Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 25759 |
| ensemblid | ENSG00000129946.11 |
| hgncid | 29869 |
| symbol | SHC2 |
| name | SHC adaptor protein 2 |
| refseq_nuc | NM_012435.3 |
| refseq_prot | NP_036567.2 |
| ensembl_nuc | ENST00000264554.11 |
| ensembl_prot | ENSP00000264554.4 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 416589 |
| end | 461033 |
| strand | - |
| ver | v1.2 |
| region | chr19:416589-461033 |
| region5000 | chr19:411589-466033 |
| regionname0 | SHC2_chr19_416589_461033 |
| regionname5000 | SHC2_chr19_411589_466033 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 582 | 179 | 46 | 35 | 75 | 5 | 18 | 45 | SHC2_chr19_411589_466033 | SHC2 | MTQGP others(577): Show |
chr19 | 411589 | 466033 |
| a0002 | 1/1 | 582 | 19 | 1 | 6 | 1 | 1 | 8 | 1 | SHC2_chr19_411589_466033 | SHC2 | MTQGP others(577): Show |
chr19 | 411589 | 466033 |
| a0003 | 0/0 | 582 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | MTQGP others(577): Show |
chr19 | 411589 | 466033 |
| a0004 | 0/0 | 582 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | MTQGP others(577): Show |
chr19 | 411589 | 466033 |
| a0005 | 0/0 | 582 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | MTQGP others(577): Show |
chr19 | 411589 | 466033 |
| a0006 | 0/0 | 582 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SHC2_chr19_411589_466033 | SHC2 | MTQGP others(577): Show |
chr19 | 411589 | 466033 |
| a0007 | 0/0 | 582 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | MTQGP others(577): Show |
chr19 | 411589 | 466033 |
| a0008 | 0/0 | 582 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | MTQGP others(577): Show |
chr19 | 411589 | 466033 |
| a0009 | 0/0 | 582 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | MTQGP others(577): Show |
chr19 | 411589 | 466033 |
| a0010 | 0/0 | 582 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | MTQGP others(577): Show |
chr19 | 411589 | 466033 |
| a0011 | 0/0 | 582 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | MTQGP others(577): Show |
chr19 | 411589 | 466033 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1746 | 88 | 27 | 18 | 35 | 2 | 6 | SHC2_chr19_411589_466033 | SHC2 | ATGAC others(1741): Show |
chr19 | 411589 | 466033 | ||
| a0001c0002 | 0/0 | 1746 | 38 | 2 | 7 | 23 | 0 | 6 | SHC2_chr19_411589_466033 | SHC2 | ATGAC others(1741): Show |
chr19 | 411589 | 466033 | ||
| a0001c0003 | 0/0 | 1746 | 23 | 0 | 2 | 17 | 0 | 4 | SHC2_chr19_411589_466033 | SHC2 | ATGAC others(1741): Show |
chr19 | 411589 | 466033 | ||
| a0001c0005 | 0/0 | 1746 | 12 | 4 | 4 | 0 | 2 | 2 | SHC2_chr19_411589_466033 | SHC2 | ATGAC others(1741): Show |
chr19 | 411589 | 466033 | ||
| a0001c0006 | 0/0 | 1746 | 6 | 4 | 1 | 0 | 1 | 0 | SHC2_chr19_411589_466033 | SHC2 | ATGAC others(1741): Show |
chr19 | 411589 | 466033 | ||
| a0001c0007 | 0/0 | 1746 | 5 | 5 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | ATGAC others(1741): Show |
chr19 | 411589 | 466033 | ||
| a0001c0013 | 0/0 | 1746 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | ATGAC others(1741): Show |
chr19 | 411589 | 466033 | ||
| a0001c0014 | 0/0 | 1746 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | ATGAC others(1741): Show |
chr19 | 411589 | 466033 | ||
| a0001c0016 | 0/0 | 1746 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | ATGAC others(1741): Show |
chr19 | 411589 | 466033 | ||
| a0001c0017 | 0/0 | 1746 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | ATGAC others(1741): Show |
chr19 | 411589 | 466033 | ||
| a0001c0018 | 0/0 | 1746 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | ATGAC others(1741): Show |
chr19 | 411589 | 466033 | ||
| a0001c0020 | 0/0 | 1746 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | ATGAC others(1741): Show |
chr19 | 411589 | 466033 | ||
| a0001c0023 | 0/0 | 1746 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | ATGAC others(1741): Show |
chr19 | 411589 | 466033 | ||
| a0002c0004 | 1/1 | 1746 | 16 | 0 | 6 | 0 | 1 | 7 | SHC2_chr19_411589_466033 | SHC2 | ATGAC others(1741): Show |
chr19 | 411589 | 466033 | ||
| a0002c0012 | 0/0 | 1746 | 2 | 0 | 0 | 1 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | ATGAC others(1741): Show |
chr19 | 411589 | 466033 | ||
| a0002c0024 | 0/0 | 1746 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | ATGAC others(1741): Show |
chr19 | 411589 | 466033 | ||
| a0003c0008 | 0/0 | 1746 | 3 | 3 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | ATGAC others(1741): Show |
chr19 | 411589 | 466033 | ||
| a0004c0011 | 0/0 | 1746 | 2 | 1 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | ATGAC others(1741): Show |
chr19 | 411589 | 466033 | ||
| a0005c0009 | 0/0 | 1746 | 2 | 2 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | ATGAC others(1741): Show |
chr19 | 411589 | 466033 | ||
| a0006c0010 | 0/0 | 1746 | 2 | 0 | 0 | 2 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | ATGAC others(1741): Show |
chr19 | 411589 | 466033 | ||
| a0007c0025 | 0/0 | 1746 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | ATGAC others(1741): Show |
chr19 | 411589 | 466033 | ||
| a0008c0015 | 0/0 | 1746 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | ATGAC others(1741): Show |
chr19 | 411589 | 466033 | ||
| a0009c0021 | 0/0 | 1746 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | ATGAC others(1741): Show |
chr19 | 411589 | 466033 | ||
| a0010c0019 | 0/0 | 1746 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | ATGAC others(1741): Show |
chr19 | 411589 | 466033 | ||
| a0011c0022 | 0/0 | 1746 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | ATGAC others(1741): Show |
chr19 | 411589 | 466033 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2525 | 52 | 0 | 12 | 35 | 2 | 3 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0001t0002 | 0/0 | 2525 | 5 | 5 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0001t0003 | 0/0 | 2525 | 7 | 6 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0001t0004 | 0/0 | 2525 | 7 | 2 | 3 | 0 | 0 | 2 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0001t0005 | 0/0 | 2525 | 6 | 5 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0001t0006 | 0/0 | 2525 | 5 | 5 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0001t0007 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0001t0008 | 0/0 | 2525 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0001t0009 | 0/0 | 2525 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0001t0011 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0001t0013 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0001t0016 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0002t0001 | 0/0 | 2525 | 21 | 1 | 2 | 14 | 0 | 4 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0002t0002 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0002t0003 | 0/0 | 2525 | 10 | 0 | 2 | 6 | 0 | 2 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0002t0004 | 0/0 | 2525 | 6 | 0 | 3 | 3 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0003t0001 | 0/0 | 2525 | 5 | 0 | 2 | 2 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0003t0002 | 0/0 | 2525 | 14 | 0 | 0 | 11 | 0 | 3 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0003t0004 | 0/0 | 2525 | 3 | 0 | 0 | 3 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0003t0010 | 0/0 | 2525 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0005t0001 | 0/0 | 2525 | 8 | 0 | 4 | 0 | 2 | 2 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0005t0005 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0005t0006 | 0/0 | 2525 | 2 | 2 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0005t0015 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0006t0001 | 0/0 | 2525 | 3 | 3 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0006t0002 | 0/0 | 2525 | 2 | 0 | 1 | 0 | 1 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0006t0006 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0007t0002 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0007t0003 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0007t0006 | 0/0 | 2525 | 3 | 3 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0013t0005 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0014t0001 | 0/0 | 2525 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0016t0001 | 0/0 | 2525 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0017t0005 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0018t0006 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0020t0001 | 0/0 | 2525 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0001c0023t0007 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0002c0004t0001 | 0/1 | 2525 | 10 | 0 | 4 | 0 | 0 | 5 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0002c0004t0004 | 0/0 | 2525 | 2 | 0 | 1 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0002c0004t0005 | 1/0 | 2525 | 4 | 0 | 1 | 0 | 1 | 1 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0002c0012t0002 | 0/0 | 2525 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0002c0012t0004 | 0/0 | 2525 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0002c0024t0003 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0003c0008t0003 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0003c0008t0005 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0003c0008t0006 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0004c0011t0005 | 0/0 | 2525 | 2 | 1 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0005c0009t0005 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0005c0009t0014 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0006c0010t0002 | 0/0 | 2525 | 2 | 0 | 0 | 2 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0007c0025t0001 | 0/0 | 2525 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0008c0015t0012 | 0/0 | 2525 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0009c0021t0002 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0010c0019t0001 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| a0011c0022t0002 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | GCAGC others(2520): Show |
