Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.138946452A>C | CA354707084 | FOXL2 | c.271T>G (p.Tyr91Asp) | |
3 | g.138946452A>G | CA354707081 | FOXL2 | c.271T>C (p.Tyr91His) | dbSNP |
3 | g.138946452A>T | CA354707082 | FOXL2 | c.271T>A (p.Tyr91Asn) | |
3 | g.138946453G>A | CA436094391 | FOXL2 | c.270C>T (p.Phe90=) | |
3 | g.138946453G>C | CA354707087 | FOXL2 | c.270C>G (p.Phe90Leu) | |
3 | g.138946453G>T | CA354707088 | FOXL2 | c.270C>A (p.Phe90Leu) | COSMIC |
3 | g.138946454A>C | CA354707090 | FOXL2 | c.269T>G (p.Phe90Cys) | |
3 | g.138946454A>G | CA354707092 | FOXL2 | c.269T>C (p.Phe90Ser) | |
3 | g.138946454A>T | CA354707094 | FOXL2 | c.269T>A (p.Phe90Tyr) | dbSNP |
3 | g.138946455A>C | CA354707097 | FOXL2 | c.268T>G (p.Phe90Val) | |
3 | g.138946455A>G | CA354707098 | FOXL2 | c.268T>C (p.Phe90Leu) | ClinVar |
3 | g.138946455A>T | CA354707099 | FOXL2 | c.268T>A (p.Phe90Ile) | |
3 | g.138946456C>A | CA436094394 | FOXL2 | c.267G>T (p.Pro89=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.138946456C= | CA1405402514 | FOXL2 | c.267G= (p.Pro89=) | |
3 | g.138946456C>G | CA436094396 | FOXL2 | c.267G>C (p.Pro89=) | dbSNP gnomAD v2 gnomAD v4 |
3 | g.138946456C>T | CA2639787 | FOXL2 | c.267G>A (p.Pro89=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.138946457G>A | CA354707102 | FOXL2 | c.266C>T (p.Pro89Leu) | dbSNP |
3 | g.138946457G>C | CA354707103 | FOXL2 | c.266C>G (p.Pro89Arg) | ClinVar dbSNP |
3 | g.138946457G= | CA1405402515 | FOXL2 | c.266C= (p.Pro89=) | |
3 | g.138946457G>T | CA354707105 | FOXL2 | c.266C>A (p.Pro89Gln) | ClinVar dbSNP |
3 | g.138946459dup | CA1054108074 | FOXL2 | c.266dup (p.Phe90ValfsTer6) | dbSNP gnomAD v3 gnomAD v4 |
3 | g.138946458G>A | CA354707110 | FOXL2 | c.265C>T (p.Pro89Ser) | |
3 | g.138946458G>C | CA354707109 | FOXL2 | c.265C>G (p.Pro89Ala) | |
3 | g.138946458G>T | CA354707108 | FOXL2 | c.265C>A (p.Pro89Thr) | |
3 | g.138946459G>A | CA436094399 | FOXL2 | c.264C>T (p.Phe88=) | dbSNP gnomAD v4 |
3 | g.138946459G>C | CA354707113 | FOXL2 | c.264C>G (p.Phe88Leu) | |
3 | g.138946459G= | CA1405402516 | FOXL2 | c.264C= (p.Phe88=) | |
3 | g.138946459G>T | CA354707111 | FOXL2 | c.264C>A (p.Phe88Leu) | |
3 | g.138946460A>C | CA354707114 | FOXL2 | c.263T>G (p.Phe88Cys) | |
3 | g.138946460A>G | CA354707118 | FOXL2 | c.263T>C (p.Phe88Ser) | |
3 | g.138946460A>T | CA354707120 | FOXL2 | c.263T>A (p.Phe88Tyr) | |
3 | g.138946461A= | CA1405402517 | FOXL2 | c.262T= (p.Phe88=) | |
3 | g.138946461A>C | CA354707123 | FOXL2 | c.262T>G (p.Phe88Val) | |
3 | g.138946461A>G | CA354707124 | FOXL2 | c.262T>C (p.Phe88Leu) | |
3 | g.138946461A>T | CA354707125 | FOXL2 | c.262T>A (p.Phe88Ile) | ClinVar dbSNP |
3 | g.138946462C>A | CA354707127 | FOXL2 | c.261G>T (p.Lys87Asn) | |
3 | g.138946462C>G | CA354707129 | FOXL2 | c.261G>C (p.Lys87Asn) | gnomAD v4 |
3 | g.138946462C>T | CA436094403 | FOXL2 | c.261G>A (p.Lys87=) | |
3 | g.138946463T>A | CA354707131 | FOXL2 | c.260A>T (p.Lys87Met) | |
3 | g.138946463T>C | CA354707133 | FOXL2 | c.260A>G (p.Lys87Arg) | gnomAD v4 |
3 | g.138946463T>G | CA354707135 | FOXL2 | c.260A>C (p.Lys87Thr) | |
3 | g.138946464T>A | CA354707139 | FOXL2 | c.259A>T (p.Lys87Ter) | |
3 | g.138946464T>C | CA354707140 | FOXL2 | c.259A>G (p.Lys87Glu) | |
3 | g.138946464T>G | CA354707137 | FOXL2 | c.259A>C (p.Lys87Gln) | |
3 | g.138946465del | CA2500598435 | FOXL2 | c.258del (p.Lys87SerfsTer?) | |
3 | g.138946465C>A | CA436094406 | FOXL2 | c.258G>T (p.Ala86=) | |
3 | g.138946465C= | CA1405402518 | FOXL2 | c.258G= (p.Ala86=) | |
3 | g.138946465C>G | CA436094407 | FOXL2 | c.258G>C (p.Ala86=) | dbSNP |
3 | g.138946465C>T | CA436094408 | FOXL2 | c.258G>A (p.Ala86=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.138946466G>A | CA354707142 | FOXL2 | c.257C>T (p.Ala86Val) |