List of variants in gene DCC studied for digestive system cancer

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_005215.4(DCC):c.91+7G>A	rs112558388	0.02064
NM_005215.4(DCC):c.1062C>T (p.Val354=)	rs141716650	0.00555
NM_005215.4(DCC):c.2053+9T>C	rs186819956	0.00534
NM_005215.4(DCC):c.2158C>T (p.Leu720=)	rs138143831
NM_005215.4(DCC):c.371C>T (p.Ser124Phe)	rs2037008530
NM_005215.4(DCC):c.3872G>A (p.Arg1291Gln)	rs768577706
NM_005215.4(DCC):c.4028G>A (p.Arg1343His)	rs149118168
NM_005215.4(DCC):c.4124C>A (p.Pro1375His)	rs387906555
NM_005215.4(DCC):c.503T>C (p.Met168Thr)	rs121912967
NM_005215.4(DCC):c.947del (p.Asn316fs)	rs2040184914

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