WARNING - Protein Allele ID and Protein Sequence HGVS API Requests Temporarily Disabled:
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32398161_32398770delinsGATGTCTTCTCCTAATTGTGAGATATATTATCAAAGTCCTTTATCACTTTGTATGGCCAAAAGGAAGTCTGTTTCCACACCTGTCTCAGCCCAGATGACTTCAAAGTCTTGTAAAGGGGAGAAAGAGATTGATGACCAAAAGAACTGCAAAAAGAGAAGAGCCTTGGATTTCTTGAGTAGACTGCCTTTACCTCCACCTGTTAGTCCCATTTGTACATTTGTTTCTCCGGCTGCACAGAAGGCATTTCAGCCACCAAGGAGTTGTGGCACCAAATACGAAACACCCATAAAGAAAAAAGAACTGAATTCTCCTCAGATGACTCCATTTAAAAAATTCAATGAAATTTCTCTTTTGGAAAGTAATTCAATAGCTGACGAAGAACTTGCATTGATAAATACCCAAGCTCTTTTGTCTGGTTCAACAGGAGAAAAACAATTTATATCTGTCAGTGAATCCACTAGGACTGCTCCCACCAGTTCAGAAGATTATCTCAGACTGAAACGACGTTGTACTACATCTCTGATCAAAGAACAGGAGAGTTCCCAGGCCAGTACGGAAGAATGTGAGAAAAATAAGCAGGACACAATTACAACTAAAAAATATATCTAA | CA2082833839 | BRCA2 | c.*172-1_*780delinsGATGTCTTCTCCTAATTGTGAGATATATTATCAAAGTCCTTTATCACTTTGTATGGCCAAAAGGAAGTCTGTTTCCACACCTGTCTCAGCCCAGATGACTTCAAAGTCTTGTAAAGGGGAGAAAGAGATTGATGACCAAAAGAACTGCAAAAAGAGAAGAGCCTTGGATTTCTTGAGTAGACTGCCTTTACCTCCACCTGTTAGTCCCATTTGTACATTTGTTTCTCCGGCTGCACAGAAGGCATTTCAGCCACCAAGGAGTTGTGGCACCAAATACGAAACACCCATAAAGAAAAAAGAACTGAATTCTCCTCAGATGACTCCATTTAAAAAATTCAATGAAATTTCTCTTTTGGAAAGTAATTCAATAGCTGACGAAGAACTTGCATTGATAAATACCCAAGCTCTTTTGTCTGGTTCAACAGGAGAAAAACAATTTATATCTGTCAGTGAATCCACTAGGACTGCTCCCACCAGTTCAGAAGATTATCTCAGACTGAAACGACGTTGTACTACATCTCTGATCAAAGAACAGGAGAGTTCCCAGGCCAGTACGGAAGAATGTGAGAAAAATAAGCAGGACACAATTACAACTAAAAAATATATCTAA c.*1016-1_*1624delinsGATGTCTTCTCCTAATTGTGAGATATATTATCAAAGTCCTTTATCACTTTGTATGGCCAAAAGGAAGTCTGTTTCCACACCTGTCTCAGCCCAGATGACTTCAAAGTCTTGTAAAGGGGAGAAAGAGATTGATGACCAAAAGAACTGCAAAAAGAGAAGAGCCTTGGATTTCTTGAGTAGACTGCCTTTACCTCCACCTGTTAGTCCCATTTGTACATTTGTTTCTCCGGCTGCACAGAAGGCATTTCAGCCACCAAGGAGTTGTGGCACCAAATACGAAACACCCATAAAGAAAAAAGAACTGAATTCTCCTCAGATGACTCCATTTAAAAAATTCAATGAAATTTCTCTTTTGGAAAGTAATTCAATAGCTGACGAAGAACTTGCATTGATAAATACCCAAGCTCTTTTGTCTGGTTCAACAGGAGAAAAACAATTTATATCTGTCAGTGAATCCACTAGGACTGCTCCCACCAGTTCAGAAGATTATCTCAGACTGAAACGACGTTGTACTACATCTCTGATCAAAGAACAGGAGAGTTCCCAGGCCAGTACGGAAGAATGTGAGAAAAATAAGCAGGACACAATTACAACTAAAAAATATATCTAA c.9280-1_9888delinsGATGTCTTCTCCTAATTGTGAGATATATTATCAAAGTCCTTTATCACTTTGTATGGCCAAAAGGAAGTCTGTTTCCACACCTGTCTCAGCCCAGATGACTTCAAAGTCTTGTAAAGGGGAGAAAGAGATTGATGACCAAAAGAACTGCAAAAAGAGAAGAGCCTTGGATTTCTTGAGTAGACTGCCTTTACCTCCACCTGTTAGTCCCATTTGTACATTTGTTTCTCCGGCTGCACAGAAGGCATTTCAGCCACCAAGGAGTTGTGGCACCAAATACGAAACACCCATAAAGAAAAAAGAACTGAATTCTCCTCAGATGACTCCATTTAAAAAATTCAATGAAATTTCTCTTTTGGAAAGTAATTCAATAGCTGACGAAGAACTTGCATTGATAAATACCCAAGCTCTTTTGTCTGGTTCAACAGGAGAAAAACAATTTATATCTGTCAGTGAATCCACTAGGACTGCTCCCACCAGTTCAGAAGATTATCTCAGACTGAAACGACGTTGTACTACATCTCTGATCAAAGAACAGGAGAGTTCCCAGGCCAGTACGGAAGAATGTGAGAAAAATAAGCAGGACACAATTACAACTAAAAAATATATCTAA c.