List of variants in gene PTF1A reported as uncertain significance for digestive system disorder

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: 28

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HGVS	dbSNP	gnomAD frequency
NM_178161.3(PTF1A):c.269G>C (p.Gly90Ala)	rs535090775	0.00423
NM_178161.3(PTF1A):c.*117A>G	rs886046911	0.00057
NM_178161.3(PTF1A):c.462G>T (p.Arg154=)	rs1056021170	0.00032
NM_178161.3(PTF1A):c.263G>A (p.Gly88Asp)	rs569569636	0.00031
NM_178161.3(PTF1A):c.*306C>G	rs769212869	0.00029
NM_178161.3(PTF1A):c.446C>T (p.Ala149Val)	rs902236805	0.00029
NM_178161.3(PTF1A):c.*265A>G	rs886046914	0.00020
NM_178161.3(PTF1A):c.960C>A (p.Asn320Lys)	rs181911810	0.00013
NM_178161.3(PTF1A):c.44C>T (p.Ala15Val)	rs140097468	0.00012
NM_178161.3(PTF1A):c.*283T>C	rs957501007	0.00010
NM_178161.3(PTF1A):c.265C>A (p.Leu89Ile)	rs1162744670	0.00008
NM_178161.3(PTF1A):c.362G>A (p.Cys121Tyr)	rs1443229654	0.00007
NM_178161.3(PTF1A):c.283G>C (p.Gly95Arg)	rs962887931	0.00004
NM_178161.3(PTF1A):c.617G>T (p.Arg206Leu)	rs886046909	0.00002
NM_178161.3(PTF1A):c.654C>A (p.Leu218=)	rs886046910	0.00002
NM_178161.3(PTF1A):c.126_129del	rs533517653
NM_178161.3(PTF1A):c.*272G>A	rs1840935977
NM_178161.3(PTF1A):c.*316T>C	rs1840936579
NM_178161.3(PTF1A):c.115G>A (p.Gly39Ser)	rs1192341489
NM_178161.3(PTF1A):c.201C>T (p.Cys67=)	rs539214102
NM_178161.3(PTF1A):c.341C>T (p.Ser114Leu)	rs1840910398
NM_178161.3(PTF1A):c.343C>T (p.Pro115Ser)	rs1840910466
NM_178161.3(PTF1A):c.440C>T (p.Ala147Val)	rs1840912525
NM_178161.3(PTF1A):c.520C>T (p.Arg174Trp)	rs1840913860
NM_178161.3(PTF1A):c.673T>G (p.Leu225Val)
NM_178161.3(PTF1A):c.703_720del (p.Gly235_Gly240del)
NM_178161.3(PTF1A):c.8C>T (p.Ala3Val)	rs146089816
NM_178161.3(PTF1A):c.987A>G (p.Ter329Trp)

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