Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.11885872_11885946del | CA2695216093 | ETV6 | c.1153-54_1173del c.1150-54_1170del c.1126-54_1146del c.889-54_909del c.532-54_552del c.1018-54_1038del | |
12 | g.11885878C>A | CA2617675055 | ETV6 | c.1153-48C>A (n.1153-48C>A) c.1150-48C>A (n.1150-48C>A) c.1126-48C>A (n.1126-48C>A) c.889-48C>A (n.889-48C>A) c.532-48C>A (n.532-48C>A) c.1018-48C>A (n.1018-48C>A) | gnomAD v4 |
12 | g.11885878C>T | CA2575169107 | ETV6 | c.1153-48C>T (n.1153-48C>T) c.1150-48C>T (n.1150-48C>T) c.1126-48C>T (n.1126-48C>T) c.889-48C>T (n.889-48C>T) c.532-48C>T (n.532-48C>T) c.1018-48C>T (n.1018-48C>T) | |
12 | g.11885879A>T | CA2725554059 | ETV6 | c.1153-47A>T (n.1153-47A>T) c.1150-47A>T (n.1150-47A>T) c.1126-47A>T (n.1126-47A>T) c.889-47A>T (n.889-47A>T) c.532-47A>T (n.532-47A>T) c.1018-47A>T (n.1018-47A>T) | dbSNP |
12 | g.11885880T>C | CA2575169108 | ETV6 | c.1153-46T>C (n.1153-46T>C) c.1150-46T>C (n.1150-46T>C) c.1126-46T>C (n.1126-46T>C) c.889-46T>C (n.889-46T>C) c.532-46T>C (n.532-46T>C) c.1018-46T>C (n.1018-46T>C) | |
12 | g.11885880_11885882delinsTTG | CA2016648560 | ETV6 | c.1153-46_1153-44delinsTTG (n.1153-46_1153-44delinsTTG) c.1150-46_1150-44delinsTTG (n.1150-46_1150-44delinsTTG) c.1126-46_1126-44delinsTTG (n.1126-46_1126-44delinsTTG) c.889-46_889-44delinsTTG (n.889-46_889-44delinsTTG) c.532-46_532-44delinsTTG (n.532-46_532-44delinsTTG) c.1018-46_1018-44delinsTTG (n.1018-46_1018-44delinsTTG) | |
12 | g.11885881T>A | CA603418298 | ETV6 | c.1153-45T>A (n.1153-45T>A) c.1150-45T>A (n.1150-45T>A) c.1126-45T>A (n.1126-45T>A) c.889-45T>A (n.889-45T>A) c.532-45T>A (n.532-45T>A) c.1018-45T>A (n.1018-45T>A) | dbSNP gnomAD v2 |
12 | g.11885881T>C | CA603418299 | ETV6 | c.1153-45T>C (n.1153-45T>C) c.1150-45T>C (n.1150-45T>C) c.1126-45T>C (n.1126-45T>C) c.889-45T>C (n.889-45T>C) c.532-45T>C (n.532-45T>C) c.1018-45T>C (n.1018-45T>C) | dbSNP gnomAD v2 gnomAD v4 |
12 | g.11885881T= | CA2016648561 | ETV6 | c.1153-45T= (n.1153-45T=) c.1150-45T= (n.1150-45T=) c.1126-45T= (n.1126-45T=) c.889-45T= (n.889-45T=) c.532-45T= (n.532-45T=) c.1018-45T= (n.1018-45T=) | |
12 | g.11885884_11885885del | CA232637420 | ETV6 | c.1153-42_1153-41del (n.1153-42_1153-41del) c.1150-42_1150-41del (n.1150-42_1150-41del) c.1126-42_1126-41del (n.1126-42_1126-41del) c.889-42_889-41del (n.889-42_889-41del) c.532-42_532-41del (n.532-42_532-41del) c.1018-42_1018-41del (n.1018-42_1018-41del) | dbSNP gnomAD v3 gnomAD v4 |
12 | g.11885882G>A | CA6454418 | ETV6 | c.1153-44G>A (n.1153-44G>A) c.1150-44G>A (n.1150-44G>A) c.1126-44G>A (n.1126-44G>A) c.889-44G>A (n.889-44G>A) c.532-44G>A (n.532-44G>A) c.1018-44G>A (n.1018-44G>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.11885882G= | CA2016648562 | ETV6 | c.1153-44G= (n.1153-44G=) c.1150-44G= (n.1150-44G=) c.1126-44G= (n.1126-44G=) c.889-44G= (n.889-44G=) c.532-44G= (n.532-44G=) c.1018-44G= (n.1018-44G=) | |
12 | g.11885882G>T | CA6454417 | ETV6 | c.1153-44G>T (n.1153-44G>T) c.1150-44G>T (n.1150-44G>T) c.1126-44G>T (n.1126-44G>T) c.889-44G>T (n.889-44G>T) c.532-44G>T (n.532-44G>T) c.1018-44G>T (n.1018-44G>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.11885883T>C | CA2617675056 | ETV6 | c.1153-43T>C (n.1153-43T>C) c.1150-43T>C (n.1150-43T>C) c.1126-43T>C (n.1126-43T>C) c.889-43T>C (n.889-43T>C) c.532-43T>C (n.532-43T>C) c.1018-43T>C (n.1018-43T>C) | gnomAD v4 |
12 | g.11885883T>G | CA2617675057 | ETV6 | c.1153-43T>G (n.1153-43T>G) c.1150-43T>G (n.1150-43T>G) c.1126-43T>G (n.1126-43T>G) c.889-43T>G (n.889-43T>G) c.532-43T>G (n.532-43T>G) c.1018-43T>G (n.1018-43T>G) | gnomAD v4 |
12 | g.11885884G>A | CA2725554060 | ETV6 | c.1153-42G>A (n.1153-42G>A) c.1150-42G>A (n.1150-42G>A) c.1126-42G>A (n.1126-42G>A) c.889-42G>A (n.889-42G>A) c.532-42G>A (n.532-42G>A) c.1018-42G>A (n.1018-42G>A) | dbSNP |
12 | g.11885884G= | CA2016648563 | ETV6 | c.1153-42G= (n.1153-42G=) c.1150-42G= (n.1150-42G=) c.1126-42G= (n.1126-42G=) c.889-42G= (n.889-42G=) c.532-42G= (n.532-42G=) c.1018-42G= (n.1018-42G=) | |
12 | g.11885886_11885889dup | CA2016648564 | ETV6 | c.1153-40_1153-37dup (n.1153-40_1153-37dup) c.1150-40_1150-37dup (n.1150-40_1150-37dup) c.1126-40_1126-37dup (n.1126-40_1126-37dup) c.889-40_889-37dup (n.889-40_889-37dup) c.532-40_532-37dup (n.532-40_532-37dup) c.1018-40_1018-37dup (n.1018-40_1018-37dup) | dbSNP |
12 | g.11885886C>A | CA2016648565 | ETV6 | c.1153-40C>A (n.1153-40C>A) c.1150-40C>A (n.1150-40C>A) c.1126-40C>A (n.1126-40C>A) c.889-40C>A (n.889-40C>A) c.532-40C>A (n.532-40C>A) c.1018-40C>A (n.1018-40C>A) | dbSNP gnomAD v4 |
12 | g.11885886C= | CA2016648566 | ETV6 | c.1153-40C= (n.1153-40C=) c.1150-40C= (n.1150-40C=) c.1126-40C= (n.1126-40C=) c.889-40C= (n.889-40C=) c.532-40C= (n.532-40C=) c.1018-40C= (n.1018-40C=) | |
12 | g.11885887T>A | CA944801864 | ETV6 | c.1153-39T>A (n.1153-39T>A) c.1150-39T>A (n.1150-39T>A) c.1126-39T>A (n.1126-39T>A) c.889-39T>A (n.889-39T>A) c.532-39T>A (n.532-39T>A) c.1018-39T>A (n.1018-39T>A) | dbSNP gnomAD v3 gnomAD v4 |
12 | g.11885887T>C | CA6454419 | ETV6 | c.1153-39T>C (n.1153-39T>C) c.1150-39T>C (n.1150-39T>C) c.1126-39T>C (n.1126-39T>C) c.889-39T>C (n.889-39T>C) c.532-39T>C (n.532-39T>C) c.1018-39T>C (n.1018-39T>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.11885887T= | CA2016648567 | ETV6 | c.1153-39T= (n.1153-39T=) c.1150-39T= (n.1150-39T=) c.1126-39T= (n.1126-39T=) c.889-39T= (n.889-39T=) c.532-39T= (n.532-39T=) c.1018-39T= (n.1018-39T=) | |
12 | g.11885888T>C | CA2617675058 | ETV6 | c.1153-38T>C (n.1153-38T>C) c.1150-38T>C (n.1150-38T>C) c.1126-38T>C (n.1126-38T>C) c.889-38T>C (n.889-38T>C) c.532-38T>C (n.532-38T>C) c.1018-38T>C (n.1018-38T>C) | gnomAD v4 |
12 | g.11885888T>G | CA603418300 | ETV6 | c.1153-38T>G (n.1153-38T>G) c.1150-38T>G (n.1150-38T>G) c.1126-38T>G (n.1126-38T>G) c.889-38T>G (n.889-38T>G) c.532-38T>G (n.532-38T>G) c.1018-38T>G (n.1018-38T>G) | dbSNP gnomAD v2 |
12 | g.11885888T= | CA2016648568 | ETV6 | c.1153-38T= (n.1153-38T=) c.1150-38T= (n.1150-38T=) c.1126-38T= (n.1126-38T=) c.889-38T= (n.889-38T=) c.532-38T= (n.532-38T=) c.1018-38T= (n.1018-38T=) | |
12 | g.11885889T>C | CA2016648570 | ETV6 | c.1153-37T>C (n.1153-37T>C) c.1150-37T>C (n.1150-37T>C) c.1126-37T>C (n.1126-37T>C) c.889-37T>C (n.889-37T>C) c.532-37T>C (n.532-37T>C) c.1018-37T>C (n.1018-37T>C) | dbSNP gnomAD v4 |
12 | g.11885889T= | CA2016648569 | ETV6 | c.1153-37T= (n.1153-37T=) c.1150-37T= (n.1150-37T=) c.1126-37T= (n.1126-37T=) c.889-37T= (n.889-37T=) c.532-37T= (n.532-37T=) c.1018-37T= (n.1018-37T=) | |
12 | g.11885890G>A | CA944801870 | ETV6 | c.1153-36G>A (n.1153-36G>A) c.1150-36G>A (n.1150-36G>A) c.1126-36G>A (n.1126-36G>A) c.889-36G>A (n.889-36G>A) c.532-36G>A (n.532-36G>A) c.1018-36G>A (n.1018-36G>A) | dbSNP gnomAD v3 gnomAD v4 |
12 | g.11885890G= | CA2016648571 | ETV6 | c.1153-36G= (n.1153-36G=) c.1150-36G= (n.1150-36G=) c.1126-36G= (n.1126-36G=) c.889-36G= (n.889-36G=) c.532-36G= (n.532-36G=) c.1018-36G= (n.1018-36G=) | |
12 | g.11885892G>A | CA603418301 | ETV6 | c.1153-34G>A (n.1153-34G>A) c.1150-34G>A (n.1150-34G>A) c.1126-34G>A (n.1126-34G>A) c.889-34G>A (n.889-34G>A) c.532-34G>A (n.532-34G>A) c.1018-34G>A (n.1018-34G>A) | dbSNP gnomAD v2 gnomAD v4 |
12 | g.11885892G>C | CA2617675059 | ETV6 | c.1153-34G>C (n.1153-34G>C) c.1150-34G>C (n.1150-34G>C) c.1126-34G>C (n.1126-34G>C) c.889-34G>C (n.889-34G>C) c.532-34G>C (n.532-34G>C) c.1018-34G>C (n.1018-34G>C) | gnomAD v4 |
