ClinVar Miner

List of variants in gene TGFBR1 reported as likely benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 38
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HGVS dbSNP
NM_004612.4(TGFBR1):c.*1183G>A rs184564501
NM_004612.4(TGFBR1):c.*1428G>C rs11568811
NM_004612.4(TGFBR1):c.*1515G>A rs11568812
NM_004612.4(TGFBR1):c.*1659T>C rs200082162
NM_004612.4(TGFBR1):c.*1710G>A rs200197062
NM_004612.4(TGFBR1):c.*1804A>G rs200656974
NM_004612.4(TGFBR1):c.*2005T>G rs144216869
NM_004612.4(TGFBR1):c.*2086T>G rs148063684
NM_004612.4(TGFBR1):c.*2100T>G rs532530728
NM_004612.4(TGFBR1):c.*2179del rs373576679
NM_004612.4(TGFBR1):c.*2645A>C rs17724567
NM_004612.4(TGFBR1):c.*2685T>G rs145043837
NM_004612.4(TGFBR1):c.*2703G>A rs76392135
NM_004612.4(TGFBR1):c.*3192T>C rs148797981
NM_004612.4(TGFBR1):c.*3261T>C rs117440593
NM_004612.4(TGFBR1):c.*3262C>T rs78385793
NM_004612.4(TGFBR1):c.*3430del rs78078491
NM_004612.4(TGFBR1):c.*360A>G rs145692006
NM_004612.4(TGFBR1):c.*3704A>G rs563433922
NM_004612.4(TGFBR1):c.*3798G>A rs141277814
NM_004612.4(TGFBR1):c.*3830T>C rs186157987
NM_004612.4(TGFBR1):c.*4202A>G rs200206515
NM_004612.4(TGFBR1):c.*4300C>T rs41283642
NM_004612.4(TGFBR1):c.*4356A>G rs201446431
NM_004612.4(TGFBR1):c.*4493G>A rs41274644
NM_004612.4(TGFBR1):c.*4499G>A rs79641064
NM_004612.4(TGFBR1):c.*4565T>C rs138721378
NM_004612.4(TGFBR1):c.*4623G>C rs200806851
NM_004612.4(TGFBR1):c.*4728G>A rs187415138
NM_004612.4(TGFBR1):c.*4809A>T rs185400896
NM_004612.4(TGFBR1):c.*566T>C rs11568808
NM_004612.4(TGFBR1):c.*789G>A rs200428927
NM_004612.4(TGFBR1):c.1032T>C (p.Asn344=) rs192662552
NM_004612.4(TGFBR1):c.1125A>C (p.Thr375=) rs7861780
NM_004612.4(TGFBR1):c.415A>G (p.Ile139Val) rs148176750
NM_004612.4(TGFBR1):c.457G>A (p.Val153Ile) rs56014374
NM_004612.4(TGFBR1):c.528G>A (p.Thr176=) rs190878719
NM_004612.4(TGFBR1):c.575-9dup rs863223798

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