List of variants in gene CC2D2A 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: 22

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HGVS	dbSNP	gnomAD frequency
NM_001378615.1(CC2D2A):c.2804G>A (p.Arg935Gln)	rs187003641	0.00142
NM_001378615.1(CC2D2A):c.3869T>C (p.Val1290Ala)	rs200427832	0.00073
NM_001378615.1(CC2D2A):c.2326G>A (p.Gly776Arg)	rs200764366	0.00067
NM_001378615.1(CC2D2A):c.2945G>A (p.Arg982His)	rs150093365	0.00057
NM_001378615.1(CC2D2A):c.3577A>G (p.Ile1193Val)	rs188891842	0.00051
NM_001378615.1(CC2D2A):c.4729G>A (p.Ala1577Thr)	rs199695154	0.00039
NM_001378615.1(CC2D2A):c.1691C>T (p.Thr564Met)	rs201954181	0.00026
NM_001378615.1(CC2D2A):c.4852C>T (p.Arg1618Cys)	rs201219078	0.00023
NM_001378615.1(CC2D2A):c.2560T>G (p.Trp854Gly)	rs747204358	0.00021
NM_001378615.1(CC2D2A):c.3135G>A (p.Val1045=)	rs371608031	0.00015
NM_001378615.1(CC2D2A):c.3751G>A (p.Gly1251Arg)	rs368180778	0.00014
NM_001378615.1(CC2D2A):c.1837G>A (p.Glu613Lys)	rs201439617	0.00010
NM_001378615.1(CC2D2A):c.2624C>T (p.Ser875Leu)	rs200904521	0.00009
NM_001378615.1(CC2D2A):c.932A>G (p.Asp311Gly)	rs375247004	0.00006
NM_001378615.1(CC2D2A):c.298A>C (p.Met100Leu)	rs370014549	0.00004
NM_001378615.1(CC2D2A):c.1994A>G (p.Gln665Arg)	rs1718235188	0.00002
NM_001378615.1(CC2D2A):c.832C>T (p.Arg278Trp)	rs372873919	0.00001
NM_001378615.1(CC2D2A):c.1127A>T (p.Glu376Val)	rs16892095
NM_001378615.1(CC2D2A):c.1817A>T (p.Glu606Val)	rs747187783
NM_001378615.1(CC2D2A):c.1946C>T (p.Thr649Met)	rs201884883
NM_001378615.1(CC2D2A):c.248-4_248-3insAAGTTTT	rs750398145
NM_001378615.1(CC2D2A):c.2993AAG[2] (p.Glu1000del)	rs764874938

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