ClinVar Miner

List of variants in gene AIP reported as likely benign for connective tissue neoplasm

Included ClinVar conditions (122):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
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NM_003977.4(AIP):c.-5G>C rs267606562
NM_003977.4(AIP):c.135C>T (p.Asp45=) rs181969066
NM_003977.4(AIP):c.145G>A (p.Val49Met) rs1063385
NM_003977.4(AIP):c.383G>A (p.Arg128His) rs267606550
NM_003977.4(AIP):c.429G>A (p.Gln143=) rs267606553
NM_003977.4(AIP):c.468+16G>T rs267607273
NM_003977.4(AIP):c.47G>A (p.Arg16His) rs145047094
NM_003977.4(AIP):c.573C>T (p.Arg191=) rs781545373
NM_003977.4(AIP):c.591G>A (p.Glu197=) rs202006716
NM_003977.4(AIP):c.609C>T (p.Tyr203=) rs146317385
NM_003977.4(AIP):c.714C>T (p.Cys238=) rs267606570
NM_003977.4(AIP):c.733G>A (p.Glu245Lys) rs150645662
NM_003977.4(AIP):c.783C>T (p.Tyr261=) rs267606576
NM_003977.4(AIP):c.807C>T (p.Phe269=) rs139407567
NM_003977.4(AIP):c.896C>T (p.Ala299Val) rs148986773
NM_003977.4(AIP):c.906G>A (p.Val302=) rs142912418
NM_003977.4(AIP):c.911G>A (p.Arg304Gln) rs104894190
NM_003977.4(AIP):c.965C>T (p.Ala322Val) rs267606586
NM_003977.4(AIP):c.987C>T (p.Ser329=) rs267606587

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