*1211-1_*1819delinsGATGTCTTCTCCTAATTGTGAGATATATTATCAAAGTCCTTTATCACTTTGTATGGCCAAAAGGAAGTCTGTTTCCACACCTGTCTCAGCCCAGATGACTTCAAAGTCTTGTAAAGGGGAGAAAGAGATTGATGACCAAAAGAACTGCAAAAAGAGAAGAGCCTTGGATTTCTTGAGTAGACTGCCTTTACCTCCACCTGTTAGTCCCATTTGTACATTTGTTTCTCCGGCTGCACAGAAGGCATTTCAGCCACCAAGGAGTTGTGGCACCAAATACGAAACACCCATAAAGAAAAAAGAACTGAATTCTCCTCAGATGACTCCATTTAAAAAATTCAATGAAATTTCTCTTTTGGAAAGTAATTCAATAGCTGACGAAGAACTTGCATTGATAAATACCCAAGCTCTTTTGTCTGGTTCAACAGGAGAAAAACAATTTATATCTGTCAGTGAATCCACTAGGACTGCTCCCACCAGTTCAGAAGATTATCTCAGACTGAAACGACGTTGTACTACATCTCTGATCAAAGAACAGGAGAGTTCCCAGGCCAGTACGGAAGAATGTGAGAAAAATAAGCAGGACACAATTACAACTAAAAAATATATCTAA c.9598-1_10206delinsGATGTCTTCTCCTAATTGTGAGATATATTATCAAAGTCCTTTATCACTTTGTATGGCCAAAAGGAAGTCTGTTTCCACACCTGTCTCAGCCCAGATGACTTCAAAGTCTTGTAAAGGGGAGAAAGAGATTGATGACCAAAAGAACTGCAAAAAGAGAAGAGCCTTGGATTTCTTGAGTAGACTGCCTTTACCTCCACCTGTTAGTCCCATTTGTACATTTGTTTCTCCGGCTGCACAGAAGGCATTTCAGCCACCAAGGAGTTGTGGCACCAAATACGAAACACCCATAAAGAAAAAAGAACTGAATTCTCCTCAGATGACTCCATTTAAAAAATTCAATGAAATTTCTCTTTTGGAAAGTAATTCAATAGCTGACGAAGAACTTGCATTGATAAATACCCAAGCTCTTTTGTCTGGTTCAACAGGAGAAAAACAATTTATATCTGTCAGTGAATCCACTAGGACTGCTCCCACCAGTTCAGAAGATTATCTCAGACTGAAACGACGTTGTACTACATCTCTGATCAAAGAACAGGAGAGTTCCCAGGCCAGTACGGAAGAATGTGAGAAAAATAAGCAGGACACAATTACAACTAAAAAATATATCTAA c.2065-1_2673delinsGATGTCTTCTCCTAATTGTGAGATATATTATCAAAGTCCTTTATCACTTTGTATGGCCAAAAGGAAGTCTGTTTCCACACCTGTCTCAGCCCAGATGACTTCAAAGTCTTGTAAAGGGGAGAAAGAGATTGATGACCAAAAGAACTGCAAAAAGAGAAGAGCCTTGGATTTCTTGAGTAGACTGCCTTTACCTCCACCTGTTAGTCCCATTTGTACATTTGTTTCTCCGGCTGCACAGAAGGCATTTCAGCCACCAAGGAGTTGTGGCACCAAATACGAAACACCCATAAAGAAAAAAGAACTGAATTCTCCTCAGATGACTCCATTTAAAAAATTCAATGAAATTTCTCTTTTGGAAAGTAATTCAATAGCTGACGAAGAACTTGCATTGATAAATACCCAAGCTCTTTTGTCTGGTTCAACAGGAGAAAAACAATTTATATCTGTCAGTGAATCCACTAGGACTGCTCCCACCAGTTCAGAAGATTATCTCAGACTGAAACGACGTTGTACTACATCTCTGATCAAAGAACAGGAGAGTTCCCAGGCCAGTACGGAAGAATGTGAGAAAAATAAGCAGGACACAATTACAACTAAAAAATATATCTAA n.1776-1_2384delinsGATGTCTTCTCCTAATTGTGAGATATATTATCAAAGTCCTTTATCACTTTGTATGGCCAAAAGGAAGTCTGTTTCCACACCTGTCTCAGCCCAGATGACTTCAAAGTCTTGTAAAGGGGAGAAAGAGATTGATGACCAAAAGAACTGCAAAAAGAGAAGAGCCTTGGATTTCTTGAGTAGACTGCCTTTACCTCCACCTGTTAGTCCCATTTGTACATTTGTTTCTCCGGCTGCACAGAAGGCATTTCAGCCACCAAGGAGTTGTGGCACCAAATACGAAACACCCATAAAGAAAAAAGAACTGAATTCTCCTCAGATGACTCCATTTAAAAAATTCAATGAAATTTCTCTTTTGGAAAGTAATTCAATAGCTGACGAAGAACTTGCATTGATAAATACCCAAGCTCTTTTGTCTGGTTCAACAGGAGAAAAACAATTTATATCTGTCAGTGAATCCACTAGGACTGCTCCCACCAGTTCAGAAGATTATCTCAGACTGAAACGACGTTGTACTACATCTCTGATCAAAGAACAGGAGAGTTCCCAGGCCAGTACGGAAGAATGTGAGAAAAATAAGCAGGACACAATTACAACTAAAAAATATATCTAA c.9649-1_10257delinsGATGTCTTCTCCTAATTGTGAGATATATTATCAAAGTCCTTTATCACTTTGTATGGCCAAAAGGAAGTCTGTTTCCACACCTGTCTCAGCCCAGATGACTTCAAAGTCTTGTAAAGGGGAGAAAGAGATTGATGACCAAAAGAACTGCAAAAAGAGAAGAGCCTTGGATTTCTTGAGTAGACTGCCTTTACCTCCACCTGTTAGTCCCATTTGTACATTTGTTTCTCCGGCTGCACAGAAGGCATTTCAGCCACCAAGGAGTTGTGGCACCAAATACGAAACACCCATAAAGAAAAAAGAACTGAATTCTCCTCAGATGACTCCATTTAAAAAATTCAATGAAATTTCTCTTTTGGAAAGTAATTCAATAGCTGACGAAGAACTTGCATTGATAAATACCCAAGCTCTTTTGTCTGGTTCAACAGGAGAAAAACAATTTATATCTGTCAGTGAATCCACTAGGACTGCTCCCACCAGTTCAGAAGATTATCTCAGACTGAAACGACGTTGTACTACATCTCTGATCAAAGAACAGGAGAGTTCCCAGGCCAGTACGGAAGAATGTGAGAAAAATAAGCAGGACACAATTACAACTAAAAAATATATCTAA