ClinVar Miner

List of variants in gene CSRP3 reported as likely benign by Ambry Genetics

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Gene type:
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Total variants: 30
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HGVS dbSNP gnomAD frequency
NM_003476.5(CSRP3):c.213C>T (p.Ile71=) rs45476991 0.00499
NM_003476.5(CSRP3):c.10T>C (p.Trp4Arg) rs45550635 0.00271
NM_003476.5(CSRP3):c.162G>A (p.Ser54=) rs112848043 0.00104
NM_003476.5(CSRP3):c.299G>A (p.Arg100His) rs138218523 0.00097
NM_003476.5(CSRP3):c.16G>A (p.Gly6Arg) rs185980145 0.00006
NM_003476.5(CSRP3):c.294G>A (p.Pro98=) rs142832902 0.00006
NM_003476.5(CSRP3):c.258G>A (p.Glu86=) rs182798086 0.00005
NM_003476.5(CSRP3):c.300C>T (p.Arg100=) rs146290726 0.00004
NM_003476.5(CSRP3):c.21C>T (p.Gly7=) rs151177504 0.00003
NM_003476.5(CSRP3):c.252G>A (p.Thr84=) rs755614464 0.00002
NM_003476.5(CSRP3):c.15C>T (p.Gly5=) rs747959696 0.00001
NM_003476.5(CSRP3):c.228C>T (p.Gly76=) rs768767452 0.00001
NM_003476.5(CSRP3):c.261T>C (p.His87=) rs773476497 0.00001
NM_003476.5(CSRP3):c.264C>A (p.Leu88=) rs758256351 0.00001
NM_003476.5(CSRP3):c.309C>G (p.Thr103=) rs1273565241 0.00001
NM_003476.5(CSRP3):c.339G>A (p.Lys113=) rs1394465819 0.00001
NM_003476.5(CSRP3):c.351C>T (p.Ser117=) rs766621810 0.00001
NM_003476.5(CSRP3):c.513C>T (p.Cys171=) rs376799144 0.00001
NM_003476.5(CSRP3):c.120C>T (p.Cys40=)
NM_003476.5(CSRP3):c.147C>A (p.Val49=) rs576346189
NM_003476.5(CSRP3):c.147C>T (p.Val49=) rs576346189
NM_003476.5(CSRP3):c.198T>C (p.Tyr66=) rs779421059
NM_003476.5(CSRP3):c.240C>T (p.Leu80=)
NM_003476.5(CSRP3):c.255C>A (p.Gly85=) rs752338221
NM_003476.5(CSRP3):c.324C>T (p.Ser108=)
NM_003476.5(CSRP3):c.381C>T (p.Val127=)
NM_003476.5(CSRP3):c.456G>A (p.Lys152=) rs397516856
NM_003476.5(CSRP3):c.54C>T (p.Tyr18=)
NM_003476.5(CSRP3):c.582A>G (p.Glu194=)
NM_003476.5(CSRP3):c.78T>C (p.Asn26=)

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