Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
21 | g.46125849C>A | CA410540007 | COL6A2 | c.2034C>A (p.Asp678Glu) c.705C>A (p.Asp235Glu) n.2111C>A n.2118C>A | |
21 | g.46125849C= | CA2392507609 | COL6A2 | c.2034C= (p.Asp678=) c.705C= (p.Asp235=) n.2111C= n.2118C= | |
21 | g.46125849C>G | CA410540012 | COL6A2 | c.2034C>G (p.Asp678Glu) c.705C>G (p.Asp235Glu) n.2111C>G n.2118C>G | |
21 | g.46125849C>T | CA10072420 | COL6A2 | c.2034C>T (p.Asp678=) c.705C>T (p.Asp235=) n.2111C>T n.2118C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
21 | g.46125850G>A | CA10072421 | COL6A2 | c.2035G>A (p.Glu679Lys) c.706G>A (p.Glu236Lys) n.2112G>A n.2119G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
21 | g.46125850G>C | CA410541274 | COL6A2 | c.2035G>C (p.Glu679Gln) c.706G>C (p.Glu236Gln) n.2112G>C n.2119G>C | |
21 | g.46125850G= | CA2392507610 | COL6A2 | c.2035G= (p.Glu679=) c.706G= (p.Glu236=) n.2112G= n.2119G= | |
21 | g.46125850G>T | CA410541278 | COL6A2 | c.2035G>T (p.Glu679Ter) c.706G>T (p.Glu236Ter) n.2112G>T n.2119G>T | gnomAD v4 |
21 | g.46125851A>C | CA410541279 | COL6A2 | c.2036A>C (p.Glu679Ala) c.707A>C (p.Glu236Ala) n.2113A>C n.2120A>C | |
21 | g.46125851A>G | CA410541281 | COL6A2 | c.2036A>G (p.Glu679Gly) c.707A>G (p.Glu236Gly) n.2113A>G n.2120A>G | |
21 | g.46125851A>T | CA410541280 | COL6A2 | c.2036A>T (p.Glu679Val) c.707A>T (p.Glu236Val) n.2113A>T n.2120A>T | |
21 | g.46125852A= | CA2392507612 | COL6A2 | c.2037A= (p.Glu679=) c.708A= (p.Glu236=) n.2114A= n.2121A= | |
21 | g.46125852A>C | CA410541284 | COL6A2 | c.2037A>C (p.Glu679Asp) c.708A>C (p.Glu236Asp) n.2114A>C n.2121A>C | |
21 | g.46125852A>G | CA513170297 | COL6A2 | c.2037A>G (p.Glu679=) c.708A>G (p.Glu236=) n.2114A>G n.2121A>G | ClinVar dbSNP gnomAD v4 |
21 | g.46125852A>T | CA410541285 | COL6A2 | c.2037A>T (p.Glu679Asp) c.708A>T (p.Glu236Asp) n.2114A>T n.2121A>T | |
21 | g.46125852_46125854delinsACG | CA2392507611 | COL6A2 | c.2037_2039delinsACG (p.Glu679=) c.708_710delinsACG (p.Glu236=) n.2114_2116delinsACG n.2121_2123delinsACG | |
21 | g.46125853C>A | CA410541287 | COL6A2 | c.2038C>A (p.Arg680Ser) c.709C>A (p.Arg237Ser) n.2115C>A n.2122C>A | |
21 | g.46125853C= | CA2392507613 | COL6A2 | c.2038C= (p.Arg680=) c.709C= (p.Arg237=) n.2115C= n.2122C= | |
21 | g.46125853C>G | CA410541289 | COL6A2 | c.2038C>G (p.Arg680Gly) c.709C>G (p.Arg237Gly) n.2115C>G n.2122C>G | |
21 | g.46125853C>T | CA10072422 | COL6A2 | c.2038C>T (p.Arg680Cys) c.709C>T (p.Arg237Cys) n.2115C>T n.2122C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC |
21 | g.46125853_46125854delinsA | CA16621031 | COL6A2 | c.2038_2039delinsA (p.Arg680IlefsTer?) c.709_710delinsA (p.Arg237IlefsTer?) n.2115_2116delinsA n.2122_2123delinsA | ClinVar dbSNP |
21 | g.46125854G>A | CA147453 | COL6A2 | c.2039G>A (p.Arg680His) c.710G>A (p.Arg237His) n.2116G>A n.2123G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
21 | g.46125854G>C | CA410541293 | COL6A2 | c.2039G>C (p.Arg680Pro) c.710G>C (p.Arg237Pro) n.2116G>C n.2123G>C | |
21 | g.46125854G= | CA2392507614 | COL6A2 | c.2039G= (p.Arg680=) c.710G= (p.Arg237=) n.2116G= n.2123G= | |
21 | g.46125854G>T | CA321972632 | COL6A2 | c.2039G>T (p.Arg680Leu) c.710G>T (p.Arg237Leu) n.2116G>T n.2123G>T | dbSNP gnomAD v3 gnomAD v4 |
21 | g.46125855T>A | CA513170299 | COL6A2 | c.2040T>A (p.Arg680=) c.711T>A (p.Arg237=) n.2117T>A n.2124T>A | |
21 | g.46125855T>C | CA513170300 | COL6A2 | c.2040T>C (p.Arg680=) c.711T>C (p.Arg237=) n.2117T>C n.2124T>C | dbSNP gnomAD v4 |
21 | g.46125855T>G | CA513170301 | COL6A2 | c.2040T>G (p.Arg680=) c.711T>G (p.Arg237=) n.2117T>G n.2124T>G | |
21 | g.46125855T= | CA2392507615 | COL6A2 | c.2040T= (p.Arg680=) c.711T= (p.Arg237=) n.2117T= n.2124T= | |
21 | g.46125855dup | CA10588991 | COL6A2 | c.2040dup (p.Ile681TyrfsTer?) c.711dup (p.Ile238TyrfsTer?) n.2117dup n.2124dup | ClinVar dbSNP gnomAD v4 |
21 | g.46125856A>C | CA410541296 | COL6A2 | c.2041A>C (p.Ile681Leu) c.712A>C (p.Ile238Leu) n.2118A>C n.2125A>C | |
21 | g.46125856A>G | CA410541298 | COL6A2 | c.2041A>G (p.Ile681Val) c.712A>G (p.Ile238Val) n.2118A>G n.2125A>G | gnomAD v4 COSMIC COSMIC COSMIC |
21 | g.46125856A>T | CA410541299 | COL6A2 | c.2041A>T (p.Ile681Phe) c.712A>T (p.Ile238Phe) n.2118A>T n.2125A>T | |
21 | g.46125857T>A | CA410541306 | COL6A2 | c.2042T>A (p.Ile681Asn) c.713T>A (p.Ile238Asn) n.2119T>A n.2126T>A | |
21 | g.46125857T>C | CA410541302 | COL6A2 | c.2042T>C (p.Ile681Thr) c.713T>C (p.Ile238Thr) n.2119T>C n.2126T>C | gnomAD v4 |
21 | g.46125857T>G | CA410541304 | COL6A2 | c.2042T>G (p.Ile681Ser) c.713T>G (p.Ile238Ser) n.2119T>G n.2126T>G | |
21 | g.46125858C>A | CA513170305 | COL6A2 | c.2043C>A (p.Ile681=) c.714C>A (p.Ile238=) n.2120C>A n.2127C>A | |
21 | g.46125858C= | CA2392507616 | COL6A2 | c.2043C= (p.Ile681=) c.714C= (p.Ile238=) n.2120C= n.2127C= | |
21 | g.46125858C>G | CA10072424 | COL6A2 | c.2043C>G (p.Ile681Met) c.714C>G (p.Ile238Met) n.2120C>G n.2127C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
21 | g.46125858C>T | CA10072423 | COL6A2 | c.2043C>T (p.Ile681=) c.714C>T (p.Ile238=) n.2120C>T n.2127C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
21 | g.46125859G>A | CA10072425 | COL6A2 | c.2044G>A (p.Asp682Asn) c.715G>A (p.Asp239Asn) n.2121G>A n.2128G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