chr19 | 411589 | 466033 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0003g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0004g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0005g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0008g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0009g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0011g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0013g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0001t0016g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0004g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0004g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0002t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0003t0010g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0005t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0005t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0005t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0005t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0005t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0005t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0005t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0005t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0005t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0005t0006g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0005t0006g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0005t0015g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0006t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0006t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0006t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0006t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0006t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0006t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0007t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0007t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0007t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0007t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0007t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0013t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0014t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0016t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0017t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0018t0006g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0020t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0001c0023t0007g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0004t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0004t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0004t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0004t0001g0194 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0004t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0004t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0004t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0004t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0004t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0004t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0004t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0004t0004g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0004t0005g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0004t0005g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0004t0005g0201 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0004t0005g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0012t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0012t0004g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0002c0024t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0003c0008t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0003c0008t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0003c0008t0006g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0004c0011t0005g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0004c0011t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0005c0009t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0005c0009t0014g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0006c0010t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0006c0010t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0007c0025t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0008c0015t0012g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0009c0021t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0010c0019t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| a0011c0022t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0005 | t0001 | g0015 | EUR | GBR | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00099 | hp2 | a0001 | c0005 | t0001 | g0020 | EUR | GBR | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | FIN | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00323 | hp2 | a0002 | c0004 | t0005 | g0204 | EUR | FIN | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0155 | EAS | CHS | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00544 | hp2 | a0001 | c0003 | t0002 | g0112 | EAS | CHS | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00558 | hp1 | a0001 | c0003 | t0002 | g0118 | EAS | CHS | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | CHS | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00621 | hp1 | a0001 | c0003 | t0010 | g0059 | EAS | CHS | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00621 | hp2 | a0001 | c0003 | t0002 | g0100 | EAS | CHS | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00639 | hp1 | a0002 | c0004 | t0001 | g0193 | AMR | PUR | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00639 | hp2 | a0001 | c0005 | t0001 | g0018 | AMR | PUR | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00733 | hp2 | a0002 | c0004 | t0001 | g0199 | AMR | PUR | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00735 | hp1 | a0001 | c0014 | t0001 | g0014 | AMR | PUR | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG00735 | hp2 | a0001 | c0005 | t0001 | g0021 | AMR | PUR | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01071 | hp2 | a0001 | c0002 | t0003 | g0149 | AMR | PUR | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0124 | AMR | PUR | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01074 | hp2 | a0001 | c0003 | t0001 | g0063 | AMR | PUR | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01099 | hp1 | a0007 | c0025 | t0001 | g0207 | AMR | PUR | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01099 | hp2 | a0001 | c0005 | t0001 | g0011 | AMR | PUR | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01109 | hp1 | a0001 | c0005 | t0001 | g0024 | AMR | PUR | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01109 | hp2 | a0004 | c0011 | t0005 | g0057 | AMR | PUR | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01256 | hp2 | a0002 | c0004 | t0001 | g0198 | AMR | CLM | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01258 | hp1 | a0002 | c0004 | t0005 | g0189 | AMR | CLM | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01358 | hp1 | a0001 | c0016 | t0001 | g0159 | AMR | CLM | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01358 | hp2 | a0002 | c0004 | t0001 | g0192 | AMR | CLM | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01361 | hp1 | a0001 | c0020 | t0001 | g0105 | AMR | CLM | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | ACB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01884 | hp2 | a0001 | c0023 | t0007 | g0187 | AFR | ACB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | ACB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0102 | AFR | ACB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01943 | hp2 | a0001 | c0006 | t0002 | g0023 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01952 | hp1 | a0008 | c0015 | t0012 | g0026 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01952 | hp2 | a0001 | c0002 | t0003 | g0150 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0082 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01981 | hp1 | a0002 | c0004 | t0004 | g0191 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0164 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0092 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02004 | hp2 | a0001 | c0002 | t0004 | g0087 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0154 | EAS | KHV | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0169 | EAS | KHV | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | ACB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | KHV | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | KHV | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02083 | hp2 | a0001 | c0002 | t0003 | g0084 | EAS | KHV | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02132 | hp2 | a0001 | c0003 | t0002 | g0071 | EAS | KHV | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | KHV | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02145 | hp1 | a0003 | c0008 | t0003 | g0184 | AFR | ACB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0037 | AFR | ACB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02148 | hp1 | a0001 | c0001 | t0008 | g0126 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0162 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CDX | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02165 | hp2 | a0001 | c0002 | t0003 | g0148 | EAS | CDX | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02258 | hp1 | a0001 | c0001 | t0013 | g0072 | AFR | ACB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0181 | AFR | ACB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02273 | hp1 | a0001 | c0002 | t0004 | g0107 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02293 | hp1 | a0001 | c0002 | t0004 | g0158 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02293 | hp2 | a0001 | c0003 | t0001 | g0114 | AMR | PEL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0031 | AFR | ACB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02451 | hp2 | a0001 | c0007 | t0006 | g0033 | AFR | ACB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0048 | AFR | GWD | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | GWD | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02622 | hp1 | a0001 | c0017 | t0005 | g0055 | AFR | GWD | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02622 | hp2 | a0001 | c0013 | t0005 | g0006 | AFR | GWD | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02698 | hp1 | a0001 | c0002 | t0003 | g0151 | SAS | PJL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0157 | SAS | PJL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02735 | hp1 | a0001 | c0005 | t0001 | g0025 | SAS | PJL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02818 | hp1 | a0003 | c0008 | t0006 | g0186 | AFR | GWD | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0038 | AFR | GWD | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02922 | hp1 | a0009 | c0021 | t0002 | g0028 | AFR | ESN | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0052 | AFR | ESN | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0049 | AFR | ESN | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0040 | AFR | ESN | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02976 | hp1 | a0001 | c0007 | t0006 | g0041 | AFR | ESN | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02976 | hp2 | a0001 | c0005 | t0015 | g0007 | AFR | ESN | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03017 | hp1 | a0002 | c0012 | t0004 | g0195 | SAS | PJL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0046 | SAS | PJL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | MSL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03098 | hp2 | a0001 | c0006 | t0006 | g0010 | AFR | MSL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03195 | hp1 | a0001 | c0007 | t0003 | g0039 | AFR | ESN | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0172 | AFR | ESN | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0050 | AFR | MSL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03209 | hp2 | a0001 | c0006 | t0001 | g0013 | AFR | MSL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03225 | hp1 | a0001 | c0005 | t0006 | g0009 | AFR | MSL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03225 | hp2 | a0004 | c0011 | t0005 | g0061 | AFR | MSL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03491 | hp1 | a0002 | c0004 | t0001 | g0196 | SAS | PJL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0042 | AFR | GWD | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03540 | hp2 | a0001 | c0005 | t0006 | g0008 | AFR | GWD | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03579 | hp1 | a0001 | c0007 | t0006 | g0054 | AFR | MSL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03579 | hp2 | a0001 | c0018 | t0006 | g0180 | AFR | MSL | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03688 | hp1 | a0001 | c0003 | t0002 | g0075 | SAS | STU | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03688 | hp2 | a0001 | c0003 | t0001 | g0140 | SAS | STU | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03831 | hp1 | a0002 | c0004 | t0001 | g0206 | SAS | BEB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0095 | SAS | BEB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0094 | SAS | BEB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03927 | hp2 | a0001 | c0005 | t0001 | g0012 | SAS | BEB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03942 | hp1 | a0002 | c0004 | t0001 | g0202 | SAS | BEB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0173 | SAS | BEB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | STU | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG04199 | hp2 | a0002 | c0004 | t0004 | g0203 | SAS | STU | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG04204 | hp1 | a0001 | c0003 | t0002 | g0182 | SAS | STU | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG04204 | hp2 | a0002 | c0004 | t0001 | g0190 | SAS | STU | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG04228 | hp1 | a0001 | c0003 | t0002 | g0074 | SAS | STU | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG04228 | hp2 | a0001 | c0002 | t0003 | g0175 | SAS | STU | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0053 | AFR | YRI | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18522 | hp2 | a0005 | c0009 | t0005 | g0047 | AFR | YRI | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | CHB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18612 | hp2 | a0001 | c0003 | t0004 | g0110 | EAS | CHB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18747 | hp1 | a0001 | c0002 | t0003 | g0160 | EAS | CHB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18906 | hp1 | a0001 | c0006 | t0001 | g0016 | AFR | YRI | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0045 | AFR | YRI | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18940 | hp2 | a0001 | c0003 | t0001 | g0060 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18947 | hp1 | a0001 | c0002 | t0004 | g0177 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18954 | hp1 | a0001 | c0003 | t0002 | g0152 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18954 | hp2 | a0001 | c0003 | t0002 | g0073 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18960 | hp1 | a0002 | c0012 | t0002 | g0205 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18960 | hp2 | a0001 | c0002 | t0003 | g0174 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18971 | hp1 | a0001 | c0002 | t0004 | g0176 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18985 | hp2 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18988 | hp2 | a0001 | c0002 | t0004 | g0096 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18989 | hp2 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18995 | hp1 | a0001 | c0002 | t0003 | g0044 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18995 | hp2 | a0001 | c0003 | t0002 | g0062 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18999 | hp1 | a0001 | c0003 | t0002 | g0068 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19009 | hp1 | a0001 | c0002 | t0003 | g0091 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19009 | hp2 | a0006 | c0010 | t0002 | g0067 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19030 | hp1 | a0001 | c0007 | t0002 | g0077 | AFR | LWK | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | LWK | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | LWK | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19043 | hp2 | a0002 | c0024 | t0003 | g0200 | AFR | LWK | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19056 | hp2 | a0001 | c0003 | t0002 | g0065 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19066 | hp2 | a0001 | c0003 | t0004 | g0111 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19074 | hp2 | a0001 | c0003 | t0001 | g0064 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19080 | hp1 | a0006 | c0010 | t0002 | g0066 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19091 | hp2 | a0001 | c0003 | t0004 | g0109 | EAS | JPT | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19240 | hp1 | a0005 | c0009 | t0014 | g0036 | AFR | YRI | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA19240 | hp2 | a0011 | c0022 | t0002 | g0185 | AFR | YRI | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | TSI | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA20752 | hp2 | a0001 | c0006 | t0002 | g0022 | EUR | TSI | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA20905 | hp1 | a0002 | c0004 | t0001 | g0197 | SAS | GIH | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA20905 | hp2 | a0002 | c0004 | t0005 | g0188 | SAS | GIH | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG01123 | hp2 | a0001 | c0001 | t0009 | g0166 | AMR | CLM | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02486 | hp1 | a0001 | c0001 | t0011 | g0034 | AFR | ACB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0030 | AFR | ACB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | ACB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG02559 | hp2 | a0003 | c0008 | t0005 | g0183 | AFR | ACB | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG06807 | hp1 | a0001 | c0006 | t0001 | g0017 | AFR | USA | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| HG06807 | hp2 | a0010 | c0019 | t0001 | g0123 | AFR | USA | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0088 | AFR | USA | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | USA | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA21309 | hp1 | a0001 | c0001 | t0016 | g0069 | AFR | LWK | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| NA21309 | hp2 | a0001 | c0005 | t0005 | g0019 | AFR | LWK | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| homoSapiens | chm13v2 | a0002 | c0004 | t0001 | g0194 | REF | REF | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| homoSapiens | grch38p0 | a0002 | c0004 | t0005 | g0201 | REF | REF | SHC2_chr19_411589_466033 | SHC2 | chr19 | 411589 | 466033 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:418948 | C | T | 1 | a0010 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.1729G>A | p.Val577Met | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/13 | 1766/2525 | 1729/1749 | 577/582 | chr19 | 418948 | |||
| chr19:422229 | C | T | 2 | a0005 a0011 |
3 | NA18522.hp2 NA19240.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.1537G>A | p.Val513Ile | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/13 | 1574/2525 | 1537/1749 | 513/582 | chr19 | 422229 | |||
| chr19:430696 | A | G | 1 | a0006 | 2 | NA19009.hp2 NA19080.hp1 |
missense_variant | MODERATE | c.1162T>C | p.Ser388Pro | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/13 | 1199/2525 | 1162/1749 | 388/582 | chr19 | 430696 | |||