12 | g.11885892G= | CA2016648572 | ETV6 | c.1153-34G= (n.1153-34G=) c.1150-34G= (n.1150-34G=) c.1126-34G= (n.1126-34G=) c.889-34G= (n.889-34G=) c.532-34G= (n.532-34G=) c.1018-34G= (n.1018-34G=) | |
12 | g.11885893C>A | CA2617675060 | ETV6 | c.1153-33C>A (n.1153-33C>A) c.1150-33C>A (n.1150-33C>A) c.1126-33C>A (n.1126-33C>A) c.889-33C>A (n.889-33C>A) c.532-33C>A (n.532-33C>A) c.1018-33C>A (n.1018-33C>A) | gnomAD v4 |
12 | g.11885893C= | CA2016648574 | ETV6 | c.1153-33C= (n.1153-33C=) c.1150-33C= (n.1150-33C=) c.1126-33C= (n.1126-33C=) c.889-33C= (n.889-33C=) c.532-33C= (n.532-33C=) c.1018-33C= (n.1018-33C=) | |
12 | g.11885893C>G | CA6454421 | ETV6 | c.1153-33C>G (n.1153-33C>G) c.1150-33C>G (n.1150-33C>G) c.1126-33C>G (n.1126-33C>G) c.889-33C>G (n.889-33C>G) c.532-33C>G (n.532-33C>G) c.1018-33C>G (n.1018-33C>G) | dbSNP ExAC gnomAD v4 |
12 | g.11885893C>T | CA684251333 | ETV6 | c.1153-33C>T (n.1153-33C>T) c.1150-33C>T (n.1150-33C>T) c.1126-33C>T (n.1126-33C>T) c.889-33C>T (n.889-33C>T) c.532-33C>T (n.532-33C>T) c.1018-33C>T (n.1018-33C>T) | dbSNP gnomAD v4 |
12 | g.11885893_11885894delinsCT | CA2016648573 | ETV6 | c.1153-33_1153-32delinsCT (n.1153-33_1153-32delinsCT) c.1150-33_1150-32delinsCT (n.1150-33_1150-32delinsCT) c.1126-33_1126-32delinsCT (n.1126-33_1126-32delinsCT) c.889-33_889-32delinsCT (n.889-33_889-32delinsCT) c.532-33_532-32delinsCT (n.532-33_532-32delinsCT) c.1018-33_1018-32delinsCT (n.1018-33_1018-32delinsCT) | |
12 | g.11885894T>C | CA2617675061 | ETV6 | c.1153-32T>C (n.1153-32T>C) c.1150-32T>C (n.1150-32T>C) c.1126-32T>C (n.1126-32T>C) c.889-32T>C (n.889-32T>C) c.532-32T>C (n.532-32T>C) c.1018-32T>C (n.1018-32T>C) | dbSNP gnomAD v4 |
12 | g.11885900dup | CA232637460 | ETV6 | c.1153-26dup (n.1153-26dup) c.1150-26dup (n.1150-26dup) c.1126-26dup (n.1126-26dup) c.889-26dup (n.889-26dup) c.532-26dup (n.532-26dup) c.1018-26dup (n.1018-26dup) | dbSNP gnomAD v2 gnomAD v4 |
12 | g.11885900del | CA6454420 | ETV6 | c.1153-26del (n.1153-26del) c.1150-26del (n.1150-26del) c.1126-26del (n.1126-26del) c.889-26del (n.889-26del) c.532-26del (n.532-26del) c.1018-26del (n.1018-26del) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.11885897T>G | CA2617675062 | ETV6 | c.1153-29T>G (n.1153-29T>G) c.1150-29T>G (n.1150-29T>G) c.1126-29T>G (n.1126-29T>G) c.889-29T>G (n.889-29T>G) c.532-29T>G (n.532-29T>G) c.1018-29T>G (n.1018-29T>G) | gnomAD v4 |
12 | g.11885898T>C | CA6454422 | ETV6 | c.1153-28T>C (n.1153-28T>C) c.1150-28T>C (n.1150-28T>C) c.1126-28T>C (n.1126-28T>C) c.889-28T>C (n.889-28T>C) c.532-28T>C (n.532-28T>C) c.1018-28T>C (n.1018-28T>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.11885898T= | CA2016648575 | ETV6 | c.1153-28T= (n.1153-28T=) c.1150-28T= (n.1150-28T=) c.1126-28T= (n.1126-28T=) c.889-28T= (n.889-28T=) c.532-28T= (n.532-28T=) c.1018-28T= (n.1018-28T=) | |
12 | g.11885898_11885899insATA | CA2725554062 | ETV6 | c.1153-28_1153-27insATA (n.1153-28_1153-27insATA) c.1150-28_1150-27insATA (n.1150-28_1150-27insATA) c.1126-28_1126-27insATA (n.1126-28_1126-27insATA) c.889-28_889-27insATA (n.889-28_889-27insATA) c.532-28_532-27insATA (n.532-28_532-27insATA) c.1018-28_1018-27insATA (n.1018-28_1018-27insATA) | dbSNP |
12 | g.11885899T>A | CA2617675063 | ETV6 | c.1153-27T>A (n.1153-27T>A) c.1150-27T>A (n.1150-27T>A) c.1126-27T>A (n.1126-27T>A) c.889-27T>A (n.889-27T>A) c.532-27T>A (n.532-27T>A) c.1018-27T>A (n.1018-27T>A) | gnomAD v4 |
12 | g.11885900T>C | CA2617675064 | ETV6 | c.1153-26T>C (n.1153-26T>C) c.1150-26T>C (n.1150-26T>C) c.1126-26T>C (n.1126-26T>C) c.889-26T>C (n.889-26T>C) c.532-26T>C (n.532-26T>C) c.1018-26T>C (n.1018-26T>C) | gnomAD v4 |
12 | g.11885900T= | CA2016648576 | ETV6 | c.1153-26T= (n.1153-26T=) c.1150-26T= (n.1150-26T=) c.1126-26T= (n.1126-26T=) c.889-26T= (n.889-26T=) c.532-26T= (n.532-26T=) c.1018-26T= (n.1018-26T=) | |
12 | g.11885900_11885901insTTTCTCT | CA2575169109 | ETV6 | c.1153-26_1153-25insTTTCTCT (n.1153-26_1153-25insTTTCTCT) c.1150-26_1150-25insTTTCTCT (n.1150-26_1150-25insTTTCTCT) c.1126-26_1126-25insTTTCTCT (n.1126-26_1126-25insTTTCTCT) c.889-26_889-25insTTTCTCT (n.889-26_889-25insTTTCTCT) c.532-26_532-25insTTTCTCT (n.532-26_532-25insTTTCTCT) c.1018-26_1018-25insTTTCTCT (n.1018-26_1018-25insTTTCTCT) | |
12 | g.11885901C>A | CA2617675065 | ETV6 | c.1153-25C>A (n.1153-25C>A) c.1150-25C>A (n.1150-25C>A) c.1126-25C>A (n.1126-25C>A) c.889-25C>A (n.889-25C>A) c.532-25C>A (n.532-25C>A) c.1018-25C>A (n.1018-25C>A) | gnomAD v4 |
12 | g.11885901C= | CA2016648577 | ETV6 | c.1153-25C= (n.1153-25C=) c.1150-25C= (n.1150-25C=) c.1126-25C= (n.1126-25C=) c.889-25C= (n.889-25C=) c.532-25C= (n.532-25C=) c.1018-25C= (n.1018-25C=) | |
12 | g.11885901C>G | CA2016648578 | ETV6 | c.1153-25C>G (n.1153-25C>G) c.1150-25C>G (n.1150-25C>G) c.1126-25C>G (n.1126-25C>G) c.889-25C>G (n.889-25C>G) c.532-25C>G (n.532-25C>G) c.1018-25C>G (n.1018-25C>G) | dbSNP gnomAD v4 |
12 | g.11885901C>T | CA603418302 | ETV6 | c.1153-25C>T (n.1153-25C>T) c.1150-25C>T (n.1150-25C>T) c.1126-25C>T (n.1126-25C>T) c.889-25C>T (n.889-25C>T) c.532-25C>T (n.532-25C>T) c.1018-25C>T (n.1018-25C>T) | dbSNP gnomAD v2 gnomAD v4 |
12 | g.11885901_11885902insACTGTCACCAAGGTTTAC | CA2725249499 | ETV6 | c.1153-25_1153-24insACTGTCACCAAGGTTTAC (n.1153-25_1153-24insACTGTCACCAAGGTTTAC) c.1150-25_1150-24insACTGTCACCAAGGTTTAC (n.1150-25_1150-24insACTGTCACCAAGGTTTAC) c.1126-25_1126-24insACTGTCACCAAGGTTTAC (n.1126-25_1126-24insACTGTCACCAAGGTTTAC) c.889-25_889-24insACTGTCACCAAGGTTTAC (n.889-25_889-24insACTGTCACCAAGGTTTAC) c.532-25_532-24insACTGTCACCAAGGTTTAC (n.532-25_532-24insACTGTCACCAAGGTTTAC) c.1018-25_1018-24insACTGTCACCAAGGTTTAC (n.1018-25_1018-24insACTGTCACCAAGGTTTAC) | dbSNP |
12 | g.11885901dup | CA6454423 | ETV6 | c.1153-25dup (n.1153-25dup) c.1150-25dup (n.1150-25dup) c.1126-25dup (n.1126-25dup) c.889-25dup (n.889-25dup) c.532-25dup (n.532-25dup) c.1018-25dup (n.1018-25dup) | dbSNP ExAC gnomAD v3 gnomAD v4 |
12 | g.11885902T>C | CA2617675066 | ETV6 | c.1153-24T>C (n.1153-24T>C) c.1150-24T>C (n.1150-24T>C) c.1126-24T>C (n.1126-24T>C) c.889-24T>C (n.889-24T>C) c.532-24T>C (n.532-24T>C) c.1018-24T>C (n.1018-24T>C) | gnomAD v4 |
12 | g.11885903C>A | CA2575169110 | ETV6 | c.1153-23C>A (n.1153-23C>A) c.1150-23C>A (n.1150-23C>A) c.1126-23C>A (n.1126-23C>A) c.889-23C>A (n.889-23C>A) c.532-23C>A (n.532-23C>A) c.1018-23C>A (n.1018-23C>A) | gnomAD v4 |
12 | g.11885903C= | CA2016648579 | ETV6 | c.1153-23C= (n.1153-23C=) c.1150-23C= (n.1150-23C=) c.1126-23C= (n.1126-23C=) c.889-23C= (n.889-23C=) c.532-23C= (n.532-23C=) c.1018-23C= (n.1018-23C=) | |
12 | g.11885903C>T | CA603418303 | ETV6 | c.1153-23C>T (n.1153-23C>T) c.1150-23C>T (n.1150-23C>T) c.1126-23C>T (n.1126-23C>T) c.889-23C>T (n.889-23C>T) c.532-23C>T (n.532-23C>T) c.1018-23C>T (n.1018-23C>T) | dbSNP gnomAD v2 gnomAD v4 |
12 | g.11885904C>A | CA2617675067 | ETV6 | c.1153-22C>A (n.1153-22C>A) c.1150-22C>A (n.1150-22C>A) c.1126-22C>A (n.1126-22C>A) c.889-22C>A (n.889-22C>A) c.532-22C>A (n.532-22C>A) c.1018-22C>A (n.1018-22C>A) | dbSNP gnomAD v4 |
12 | g.11885904C= | CA2016648580 | ETV6 | c.1153-22C= (n.1153-22C=) c.1150-22C= (n.1150-22C=) c.1126-22C= (n.1126-22C=) c.889-22C= (n.889-22C=) c.532-22C= (n.532-22C=) c.1018-22C= (n.1018-22C=) | |