21 | g.46125859G>C | CA10072426 | COL6A2 | c.2044G>C (p.Asp682His) c.715G>C (p.Asp239His) n.2121G>C n.2128G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
21 | g.46125859G= | CA2392507617 | COL6A2 | c.2044G= (p.Asp682=) c.715G= (p.Asp239=) n.2121G= n.2128G= | |
21 | g.46125859G>T | CA410541313 | COL6A2 | c.2044G>T (p.Asp682Tyr) c.715G>T (p.Asp239Tyr) n.2121G>T n.2128G>T | |
21 | g.46125860A= | CA2392507618 | COL6A2 | c.2045A= (p.Asp682=) c.716A= (p.Asp239=) n.2122A= n.2129A= | |
21 | g.46125860A>C | CA410541314 | COL6A2 | c.2045A>C (p.Asp682Ala) c.716A>C (p.Asp239Ala) n.2122A>C n.2129A>C | dbSNP gnomAD v3 gnomAD v4 |
21 | g.46125860A>G | CA410541316 | COL6A2 | c.2045A>G (p.Asp682Gly) c.716A>G (p.Asp239Gly) n.2122A>G n.2129A>G | |
21 | g.46125860A>T | CA410541318 | COL6A2 | c.2045A>T (p.Asp682Val) c.716A>T (p.Asp239Val) n.2122A>T n.2129A>T | |
21 | g.46125861C>A | CA410541319 | COL6A2 | c.2046C>A (p.Asp682Glu) c.717C>A (p.Asp239Glu) n.2123C>A n.2130C>A | |
21 | g.46125861C= | CA2392507619 | COL6A2 | c.2046C= (p.Asp682=) c.717C= (p.Asp239=) n.2123C= n.2130C= | |
21 | g.46125861C>G | CA410541320 | COL6A2 | c.2046C>G (p.Asp682Glu) c.717C>G (p.Asp239Glu) n.2123C>G n.2130C>G | dbSNP gnomAD v3 gnomAD v4 |
21 | g.46125861C>T | CA513170308 | COL6A2 | c.2046C>T (p.Asp682=) c.717C>T (p.Asp239=) n.2123C>T n.2130C>T | dbSNP gnomAD v3 gnomAD v4 |
21 | g.46125862T>A | CA410541324 | COL6A2 | c.2047T>A (p.Ser683Thr) c.718T>A (p.Ser240Thr) n.2124T>A n.2131T>A | |
21 | g.46125862T>C | CA410541325 | COL6A2 | c.2047T>C (p.Ser683Pro) c.718T>C (p.Ser240Pro) n.2124T>C n.2131T>C | ClinVar |
21 | g.46125862T>G | CA410541323 | COL6A2 | c.2047T>G (p.Ser683Ala) c.718T>G (p.Ser240Ala) n.2124T>G n.2131T>G | |
21 | g.46125863C>A | CA410541328 | COL6A2 | c.2048C>A (p.Ser683Tyr) c.719C>A (p.Ser240Tyr) n.2125C>A n.2132C>A | |
21 | g.46125863C= | CA2392507620 | COL6A2 | c.2048C= (p.Ser683=) c.719C= (p.Ser240=) n.2125C= n.2132C= | |
21 | g.46125863C>G | CA410541329 | COL6A2 | c.2048C>G (p.Ser683Cys) c.719C>G (p.Ser240Cys) n.2125C>G n.2132C>G | |
21 | g.46125863C>T | CA410541331 | COL6A2 | c.2048C>T (p.Ser683Phe) c.719C>T (p.Ser240Phe) n.2125C>T n.2132C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC |
21 | g.46125864C>A | CA513170312 | COL6A2 | c.2049C>A (p.Ser683=) c.720C>A (p.Ser240=) n.2126C>A n.2133C>A | |
21 | g.46125864C= | CA2392507621 | COL6A2 | c.2049C= (p.Ser683=) c.720C= (p.Ser240=) n.2126C= n.2133C= | |
21 | g.46125864C>G | CA513170313 | COL6A2 | c.2049C>G (p.Ser683=) c.720C>G (p.Ser240=) n.2126C>G n.2133C>G | |
21 | g.46125864C>T | CA513170314 | COL6A2 | c.2049C>T (p.Ser683=) c.720C>T (p.Ser240=) n.2126C>T n.2133C>T | dbSNP |
21 | g.46125865C>A | CA410541333 | COL6A2 | c.2050C>A (p.Leu684Met) c.721C>A (p.Leu241Met) n.2127C>A n.2134C>A | |
21 | g.46125865C>G | CA410541335 | COL6A2 | c.2050C>G (p.Leu684Val) c.721C>G (p.Leu241Val) n.2127C>G n.2134C>G | |
21 | g.46125865C>T | CA513170317 | COL6A2 | c.2050C>T (p.Leu684=) c.721C>T (p.Leu241=) n.2127C>T n.2134C>T | gnomAD v4 |
21 | g.46125865_46125866del | CA2577630030 | COL6A2 | c.2050_2051del (p.Leu684ValfsTer?) c.721_722del (p.Leu241ValfsTer?) n.2127_2128del n.2134_2135del | |
21 | g.46125866T>A | CA410541337 | COL6A2 | c.2051T>A (p.Leu684Gln) c.722T>A (p.Leu241Gln) n.2128T>A n.2135T>A | |
21 | g.46125866T>C | CA410541338 | COL6A2 | c.2051T>C (p.Leu684Pro) c.722T>C (p.Leu241Pro) n.2128T>C n.2135T>C | dbSNP gnomAD v3 gnomAD v4 |
21 | g.46125866T>G | CA410541340 | COL6A2 | c.2051T>G (p.Leu684Arg) c.722T>G (p.Leu241Arg) n.2128T>G n.2135T>G | dbSNP gnomAD v2 gnomAD v4 |
21 | g.46125866T= | CA2392507622 | COL6A2 | c.2051T= (p.Leu684=) c.722T= (p.Leu241=) n.2128T= n.2135T= | |
21 | g.46125867G>A | CA10072427 | COL6A2 | c.2052G>A (p.Leu684=) c.723G>A (p.Leu241=) n.2129G>A n.2136G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
21 | g.46125867G>C | CA513170319 | COL6A2 | c.2052G>C (p.Leu684=) c.723G>C (p.Leu241=) n.2129G>C n.2136G>C | |
21 | g.46125867G= | CA2392507623 | COL6A2 | c.2052G= (p.Leu684=) c.723G= (p.Leu241=) n.2129G= n.2136G= | |
21 | g.46125867G>T | CA513170320 | COL6A2 | c.2052G>T (p.Leu684=) c.723G>T (p.Leu241=) n.2129G>T n.2136G>T | |
21 | g.46125868T>A | CA410541343 | COL6A2 | c.2053T>A (p.Ser685Thr) c.724T>A (p.Ser242Thr) n.2130T>A n.2137T>A | |
21 | g.46125868T>C | CA410541344 | COL6A2 | c.2053T>C (p.Ser685Pro) c.724T>C (p.Ser242Pro) n.2130T>C n.2137T>C | |
21 | g.46125868T>G | CA410541345 | COL6A2 | c.2053T>G (p.Ser685Ala) c.724T>G (p.Ser242Ala) n.2130T>G n.2137T>G | |
21 | g.46125869C>A | CA410541349 | COL6A2 | c.2054C>A (p.Ser685Ter) c.725C>A (p.Ser242Ter) n.2131C>A n.2138C>A | dbSNP gnomAD v2 gnomAD v4 |
21 | g.46125869C= | CA2392507624 | COL6A2 | c.2054C= (p.Ser685=) c.725C= (p.Ser242=) n.2131C= n.2138C= | |
21 | g.46125869C>G | CA410541347 | COL6A2 | c.2054C>G (p.Ser685Trp) c.725C>G (p.Ser242Trp) n.2131C>G n.2138C>G | ClinVar dbSNP |
21 | g.46125869C>T | CA321972637 | COL6A2 | c.2054C>T (p.Ser685Leu) c.725C>T (p.Ser242Leu) n.2131C>T n.2138C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
21 | g.46125870G>A | CA10072428 | COL6A2 | c.2055G>A (p.Ser685=) c.726G>A (p.Ser242=) n.2132G>A n.2139G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
21 | g.46125870G>C | CA513170321 | COL6A2 | c.2055G>C (p.Ser685=) c.726G>C (p.Ser242=) n.2132G>C n.2139G>C | gnomAD v4 |
