ClinVar Miner

List of variants in gene SIL1 reported as uncertain significance by Athena Diagnostics Inc

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Total variants: 33
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HGVS dbSNP gnomAD frequency
NM_022464.5(SIL1):c.310C>G (p.Leu104Val) rs150892227 0.00018
NM_022464.5(SIL1):c.424G>C (p.Ala142Pro) rs142987777 0.00016
NM_022464.5(SIL1):c.724G>A (p.Val242Met) rs545999438 0.00010
NM_022464.5(SIL1):c.142A>C (p.Thr48Pro) rs185697854 0.00009
NM_022464.5(SIL1):c.1022C>T (p.Thr341Met) rs372399027 0.00008
NM_022464.5(SIL1):c.1088A>C (p.Gln363Pro) rs563414935 0.00004
NM_022464.5(SIL1):c.902C>T (p.Pro301Leu) rs1478296366 0.00004
NM_022464.5(SIL1):c.1321G>A (p.Glu441Lys) rs779649580 0.00003
NM_022464.5(SIL1):c.355C>G (p.Leu119Val) rs758512287 0.00003
NM_022464.5(SIL1):c.937C>A (p.Leu313Met) rs374933348 0.00003
NM_022464.5(SIL1):c.991C>T (p.Arg331Cys) rs765721225 0.00003
NM_022464.5(SIL1):c.288G>T (p.Gln96His) rs368830878 0.00002
NM_022464.5(SIL1):c.272T>C (p.Val91Ala) rs1461916800 0.00001
NM_022464.5(SIL1):c.-10G>T rs199951755
NM_022464.5(SIL1):c.1036G>A (p.Ala346Thr) rs377150029
NM_022464.5(SIL1):c.1094G>A (p.Arg365His)
NM_022464.5(SIL1):c.1100T>C (p.Val367Ala)
NM_022464.5(SIL1):c.1120T>C (p.Trp374Arg) rs1021273983
NM_022464.5(SIL1):c.1168G>A (p.Glu390Lys)
NM_022464.5(SIL1):c.1177G>T (p.Ala393Ser)
NM_022464.5(SIL1):c.1238G>A (p.Arg413His)
NM_022464.5(SIL1):c.1255G>A (p.Gly419Ser) rs398124389
NM_022464.5(SIL1):c.1358T>C (p.Val453Ala)
NM_022464.5(SIL1):c.135G>A (p.Lys45=)
NM_022464.5(SIL1):c.221A>C (p.His74Pro)
NM_022464.5(SIL1):c.475C>T (p.Arg159Trp)
NM_022464.5(SIL1):c.527T>C (p.Val176Ala) rs1768669040
NM_022464.5(SIL1):c.715G>C (p.Glu239Gln) rs2150428182
NM_022464.5(SIL1):c.74G>A (p.Cys25Tyr) rs1750782507
NM_022464.5(SIL1):c.836C>T (p.Thr279Met) rs535287958
NM_022464.5(SIL1):c.903C>G (p.Pro301=) rs1561801612
NM_022464.5(SIL1):c.913C>A (p.Arg305=) rs758782317
NM_022464.5(SIL1):c.9C>G (p.Pro3=)

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