Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.39589885T>ACA391670230FSIP1,THBS1c.2007T>A (p.Tyr669Ter)
c.771-1311A>T
c.1833T>A (p.Tyr611Ter)
n.2182T>A
15g.39589885T>CCA7472121FSIP1,THBS1c.2007T>C (p.Tyr669=)
c.771-1311A>G
c.1833T>C (p.Tyr611=)
n.2182T>C
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.39589885T>GCA391670229FSIP1,THBS1c.2007T>G (p.Tyr669Ter)
c.771-1311A>C
c.1833T>G (p.Tyr611Ter)
n.2182T>G
15g.39589885T=CA2171400152FSIP1,THBS1c.2007T= (p.Tyr669=)
c.771-1311A=
c.1833T= (p.Tyr611=)
n.2182T=
15g.39589886A=CA2171400153FSIP1,THBS1c.2008A= (p.Ser670=)
c.771-1312T=
c.1834A= (p.Ser612=)
n.2183A=
15g.39589886A>CCA391670231FSIP1,THBS1c.2008A>C (p.Ser670Arg)
c.771-1312T>G
c.1834A>C (p.Ser612Arg)
n.2183A>C
 dbSNP
15g.39589886A>GCA391670233FSIP1,THBS1c.2008A>G (p.Ser670Gly)
c.771-1312T>C
c.1834A>G (p.Ser612Gly)
n.2183A>G
15g.39589886A>TCA391670232FSIP1,THBS1c.2008A>T (p.Ser670Cys)
c.771-1312T>A
c.1834A>T (p.Ser612Cys)
n.2183A>T
15g.39589887G>ACA391670234FSIP1,THBS1c.2009G>A (p.Ser670Asn)
c.771-1313C>T
c.1835G>A (p.Ser612Asn)
n.2184G>A
15g.39589887G>CCA391670235FSIP1,THBS1c.2009G>C (p.Ser670Thr)
c.771-1313C>G
c.1835G>C (p.Ser612Thr)
n.2184G>C
15g.39589887G>TCA391670236FSIP1,THBS1c.2009G>T (p.Ser670Ile)
c.771-1313C>A
c.1835G>T (p.Ser612Ile)
n.2184G>T
15g.39589888C>ACA391670237FSIP1,THBS1c.2010C>A (p.Ser670Arg)
c.771-1314G>T
c.1836C>A (p.Ser612Arg)
n.2185C>A
15g.39589888C=CA2171400154FSIP1,THBS1c.2010C= (p.Ser670=)
c.771-1314G=
c.1836C= (p.Ser612=)
n.2185C=
15g.39589888C>GCA391670238FSIP1,THBS1c.2010C>G (p.Ser670Arg)
c.771-1314G>C
c.1836C>G (p.Ser612Arg)
n.2185C>G
15g.39589888C>TCA7472122FSIP1,THBS1c.2010C>T (p.Ser670=)
c.771-1314G>A
c.1836C>T (p.Ser612=)
n.2185C>T
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.39589889G>ACA7472123FSIP1,THBS1c.2011G>A (p.Asp671Asn)
c.771-1315C>T
c.1837G>A (p.Asp613Asn)
n.2186G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
15g.39589889G>CCA391670239FSIP1,THBS1c.2011G>C (p.Asp671His)
c.771-1315C>G
c.1837G>C (p.Asp613His)
n.2186G>C
 dbSNP
15g.39589889G=CA2171400155FSIP1,THBS1c.2011G= (p.Asp671=)
c.771-1315C=
c.1837G= (p.Asp613=)
n.2186G=
15g.39589889G>TCA391670240FSIP1,THBS1c.2011G>T (p.Asp671Tyr)
c.771-1315C>A
c.1837G>T (p.Asp613Tyr)
n.2186G>T
 gnomAD v4
15g.39589890A=CA2171400156FSIP1,THBS1c.2012A= (p.Asp671=)
c.771-1316T=
c.1838A= (p.Asp613=)
n.2187A=
15g.39589890A>CCA391670241FSIP1,THBS1c.2012A>C (p.Asp671Ala)
c.771-1316T>G
c.1838A>C (p.Asp613Ala)
n.2187A>C
15g.39589890A>GCA391670242FSIP1,THBS1c.2012A>G (p.Asp671Gly)
c.771-1316T>C
c.1838A>G (p.Asp613Gly)
n.2187A>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
15g.39589890A>TCA391670243FSIP1,THBS1c.2012A>T (p.Asp671Val)
c.771-1316T>A
c.1838A>T (p.Asp613Val)
n.2187A>T
15g.39589891C>ACA391670244FSIP1,THBS1c.2013C>A (p.Asp671Glu)
c.771-1317G>T
c.1839C>A (p.Asp613Glu)
n.2188C>A
 gnomAD v4
15g.39589891C=CA2171400157FSIP1,THBS1c.2013C= (p.Asp671=)
c.771-1317G=
c.1839C= (p.Asp613=)
n.2188C=
15g.39589891C>GCA391670245FSIP1,THBS1c.2013C>G (p.Asp671Glu)
c.771-1317G>C
c.1839C>G (p.Asp613Glu)
n.2188C>G
15g.39589891C>TCA7472124FSIP1,THBS1c.2013C>T (p.Asp671=)
c.771-1317G>A
c.1839C>T (p.Asp613=)
n.2188C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.39589892C>ACA391670246FSIP1,THBS1c.2014C>A (p.Pro672Thr)
c.771-1318G>T
c.1840C>A (p.Pro614Thr)
n.2189C>A
15g.39589892C>GCA391670247FSIP1,THBS1c.2014C>G (p.Pro672Ala)
c.771-1318G>C
c.1840C>G (p.Pro614Ala)
n.2189C>G
15g.39589892C>TCA391670248FSIP1,THBS1c.2014C>T (p.Pro672Ser)
c.771-1318G>A
c.1840C>T (p.Pro614Ser)
n.2189C>T
15g.39589893C>ACA7472125FSIP1,THBS1c.2015C>A (p.Pro672His)
c.771-1319G>T
c.1841C>A (p.Pro614His)
n.2190C>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.39589893C=CA2171400158FSIP1,THBS1c.2015C= (p.Pro672=)
c.771-1319G=
c.1841C= (p.Pro614=)
n.2190C=
15g.39589893C>GCA391670249FSIP1,THBS1c.2015C>G (p.Pro672Arg)
c.771-1319G>C
c.1841C>G (p.Pro614Arg)
n.2190C>G
15g.39589893C>TCA391670250FSIP1,THBS1c.2015C>T (p.Pro672Leu)
c.771-1319G>A
c.1841C>T (p.Pro614Leu)
n.2190C>T
15g.39589894C>ACA489673261FSIP1,THBS1c.2016C>A (p.Pro672=)
c.771-1320G>T
c.1842C>A (p.Pro614=)
n.2191C>A
15g.39589894C>GCA489673264FSIP1,THBS1c.2016C>G (p.Pro672=)
c.771-1320G>C
c.1842C>G (p.Pro614=)
n.2191C>G
 COSMIC
15g.39589894C>TCA489673266FSIP1,THBS1c.2016C>T (p.Pro672=)
c.771-1320G>A
c.1842C>T (p.Pro614=)
n.2191C>T
15g.39589895A=CA2171400159FSIP1,THBS1c.2017A= (p.Met673=)
c.771-1321T=
c.1843A= (p.Met615=)
n.2192A=
15g.39589895A>CCA7472126FSIP1,THBS1c.2017A>C (p.Met673Leu)
c.771-1321T>G
c.1843A>C (p.Met615Leu)
n.2192A>C
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.39589895A>GCA268725276FSIP1,THBS1c.2017A>G (p.Met673Val)
c.771-1321T>C
c.1843A>G (p.Met615Val)
n.2192A>G
 dbSNP
15g.39589895A>TCA391670251FSIP1,THBS1c.2017A>T (p.Met673Leu)
c.771-1321T>A
c.1843A>T (p.Met615Leu)
n.2192A>T
15g.39589896T>ACA391670253FSIP1,THBS1c.2018T>A (p.Met673Lys)
c.771-1322A>T
c.1844T>A (p.Met615Lys)
n.2193T>A