21 | g.46125870G= | CA2392507625 | COL6A2 | c.2055G= (p.Ser685=) c.726G= (p.Ser242=) n.2132G= n.2139G= | |
21 | g.46125870G>T | CA513170322 | COL6A2 | c.2055G>T (p.Ser685=) c.726G>T (p.Ser242=) n.2132G>T n.2139G>T | |
21 | g.46125871A>C | CA410541353 | COL6A2 | c.2056A>C (p.Ser686Arg) c.727A>C (p.Ser243Arg) n.2133A>C n.2140A>C | ClinVar |
21 | g.46125871A>G | CA410541355 | COL6A2 | c.2056A>G (p.Ser686Gly) c.727A>G (p.Ser243Gly) n.2133A>G n.2140A>G | gnomAD v4 |
21 | g.46125871A>T | CA410541357 | COL6A2 | c.2056A>T (p.Ser686Cys) c.727A>T (p.Ser243Cys) n.2133A>T n.2140A>T | |
21 | g.46125872G>A | CA410541359 | COL6A2 | c.2057G>A (p.Ser686Asn) c.728G>A (p.Ser243Asn) n.2134G>A n.2141G>A | gnomAD v4 |
21 | g.46125872G>C | CA410541361 | COL6A2 | c.2057G>C (p.Ser686Thr) c.728G>C (p.Ser243Thr) n.2134G>C n.2141G>C | |
21 | g.46125872G>T | CA410541363 | COL6A2 | c.2057G>T (p.Ser686Ile) c.728G>T (p.Ser243Ile) n.2134G>T n.2141G>T | |
21 | g.46125873C>A | CA410541365 | COL6A2 | c.2058C>A (p.Ser686Arg) c.729C>A (p.Ser243Arg) n.2135C>A n.2142C>A | |
21 | g.46125873C= | CA2392507626 | COL6A2 | c.2058C= (p.Ser686=) c.729C= (p.Ser243=) n.2135C= n.2142C= | |
21 | g.46125873C>G | CA410541367 | COL6A2 | c.2058C>G (p.Ser686Arg) c.729C>G (p.Ser243Arg) n.2135C>G n.2142C>G | |
21 | g.46125873C>T | CA10072429 | COL6A2 | c.2058C>T (p.Ser686=) c.729C>T (p.Ser243=) n.2135C>T n.2142C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
21 | g.46125874T>A | CA410541370 | COL6A2 | c.2059T>A (p.Phe687Ile) c.730T>A (p.Phe244Ile) n.2136T>A n.2143T>A | |
21 | g.46125874T>C | CA410541371 | COL6A2 | c.2059T>C (p.Phe687Leu) c.730T>C (p.Phe244Leu) n.2136T>C n.2143T>C | |
21 | g.46125874T>G | CA410541372 | COL6A2 | c.2059T>G (p.Phe687Val) c.730T>G (p.Phe244Val) n.2136T>G n.2143T>G | |
21 | g.46125875T>A | CA410541376 | COL6A2 | c.2060T>A (p.Phe687Tyr) c.731T>A (p.Phe244Tyr) n.2137T>A n.2144T>A | |
21 | g.46125875T>C | CA10072430 | COL6A2 | c.2060T>C (p.Phe687Ser) c.731T>C (p.Phe244Ser) n.2137T>C n.2144T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
21 | g.46125875T>G | CA410541374 | COL6A2 | c.2060T>G (p.Phe687Cys) c.731T>G (p.Phe244Cys) n.2137T>G n.2144T>G | |
21 | g.46125875T= | CA2392507627 | COL6A2 | c.2060T= (p.Phe687=) c.731T= (p.Phe244=) n.2137T= n.2144T= | |
21 | g.46125876C>A | CA410541381 | COL6A2 | c.2061C>A (p.Phe687Leu) c.732C>A (p.Phe244Leu) n.2138C>A n.2145C>A | |
21 | g.46125876C>G | CA410541379 | COL6A2 | c.2061C>G (p.Phe687Leu) c.732C>G (p.Phe244Leu) n.2138C>G n.2145C>G | |
21 | g.46125876C>T | CA513170326 | COL6A2 | c.2061C>T (p.Phe687=) c.732C>T (p.Phe244=) n.2138C>T n.2145C>T | gnomAD v4 |
21 | g.46125877A>C | CA410541383 | COL6A2 | c.2062A>C (p.Lys688Gln) c.733A>C (p.Lys245Gln) n.2139A>C n.2146A>C | |
21 | g.46125877A>G | CA410541384 | COL6A2 | c.2062A>G (p.Lys688Glu) c.733A>G (p.Lys245Glu) n.2139A>G n.2146A>G | gnomAD v4 |
21 | g.46125877A>T | CA410541385 | COL6A2 | c.2062A>T (p.Lys688Ter) c.733A>T (p.Lys245Ter) n.2139A>T n.2146A>T | |
21 | g.46125878A= | CA2392507628 | COL6A2 | c.2063A= (p.Lys688=) c.734A= (p.Lys245=) n.2140A= n.2147A= | |
21 | g.46125878A>C | CA410541386 | COL6A2 | c.2063A>C (p.Lys688Thr) c.734A>C (p.Lys245Thr) n.2140A>C n.2147A>C | |
21 | g.46125878A>G | CA410541388 | COL6A2 | c.2063A>G (p.Lys688Arg) c.734A>G (p.Lys245Arg) n.2140A>G n.2147A>G | dbSNP gnomAD v3 gnomAD v4 |
21 | g.46125878A>T | CA410541390 | COL6A2 | c.2063A>T (p.Lys688Met) c.734A>T (p.Lys245Met) n.2140A>T n.2147A>T | |
21 | g.46125879G>A | CA513170327 | COL6A2 | c.2064G>A (p.Lys688=) c.735G>A (p.Lys245=) n.2141G>A n.2148G>A | gnomAD v4 |
21 | g.46125879G>C | CA10072431 | COL6A2 | c.2064G>C (p.Lys688Asn) c.735G>C (p.Lys245Asn) n.2141G>C n.2148G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
21 | g.46125879G= | CA2392507629 | COL6A2 | c.2064G= (p.Lys688=) c.735G= (p.Lys245=) n.2141G= n.2148G= | |
21 | g.46125879G>T | CA410541393 | COL6A2 | c.2064G>T (p.Lys688Asn) c.735G>T (p.Lys245Asn) n.2141G>T n.2148G>T | |
21 | g.46125880G>A | CA10072432 | COL6A2 | c.2065G>A (p.Glu689Lys) c.736G>A (p.Glu246Lys) n.2142G>A n.2149G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
21 | g.46125880G>C | CA410541395 | COL6A2 | c.2065G>C (p.Glu689Gln) c.736G>C (p.Glu246Gln) n.2142G>C n.2149G>C | |
21 | g.46125880G= | CA2392507630 | COL6A2 | c.2065G= (p.Glu689=) c.736G= (p.Glu246=) n.2142G= n.2149G= | |
21 | g.46125880G>T | CA410541397 | COL6A2 | c.2065G>T (p.Glu689Ter) c.736G>T (p.Glu246Ter) n.2142G>T n.2149G>T | |
21 | g.46125881A= | CA2392507631 | COL6A2 | c.2066A= (p.Glu689=) c.737A= (p.Glu246=) n.2143A= n.2150A= | |
21 | g.46125881A>C | CA410541403 | COL6A2 | c.2066A>C (p.Glu689Ala) c.737A>C (p.Glu246Ala) n.2143A>C n.2150A>C | dbSNP |
21 | g.46125881A>G | CA410541400 | COL6A2 | c.2066A>G (p.Glu689Gly) c.737A>G (p.Glu246Gly) n.2143A>G n.2150A>G | |
21 | g.46125881A>T | CA410541402 | COL6A2 | c.2066A>T (p.Glu689Val) c.737A>T (p.Glu246Val) n.2143A>T n.2150A>T | |
21 | g.46125882G>A | CA513170331 | COL6A2 | c.2067G>A (p.Glu689=) c.738G>A (p.Glu246=) n.2144G>A n.2151G>A | dbSNP gnomAD v4 |
21 | g.46125882G>C | CA410541406 | COL6A2 | c.2067G>C (p.Glu689Asp) c.738G>C (p.Glu246Asp) n.2144G>C n.2151G>C | |
21 | g.46125882G= | CA2392507632 | COL6A2 | c.2067G= (p.Glu689=) c.738G= (p.Glu246=) n.2144G= n.2151G= | |