12 | g.11885904C>T | CA603418304 | ETV6 | c.1153-22C>T (n.1153-22C>T) c.1150-22C>T (n.1150-22C>T) c.1126-22C>T (n.1126-22C>T) c.889-22C>T (n.889-22C>T) c.532-22C>T (n.532-22C>T) c.1018-22C>T (n.1018-22C>T) | dbSNP gnomAD v2 gnomAD v4 |
12 | g.11885905C>A | CA2617675068 | ETV6 | c.1153-21C>A (n.1153-21C>A) c.1150-21C>A (n.1150-21C>A) c.1126-21C>A (n.1126-21C>A) c.889-21C>A (n.889-21C>A) c.532-21C>A (n.532-21C>A) c.1018-21C>A (n.1018-21C>A) | gnomAD v4 |
12 | g.11885905C= | CA2016648581 | ETV6 | c.1153-21C= (n.1153-21C=) c.1150-21C= (n.1150-21C=) c.1126-21C= (n.1126-21C=) c.889-21C= (n.889-21C=) c.532-21C= (n.532-21C=) c.1018-21C= (n.1018-21C=) | |
12 | g.11885905C>T | CA603418305 | ETV6 | c.1153-21C>T (n.1153-21C>T) c.1150-21C>T (n.1150-21C>T) c.1126-21C>T (n.1126-21C>T) c.889-21C>T (n.889-21C>T) c.532-21C>T (n.532-21C>T) c.1018-21C>T (n.1018-21C>T) | dbSNP gnomAD v2 gnomAD v4 |
12 | g.11885906T>C | CA6454424 | ETV6 | c.1153-20T>C (n.1153-20T>C) c.1150-20T>C (n.1150-20T>C) c.1126-20T>C (n.1126-20T>C) c.889-20T>C (n.889-20T>C) c.532-20T>C (n.532-20T>C) c.1018-20T>C (n.1018-20T>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.11885906T>G | CA2617675069 | ETV6 | c.1153-20T>G (n.1153-20T>G) c.1150-20T>G (n.1150-20T>G) c.1126-20T>G (n.1126-20T>G) c.889-20T>G (n.889-20T>G) c.532-20T>G (n.532-20T>G) c.1018-20T>G (n.1018-20T>G) | gnomAD v4 |
12 | g.11885906T= | CA2016648582 | ETV6 | c.1153-20T= (n.1153-20T=) c.1150-20T= (n.1150-20T=) c.1126-20T= (n.1126-20T=) c.889-20T= (n.889-20T=) c.532-20T= (n.532-20T=) c.1018-20T= (n.1018-20T=) | |
12 | g.11885907T>C | CA2617675070 | ETV6 | c.1153-19T>C (n.1153-19T>C) c.1150-19T>C (n.1150-19T>C) c.1126-19T>C (n.1126-19T>C) c.889-19T>C (n.889-19T>C) c.532-19T>C (n.532-19T>C) c.1018-19T>C (n.1018-19T>C) | gnomAD v4 |
12 | g.11885911_11885913dup | CA2016648583 | ETV6 | c.1153-15_1153-13dup (n.1153-15_1153-13dup) c.1150-15_1150-13dup (n.1150-15_1150-13dup) c.1126-15_1126-13dup (n.1126-15_1126-13dup) c.889-15_889-13dup (n.889-15_889-13dup) c.532-15_532-13dup (n.532-15_532-13dup) c.1018-15_1018-13dup (n.1018-15_1018-13dup) | dbSNP |
12 | g.11885908C>A | CA2617675071 | ETV6 | c.1153-18C>A (n.1153-18C>A) c.1150-18C>A (n.1150-18C>A) c.1126-18C>A (n.1126-18C>A) c.889-18C>A (n.889-18C>A) c.532-18C>A (n.532-18C>A) c.1018-18C>A (n.1018-18C>A) | gnomAD v4 |
12 | g.11885908C= | CA2016648584 | ETV6 | c.1153-18C= (n.1153-18C=) c.1150-18C= (n.1150-18C=) c.1126-18C= (n.1126-18C=) c.889-18C= (n.889-18C=) c.532-18C= (n.532-18C=) c.1018-18C= (n.1018-18C=) | |
12 | g.11885908C>T | CA603418306 | ETV6 | c.1153-18C>T (n.1153-18C>T) c.1150-18C>T (n.1150-18C>T) c.1126-18C>T (n.1126-18C>T) c.889-18C>T (n.889-18C>T) c.532-18C>T (n.532-18C>T) c.1018-18C>T (n.1018-18C>T) | dbSNP gnomAD v2 gnomAD v4 |
12 | g.11885909C>A | CA2617675072 | ETV6 | c.1153-17C>A (n.1153-17C>A) c.1150-17C>A (n.1150-17C>A) c.1126-17C>A (n.1126-17C>A) c.889-17C>A (n.889-17C>A) c.532-17C>A (n.532-17C>A) c.1018-17C>A (n.1018-17C>A) | gnomAD v4 |
12 | g.11885909C= | CA2016648585 | ETV6 | c.1153-17C= (n.1153-17C=) c.1150-17C= (n.1150-17C=) c.1126-17C= (n.1126-17C=) c.889-17C= (n.889-17C=) c.532-17C= (n.532-17C=) c.1018-17C= (n.1018-17C=) | |
12 | g.11885909C>G | CA684251355 | ETV6 | c.1153-17C>G (n.1153-17C>G) c.1150-17C>G (n.1150-17C>G) c.1126-17C>G (n.1126-17C>G) c.889-17C>G (n.889-17C>G) c.532-17C>G (n.532-17C>G) c.1018-17C>G (n.1018-17C>G) | dbSNP gnomAD v4 |
12 | g.11885909C>T | CA603418307 | ETV6 | c.1153-17C>T (n.1153-17C>T) c.1150-17C>T (n.1150-17C>T) c.1126-17C>T (n.1126-17C>T) c.889-17C>T (n.889-17C>T) c.532-17C>T (n.532-17C>T) c.1018-17C>T (n.1018-17C>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.11885911C>T | CA2725554063 | ETV6 | c.1153-15C>T (n.1153-15C>T) c.1150-15C>T (n.1150-15C>T) c.1126-15C>T (n.1126-15C>T) c.889-15C>T (n.889-15C>T) c.532-15C>T (n.532-15C>T) c.1018-15C>T (n.1018-15C>T) | dbSNP |
12 | g.11885912C>A | CA2617675073 | ETV6 | c.1153-14C>A (n.1153-14C>A) c.1150-14C>A (n.1150-14C>A) c.1126-14C>A (n.1126-14C>A) c.889-14C>A (n.889-14C>A) c.532-14C>A (n.532-14C>A) c.1018-14C>A (n.1018-14C>A) | gnomAD v4 |
12 | g.11885914T>A | CA603418308 | ETV6 | c.1153-12T>A (n.1153-12T>A) c.1150-12T>A (n.1150-12T>A) c.1126-12T>A (n.1126-12T>A) c.889-12T>A (n.889-12T>A) c.532-12T>A (n.532-12T>A) c.1018-12T>A (n.1018-12T>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.11885914T>C | CA6454425 | ETV6 | c.1153-12T>C (n.1153-12T>C) c.1150-12T>C (n.1150-12T>C) c.1126-12T>C (n.1126-12T>C) c.889-12T>C (n.889-12T>C) c.532-12T>C (n.532-12T>C) c.1018-12T>C (n.1018-12T>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.11885914T>G | CA2794567723 | ETV6 | c.1153-12T>G (n.1153-12T>G) c.1150-12T>G (n.1150-12T>G) c.1126-12T>G (n.1126-12T>G) c.889-12T>G (n.889-12T>G) c.532-12T>G (n.532-12T>G) c.1018-12T>G (n.1018-12T>G) | |
12 | g.11885914T= | CA2016648586 | ETV6 | c.1153-12T= (n.1153-12T=) c.1150-12T= (n.1150-12T=) c.1126-12T= (n.1126-12T=) c.889-12T= (n.889-12T=) c.532-12T= (n.532-12T=) c.1018-12T= (n.1018-12T=) | |
12 | g.11885925_11885938del | CA913184887 | ETV6 | c.1153-1_1165del c.1150-1_1162del c.1126-1_1138del c.889-1_901del c.532-1_544del c.1018-1_1030del | ClinVar dbSNP |
12 | g.11885917A>T | CA2725554066 | ETV6 | c.1153-9A>T (n.1153-9A>T) c.1150-9A>T (n.1150-9A>T) c.1126-9A>T (n.1126-9A>T) c.889-9A>T (n.889-9A>T) c.532-9A>T (n.532-9A>T) c.1018-9A>T (n.1018-9A>T) | dbSNP |
12 | g.11885918A>G | CA2617675074 | ETV6 | c.1153-8A>G (n.1153-8A>G) c.1150-8A>G (n.1150-8A>G) c.1126-8A>G (n.1126-8A>G) c.889-8A>G (n.889-8A>G) c.532-8A>G (n.532-8A>G) c.1018-8A>G (n.1018-8A>G) | gnomAD v4 |
12 | g.11885919C>A | CA2575169111 | ETV6 | c.1153-7C>A (n.1153-7C>A) c.1150-7C>A (n.1150-7C>A) c.1126-7C>A (n.1126-7C>A) c.889-7C>A (n.889-7C>A) c.532-7C>A (n.532-7C>A) c.1018-7C>A (n.1018-7C>A) | gnomAD v4 |
12 | g.11885919C= | CA2016648587 | ETV6 | c.1153-7C= (n.1153-7C=) c.1150-7C= (n.1150-7C=) c.1126-7C= (n.1126-7C=) c.889-7C= (n.889-7C=) c.532-7C= (n.532-7C=) c.1018-7C= (n.1018-7C=) | |
12 | g.11885919C>T | CA6454426 | ETV6 | c.1153-7C>T (n.1153-7C>T) c.1150-7C>T (n.1150-7C>T) c.1126-7C>T (n.1126-7C>T) c.889-7C>T (n.889-7C>T) c.532-7C>T (n.532-7C>T) c.1018-7C>T (n.1018-7C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.11885919_11885921delinsCAA | CA2016648588 | ETV6 | c.1153-7_1153-5delinsCAA (n.1153-7_1153-5delinsCAA) c.1150-7_1150-5delinsCAA (n.1150-7_1150-5delinsCAA) c.1126-7_1126-5delinsCAA (n.1126-7_1126-5delinsCAA) c.889-7_889-5delinsCAA (n.889-7_889-5delinsCAA) c.532-7_532-5delinsCAA (n.532-7_532-5delinsCAA) c.1018-7_1018-5delinsCAA (n.1018-7_1018-5delinsCAA) | |
12 | g.11885921_11885922del | CA2016648589 | ETV6 | c.1153-5_1153-4del (n.1153-5_1153-4del) c.1150-5_1150-4del (n.1150-5_1150-4del) c.1126-5_1126-4del (n.1126-5_1126-4del) c.889-5_889-4del (n.889-5_889-4del) c.532-5_532-4del (n.532-5_532-4del) c.1018-5_1018-4del (n.1018-5_1018-4del) | dbSNP |
12 | g.11885930_11885934del | CA199643 | ETV6 | c.1157_1161del c.1154_1158del c.1130_1134del c.893_897del c.536_540del c.1022_1026del | ClinVar gnomAD v4 |
12 | g.11885923C>A | CA232637494 | ETV6 | c.1153-3C>A (n.1153-3C>A) c.1150-3C>A (n.1150-3C>A) c.1126-3C>A (n.1126-3C>A) c.889-3C>A (n.889-3C>A) c.532-3C>A (n.532-3C>A) c.1018-3C>A (n.1018-3C>A) | dbSNP gnomAD v4 |
12 | g.11885923C= | CA2016648590 | ETV6 | c.1153-3C= (n.1153-3C=) c.1150-3C= (n.1150-3C=) c.1126-3C= (n.1126-3C=) c.889-3C= (n.889-3C=) c.532-3C= (n.532-3C=) c.1018-3C= (n.1018-3C=) | |
