List of variants in gene DLX3 reported as uncertain significance for Hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism

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: 35

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HGVS	dbSNP	gnomAD frequency
NM_005220.3(DLX3):c.710A>G (p.Tyr237Cys)	rs142563930	0.00179
NM_005220.3(DLX3):c.-135C>T	rs532523216	0.00043
NM_005220.3(DLX3):c.*1272T>C	rs192378506	0.00042
NM_005220.3(DLX3):c.*437G>A	rs111413176	0.00034
NM_005220.3(DLX3):c.*726T>C	rs190429946	0.00026
NM_005220.3(DLX3):c.90T>C (p.Pro30=)	rs145424773	0.00025
NM_005220.3(DLX3):c.*988G>A	rs555823151	0.00021
NM_005220.3(DLX3):c.-190C>T	rs886053136	0.00021
NM_005220.3(DLX3):c.-121C>T	rs756924776	0.00020
NM_005220.3(DLX3):c.-225G>A	rs546133632	0.00008
NM_005220.3(DLX3):c.*1164A>G	rs1024414003	0.00007
NM_005220.3(DLX3):c.*548C>T	rs997326806	0.00007
NM_005220.3(DLX3):c.798G>A (p.Pro266=)	rs569475772	0.00006
NM_005220.3(DLX3):c.*1252C>G	rs3803879	0.00004
NM_005220.3(DLX3):c.140A>G (p.Gln47Arg)	rs773002632	0.00004
NM_005220.3(DLX3):c.698C>T (p.Pro233Leu)	rs146899668	0.00004
NM_005220.3(DLX3):c.*75G>A	rs1051660674	0.00003
NM_005220.3(DLX3):c.*124C>A	rs886053133	0.00001
NM_005220.3(DLX3):c.*429C>G	rs1358552045	0.00001
NM_005220.3(DLX3):c.*812G>A	rs1906056965	0.00001
NM_005220.3(DLX3):c.*821C>A	rs886053131	0.00001
NM_005220.3(DLX3):c.-62C>A	rs1489241968	0.00001
NM_005220.3(DLX3):c.326-15G>T	rs778835890	0.00001
NM_005220.3(DLX3):c.*1025G>T	rs1224971346
NM_005220.3(DLX3):c.*1205A>C	rs886053129
NM_005220.3(DLX3):c.*1408G>A	rs772459781
NM_005220.3(DLX3):c.*1505G>A	rs768920190
NM_005220.3(DLX3):c.*714C>T	rs886053132
NM_005220.3(DLX3):c.*83G>A	rs886053134
NM_005220.3(DLX3):c.-131C>A	rs543871008
NM_005220.3(DLX3):c.-131C>G	rs543871008
NM_005220.3(DLX3):c.-132C>A	rs150591955
NM_005220.3(DLX3):c.746A>C (p.Asn249Thr)	rs1906092898
NM_005220.3(DLX3):c.846C>A (p.Asn282Lys)	rs886053135
NM_005220.3(DLX3):c.92C>G (p.Thr31Ser)

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