ClinVar Miner

List of variants in gene NOTCH1 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 45
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HGVS dbSNP
GRCh37/hg19 9q34.3(chr9:139390822-139391737)x1
GRCh37/hg19 9q34.3(chr9:139390822-139403378)x1
NC_000009.12:g.136508789dup
NC_000009.12:g.136515849_136515856del
NM_017617.5(NOTCH1):c.-152T>C
NM_017617.5(NOTCH1):c.1100-140G>A
NM_017617.5(NOTCH1):c.1100-85T>C
NM_017617.5(NOTCH1):c.141-230T>C
NM_017617.5(NOTCH1):c.1441+131A>G
NM_017617.5(NOTCH1):c.1442-43C>T
NM_017617.5(NOTCH1):c.1555+102C>T
NM_017617.5(NOTCH1):c.1555+245C>T
NM_017617.5(NOTCH1):c.1555+272C>T
NM_017617.5(NOTCH1):c.1556-133A>G
NM_017617.5(NOTCH1):c.1556-43T>C
NM_017617.5(NOTCH1):c.2207+206T>C
NM_017617.5(NOTCH1):c.2207+70G>A
NM_017617.5(NOTCH1):c.2467+21G>A
NM_017617.5(NOTCH1):c.2467+34C>G
NM_017617.5(NOTCH1):c.2587+103T>C
NM_017617.5(NOTCH1):c.2588-104T>C
NM_017617.5(NOTCH1):c.2970-31A>G
NM_017617.5(NOTCH1):c.3171+220A>G
NM_017617.5(NOTCH1):c.3171+54A>G
NM_017617.5(NOTCH1):c.3172-122T>C
NM_017617.5(NOTCH1):c.3172-71A>G
NM_017617.5(NOTCH1):c.3325+21A>G
NM_017617.5(NOTCH1):c.3644-152G>C
NM_017617.5(NOTCH1):c.3644-79C>T
NM_017617.5(NOTCH1):c.4014+75G>A
NM_017617.5(NOTCH1):c.4015-73G>A
NM_017617.5(NOTCH1):c.4823G>A (p.Arg1608His) rs76371972
NM_017617.5(NOTCH1):c.5167+189C>A
NM_017617.5(NOTCH1):c.5167+208C>T rs11574905
NM_017617.5(NOTCH1):c.5385-70C>T
NM_017617.5(NOTCH1):c.5473-43T>C
NM_017617.5(NOTCH1):c.5639-174G>A
NM_017617.5(NOTCH1):c.5934+45G>A
NM_017617.5(NOTCH1):c.5935-148G>A
NM_017617.5(NOTCH1):c.5935-209G>A
NM_017617.5(NOTCH1):c.6180+176T>C
NM_017617.5(NOTCH1):c.6180+189C>T
NM_017617.5(NOTCH1):c.6180+284G>A
NM_017617.5(NOTCH1):c.866-257G>A
NM_017617.5(NOTCH1):c.866-263G>A

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