12 | g.11885923C>G | CA603418309 | ETV6 | c.1153-3C>G (n.1153-3C>G) c.1150-3C>G (n.1150-3C>G) c.1126-3C>G (n.1126-3C>G) c.889-3C>G (n.889-3C>G) c.532-3C>G (n.532-3C>G) c.1018-3C>G (n.1018-3C>G) | dbSNP gnomAD v2 gnomAD v4 |
12 | g.11885923C>T | CA2725256346 | ETV6 | c.1153-3C>T (n.1153-3C>T) c.1150-3C>T (n.1150-3C>T) c.1126-3C>T (n.1126-3C>T) c.889-3C>T (n.889-3C>T) c.532-3C>T (n.532-3C>T) c.1018-3C>T (n.1018-3C>T) | dbSNP |
12 | g.11885924A>C | CA384044790 | ETV6 | c.1153-2A>C (n.1153-2A>C) c.1150-2A>C (n.1150-2A>C) c.1126-2A>C (n.1126-2A>C) c.889-2A>C (n.889-2A>C) c.532-2A>C (n.532-2A>C) c.1018-2A>C (n.1018-2A>C) | |
12 | g.11885924A>G | CA384044791 | ETV6 | c.1153-2A>G (n.1153-2A>G) c.1150-2A>G (n.1150-2A>G) c.1126-2A>G (n.1126-2A>G) c.889-2A>G (n.889-2A>G) c.532-2A>G (n.532-2A>G) c.1018-2A>G (n.1018-2A>G) | |
12 | g.11885924A>T | CA384044792 | ETV6 | c.1153-2A>T (n.1153-2A>T) c.1150-2A>T (n.1150-2A>T) c.1126-2A>T (n.1126-2A>T) c.889-2A>T (n.889-2A>T) c.532-2A>T (n.532-2A>T) c.1018-2A>T (n.1018-2A>T) | |
12 | g.11885925_11885926del | CA2580085156 | ETV6 | c.1153-1_1153del c.1150-1_1150del c.1126-1_1126del c.889-1_889del c.532-1_532del c.1018-1_1018del | ClinVar |
12 | g.11885924_11885938del | CA2573053612 | ETV6 | c.1153-2_1165del c.1150-2_1162del c.1126-2_1138del c.889-2_901del c.532-2_544del c.1018-2_1030del | ClinVar dbSNP |
12 | g.11885925G>A | CA384044793 | ETV6 | c.1153-1G>A (n.1153-1G>A) c.1150-1G>A (n.1150-1G>A) c.1126-1G>A (n.1126-1G>A) c.889-1G>A (n.889-1G>A) c.532-1G>A (n.532-1G>A) c.1018-1G>A (n.1018-1G>A) | |
12 | g.11885925G>C | CA384044794 | ETV6 | c.1153-1G>C (n.1153-1G>C) c.1150-1G>C (n.1150-1G>C) c.1126-1G>C (n.1126-1G>C) c.889-1G>C (n.889-1G>C) c.532-1G>C (n.532-1G>C) c.1018-1G>C (n.1018-1G>C) | dbSNP gnomAD v3 gnomAD v4 |
12 | g.11885925G= | CA2016648591 | ETV6 | c.1153-1G= (n.1153-1G=) c.1150-1G= (n.1150-1G=) c.1126-1G= (n.1126-1G=) c.889-1G= (n.889-1G=) c.532-1G= (n.532-1G=) c.1018-1G= (n.1018-1G=) | |
12 | g.11885925G>T | CA384044795 | ETV6 | c.1153-1G>T (n.1153-1G>T) c.1150-1G>T (n.1150-1G>T) c.1126-1G>T (n.1126-1G>T) c.889-1G>T (n.889-1G>T) c.532-1G>T (n.532-1G>T) c.1018-1G>T (n.1018-1G>T) | COSMIC |
12 | g.11885926A>C | CA384044796 | ETV6 | c.1153A>C (p.Asn385His) c.1150A>C (p.Asn384His) c.1126A>C (p.Asn376His) c.889A>C (p.Asn297His) c.532A>C (p.Asn178His) c.1018A>C (p.Asn340His) | |
12 | g.11885926A>G | CA384044797 | ETV6 | c.1153A>G (p.Asn385Asp) c.1150A>G (p.Asn384Asp) c.1126A>G (p.Asn376Asp) c.889A>G (p.Asn297Asp) c.532A>G (p.Asn178Asp) c.1018A>G (p.Asn340Asp) | |
12 | g.11885926A>T | CA384044798 | ETV6 | c.1153A>T (p.Asn385Tyr) c.1150A>T (p.Asn384Tyr) c.1126A>T (p.Asn376Tyr) c.889A>T (p.Asn297Tyr) c.532A>T (p.Asn178Tyr) c.1018A>T (p.Asn340Tyr) | ClinVar dbSNP |
12 | g.11885927A>C | CA384044801 | ETV6 | c.1154A>C (p.Asn385Thr) c.1151A>C (p.Asn384Thr) c.1127A>C (p.Asn376Thr) c.890A>C (p.Asn297Thr) c.533A>C (p.Asn178Thr) c.1019A>C (p.Asn340Thr) | |
12 | g.11885927A>G | CA384044799 | ETV6 | c.1154A>G (p.Asn385Ser) c.1151A>G (p.Asn384Ser) c.1127A>G (p.Asn376Ser) c.890A>G (p.Asn297Ser) c.533A>G (p.Asn178Ser) c.1019A>G (p.Asn340Ser) | COSMIC |
12 | g.11885927A>T | CA384044800 | ETV6 | c.1154A>T (p.Asn385Ile) c.1151A>T (p.Asn384Ile) c.1127A>T (p.Asn376Ile) c.890A>T (p.Asn297Ile) c.533A>T (p.Asn178Ile) c.1019A>T (p.Asn340Ile) | |
12 | g.11885929_11885942del | CA2617675075 | ETV6 | c.1156_1169del (p.Arg386LeufsTer2) c.1153_1166del (p.Arg385LeufsTer2) c.1129_1142del (p.Arg377LeufsTer2) c.892_905del (p.Arg298LeufsTer2) c.535_548del (p.Arg179LeufsTer2) c.1021_1034del (p.Arg341LeufsTer2) | gnomAD v4 |
12 | g.11885928C>A | CA384044802 | ETV6 | c.1155C>A (p.Asn385Lys) c.1152C>A (p.Asn384Lys) c.1128C>A (p.Asn376Lys) c.891C>A (p.Asn297Lys) c.534C>A (p.Asn178Lys) c.1020C>A (p.Asn340Lys) | |
12 | g.11885928C>G | CA384044803 | ETV6 | c.1155C>G (p.Asn385Lys) c.1152C>G (p.Asn384Lys) c.1128C>G (p.Asn376Lys) c.891C>G (p.Asn297Lys) c.534C>G (p.Asn178Lys) c.1020C>G (p.Asn340Lys) | |
12 | g.11885928C>T | CA478767192 | ETV6 | c.1155C>T (p.Asn385=) c.1152C>T (p.Asn384=) c.1128C>T (p.Asn376=) c.891C>T (p.Asn297=) c.534C>T (p.Asn178=) c.1020C>T (p.Asn340=) | |
12 | g.11885929A>C | CA478767193 | ETV6 | c.1156A>C (p.Arg386=) c.1153A>C (p.Arg385=) c.1129A>C (p.Arg377=) c.892A>C (p.Arg298=) c.535A>C (p.Arg179=) c.1021A>C (p.Arg341=) | |
12 | g.11885929A>G | CA384044804 | ETV6 | c.1156A>G (p.Arg386Gly) c.1153A>G (p.Arg385Gly) c.1129A>G (p.Arg377Gly) c.892A>G (p.Arg298Gly) c.535A>G (p.Arg179Gly) c.1021A>G (p.Arg341Gly) | |
12 | g.11885929A>T | CA384044805 | ETV6 | c.1156A>T (p.Arg386Ter) c.1153A>T (p.Arg385Ter) c.1129A>T (p.Arg377Ter) c.892A>T (p.Arg298Ter) c.535A>T (p.Arg179Ter) c.1021A>T (p.Arg341Ter) | |
12 | g.11885930G>A | CA384044806 | ETV6 | c.1157G>A (p.Arg386Lys) c.1154G>A (p.Arg385Lys) c.1130G>A (p.Arg377Lys) c.893G>A (p.Arg298Lys) c.536G>A (p.Arg179Lys) c.1022G>A (p.Arg341Lys) | dbSNP |
12 | g.11885930G>C | CA384044807 | ETV6 | c.1157G>C (p.Arg386Thr) c.1154G>C (p.Arg385Thr) c.1130G>C (p.Arg377Thr) c.893G>C (p.Arg298Thr) c.536G>C (p.Arg179Thr) c.1022G>C (p.Arg341Thr) | |
12 | g.11885930G>T | CA384044808 | ETV6 | c.1157G>T (p.Arg386Ile) c.1154G>T (p.Arg385Ile) c.1130G>T (p.Arg377Ile) c.893G>T (p.Arg298Ile) c.536G>T (p.Arg179Ile) c.1022G>T (p.Arg341Ile) | |
12 | g.11885931A>C | CA384044809 | ETV6 | c.1158A>C (p.Arg386Ser) c.1155A>C (p.Arg385Ser) c.1131A>C (p.Arg377Ser) c.894A>C (p.Arg298Ser) c.537A>C (p.Arg179Ser) c.1023A>C (p.Arg341Ser) | |
12 | g.11885931A>G | CA478767194 | ETV6 | c.1158A>G (p.Arg386=) c.1155A>G (p.Arg385=) c.1131A>G (p.Arg377=) c.894A>G (p.Arg298=) c.537A>G (p.Arg179=) c.1023A>G (p.Arg341=) | |
12 | g.11885931A>T | CA384044810 | ETV6 | c.1158A>T (p.Arg386Ser) c.1155A>T (p.Arg385Ser) c.1131A>T (p.Arg377Ser) c.894A>T (p.Arg298Ser) c.537A>T (p.Arg179Ser) c.1023A>T (p.Arg341Ser) | |
12 | g.11885932A>C | CA384044811 | ETV6 | c.1159A>C (p.Thr387Pro) c.1156A>C (p.Thr386Pro) c.1132A>C (p.Thr378Pro) c.895A>C (p.Thr299Pro) c.538A>C (p.Thr180Pro) c.1024A>C (p.Thr342Pro) | |
12 | g.11885932A>G | CA384044812 | ETV6 | c.1159A>G (p.Thr387Ala) c.1156A>G (p.Thr386Ala) c.1132A>G (p.Thr378Ala) c.895A>G (p.Thr299Ala) c.538A>G (p.Thr180Ala) c.1024A>G (p.Thr342Ala) | dbSNP gnomAD v3 |
12 | g.11885932A>T | CA384044813 | ETV6 | c.1159A>T (p.Thr387Ser) c.1156A>T (p.Thr386Ser) c.1132A>T (p.Thr378Ser) c.895A>T (p.Thr299Ser) c.538A>T (p.Thr180Ser) c.1024A>T (p.Thr342Ser) | |
12 | g.11885933C>A | CA384044815 | ETV6 | c.1160C>A (p.Thr387Lys) c.1157C>A (p.Thr386Lys) c.1133C>A (p.Thr378Lys) c.896C>A (p.Thr299Lys) c.539C>A (p.Thr180Lys) c.1025C>A (p.Thr342Lys) | |
12 | g.11885933C= | CA2016648592 | ETV6 | c.1160C= (p.Thr387=) c.1157C= (p.Thr386=) c.1133C= (p.Thr378=) c.896C= (p.Thr299=) c.539C= (p.Thr180=) c.1025C= (p.Thr342=) | |
12 | g.11885933C>G | CA384044816 | ETV6 | c.1160C>G (p.Thr387Arg) c.1157C>G (p.Thr386Arg) c.1133C>G (p.Thr378Arg) c.896C>G (p.Thr299Arg) c.539C>G (p.Thr180Arg) c.1025C>G (p.Thr342Arg) | |
12 | g.11885933C>T | CA384044814 | ETV6 | c.1160C>T (p.Thr387Ile) c.1157C>T (p.Thr386Ile) c.1133C>T (p.Thr378Ile) c.896C>T (p.Thr299Ile) c.539C>T (p.Thr180Ile) c.1025C>T (p.Thr342Ile) | dbSNP gnomAD v2 gnomAD v4 |
12 | g.11885934A>C | CA478767195 | ETV6 | c.1161A>C (p.Thr387=) c.1158A>C (p.Thr386=) c.1134A>C (p.Thr378=) c.897A>C (p.Thr299=) c.540A>C (p.Thr180=) c.1026A>C (p.Thr342=) | |