21 | g.46125882G>T | CA410541408 | COL6A2 | c.2067G>T (p.Glu689Asp) c.738G>T (p.Glu246Asp) n.2144G>T n.2151G>T | |
21 | g.46125883dup | CA2654974008 | COL6A2 | c.2068dup (p.Ala690GlyfsTer?) c.739dup (p.Ala247GlyfsTer?) n.2145dup n.2152dup | gnomAD v4 |
21 | g.46125883G>A | CA321972648 | COL6A2 | c.2068G>A (p.Ala690Thr) c.739G>A (p.Ala247Thr) n.2145G>A n.2152G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
21 | g.46125883G>C | CA410541410 | COL6A2 | c.2068G>C (p.Ala690Pro) c.739G>C (p.Ala247Pro) n.2145G>C n.2152G>C | |
21 | g.46125883G= | CA2392507633 | COL6A2 | c.2068G= (p.Ala690=) c.739G= (p.Ala247=) n.2145G= n.2152G= | |
21 | g.46125883G>T | CA410541412 | COL6A2 | c.2068G>T (p.Ala690Ser) c.739G>T (p.Ala247Ser) n.2145G>T n.2152G>T | gnomAD v4 |
21 | g.46125884C>A | CA410541415 | COL6A2 | c.2069C>A (p.Ala690Asp) c.740C>A (p.Ala247Asp) n.2146C>A n.2153C>A | |
21 | g.46125884C= | CA2392507634 | COL6A2 | c.2069C= (p.Ala690=) c.740C= (p.Ala247=) n.2146C= n.2153C= | |
21 | g.46125884C>G | CA410541416 | COL6A2 | c.2069C>G (p.Ala690Gly) c.740C>G (p.Ala247Gly) n.2146C>G n.2153C>G | ClinVar dbSNP |
21 | g.46125884C>T | CA410541418 | COL6A2 | c.2069C>T (p.Ala690Val) c.740C>T (p.Ala247Val) n.2146C>T n.2153C>T | gnomAD v4 |
21 | g.46125885T>A | CA513170335 | COL6A2 | c.2070T>A (p.Ala690=) c.741T>A (p.Ala247=) n.2147T>A n.2154T>A | |
21 | g.46125885T>C | CA10072433 | COL6A2 | c.2070T>C (p.Ala690=) c.741T>C (p.Ala247=) n.2147T>C n.2154T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
21 | g.46125885T>G | CA513170336 | COL6A2 | c.2070T>G (p.Ala690=) c.741T>G (p.Ala247=) n.2147T>G n.2154T>G | gnomAD v4 |
21 | g.46125885T= | CA2392507635 | COL6A2 | c.2070T= (p.Ala690=) c.741T= (p.Ala247=) n.2147T= n.2154T= | |
21 | g.46125886G>A | CA410541422 | COL6A2 | c.2071G>A (p.Val691Ile) c.742G>A (p.Val248Ile) n.2148G>A n.2155G>A | dbSNP gnomAD v4 |
21 | g.46125886G>C | CA410541424 | COL6A2 | c.2071G>C (p.Val691Leu) c.742G>C (p.Val248Leu) n.2148G>C n.2155G>C | |
21 | g.46125886G= | CA2392507636 | COL6A2 | c.2071G= (p.Val691=) c.742G= (p.Val248=) n.2148G= n.2155G= | |
21 | g.46125886G>T | CA410541425 | COL6A2 | c.2071G>T (p.Val691Phe) c.742G>T (p.Val248Phe) n.2148G>T n.2155G>T | |
21 | g.46125887T>A | CA410541427 | COL6A2 | c.2072T>A (p.Val691Asp) c.743T>A (p.Val248Asp) n.2149T>A n.2156T>A | |
21 | g.46125887T>C | CA410541429 | COL6A2 | c.2072T>C (p.Val691Ala) c.743T>C (p.Val248Ala) n.2149T>C n.2156T>C | |
21 | g.46125887T>G | CA410541426 | COL6A2 | c.2072T>G (p.Val691Gly) c.743T>G (p.Val248Gly) n.2149T>G n.2156T>G | |
21 | g.46125888C>A | CA513170340 | COL6A2 | c.2073C>A (p.Val691=) c.744C>A (p.Val248=) n.2150C>A n.2157C>A | |
21 | g.46125888C= | CA2392507637 | COL6A2 | c.2073C= (p.Val691=) c.744C= (p.Val248=) n.2150C= n.2157C= | |
21 | g.46125888C>G | CA10072434 | COL6A2 | c.2073C>G (p.Val691=) c.744C>G (p.Val248=) n.2150C>G n.2157C>G | dbSNP ExAC gnomAD v2 |
21 | g.46125888C>T | CA513170341 | COL6A2 | c.2073C>T (p.Val691=) c.744C>T (p.Val248=) n.2150C>T n.2157C>T | |
21 | g.46125888_46125891delinsCAAG | CA2392507638 | COL6A2 | c.2073_2076delinsCAAG (p.Val691=) c.744_747delinsCAAG (p.Val248=) n.2150_2153delinsCAAG n.2157_2160delinsCAAG | |
21 | g.46125889A= | CA2392507639 | COL6A2 | c.2074A= (p.Lys692=) c.745A= (p.Lys249=) n.2151A= n.2158A= | |
21 | g.46125889A>C | CA410541431 | COL6A2 | c.2074A>C (p.Lys692Gln) c.745A>C (p.Lys249Gln) n.2151A>C n.2158A>C | |
21 | g.46125889A>G | CA321972651 | COL6A2 | c.2074A>G (p.Lys692Glu) c.745A>G (p.Lys249Glu) n.2151A>G n.2158A>G | dbSNP |
21 | g.46125889A>T | CA410541434 | COL6A2 | c.2074A>T (p.Lys692Ter) c.745A>T (p.Lys249Ter) n.2151A>T n.2158A>T | |
21 | g.46125891_46125893del | CA1139666904 | COL6A2 | c.2076_2078del (p.Lys692del) c.747_749del (p.Lys249del) n.2153_2155del n.2160_2162del | ClinVar dbSNP |
21 | g.46125890A>C | CA410541438 | COL6A2 | c.2075A>C (p.Lys692Thr) c.746A>C (p.Lys249Thr) n.2152A>C n.2159A>C | |
21 | g.46125890A>G | CA410541439 | COL6A2 | c.2075A>G (p.Lys692Arg) c.746A>G (p.Lys249Arg) n.2152A>G n.2159A>G | gnomAD v4 |
21 | g.46125890A>T | CA410541441 | COL6A2 | c.2075A>T (p.Lys692Met) c.746A>T (p.Lys249Met) n.2152A>T n.2159A>T | |
21 | g.46125891G>A | CA10072435 | COL6A2 | c.2076G>A (p.Lys692=) c.747G>A (p.Lys249=) n.2153G>A n.2160G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
21 | g.46125891G>C | CA410541444 | COL6A2 | c.2076G>C (p.Lys692Asn) c.747G>C (p.Lys249Asn) n.2153G>C n.2160G>C | |
21 | g.46125891G= | CA2392507640 | COL6A2 | c.2076G= (p.Lys692=) c.747G= (p.Lys249=) n.2153G= n.2160G= | |
21 | g.46125891G>T | CA410541446 | COL6A2 | c.2076G>T (p.Lys692Asn) c.747G>T (p.Lys249Asn) n.2153G>T n.2160G>T | |
21 | g.46125892A>C | CA410541448 | COL6A2 | c.2077A>C (p.Asn693His) c.748A>C (p.Asn250His) n.2154A>C n.2161A>C | |
21 | g.46125892A>G | CA410541449 | COL6A2 | c.2077A>G (p.Asn693Asp) c.748A>G (p.Asn250Asp) n.2154A>G n.2161A>G | |
21 | g.46125892A>T | CA410541451 | COL6A2 | c.2077A>T (p.Asn693Tyr) c.748A>T (p.Asn250Tyr) n.2154A>T n.2161A>T | |
21 | g.46125893A>C | CA410541455 | COL6A2 | c.2078A>C (p.Asn693Thr) c.749A>C (p.Asn250Thr) n.2155A>C n.2162A>C | |
21 | g.46125893A>G | CA410541456 | COL6A2 | c.2078A>G (p.Asn693Ser) c.749A>G (p.Asn250Ser) n.2155A>G n.2162A>G | |
21 | g.46125893A>T | CA410541454 | COL6A2 | c.2078A>T (p.Asn693Ile) c.749A>T (p.Asn250Ile) n.2155A>T n.2162A>T | |
