List of variants in gene IQCB1 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 41

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HGVS	dbSNP	gnomAD frequency
NM_001023570.4(IQCB1):c.322C>T (p.Leu108Phe)	rs146580215	0.00036
NM_001023570.4(IQCB1):c.1153G>C (p.Glu385Gln)	rs772153735	0.00015
NM_001023570.4(IQCB1):c.1000A>C (p.Lys334Gln)	rs532987681	0.00010
NM_001023570.4(IQCB1):c.1123C>A (p.His375Asn)	rs137890014	0.00009
NM_001023570.4(IQCB1):c.1324G>T (p.Ala442Ser)	rs780327292	0.00008
NM_001023570.4(IQCB1):c.1727T>C (p.Ile576Thr)	rs150073223	0.00007
NM_001023570.4(IQCB1):c.1151G>A (p.Arg384Gln)	rs773223673	0.00004
NM_001023570.4(IQCB1):c.118C>T (p.Pro40Ser)	rs750396752	0.00004
NM_001023570.4(IQCB1):c.1466G>A (p.Arg489Gln)	rs778777318	0.00004
NM_001023570.4(IQCB1):c.1594G>A (p.Gly532Arg)	rs149207095	0.00004
NM_001023570.4(IQCB1):c.458T>C (p.Leu153Ser)	rs368772723	0.00004
NM_001023570.4(IQCB1):c.482A>G (p.Gln161Arg)	rs376700204	0.00004
NM_001023570.4(IQCB1):c.1279G>A (p.Ala427Thr)	rs776989189	0.00003
NM_001023570.4(IQCB1):c.1567+3A>G	rs1403759372	0.00003
NM_001023570.4(IQCB1):c.445C>A (p.Leu149Ile)	rs1001594561	0.00003
NM_001023570.4(IQCB1):c.826C>G (p.Gln276Glu)	rs141949168	0.00003
NM_001023570.4(IQCB1):c.904C>G (p.Gln302Glu)	rs756776335	0.00003
NM_001023570.4(IQCB1):c.1003A>G (p.Met335Val)	rs143553764	0.00002
NM_001023570.4(IQCB1):c.1046A>G (p.Lys349Arg)	rs200158965	0.00002
NM_001023570.4(IQCB1):c.1271A>G (p.Gln424Arg)	rs545361604	0.00002
NM_001023570.4(IQCB1):c.1334G>A (p.Arg445Gln)	rs377265463	0.00002
NM_001023570.4(IQCB1):c.1741G>C (p.Asp581His)	rs1283756243	0.00002
NM_001023570.4(IQCB1):c.814C>G (p.Gln272Glu)	rs760296374	0.00002
NM_001023570.4(IQCB1):c.884A>G (p.His295Arg)	rs377524012	0.00002
NM_001023570.4(IQCB1):c.1150C>T (p.Arg384Trp)	rs760548277	0.00001
NM_001023570.4(IQCB1):c.1364G>A (p.Arg455Gln)	rs766072332	0.00001
NM_001023570.4(IQCB1):c.1420A>G (p.Met474Val)	rs764720012	0.00001
NM_001023570.4(IQCB1):c.1505G>A (p.Arg502Gln)	rs200367729	0.00001
NM_001023570.4(IQCB1):c.1576A>C (p.Ser526Arg)	rs1390983530	0.00001
NM_001023570.4(IQCB1):c.157A>G (p.Ile53Val)	rs542335278	0.00001
NM_001023570.4(IQCB1):c.272G>A (p.Cys91Tyr)	rs370233738	0.00001
NM_001023570.4(IQCB1):c.532G>A (p.Val178Ile)	rs1272185942	0.00001
NM_001023570.4(IQCB1):c.692C>T (p.Thr231Ile)	rs1278873318	0.00001
NM_001023570.4(IQCB1):c.880C>G (p.Leu294Val)	rs756107852	0.00001
NM_001023570.4(IQCB1):c.952C>G (p.Pro318Ala)	rs749043070	0.00001
NM_001023570.4(IQCB1):c.1250A>T (p.Tyr417Phe)	rs777697438
NM_001023570.4(IQCB1):c.1319T>C (p.Leu440Pro)	rs749515337
NM_001023570.4(IQCB1):c.1450G>A (p.Ala484Thr)	rs776788131
NM_001023570.4(IQCB1):c.214C>G (p.Arg72Gly)	rs201405662
NM_001023570.4(IQCB1):c.491T>C (p.Leu164Pro)	rs746194022
NM_001023570.4(IQCB1):c.580A>T (p.Ile194Phe)	rs1412812453

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