12 | g.11885934A>G | CA478767196 | ETV6 | c.1161A>G (p.Thr387=) c.1158A>G (p.Thr386=) c.1134A>G (p.Thr378=) c.897A>G (p.Thr299=) c.540A>G (p.Thr180=) c.1026A>G (p.Thr342=) | |
12 | g.11885934A>T | CA478767197 | ETV6 | c.1161A>T (p.Thr387=) c.1158A>T (p.Thr386=) c.1134A>T (p.Thr378=) c.897A>T (p.Thr299=) c.540A>T (p.Thr180=) c.1026A>T (p.Thr342=) | |
12 | g.11885935A>C | CA384044817 | ETV6 | c.1162A>C (p.Asn388His) c.1159A>C (p.Asn387His) c.1135A>C (p.Asn379His) c.898A>C (p.Asn300His) c.541A>C (p.Asn181His) c.1027A>C (p.Asn343His) | |
12 | g.11885935A>G | CA384044818 | ETV6 | c.1162A>G (p.Asn388Asp) c.1159A>G (p.Asn387Asp) c.1135A>G (p.Asn379Asp) c.898A>G (p.Asn300Asp) c.541A>G (p.Asn181Asp) c.1027A>G (p.Asn343Asp) | |
12 | g.11885935A>T | CA384044819 | ETV6 | c.1162A>T (p.Asn388Tyr) c.1159A>T (p.Asn387Tyr) c.1135A>T (p.Asn379Tyr) c.898A>T (p.Asn300Tyr) c.541A>T (p.Asn181Tyr) c.1027A>T (p.Asn343Tyr) | |
12 | g.11885936A>C | CA384044820 | ETV6 | c.1163A>C (p.Asn388Thr) c.1160A>C (p.Asn387Thr) c.1136A>C (p.Asn379Thr) c.899A>C (p.Asn300Thr) c.542A>C (p.Asn181Thr) c.1028A>C (p.Asn343Thr) | |
12 | g.11885936A>G | CA384044821 | ETV6 | c.1163A>G (p.Asn388Ser) c.1160A>G (p.Asn387Ser) c.1136A>G (p.Asn379Ser) c.899A>G (p.Asn300Ser) c.542A>G (p.Asn181Ser) c.1028A>G (p.Asn343Ser) | |
12 | g.11885936A>T | CA384044822 | ETV6 | c.1163A>T (p.Asn388Ile) c.1160A>T (p.Asn387Ile) c.1136A>T (p.Asn379Ile) c.899A>T (p.Asn300Ile) c.542A>T (p.Asn181Ile) c.1028A>T (p.Asn343Ile) | |
12 | g.11885937C>A | CA384044824 | ETV6 | c.1164C>A (p.Asn388Lys) c.1C>A c.1161C>A (p.Asn387Lys) c.1137C>A (p.Asn379Lys) c.900C>A (p.Asn300Lys) c.543C>A (p.Asn181Lys) c.1029C>A (p.Asn343Lys) | |
12 | g.11885937C>G | CA384044823 | ETV6 | c.1164C>G (p.Asn388Lys) c.1C>G c.1161C>G (p.Asn387Lys) c.1137C>G (p.Asn379Lys) c.900C>G (p.Asn300Lys) c.543C>G (p.Asn181Lys) c.1029C>G (p.Asn343Lys) | |
12 | g.11885937C>T | CA478767198 | ETV6 | c.1164C>T (p.Asn388=) c.1C>T c.1161C>T (p.Asn387=) c.1137C>T (p.Asn379=) c.900C>T (p.Asn300=) c.543C>T (p.Asn181=) c.1029C>T (p.Asn343=) | gnomAD v4 |
12 | g.11885938A>C | CA384044825 | ETV6 | c.1165A>C (p.Met389Leu) c.2A>C c.1162A>C (p.Met388Leu) c.1138A>C (p.Met380Leu) c.901A>C (p.Met301Leu) c.544A>C (p.Met182Leu) c.1030A>C (p.Met344Leu) | |
12 | g.11885938A>G | CA384044826 | ETV6 | c.1165A>G (p.Met389Val) c.2A>G c.1162A>G (p.Met388Val) c.1138A>G (p.Met380Val) c.901A>G (p.Met301Val) c.544A>G (p.Met182Val) c.1030A>G (p.Met344Val) | |
12 | g.11885938A>T | CA384044827 | ETV6 | c.1165A>T (p.Met389Leu) c.2A>T c.1162A>T (p.Met388Leu) c.1138A>T (p.Met380Leu) c.901A>T (p.Met301Leu) c.544A>T (p.Met182Leu) c.1030A>T (p.Met344Leu) | |
12 | g.11885939T>A | CA384044828 | ETV6 | c.1166T>A (p.Met389Lys) c.3T>A c.1163T>A (p.Met388Lys) c.1139T>A (p.Met380Lys) c.902T>A (p.Met301Lys) c.545T>A (p.Met182Lys) c.1031T>A (p.Met344Lys) | |
12 | g.11885939T>C | CA384044829 | ETV6 | c.1166T>C (p.Met389Thr) c.3T>C c.1163T>C (p.Met388Thr) c.1139T>C (p.Met380Thr) c.902T>C (p.Met301Thr) c.545T>C (p.Met182Thr) c.1031T>C (p.Met344Thr) | |
12 | g.11885939T>G | CA384044830 | ETV6 | c.1166T>G (p.Met389Arg) c.3T>G c.1163T>G (p.Met388Arg) c.1139T>G (p.Met380Arg) c.902T>G (p.Met301Arg) c.545T>G (p.Met182Arg) c.1031T>G (p.Met344Arg) | |
12 | g.11885940G>A | CA384044831 | ETV6 | c.1167G>A (p.Met389Ile) c.4G>A c.1164G>A (p.Met388Ile) c.1140G>A (p.Met380Ile) c.903G>A (p.Met301Ile) c.546G>A (p.Met182Ile) c.1032G>A (p.Met344Ile) | COSMIC |
12 | g.11885940G>C | CA384044833 | ETV6 | c.1167G>C (p.Met389Ile) c.4G>C c.1164G>C (p.Met388Ile) c.1140G>C (p.Met380Ile) c.903G>C (p.Met301Ile) c.546G>C (p.Met182Ile) c.1032G>C (p.Met344Ile) | dbSNP |
12 | g.11885940G>T | CA384044832 | ETV6 | c.1167G>T (p.Met389Ile) c.4G>T c.1164G>T (p.Met388Ile) c.1140G>T (p.Met380Ile) c.903G>T (p.Met301Ile) c.546G>T (p.Met182Ile) c.1032G>T (p.Met344Ile) | gnomAD v4 |
12 | g.11885942_11885950del | CA645595229 | ETV6 | c.1169_1177del (p.Thr390_Glu392del) c.6_14del c.1166_1174del (p.Thr389_Glu391del) c.1142_1150del (p.Thr381_Glu383del) c.905_913del (p.Thr302_Glu304del) c.548_556del (p.Thr183_Glu185del) c.1034_1042del (p.Thr345_Glu347del) | COSMIC |
12 | g.11885941A>C | CA384044834 | ETV6 | c.1168A>C (p.Thr390Pro) c.5A>C c.1165A>C (p.Thr389Pro) c.1141A>C (p.Thr381Pro) c.904A>C (p.Thr302Pro) c.547A>C (p.Thr183Pro) c.1033A>C (p.Thr345Pro) | |
12 | g.11885941A>G | CA384044835 | ETV6 | c.1168A>G (p.Thr390Ala) c.5A>G c.1165A>G (p.Thr389Ala) c.1141A>G (p.Thr381Ala) c.904A>G (p.Thr302Ala) c.547A>G (p.Thr183Ala) c.1033A>G (p.Thr345Ala) | |
12 | g.11885941A>T | CA384044836 | ETV6 | c.1168A>T (p.Thr390Ser) c.5A>T c.1165A>T (p.Thr389Ser) c.1141A>T (p.Thr381Ser) c.904A>T (p.Thr302Ser) c.547A>T (p.Thr183Ser) c.1033A>T (p.Thr345Ser) | |
12 | g.11885942C>A | CA384044837 | ETV6 | c.1169C>A (p.Thr390Asn) c.6C>A c.1166C>A (p.Thr389Asn) c.1142C>A (p.Thr381Asn) c.905C>A (p.Thr302Asn) c.548C>A (p.Thr183Asn) c.1034C>A (p.Thr345Asn) | |
12 | g.11885942C>G | CA384044838 | ETV6 | c.1169C>G (p.Thr390Ser) c.6C>G c.1166C>G (p.Thr389Ser) c.1142C>G (p.Thr381Ser) c.905C>G (p.Thr302Ser) c.548C>G (p.Thr183Ser) c.1034C>G (p.Thr345Ser) | |
12 | g.11885942C>T | CA384044839 | ETV6 | c.1169C>T (p.Thr390Ile) c.6C>T c.1166C>T (p.Thr389Ile) c.1142C>T (p.Thr381Ile) c.905C>T (p.Thr302Ile) c.548C>T (p.Thr183Ile) c.1034C>T (p.Thr345Ile) | ClinVar |
12 | g.11885943C>A | CA478767199 | ETV6 | c.1170C>A (p.Thr390=) c.7C>A c.1167C>A (p.Thr389=) c.1143C>A (p.Thr381=) c.906C>A (p.Thr302=) c.549C>A (p.Thr183=) c.1035C>A (p.Thr345=) | |
12 | g.11885943C>G | CA478767200 | ETV6 | c.1170C>G (p.Thr390=) c.7C>G c.1167C>G (p.Thr389=) c.1143C>G (p.Thr381=) c.906C>G (p.Thr302=) c.549C>G (p.Thr183=) c.1035C>G (p.Thr345=) | |
12 | g.11885943C>T | CA478767201 | ETV6 | c.1170C>T (p.Thr390=) c.7C>T c.1167C>T (p.Thr389=) c.1143C>T (p.Thr381=) c.906C>T (p.Thr302=) c.549C>T (p.Thr183=) c.1035C>T (p.Thr345=) | |
12 | g.11885944del | CA645595230 | ETV6 | c.1171del (p.Tyr391MetfsTer14) c.8del c.1168del (p.Tyr390MetfsTer14) c.1144del (p.Tyr382MetfsTer14) c.907del (p.Tyr303MetfsTer14) c.550del (p.Tyr184MetfsTer14) c.1036del (p.Tyr346MetfsTer14) | COSMIC |
12 | g.11885944T>A | CA384044840 | ETV6 | c.1171T>A (p.Tyr391Asn) c.8T>A c.1168T>A (p.Tyr390Asn) c.1144T>A (p.Tyr382Asn) c.907T>A (p.Tyr303Asn) c.550T>A (p.Tyr184Asn) c.1036T>A (p.Tyr346Asn) | |
12 | g.11885944T>C | CA384044841 | ETV6 | c.1171T>C (p.Tyr391His) c.8T>C c.1168T>C (p.Tyr390His) c.1144T>C (p.Tyr382His) c.907T>C (p.Tyr303His) c.550T>C (p.Tyr184His) c.1036T>C (p.Tyr346His) | |
12 | g.11885944T>G | CA384044842 | ETV6 | c.1171T>G (p.Tyr391Asp) c.8T>G c.1168T>G (p.Tyr390Asp) c.1144T>G (p.Tyr382Asp) c.907T>G (p.Tyr303Asp) c.550T>G (p.Tyr184Asp) c.1036T>G (p.Tyr346Asp) | |
12 | g.11885945A>C | CA384044843 | ETV6 | c.1172A>C (p.Tyr391Ser) c.9A>C c.1169A>C (p.Tyr390Ser) c.1145A>C (p.Tyr382Ser) c.908A>C (p.Tyr303Ser) c.551A>C (p.Tyr184Ser) c.1037A>C (p.Tyr346Ser) | |
12 | g.11885945A>G | CA384044844 | ETV6 | c.1172A>G (p.Tyr391Cys) c.9A>G c.1169A>G (p.Tyr390Cys) c.1145A>G (p.Tyr382Cys) c.908A>G (p.Tyr303Cys) c.551A>G (p.Tyr184Cys) c.1037A>G (p.Tyr346Cys) | dbSNP COSMIC |
12 | g.11885945A>T | CA384044845 | ETV6 | c.1172A>T (p.Tyr391Phe) c.9A>T c.1169A>T (p.Tyr390Phe) c.1145A>T (p.Tyr382Phe) c.908A>T (p.Tyr303Phe) c.551A>T (p.Tyr184Phe) c.1037A>T (p.Tyr346Phe) | |
12 | g.11885946T>A | CA384044846 | ETV6 | c.1173T>A (p.Tyr391Ter) c.10T>A c.1170T>A (p.Tyr390Ter) c.1146T>A (p.Tyr382Ter) c.909T>A (p.Tyr303Ter) c.552T>A (p.Tyr184Ter) c.1038T>A (p.Tyr346Ter) | COSMIC |