21 | g.46125894C>A | CA10072436 | COL6A2 | c.2079C>A (p.Asn693Lys) c.750C>A (p.Asn250Lys) n.2156C>A n.2163C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
21 | g.46125894C= | CA2392507641 | COL6A2 | c.2079C= (p.Asn693=) c.750C= (p.Asn250=) n.2156C= n.2163C= | |
21 | g.46125894C>G | CA410541458 | COL6A2 | c.2079C>G (p.Asn693Lys) c.750C>G (p.Asn250Lys) n.2156C>G n.2163C>G | |
21 | g.46125894C>T | CA513170343 | COL6A2 | c.2079C>T (p.Asn693=) c.750C>T (p.Asn250=) n.2156C>T n.2163C>T | |
21 | g.46125895C>A | CA410541460 | COL6A2 | c.2080C>A (p.Leu694Ile) n.2157C>A n.2164C>A | |
21 | g.46125895C>G | CA410541461 | COL6A2 | c.2080C>G (p.Leu694Val) n.2157C>G n.2164C>G | gnomAD v4 |
21 | g.46125895C>T | CA410541463 | COL6A2 | c.2080C>T (p.Leu694Phe) n.2157C>T n.2164C>T | gnomAD v4 COSMIC COSMIC COSMIC |
21 | g.46125896T>A | CA410541469 | COL6A2 | c.2081T>A (p.Leu694His) n.2158T>A n.2165T>A | |
21 | g.46125896T>C | CA410541467 | COL6A2 | c.2081T>C (p.Leu694Pro) n.2158T>C n.2165T>C | |
21 | g.46125896T>G | CA410541466 | COL6A2 | c.2081T>G (p.Leu694Arg) n.2158T>G n.2165T>G | |
21 | g.46125897C>A | CA513170347 | COL6A2 | c.2082C>A (p.Leu694=) n.2159C>A n.2166C>A | |
21 | g.46125897C= | CA2392507642 | COL6A2 | c.2082C= (p.Leu694=) n.2159C= n.2166C= | |
21 | g.46125897C>G | CA513170348 | COL6A2 | c.2082C>G (p.Leu694=) n.2159C>G n.2166C>G | |
21 | g.46125897C>T | CA10072437 | COL6A2 | c.2082C>T (p.Leu694=) n.2159C>T n.2166C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
21 | g.46125897_46125898dup | CA2573054956 | COL6A2 | c.2082_2083dup (p.Glu695AlafsTer?) n.2159_2160dup n.2166_2167dup | ClinVar dbSNP |
21 | g.46125898G>A | CA10072438 | COL6A2 | c.2083G>A (p.Glu695Lys) n.2160G>A n.2167G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
21 | g.46125898G>C | CA410541473 | COL6A2 | c.2083G>C (p.Glu695Gln) n.2160G>C n.2167G>C | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
21 | g.46125898G= | CA2392507643 | COL6A2 | c.2083G= (p.Glu695=) n.2160G= n.2167G= | |
21 | g.46125898G>T | CA410541475 | COL6A2 | c.2083G>T (p.Glu695Ter) n.2160G>T n.2167G>T | |
21 | g.46125899A= | CA2392507644 | COL6A2 | c.2084A= (p.Glu695=) n.2161A= n.2168A= | |
21 | g.46125899A>C | CA10072439 | COL6A2 | c.2084A>C (p.Glu695Ala) n.2161A>C n.2168A>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
21 | g.46125899A>G | CA410541478 | COL6A2 | c.2084A>G (p.Glu695Gly) n.2161A>G n.2168A>G | gnomAD v4 |
21 | g.46125899A>T | CA410541479 | COL6A2 | c.2084A>T (p.Glu695Val) n.2161A>T n.2168A>T | |
21 | g.46125900G>A | CA513170351 | COL6A2 | c.2085G>A (p.Glu695=) n.2162G>A n.2169G>A | |
21 | g.46125900G>C | CA410541481 | COL6A2 | c.2085G>C (p.Glu695Asp) n.2162G>C n.2169G>C | |
21 | g.46125900G>T | CA410541480 | COL6A2 | c.2085G>T (p.Glu695Asp) n.2162G>T n.2169G>T | |
21 | g.46125901T>A | CA410541483 | COL6A2 | c.2086T>A (p.Trp696Arg) n.2163T>A n.2170T>A | dbSNP |
21 | g.46125901T>C | CA410541486 | COL6A2 | c.2086T>C (p.Trp696Arg) n.2163T>C n.2170T>C | |
21 | g.46125901T>G | CA410541484 | COL6A2 | c.2086T>G (p.Trp696Gly) n.2163T>G n.2170T>G | |
21 | g.46125902G>A | CA410541489 | COL6A2 | c.2087G>A (p.Trp696Ter) n.2164G>A n.2171G>A | dbSNP |
21 | g.46125902G>C | CA410541490 | COL6A2 | c.2087G>C (p.Trp696Ser) n.2164G>C n.2171G>C | |
21 | g.46125902G= | CA2392507645 | COL6A2 | c.2087G= (p.Trp696=) n.2164G= n.2171G= | |
21 | g.46125902G>T | CA410541492 | COL6A2 | c.2087G>T (p.Trp696Leu) n.2164G>T n.2171G>T | |
21 | g.46125903G>A | CA410541494 | COL6A2 | c.2088G>A (p.Trp696Ter) n.2165G>A n.2172G>A | |
21 | g.46125903G>C | CA410541496 | COL6A2 | c.2088G>C (p.Trp696Cys) n.2165G>C n.2172G>C | ClinVar |
21 | g.46125903G>T | CA410541498 | COL6A2 | c.2088G>T (p.Trp696Cys) n.2165G>T n.2172G>T | |
21 | g.46125904A>C | CA410541500 | COL6A2 | c.2089A>C (p.Ile697Leu) n.2166A>C n.2173A>C | gnomAD v4 |
21 | g.46125904A>G | CA410541502 | COL6A2 | c.2089A>G (p.Ile697Val) n.2166A>G n.2173A>G | |
21 | g.46125904A>T | CA410541504 | COL6A2 | c.2089A>T (p.Ile697Phe) n.2166A>T n.2173A>T | |
21 | g.46125905T>A | CA410541506 | COL6A2 | c.2090T>A (p.Ile697Asn) n.2167T>A n.2174T>A | |
21 | g.46125905T>C | CA410541508 | COL6A2 | c.2090T>C (p.Ile697Thr) n.2167T>C n.2174T>C | |
21 | g.46125905T>G | CA410541510 | COL6A2 | c.2090T>G (p.Ile697Ser) n.2167T>G n.2174T>G | |
21 | g.46125906T>A | CA513170358 | COL6A2 | c.2091T>A (p.Ile697=) n.2168T>A n.2175T>A | |
21 | g.46125906T>C | CA513170360 | COL6A2 | c.2091T>C (p.Ile697=) n.2168T>C n.2175T>C | |
21 | g.46125906T>G | CA410541512 | COL6A2 | c.2091T>G (p.Ile697Met) n.2168T>G n.2175T>G | |
21 | g.46125907G>A | CA410541513 | COL6A2 | c.2092G>A (p.Ala698Thr) n.2169G>A n.2176G>A | gnomAD v4 |
21 | g.46125907G>C | CA410541516 | COL6A2 | c.2092G>C (p.Ala698Pro) n.2169G>C n.2176G>C | |
21 | g.46125907G>T | CA410541514 | COL6A2 | c.2092G>T (p.Ala698Ser) n.2169G>T n.2176G>T | gnomAD v4 |
21 | g.46125908C>A | CA410541519 | COL6A2 | c.2093C>A (p.Ala698Glu) n.2170C>A n.2177C>A | |
21 | g.46125908C= | CA2392507646 | COL6A2 | c.2093C= (p.Ala698=) n.2170C= n.2177C= | |
21 | g.46125908C>G | CA410541520 | COL6A2 | c.2093C>G (p.Ala698Gly) n.2170C>G n.2177C>G | |
21 | g.46125908C>T | CA410541522 | COL6A2 | c.2093C>T (p.Ala698Val) n.2170C>T n.2177C>T | ClinVar dbSNP |
21 | g.46125908_46125909delinsTA | CA2580098916 | COL6A2 | c.2093_2094delinsTA (p.Ala698Val) n.2170_2171delinsTA n.2177_2178delinsTA | ClinVar |