c.9657-1_10265delinsGATGTCTTCTCCTAATTGTGAGATATATTATCAAAGTCCTTTATCACTTTGTATGGCCAAAAGGAAGTCTGTTTCCACACCTGTCTCAGCCCAGATGACTTCAAAGTCTTGTAAAGGGGAGAAAGAGATTGATGACCAAAAGAACTGCAAAAAGAGAAGAGCCTTGGATTTCTTGAGTAGACTGCCTTTACCTCCACCTGTTAGTCCCATTTGTACATTTGTTTCTCCGGCTGCACAGAAGGCATTTCAGCCACCAAGGAGTTGTGGCACCAAATACGAAACACCCATAAAGAAAAAAGAACTGAATTCTCCTCAGATGACTCCATTTAAAAAATTCAATGAAATTTCTCTTTTGGAAAGTAATTCAATAGCTGACGAAGAACTTGCATTGATAAATACCCAAGCTCTTTTGTCTGGTTCAACAGGAGAAAAACAATTTATATCTGTCAGTGAATCCACTAGGACTGCTCCCACCAGTTCAGAAGATTATCTCAGACTGAAACGACGTTGTACTACATCTCTGATCAAAGAACAGGAGAGTTCCCAGGCCAGTACGGAAGAATGTGAGAAAAATAAGCAGGACACAATTACAACTAAAAAATATATCTAA c.9553-1_10161delinsGATGTCTTCTCCTAATTGTGAGATATATTATCAAAGTCCTTTATCACTTTGTATGGCCAAAAGGAAGTCTGTTTCCACACCTGTCTCAGCCCAGATGACTTCAAAGTCTTGTAAAGGGGAGAAAGAGATTGATGACCAAAAGAACTGCAAAAAGAGAAGAGCCTTGGATTTCTTGAGTAGACTGCCTTTACCTCCACCTGTTAGTCCCATTTGTACATTTGTTTCTCCGGCTGCACAGAAGGCATTTCAGCCACCAAGGAGTTGTGGCACCAAATACGAAACACCCATAAAGAAAAAAGAACTGAATTCTCCTCAGATGACTCCATTTAAAAAATTCAATGAAATTTCTCTTTTGGAAAGTAATTCAATAGCTGACGAAGAACTTGCATTGATAAATACCCAAGCTCTTTTGTCTGGTTCAACAGGAGAAAAACAATTTATATCTGTCAGTGAATCCACTAGGACTGCTCCCACCAGTTCAGAAGATTATCTCAGACTGAAACGACGTTGTACTACATCTCTGATCAAAGAACAGGAGAGTTCCCAGGCCAGTACGGAAGAATGTGAGAAAAATAAGCAGGACACAATTACAACTAAAAAATATATCTAA | |
| 13 | g.32398162_32398770del | CA913190737 | BRCA2 | c.*172_*780del (n.*172_*780del) c.*1016_*1624del (n.*1016_*1624del) c.9280_9888del (p.Met3094_Ter3296del) c.*1211_*1819del (n.*1211_*1819del) c.9598_10206del (p.Met3200_Ter3402del) c.2065_2673del (p.Met689_Ter891del) n.1776_2384del c.9649_10257del (p.Met3217_Ter3419del) c.9657_10265del (n.9657_10265del) c.9553_10161del (p.Met3185_Ter3387del) | ClinVar dbSNP |
| 13 | g.32398162_32399672del | CA658798102 | BRCA2 | c.*172_*1682del (n.*172_*1682del) c.9280_*902del (n.[c.9280_*902del;Met3094LeufsTer18]) c.9649_*902del (n.[c.9649_*902del;Met3217LeufsTer18]) c.9657_11167del (n.9657_11167del) c.9649_*902del (n.[c.9649_*902del;Met3217=]) c.9553_*902del (n.[c.9553_*902del;Met3185LeufsTer18]) | ClinVar |
| 13 | g.32398265_32398266delinsAG | CA2082834827 | BRCA2 | c.*275_*276delinsAG (n.*275_*276delinsAG) c.*1119_*1120delinsAG (n.*1119_*1120delinsAG) c.9383_9384delinsAG (p.Lys3128=) c.*1314_*1315delinsAG (n.*1314_*1315delinsAG) c.9701_9702delinsAG (p.Lys3234=) c.2168_2169delinsAG (p.Lys723=) n.1879_1880delinsAG c.9752_9753delinsAG (p.Lys3251=) c.9760_9761delinsAG (n.9760_9761delinsAG) c.835_836delinsAG n.340_341delinsAG c.9656_9657delinsAG (p.Lys3219=) | |
| 13 | g.32398266del | CA10575936 | BRCA2 | c.*276del (n.*276del) c.*1120del (n.*1120del) c.9384del (p.Lys3128AsnfsTer24) c.*1315del (n.*1315del) c.9702del (p.Lys3234AsnfsTer24) c.2169del (p.Lys723AsnfsTer24) n.1880del c.9753del (p.Lys3251AsnfsTer24) c.9761del (n.9761del) c.836del n.341del c.9657del (p.Lys3219AsnfsTer24) | ClinVar dbSNP |