15g.39589896T>CCA7472127FSIP1,THBS1c.2018T>C (p.Met673Thr)
c.771-1322A>G
c.1844T>C (p.Met615Thr)
n.2193T>C
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.39589896T>GCA391670252FSIP1,THBS1c.2018T>G (p.Met673Arg)
c.771-1322A>C
c.1844T>G (p.Met615Arg)
n.2193T>G
15g.39589896T=CA2171400160FSIP1,THBS1c.2018T= (p.Met673=)
c.771-1322A=
c.1844T= (p.Met615=)
n.2193T=
15g.39589897G>ACA391670254FSIP1,THBS1c.2019G>A (p.Met673Ile)
c.771-1323C>T
c.1845G>A (p.Met615Ile)
n.2194G>A
 dbSNP gnomAD v2 gnomAD v4
15g.39589897G>CCA391670255FSIP1,THBS1c.2019G>C (p.Met673Ile)
c.771-1323C>G
c.1845G>C (p.Met615Ile)
n.2194G>C
15g.39589897G=CA2171400161FSIP1,THBS1c.2019G= (p.Met673=)
c.771-1323C=
c.1845G= (p.Met615=)
n.2194G=
15g.39589897G>TCA391670256FSIP1,THBS1c.2019G>T (p.Met673Ile)
c.771-1323C>A
c.1845G>T (p.Met615Ile)
n.2194G>T
15g.39589898T>ACA391670257FSIP1,THBS1c.2020T>A (p.Tyr674Asn)
c.771-1324A>T
c.1846T>A (p.Tyr616Asn)
n.2195T>A
15g.39589898T>CCA7472128FSIP1,THBS1c.2020T>C (p.Tyr674His)
c.771-1324A>G
c.1846T>C (p.Tyr616His)
n.2195T>C
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.39589898T>GCA391670258FSIP1,THBS1c.2020T>G (p.Tyr674Asp)
c.771-1324A>C
c.1846T>G (p.Tyr616Asp)
n.2195T>G
15g.39589898T=CA2171400162FSIP1,THBS1c.2020T= (p.Tyr674=)
c.771-1324A=
c.1846T= (p.Tyr616=)
n.2195T=
15g.39589899A>CCA391670261FSIP1,THBS1c.2021A>C (p.Tyr674Ser)
c.771-1325T>G
c.1847A>C (p.Tyr616Ser)
n.2196A>C
15g.39589899A>GCA391670259FSIP1,THBS1c.2021A>G (p.Tyr674Cys)
c.771-1325T>C
c.1847A>G (p.Tyr616Cys)
n.2196A>G
15g.39589899A>TCA391670260FSIP1,THBS1c.2021A>T (p.Tyr674Phe)
c.771-1325T>A
c.1847A>T (p.Tyr616Phe)
n.2196A>T
 dbSNP
15g.39589900C>ACA391670262FSIP1,THBS1c.2022C>A (p.Tyr674Ter)
c.771-1326G>T
c.1848C>A (p.Tyr616Ter)
n.2197C>A
15g.39589900C>GCA391670263FSIP1,THBS1c.2022C>G (p.Tyr674Ter)
c.771-1326G>C
c.1848C>G (p.Tyr616Ter)
n.2197C>G
15g.39589900C>TCA489673290FSIP1,THBS1c.2022C>T (p.Tyr674=)
c.771-1326G>A
c.1848C>T (p.Tyr616=)
n.2197C>T
 gnomAD v4 COSMIC
15g.39589901C>ACA391670264FSIP1,THBS1c.2023C>A (p.Arg675Ser)
c.771-1327G>T
c.1849C>A (p.Arg617Ser)
n.2198C>A
15g.39589901C=CA2171400163FSIP1,THBS1c.2023C= (p.Arg675=)
c.771-1327G=
c.1849C= (p.Arg617=)
n.2198C=
15g.39589901C>GCA391670265FSIP1,THBS1c.2023C>G (p.Arg675Gly)
c.771-1327G>C
c.1849C>G (p.Arg617Gly)
n.2198C>G
15g.39589901C>TCA391670266FSIP1,THBS1c.2023C>T (p.Arg675Cys)
c.771-1327G>A
c.1849C>T (p.Arg617Cys)
n.2198C>T
 dbSNP gnomAD v3 gnomAD v4
15g.39589902G>ACA391670267FSIP1,THBS1c.2024G>A (p.Arg675His)
c.771-1328C>T
c.1850G>A (p.Arg617His)
n.2199G>A
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.39589902G>CCA391670269FSIP1,THBS1c.2024G>C (p.Arg675Pro)
c.771-1328C>G
c.1850G>C (p.Arg617Pro)
n.2199G>C
15g.39589902G=CA2171400164FSIP1,THBS1c.2024G= (p.Arg675=)
c.771-1328C=
c.1850G= (p.Arg617=)
n.2199G=
15g.39589902G>TCA391670268FSIP1,THBS1c.2024G>T (p.Arg675Leu)
c.771-1328C>A
c.1850G>T (p.Arg617Leu)
n.2199G>T
 gnomAD v4
15g.39589903C>ACA489673301FSIP1,THBS1c.2025C>A (p.Arg675=)
c.771-1329G>T
c.1851C>A (p.Arg617=)
n.2200C>A
15g.39589903C>GCA489673304FSIP1,THBS1c.2025C>G (p.Arg675=)
c.771-1329G>C
c.1851C>G (p.Arg617=)
n.2200C>G
15g.39589903C>TCA489673306FSIP1,THBS1c.2025C>T (p.Arg675=)
c.771-1329G>A
c.1851C>T (p.Arg617=)
n.2200C>T
15g.39589904T>ACA391670270FSIP1,THBS1c.2026T>A (p.Cys676Ser)
c.771-1330A>T
c.1852T>A (p.Cys618Ser)
n.2201T>A
15g.39589904T>CCA391670271FSIP1,THBS1c.2026T>C (p.Cys676Arg)
c.771-1330A>G
c.1852T>C (p.Cys618Arg)
n.2201T>C
15g.39589904T>GCA391670272FSIP1,THBS1c.2026T>G (p.Cys676Gly)
c.771-1330A>C
c.1852T>G (p.Cys618Gly)
n.2201T>G
15g.39589905G>ACA391670273FSIP1,THBS1c.2027G>A (p.Cys676Tyr)
c.771-1331C>T
c.1853G>A (p.Cys618Tyr)
n.2202G>A
15g.39589905G>CCA391670274FSIP1,THBS1c.2027G>C (p.Cys676Ser)
c.771-1331C>G
c.1853G>C (p.Cys618Ser)
n.2202G>C
15g.39589905G>TCA391670275FSIP1,THBS1c.2027G>T (p.Cys676Phe)
c.771-1331C>A
c.1853G>T (p.Cys618Phe)
n.2202G>T
15g.39589906C>ACA391670276FSIP1,THBS1c.2028C>A (p.Cys676Ter)
c.771-1332G>T
c.1854C>A (p.Cys618Ter)
n.2203C>A
15g.39589906C=CA2171400165FSIP1,THBS1c.2028C= (p.Cys676=)
c.771-1332G=
c.1854C= (p.Cys618=)
n.2203C=
15g.39589906C>GCA391670277FSIP1,THBS1c.2028C>G (p.Cys676Trp)
c.771-1332G>C
c.1854C>G (p.Cys618Trp)
n.2203C>G
15g.39589906C>TCA7472129FSIP1,THBS1c.2028C>T (p.Cys676=)
c.771-1332G>A
c.1854C>T (p.Cys618=)
n.2203C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.39589907G>ACA7472130FSIP1,THBS1c.2029G>A (p.Glu677Lys)
c.771-1333C>T
c.1855G>A (p.Glu619Lys)
n.2204G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.39589907G>CCA391670278FSIP1,THBS1c.2029G>C (p.Glu677Gln)
c.771-1333C>G
c.1855G>C (p.Glu619Gln)
n.2204G>C
15g.39589907G=CA2171400166FSIP1,THBS1c.2029G= (p.Glu677=)
c.771-1333C=
c.1855G= (p.Glu619=)
n.2204G=
15g.39589907G>TCA391670279FSIP1,THBS1c.2029G>T (p.Glu677Ter)
c.771-1333C>A
c.1855G>T (p.Glu619Ter)
n.2204G>T
 COSMIC
15g.39589908A>CCA391670281FSIP1,THBS1c.2030A>C (p.Glu677Ala)
c.771-1334T>G
c.1856A>C (p.Glu619Ala)
n.2205A>C
