List of variants in gene CDON reported as likely benign by Illumina Laboratory Services, Illumina

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: 31

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HGVS	dbSNP	gnomAD frequency
NM_016952.4(CDON):c.-131G>A	rs79446614	0.15824
NM_001378964.1(CDON):c.*3972C>G	rs142923654	0.00828
NM_001378964.1(CDON):c.*3919T>C	rs61917811	0.00390
NM_001378964.1(CDON):c.*3176C>G	rs187258536	0.00283
NM_001378964.1(CDON):c.2462G>A (p.Arg821His)	rs146660717	0.00102
NM_001378964.1(CDON):c.-48G>A	rs374433009	0.00085
NM_001378964.1(CDON):c.350-11A>G	rs199981607	0.00072
NM_001378964.1(CDON):c.1263T>C (p.Phe421=)	rs191544852	0.00056
NM_001378964.1(CDON):c.1855G>C (p.Asp619His)	rs141081456	0.00056
NM_001378964.1(CDON):c.3726A>C (p.Thr1242=)	rs139588649	0.00046
NM_001378964.1(CDON):c.1041C>T (p.His347=)	rs201963480	0.00031
NM_001378964.1(CDON):c.1940C>T (p.Pro647Leu)	rs200961603	0.00021
NM_001378964.1(CDON):c.3190A>G (p.Ser1064Gly)	rs143111106	0.00019
NM_001378964.1(CDON):c.3754G>C (p.Asp1252His)	rs150974313	0.00016
NM_001378964.1(CDON):c.1302G>A (p.Pro434=)	rs375157917	0.00014
NM_001378964.1(CDON):c.791C>A (p.Pro264Gln)	rs140542787	0.00012
NM_001378964.1(CDON):c.1414C>G (p.Pro472Ala)	rs750020763	0.00009
NM_001378964.1(CDON):c.3602G>A (p.Gly1201Asp)	rs200042535	0.00009
NM_001378964.1(CDON):c.3574G>A (p.Asp1192Asn)	rs181749265	0.00006
NM_001378964.1(CDON):c.1906A>G (p.Ser636Gly)	rs758389908	0.00005
NM_001378964.1(CDON):c.1501G>A (p.Glu501Lys)	rs761054118	0.00004
NM_001378964.1(CDON):c.1889C>T (p.Thr630Met)	rs559379897	0.00004
NM_001378964.1(CDON):c.1977C>T (p.Ser659=)	rs563267429	0.00004
NM_001378964.1(CDON):c.2026+15C>T	rs143813933	0.00004
NM_001378964.1(CDON):c.*3221A>G	rs539903009	0.00003
NM_001378964.1(CDON):c.2159-8G>A	rs759480175	0.00003
NM_001378964.1(CDON):c.1057C>T (p.His353Tyr)	rs772141487	0.00001
NM_001378964.1(CDON):c.1665G>A (p.Pro555=)	rs537471531	0.00001
NM_001378964.1(CDON):c.*1311GTTT[2]	rs567351832
NM_001378964.1(CDON):c.*1457G>A	rs141994408
NM_001378964.1(CDON):c.1253A>T (p.Asp418Val)	rs753627841

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