| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.22625384C>A | CA380059074 | FANCF | c.427G>T (p.Val143Leu) | |
| 11 | g.22625384C= | CA1957607170 | FANCF | c.427G= (p.Val143=) | |
| 11 | g.22625384C>G | CA380059075 | FANCF | c.427G>C (p.Val143Leu) | |
| 11 | g.22625384C>T | CA380059076 | FANCF | c.427G>A (p.Val143Met) | dbSNP gnomAD v3 gnomAD v4 |
| 11 | g.22625385C>A | CA473533592 | FANCF | c.426G>T (p.Ala142=) | dbSNP gnomAD v2 gnomAD v4 |
| 11 | g.22625385C= | CA1957607171 | FANCF | c.426G= (p.Ala142=) | |
| 11 | g.22625385C>G | CA473533590 | FANCF | c.426G>C (p.Ala142=) | |
| 11 | g.22625385C>T | CA473533591 | FANCF | c.426G>A (p.Ala142=) | dbSNP gnomAD v4 |
| 11 | g.22625386G>A | CA380059077 | FANCF | c.425C>T (p.Ala142Val) | dbSNP |
| 11 | g.22625386G>C | CA380059078 | FANCF | c.425C>G (p.Ala142Gly) | |
| 11 | g.22625386G= | CA1957607172 | FANCF | c.425C= (p.Ala142=) | |
| 11 | g.22625386G>T | CA5924335 | FANCF | c.425C>A (p.Ala142Glu) | dbSNP ExAC gnomAD v4 COSMIC |
| 11 | g.22625387C>A | CA380059079 | FANCF | c.424G>T (p.Ala142Ser) | dbSNP |
| 11 | g.22625387C>G | CA380059080 | FANCF | c.424G>C (p.Ala142Pro) | |
| 11 | g.22625387C>T | CA380059081 | FANCF | c.424G>A (p.Ala142Thr) | |
| 11 | g.22625388A>C | CA473533595 | FANCF | c.423T>G (p.Ser141=) | |
| 11 | g.22625388A>G | CA473533596 | FANCF | c.423T>C (p.Ser141=) | dbSNP |
| 11 | g.22625388A>T | CA473533597 | FANCF | c.423T>A (p.Ser141=) | |
| 11 | g.22625389G>A | CA380059083 | FANCF | c.422C>T (p.Ser141Phe) | dbSNP gnomAD v4 |
| 11 | g.22625389G>C | CA380059084 | FANCF | c.422C>G (p.Ser141Cys) | dbSNP |
| 11 | g.22625389G= | CA1957607173 | FANCF | c.422C= (p.Ser141=) | |
| 11 | g.22625389G>T | CA380059082 | FANCF | c.422C>A (p.Ser141Tyr) | gnomAD v4 |
| 11 | g.22625390A= | CA1957607174 | FANCF | c.421T= (p.Ser141=) | |
| 11 | g.22625390A>C | CA380059085 | FANCF | c.421T>G (p.Ser141Ala) | dbSNP |
| 11 | g.22625390A>G | CA380059086 | FANCF | c.421T>C (p.Ser141Pro) | |
| 11 | g.22625390A>T | CA380059087 | FANCF | c.421T>A (p.Ser141Thr) | |
| 11 | g.22625391C>A | CA473533598 | FANCF | c.420G>T (p.Arg140=) | |
| 11 | g.22625391C>G | CA473533599 | FANCF | c.420G>C (p.Arg140=) | |
| 11 | g.22625391C>T | CA473533600 | FANCF | c.420G>A (p.Arg140=) | ClinVar dbSNP gnomAD v4 |
| 11 | g.22625392C>A | CA380059088 | FANCF | c.419G>T (p.Arg140Leu) | |
| 11 | g.22625392C= | CA1957607175 | FANCF | c.419G= (p.Arg140=) | |
| 11 | g.22625392C>G | CA380059089 | FANCF | c.419G>C (p.Arg140Pro) | dbSNP |
| 11 | g.22625392C>T | CA219086645 | FANCF | c.419G>A (p.Arg140Gln) | ClinVar dbSNP gnomAD v4 |
| 11 | g.22625393G>A | CA380059090 | FANCF | c.418C>T (p.Arg140Trp) | dbSNP gnomAD v4 |
| 11 | g.22625393G>C | CA380059091 | FANCF | c.418C>G (p.Arg140Gly) | |
| 11 | g.22625393G>T | CA473533604 | FANCF | c.418C>A (p.Arg140=) | |
| 11 | g.22625394C>A | CA473533607 | FANCF | c.417G>T (p.Arg139=) | |
| 11 | g.22625394C>G | CA473533606 | FANCF | c.417G>C (p.Arg139=) | dbSNP |
| 11 | g.22625394C>T | CA473533605 | FANCF | c.417G>A (p.Arg139=) | |
| 11 | g.22625395C>A | CA380059092 | FANCF | c.416G>T (p.Arg139Leu) | |
| 11 | g.22625395C= | CA1957607176 | FANCF | c.416G= (p.Arg139=) | |
| 11 | g.22625395C>G | CA380059093 | FANCF | c.416G>C (p.Arg139Pro) | gnomAD v4 |
| 11 | g.22625395C>T | CA380059094 | FANCF | c.416G>A (p.Arg139Gln) | dbSNP gnomAD v4 |
| 11 | g.22625396G>A | CA380059095 | FANCF | c.415C>T (p.Arg139Trp) | gnomAD v4 |
| 11 | g.22625396G>C | CA5924337 | FANCF | c.415C>G (p.Arg139Gly) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.22625396G= | CA1957607177 | FANCF | c.415C= (p.Arg139=) | |
| 11 | g.22625396G>T | CA473533609 | FANCF | c.415C>A (p.Arg139=) | |
| 11 | g.22625403_22625411dup | CA5924336 | FANCF | c.407_415dup (p.Arg138_Arg139insLeuAlaArg) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.22625397G>A | CA5924338 | FANCF | c.414C>T (p.Arg138=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.22625397G>C | CA473533611 | FANCF | c.414C>G (p.Arg138=) |