12 | g.11885946T>C | CA6454427 | ETV6 | c.1173T>C (p.Tyr391=) c.10T>C c.1170T>C (p.Tyr390=) c.1146T>C (p.Tyr382=) c.909T>C (p.Tyr303=) c.552T>C (p.Tyr184=) c.1038T>C (p.Tyr346=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.11885946T>G | CA384044847 | ETV6 | c.1173T>G (p.Tyr391Ter) c.10T>G c.1170T>G (p.Tyr390Ter) c.1146T>G (p.Tyr382Ter) c.909T>G (p.Tyr303Ter) c.552T>G (p.Tyr184Ter) c.1038T>G (p.Tyr346Ter) | gnomAD v4 |
12 | g.11885946T= | CA2016648593 | ETV6 | c.1173T= (p.Tyr391=) c.10T= c.1170T= (p.Tyr390=) c.1146T= (p.Tyr382=) c.909T= (p.Tyr303=) c.552T= (p.Tyr184=) c.1038T= (p.Tyr346=) | |
12 | g.11885947G>A | CA384044848 | ETV6 | c.1174G>A (p.Glu392Lys) c.11G>A c.1171G>A (p.Glu391Lys) c.1147G>A (p.Glu383Lys) c.910G>A (p.Glu304Lys) c.553G>A (p.Glu185Lys) c.1039G>A (p.Glu347Lys) | dbSNP COSMIC |
12 | g.11885947G>C | CA384044849 | ETV6 | c.1174G>C (p.Glu392Gln) c.11G>C c.1171G>C (p.Glu391Gln) c.1147G>C (p.Glu383Gln) c.910G>C (p.Glu304Gln) c.553G>C (p.Glu185Gln) c.1039G>C (p.Glu347Gln) | |
12 | g.11885947G>T | CA384044850 | ETV6 | c.1174G>T (p.Glu392Ter) c.11G>T c.1171G>T (p.Glu391Ter) c.1147G>T (p.Glu383Ter) c.910G>T (p.Glu304Ter) c.553G>T (p.Glu185Ter) c.1039G>T (p.Glu347Ter) | |
12 | g.11885948A>C | CA384044851 | ETV6 | c.1175A>C (p.Glu392Ala) c.12A>C c.1172A>C (p.Glu391Ala) c.1148A>C (p.Glu383Ala) c.911A>C (p.Glu304Ala) c.554A>C (p.Glu185Ala) c.1040A>C (p.Glu347Ala) | |
12 | g.11885948A>G | CA384044852 | ETV6 | c.1175A>G (p.Glu392Gly) c.12A>G c.1172A>G (p.Glu391Gly) c.1148A>G (p.Glu383Gly) c.911A>G (p.Glu304Gly) c.554A>G (p.Glu185Gly) c.1040A>G (p.Glu347Gly) | |
12 | g.11885948A>T | CA384044853 | ETV6 | c.1175A>T (p.Glu392Val) c.12A>T c.1172A>T (p.Glu391Val) c.1148A>T (p.Glu383Val) c.911A>T (p.Glu304Val) c.554A>T (p.Glu185Val) c.1040A>T (p.Glu347Val) | |
12 | g.11885949G>A | CA478767202 | ETV6 | c.1176G>A (p.Glu392=) c.13G>A c.1173G>A (p.Glu391=) c.1149G>A (p.Glu383=) c.912G>A (p.Glu304=) c.555G>A (p.Glu185=) c.1041G>A (p.Glu347=) | gnomAD v4 |
12 | g.11885949G>C | CA384044854 | ETV6 | c.1176G>C (p.Glu392Asp) c.13G>C c.1173G>C (p.Glu391Asp) c.1149G>C (p.Glu383Asp) c.912G>C (p.Glu304Asp) c.555G>C (p.Glu185Asp) c.1041G>C (p.Glu347Asp) | |
12 | g.11885949G>T | CA384044855 | ETV6 | c.1176G>T (p.Glu392Asp) c.13G>T c.1173G>T (p.Glu391Asp) c.1149G>T (p.Glu383Asp) c.912G>T (p.Glu304Asp) c.555G>T (p.Glu185Asp) c.1041G>T (p.Glu347Asp) | |
12 | g.11885950A>C | CA384044856 | ETV6 | c.1177A>C (p.Lys393Gln) c.14A>C c.1174A>C (p.Lys392Gln) c.1150A>C (p.Lys384Gln) c.913A>C (p.Lys305Gln) c.556A>C (p.Lys186Gln) c.1042A>C (p.Lys348Gln) | |
12 | g.11885950A>G | CA384044857 | ETV6 | c.1177A>G (p.Lys393Glu) c.14A>G c.1174A>G (p.Lys392Glu) c.1150A>G (p.Lys384Glu) c.913A>G (p.Lys305Glu) c.556A>G (p.Lys186Glu) c.1042A>G (p.Lys348Glu) | |
12 | g.11885950A>T | CA384044858 | ETV6 | c.1177A>T (p.Lys393Ter) c.14A>T c.1174A>T (p.Lys392Ter) c.1150A>T (p.Lys384Ter) c.913A>T (p.Lys305Ter) c.556A>T (p.Lys186Ter) c.1042A>T (p.Lys348Ter) | |
12 | g.11885951A>C | CA384044859 | ETV6 | c.1178A>C (p.Lys393Thr) c.15A>C c.1175A>C (p.Lys392Thr) c.1151A>C (p.Lys384Thr) c.914A>C (p.Lys305Thr) c.557A>C (p.Lys186Thr) c.1043A>C (p.Lys348Thr) | |
12 | g.11885951A>G | CA384044860 | ETV6 | c.1178A>G (p.Lys393Arg) c.15A>G c.1175A>G (p.Lys392Arg) c.1151A>G (p.Lys384Arg) c.914A>G (p.Lys305Arg) c.557A>G (p.Lys186Arg) c.1043A>G (p.Lys348Arg) | |
12 | g.11885951A>T | CA384044861 | ETV6 | c.1178A>T (p.Lys393Ile) c.15A>T c.1175A>T (p.Lys392Ile) c.1151A>T (p.Lys384Ile) c.914A>T (p.Lys305Ile) c.557A>T (p.Lys186Ile) c.1043A>T (p.Lys348Ile) | |
12 | g.11885952A= | CA2016648594 | ETV6 | c.1179A= (p.Lys393=) c.16A= c.1176A= (p.Lys392=) c.1152A= (p.Lys384=) c.915A= (p.Lys305=) c.558A= (p.Lys186=) c.1044A= (p.Lys348=) | |
12 | g.11885952A>C | CA384044862 | ETV6 | c.1179A>C (p.Lys393Asn) c.16A>C c.1176A>C (p.Lys392Asn) c.1152A>C (p.Lys384Asn) c.915A>C (p.Lys305Asn) c.558A>C (p.Lys186Asn) c.1044A>C (p.Lys348Asn) | |
12 | g.11885952A>G | CA478767203 | ETV6 | c.1179A>G (p.Lys393=) c.16A>G c.1176A>G (p.Lys392=) c.1152A>G (p.Lys384=) c.915A>G (p.Lys305=) c.558A>G (p.Lys186=) c.1044A>G (p.Lys348=) | dbSNP gnomAD v4 |
12 | g.11885952A>T | CA384044863 | ETV6 | c.1179A>T (p.Lys393Asn) c.16A>T c.1176A>T (p.Lys392Asn) c.1152A>T (p.Lys384Asn) c.915A>T (p.Lys305Asn) c.558A>T (p.Lys186Asn) c.1044A>T (p.Lys348Asn) | |
12 | g.11885953A>C | CA384044864 | ETV6 | c.1180A>C (p.Met394Leu) c.17A>C c.1177A>C (p.Met393Leu) c.1153A>C (p.Met385Leu) c.916A>C (p.Met306Leu) c.559A>C (p.Met187Leu) c.1045A>C (p.Met349Leu) | |
12 | g.11885953A>G | CA384044865 | ETV6 | c.1180A>G (p.Met394Val) c.17A>G c.1177A>G (p.Met393Val) c.1153A>G (p.Met385Val) c.916A>G (p.Met306Val) c.559A>G (p.Met187Val) c.1045A>G (p.Met349Val) | gnomAD v4 |
12 | g.11885953A>T | CA384044866 | ETV6 | c.1180A>T (p.Met394Leu) c.17A>T c.1177A>T (p.Met393Leu) c.1153A>T (p.Met385Leu) c.916A>T (p.Met306Leu) c.559A>T (p.Met187Leu) c.1045A>T (p.Met349Leu) | |
12 | g.11885954T>A | CA384044867 | ETV6 | c.1181T>A (p.Met394Lys) c.18T>A c.1178T>A (p.Met393Lys) c.1154T>A (p.Met385Lys) c.917T>A (p.Met306Lys) c.560T>A (p.Met187Lys) c.1046T>A (p.Met349Lys) | |
12 | g.11885954T>C | CA384044868 | ETV6 | c.1181T>C (p.Met394Thr) c.18T>C c.1178T>C (p.Met393Thr) c.1154T>C (p.Met385Thr) c.917T>C (p.Met306Thr) c.560T>C (p.Met187Thr) c.1046T>C (p.Met349Thr) | |
12 | g.11885954T>G | CA384044869 | ETV6 | c.1181T>G (p.Met394Arg) c.18T>G c.1178T>G (p.Met393Arg) c.1154T>G (p.Met385Arg) c.917T>G (p.Met306Arg) c.560T>G (p.Met187Arg) c.1046T>G (p.Met349Arg) | |
12 | g.11885955G>A | CA384044870 | ETV6 | c.1182G>A (p.Met394Ile) c.19G>A c.1179G>A (p.Met393Ile) c.1155G>A (p.Met385Ile) c.918G>A (p.Met306Ile) c.561G>A (p.Met187Ile) c.1047G>A (p.Met349Ile) | dbSNP gnomAD v3 gnomAD v4 |
12 | g.11885955G>C | CA384044871 | ETV6 | c.1182G>C (p.Met394Ile) c.19G>C c.1179G>C (p.Met393Ile) c.1155G>C (p.Met385Ile) c.918G>C (p.Met306Ile) c.561G>C (p.Met187Ile) c.1047G>C (p.Met349Ile) | |
12 | g.11885955G= | CA2016648595 | ETV6 | c.1182G= (p.Met394=) c.19G= c.1179G= (p.Met393=) c.1155G= (p.Met385=) c.918G= (p.Met306=) c.561G= (p.Met187=) c.1047G= (p.Met349=) | |
12 | g.11885955G>T | CA384044872 | ETV6 | c.1182G>T (p.Met394Ile) c.19G>T c.1179G>T (p.Met393Ile) c.1155G>T (p.Met385Ile) c.918G>T (p.Met306Ile) c.561G>T (p.Met187Ile) c.1047G>T (p.Met349Ile) | |
12 | g.11885956T>A | CA384044873 | ETV6 | c.1183T>A (p.Ser395Thr) c.20T>A c.1180T>A (p.Ser394Thr) c.1156T>A (p.Ser386Thr) c.919T>A (p.Ser307Thr) c.562T>A (p.Ser188Thr) c.1048T>A (p.Ser350Thr) | dbSNP |
12 | g.11885956T>C | CA384044874 | ETV6 | c.1183T>C (p.Ser395Pro) c.20T>C c.1180T>C (p.Ser394Pro) c.1156T>C (p.Ser386Pro) c.919T>C (p.Ser307Pro) c.562T>C (p.Ser188Pro) c.1048T>C (p.Ser350Pro) | |
12 | g.11885956T>G | CA384044875 | ETV6 | c.1183T>G (p.Ser395Ala) c.20T>G c.1180T>G (p.Ser394Ala) c.1156T>G (p.Ser386Ala) c.919T>G (p.Ser307Ala) c.562T>G (p.Ser188Ala) c.1048T>G (p.Ser350Ala) | |
12 | g.11885957C>A | CA384044877 | ETV6 | c.1184C>A (p.Ser395Tyr) c.21C>A c.1181C>A (p.Ser394Tyr) c.1157C>A (p.Ser386Tyr) c.920C>A (p.Ser307Tyr) c.563C>A (p.Ser188Tyr) c.1049C>A (p.Ser350Tyr) | |
12 | g.11885957C>G | CA384044878 | ETV6 | c.1184C>G (p.Ser395Cys) c.21C>G c.1181C>G (p.Ser394Cys) c.1157C>G (p.Ser386Cys) c.920C>G (p.Ser307Cys) c.563C>G (p.Ser188Cys) c.1049C>G (p.Ser350Cys) | |