| chr19:434848 | T | C | 1 | a0011 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.971A>G | p.Glu324Gly | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/13 | 1008/2525 | 971/1749 | 324/582 | chr19 | 434848 | |||
| chr19:436181 | C | A | 1 | a0009 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.937G>T | p.Ala313Ser | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/13 | 974/2525 | 937/1749 | 313/582 | chr19 | 436181 | |||
| chr19:438830 | T | C | 1 | a0004 | 2 | HG01109.hp2 HG03225.hp2 |
missense_variant | MODERATE | c.608A>G | p.Asn203Ser | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/13 | 645/2525 | 608/1749 | 203/582 | chr19 | 438830 | |||
| chr19:460636 | C | T | 1 | a0008 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.361G>A | p.Ala121Thr | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/13 | 398/2525 | 361/1749 | 121/582 | chr19 | 460636 | |||
| chr19:460642 | C | A | 2 | a0003 a0011 |
4 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(1): Show |
missense_variant | MODERATE | c.355G>T | p.Ala119Ser | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/13 | 392/2525 | 355/1749 | 119/582 | chr19 | 460642 | |||
| chr19:460668 | C | G | 10 | a0001 a0003 a0004 others(7): Show |
193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
missense_variant | MODERATE | c.329G>C | p.Gly110Ala | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/13 | 366/2525 | 329/1749 | 110/582 | chr19 | 460668 | |||
| chr19:460729 | G | A | 1 | a0007 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.268C>T | p.Pro90Ser | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/13 | 305/2525 | 268/1749 | 90/582 | chr19 | 460729 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:418973 | G | A | 1 | a0001c0018 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.1704C>T | p.Ala568Ala | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/13 | 1741/2525 | 1704/1749 | 568/582 | chr19 | 418973 | |||
| chr19:422238 | G | T | 1 | a0001c0002 | 38 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(35): Show |
synonymous_variant | LOW | c.1528C>A | p.Arg510Arg | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/13 | 1565/2525 | 1528/1749 | 510/582 | chr19 | 422238 | |||
| chr19:422452 | G | C | 4 | a0001c0007 a0001c0023 a0002c0024 others(1): Show |
9 | HG01109.hp2 HG01884.hp2 HG02451.hp2 others(6): Show |
synonymous_variant | LOW | c.1314C>G | p.Pro438Pro | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/13 | 1351/2525 | 1314/1749 | 438/582 | chr19 | 422452 | |||
| chr19:425131 | C | T | 3 | a0001c0013 a0001c0017 a0001c0018 |
3 | HG02622.hp1 HG02622.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.1275G>A | p.Pro425Pro | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/13 | 1312/2525 | 1275/1749 | 425/582 | chr19 | 425131 | |||
| chr19:425182 | G | A | 3 | a0001c0014 a0001c0020 a0007c0025 |
3 | HG00735.hp1 HG01099.hp1 HG01361.hp1 |
synonymous_variant | LOW | c.1224C>T | p.Asp408Asp | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/13 | 1261/2525 | 1224/1749 | 408/582 | chr19 | 425182 | |||
| chr19:425224 | C | T | 1 | a0001c0016 | 1 | HG01358.hp1 | synonymous_variant | LOW | c.1182G>A | p.Pro394Pro | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/13 | 1219/2525 | 1182/1749 | 394/582 | chr19 | 425224 | |||
| chr19:434718 | G | A | 5 | a0001c0003 a0001c0006 a0002c0012 others(2): Show |
34 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(31): Show |
synonymous_variant | LOW | c.1101C>T | p.Ala367Ala | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/13 | 1138/2525 | 1101/1749 | 367/582 | chr19 | 434718 | |||
| chr19:460658 | C | A | 1 | a0001c0023 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.339G>T | p.Ala113Ala | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/13 | 376/2525 | 339/1749 | 113/582 | chr19 | 460658 | |||
| chr19:460883 | C | T | 4 | a0001c0005 a0001c0006 a0001c0013 others(1): Show |
20 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(17): Show |
synonymous_variant | LOW | c.114G>A | p.Ala38Ala | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/13 | 151/2525 | 114/1749 | 38/582 | chr19 | 460883 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:416616 | C | T | 1 | a0001c0003t0010 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*712G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 13/13 | 2312 | chr19 | 416616 | ||||||
| chr19:416664 | C | T | 45 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(42): Show |
192 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*664G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 13/13 | 2264 | chr19 | 416664 | ||||||
| chr19:416666 | G | C | 7 | a0001c0001t0006 a0001c0001t0013 a0001c0005t0006 others(4): Show |
14 | HG02258.hp1 HG02451.hp2 HG02486.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*662C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 13/13 | 2262 | chr19 | 416666 | ||||||
| chr19:416694 | C | T | 1 | a0001c0005t0015 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*634G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 13/13 | 2234 | chr19 | 416694 | ||||||
| chr19:416834 | A | G | 20 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(17): Show |
54 | HG00544.hp2 HG00558.hp1 HG00621.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*494T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 13/13 | 2094 | chr19 | 416834 | ||||||
| chr19:416950 | G | A | 1 | a0001c0001t0016 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*378C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 13/13 | 1978 | chr19 | 416950 | ||||||
| chr19:416963 | C | T | 14 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(11): Show |
106 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*365G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 13/13 | 1965 | chr19 | 416963 | ||||||
| chr19:417014 | A | C | 46 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(43): Show |
193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*314T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 13/13 | 1914 | chr19 | 417014 | ||||||
| chr19:417157 | C | T | 10 | a0001c0001t0002 a0001c0002t0002 a0001c0003t0002 others(7): Show |
29 | HG00544.hp2 HG00558.hp1 HG00621.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*171G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 13/13 | 1771 | chr19 | 417157 | ||||||
| chr19:417196 | C | T | 1 | a0001c0001t0009 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*132G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 13/13 | 1732 | chr19 | 417196 | ||||||
| chr19:417214 | C | T | 1 | a0001c0001t0008 | 1 | HG02148.hp1 | 3_prime_UTR_variant | MODIFIER | c.*114G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 13/13 | 1714 | chr19 | 417214 | ||||||
| chr19:417256 | C | T | 1 | a0008c0015t0012 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*72G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 13/13 | 1672 | chr19 | 417256 | ||||||
| chr19:417262 | G | A | 6 | a0001c0001t0003 a0001c0001t0016 a0001c0002t0003 others(3): Show |
21 | HG01071.hp2 HG01952.hp2 HG01978.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*66C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 13/13 | 1666 | chr19 | 417262 | ||||||
| chr19:417281 | C | T | 15 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(12): Show |
107 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*47G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 13/13 | 1647 | chr19 | 417281 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:417396 | T | C | 188 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0058 others(185): Show |
193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.*6-74A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 417396 | |||||||
| chr19:417556 | A | G | 146 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0058 others(143): Show |
150 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.*6-234T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 417556 | |||||||
| chr19:417588 | C | T | 18 | a0001c0001t0004g0002 a0001c0001t0004g0031 a0001c0001t0004g0124 others(15): Show |
19 | HG01074.hp1 HG01981.hp1 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.*6-266G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 417588 | |||||||
| chr19:417621 | C | T | 1 | a0001c0001t0004g0031 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.*6-299G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 417621 | |||||||
| chr19:417633 | C | G | 1 | a0001c0001t0004g0031 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.*6-311G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 417633 | |||||||
| chr19:417705 | C | T | 1 | a0001c0002t0001g0088 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.*6-383G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 417705 | |||||||
| chr19:417706 | G | A | 1 | a0001c0002t0001g0157 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.*6-384C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 417706 | |||||||
| chr19:417714 | C | T | 4 | a0001c0001t0003g0032 a0001c0001t0003g0049 a0001c0001t0003g0070 others(1): Show |
4 | HG02055.hp2 HG02486.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.*6-392G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 417714 | |||||||
| chr19:417729 | C | T | 1 | a0001c0005t0001g0024 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.*6-407G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 417729 | |||||||
| chr19:417737 | A | G | 188 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0058 others(185): Show |
193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.*6-415T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 417737 | |||||||
| chr19:417826 | TGGGTGGA others(15): Show |
T | 1 | a0001c0001t0001g0003 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.*6-526_*6-505delTA others(20): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 417826 | |||||||
