Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.93103944A= | CA1726201152 | SAMD9 | c.2154T= (p.Ile718=) | |
7 | g.93103944A>C | CA368192644 | SAMD9 | c.2154T>G (p.Ile718Met) | |
7 | g.93103944A>G | CA4342882 | SAMD9 | c.2154T>C (p.Ile718=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.93103944A>T | CA456626155 | SAMD9 | c.2154T>A (p.Ile718=) | |
7 | g.93103945A= | CA1726201156 | SAMD9 | c.2153T= (p.Ile718=) | |
7 | g.93103945A>C | CA368192661 | SAMD9 | c.2153T>G (p.Ile718Ser) | |
7 | g.93103945A>G | CA368192667 | SAMD9 | c.2153T>C (p.Ile718Thr) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
7 | g.93103945A>T | CA368192664 | SAMD9 | c.2153T>A (p.Ile718Asn) | |
7 | g.93103946T>A | CA368192669 | SAMD9 | c.2152A>T (p.Ile718Phe) | |
7 | g.93103946T>C | CA368192670 | SAMD9 | c.2152A>G (p.Ile718Val) | |
7 | g.93103946T>G | CA368192672 | SAMD9 | c.2152A>C (p.Ile718Leu) | |
7 | g.93103947C>A | CA368192675 | SAMD9 | c.2151G>T (p.Met717Ile) | |
7 | g.93103947C= | CA1726201159 | SAMD9 | c.2151G= (p.Met717=) | |
7 | g.93103947C>G | CA368192679 | SAMD9 | c.2151G>C (p.Met717Ile) | |
7 | g.93103947C>T | CA4342883 | SAMD9 | c.2151G>A (p.Met717Ile) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
7 | g.93103948A= | CA1726201162 | SAMD9 | c.2150T= (p.Met717=) | |
7 | g.93103948A>C | CA368192687 | SAMD9 | c.2150T>G (p.Met717Arg) | |
7 | g.93103948A>G | CA368192690 | SAMD9 | c.2150T>C (p.Met717Thr) | dbSNP gnomAD v4 |
7 | g.93103948A>T | CA368192692 | SAMD9 | c.2150T>A (p.Met717Lys) | ClinVar dbSNP |
7 | g.93103948_93103950del | CA2739278680 | SAMD9 | c.2148_2150del (p.Met717del) | ClinVar |
7 | g.93103949T>A | CA368192698 | SAMD9 | c.2149A>T (p.Met717Leu) | |
7 | g.93103949T>C | CA368192701 | SAMD9 | c.2149A>G (p.Met717Val) | dbSNP |
7 | g.93103949T>G | CA368192703 | SAMD9 | c.2149A>C (p.Met717Leu) | |
7 | g.93103949T= | CA1726201165 | SAMD9 | c.2149A= (p.Met717=) | |
7 | g.93103950T>A | CA456626173 | SAMD9 | c.2148A>T (p.Ala716=) | |
7 | g.93103950T>C | CA4342884 | SAMD9 | c.2148A>G (p.Ala716=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.93103950T>G | CA456626171 | SAMD9 | c.2148A>C (p.Ala716=) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.93103950T= | CA1726201166 | SAMD9 | c.2148A= (p.Ala716=) | |
7 | g.93103951G>A | CA368192731 | SAMD9 | c.2147C>T (p.Ala716Val) | |
7 | g.93103951G>C | CA368192724 | SAMD9 | c.2147C>G (p.Ala716Gly) | gnomAD v4 |
7 | g.93103951G= | CA1726201169 | SAMD9 | c.2147C= (p.Ala716=) | |
7 | g.93103951G>T | CA368192727 | SAMD9 | c.2147C>A (p.Ala716Glu) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.93103952C>A | CA368192734 | SAMD9 | c.2146G>T (p.Ala716Ser) | |
7 | g.93103952C= | CA1726201171 | SAMD9 | c.2146G= (p.Ala716=) | |
7 | g.93103952C>G | CA368192736 | SAMD9 | c.2146G>C (p.Ala716Pro) | |
7 | g.93103952C>T | CA368192738 | SAMD9 | c.2146G>A (p.Ala716Thr) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
7 | g.93103953T>A | CA161992113 | SAMD9 | c.2145A>T (p.Glu715Asp) | dbSNP |
7 | g.93103953T>C | CA456626180 | SAMD9 | c.2145A>G (p.Glu715=) | |
7 | g.93103953T>G | CA368192744 | SAMD9 | c.2145A>C (p.Glu715Asp) | |
7 | g.93103953T= | CA1726201175 | SAMD9 | c.2145A= (p.Glu715=) | |
7 | g.93103954T>A | CA368192750 | SAMD9 | c.2144A>T (p.Glu715Val) | |
7 | g.93103954T>C | CA368192752 | SAMD9 | c.2144A>G (p.Glu715Gly) | ClinVar |
7 | g.93103954T>G | CA368192756 | SAMD9 | c.2144A>C (p.Glu715Ala) | |
7 | g.93103955C>A | CA368192776 | SAMD9 | c.2143G>T (p.Glu715Ter) | |
7 | g.93103955C>G | CA368192782 | SAMD9 | c.2143G>C (p.Glu715Gln) | |
7 | g.93103955C>T | CA368192785 | SAMD9 | c.2143G>A (p.Glu715Lys) | gnomAD v4 |
7 | g.93103956A= | CA1726201179 | SAMD9 | c.2142T= (p.Leu714=) | |
7 | g.93103956A>C | CA456626184 | SAMD9 | c.2142T>G (p.Leu714=) | |
7 | g.93103956A>G | CA456626187 | SAMD9 | c.2142T>C (p.Leu714=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
7 | g.93103956A>T | CA456626188 | SAMD9 | c.2142T>A (p.Leu714=) |