12 | g.11885957C>T | CA384044876 | ETV6 | c.1184C>T (p.Ser395Phe) c.21C>T c.1181C>T (p.Ser394Phe) c.1157C>T (p.Ser386Phe) c.920C>T (p.Ser307Phe) c.563C>T (p.Ser188Phe) c.1049C>T (p.Ser350Phe) | dbSNP |
12 | g.11885958C>A | CA478767204 | ETV6 | c.1185C>A (p.Ser395=) c.22C>A c.1182C>A (p.Ser394=) c.1158C>A (p.Ser386=) c.921C>A (p.Ser307=) c.564C>A (p.Ser188=) c.1050C>A (p.Ser350=) | |
12 | g.11885958C>G | CA478767205 | ETV6 | c.1185C>G (p.Ser395=) c.22C>G c.1182C>G (p.Ser394=) c.1158C>G (p.Ser386=) c.921C>G (p.Ser307=) c.564C>G (p.Ser188=) c.1050C>G (p.Ser350=) | gnomAD v4 |
12 | g.11885958C>T | CA478767206 | ETV6 | c.1185C>T (p.Ser395=) c.22C>T c.1182C>T (p.Ser394=) c.1158C>T (p.Ser386=) c.921C>T (p.Ser307=) c.564C>T (p.Ser188=) c.1050C>T (p.Ser350=) | gnomAD v4 |
12 | g.11885959A>C | CA478767207 | ETV6 | c.1186A>C (p.Arg396=) c.23A>C c.1183A>C (p.Arg395=) c.1159A>C (p.Arg387=) c.922A>C (p.Arg308=) c.565A>C (p.Arg189=) c.1051A>C (p.Arg351=) | |
12 | g.11885959A>G | CA384044880 | ETV6 | c.1186A>G (p.Arg396Gly) c.23A>G c.1183A>G (p.Arg395Gly) c.1159A>G (p.Arg387Gly) c.922A>G (p.Arg308Gly) c.565A>G (p.Arg189Gly) c.1051A>G (p.Arg351Gly) | dbSNP COSMIC |
12 | g.11885959A>T | CA384044879 | ETV6 | c.1186A>T (p.Arg396Ter) c.23A>T c.1183A>T (p.Arg395Ter) c.1159A>T (p.Arg387Ter) c.922A>T (p.Arg308Ter) c.565A>T (p.Arg189Ter) c.1051A>T (p.Arg351Ter) | |
12 | g.11885960G>A | CA384044883 | ETV6 | c.1187G>A (p.Arg396Lys) c.24G>A c.1184G>A (p.Arg395Lys) c.1160G>A (p.Arg387Lys) c.923G>A (p.Arg308Lys) c.566G>A (p.Arg189Lys) c.1052G>A (p.Arg351Lys) | |
12 | g.11885960G>C | CA384044881 | ETV6 | c.1187G>C (p.Arg396Thr) c.24G>C c.1184G>C (p.Arg395Thr) c.1160G>C (p.Arg387Thr) c.923G>C (p.Arg308Thr) c.566G>C (p.Arg189Thr) c.1052G>C (p.Arg351Thr) | COSMIC |
12 | g.11885960G>T | CA384044882 | ETV6 | c.1187G>T (p.Arg396Ile) c.24G>T c.1184G>T (p.Arg395Ile) c.1160G>T (p.Arg387Ile) c.923G>T (p.Arg308Ile) c.566G>T (p.Arg189Ile) c.1052G>T (p.Arg351Ile) | |
12 | g.11885961A>C | CA384044884 | ETV6 | c.1188A>C (p.Arg396Ser) c.25A>C c.1185A>C (p.Arg395Ser) c.1161A>C (p.Arg387Ser) c.924A>C (p.Arg308Ser) c.567A>C (p.Arg189Ser) c.1053A>C (p.Arg351Ser) | |
12 | g.11885961A>G | CA478767208 | ETV6 | c.1188A>G (p.Arg396=) c.25A>G c.1185A>G (p.Arg395=) c.1161A>G (p.Arg387=) c.924A>G (p.Arg308=) c.567A>G (p.Arg189=) c.1053A>G (p.Arg351=) | |
12 | g.11885961A>T | CA384044885 | ETV6 | c.1188A>T (p.Arg396Ser) c.25A>T c.1185A>T (p.Arg395Ser) c.1161A>T (p.Arg387Ser) c.924A>T (p.Arg308Ser) c.567A>T (p.Arg189Ser) c.1053A>T (p.Arg351Ser) | |
12 | g.11885962G>A | CA384044886 | ETV6 | c.1189G>A (p.Ala397Thr) c.26G>A c.1186G>A (p.Ala396Thr) c.1162G>A (p.Ala388Thr) c.925G>A (p.Ala309Thr) c.568G>A (p.Ala190Thr) c.1054G>A (p.Ala352Thr) | |
12 | g.11885962G>C | CA384044887 | ETV6 | c.1189G>C (p.Ala397Pro) c.26G>C c.1186G>C (p.Ala396Pro) c.1162G>C (p.Ala388Pro) c.925G>C (p.Ala309Pro) c.568G>C (p.Ala190Pro) c.1054G>C (p.Ala352Pro) | dbSNP |
12 | g.11885962G>T | CA384044888 | ETV6 | c.1189G>T (p.Ala397Ser) c.26G>T c.1186G>T (p.Ala396Ser) c.1162G>T (p.Ala388Ser) c.925G>T (p.Ala309Ser) c.568G>T (p.Ala190Ser) c.1054G>T (p.Ala352Ser) | |
12 | g.11885963C>A | CA384044889 | ETV6 | c.1190C>A (p.Ala397Asp) c.27C>A c.1187C>A (p.Ala396Asp) c.1163C>A (p.Ala388Asp) c.926C>A (p.Ala309Asp) c.569C>A (p.Ala190Asp) c.1055C>A (p.Ala352Asp) | |
12 | g.11885963C>G | CA384044890 | ETV6 | c.1190C>G (p.Ala397Gly) c.27C>G c.1187C>G (p.Ala396Gly) c.1163C>G (p.Ala388Gly) c.926C>G (p.Ala309Gly) c.569C>G (p.Ala190Gly) c.1055C>G (p.Ala352Gly) | dbSNP |
12 | g.11885963C>T | CA384044891 | ETV6 | c.1190C>T (p.Ala397Val) c.27C>T c.1187C>T (p.Ala396Val) c.1163C>T (p.Ala388Val) c.926C>T (p.Ala309Val) c.569C>T (p.Ala190Val) c.1055C>T (p.Ala352Val) | ClinVar dbSNP COSMIC |
12 | g.11885964C>A | CA478767209 | ETV6 | c.1191C>A (p.Ala397=) c.28C>A c.1188C>A (p.Ala396=) c.1164C>A (p.Ala388=) c.927C>A (p.Ala309=) c.570C>A (p.Ala190=) c.1056C>A (p.Ala352=) | dbSNP |
12 | g.11885964C>G | CA478767210 | ETV6 | c.1191C>G (p.Ala397=) c.28C>G c.1188C>G (p.Ala396=) c.1164C>G (p.Ala388=) c.927C>G (p.Ala309=) c.570C>G (p.Ala190=) c.1056C>G (p.Ala352=) | |
12 | g.11885964C>T | CA478767211 | ETV6 | c.1191C>T (p.Ala397=) c.28C>T c.1188C>T (p.Ala396=) c.1164C>T (p.Ala388=) c.927C>T (p.Ala309=) c.570C>T (p.Ala190=) c.1056C>T (p.Ala352=) | |
12 | g.11885965C>A | CA384044892 | ETV6 | c.1192C>A (p.Leu398Met) c.29C>A c.1189C>A (p.Leu397Met) c.1165C>A (p.Leu389Met) c.928C>A (p.Leu310Met) c.571C>A (p.Leu191Met) c.1057C>A (p.Leu353Met) | |
12 | g.11885965C>G | CA384044893 | ETV6 | c.1192C>G (p.Leu398Val) c.29C>G c.1189C>G (p.Leu397Val) c.1165C>G (p.Leu389Val) c.928C>G (p.Leu310Val) c.571C>G (p.Leu191Val) c.1057C>G (p.Leu353Val) | |
12 | g.11885965C>T | CA478767212 | ETV6 | c.1192C>T (p.Leu398=) c.29C>T c.1189C>T (p.Leu397=) c.1165C>T (p.Leu389=) c.928C>T (p.Leu310=) c.571C>T (p.Leu191=) c.1057C>T (p.Leu353=) | |
12 | g.11885966T>A | CA384044894 | ETV6 | c.1193T>A (p.Leu398Gln) c.30T>A c.1190T>A (p.Leu397Gln) c.1166T>A (p.Leu389Gln) c.929T>A (p.Leu310Gln) c.572T>A (p.Leu191Gln) c.1058T>A (p.Leu353Gln) | COSMIC |
12 | g.11885966T>C | CA384044896 | ETV6 | c.1193T>C (p.Leu398Pro) c.30T>C c.1190T>C (p.Leu397Pro) c.1166T>C (p.Leu389Pro) c.929T>C (p.Leu310Pro) c.572T>C (p.Leu191Pro) c.1058T>C (p.Leu353Pro) | dbSNP |
12 | g.11885966T>G | CA384044895 | ETV6 | c.1193T>G (p.Leu398Arg) c.30T>G c.1190T>G (p.Leu397Arg) c.1166T>G (p.Leu389Arg) c.929T>G (p.Leu310Arg) c.572T>G (p.Leu191Arg) c.1058T>G (p.Leu353Arg) | |
12 | g.11885967G>A | CA6454428 | ETV6 | c.1194G>A (p.Leu398=) c.31G>A c.1191G>A (p.Leu397=) c.1167G>A (p.Leu389=) c.930G>A (p.Leu310=) c.573G>A (p.Leu191=) c.1059G>A (p.Leu353=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.11885967G>C | CA478767214 | ETV6 | c.1194G>C (p.Leu398=) c.31G>C c.1191G>C (p.Leu397=) c.1167G>C (p.Leu389=) c.930G>C (p.Leu310=) c.573G>C (p.Leu191=) c.1059G>C (p.Leu353=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.11885967G= | CA2016648596 | ETV6 | c.1194G= (p.Leu398=) c.31G= c.1191G= (p.Leu397=) c.1167G= (p.Leu389=) c.930G= (p.Leu310=) c.573G= (p.Leu191=) c.1059G= (p.Leu353=) | |
12 | g.11885967G>T | CA478767213 | ETV6 | c.1194G>T (p.Leu398=) c.31G>T c.1191G>T (p.Leu397=) c.1167G>T (p.Leu389=) c.930G>T (p.Leu310=) c.573G>T (p.Leu191=) c.1059G>T (p.Leu353=) | |
12 | g.11885968C>A | CA384044897 | ETV6 | c.1195C>A (p.Arg399Ser) c.32C>A c.1192C>A (p.Arg398Ser) c.1168C>A (p.Arg390Ser) c.931C>A (p.Arg311Ser) c.574C>A (p.Arg192Ser) c.1060C>A (p.Arg354Ser) | dbSNP gnomAD v2 COSMIC |
12 | g.11885968C= | CA2016648597 | ETV6 | c.1195C= (p.Arg399=) c.32C= c.1192C= (p.Arg398=) c.1168C= (p.Arg390=) c.931C= (p.Arg311=) c.574C= (p.Arg192=) c.1060C= (p.Arg354=) | |
12 | g.11885968C>G | CA384044898 | ETV6 | c.1195C>G (p.Arg399Gly) c.32C>G c.1192C>G (p.Arg398Gly) c.1168C>G (p.Arg390Gly) c.931C>G (p.Arg311Gly) c.574C>G (p.Arg192Gly) c.1060C>G (p.Arg354Gly) | COSMIC |
12 | g.11885968C>T | CA175025 | ETV6 | c.1195C>T (p.Arg399Cys) c.32C>T c.1192C>T (p.Arg398Cys) c.1168C>T (p.Arg390Cys) c.931C>T (p.Arg311Cys) c.574C>T (p.Arg192Cys) c.1060C>T (p.Arg354Cys) | ClinVar dbSNP |
12 | g.11885969G>A | CA384044899 | ETV6 | c.1196G>A (p.Arg399His) c.33G>A c.1193G>A (p.Arg398His) c.1169G>A (p.Arg390His) c.932G>A (p.Arg311His) c.575G>A (p.Arg192His) c.1061G>A (p.Arg354His) | ClinVar dbSNP gnomAD v4 COSMIC |