| chr19:417870 | G | C | 21 | a0001c0001t0001g0165 a0001c0001t0002g0051 a0001c0003t0002g0001 others(18): Show |
22 | HG00544.hp2 HG00558.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.*6-548C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 417870 | |||||||
| chr19:417989 | G | A | 1 | a0001c0003t0001g0060 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.*6-667C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 417989 | |||||||
| chr19:418056 | A | G | 33 | a0001c0001t0001g0171 a0001c0001t0003g0005 a0001c0001t0003g0172 others(30): Show |
35 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.*6-734T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418056 | |||||||
| chr19:418065 | A | G | 14 | a0001c0001t0001g0135 a0001c0001t0007g0038 a0001c0002t0001g0079 others(11): Show |
14 | HG00558.hp2 HG01993.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.*6-743T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418065 | |||||||
| chr19:418126 | C | G | 1 | a0001c0001t0003g0032 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.*5+797G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418126 | |||||||
| chr19:418131 | C | T | 54 | a0001c0001t0001g0171 a0001c0001t0003g0005 a0001c0001t0003g0172 others(51): Show |
57 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.*5+792G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418131 | |||||||
| chr19:418133 | C | T | 1 | a0001c0001t0004g0164 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.*5+790G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418133 | |||||||
| chr19:418178 | A | G | 194 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0058 others(191): Show |
199 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.*5+745T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418178 | |||||||
| chr19:418232 | C | T | 3 | a0002c0004t0001g0190 a0002c0004t0001g0193 a0002c0004t0001g0202 |
3 | HG00639.hp1 HG03942.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.*5+691G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418232 | |||||||
| chr19:418250 | C | T | 1 | a0001c0002t0001g0154 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.*5+673G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418250 | |||||||
| chr19:418323 | C | T | 12 | a0001c0001t0002g0056 a0001c0001t0004g0002 a0001c0001t0004g0124 others(9): Show |
13 | HG01074.hp1 HG01358.hp2 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.*5+600G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418323 | |||||||
| chr19:418433 | C | T | 1 | a0001c0003t0002g0118 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.*5+490G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418433 | |||||||
| chr19:418436 | C | T | 20 | a0001c0001t0004g0002 a0001c0001t0004g0031 a0001c0001t0004g0124 others(17): Show |
22 | HG01074.hp1 HG01109.hp2 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.*5+487G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418436 | |||||||
| chr19:418507 | C | T | 16 | a0001c0001t0002g0101 a0001c0001t0004g0162 a0001c0001t0004g0164 others(13): Show |
17 | HG00544.hp2 HG01358.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.*5+416G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418507 | |||||||
| chr19:418549 | G | A | 2 | a0001c0003t0002g0062 a0002c0012t0002g0205 |
2 | NA18960.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.*5+374C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418549 | |||||||
| chr19:418556 | G | A | 18 | a0001c0001t0002g0101 a0001c0001t0003g0049 a0001c0001t0004g0002 others(15): Show |
19 | HG00544.hp2 HG01074.hp1 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.*5+367C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418556 | |||||||
| chr19:418624 | A | G | 7 | a0001c0001t0004g0031 a0001c0001t0005g0027 a0001c0001t0005g0037 others(4): Show |
7 | HG01891.hp1 HG01891.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.*5+299T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418624 | |||||||
| chr19:418701 | AGGGGACA others(16): Show |
A | 14 | a0001c0001t0002g0051 a0001c0001t0003g0049 a0001c0001t0011g0034 others(11): Show |
14 | HG01109.hp2 HG02258.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.*5+199_*5+221delAC others(21): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418701 | |||||||
| chr19:418769 | G | A | 67 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0058 others(64): Show |
68 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.*5+154C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418769 | |||||||
| chr19:418786 | G | A | 51 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0002g0051 others(48): Show |
52 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.*5+137C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418786 | |||||||
| chr19:418790 | C | T | 3 | a0001c0001t0002g0051 a0001c0001t0003g0049 a0005c0009t0014g0036 |
3 | HG02559.hp1 HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.*5+133G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418790 | |||||||
| chr19:418791 | G | A | 4 | a0001c0001t0002g0101 a0001c0001t0007g0038 a0001c0005t0006g0008 others(1): Show |
4 | HG02572.hp2 HG02818.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.*5+132C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418791 | |||||||
| chr19:418805 | CCT | C | 6 | a0001c0001t0002g0076 a0001c0001t0004g0031 a0001c0001t0005g0027 others(3): Show |
6 | HG01884.hp1 HG01891.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.*5+116_*5+117delAG | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418805 | |||||||
| chr19:418835 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.*5+88G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418835 | |||||||
| chr19:418892 | A | G | 1 | a0002c0004t0004g0191 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.*5+31T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418892 | |||||||
| chr19:418914 | G | C | 1 | a0002c0012t0004g0195 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.*5+9C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418914 | |||||||
| chr19:418915 | C | G | 4 | a0001c0003t0001g0063 a0001c0006t0001g0013 a0001c0006t0001g0016 others(1): Show |
4 | HG01074.hp2 HG03209.hp2 HG06807.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.*5+8G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 12/12 | chr19 | 418915 | |||||||
| chr19:419075 | G | A | 22 | a0001c0003t0001g0060 a0001c0003t0001g0063 a0001c0003t0002g0001 others(19): Show |
23 | HG00544.hp2 HG00558.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.1621-19C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 419075 | |||||||
| chr19:419167 | C | T | 1 | a0001c0018t0006g0180 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1621-111G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 419167 | |||||||
| chr19:419204 | A | C | 8 | a0001c0001t0002g0076 a0001c0001t0003g0070 a0001c0001t0004g0031 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1621-148T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 419204 | |||||||
| chr19:419232 | C | A | 1 | a0011c0022t0002g0185 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1621-176G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 419232 | |||||||
| chr19:419246 | C | T | 3 | a0001c0001t0003g0070 a0001c0001t0011g0034 a0001c0007t0003g0039 |
3 | HG02486.hp1 HG03195.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1621-190G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 419246 | |||||||
| chr19:419407 | A | G | 189 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0058 others(186): Show |
194 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(191): Show |
intron_variant | MODIFIER | c.1621-351T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 419407 | |||||||
| chr19:419471 | T | C | 189 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0058 others(186): Show |
194 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(191): Show |
intron_variant | MODIFIER | c.1621-415A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 419471 | |||||||
| chr19:419498 | T | C | 56 | a0001c0001t0002g0076 a0001c0001t0003g0070 a0001c0001t0004g0031 others(53): Show |
57 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.1621-442A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 419498 | |||||||
| chr19:419531 | G | A | 2 | a0001c0001t0002g0076 a0001c0001t0005g0053 |
2 | HG01884.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1621-475C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 419531 | |||||||
| chr19:419561 | G | A | 1 | a0001c0007t0003g0039 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1621-505C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 419561 | |||||||
| chr19:419593 | G | A | 5 | a0001c0002t0001g0004 a0001c0002t0004g0087 a0001c0002t0004g0096 others(2): Show |
6 | HG02004.hp2 HG02273.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.1621-537C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 419593 | |||||||
| chr19:419788 | C | T | 25 | a0001c0002t0001g0079 a0001c0002t0001g0080 a0001c0002t0001g0082 others(22): Show |
25 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.1621-732G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 419788 | |||||||
| chr19:419799 | T | TA | 9 | a0001c0001t0002g0076 a0001c0001t0004g0031 a0001c0001t0005g0027 others(6): Show |
9 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1621-744dupT | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 419799 | |||||||
| chr19:419874 | T | C | 1 | a0001c0001t0001g0078 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1621-818A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 419874 | |||||||
| chr19:420118 | C | T | 1 | a0001c0002t0001g0095 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1621-1062G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 420118 | |||||||
| chr19:420349 | C | A | 5 | a0001c0007t0002g0077 a0001c0007t0006g0033 a0001c0007t0006g0054 others(2): Show |