15g.39589908A>GCA391670282FSIP1,THBS1c.2030A>G (p.Glu677Gly)
c.771-1334T>C
c.1856A>G (p.Glu619Gly)
n.2205A>G
15g.39589908A>TCA391670280FSIP1,THBS1c.2030A>T (p.Glu677Val)
c.771-1334T>A
c.1856A>T (p.Glu619Val)
n.2205A>T
15g.39589909G>ACA7472131FSIP1,THBS1c.2031G>A (p.Glu677=)
c.771-1335C>T
c.1857G>A (p.Glu619=)
n.2206G>A
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.39589909G>CCA391670283FSIP1,THBS1c.2031G>C (p.Glu677Asp)
c.771-1335C>G
c.1857G>C (p.Glu619Asp)
n.2206G>C
 dbSNP gnomAD v3 gnomAD v4
15g.39589909G=CA2171400167FSIP1,THBS1c.2031G= (p.Glu677=)
c.771-1335C=
c.1857G= (p.Glu619=)
n.2206G=
15g.39589909G>TCA391670284FSIP1,THBS1c.2031G>T (p.Glu677Asp)
c.771-1335C>A
c.1857G>T (p.Glu619Asp)
n.2206G>T
15g.39589910T>ACA391670285FSIP1,THBS1c.2032T>A (p.Cys678Ser)
c.771-1336A>T
c.1858T>A (p.Cys620Ser)
n.2207T>A
15g.39589910T>CCA391670286FSIP1,THBS1c.2032T>C (p.Cys678Arg)
c.771-1336A>G
c.1858T>C (p.Cys620Arg)
n.2207T>C
15g.39589910T>GCA391670287FSIP1,THBS1c.2032T>G (p.Cys678Gly)
c.771-1336A>C
c.1858T>G (p.Cys620Gly)
n.2207T>G
15g.39589911G>ACA391670288FSIP1,THBS1c.2033G>A (p.Cys678Tyr)
c.771-1337C>T
c.1859G>A (p.Cys620Tyr)
n.2208G>A
 gnomAD v4
15g.39589911G>CCA391670289FSIP1,THBS1c.2033G>C (p.Cys678Ser)
c.771-1337C>G
c.1859G>C (p.Cys620Ser)
n.2208G>C
15g.39589911G>TCA391670290FSIP1,THBS1c.2033G>T (p.Cys678Phe)
c.771-1337C>A
c.1859G>T (p.Cys620Phe)
n.2208G>T
15g.39589912C>ACA391670291FSIP1,THBS1c.2034C>A (p.Cys678Ter)
c.771-1338G>T
c.1860C>A (p.Cys620Ter)
n.2209C>A
15g.39589912C>GCA391670292FSIP1,THBS1c.2034C>G (p.Cys678Trp)
c.771-1338G>C
c.1860C>G (p.Cys620Trp)
n.2209C>G
15g.39589912C>TCA489673340FSIP1,THBS1c.2034C>T (p.Cys678=)
c.771-1338G>A
c.1860C>T (p.Cys620=)
n.2209C>T
15g.39589913A>CCA391670293FSIP1,THBS1c.2035A>C (p.Lys679Gln)
c.771-1339T>G
c.1861A>C (p.Lys621Gln)
n.2210A>C
15g.39589913A>GCA391670294FSIP1,THBS1c.2035A>G (p.Lys679Glu)
c.771-1339T>C
c.1861A>G (p.Lys621Glu)
n.2210A>G
 gnomAD v4
15g.39589913A>TCA391670295FSIP1,THBS1c.2035A>T (p.Lys679Ter)
c.771-1339T>A
c.1861A>T (p.Lys621Ter)
n.2210A>T
15g.39589914A>CCA391670298FSIP1,THBS1c.2036A>C (p.Lys679Thr)
c.771-1340T>G
c.1862A>C (p.Lys621Thr)
n.2211A>C
15g.39589914A>GCA391670297FSIP1,THBS1c.2036A>G (p.Lys679Arg)
c.771-1340T>C
c.1862A>G (p.Lys621Arg)
n.2211A>G
15g.39589914A>TCA391670296FSIP1,THBS1c.2036A>T (p.Lys679Met)
c.771-1340T>A
c.1862A>T (p.Lys621Met)
n.2211A>T
 gnomAD v4
15g.39589915G>ACA489673348FSIP1,THBS1c.2037G>A (p.Lys679=)
c.771-1341C>T
c.1863G>A (p.Lys621=)
n.2212G>A
15g.39589915G>CCA391670299FSIP1,THBS1c.2037G>C (p.Lys679Asn)
c.771-1341C>G
c.1863G>C (p.Lys621Asn)
n.2212G>C
15g.39589915G>TCA391670300FSIP1,THBS1c.2037G>T (p.Lys679Asn)
c.771-1341C>A
c.1863G>T (p.Lys621Asn)
n.2212G>T
15g.39589916C>ACA391670301FSIP1,THBS1c.2038C>A (p.Pro680Thr)
c.771-1342G>T
c.1864C>A (p.Pro622Thr)
n.2213C>A
15g.39589916C>GCA391670302FSIP1,THBS1c.2038C>G (p.Pro680Ala)
c.771-1342G>C
c.1864C>G (p.Pro622Ala)
n.2213C>G
15g.39589916C>TCA391670303FSIP1,THBS1c.2038C>T (p.Pro680Ser)
c.771-1342G>A
c.1864C>T (p.Pro622Ser)
n.2213C>T
15g.39589917C>ACA391670304FSIP1,THBS1c.2039C>A (p.Pro680His)
c.771-1343G>T
c.1865C>A (p.Pro622His)
n.2214C>A
15g.39589917C>GCA391670305FSIP1,THBS1c.2039C>G (p.Pro680Arg)
c.771-1343G>C
c.1865C>G (p.Pro622Arg)
n.2214C>G
15g.39589917C>TCA391670306FSIP1,THBS1c.2039C>T (p.Pro680Leu)
c.771-1343G>A
c.1865C>T (p.Pro622Leu)
n.2214C>T
15g.39589918T>ACA489673360FSIP1,THBS1c.2040T>A (p.Pro680=)
c.771-1344A>T
c.1866T>A (p.Pro622=)
n.2215T>A
15g.39589918T>CCA489673362FSIP1,THBS1c.2040T>C (p.Pro680=)
c.771-1344A>G
c.1866T>C (p.Pro622=)
n.2215T>C
15g.39589918T>GCA489673364FSIP1,THBS1c.2040T>G (p.Pro680=)
c.771-1344A>C
c.1866T>G (p.Pro622=)
n.2215T>G
15g.39589919G>ACA391670307FSIP1,THBS1c.2041G>A (p.Gly681Ser)
c.771-1345C>T
c.1867G>A (p.Gly623Ser)
n.2216G>A
 dbSNP
15g.39589919G>CCA391670308FSIP1,THBS1c.2041G>C (p.Gly681Arg)
c.771-1345C>G
c.1867G>C (p.Gly623Arg)
n.2216G>C
15g.39589919G=CA2171400168FSIP1,THBS1c.2041G= (p.Gly681=)
c.771-1345C=
c.1867G= (p.Gly623=)
n.2216G=
15g.39589919G>TCA391670309FSIP1,THBS1c.2041G>T (p.Gly681Cys)
c.771-1345C>A
c.1867G>T (p.Gly623Cys)
n.2216G>T
15g.39589920G>ACA391670310FSIP1,THBS1c.2042G>A (p.Gly681Asp)
c.771-1346C>T
c.1868G>A (p.Gly623Asp)
n.2217G>A
15g.39589920G>CCA391670311FSIP1,THBS1c.2042G>C (p.Gly681Ala)
c.771-1346C>G
c.1868G>C (p.Gly623Ala)
n.2217G>C
15g.39589920G>TCA391670312FSIP1,THBS1c.2042G>T (p.Gly681Val)
c.771-1346C>A
c.1868G>T (p.Gly623Val)
n.2217G>T
15g.39589921C>ACA489673373FSIP1,THBS1c.2043C>A (p.Gly681=)
c.771-1347G>T
c.1869C>A (p.Gly623=)
n.2218C>A
15g.39589921C>GCA489673374FSIP1,THBS1c.2043C>G (p.Gly681=)
c.771-1347G>C
c.1869C>G (p.Gly623=)
n.2218C>G
15g.39589921C>TCA489673377FSIP1,THBS1c.2043C>T (p.Gly681=)
c.771-1347G>A
c.1869C>T (p.Gly623=)
n.2218C>T
 COSMIC
15g.39589922T>ACA391670315FSIP1,THBS1c.2044T>A (p.Tyr682Asn)
c.771-1348A>T
c.1870T>A (p.Tyr624Asn)
n.2219T>A
15g.39589922T>CCA391670314FSIP1,THBS1c.2044T>C (p.Tyr682His)
c.771-1348A>G
c.1870T>C (p.Tyr624His)
n.2219T>C
