List of variants in gene PSAT1 reported as benign for not provided

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: 38

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HGVS	dbSNP	gnomAD frequency
NM_058179.4(PSAT1):c.-12G>C	rs2277148	0.80020
NM_058179.4(PSAT1):c.397+100dup	rs3842207	0.79210
NM_058179.4(PSAT1):c.740+176T>C	rs2039325	0.79176
NM_058179.4(PSAT1):c.570+44G>T	rs944513	0.77720
NM_058179.4(PSAT1):c.60+211C>G	rs10746571	0.76528
NM_058179.4(PSAT1):c.398-142T>G	rs1537173	0.74941
NM_058179.4(PSAT1):c.869+278T>C	rs7028807	0.74879
NM_058179.4(PSAT1):c.741-18T>A	rs3780194	0.74689
NM_058179.4(PSAT1):c.869+167C>T	rs7043123	0.74676
NM_058179.4(PSAT1):c.869+300C>T	rs10735532	0.74600
NM_058179.4(PSAT1):c.61-115A>T	rs10121107	0.69182
NM_058179.4(PSAT1):c.122-255G>A	rs7855063	0.65693
NM_058179.4(PSAT1):c.191+157C>T	rs3739473	0.65559
NM_058179.4(PSAT1):c.297T>G (p.Ala99=)	rs3739474	0.62693
NM_058179.4(PSAT1):c.570+197C>T	rs10116231	0.41776
NM_058179.4(PSAT1):c.1008-277C>T	rs10780231	0.40258
NM_058179.4(PSAT1):c.740+111A>G	rs2039324	0.30400
NM_058179.4(PSAT1):c.740+110C>T	rs2039323	0.30238
NM_058179.4(PSAT1):c.741-77C>A	rs3780193	0.20347
NM_058179.4(PSAT1):c.740+130T>G	rs61143519	0.17843
NM_058179.4(PSAT1):c.571-165G>A	rs3739475	0.14943
NM_058179.4(PSAT1):c.571-80C>T	rs3739476	0.14904
NM_058179.4(PSAT1):c.61-126G>A	rs3824360	0.13640
NM_058179.4(PSAT1):c.191+131C>T	rs3739472	0.13627
NM_058179.4(PSAT1):c.398-209G>A	rs17064299	0.12959
NM_058179.4(PSAT1):c.571-283G>A	rs3824361	0.12545
NM_058179.4(PSAT1):c.*422C>T	rs10867185	0.12240
NM_058179.4(PSAT1):c.398-85C>T	rs41277899	0.11667
NM_058179.4(PSAT1):c.1008-296G>A	rs12379053	0.10800
NM_058179.4(PSAT1):c.1007+167A>C	rs3758203	0.10571
NM_058179.4(PSAT1):c.870-138G>A	rs79095858	0.07620
NM_058179.4(PSAT1):c.*252G>C	rs17064358	0.02208
NM_058179.4(PSAT1):c.*836A>G	rs41277905	0.00996
NM_058179.4(PSAT1):c.348G>A (p.Lys116=)	rs41277897	0.00971
NM_058179.4(PSAT1):c.696G>A (p.Val232=)	rs140331840	0.00097
NM_058179.4(PSAT1):c.122-17T>C	rs3739471	0.00021
NM_058179.4(PSAT1):c.869+69T>G	rs7028509
NM_058179.4(PSAT1):c.870-139G>C	rs10867184

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