| 13 | g.32398266G>A | CA483439958 | BRCA2 | c.*276G>A (n.*276G>A) c.*1120G>A (n.*1120G>A) c.9384G>A (p.Lys3128=) c.*1315G>A (n.*1315G>A) c.9702G>A (p.Lys3234=) c.2169G>A (p.Lys723=) n.1880G>A c.9753G>A (p.Lys3251=) c.9761G>A (n.9761G>A) c.836G>A n.341G>A c.9657G>A (p.Lys3219=) | ClinVar dbSNP |
| 13 | g.32398266G>C | CA387765702 | BRCA2 | c.*276G>C (n.*276G>C) c.*1120G>C (n.*1120G>C) c.9384G>C (p.Lys3128Asn) c.*1315G>C (n.*1315G>C) c.9702G>C (p.Lys3234Asn) c.2169G>C (p.Lys723Asn) n.1880G>C c.9753G>C (p.Lys3251Asn) c.9761G>C (n.9761G>C) c.836G>C n.341G>C c.9657G>C (p.Lys3219Asn) | dbSNP |
| 13 | g.32398266G= | CA2082834853 | BRCA2 | c.*276G= (n.*276G=) c.*1120G= (n.*1120G=) c.9384G= (p.Lys3128=) c.*1315G= (n.*1315G=) c.9702G= (p.Lys3234=) c.2169G= (p.Lys723=) n.1880G= c.9753G= (p.Lys3251=) c.9761G= (n.9761G=) c.836G= n.341G= c.9657G= (p.Lys3219=) | |
| 13 | g.32398266G>T | CA026291 | BRCA2 | c.*276G>T (n.*276G>T) c.*1120G>T (n.*1120G>T) c.9384G>T (p.Lys3128Asn) c.*1315G>T (n.*1315G>T) c.9702G>T (p.Lys3234Asn) c.2169G>T (p.Lys723Asn) n.1880G>T c.9753G>T (p.Lys3251Asn) c.9761G>T (n.9761G>T) c.836G>T n.341G>T c.9657G>T (p.Lys3219Asn) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32398266_32398267delinsGT | CA2082834841 | BRCA2 | c.*276_*277delinsGT (n.*276_*277delinsGT) c.*1120_*1121delinsGT (n.*1120_*1121delinsGT) c.9384_9385delinsGT (p.Lys3128=) c.*1315_*1316delinsGT (n.*1315_*1316delinsGT) c.9702_9703delinsGT (p.Lys3234=) c.2169_2170delinsGT (p.Lys723=) n.1880_1881delinsGT c.9753_9754delinsGT (p.Lys3251=) c.9761_9762delinsGT (n.9761_9762delinsGT) c.836_837delinsGT n.341_342delinsGT c.9657_9658delinsGT (p.Lys3219=) | |
| 13 | g.32398266_32398267delinsTC | CA891843584 | BRCA2 | c.*276_*277delinsTC (n.*276_*277delinsTC) c.*1120_*1121delinsTC (n.*1120_*1121delinsTC) c.9384_9385delinsTC (p.Lys3128_Ser3129delinsAsnPro) c.*1315_*1316delinsTC (n.*1315_*1316delinsTC) c.9702_9703delinsTC (p.Lys3234_Ser3235delinsAsnPro) c.2169_2170delinsTC (p.Lys723_Ser724delinsAsnPro) n.1880_1881delinsTC c.9753_9754delinsTC (p.Lys3251_Ser3252delinsAsnPro) c.9761_9762delinsTC (n.9761_9762delinsTC) c.836_837delinsTC n.341_342delinsTC c.9657_9658delinsTC (p.Lys3219_Ser3220delinsAsnPro) | ClinVar dbSNP |
| 13 | g.32398267_32398278del | CA645586594 | BRCA2 | c.*277_*288del (n.*277_*288del) c.*1121_*1132del (n.*1121_*1132del) c.9385_9396del (p.Ser3129_Gly3132del) c.*1316_*1327del (n.*1316_*1327del) c.9703_9714del (p.Ser3235_Gly3238del) c.2170_2181del (p.Ser724_Gly727del) n.1881_1892del c.9754_9765del (p.Ser3252_Gly3255del) c.9762_9773del (n.9762_9773del) n.342_353del c.9658_9669del (p.Ser3220_Gly3223del) | ClinVar dbSNP COSMIC COSMIC |