15g.39589922T>GCA391670313FSIP1,THBS1c.2044T>G (p.Tyr682Asp)
c.771-1348A>C
c.1870T>G (p.Tyr624Asp)
n.2219T>G
15g.39589923A=CA2171400169FSIP1,THBS1c.2045A= (p.Tyr682=)
c.771-1349T=
c.1871A= (p.Tyr624=)
n.2220A=
15g.39589923A>CCA391670316FSIP1,THBS1c.2045A>C (p.Tyr682Ser)
c.771-1349T>G
c.1871A>C (p.Tyr624Ser)
n.2220A>C
15g.39589923A>GCA391670317FSIP1,THBS1c.2045A>G (p.Tyr682Cys)
c.771-1349T>C
c.1871A>G (p.Tyr624Cys)
n.2220A>G
 dbSNP
15g.39589923A>TCA391670318FSIP1,THBS1c.2045A>T (p.Tyr682Phe)
c.771-1349T>A
c.1871A>T (p.Tyr624Phe)
n.2220A>T
 dbSNP gnomAD v2 gnomAD v4
15g.39589924C>ACA391670319FSIP1,THBS1c.2046C>A (p.Tyr682Ter)
c.771-1350G>T
c.1872C>A (p.Tyr624Ter)
n.2221C>A
15g.39589924C=CA2171400170FSIP1,THBS1c.2046C= (p.Tyr682=)
c.771-1350G=
c.1872C= (p.Tyr624=)
n.2221C=
15g.39589924C>GCA391670320FSIP1,THBS1c.2046C>G (p.Tyr682Ter)
c.771-1350G>C
c.1872C>G (p.Tyr624Ter)
n.2221C>G
15g.39589924C>TCA7472132FSIP1,THBS1c.2046C>T (p.Tyr682=)
c.771-1350G>A
c.1872C>T (p.Tyr624=)
n.2221C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.39589925G>ACA7472133FSIP1,THBS1c.2047G>A (p.Ala683Thr)
c.771-1351C>T
c.1873G>A (p.Ala625Thr)
n.2222G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.39589925G>CCA391670322FSIP1,THBS1c.2047G>C (p.Ala683Pro)
c.771-1351C>G
c.1873G>C (p.Ala625Pro)
n.2222G>C
15g.39589925G=CA2171400171FSIP1,THBS1c.2047G= (p.Ala683=)
c.771-1351C=
c.1873G= (p.Ala625=)
n.2222G=
15g.39589925G>TCA391670321FSIP1,THBS1c.2047G>T (p.Ala683Ser)
c.771-1351C>A
c.1873G>T (p.Ala625Ser)
n.2222G>T
15g.39589926C>ACA391670323FSIP1,THBS1c.2048C>A (p.Ala683Asp)
c.771-1352G>T
c.1874C>A (p.Ala625Asp)
n.2223C>A
15g.39589926C>GCA391670324FSIP1,THBS1c.2048C>G (p.Ala683Gly)
c.771-1352G>C
c.1874C>G (p.Ala625Gly)
n.2223C>G
15g.39589926C>TCA391670325FSIP1,THBS1c.2048C>T (p.Ala683Val)
c.771-1352G>A
c.1874C>T (p.Ala625Val)
n.2223C>T
15g.39589927T>ACA489673401FSIP1,THBS1c.2049T>A (p.Ala683=)
c.771-1353A>T
c.1875T>A (p.Ala625=)
n.2224T>A
15g.39589927T>CCA489673398FSIP1,THBS1c.2049T>C (p.Ala683=)
c.771-1353A>G
c.1875T>C (p.Ala625=)
n.2224T>C
15g.39589927T>GCA489673399FSIP1,THBS1c.2049T>G (p.Ala683=)
c.771-1353A>C
c.1875T>G (p.Ala625=)
n.2224T>G
15g.39589928G>ACA7472134FSIP1,THBS1c.2050G>A (p.Gly684Ser)
c.771-1354C>T
c.1876G>A (p.Gly626Ser)
n.2225G>A
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.39589928G>CCA391670326FSIP1,THBS1c.2050G>C (p.Gly684Arg)
c.771-1354C>G
c.1876G>C (p.Gly626Arg)
n.2225G>C
15g.39589928G=CA2171400172FSIP1,THBS1c.2050G= (p.Gly684=)
c.771-1354C=
c.1876G= (p.Gly626=)
n.2225G=
15g.39589928G>TCA391670327FSIP1,THBS1c.2050G>T (p.Gly684Cys)
c.771-1354C>A
c.1876G>T (p.Gly626Cys)
n.2225G>T
15g.39589929G>ACA391670328FSIP1,THBS1c.2051G>A (p.Gly684Asp)
c.771-1355C>T
c.1877G>A (p.Gly626Asp)
n.2226G>A
15g.39589929G>CCA391670330FSIP1,THBS1c.2051G>C (p.Gly684Ala)
c.771-1355C>G
c.1877G>C (p.Gly626Ala)
n.2226G>C
15g.39589929G>TCA391670329FSIP1,THBS1c.2051G>T (p.Gly684Val)
c.771-1355C>A
c.1877G>T (p.Gly626Val)
n.2226G>T
15g.39589930C>ACA489673410FSIP1,THBS1c.2052C>A (p.Gly684=)
c.771-1356G>T
c.1878C>A (p.Gly626=)
n.2227C>A
 dbSNP
15g.39589930C=CA2171400173FSIP1,THBS1c.2052C= (p.Gly684=)
c.771-1356G=
c.1878C= (p.Gly626=)
n.2227C=
15g.39589930C>GCA489673411FSIP1,THBS1c.2052C>G (p.Gly684=)
c.771-1356G>C
c.1878C>G (p.Gly626=)
n.2227C>G
15g.39589930C>TCA489673413FSIP1,THBS1c.2052C>T (p.Gly684=)
c.771-1356G>A
c.1878C>T (p.Gly626=)
n.2227C>T
15g.39589931A>CCA391670331FSIP1,THBS1c.2053A>C (p.Asn685His)
c.771-1357T>G
c.1879A>C (p.Asn627His)
n.2228A>C
15g.39589931A>GCA391670332FSIP1,THBS1c.2053A>G (p.Asn685Asp)
c.771-1357T>C
c.1879A>G (p.Asn627Asp)
n.2228A>G
15g.39589931A>TCA391670333FSIP1,THBS1c.2053A>T (p.Asn685Tyr)
c.771-1357T>A
c.1879A>T (p.Asn627Tyr)
n.2228A>T
15g.39589932A>CCA391670334FSIP1,THBS1c.2054A>C (p.Asn685Thr)
c.771-1358T>G
c.1880A>C (p.Asn627Thr)
n.2229A>C
15g.39589932A>GCA391670335FSIP1,THBS1c.2054A>G (p.Asn685Ser)
c.771-1358T>C
c.1880A>G (p.Asn627Ser)
n.2229A>G
 gnomAD v4
15g.39589932A>TCA391670336FSIP1,THBS1c.2054A>T (p.Asn685Ile)
c.771-1358T>A
c.1880A>T (p.Asn627Ile)
n.2229A>T
15g.39589933T>ACA391670337FSIP1,THBS1c.2055T>A (p.Asn685Lys)
c.771-1359A>T
c.1881T>A (p.Asn627Lys)
n.2230T>A
15g.39589933T>CCA489673423FSIP1,THBS1c.2055T>C (p.Asn685=)
c.771-1359A>G
c.1881T>C (p.Asn627=)
n.2230T>C
 dbSNP gnomAD v4
15g.39589933T>GCA391670338FSIP1,THBS1c.2055T>G (p.Asn685Lys)
c.771-1359A>C
c.1881T>G (p.Asn627Lys)
n.2230T>G
15g.39589933T=CA2171400174FSIP1,THBS1c.2055T= (p.Asn685=)
c.771-1359A=
c.1881T= (p.Asn627=)
n.2230T=
15g.39589934G>ACA391670339FSIP1,THBS1c.2056G>A (p.Gly686Ser)
c.771-1360C>T
c.1882G>A (p.Gly628Ser)
n.2231G>A
15g.39589934G>CCA391670340FSIP1,THBS1c.2056G>C (p.Gly686Arg)
c.771-1360C>G
c.1882G>C (p.Gly628Arg)
n.2231G>C
15g.39589934G>TCA391670341FSIP1,THBS1c.2056G>T (p.Gly686Cys)
c.771-1360C>A
c.1882G>T (p.Gly628Cys)
n.2231G>T
15g.39589935G>ACA391670344FSIP1,THBS1c.2057G>A (p.Gly686Asp)
c.771-1361C>T
c.1883G>A (p.Gly628Asp)
n.2232G>A