5 | HG02451.hp2 HG02559.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1621-1293G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 420349 | |||||||
| chr19:420393 | C | T | 1 | a0003c0008t0005g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1621-1337G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 420393 | |||||||
| chr19:420436 | C | T | 4 | a0001c0007t0002g0077 a0001c0007t0006g0033 a0001c0007t0006g0054 others(1): Show |
4 | HG02451.hp2 HG03579.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1621-1380G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 420436 | |||||||
| chr19:420619 | T | C | 3 | a0001c0003t0002g0001 a0001c0003t0002g0112 a0001c0003t0002g0152 |
4 | HG00544.hp2 NA18954.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.1620+1527A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 420619 | |||||||
| chr19:420636 | G | C | 1 | a0001c0005t0006g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1620+1510C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 420636 | |||||||
| chr19:420751 | C | T | 2 | a0001c0002t0003g0084 a0001c0002t0003g0160 |
2 | HG02083.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.1620+1395G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 420751 | |||||||
| chr19:420755 | G | A | 144 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0058 others(141): Show |
149 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.1620+1391C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 420755 | |||||||
| chr19:420780 | G | A | 1 | a0001c0001t0002g0051 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1620+1366C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 420780 | |||||||
| chr19:420834 | A | G | 2 | a0001c0002t0004g0176 a0001c0002t0004g0177 |
2 | NA18947.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1620+1312T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 420834 | |||||||
| chr19:420918 | T | C | 22 | a0001c0001t0002g0035 a0001c0001t0002g0056 a0001c0001t0003g0005 others(19): Show |
23 | HG01891.hp2 HG01978.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1620+1228A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 420918 | |||||||
| chr19:420922 | C | T | 22 | a0001c0001t0002g0035 a0001c0001t0002g0056 a0001c0001t0003g0005 others(19): Show |
23 | HG01891.hp2 HG01978.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1620+1224G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 420922 | |||||||
| chr19:420941 | T | G | 5 | a0001c0003t0001g0114 a0001c0003t0004g0109 a0001c0003t0004g0110 others(2): Show |
5 | HG01952.hp1 HG02293.hp2 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.1620+1205A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 420941 | |||||||
| chr19:420975 | G | A | 13 | a0001c0001t0004g0002 a0001c0001t0004g0162 a0001c0001t0004g0164 others(10): Show |
15 | HG01358.hp2 HG01981.hp1 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.1620+1171C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 420975 | |||||||
| chr19:421297 | A | G | 2 | a0001c0002t0004g0176 a0001c0002t0004g0177 |
2 | NA18947.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1620+849T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421297 | |||||||
| chr19:421305 | C | T | 30 | a0001c0003t0001g0060 a0001c0003t0001g0063 a0001c0003t0001g0114 others(27): Show |
31 | HG00544.hp2 HG00558.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.1620+841G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421305 | |||||||
| chr19:421397 | CA | C | 32 | a0001c0002t0001g0004 a0001c0002t0001g0079 a0001c0002t0001g0080 others(29): Show |
33 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1620+748delT | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421397 | |||||||
| chr19:421397 | CAA | C | 127 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0058 others(124): Show |
130 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.1620+747_1620+748d others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421397 | |||||||
| chr19:421408 | A | AAAAG | 7 | a0001c0007t0002g0077 a0001c0007t0006g0033 a0001c0007t0006g0054 others(4): Show |
7 | HG01109.hp2 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1620+737_1620+738i others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421408 | |||||||
| chr19:421412 | A | G | 7 | a0001c0007t0002g0077 a0001c0007t0006g0033 a0001c0007t0006g0054 others(4): Show |
7 | HG01109.hp2 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1620+734T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421412 | |||||||
| chr19:421413 | A | G | 162 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0058 others(159): Show |
166 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.1620+733T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421413 | |||||||
| chr19:421430 | A | G | 5 | a0001c0001t0002g0076 a0001c0001t0003g0032 a0001c0001t0003g0070 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1620+716T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421430 | |||||||
| chr19:421433 | G | A | 163 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0058 others(160): Show |
167 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.1620+713C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421433 | |||||||
| chr19:421454 | G | T | 2 | a0004c0011t0005g0057 a0004c0011t0005g0061 |
2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1620+692C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421454 | |||||||
| chr19:421459 | G | A | 1 | a0001c0002t0003g0148 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1620+687C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421459 | |||||||
| chr19:421467 | G | GAGGA | 171 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0058 others(168): Show |
175 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.1620+675_1620+678d others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421467 | |||||||
| chr19:421499 | T | G | 1 | a0003c0008t0003g0184 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1620+647A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421499 | |||||||
| chr19:421567 | A | G | 4 | a0001c0001t0011g0034 a0005c0009t0005g0047 a0005c0009t0014g0036 others(1): Show |
4 | HG02486.hp1 NA18522.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1620+579T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421567 | |||||||
| chr19:421571 | T | C | 1 | a0002c0012t0002g0205 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1620+575A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421571 | |||||||
| chr19:421597 | T | C | 1 | a0001c0001t0002g0051 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1620+549A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421597 | |||||||
| chr19:421661 | G | A | 1 | a0001c0003t0001g0063 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1620+485C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421661 | |||||||
| chr19:421825 | A | G | 137 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0058 others(134): Show |
140 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.1620+321T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421825 | |||||||
| chr19:421842 | C | T | 35 | a0001c0001t0002g0076 a0001c0001t0003g0032 a0001c0001t0003g0070 others(32): Show |
36 | HG00544.hp2 HG00558.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.1620+304G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421842 | |||||||
| chr19:421976 | T | C | 1 | a0001c0001t0001g0058 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1620+170A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 421976 | |||||||
| chr19:422023 | TCGAGACC others(44): Show |
T | 35 | a0001c0002t0001g0004 a0001c0002t0001g0079 a0001c0002t0001g0080 others(32): Show |
36 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.1620+72_1620+122de others(52): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 422023 | |||||||
| chr19:422033 | TGAGACCC others(35): Show |
T | 127 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0058 others(124): Show |
130 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.1620+71_1620+112de others(43): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 422033 | |||||||
| chr19:422118 | G | A | 2 | a0001c0001t0003g0172 a0003c0008t0003g0184 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1620+28C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 11/12 | chr19 | 422118 | |||||||
| chr19:422481 | G | A | 30 | a0001c0003t0001g0060 a0001c0003t0001g0063 a0001c0003t0001g0114 others(27): Show |
31 | HG00544.hp2 HG00558.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.1310-25C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422481 | |||||||
| chr19:422512 | C | T | 2 | a0001c0001t0003g0032 a0001c0005t0006g0009 |
2 | HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1310-56G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422512 | |||||||
| chr19:422534 | G | A | 99 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0058 others(96): Show |
101 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.1310-78C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422534 | |||||||
| chr19:422537 | T | A | 1 | a0001c0001t0002g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1310-81A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422537 | |||||||
| chr19:422543 | G | A | 134 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0058 others(131): Show |
137 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.1310-87C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422543 | |||||||
| chr19:422555 | G | A | 134 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0058 others(131): Show |
137 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.1310-99C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422555 | |||||||
| chr19:422579 | C | T | 97 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0058 others(94): Show |
99 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1310-123G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422579 | |||||||