| 13 | g.32398267T>A | CA387765710 | BRCA2 | c.*277T>A (n.*277T>A) c.*1121T>A (n.*1121T>A) c.9385T>A (p.Ser3129Thr) c.*1316T>A (n.*1316T>A) c.9703T>A (p.Ser3235Thr) c.2170T>A (p.Ser724Thr) n.1881T>A c.9754T>A (p.Ser3252Thr) c.9762T>A (n.9762T>A) c.837T>A n.342T>A c.9658T>A (p.Ser3220Thr) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32398267T>C | CA16613984 | BRCA2 | c.*277T>C (n.*277T>C) c.*1121T>C (n.*1121T>C) c.9385T>C (p.Ser3129Pro) c.*1316T>C (n.*1316T>C) c.9703T>C (p.Ser3235Pro) c.2170T>C (p.Ser724Pro) n.1881T>C c.9754T>C (p.Ser3252Pro) c.9762T>C (n.9762T>C) c.837T>C n.342T>C c.9658T>C (p.Ser3220Pro) | ClinVar dbSNP gnomAD v4 |
| 13 | g.32398267T>G | CA387765711 | BRCA2 | c.*277T>G (n.*277T>G) c.*1121T>G (n.*1121T>G) c.9385T>G (p.Ser3129Ala) c.*1316T>G (n.*1316T>G) c.9703T>G (p.Ser3235Ala) c.2170T>G (p.Ser724Ala) n.1881T>G c.9754T>G (p.Ser3252Ala) c.9762T>G (n.9762T>G) c.837T>G n.342T>G c.9658T>G (p.Ser3220Ala) | ClinVar dbSNP |
| 13 | g.32398267T= | CA2082834870 | BRCA2 | c.*277T= (n.*277T=) c.*1121T= (n.*1121T=) c.9385T= (p.Ser3129=) c.*1316T= (n.*1316T=) c.9703T= (p.Ser3235=) c.2170T= (p.Ser724=) n.1881T= c.9754T= (p.Ser3252=) c.9762T= (n.9762T=) c.837T= n.342T= c.9658T= (p.Ser3220=) | |
| 13 | g.32398268C>A | CA387765715 | BRCA2 | c.*278C>A (n.*278C>A) c.*1122C>A (n.*1122C>A) c.9386C>A (p.Ser3129Tyr) c.*1317C>A (n.*1317C>A) c.9704C>A (p.Ser3235Tyr) c.2171C>A (p.Ser724Tyr) n.1882C>A c.9755C>A (p.Ser3252Tyr) c.9763C>A (n.9763C>A) c.838C>A n.343C>A c.9659C>A (p.Ser3220Tyr) | dbSNP |
| 13 | g.32398268C>G | CA387765718 | BRCA2 | c.*278C>G (n.*278C>G) c.*1122C>G (n.*1122C>G) c.9386C>G (p.Ser3129Cys) c.*1317C>G (n.*1317C>G) c.9704C>G (p.Ser3235Cys) c.2171C>G (p.Ser724Cys) n.1882C>G c.9755C>G (p.Ser3252Cys) c.9763C>G (n.9763C>G) c.838C>G n.343C>G c.9659C>G (p.Ser3220Cys) | dbSNP |
| 13 | g.32398268C>T | CA387765720 | BRCA2 | c.*278C>T (n.*278C>T) c.*1122C>T (n.*1122C>T) c.9386C>T (p.Ser3129Phe) c.*1317C>T (n.*1317C>T) c.9704C>T (p.Ser3235Phe) c.2171C>T (p.Ser724Phe) n.1882C>T c.9755C>T (p.Ser3252Phe) c.9763C>T (n.9763C>T) c.838C>T n.343C>T c.9659C>T (p.Ser3220Phe) | dbSNP COSMIC COSMIC |
| 13 | g.32398269T>A | CA483439962 | BRCA2 | c.*279T>A (n.*279T>A) c.*1123T>A (n.*1123T>A) c.9387T>A (p.Ser3129=) c.*1318T>A (n.*1318T>A) c.9705T>A (p.Ser3235=) c.2172T>A (p.Ser724=) n.1883T>A c.9756T>A (p.Ser3252=) c.9764T>A (n.9764T>A) c.839T>A n.344T>A c.9660T>A (p.Ser3220=) | dbSNP |
| 13 | g.32398269T>C | CA483439963 | BRCA2 | c.*279T>C (n.*279T>C) c.*1123T>C (n.*1123T>C) c.9387T>C (p.Ser3129=) c.*1318T>C (n.*1318T>C) c.9705T>C (p.Ser3235=) c.2172T>C (p.Ser724=) n.1883T>C c.9756T>C (p.Ser3252=) c.9764T>C (n.9764T>C) c.839T>C n.344T>C c.9660T>C (p.Ser3220=) | dbSNP |