21 | g.46125908_46125909insA | CA2818101900 | COL6A2 | c.2093_2094insA (p.Gly700ArgfsTer?) n.2170_2171insA n.2177_2178insA | |
21 | g.46125909G>A | CA147456 | COL6A2 | c.2094G>A (p.Ala698=) n.2171G>A n.2178G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
21 | g.46125909G>C | CA513170362 | COL6A2 | c.2094G>C (p.Ala698=) n.2171G>C n.2178G>C | dbSNP gnomAD v4 |
21 | g.46125909G= | CA2392507647 | COL6A2 | c.2094G= (p.Ala698=) n.2171G= n.2178G= | |
21 | g.46125909G>T | CA513170363 | COL6A2 | c.2094G>T (p.Ala698=) n.2171G>T n.2178G>T | |
21 | g.46125910G>A | CA410541525 | COL6A2 | c.2095G>A (p.Gly699Ser) n.2172G>A n.2179G>A | dbSNP |
21 | g.46125910G>C | CA410541527 | COL6A2 | c.2095G>C (p.Gly699Arg) n.2172G>C n.2179G>C | gnomAD v3 gnomAD v4 |
21 | g.46125910G= | CA2392507648 | COL6A2 | c.2095G= (p.Gly699=) n.2172G= n.2179G= | |
21 | g.46125910G>T | CA410541529 | COL6A2 | c.2095G>T (p.Gly699Cys) n.2172G>T n.2179G>T | |
21 | g.46125910_46125911insTG | CA2818101901 | COL6A2 | c.2095_2096insTG (p.Gly699ValfsTer?) n.2172_2173insTG n.2179_2180insTG | |
21 | g.46125911G>A | CA278956 | COL6A2 | c.2096G>A (p.Gly699Asp) n.2173G>A n.2180G>A | ClinVar dbSNP |
21 | g.46125911G>C | CA410541533 | COL6A2 | c.2096G>C (p.Gly699Ala) n.2173G>C n.2180G>C | |
21 | g.46125911G= | CA2392507649 | COL6A2 | c.2096G= (p.Gly699=) n.2173G= n.2180G= | |
21 | g.46125911G>T | CA410541534 | COL6A2 | c.2096G>T (p.Gly699Val) n.2173G>T n.2180G>T | |
21 | g.46125912C>A | CA513170364 | COL6A2 | c.2097C>A (p.Gly699=) n.2174C>A n.2181C>A | dbSNP |
21 | g.46125912C= | CA2392507650 | COL6A2 | c.2097C= (p.Gly699=) n.2174C= n.2181C= | |
21 | g.46125912C>G | CA513170365 | COL6A2 | c.2097C>G (p.Gly699=) n.2174C>G n.2181C>G | dbSNP |
21 | g.46125912C>T | CA147459 | COL6A2 | c.2097C>T (p.Gly699=) n.2174C>T n.2181C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
21 | g.46125912_46125913delinsTA | CA2499225995 | COL6A2 | c.2097_2098delinsTA (p.Gly700Ser) n.2174_2175delinsTA n.2181_2182delinsTA | ClinVar dbSNP |
21 | g.46125912_46125913insACCTGGACACCCTCCCTGTCGAGCTTCAAGGAGGCTGTCAAGAACCTCGAGGGGAGTGCAGGT | CA2818101902 | COL6A2 | c.2097_2098insACCTGGACACCCTCCCTGTCGAGCTTCAAGGAGGCTGTCAAGAACCTCGAGGGGAGTGCAGGT (p.Gly699_Gly700insThrTrpThrProSerLeuSerSerPheLysGluAlaValLysAsnLeuGluGlySerAlaGly) n.2174_2175insACCTGGACACCCTCCCTGTCGAGCTTCAAGGAGGCTGTCAAGAACCTCGAGGGGAGTGCAGGT n.2181_2182insACCTGGACACCCTCCCTGTCGAGCTTCAAGGAGGCTGTCAAGAACCTCGAGGGGAGTGCAGGT | |
21 | g.46125913G>A | CA242678 | COL6A2 | c.2098G>A (p.Gly700Ser) n.2175G>A n.2182G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
21 | g.46125913G>C | CA410541541 | COL6A2 | c.2098G>C (p.Gly700Arg) n.2175G>C n.2182G>C | |
21 | g.46125913G= | CA2392507651 | COL6A2 | c.2098G= (p.Gly700=) n.2175G= n.2182G= | |
21 | g.46125913G>T | CA410541538 | COL6A2 | c.2098G>T (p.Gly700Cys) n.2175G>T n.2182G>T | |
21 | g.46125914G>A | CA410541548 | COL6A2 | c.2099G>A (p.Gly700Asp) n.2176G>A n.2183G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
21 | g.46125914G>C | CA410541544 | COL6A2 | c.2099G>C (p.Gly700Ala) n.2176G>C n.2183G>C | |
21 | g.46125914G= | CA2392507652 | COL6A2 | c.2099G= (p.Gly700=) n.2176G= n.2183G= | |
21 | g.46125914G>T | CA410541546 | COL6A2 | c.2099G>T (p.Gly700Val) n.2176G>T n.2183G>T | |
21 | g.46125915C>A | CA513170369 | COL6A2 | c.2100C>A (p.Gly700=) n.2177C>A n.2184C>A | |
21 | g.46125915C= | CA2392507653 | COL6A2 | c.2100C= (p.Gly700=) n.2177C= n.2184C= | |
21 | g.46125915C>G | CA513170371 | COL6A2 | c.2100C>G (p.Gly700=) n.2177C>G n.2184C>G | dbSNP |
21 | g.46125915C>T | CA513170373 | COL6A2 | c.2100C>T (p.Gly700=) n.2177C>T n.2184C>T | gnomAD v4 |
21 | g.46125916A>C | CA410541549 | COL6A2 | c.2101A>C (p.Thr701Pro) n.2178A>C n.2185A>C | |
21 | g.46125916A>G | CA410541551 | COL6A2 | c.2101A>G (p.Thr701Ala) n.2178A>G n.2185A>G | |
21 | g.46125916A>T | CA410541553 | COL6A2 | c.2101A>T (p.Thr701Ser) n.2178A>T n.2185A>T | |
21 | g.46125917C>A | CA410541559 | COL6A2 | c.2102C>A (p.Thr701Asn) n.2179C>A n.2186C>A | |
21 | g.46125917C= | CA2392507654 | COL6A2 | c.2102C= (p.Thr701=) n.2179C= n.2186C= | |
21 | g.46125917C>G | CA321972669 | COL6A2 | c.2102C>G (p.Thr701Ser) n.2179C>G n.2186C>G | dbSNP gnomAD v2 gnomAD v4 |
21 | g.46125917C>T | CA410541556 | COL6A2 | c.2102C>T (p.Thr701Ile) n.2179C>T n.2186C>T | |
21 | g.46125918C>A | CA513170375 | COL6A2 | c.2103C>A (p.Thr701=) n.2180C>A n.2187C>A | |
21 | g.46125918C>G | CA513170377 | COL6A2 | c.2103C>G (p.Thr701=) n.2180C>G n.2187C>G | |
21 | g.46125918C>T | CA513170379 | COL6A2 | c.2103C>T (p.Thr701=) n.2180C>T n.2187C>T | |
21 | g.46125919T>A | CA410541561 | COL6A2 | c.2104T>A (p.Trp702Arg) n.2181T>A n.2188T>A | |
21 | g.46125919T>C | CA410541563 | COL6A2 | c.2104T>C (p.Trp702Arg) n.2181T>C n.2188T>C | dbSNP gnomAD v4 |
21 | g.46125919T>G | CA410541565 | COL6A2 | c.2104T>G (p.Trp702Gly) n.2181T>G n.2188T>G | gnomAD v4 |
21 | g.46125919T= | CA2392507655 | COL6A2 | c.2104T= (p.Trp702=) n.2181T= n.2188T= | |
21 | g.46125920G>A | CA410541567 | COL6A2 | c.2105G>A (p.Trp702Ter) n.2182G>A n.2189G>A | |
21 | g.46125920G>C | CA410541569 | COL6A2 | c.2105G>C (p.Trp702Ser) n.2182G>C n.2189G>C | |
21 | g.46125920G>T | CA410541570 | COL6A2 | c.2105G>T (p.Trp702Leu) n.2182G>T n.2189G>T | |