| chr19:422584 | G | A | 134 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0058 others(131): Show |
137 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.1310-128C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422584 | |||||||
| chr19:422592 | C | T | 97 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0058 others(94): Show |
99 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1310-136G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422592 | |||||||
| chr19:422625 | G | A | 2 | a0001c0002t0004g0176 a0001c0002t0004g0177 |
2 | NA18947.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1310-169C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422625 | |||||||
| chr19:422625 | G | C | 68 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0058 others(65): Show |
69 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.1310-169C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422625 | |||||||
| chr19:422665 | G | A | 34 | a0001c0002t0001g0004 a0001c0002t0001g0079 a0001c0002t0001g0080 others(31): Show |
35 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.1310-209C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422665 | |||||||
| chr19:422730 | T | G | 1 | a0002c0004t0004g0203 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1310-274A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422730 | |||||||
| chr19:422738 | A | G | 2 | a0001c0001t0002g0076 a0001c0001t0013g0072 |
2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1310-282T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422738 | |||||||
| chr19:422755 | T | C | 1 | a0003c0008t0005g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1310-299A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422755 | |||||||
| chr19:422770 | C | A | 1 | a0001c0001t0001g0081 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1310-314G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422770 | |||||||
| chr19:422904 | G | C | 1 | a0001c0002t0002g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1310-448C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422904 | |||||||
| chr19:422938 | C | T | 88 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0058 others(85): Show |
90 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.1310-482G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 422938 | |||||||
| chr19:423099 | T | TCCTCCAG others(298): Show |
1 | a0001c0001t0008g0126 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1310-948_1310-644d others(307): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423099 | |||||||
| chr19:423099 | TCCTCCAG others(237): Show |
T | 1 | a0001c0002t0001g0094 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1310-887_1310-644d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423099 | |||||||
| chr19:423099 | TCCTCCAG others(298): Show |
T | 33 | a0001c0002t0001g0004 a0001c0002t0001g0079 a0001c0002t0001g0080 others(30): Show |
34 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.1310-948_1310-644d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423099 | |||||||
| chr19:423099 | TCCTCCAG others(481): Show |
T | 5 | a0001c0001t0002g0076 a0001c0001t0003g0032 a0001c0001t0003g0070 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1310-1131_1310-644 others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423099 | |||||||
| chr19:423131 | G | GCCCTGAC others(54): Show |
20 | a0001c0001t0002g0035 a0001c0001t0002g0056 a0001c0001t0003g0005 others(17): Show |
21 | HG01891.hp2 HG01978.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1310-676_1310-675i others(63): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423131 | |||||||
| chr19:423131 | GCCCTGAC others(420): Show |
G | 35 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0002g0101 others(32): Show |
36 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.1310-1102_1310-676 others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423131 | |||||||
| chr19:423142 | C | T | 31 | a0001c0003t0001g0060 a0001c0003t0001g0063 a0001c0003t0001g0064 others(28): Show |
32 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1310-686G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423142 | |||||||
| chr19:423143 | ACTCCCTG others(359): Show |
A | 1 | a0001c0001t0002g0051 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1310-1053_1310-688 others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423143 | |||||||
| chr19:423157 | C | A | 31 | a0001c0003t0001g0060 a0001c0003t0001g0063 a0001c0003t0001g0064 others(28): Show |
32 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1310-701G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423157 | |||||||
| chr19:423192 | G | C | 1 | a0001c0002t0002g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1310-736C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423192 | |||||||
| chr19:423192 | GCCCTGAC others(359): Show |
C | 1 | a0003c0008t0005g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1310-1101_1310-736 others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423192 | |||||||
| chr19:423192 | GCCCTGAC others(359): Show |
G | 41 | a0001c0003t0001g0060 a0001c0003t0001g0063 a0001c0003t0001g0064 others(38): Show |
42 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.1310-1102_1310-737 others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423192 | |||||||
| chr19:423204 | ACTCCCTG others(420): Show |
A | 1 | a0001c0002t0002g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1310-1175_1310-749 others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423204 | |||||||
| chr19:423241 | G | A | 3 | a0001c0001t0001g0089 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | HG00609.hp1 NA18985.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1310-785C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423241 | |||||||
| chr19:423279 | G | GGCCCCTC others(115): Show |
1 | a0001c0001t0001g0147 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1310-945_1310-824d others(124): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423279 | |||||||
| chr19:423279 | GGCCCCTC others(54): Show |
G | 1 | a0001c0001t0001g0144 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1310-884_1310-824d others(63): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423279 | |||||||
| chr19:423279 | GGCCCCTC others(115): Show |
G | 1 | a0001c0001t0001g0145 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1310-945_1310-824d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423279 | |||||||
| chr19:423340 | C | CGCCCCTC others(54): Show |
4 | a0001c0005t0001g0015 a0001c0014t0001g0014 a0001c0020t0001g0105 others(1): Show |
4 | HG00099.hp1 HG00735.hp1 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.1310-885_1310-884i others(63): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423340 | |||||||
| chr19:423401 | C | G | 20 | a0001c0001t0002g0035 a0001c0001t0002g0056 a0001c0001t0003g0005 others(17): Show |
21 | HG01891.hp2 HG01978.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1310-945G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423401 | |||||||
| chr19:423436 | G | GCCCTGAC others(115): Show |
4 | a0001c0001t0001g0085 a0001c0001t0001g0120 a0001c0001t0001g0127 others(1): Show |
4 | HG00639.hp2 HG01071.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1310-1102_1310-981 others(125): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423436 | |||||||
| chr19:423436 | GCCCTGAC others(115): Show |
G | 1 | a0001c0001t0001g0058 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1310-1102_1310-981 others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423436 | |||||||
| chr19:423462 | C | A | 1 | a0001c0002t0001g0095 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1310-1006G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423462 | |||||||
| chr19:423462 | C | G | 33 | a0001c0002t0001g0004 a0001c0002t0001g0079 a0001c0002t0001g0080 others(30): Show |
34 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.1310-1006G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423462 | |||||||
| chr19:423509 | G | A | 20 | a0001c0001t0002g0035 a0001c0001t0002g0056 a0001c0001t0003g0005 others(17): Show |
21 | HG01891.hp2 HG01978.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1310-1053C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423509 | |||||||
| chr19:423509 | GCTCCCTG others(54): Show |
G | 1 | a0001c0001t0001g0171 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1310-1114_1310-105 others(65): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423509 | |||||||
| chr19:423558 | C | G | 55 | a0001c0001t0001g0113 a0001c0001t0002g0035 a0001c0001t0002g0056 others(52): Show |
57 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(54): Show |
intron_variant | MODIFIER | c.1310-1102G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423558 | |||||||
| chr19:423569 | C | T | 3 | a0001c0002t0001g0079 a0001c0002t0001g0080 a0008c0015t0012g0026 |
3 | HG00558.hp2 HG01952.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1310-1113G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423569 | |||||||
| chr19:423570 | A | G | 32 | a0001c0002t0001g0094 a0001c0003t0001g0060 a0001c0003t0001g0063 others(29): Show |
33 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.1310-1114T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423570 | |||||||
| chr19:423570 | ACTCCCTG others(54): Show |
A | 1 | a0001c0001t0001g0103 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1310-1175_1310-111 others(65): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423570 | |||||||
| chr19:423618 | C | A | 32 | a0001c0003t0001g0060 a0001c0003t0001g0063 a0001c0003t0001g0064 others(29): Show |
33 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.1310-1162G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423618 | |||||||
| chr19:423619 | G | C | 35 | a0001c0002t0001g0004 a0001c0002t0001g0079 a0001c0002t0001g0080 others(32): Show |