| 13 | g.32398269T>G | CA483439964 | BRCA2 | c.*279T>G (n.*279T>G) c.*1123T>G (n.*1123T>G) c.9387T>G (p.Ser3129=) c.*1318T>G (n.*1318T>G) c.9705T>G (p.Ser3235=) c.2172T>G (p.Ser724=) n.1883T>G c.9756T>G (p.Ser3252=) c.9764T>G (n.9764T>G) c.839T>G n.344T>G c.9660T>G (p.Ser3220=) | |
| 13 | g.32398269_32398272dup | CA2580087450 | BRCA2 | c.*279_*282dup (n.*279_*282dup) c.*1123_*1126dup (n.*1123_*1126dup) c.9387_9390dup (p.Lys3131LeufsTer2) c.*1318_*1321dup (n.*1318_*1321dup) c.9705_9708dup (p.Lys3237LeufsTer2) c.2172_2175dup (p.Lys726LeufsTer2) n.1883_1886dup c.9756_9759dup (p.Lys3254LeufsTer2) c.9764_9767dup (n.9764_9767dup) n.344_347dup c.9660_9663dup (p.Lys3222LeufsTer2) | ClinVar |
| 13 | g.32398270T>A | CA387765721 | BRCA2 | c.*280T>A (n.*280T>A) c.*1124T>A (n.*1124T>A) c.9388T>A (p.Cys3130Ser) c.*1319T>A (n.*1319T>A) c.9706T>A (p.Cys3236Ser) c.2173T>A (p.Cys725Ser) n.1884T>A c.9757T>A (p.Cys3253Ser) c.9765T>A (n.9765T>A) c.840T>A n.345T>A c.9661T>A (p.Cys3221Ser) | dbSNP |
| 13 | g.32398270T>C | CA387765722 | BRCA2 | c.*280T>C (n.*280T>C) c.*1124T>C (n.*1124T>C) c.9388T>C (p.Cys3130Arg) c.*1319T>C (n.*1319T>C) c.9706T>C (p.Cys3236Arg) c.2173T>C (p.Cys725Arg) n.1884T>C c.9757T>C (p.Cys3253Arg) c.9765T>C (n.9765T>C) c.840T>C n.345T>C c.9661T>C (p.Cys3221Arg) | dbSNP |
| 13 | g.32398270T>G | CA387765726 | BRCA2 | c.*280T>G (n.*280T>G) c.*1124T>G (n.*1124T>G) c.9388T>G (p.Cys3130Gly) c.*1319T>G (n.*1319T>G) c.9706T>G (p.Cys3236Gly) c.2173T>G (p.Cys725Gly) n.1884T>G c.9757T>G (p.Cys3253Gly) c.9765T>G (n.9765T>G) c.840T>G n.345T>G c.9661T>G (p.Cys3221Gly) | |
| 13 | g.32398271G>A | CA026292 | BRCA2 | c.*281G>A (n.*281G>A) c.*1125G>A (n.*1125G>A) c.9389G>A (p.Cys3130Tyr) c.*1320G>A (n.*1320G>A) c.9707G>A (p.Cys3236Tyr) c.2174G>A (p.Cys725Tyr) n.1885G>A c.9758G>A (p.Cys3253Tyr) c.9766G>A (n.9766G>A) c.841G>A n.346G>A c.9662G>A (p.Cys3221Tyr) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32398271G>C | CA387765734 | BRCA2 | c.*281G>C (n.*281G>C) c.*1125G>C (n.*1125G>C) c.9389G>C (p.Cys3130Ser) c.*1320G>C (n.*1320G>C) c.9707G>C (p.Cys3236Ser) c.2174G>C (p.Cys725Ser) n.1885G>C c.9758G>C (p.Cys3253Ser) c.9766G>C (n.9766G>C) c.841G>C n.346G>C c.9662G>C (p.Cys3221Ser) | ClinVar dbSNP |
| 13 | g.32398271G= | CA2082834882 | BRCA2 | c.*281G= (n.*281G=) c.*1125G= (n.*1125G=) c.9389G= (p.Cys3130=) c.*1320G= (n.*1320G=) c.9707G= (p.Cys3236=) c.2174G= (p.Cys725=) n.1885G= c.9758G= (p.Cys3253=) c.9766G= (n.9766G=) c.841G= n.346G= c.9662G= (p.Cys3221=) | |
| 13 | g.32398271G>T | CA387765730 | BRCA2 | c.*281G>T (n.*281G>T) c.*1125G>T (n.*1125G>T) c.9389G>T (p.Cys3130Phe) c.*1320G>T (n.*1320G>T) c.9707G>T (p.Cys3236Phe) c.2174G>T (p.Cys725Phe) n.1885G>T c.9758G>T (p.Cys3253Phe) c.9766G>T (n.9766G>T) c.841G>T n.346G>T c.9662G>T (p.Cys3221Phe) | dbSNP |
| 13 | g.32398272T>A | CA387765736 | BRCA2 | c.*282T>A (n.*282T>A) c.*1126T>A (n.*1126T>A) c.9390T>A (p.Cys3130Ter) c.*1321T>A (n.*1321T>A) c.9708T>A (p.Cys3236Ter) c.2175T>A (p.Cys725Ter) n.1886T>A c.9759T>A (p.Cys3253Ter) c.9767T>A (n.9767T>A) c.842T>A n.347T>A c.9663T>A (p.Cys3221Ter) | |