21 | g.46125921G>A | CA410541572 | COL6A2 | c.2106G>A (p.Trp702Ter) n.2183G>A n.2190G>A | gnomAD v4 |
21 | g.46125921G>C | CA410541576 | COL6A2 | c.2106G>C (p.Trp702Cys) n.2183G>C n.2190G>C | |
21 | g.46125921G>T | CA410541574 | COL6A2 | c.2106G>T (p.Trp702Cys) n.2183G>T n.2190G>T | |
21 | g.46125922A>C | CA410541578 | COL6A2 | c.2107A>C (p.Thr703Pro) n.2184A>C n.2191A>C | ClinVar gnomAD v4 |
21 | g.46125922A>G | CA410541580 | COL6A2 | c.2107A>G (p.Thr703Ala) n.2184A>G n.2191A>G | |
21 | g.46125922A>T | CA410541582 | COL6A2 | c.2107A>T (p.Thr703Ser) n.2184A>T n.2191A>T | |
21 | g.46125923C>A | CA410541583 | COL6A2 | c.2108C>A (p.Thr703Lys) n.2185C>A n.2192C>A | |
21 | g.46125923C>G | CA410541584 | COL6A2 | c.2108C>G (p.Thr703Arg) n.2185C>G n.2192C>G | |
21 | g.46125923C>T | CA410541586 | COL6A2 | c.2108C>T (p.Thr703Ile) n.2185C>T n.2192C>T | |
21 | g.46125924A= | CA2392507656 | COL6A2 | c.2109A= (p.Thr703=) n.2186A= n.2193A= | |
21 | g.46125924A>C | CA513170383 | COL6A2 | c.2109A>C (p.Thr703=) n.2186A>C n.2193A>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
21 | g.46125924A>G | CA513170385 | COL6A2 | c.2109A>G (p.Thr703=) n.2186A>G n.2193A>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
21 | g.46125924A>T | CA513170384 | COL6A2 | c.2109A>T (p.Thr703=) n.2186A>T n.2193A>T | |
21 | g.46125925C>A | CA410541588 | COL6A2 | c.2110C>A (p.Pro704Thr) n.2187C>A n.2194C>A | |
21 | g.46125925C>G | CA410541589 | COL6A2 | c.2110C>G (p.Pro704Ala) n.2187C>G n.2194C>G | |
21 | g.46125925C>T | CA410541591 | COL6A2 | c.2110C>T (p.Pro704Ser) n.2187C>T n.2194C>T | |
21 | g.46125926C>A | CA410541593 | COL6A2 | c.2111C>A (p.Pro704His) n.2188C>A n.2195C>A | dbSNP |
21 | g.46125926C>G | CA410541594 | COL6A2 | c.2111C>G (p.Pro704Arg) n.2188C>G n.2195C>G | |
21 | g.46125926C>T | CA410541595 | COL6A2 | c.2111C>T (p.Pro704Leu) n.2188C>T n.2195C>T | |
21 | g.46125927C>A | CA513170389 | COL6A2 | c.2112C>A (p.Pro704=) n.2189C>A n.2196C>A | |
21 | g.46125927C>G | CA513170388 | COL6A2 | c.2112C>G (p.Pro704=) n.2189C>G n.2196C>G | |
21 | g.46125927C>T | CA513170387 | COL6A2 | c.2112C>T (p.Pro704=) n.2189C>T n.2196C>T | |
21 | g.46125928T>A | CA410541600 | COL6A2 | c.2113T>A (p.Ser705Thr) n.2190T>A n.2197T>A | |
21 | g.46125928T>C | CA221819 | COL6A2 | c.2113T>C (p.Ser705Pro) n.2190T>C n.2197T>C | ClinVar dbSNP |
21 | g.46125928T>G | CA410541597 | COL6A2 | c.2113T>G (p.Ser705Ala) n.2190T>G n.2197T>G | |
21 | g.46125928T= | CA2392507657 | COL6A2 | c.2113T= (p.Ser705=) n.2190T= n.2197T= | |
21 | g.46125929C>A | CA410541603 | COL6A2 | c.2114C>A (p.Ser705Ter) n.2191C>A n.2198C>A | |
21 | g.46125929C= | CA2392507658 | COL6A2 | c.2114C= (p.Ser705=) n.2191C= n.2198C= | |
21 | g.46125929C>G | CA410541606 | COL6A2 | c.2114C>G (p.Ser705Ter) n.2191C>G n.2198C>G | |
21 | g.46125929C>T | CA10072440 | COL6A2 | c.2114C>T (p.Ser705Leu) n.2191C>T n.2198C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
21 | g.46125930A>C | CA513170392 | COL6A2 | c.2115A>C (p.Ser705=) n.2192A>C n.2199A>C | |
21 | g.46125930A>G | CA513170393 | COL6A2 | c.2115A>G (p.Ser705=) n.2192A>G n.2199A>G | dbSNP gnomAD v4 |
21 | g.46125930A>T | CA513170394 | COL6A2 | c.2115A>T (p.Ser705=) n.2192A>T n.2199A>T | |
21 | g.46125931G>A | CA410541608 | COL6A2 | c.2116G>A (p.Ala706Thr) n.2193G>A n.2200G>A | ClinVar gnomAD v4 |
21 | g.46125931G>C | CA242675 | COL6A2 | c.2116G>C (p.Ala706Pro) n.2193G>C n.2200G>C | ClinVar dbSNP |
21 | g.46125931G= | CA2392507659 | COL6A2 | c.2116G= (p.Ala706=) n.2193G= n.2200G= | |
21 | g.46125931G>T | CA410541609 | COL6A2 | c.2116G>T (p.Ala706Ser) n.2193G>T n.2200G>T | |
21 | g.46125932C>A | CA410541611 | COL6A2 | c.2117C>A (p.Ala706Asp) n.2194C>A n.2201C>A | |
21 | g.46125932C= | CA2392507660 | COL6A2 | c.2117C= (p.Ala706=) n.2194C= n.2201C= | |
21 | g.46125932C>G | CA410541613 | COL6A2 | c.2117C>G (p.Ala706Gly) n.2194C>G n.2201C>G | |
21 | g.46125932C>T | CA410541615 | COL6A2 | c.2117C>T (p.Ala706Val) n.2194C>T n.2201C>T | dbSNP gnomAD v3 gnomAD v4 |
21 | g.46125933C>A | CA513170397 | COL6A2 | c.2118C>A (p.Ala706=) n.2195C>A n.2202C>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
21 | g.46125933C= | CA2392507661 | COL6A2 | c.2118C= (p.Ala706=) n.2195C= n.2202C= | |
21 | g.46125933C>G | CA513170398 | COL6A2 | c.2118C>G (p.Ala706=) n.2195C>G n.2202C>G | |
21 | g.46125933C>T | CA10072441 | COL6A2 | c.2118C>T (p.Ala706=) n.2195C>T n.2202C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
21 | g.46125934C>A | CA410541618 | COL6A2 | c.2119C>A (p.Leu707Ile) n.2196C>A n.2203C>A | |
21 | g.46125934C= | CA2392507662 | COL6A2 | c.2119C= (p.Leu707=) n.2196C= n.2203C= | |
21 | g.46125934C>G | CA410541620 | COL6A2 | c.2119C>G (p.Leu707Val) n.2196C>G n.2203C>G | dbSNP |
21 | g.46125934C>T | CA410541622 | COL6A2 | c.2119C>T (p.Leu707Phe) n.2196C>T n.2203C>T | |
21 | g.46125935T>A | CA410541627 | COL6A2 | c.2120T>A (p.Leu707His) n.2197T>A n.2204T>A | |
21 | g.46125935T>C | CA410541626 | COL6A2 | c.2120T>C (p.Leu707Pro) n.2197T>C n.2204T>C | ClinVar dbSNP |
21 | g.46125935T>G | CA410541624 | COL6A2 | c.2120T>G (p.Leu707Arg) n.2197T>G n.2204T>G | |
21 | g.46125936C>A | CA513170400 | COL6A2 | c.2121C>A (p.Leu707=) n.2198C>A n.2205C>A | |
21 | g.46125936C= | CA2392507663 | COL6A2 | c.2121C= (p.Leu707=) n.2198C= n.2205C= | |
