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.241A>G (p.Met81Val) rs763781326
NM_022455.4(NSD1):c.2450C>T (p.Ser817Phe) rs115722008
NM_022455.4(NSD1):c.2465C>G (p.Ser822Cys) rs377684553
NM_022455.4(NSD1):c.2776C>A (p.Arg926=) rs886038674
NM_022455.4(NSD1):c.2835T>C (p.Ser945=) rs145987330
NM_022455.4(NSD1):c.2968G>A (p.Glu990Lys)
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.3150C>T (p.Thr1050=) rs144257298
NM_022455.4(NSD1):c.3187A>G (p.Thr1063Ala) rs193290006
NM_022455.4(NSD1):c.3215G>A (p.Arg1072Gln) rs28932180
NM_022455.4(NSD1):c.3221G>A (p.Arg1074His)
NM_022455.4(NSD1):c.3224G>A (p.Gly1075Glu) rs1562212091
NM_022455.4(NSD1):c.3393C>T (p.Asn1131=) rs150296373
NM_022455.4(NSD1):c.339C>T (p.Cys113=) rs77093936
NM_022455.4(NSD1):c.3564G>C (p.Arg1188Ser) rs199814669
NM_022455.4(NSD1):c.3705T>C (p.Asn1235=) rs28932181
NM_022455.4(NSD1):c.3722G>C (p.Ser1241Thr) rs138641637
NM_022455.4(NSD1):c.3741G>A (p.Met1247Ile)
NM_022455.4(NSD1):c.436A>G (p.Ile146Val)
NM_022455.4(NSD1):c.4473G>T (p.Ser1491=) rs150920473
NM_022455.4(NSD1):c.4520C>T (p.Thr1507Met) rs144900277
NM_022455.4(NSD1):c.4564G>A (p.Asp1522Asn) rs201483724
NM_022455.4(NSD1):c.4564G>T (p.Asp1522Tyr) rs201483724
NM_022455.4(NSD1):c.4605C>T (p.Arg1535=) rs140229717
NM_022455.4(NSD1):c.5031T>C (p.Ala1677=)
NM_022455.4(NSD1):c.5520A>G (p.Glu1840=) rs140815139
NM_022455.4(NSD1):c.5623-4C>T
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.682C>G (p.Pro228Ala)
NM_022455.4(NSD1):c.6848T>C (p.Leu2283Pro)
NM_022455.4(NSD1):c.6903G>C (p.Gly2301=) rs11740250
NM_022455.4(NSD1):c.7137A>G (p.Ser2379=)
NM_022455.4(NSD1):c.7402C>T (p.Arg2468Trp)
NM_022455.4(NSD1):c.760C>T (p.Leu254Phe) rs149334244
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.7908C>T (p.Leu2636=) rs143159630
NM_022455.4(NSD1):c.8014A>G (p.Lys2672Glu)
NM_022455.4(NSD1):c.887C>G (p.Pro296Arg) rs1189702665

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