12 | g.11885969G>C | CA384044900 | ETV6 | c.1196G>C (p.Arg399Pro) c.33G>C c.1193G>C (p.Arg398Pro) c.1169G>C (p.Arg390Pro) c.932G>C (p.Arg311Pro) c.575G>C (p.Arg192Pro) c.1061G>C (p.Arg354Pro) | dbSNP |
12 | g.11885969G>T | CA384044901 | ETV6 | c.1196G>T (p.Arg399Leu) c.33G>T c.1193G>T (p.Arg398Leu) c.1169G>T (p.Arg390Leu) c.932G>T (p.Arg311Leu) c.575G>T (p.Arg192Leu) c.1061G>T (p.Arg354Leu) | |
12 | g.11885969_11885970insGGAG | CA2725554085 | ETV6 | c.1196_1197insGGAG (p.His400GlufsTer27) c.33_34insGGAG c.1193_1194insGGAG (p.His399GlufsTer27) c.1169_1170insGGAG (p.His391GlufsTer27) c.932_933insGGAG (p.His312GlufsTer27) c.575_576insGGAG (p.His193GlufsTer27) c.1061_1062insGGAG (p.His355GlufsTer27) | dbSNP |
12 | g.11885970C>A | CA478767215 | ETV6 | c.1197C>A (p.Arg399=) c.34C>A c.1194C>A (p.Arg398=) c.1170C>A (p.Arg390=) c.933C>A (p.Arg311=) c.576C>A (p.Arg192=) c.1062C>A (p.Arg354=) | |
12 | g.11885970C>G | CA478767216 | ETV6 | c.1197C>G (p.Arg399=) c.34C>G c.1194C>G (p.Arg398=) c.1170C>G (p.Arg390=) c.933C>G (p.Arg311=) c.576C>G (p.Arg192=) c.1062C>G (p.Arg354=) | |
12 | g.11885970C>T | CA478767217 | ETV6 | c.1197C>T (p.Arg399=) c.34C>T c.1194C>T (p.Arg398=) c.1170C>T (p.Arg390=) c.933C>T (p.Arg311=) c.576C>T (p.Arg192=) c.1062C>T (p.Arg354=) | |
12 | g.11885971C>A | CA384044902 | ETV6 | c.1198C>A (p.His400Asn) c.35C>A c.1195C>A (p.His399Asn) c.1171C>A (p.His391Asn) c.934C>A (p.His312Asn) c.577C>A (p.His193Asn) c.1063C>A (p.His355Asn) | COSMIC |
12 | g.11885971C= | CA2016648598 | ETV6 | c.1198C= (p.His400=) c.35C= c.1195C= (p.His399=) c.1171C= (p.His391=) c.934C= (p.His312=) c.577C= (p.His193=) c.1063C= (p.His355=) | |
12 | g.11885971C>G | CA384044903 | ETV6 | c.1198C>G (p.His400Asp) c.35C>G c.1195C>G (p.His399Asp) c.1171C>G (p.His391Asp) c.934C>G (p.His312Asp) c.577C>G (p.His193Asp) c.1063C>G (p.His355Asp) | |
12 | g.11885971C>T | CA384044904 | ETV6 | c.1198C>T (p.His400Tyr) c.35C>T c.1195C>T (p.His399Tyr) c.1171C>T (p.His391Tyr) c.934C>T (p.His312Tyr) c.577C>T (p.His193Tyr) c.1063C>T (p.His355Tyr) | |
12 | g.11885972A>C | CA384044906 | ETV6 | c.1199A>C (p.His400Pro) c.36A>C c.1196A>C (p.His399Pro) c.1172A>C (p.His391Pro) c.935A>C (p.His312Pro) c.578A>C (p.His193Pro) c.1064A>C (p.His355Pro) | |
12 | g.11885972A>G | CA384044907 | ETV6 | c.1199A>G (p.His400Arg) c.36A>G c.1196A>G (p.His399Arg) c.1172A>G (p.His391Arg) c.935A>G (p.His312Arg) c.578A>G (p.His193Arg) c.1064A>G (p.His355Arg) | |
12 | g.11885972A>T | CA384044905 | ETV6 | c.1199A>T (p.His400Leu) c.36A>T c.1196A>T (p.His399Leu) c.1172A>T (p.His391Leu) c.935A>T (p.His312Leu) c.578A>T (p.His193Leu) c.1064A>T (p.His355Leu) | |
12 | g.11885972_11885995dup | CA658797843 | ETV6 | c.1199_1222dup (p.Ile407_Arg408insAsnTyrTyrLysLeuAsnIleIle) c.36_59dup c.1196_1219dup (p.Ile406_Arg407insAsnTyrTyrLysLeuAsnIleIle) c.1172_1195dup (p.Ile398_Arg399insAsnTyrTyrLysLeuAsnIleIle) c.935_958dup (p.Ile319_Arg320insAsnTyrTyrLysLeuAsnIleIle) c.578_601dup (p.Ile200_Arg201insAsnTyrTyrLysLeuAsnIleIle) c.1064_1087dup (p.Ile362_Arg363insAsnTyrTyrLysLeuAsnIleIle) | ClinVar dbSNP |
12 | g.11885972_11885973insTTAAAATAAAAG | CA2725554086 | ETV6 | c.1199_1200insTTAAAATAAAAG (p.His401Ter) c.36_37insTTAAAATAAAAG c.1196_1197insTTAAAATAAAAG (p.His400Ter) c.1172_1173insTTAAAATAAAAG (p.His392Ter) c.935_936insTTAAAATAAAAG (p.His313Ter) c.578_579insTTAAAATAAAAG (p.His194Ter) c.1064_1065insTTAAAATAAAAG (p.His356Ter) | dbSNP |
12 | g.11885973C>A | CA384044908 | ETV6 | c.1200C>A (p.His400Gln) c.37C>A c.1197C>A (p.His399Gln) c.1173C>A (p.His391Gln) c.936C>A (p.His312Gln) c.579C>A (p.His193Gln) c.1065C>A (p.His355Gln) | |
12 | g.11885973C>G | CA384044909 | ETV6 | c.1200C>G (p.His400Gln) c.37C>G c.1197C>G (p.His399Gln) c.1173C>G (p.His391Gln) c.936C>G (p.His312Gln) c.579C>G (p.His193Gln) c.1065C>G (p.His355Gln) | |
12 | g.11885973C>T | CA478767218 | ETV6 | c.1200C>T (p.His400=) c.37C>T c.1197C>T (p.His399=) c.1173C>T (p.His391=) c.936C>T (p.His312=) c.579C>T (p.His193=) c.1065C>T (p.His355=) | gnomAD v4 |
12 | g.11885973dup | CA645595231 | ETV6 | c.1200dup (p.Tyr401LeufsTer25) c.37dup c.1197dup (p.Tyr400LeufsTer25) c.1173dup (p.Tyr392LeufsTer25) c.936dup (p.Tyr313LeufsTer25) c.579dup (p.Tyr194LeufsTer25) c.1065dup (p.Tyr356LeufsTer25) | COSMIC |
12 | g.11885974T>A | CA384044910 | ETV6 | c.1201T>A (p.Tyr401Asn) c.38T>A c.1198T>A (p.Tyr400Asn) c.1174T>A (p.Tyr392Asn) c.937T>A (p.Tyr313Asn) c.580T>A (p.Tyr194Asn) c.1066T>A (p.Tyr356Asn) | |
12 | g.11885974T>C | CA384044911 | ETV6 | c.1201T>C (p.Tyr401His) c.38T>C c.1198T>C (p.Tyr400His) c.1174T>C (p.Tyr392His) c.937T>C (p.Tyr313His) c.580T>C (p.Tyr194His) c.1066T>C (p.Tyr356His) | ClinVar dbSNP |
12 | g.11885974T>G | CA384044912 | ETV6 | c.1201T>G (p.Tyr401Asp) c.38T>G c.1198T>G (p.Tyr400Asp) c.1174T>G (p.Tyr392Asp) c.937T>G (p.Tyr313Asp) c.580T>G (p.Tyr194Asp) c.1066T>G (p.Tyr356Asp) | |
12 | g.11885974T= | CA2016648599 | ETV6 | c.1201T= (p.Tyr401=) c.38T= c.1198T= (p.Tyr400=) c.1174T= (p.Tyr392=) c.937T= (p.Tyr313=) c.580T= (p.Tyr194=) c.1066T= (p.Tyr356=) | |
12 | g.11885975A>C | CA384044913 | ETV6 | c.1202A>C (p.Tyr401Ser) c.39A>C c.1199A>C (p.Tyr400Ser) c.1175A>C (p.Tyr392Ser) c.938A>C (p.Tyr313Ser) c.581A>C (p.Tyr194Ser) c.1067A>C (p.Tyr356Ser) | |
12 | g.11885975A>G | CA384044914 | ETV6 | c.1202A>G (p.Tyr401Cys) c.39A>G c.1199A>G (p.Tyr400Cys) c.1175A>G (p.Tyr392Cys) c.938A>G (p.Tyr313Cys) c.581A>G (p.Tyr194Cys) c.1067A>G (p.Tyr356Cys) | ClinVar COSMIC |
12 | g.11885975A>T | CA384044915 | ETV6 | c.1202A>T (p.Tyr401Phe) c.39A>T c.1199A>T (p.Tyr400Phe) c.1175A>T (p.Tyr392Phe) c.938A>T (p.Tyr313Phe) c.581A>T (p.Tyr194Phe) c.1067A>T (p.Tyr356Phe) | |
12 | g.11885976C>A | CA384044916 | ETV6 | c.1203C>A (p.Tyr401Ter) c.40C>A c.1200C>A (p.Tyr400Ter) c.1176C>A (p.Tyr392Ter) c.939C>A (p.Tyr313Ter) c.582C>A (p.Tyr194Ter) c.1068C>A (p.Tyr356Ter) | |
12 | g.11885976C>G | CA384044917 | ETV6 | c.1203C>G (p.Tyr401Ter) c.40C>G c.1200C>G (p.Tyr400Ter) c.1176C>G (p.Tyr392Ter) c.939C>G (p.Tyr313Ter) c.582C>G (p.Tyr194Ter) c.1068C>G (p.Tyr356Ter) | |
12 | g.11885976C>T | CA478767219 | ETV6 | c.1203C>T (p.Tyr401=) c.40C>T c.1200C>T (p.Tyr400=) c.1176C>T (p.Tyr392=) c.939C>T (p.Tyr313=) c.582C>T (p.Tyr194=) c.1068C>T (p.Tyr356=) | |
12 | g.11885977T>A | CA384044918 | ETV6 | c.1204T>A (p.Tyr402Asn) c.41T>A c.1201T>A (p.Tyr401Asn) c.1177T>A (p.Tyr393Asn) c.940T>A (p.Tyr314Asn) c.583T>A (p.Tyr195Asn) c.1069T>A (p.Tyr357Asn) | |
12 | g.11885977T>C | CA384044919 | ETV6 | c.1204T>C (p.Tyr402His) c.41T>C c.1201T>C (p.Tyr401His) c.1177T>C (p.Tyr393His) c.940T>C (p.Tyr314His) c.583T>C (p.Tyr195His) c.1069T>C (p.Tyr357His) | |
12 | g.11885977T>G | CA384044920 | ETV6 | c.1204T>G (p.Tyr402Asp) c.41T>G c.1201T>G (p.Tyr401Asp) c.1177T>G (p.Tyr393Asp) c.940T>G (p.Tyr314Asp) c.583T>G (p.Tyr195Asp) c.1069T>G (p.Tyr357Asp) | |
12 | g.11885978A>C | CA384044923 | ETV6 | c.1205A>C (p.Tyr402Ser) c.42A>C c.1202A>C (p.Tyr401Ser) c.1178A>C (p.Tyr393Ser) c.941A>C (p.Tyr314Ser) c.584A>C (p.Tyr195Ser) c.1070A>C (p.Tyr357Ser) | |
12 | g.11885978A>G | CA384044922 | ETV6 | c.1205A>G (p.Tyr402Cys) c.42A>G c.1202A>G (p.Tyr401Cys) c.1178A>G (p.Tyr393Cys) c.941A>G (p.Tyr314Cys) c.584A>G (p.Tyr195Cys) c.1070A>G (p.Tyr357Cys) | |
12 | g.11885978A>T | CA384044921 | ETV6 | c.1205A>T (p.Tyr402Phe) c.42A>T c.1202A>T (p.Tyr401Phe) c.1178A>T (p.Tyr393Phe) c.941A>T (p.Tyr314Phe) c.584A>T (p.Tyr195Phe) c.1070A>T (p.Tyr357Phe) |