21 | g.46125936C>G | CA10072442 | COL6A2 | c.2121C>G (p.Leu707=) n.2198C>G n.2205C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
21 | g.46125936C>T | CA513170401 | COL6A2 | c.2121C>T (p.Leu707=) n.2198C>T n.2205C>T | |
21 | g.46125937A>C | CA410541630 | COL6A2 | c.2122A>C (p.Lys708Gln) n.2199A>C n.2206A>C | |
21 | g.46125937A>G | CA410541631 | COL6A2 | c.2122A>G (p.Lys708Glu) n.2199A>G n.2206A>G | |
21 | g.46125937A>T | CA410541632 | COL6A2 | c.2122A>T (p.Lys708Ter) n.2199A>T n.2206A>T | |
21 | g.46125938del | CA2654974009 | COL6A2 | c.2123del (p.Lys708SerfsTer?) n.2200del n.2207del | gnomAD v4 |
21 | g.46125938A>C | CA410541635 | COL6A2 | c.2123A>C (p.Lys708Thr) n.2200A>C n.2207A>C | |
21 | g.46125938A>G | CA410541636 | COL6A2 | c.2123A>G (p.Lys708Arg) n.2200A>G n.2207A>G | |
21 | g.46125938A>T | CA410541638 | COL6A2 | c.2123A>T (p.Lys708Met) n.2200A>T n.2207A>T | |
21 | g.46125939G>A | CA513170402 | COL6A2 | c.2124G>A (p.Lys708=) n.2201G>A n.2208G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
21 | g.46125939G>C | CA410541641 | COL6A2 | c.2124G>C (p.Lys708Asn) n.2201G>C n.2208G>C | |
21 | g.46125939G= | CA2392507664 | COL6A2 | c.2124G= (p.Lys708=) n.2201G= n.2208G= | |
21 | g.46125939G>T | CA410541642 | COL6A2 | c.2124G>T (p.Lys708Asn) n.2201G>T n.2208G>T | |
21 | g.46125940T>A | CA410541644 | COL6A2 | c.2125T>A (p.Phe709Ile) n.2202T>A n.2209T>A | gnomAD v4 |
21 | g.46125940T>C | CA410541646 | COL6A2 | c.2125T>C (p.Phe709Leu) n.2202T>C n.2209T>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
21 | g.46125940T>G | CA10072443 | COL6A2 | c.2125T>G (p.Phe709Val) n.2202T>G n.2209T>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
21 | g.46125940T= | CA2392507665 | COL6A2 | c.2125T= (p.Phe709=) n.2202T= n.2209T= | |
21 | g.46125941T>A | CA410541650 | COL6A2 | c.2126T>A (p.Phe709Tyr) n.2203T>A n.2210T>A | |
21 | g.46125941T>C | CA410541652 | COL6A2 | c.2126T>C (p.Phe709Ser) n.2203T>C n.2210T>C | |
21 | g.46125941T>G | CA410541648 | COL6A2 | c.2126T>G (p.Phe709Cys) n.2203T>G n.2210T>G | |
21 | g.46125941_46125964dup | CA2654974010 | COL6A2 | c.2126_2149dup (p.Lys716_Glu717insValAlaTyrAspArgLeuIleLys) n.2203_2226dup n.2210_2233dup | gnomAD v4 |
21 | g.46125942T>A | CA410541654 | COL6A2 | c.2127T>A (p.Phe709Leu) n.2204T>A n.2211T>A | |
21 | g.46125942T>C | CA10072444 | COL6A2 | c.2127T>C (p.Phe709=) n.2204T>C n.2211T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
21 | g.46125942T>G | CA410541657 | COL6A2 | c.2127T>G (p.Phe709Leu) n.2204T>G n.2211T>G | |
21 | g.46125942T= | CA2392507666 | COL6A2 | c.2127T= (p.Phe709=) n.2204T= n.2211T= | |
21 | g.46125943G>A | CA410541659 | COL6A2 | c.2128G>A (p.Ala710Thr) n.2205G>A n.2212G>A | |
21 | g.46125943G>C | CA410541661 | COL6A2 | c.2128G>C (p.Ala710Pro) n.2205G>C n.2212G>C | |
21 | g.46125943G>T | CA410541662 | COL6A2 | c.2128G>T (p.Ala710Ser) n.2205G>T n.2212G>T | ClinVar |
21 | g.46125944C>A | CA410541665 | COL6A2 | c.2129C>A (p.Ala710Asp) n.2206C>A n.2213C>A | ClinVar dbSNP |
21 | g.46125944C= | CA2392507667 | COL6A2 | c.2129C= (p.Ala710=) n.2206C= n.2213C= | |
21 | g.46125944C>G | CA410541666 | COL6A2 | c.2129C>G (p.Ala710Gly) n.2206C>G n.2213C>G | |
21 | g.46125944C>T | CA410541667 | COL6A2 | c.2129C>T (p.Ala710Val) n.2206C>T n.2213C>T | ClinVar dbSNP |
21 | g.46125945C>A | CA513170406 | COL6A2 | c.2130C>A (p.Ala710=) n.2207C>A n.2214C>A | dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC |
21 | g.46125945C= | CA2392507668 | COL6A2 | c.2130C= (p.Ala710=) n.2207C= n.2214C= | |
21 | g.46125945C>G | CA513170407 | COL6A2 | c.2130C>G (p.Ala710=) n.2207C>G n.2214C>G | gnomAD v4 |
21 | g.46125945C>T | CA513170408 | COL6A2 | c.2130C>T (p.Ala710=) n.2207C>T n.2214C>T | gnomAD v3 gnomAD v4 |
21 | g.46125946T>A | CA410541669 | COL6A2 | c.2131T>A (p.Tyr711Asn) n.2208T>A n.2215T>A | |
21 | g.46125946T>C | CA410541671 | COL6A2 | c.2131T>C (p.Tyr711His) n.2208T>C n.2215T>C | gnomAD v4 |
21 | g.46125946T>G | CA410541673 | COL6A2 | c.2131T>G (p.Tyr711Asp) n.2208T>G n.2215T>G | |
21 | g.46125947A= | CA2392507669 | COL6A2 | c.2132A= (p.Tyr711=) n.2209A= n.2216A= | |
21 | g.46125947A>C | CA410541676 | COL6A2 | c.2132A>C (p.Tyr711Ser) n.2209A>C n.2216A>C | |
21 | g.46125947A>G | CA10072445 | COL6A2 | c.2132A>G (p.Tyr711Cys) n.2209A>G n.2216A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
21 | g.46125947A>T | CA410541674 | COL6A2 | c.2132A>T (p.Tyr711Phe) n.2209A>T n.2216A>T | ClinVar |
21 | g.46125948C>A | CA410541679 | COL6A2 | c.2133C>A (p.Tyr711Ter) n.2210C>A n.2217C>A | ClinVar dbSNP |
21 | g.46125948C= | CA2392507670 | COL6A2 | c.2133C= (p.Tyr711=) n.2210C= n.2217C= | |
21 | g.46125948C>G | CA410541681 | COL6A2 | c.2133C>G (p.Tyr711Ter) n.2210C>G n.2217C>G | ClinVar dbSNP |
21 | g.46125948C>T | CA10072446 | COL6A2 | c.2133C>T (p.Tyr711=) n.2210C>T n.2217C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
21 | g.46125949G>A | CA10072447 | COL6A2 | c.2134G>A (p.Asp712Asn) n.2211G>A n.2218G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
21 | g.46125949G>C | CA410541685 | COL6A2 | c.2134G>C (p.Asp712His) n.2211G>C n.2218G>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
21 | g.46125949G= | CA2392507671 | COL6A2 | c.2134G= (p.Asp712=) n.2211G= n.2218G= | |
21 | g.46125949G>T | CA10653709 | COL6A2 | c.2134G>T (p.Asp712Tyr) n.2211G>T n.2218G>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |