List of variants in gene IMMP1L reported as uncertain significance

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001304274.2(IMMP1L):c.223A>G (p.Ser75Gly)	rs142948682	0.00039
NM_001304274.2(IMMP1L):c.121A>G (p.Met41Val)	rs370083551	0.00009
NM_001304274.2(IMMP1L):c.88G>A (p.Val30Ile)	rs141910560	0.00007
NM_001304274.2(IMMP1L):c.182A>G (p.Tyr61Cys)	rs755501262	0.00002
NM_001304274.2(IMMP1L):c.115C>A (p.Pro39Thr)	rs1954109437	0.00001
NM_001304274.2(IMMP1L):c.221C>T (p.Pro74Leu)	rs147462733	0.00001
NM_001304274.2(IMMP1L):c.313C>G (p.His105Asp)	rs1200883522	0.00001
NM_001304274.2(IMMP1L):c.76G>C (p.Ala26Pro)	rs372148769	0.00001
NM_001304274.2(IMMP1L):c.100G>C (p.Val34Leu)
NM_001304274.2(IMMP1L):c.241A>G (p.Ile81Val)
NM_001304274.2(IMMP1L):c.295T>C (p.Ser99Pro)
NM_001304274.2(IMMP1L):c.346G>C (p.Glu116Gln)	rs146915142
NM_001304274.2(IMMP1L):c.386A>G (p.Tyr129Cys)	rs1368889070
NM_001304274.2(IMMP1L):c.419G>A (p.Arg140Gln)
NM_001304274.2(IMMP1L):c.81T>G (p.Phe27Leu)

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