15g.39589935G>CCA391670342FSIP1,THBS1c.2057G>C (p.Gly686Ala)
c.771-1361C>G
c.1883G>C (p.Gly628Ala)
n.2232G>C
 dbSNP gnomAD v2 gnomAD v4
15g.39589935G=CA2171400175FSIP1,THBS1c.2057G= (p.Gly686=)
c.771-1361C=
c.1883G= (p.Gly628=)
n.2232G=
15g.39589935G>TCA391670343FSIP1,THBS1c.2057G>T (p.Gly686Val)
c.771-1361C>A
c.1883G>T (p.Gly628Val)
n.2232G>T
15g.39589936C>ACA489673445FSIP1,THBS1c.2058C>A (p.Gly686=)
c.771-1362G>T
c.1884C>A (p.Gly628=)
n.2233C>A
 gnomAD v4
15g.39589936C>GCA489673446FSIP1,THBS1c.2058C>G (p.Gly686=)
c.771-1362G>C
c.1884C>G (p.Gly628=)
n.2233C>G
15g.39589936C>TCA489673448FSIP1,THBS1c.2058C>T (p.Gly686=)
c.771-1362G>A
c.1884C>T (p.Gly628=)
n.2233C>T
 gnomAD v4
15g.39589937A=CA2171400176FSIP1,THBS1c.2059A= (p.Ile687=)
c.771-1363T=
c.1885A= (p.Ile629=)
n.2234A=
15g.39589937A>CCA391670345FSIP1,THBS1c.2059A>C (p.Ile687Leu)
c.771-1363T>G
c.1885A>C (p.Ile629Leu)
n.2234A>C
15g.39589937A>GCA7472135FSIP1,THBS1c.2059A>G (p.Ile687Val)
c.771-1363T>C
c.1885A>G (p.Ile629Val)
n.2234A>G
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.39589937A>TCA391670346FSIP1,THBS1c.2059A>T (p.Ile687Phe)
c.771-1363T>A
c.1885A>T (p.Ile629Phe)
n.2234A>T
 dbSNP gnomAD v2 gnomAD v4
15g.39589938T>ACA7472136FSIP1,THBS1c.2060T>A (p.Ile687Asn)
c.771-1364A>T
c.1886T>A (p.Ile629Asn)
n.2235T>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.39589938T>CCA391670347FSIP1,THBS1c.2060T>C (p.Ile687Thr)
c.771-1364A>G
c.1886T>C (p.Ile629Thr)
n.2235T>C
15g.39589938T>GCA391670348FSIP1,THBS1c.2060T>G (p.Ile687Ser)
c.771-1364A>C
c.1886T>G (p.Ile629Ser)
n.2235T>G
15g.39589938T=CA2171400177FSIP1,THBS1c.2060T= (p.Ile687=)
c.771-1364A=
c.1886T= (p.Ile629=)
n.2235T=
15g.39589939C>ACA489673463FSIP1,THBS1c.2061C>A (p.Ile687=)
c.771-1365G>T
c.1887C>A (p.Ile629=)
n.2236C>A
15g.39589939C>GCA391670349FSIP1,THBS1c.2061C>G (p.Ile687Met)
c.771-1365G>C
c.1887C>G (p.Ile629Met)
n.2236C>G
15g.39589939C>TCA489673468FSIP1,THBS1c.2061C>T (p.Ile687=)
c.771-1365G>A
c.1887C>T (p.Ile629=)
n.2236C>T
 gnomAD v4
15g.39589940A=CA2171400178FSIP1,THBS1c.2062A= (p.Ile688=)
c.771-1366T=
c.1888A= (p.Ile630=)
n.2237A=
15g.39589940A>CCA391670350FSIP1,THBS1c.2062A>C (p.Ile688Leu)
c.771-1366T>G
c.1888A>C (p.Ile630Leu)
n.2237A>C
15g.39589940A>GCA391670351FSIP1,THBS1c.2062A>G (p.Ile688Val)
c.771-1366T>C
c.1888A>G (p.Ile630Val)
n.2237A>G
 dbSNP
15g.39589940A>TCA7472137FSIP1,THBS1c.2062A>T (p.Ile688Phe)
c.771-1366T>A
c.1888A>T (p.Ile630Phe)
n.2237A>T
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.39589941T>ACA391670352FSIP1,THBS1c.2063T>A (p.Ile688Asn)
c.771-1367A>T
c.1889T>A (p.Ile630Asn)
n.2238T>A
15g.39589941T>CCA391670353FSIP1,THBS1c.2063T>C (p.Ile688Thr)
c.771-1367A>G
c.1889T>C (p.Ile630Thr)
n.2238T>C
15g.39589941T>GCA391670354FSIP1,THBS1c.2063T>G (p.Ile688Ser)
c.771-1367A>C
c.1889T>G (p.Ile630Ser)
n.2238T>G
15g.39589942C>ACA489673480FSIP1,THBS1c.2064C>A (p.Ile688=)
c.771-1368G>T
c.1890C>A (p.Ile630=)
n.2239C>A
15g.39589942C>GCA391670355FSIP1,THBS1c.2064C>G (p.Ile688Met)
c.771-1368G>C
c.1890C>G (p.Ile630Met)
n.2239C>G
15g.39589942C>TCA489673481FSIP1,THBS1c.2064C>T (p.Ile688=)
c.771-1368G>A
c.1890C>T (p.Ile630=)
n.2239C>T
15g.39589943T>ACA391670358FSIP1,THBS1c.2065T>A (p.Cys689Ser)
c.771-1369A>T
c.1891T>A (p.Cys631Ser)
n.2240T>A
15g.39589943T>CCA391670357FSIP1,THBS1c.2065T>C (p.Cys689Arg)
c.771-1369A>G
c.1891T>C (p.Cys631Arg)
n.2240T>C
15g.39589943T>GCA391670356FSIP1,THBS1c.2065T>G (p.Cys689Gly)
c.771-1369A>C
c.1891T>G (p.Cys631Gly)
n.2240T>G
15g.39589944G>ACA391670359FSIP1,THBS1c.2066G>A (p.Cys689Tyr)
c.771-1370C>T
c.1892G>A (p.Cys631Tyr)
n.2241G>A
15g.39589944G>CCA391670360FSIP1,THBS1c.2066G>C (p.Cys689Ser)
c.771-1370C>G
c.1892G>C (p.Cys631Ser)
n.2241G>C
15g.39589944G>TCA391670361FSIP1,THBS1c.2066G>T (p.Cys689Phe)
c.771-1370C>A
c.1892G>T (p.Cys631Phe)
n.2241G>T
15g.39589945C>ACA391670362FSIP1,THBS1c.2067C>A (p.Cys689Ter)
c.771-1371G>T
c.1893C>A (p.Cys631Ter)
n.2242C>A
15g.39589945C=CA2171400179FSIP1,THBS1c.2067C= (p.Cys689=)
c.771-1371G=
c.1893C= (p.Cys631=)
n.2242C=
15g.39589945C>GCA391670363FSIP1,THBS1c.2067C>G (p.Cys689Trp)
c.771-1371G>C
c.1893C>G (p.Cys631Trp)
n.2242C>G
15g.39589945C>TCA7472138FSIP1,THBS1c.2067C>T (p.Cys689=)
c.771-1371G>A
c.1893C>T (p.Cys631=)
n.2242C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.39589946G>ACA7472139FSIP1,THBS1c.2068G>A (p.Gly690Arg)
c.771-1372C>T
c.1894G>A (p.Gly632Arg)
n.2243G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.39589946G>CCA391670364FSIP1,THBS1c.2068G>C (p.Gly690Arg)
c.771-1372C>G
c.1894G>C (p.Gly632Arg)
n.2243G>C
15g.39589946G=CA2171400180FSIP1,THBS1c.2068G= (p.Gly690=)
c.771-1372C=
c.1894G= (p.Gly632=)
n.2243G=
15g.39589946G>TCA391670365FSIP1,THBS1c.2068G>T (p.Gly690Trp)
c.771-1372C>A
c.1894G>T (p.Gly632Trp)
n.2243G>T
 gnomAD v4
15g.39589947G>ACA391670366FSIP1,THBS1c.2069G>A (p.Gly690Glu)
c.771-1373C>T
c.1895G>A (p.Gly632Glu)
n.2244G>A
15g.39589947G>CCA391670367FSIP1,THBS1c.2069G>C (p.Gly690Ala)
c.771-1373C>G
c.1895G>C (p.Gly632Ala)
n.2244G>C
15g.39589947G>TCA391670368FSIP1,THBS1c.2069G>T (p.Gly690Val)
c.771-1373C>A
c.1895G>T (p.Gly632Val)
n.2244G>T
15g.39589948G>ACA489673504FSIP1,THBS1c.2070G>A (p.Gly690=)
c.771-1374C>T
c.1896G>A (p.Gly632=)
n.2245G>A
15g.39589948G>CCA489673506FSIP1,THBS1c.2070G>C (p.Gly690=)
c.771-1374C>G
c.1896G>C (p.Gly632=)
n.2245G>C
 dbSNP
15g.39589948G=CA2171400181FSIP1,THBS1c.2070G= (p.Gly690=)
c.771-1374C=
c.1896G= (p.Gly632=)
n.2245G=
15g.39589948G>TCA489673507FSIP1,THBS1c.2070G>T (p.Gly690=)
c.771-1374C>A
c.1896G>T (p.Gly632=)
n.2245G>T
 COSMIC
15g.39589949G>ACA391670371FSIP1,THBS1c.2071G>A (p.Glu691Lys)
c.771-1375C>T
c.1897G>A (p.Glu633Lys)
n.2246G>A
15g.39589949G>CCA391670370FSIP1,THBS1c.2071G>C (p.Glu691Gln)
c.771-1375C>G
c.1897G>C (p.Glu633Gln)
n.2246G>C
15g.39589949G>TCA391670369FSIP1,THBS1c.2071G>T (p.Glu691Ter)
c.771-1375C>A
c.1897G>T (p.Glu633Ter)
n.2246G>T
15g.39589950A>CCA391670374FSIP1,THBS1c.2072A>C (p.Glu691Ala)
c.771-1376T>G
c.1898A>C (p.Glu633Ala)
n.2247A>C
15g.39589950A>GCA391670372FSIP1,THBS1c.2072A>G (p.Glu691Gly)
c.771-1376T>C
c.1898A>G (p.Glu633Gly)
n.2247A>G
15g.39589950A>TCA391670373FSIP1,THBS1c.2072A>T (p.Glu691Val)
c.771-1376T>A
c.1898A>T (p.Glu633Val)
n.2247A>T
15g.39589951G>ACA489673517FSIP1,THBS1c.2073G>A (p.Glu691=)
c.771-1377C>T
c.1899G>A (p.Glu633=)
n.2248G>A
15g.39589951G>CCA268725407FSIP1,THBS1c.2073G>C (p.Glu691Asp)
c.771-1377C>G
c.1899G>C (p.Glu633Asp)
n.2248G>C
 dbSNP
15g.39589951G=CA2171400182FSIP1,THBS1c.2073G= (p.Glu691=)
c.771-1377C=
c.1899G= (p.Glu633=)
n.2248G=
15g.39589951G>TCA391670375FSIP1,THBS1c.2073G>T (p.Glu691Asp)
c.771-1377C>A
c.1899G>T (p.Glu633Asp)
n.2248G>T
15g.39589952G>ACA391670376FSIP1,THBS1c.2074G>A (p.Asp692Asn)
c.771-1378C>T
c.1900G>A (p.Asp634Asn)
n.2249G>A
15g.39589952G>CCA391670377FSIP1,THBS1c.2074G>C (p.Asp692His)
c.771-1378C>G
c.1900G>C (p.Asp634His)
n.2249G>C
15g.39589952G>TCA391670378FSIP1,THBS1c.2074G>T (p.Asp692Tyr)
c.771-1378C>A
c.1900G>T (p.Asp634Tyr)
n.2249G>T
15g.39589953A>CCA391670379FSIP1,THBS1c.2075A>C (p.Asp692Ala)
c.771-1379T>G
c.1901A>C (p.Asp634Ala)
n.2250A>C
15g.39589953A>GCA391670380FSIP1,THBS1c.2075A>G (p.Asp692Gly)
c.771-1379T>C
c.1901A>G (p.Asp634Gly)
n.2250A>G
15g.39589953A>TCA391670381FSIP1,THBS1c.2075A>T (p.Asp692Val)
c.771-1379T>A
c.1901A>T (p.Asp634Val)
n.2250A>T
15g.39589954C>ACA391670382FSIP1,THBS1c.2076C>A (p.Asp692Glu)
c.771-1380G>T
c.1902C>A (p.Asp634Glu)
n.2251C>A
15g.39589954C=CA2171400183FSIP1,THBS1c.2076C= (p.Asp692=)
c.771-1380G=
c.1902C= (p.Asp634=)
n.2251C=
15g.39589954C>GCA391670383FSIP1,THBS1c.2076C>G (p.Asp692Glu)
c.771-1380G>C
c.1902C>G (p.Asp634Glu)
n.2251C>G
15g.39589954C>TCA489673527FSIP1,THBS1c.2076C>T (p.Asp692=)
c.771-1380G>A
c.1902C>T (p.Asp634=)
n.2251C>T
 dbSNP gnomAD v2 gnomAD v4
15g.39589955A=CA2171400184FSIP1,THBS1c.2077A= (p.Thr693=)
c.771-1381T=
c.1903A= (p.Thr635=)
n.2252A=
15g.39589955A>CCA391670386FSIP1,THBS1c.2077A>C (p.Thr693Pro)
c.771-1381T>G
c.1903A>C (p.Thr635Pro)
n.2252A>C
15g.39589955A>GCA391670385FSIP1,THBS1c.2077A>G (p.Thr693Ala)
c.771-1381T>C
c.1903A>G (p.Thr635Ala)
n.2252A>G
 dbSNP gnomAD v3 gnomAD v4
15g.39589955A>TCA391670384FSIP1,THBS1c.2077A>T (p.Thr693Ser)
c.771-1381T>A
c.1903A>T (p.Thr635Ser)
n.2252A>T
15g.39589956C>ACA391670387FSIP1,THBS1c.2078C>A (p.Thr693Lys)
c.771-1382G>T
c.1904C>A (p.Thr635Lys)
n.2253C>A
15g.39589956C=CA2171400185FSIP1,THBS1c.2078C= (p.Thr693=)
c.771-1382G=
c.1904C= (p.Thr635=)
n.2253C=
15g.39589956C>GCA391670388FSIP1,THBS1c.2078C>G (p.Thr693Arg)
c.771-1382G>C
c.1904C>G (p.Thr635Arg)
n.2253C>G
15g.39589956C>TCA391670389FSIP1,THBS1c.2078C>T (p.Thr693Ile)
c.771-1382G>A
c.1904C>T (p.Thr635Ile)
n.2253C>T
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
15g.39589957A>CCA489673542FSIP1,THBS1c.2079A>C (p.Thr693=)
c.771-1383T>G
c.1905A>C (p.Thr635=)
n.2254A>C
15g.39589957A>GCA489673540FSIP1,THBS1c.2079A>G (p.Thr693=)
c.771-1383T>C
c.1905A>G (p.Thr635=)
n.2254A>G
15g.39589957A>TCA489673538FSIP1,THBS1c.2079A>T (p.Thr693=)
c.771-1383T>A
c.1905A>T (p.Thr635=)
n.2254A>T
15g.39589958G>ACA391670390FSIP1,THBS1c.2080G>A (p.Asp694Asn)
c.771-1384C>T
c.1906G>A (p.Asp636Asn)
n.2255G>A
 gnomAD v4
15g.39589958G>CCA391670391FSIP1,THBS1c.2080G>C (p.Asp694His)
c.771-1384C>G
c.1906G>C (p.Asp636His)
n.2255G>C
15g.39589958G>TCA391670392FSIP1,THBS1c.2080G>T (p.Asp694Tyr)
c.771-1384C>A
c.1906G>T (p.Asp636Tyr)
n.2255G>T
15g.39589959A>CCA391670393FSIP1,THBS1c.2081A>C (p.Asp694Ala)
c.771-1385T>G
c.1907A>C (p.Asp636Ala)
n.2256A>C
15g.39589959A>GCA391670394FSIP1,THBS1c.2081A>G (p.Asp694Gly)
c.771-1385T>C
c.1907A>G (p.Asp636Gly)
n.2256A>G
15g.39589959A>TCA391670395FSIP1,THBS1c.2081A>T (p.Asp694Val)
c.771-1385T>A
c.1907A>T (p.Asp636Val)
n.2256A>T
15g.39589960C>ACA391670396FSIP1,THBS1c.2082C>A (p.Asp694Glu)
c.771-1386G>T
c.1908C>A (p.Asp636Glu)
n.2257C>A
 dbSNP gnomAD v2 gnomAD v4
15g.39589960C=CA2171400186FSIP1,THBS1c.2082C= (p.Asp694=)
c.771-1386G=
c.1908C= (p.Asp636=)
n.2257C=
15g.39589960C>GCA391670397FSIP1,THBS1c.2082C>G (p.Asp694Glu)
c.771-1386G>C
c.1908C>G (p.Asp636Glu)