| 13 | g.32398272T>C | CA483439965 | BRCA2 | c.*282T>C (n.*282T>C) c.*1126T>C (n.*1126T>C) c.9390T>C (p.Cys3130=) c.*1321T>C (n.*1321T>C) c.9708T>C (p.Cys3236=) c.2175T>C (p.Cys725=) n.1886T>C c.9759T>C (p.Cys3253=) c.9767T>C (n.9767T>C) c.842T>C n.347T>C c.9663T>C (p.Cys3221=) | |
| 13 | g.32398272T>G | CA387765737 | BRCA2 | c.*282T>G (n.*282T>G) c.*1126T>G (n.*1126T>G) c.9390T>G (p.Cys3130Trp) c.*1321T>G (n.*1321T>G) c.9708T>G (p.Cys3236Trp) c.2175T>G (p.Cys725Trp) n.1886T>G c.9759T>G (p.Cys3253Trp) c.9767T>G (n.9767T>G) c.842T>G n.347T>G c.9663T>G (p.Cys3221Trp) | dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32398272T= | CA2082834894 | BRCA2 | c.*282T= (n.*282T=) c.*1126T= (n.*1126T=) c.9390T= (p.Cys3130=) c.*1321T= (n.*1321T=) c.9708T= (p.Cys3236=) c.2175T= (p.Cys725=) n.1886T= c.9759T= (p.Cys3253=) c.9767T= (n.9767T=) c.842T= n.347T= c.9663T= (p.Cys3221=) | |
| 13 | g.32398273A= | CA2082834898 | BRCA2 | c.*283A= (n.*283A=) c.*1127A= (n.*1127A=) c.9391A= (p.Lys3131=) c.*1322A= (n.*1322A=) c.9709A= (p.Lys3237=) c.2176A= (p.Lys726=) n.1887A= c.9760A= (p.Lys3254=) c.9768A= (n.9768A=) n.348A= c.9664A= (p.Lys3222=) | |
| 13 | g.32398273A>C | CA387765742 | BRCA2 | c.*283A>C (n.*283A>C) c.*1127A>C (n.*1127A>C) c.9391A>C (p.Lys3131Gln) c.*1322A>C (n.*1322A>C) c.9709A>C (p.Lys3237Gln) c.2176A>C (p.Lys726Gln) n.1887A>C c.9760A>C (p.Lys3254Gln) c.9768A>C (n.9768A>C) n.348A>C c.9664A>C (p.Lys3222Gln) | |
| 13 | g.32398273A>G | CA387765743 | BRCA2 | c.*283A>G (n.*283A>G) c.*1127A>G (n.*1127A>G) c.9391A>G (p.Lys3131Glu) c.*1322A>G (n.*1322A>G) c.9709A>G (p.Lys3237Glu) c.2176A>G (p.Lys726Glu) n.1887A>G c.9760A>G (p.Lys3254Glu) c.9768A>G (n.9768A>G) n.348A>G c.9664A>G (p.Lys3222Glu) | ClinVar dbSNP |
| 13 | g.32398273A>T | CA387765746 | BRCA2 | c.*283A>T (n.*283A>T) c.*1127A>T (n.*1127A>T) c.9391A>T (p.Lys3131Ter) c.*1322A>T (n.*1322A>T) c.9709A>T (p.Lys3237Ter) c.2176A>T (p.Lys726Ter) n.1887A>T c.9760A>T (p.Lys3254Ter) c.9768A>T (n.9768A>T) n.348A>T c.9664A>T (p.Lys3222Ter) | dbSNP |
| 13 | g.32398275del | CA2727928013 | BRCA2 | c.*285del (n.*285del) c.*1129del (n.*1129del) c.9393del (p.Glu3133ArgfsTer19) c.*1324del (n.*1324del) c.9711del (p.Glu3239ArgfsTer19) c.2178del (p.Glu728ArgfsTer19) n.1889del c.9762del (p.Glu3256ArgfsTer19) c.9770del (n.9770del) n.350del c.9666del (p.Glu3224ArgfsTer19) | dbSNP |
| 13 | g.32398274A>C | CA387765748 | BRCA2 | c.*284A>C (n.*284A>C) c.*1128A>C (n.*1128A>C) c.9392A>C (p.Lys3131Thr) c.*1323A>C (n.*1323A>C) c.9710A>C (p.Lys3237Thr) c.2177A>C (p.Lys726Thr) n.1888A>C c.9761A>C (p.Lys3254Thr) c.9769A>C (n.9769A>C) n.349A>C c.9665A>C (p.Lys3222Thr) | |
