| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.108250410_108250412delinsCTT | CA2061868553 | WSCD2 | c.*2067_*2069delinsCTT (n.*2067_*2069delinsCTT) | |
| 12 | g.108250412_108250413del | CA2061868555 | WSCD2 | c.*2069_*2070del (n.*2069_*2070del) | dbSNP |
| 12 | g.108250412T>A | CA951585958 | WSCD2 | c.*2069T>A (n.*2069T>A) | gnomAD v3 gnomAD v4 |
| 12 | g.108250412T>C | CA13631809 | WSCD2 | c.*2069T>C (n.*2069T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.108250412T>G | CA243281246 | WSCD2 | c.*2069T>G (n.*2069T>G) | dbSNP |
| 12 | g.108250412T= | CA2061868559 | WSCD2 | c.*2069T= (n.*2069T=) | |
| 12 | g.108250413T>C | CA2061868561 | WSCD2 | c.*2070T>C (n.*2070T>C) | dbSNP |
| 12 | g.108250413T>G | CA607236459 | WSCD2 | c.*2070T>G (n.*2070T>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.108250413T= | CA2061868560 | WSCD2 | c.*2070T= (n.*2070T=) | |
| 12 | g.108250414_108250415insA | CA951585966 | WSCD2 | c.*2071_*2072insA (n.*2071_*2072insA) | gnomAD v3 gnomAD v4 |
| 12 | g.108250415T>C | CA2061868564 | WSCD2 | c.*2072T>C (n.*2072T>C) | dbSNP gnomAD v4 |
| 12 | g.108250415T= | CA2061868563 | WSCD2 | c.*2072T= (n.*2072T=) | |
| 12 | g.108250415_108250416insTAAAAA | CA951585971 | WSCD2 | c.*2072_*2073insTAAAAA (n.*2072_*2073insTAAAAA) | gnomAD v3 gnomAD v4 |
| 12 | g.108250416A= | CA2061868566 | WSCD2 | c.*2073A= (n.*2073A=) | |
| 12 | g.108250416A>C | CA607236460 | WSCD2 | c.*2073A>C (n.*2073A>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.108250416A>G | CA243281255 | WSCD2 | c.*2073A>G (n.*2073A>G) | dbSNP gnomAD v4 |
| 12 | g.108250417T>A | CA2620705861 | WSCD2 | c.*2074T>A (n.*2074T>A) | gnomAD v4 |
| 12 | g.108250417T>C | CA2061868569 | WSCD2 | c.*2074T>C (n.*2074T>C) | dbSNP |
| 12 | g.108250417T= | CA2061868568 | WSCD2 | c.*2074T= (n.*2074T=) | |
| 12 | g.108250418G>T | CA2620705862 | WSCD2 | c.*2075G>T (n.*2075G>T) | gnomAD v4 |
| 12 | g.108250419_108250420insCTCTGTTGTC | CA2533831898 | WSCD2 | c.*2076_*2077insCTCTGTTGTC (n.*2076_*2077insCTCTGTTGTC) | |
| 12 | g.108250421T>C | CA607236461 | WSCD2 | c.*2078T>C (n.*2078T>C) | dbSNP gnomAD v2 |
| 12 | g.108250421T>G | CA243281256 | WSCD2 | c.*2078T>G (n.*2078T>G) | dbSNP gnomAD v3 gnomAD v4 |
| 12 | g.108250421T= | CA2061868571 | WSCD2 | c.*2078T= (n.*2078T=) | |
| 12 | g.108250422T>A | CA2620705863 | WSCD2 | c.*2079T>A (n.*2079T>A) | gnomAD v4 |
| 12 | g.108250422T>C | CA2061868574 | WSCD2 | c.*2079T>C (n.*2079T>C) | dbSNP |
| 12 | g.108250422T= | CA2061868573 | WSCD2 | c.*2079T= (n.*2079T=) | |
| 12 | g.108250423G>C | CA607236462 | WSCD2 | c.*2080G>C (n.*2080G>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.108250423G= | CA2061868575 | WSCD2 | c.*2080G= (n.*2080G=) | |
| 12 | g.108250426A= | CA2061868576 | WSCD2 | c.*2083A= (n.*2083A=) | |
| 12 | g.108250426A>G | CA2061868577 | WSCD2 | c.*2083A>G (n.*2083A>G) | dbSNP gnomAD v4 |
| 12 | g.108250427C>A | CA2620705864 | WSCD2 | c.*2084C>A (n.*2084C>A) | gnomAD v4 |
| 12 | g.108250427C= | CA2061868579 | WSCD2 | c.*2084C= (n.*2084C=) | |
| 12 | g.108250427C>T | CA2061868580 | WSCD2 | c.*2084C>T (n.*2084C>T) | dbSNP |
| 12 | g.108250429G>A | CA2620705865 | WSCD2 | c.*2086G>A (n.*2086G>A) | gnomAD v4 |
| 12 | g.108250429G>T | CA2620705866 | WSCD2 | c.*2086G>T (n.*2086G>T) | gnomAD v4 |
| 12 | g.108250430T>C | CA2061868581 | WSCD2 | c.*2087T>C (n.*2087T>C) | dbSNP gnomAD v4 |
| 12 | g.108250430T= | CA2061868582 | WSCD2 | c.*2087T= (n.*2087T=) | |
| 12 | g.108250431A>G | CA2620705867 | WSCD2 | c.*2088A>G (n.*2088A>G) | gnomAD v4 |
| 12 | g.108250433C>A | CA2061868584 | WSCD2 | c.*2090C>A (n.*2090C>A) | dbSNP gnomAD v4 |
| 12 | g.108250433C= | CA2061868583 | WSCD2 | c.*2090C= (n.*2090C=) | |
| 12 | g.108250433C>G | CA683317562 | WSCD2 | c.*2090C>G (n.*2090C>G) | dbSNP gnomAD v3 gnomAD v4 |
| 12 | g.108250434C>A | CA2620705868 | WSCD2 | c.*2091C>A (n.*2091C>A) | gnomAD v4 |
| 12 | g.108250435C>A | CA2620705869 | WSCD2 | c.*2092C>A (n.*2092C>A) | gnomAD v4 |
| 12 | g.108250436A>G | CA2620705870 | WSCD2 | c.*2093A>G (n.*2093A>G) | gnomAD v4 |
| 12 | g.108250437C>A | CA2620705871 | WSCD2 | c.*2094C>A (n.*2094C>A) | gnomAD v4 |
| 12 | g.108250441T>C | CA2620705872 | WSCD2 | c.*2098T>C (n.*2098T>C) | gnomAD v4 |
| 12 | g.108250442T>C | CA2620705873 | WSCD2 | c.*2099T>C (n.*2099T>C) | gnomAD v4 |
| 12 | g.108250443G= | CA2061868585 | WSCD2 | c.*2100G= (n.*2100G=) | |
| 12 | g.108250443G>T | CA2061868587 | WSCD2 | c.*2100G>T (n.*2100G>T) | dbSNP gnomAD v4 |