n.2257C>G
15g.39589960C>TCA489673544FSIP1,THBS1c.2082C>T (p.Asp694=)
c.771-1386G>A
c.1908C>T (p.Asp636=)
n.2257C>T
 dbSNP
15g.39589961C>ACA391670398FSIP1,THBS1c.2083C>A (p.Leu695Met)
c.771-1387G>T
c.1909C>A (p.Leu637Met)
n.2258C>A
15g.39589961C>GCA391670399FSIP1,THBS1c.2083C>G (p.Leu695Val)
c.771-1387G>C
c.1909C>G (p.Leu637Val)
n.2258C>G
15g.39589961C>TCA489673548FSIP1,THBS1c.2083C>T (p.Leu695=)
c.771-1387G>A
c.1909C>T (p.Leu637=)
n.2258C>T
15g.39589962T>ACA391670401FSIP1,THBS1c.2084T>A (p.Leu695Gln)
c.771-1388A>T
c.1910T>A (p.Leu637Gln)
n.2259T>A
15g.39589962T>CCA391670402FSIP1,THBS1c.2084T>C (p.Leu695Pro)
c.771-1388A>G
c.1910T>C (p.Leu637Pro)
n.2259T>C
15g.39589962T>GCA391670400FSIP1,THBS1c.2084T>G (p.Leu695Arg)
c.771-1388A>C
c.1910T>G (p.Leu637Arg)
n.2259T>G
15g.39589963G>ACA7472140FSIP1,THBS1c.2085G>A (p.Leu695=)
c.771-1389C>T
c.1911G>A (p.Leu637=)
n.2260G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.39589963G>CCA489673553FSIP1,THBS1c.2085G>C (p.Leu695=)
c.771-1389C>G
c.1911G>C (p.Leu637=)
n.2260G>C
15g.39589963G=CA2171400187FSIP1,THBS1c.2085G= (p.Leu695=)
c.771-1389C=
c.1911G= (p.Leu637=)
n.2260G=
15g.39589963G>TCA489673555FSIP1,THBS1c.2085G>T (p.Leu695=)
c.771-1389C>A
c.1911G>T (p.Leu637=)
n.2260G>T
15g.39589964G>ACA391670403FSIP1,THBS1c.2086G>A (p.Asp696Asn)
c.771-1390C>T
c.1912G>A (p.Asp638Asn)
n.2261G>A
15g.39589964G>CCA391670404FSIP1,THBS1c.2086G>C (p.Asp696His)
c.771-1390C>G
c.1912G>C (p.Asp638His)
n.2261G>C
15g.39589964G>TCA391670405FSIP1,THBS1c.2086G>T (p.Asp696Tyr)
c.771-1390C>A
c.1912G>T (p.Asp638Tyr)
n.2261G>T
15g.39589965A>CCA391670406FSIP1,THBS1c.2087A>C (p.Asp696Ala)
c.771-1391T>G
c.1913A>C (p.Asp638Ala)
n.2262A>C
15g.39589965A>GCA391670407FSIP1,THBS1c.2087A>G (p.Asp696Gly)
c.771-1391T>C
c.1913A>G (p.Asp638Gly)
n.2262A>G
15g.39589965A>TCA391670408FSIP1,THBS1c.2087A>T (p.Asp696Val)
c.771-1391T>A
c.1913A>T (p.Asp638Val)
n.2262A>T
15g.39589966T>ACA391670410FSIP1,THBS1c.2088T>A (p.Asp696Glu)
c.771-1392A>T
c.1914T>A (p.Asp638Glu)
n.2263T>A
15g.39589966T>CCA489673562FSIP1,THBS1c.2088T>C (p.Asp696=)
c.771-1392A>G
c.1914T>C (p.Asp638=)
n.2263T>C
 gnomAD v4
15g.39589966T>GCA391670409FSIP1,THBS1c.2088T>G (p.Asp696Glu)
c.771-1392A>C
c.1914T>G (p.Asp638Glu)
n.2263T>G
15g.39589967G>ACA391670411FSIP1,THBS1c.2089G>A (p.Gly697Ser)
c.771-1393C>T
c.1915G>A (p.Gly639Ser)
n.2264G>A
15g.39589967G>CCA391670412FSIP1,THBS1c.2089G>C (p.Gly697Arg)
c.771-1393C>G
c.1915G>C (p.Gly639Arg)
n.2264G>C
15g.39589967G>TCA391670413FSIP1,THBS1c.2089G>T (p.Gly697Cys)
c.771-1393C>A
c.1915G>T (p.Gly639Cys)
n.2264G>T
15g.39589968G>ACA391670414FSIP1,THBS1c.2090G>A (p.Gly697Asp)
c.771-1394C>T
c.1916G>A (p.Gly639Asp)
n.2265G>A
 gnomAD v4
15g.39589968G>CCA391670415FSIP1,THBS1c.2090G>C (p.Gly697Ala)
c.771-1394C>G
c.1916G>C (p.Gly639Ala)
n.2265G>C
15g.39589968G>TCA391670416FSIP1,THBS1c.2090G>T (p.Gly697Val)
c.771-1394C>A
c.1916G>T (p.Gly639Val)
n.2265G>T
15g.39589969C>ACA489673574FSIP1,THBS1c.2091C>A (p.Gly697=)
c.771-1395G>T
c.1917C>A (p.Gly639=)
n.2266C>A
 gnomAD v4
15g.39589969C>GCA489673575FSIP1,THBS1c.2091C>G (p.Gly697=)
c.771-1395G>C
c.1917C>G (p.Gly639=)
n.2266C>G
15g.39589969C>TCA489673577FSIP1,THBS1c.2091C>T (p.Gly697=)
c.771-1395G>A
c.1917C>T (p.Gly639=)
n.2266C>T
 gnomAD v4
15g.39589970T>ACA391670417FSIP1,THBS1c.2092T>A (p.Trp698Arg)
c.771-1396A>T
c.1918T>A (p.Trp640Arg)
n.2267T>A
15g.39589970T>CCA391670419FSIP1,THBS1c.2092T>C (p.Trp698Arg)
c.771-1396A>G
c.1918T>C (p.Trp640Arg)
n.2267T>C
 dbSNP
15g.39589970T>GCA391670418FSIP1,THBS1c.2092T>G (p.Trp698Gly)
c.771-1396A>C
c.1918T>G (p.Trp640Gly)
n.2267T>G
15g.39589970T=CA2171400188FSIP1,THBS1c.2092T= (p.Trp698=)
c.771-1396A=
c.1918T= (p.Trp640=)
n.2267T=
15g.39589971G>ACA391670420FSIP1,THBS1c.2093G>A (p.Trp698Ter)
c.771-1397C>T
c.1919G>A (p.Trp640Ter)
n.2268G>A
 dbSNP gnomAD v2
15g.39589971G>CCA391670421FSIP1,THBS1c.2093G>C (p.Trp698Ser)
c.771-1397C>G
c.1919G>C (p.Trp640Ser)
n.2268G>C
 gnomAD v4
15g.39589971G=CA2171400189FSIP1,THBS1c.2093G= (p.Trp698=)
c.771-1397C=
c.1919G= (p.Trp640=)
n.2268G=
15g.39589971G>TCA391670422FSIP1,THBS1c.2093G>T (p.Trp698Leu)
c.771-1397C>A
c.1919G>T (p.Trp640Leu)
n.2268G>T
15g.39589972G>ACA391670423FSIP1,THBS1c.2094G>A (p.Trp698Ter)
c.771-1398C>T
c.1920G>A (p.Trp640Ter)
n.2269G>A
15g.39589972G>CCA391670424FSIP1,THBS1c.2094G>C (p.Trp698Cys)
c.771-1398C>G
c.1920G>C (p.Trp640Cys)
n.2269G>C
15g.39589972G>TCA391670425FSIP1,THBS1c.2094G>T (p.Trp698Cys)
c.771-1398C>A
c.1920G>T (p.Trp640Cys)
n.2269G>T
15g.39589973C>ACA7472141FSIP1,THBS1c.2095C>A (p.Pro699Thr)
c.771-1399G>T
c.1921C>A (p.Pro641Thr)
n.2270C>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.39589973C=CA2171400190FSIP1,THBS1c.2095C= (p.Pro699=)
c.771-1399G=
c.1921C= (p.Pro641=)
n.2270C=
15g.39589973C>GCA391670426FSIP1,THBS1c.2095C>G (p.Pro699Ala)
c.771-1399G>C
c.1921C>G (p.Pro641Ala)
n.2270C>G
15g.39589973C>TCA391670427FSIP1,THBS1c.2095C>T (p.Pro699Ser)
c.771-1399G>A
c.1921C>T (p.Pro641Ser)
n.2270C>T
15g.39589974C>ACA391670428FSIP1,THBS1c.2096C>A (p.Pro699His)