| 13 | g.32398274A>G | CA387765750 | BRCA2 | c.*284A>G (n.*284A>G) c.*1128A>G (n.*1128A>G) c.9392A>G (p.Lys3131Arg) c.*1323A>G (n.*1323A>G) c.9710A>G (p.Lys3237Arg) c.2177A>G (p.Lys726Arg) n.1888A>G c.9761A>G (p.Lys3254Arg) c.9769A>G (n.9769A>G) n.349A>G c.9665A>G (p.Lys3222Arg) | |
| 13 | g.32398274A>T | CA387765754 | BRCA2 | c.*284A>T (n.*284A>T) c.*1128A>T (n.*1128A>T) c.9392A>T (p.Lys3131Ile) c.*1323A>T (n.*1323A>T) c.9710A>T (p.Lys3237Ile) c.2177A>T (p.Lys726Ile) n.1888A>T c.9761A>T (p.Lys3254Ile) c.9769A>T (n.9769A>T) n.349A>T c.9665A>T (p.Lys3222Ile) | |
| 13 | g.32398275A>C | CA387765755 | BRCA2 | c.*285A>C (n.*285A>C) c.*1129A>C (n.*1129A>C) c.9393A>C (p.Lys3131Asn) c.*1324A>C (n.*1324A>C) c.9711A>C (p.Lys3237Asn) c.2178A>C (p.Lys726Asn) n.1889A>C c.9762A>C (p.Lys3254Asn) c.9770A>C (n.9770A>C) n.350A>C c.9666A>C (p.Lys3222Asn) | |
| 13 | g.32398275A>G | CA483440042 | BRCA2 | c.*285A>G (n.*285A>G) c.*1129A>G (n.*1129A>G) c.9393A>G (p.Lys3131=) c.*1324A>G (n.*1324A>G) c.9711A>G (p.Lys3237=) c.2178A>G (p.Lys726=) n.1889A>G c.9762A>G (p.Lys3254=) c.9770A>G (n.9770A>G) n.350A>G c.9666A>G (p.Lys3222=) | |
| 13 | g.32398275A>T | CA387765756 | BRCA2 | c.*285A>T (n.*285A>T) c.*1129A>T (n.*1129A>T) c.9393A>T (p.Lys3131Asn) c.*1324A>T (n.*1324A>T) c.9711A>T (p.Lys3237Asn) c.2178A>T (p.Lys726Asn) n.1889A>T c.9762A>T (p.Lys3254Asn) c.9770A>T (n.9770A>T) n.350A>T c.9666A>T (p.Lys3222Asn) | |
| 13 | g.32398276G>A | CA6941446 | BRCA2 | c.*286G>A (n.*286G>A) c.*1130G>A (n.*1130G>A) c.9394G>A (p.Gly3132Arg) c.*1325G>A (n.*1325G>A) c.9712G>A (p.Gly3238Arg) c.2179G>A (p.Gly727Arg) n.1890G>A c.9763G>A (p.Gly3255Arg) c.9771G>A (n.9771G>A) n.351G>A c.9667G>A (p.Gly3223Arg) | ClinVar dbSNP ExAC gnomAD v3 gnomAD v4 |
| 13 | g.32398276G>C | CA387765759 | BRCA2 | c.*286G>C (n.*286G>C) c.*1130G>C (n.*1130G>C) c.9394G>C (p.Gly3132Arg) c.*1325G>C (n.*1325G>C) c.9712G>C (p.Gly3238Arg) c.2179G>C (p.Gly727Arg) n.1890G>C c.9763G>C (p.Gly3255Arg) c.9771G>C (n.9771G>C) n.351G>C c.9667G>C (p.Gly3223Arg) | ClinVar dbSNP gnomAD v4 |
| 13 | g.32398276G= | CA2082834906 | BRCA2 | c.*286G= (n.*286G=) c.*1130G= (n.*1130G=) c.9394G= (p.Gly3132=) c.*1325G= (n.*1325G=) c.9712G= (p.Gly3238=) c.2179G= (p.Gly727=) n.1890G= c.9763G= (p.Gly3255=) c.9771G= (n.9771G=) n.351G= c.9667G= (p.Gly3223=) | |
| 13 | g.32398276G>T | CA387765758 | BRCA2 | c.*286G>T (n.*286G>T) c.*1130G>T (n.*1130G>T) c.9394G>T (p.Gly3132Trp) c.*1325G>T (n.*1325G>T) c.9712G>T (p.Gly3238Trp) c.2179G>T (p.Gly727Trp) n.1890G>T c.9763G>T (p.Gly3255Trp) c.9771G>T (n.9771G>T) n.351G>T c.9667G>T (p.Gly3223Trp) | ClinVar dbSNP |
| 13 | g.32398279del | CA645586595 | BRCA2 | c.*289del (n.*289del) c.*1133del (n.*1133del) c.9397del (p.Glu3133ArgfsTer19) c.*1328del (n.*1328del) c.9715del (p.Glu3239ArgfsTer19) c.2182del (p.Glu728ArgfsTer19) n.1893del c.9766del (p.Glu3256ArgfsTer19) c.9774del (n.9774del) n.354del c.9670del (p.Glu3224ArgfsTer19) | COSMIC COSMIC |