c.771-1400G>T
c.1922C>A (p.Pro641His)
n.2271C>A
15g.39589974C>GCA391670429FSIP1,THBS1c.2096C>G (p.Pro699Arg)
c.771-1400G>C
c.1922C>G (p.Pro641Arg)
n.2271C>G
15g.39589974C>TCA391670430FSIP1,THBS1c.2096C>T (p.Pro699Leu)
c.771-1400G>A
c.1922C>T (p.Pro641Leu)
n.2271C>T
15g.39589975C>ACA489673609FSIP1,THBS1c.2097C>A (p.Pro699=)
c.771-1401G>T
c.1923C>A (p.Pro641=)
n.2272C>A
15g.39589975C=CA2171400191FSIP1,THBS1c.2097C= (p.Pro699=)
c.771-1401G=
c.1923C= (p.Pro641=)
n.2272C=
15g.39589975C>GCA489673612FSIP1,THBS1c.2097C>G (p.Pro699=)
c.771-1401G>C
c.1923C>G (p.Pro641=)
n.2272C>G
15g.39589975C>TCA489673610FSIP1,THBS1c.2097C>T (p.Pro699=)
c.771-1401G>A
c.1923C>T (p.Pro641=)
n.2272C>T
15g.39589976A=CA2171400192FSIP1,THBS1c.2098A= (p.Asn700=)
c.771-1402T=
c.1924A= (p.Asn642=)
n.2273A=
15g.39589976A>CCA391670432FSIP1,THBS1c.2098A>C (p.Asn700His)
c.771-1402T>G
c.1924A>C (p.Asn642His)
n.2273A>C
15g.39589976A>GCA7472142FSIP1,THBS1c.2098A>G (p.Asn700Asp)
c.771-1402T>C
c.1924A>G (p.Asn642Asp)
n.2273A>G
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.39589976A>TCA391670431FSIP1,THBS1c.2098A>T (p.Asn700Tyr)
c.771-1402T>A
c.1924A>T (p.Asn642Tyr)
n.2273A>T
15g.39589977dupCA919535973FSIP1,THBS1c.2099dup (p.Asn700LysfsTer2)
c.771-1402dup
c.1925dup (p.Asn642LysfsTer2)
n.2274dup
 dbSNP gnomAD v4
15g.39589977A=CA2171400193FSIP1,THBS1c.2099A= (p.Asn700=)
c.771-1403T=
c.1925A= (p.Asn642=)
n.2274A=
15g.39589977A>CCA391670433FSIP1,THBS1c.2099A>C (p.Asn700Thr)
c.771-1403T>G
c.1925A>C (p.Asn642Thr)
n.2274A>C
15g.39589977A>GCA7472143FSIP1,THBS1c.2099A>G (p.Asn700Ser)
c.771-1403T>C
c.1925A>G (p.Asn642Ser)
n.2274A>G
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.39589977A>TCA391670434FSIP1,THBS1c.2099A>T (p.Asn700Ile)
c.771-1403T>A
c.1925A>T (p.Asn642Ile)
n.2274A>T
15g.39589978T>ACA391670435FSIP1,THBS1c.2100T>A (p.Asn700Lys)
c.771-1404A>T
c.1926T>A (p.Asn642Lys)
n.2275T>A
15g.39589978T>CCA489673624FSIP1,THBS1c.2100T>C (p.Asn700=)
c.771-1404A>G
c.1926T>C (p.Asn642=)
n.2275T>C
 dbSNP
15g.39589978T>GCA391670436FSIP1,THBS1c.2100T>G (p.Asn700Lys)
c.771-1404A>C
c.1926T>G (p.Asn642Lys)
n.2275T>G
 gnomAD v4
15g.39589978T=CA2171400194FSIP1,THBS1c.2100T= (p.Asn700=)
c.771-1404A=
c.1926T= (p.Asn642=)
n.2275T=
15g.39589979G>ACA391670437FSIP1,THBS1c.2101G>A (p.Glu701Lys)
c.771-1405C>T
c.1927G>A (p.Glu643Lys)
n.2276G>A
15g.39589979G>CCA391670438FSIP1,THBS1c.2101G>C (p.Glu701Gln)
c.771-1405C>G
c.1927G>C (p.Glu643Gln)
n.2276G>C
15g.39589979G>TCA391670439FSIP1,THBS1c.2101G>T (p.Glu701Ter)
c.771-1405C>A
c.1927G>T (p.Glu643Ter)
n.2276G>T
15g.39589980A=CA2171400195FSIP1,THBS1c.2102A= (p.Glu701=)
c.771-1406T=
c.1928A= (p.Glu643=)
n.2277A=
15g.39589980A>CCA391670440FSIP1,THBS1c.2102A>C (p.Glu701Ala)
c.771-1406T>G
c.1928A>C (p.Glu643Ala)
n.2277A>C
15g.39589980A>GCA7472144FSIP1,THBS1c.2102A>G (p.Glu701Gly)
c.771-1406T>C
c.1928A>G (p.Glu643Gly)
n.2277A>G
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.39589980A>TCA391670441FSIP1,THBS1c.2102A>T (p.Glu701Val)
c.771-1406T>A
c.1928A>T (p.Glu643Val)
n.2277A>T
15g.39589981G>ACA489673651FSIP1,THBS1c.2103G>A (p.Glu701=)
c.771-1407C>T
c.1929G>A (p.Glu643=)
n.2278G>A
15g.39589981G>CCA7472145FSIP1,THBS1c.2103G>C (p.Glu701Asp)
c.771-1407C>G
c.1929G>C (p.Glu643Asp)
n.2278G>C
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.39589981G=CA2171400196FSIP1,THBS1c.2103G= (p.Glu701=)
c.771-1407C=
c.1929G= (p.Glu643=)
n.2278G=
15g.39589981G>TCA391670442FSIP1,THBS1c.2103G>T (p.Glu701Asp)
c.771-1407C>A
c.1929G>T (p.Glu643Asp)
n.2278G>T
15g.39589982A>CCA391670445FSIP1,THBS1c.2104A>C (p.Asn702His)
c.771-1408T>G
c.1930A>C (p.Asn644His)
n.2279A>C
15g.39589982A>GCA391670444FSIP1,THBS1c.2104A>G (p.Asn702Asp)
c.771-1408T>C
c.1930A>G (p.Asn644Asp)
n.2279A>G
15g.39589982A>TCA391670443FSIP1,THBS1c.2104A>T (p.Asn702Tyr)
c.771-1408T>A
c.1930A>T (p.Asn644Tyr)
n.2279A>T
15g.39589983A>CCA391670446FSIP1,THBS1c.2105A>C (p.Asn702Thr)
c.771-1409T>G
c.1931A>C (p.Asn644Thr)
n.2280A>C
15g.39589983A>GCA391670447FSIP1,THBS1c.2105A>G (p.Asn702Ser)
c.771-1409T>C
c.1931A>G (p.Asn644Ser)
n.2280A>G
15g.39589983A>TCA391670448FSIP1,THBS1c.2105A>T (p.Asn702Ile)
c.771-1409T>A
c.1931A>T (p.Asn644Ile)
n.2280A>T
15g.39589984C>ACA391670449FSIP1,THBS1c.2106C>A (p.Asn702Lys)
c.771-1410G>T
c.1932C>A (p.Asn644Lys)
n.2281C>A
15g.39589984C=CA2171400197FSIP1,THBS1c.2106C= (p.Asn702=)
c.771-1410G=
c.1932C= (p.Asn644=)
n.2281C=
15g.39589984C>GCA391670450FSIP1,THBS1c.2106C>G (p.Asn702Lys)
c.771-1410G>C
c.1932C>G (p.Asn644Lys)
n.2281C>G
15g.39589984C>TCA489673681FSIP1,THBS1c.2106C>T (p.Asn702=)
c.771-1410G>A
c.1932C>T (p.Asn644=)
n.2281C>T
 dbSNP
15g.39589985C>ACA391670451FSIP1,THBS1c.2107C>A (p.Leu703Met)
c.771-1411G>T
c.1933C>A (p.Leu645Met)
n.2282C>A
15g.39589985C>GCA391670452FSIP1,THBS1c.2107C>G (p.Leu703Val)
c.771-1411G>C
c.1933C>G (p.Leu645Val)
n.2282C>G
15g.39589985C>TCA489673689FSIP1,THBS1c.2107C>T (p.Leu703=)
c.771-1411G>A
c.1933C>T (p.Leu645=)
n.2282C>T

Number of alleles fetched