36 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.1310-1163C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423619 | |||||||
| chr19:423622 | C | T | 1 | a0001c0002t0001g0095 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1310-1166G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423622 | |||||||
| chr19:423631 | G | A | 34 | a0001c0002t0001g0004 a0001c0002t0001g0079 a0001c0002t0001g0080 others(31): Show |
35 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.1310-1175C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423631 | |||||||
| chr19:423734 | G | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1310-1278C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423734 | |||||||
| chr19:423933 | G | A | 32 | a0001c0003t0001g0060 a0001c0003t0001g0063 a0001c0003t0001g0064 others(29): Show |
33 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.1309+1164C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 423933 | |||||||
| chr19:424074 | T | A | 2 | a0001c0002t0003g0084 a0001c0002t0003g0160 |
2 | HG02083.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.1309+1023A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 424074 | |||||||
| chr19:424142 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1309+955A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 424142 | |||||||
| chr19:424168 | G | A | 1 | a0001c0001t0007g0038 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1309+929C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 424168 | |||||||
| chr19:424216 | G | A | 1 | a0001c0001t0001g0003 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1309+881C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 424216 | |||||||
| chr19:424267 | G | A | 1 | a0001c0006t0006g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1309+830C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 424267 | |||||||
| chr19:424326 | C | T | 1 | a0001c0003t0002g0182 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1309+771G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 424326 | |||||||
| chr19:424416 | G | A | 4 | a0001c0001t0011g0034 a0005c0009t0005g0047 a0005c0009t0014g0036 others(1): Show |
4 | HG02486.hp1 NA18522.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1309+681C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 424416 | |||||||
| chr19:424505 | G | A | 1 | a0003c0008t0005g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1309+592C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 424505 | |||||||
| chr19:424531 | C | T | 26 | a0001c0003t0001g0063 a0001c0003t0001g0114 a0001c0003t0002g0062 others(23): Show |
26 | HG00558.hp1 HG00621.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.1309+566G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 424531 | |||||||
| chr19:424559 | G | A | 1 | a0001c0002t0001g0157 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1309+538C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 424559 | |||||||
| chr19:424806 | G | A | 36 | a0001c0002t0001g0004 a0001c0002t0001g0079 a0001c0002t0001g0080 others(33): Show |
37 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1309+291C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 424806 | |||||||
| chr19:425020 | T | G | 1 | a0001c0002t0001g0004 | 2 | NA18939.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.1309+77A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 10/12 | chr19 | 425020 | |||||||
| chr19:425250 | G | C | 1 | a0001c0002t0002g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1175-19C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 425250 | |||||||
| chr19:425290 | G | A | 3 | a0001c0001t0003g0032 a0001c0001t0003g0070 a0001c0005t0006g0009 |
3 | HG02055.hp2 HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1175-59C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 425290 | |||||||
| chr19:425305 | C | T | 10 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0005t0001g0011 others(7): Show |
10 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.1175-74G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 425305 | |||||||
| chr19:425343 | C | A | 2 | a0001c0002t0004g0176 a0001c0002t0004g0177 |
2 | NA18947.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1175-112G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 425343 | |||||||
| chr19:425370 | C | A | 32 | a0001c0003t0001g0060 a0001c0003t0001g0063 a0001c0003t0001g0064 others(29): Show |
33 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.1175-139G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 425370 | |||||||
| chr19:425383 | G | A | 1 | a0001c0001t0006g0052 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1175-152C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 425383 | |||||||
| chr19:425413 | T | C | 2 | a0001c0001t0006g0052 a0003c0008t0006g0186 |
2 | HG02818.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1175-182A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 425413 | |||||||
| chr19:425460 | G | A | 1 | a0001c0002t0001g0088 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1175-229C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 425460 | |||||||
| chr19:425469 | G | A | 31 | a0001c0003t0001g0060 a0001c0003t0001g0063 a0001c0003t0001g0064 others(28): Show |
32 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1175-238C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 425469 | |||||||
| chr19:425530 | A | C | 1 | a0001c0001t0001g0097 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1175-299T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 425530 | |||||||
| chr19:425559 | T | C | 37 | a0001c0002t0001g0004 a0001c0002t0001g0079 a0001c0002t0001g0080 others(34): Show |
38 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.1175-328A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 425559 | |||||||
| chr19:425581 | A | G | 2 | a0001c0002t0004g0176 a0001c0002t0004g0177 |
2 | NA18947.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1175-350T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 425581 | |||||||
| chr19:425755 | G | A | 32 | a0001c0003t0001g0060 a0001c0003t0001g0063 a0001c0003t0001g0064 others(29): Show |
33 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.1175-524C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 425755 | |||||||
| chr19:425895 | G | A | 1 | a0001c0001t0002g0051 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1175-664C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 425895 | |||||||
| chr19:426029 | C | CA | 19 | a0001c0001t0001g0115 a0001c0001t0001g0132 a0001c0001t0002g0056 others(16): Show |
19 | HG00621.hp2 HG01071.hp2 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.1175-799dupT | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426029 | |||||||
| chr19:426029 | CA | C | 5 | a0001c0001t0002g0076 a0001c0001t0003g0032 a0001c0001t0003g0070 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1175-799delT | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426029 | |||||||
| chr19:426043 | A | C | 1 | a0001c0013t0005g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1175-812T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426043 | |||||||
| chr19:426219 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1175-988C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426219 | |||||||
| chr19:426331 | AAGAGTCC others(98): Show |
A | 1 | a0007c0025t0001g0207 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1175-1205_1175-110 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426331 | |||||||
| chr19:426359 | CGAGAGGC others(168): Show |
C | 2 | a0001c0001t0001g0134 a0001c0001t0002g0051 |
2 | HG01361.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1175-1303_1175-112 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426359 | |||||||
| chr19:426363 | A | AGGCAGAG others(28): Show |
1 | a0002c0004t0001g0198 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1175-1167_1175-113 others(39): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426363 | |||||||
| chr19:426363 | AGGCAGAG others(203): Show |
A | 5 | a0001c0001t0002g0076 a0001c0001t0003g0032 a0001c0001t0003g0070 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1175-1342_1175-113 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426363 | |||||||
| chr19:426363 | AGGCAGAG others(378): Show |
A | 1 | a0001c0001t0001g0003 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1175-1517_1175-113 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426363 | |||||||
| chr19:426428 | G | T | 1 | a0001c0002t0002g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1175-1197C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426428 | |||||||
| chr19:426433 | GGGCAGAG others(63): Show |
G | 2 | a0001c0002t0004g0176 a0001c0002t0004g0177 |
2 | NA18947.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1175-1272_1175-120 others(74): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426433 | |||||||
| chr19:426440 | G | C | 34 | a0001c0002t0001g0004 a0001c0002t0001g0079 a0001c0002t0001g0080 others(31): Show |
35 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.1175-1209C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426440 | |||||||
| chr19:426463 | G | T | 1 | a0001c0002t0002g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1175-1232C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426463 | |||||||
| chr19:426464 | AGAGAGGC others(28): Show |
A | 33 | a0001c0002t0002g0045 a0001c0003t0001g0060 a0001c0003t0001g0063 others(30): Show |
34 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.1175-1268_1175-123 others(39): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426464 | |||||||
| chr19:426468 | A | G | 2 | a0001c0001t0003g0172 a0003c0008t0003g0184 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1175-1237T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426468 | |||||||
| chr19:426503 | A | G | 33 | a0001c0002t0002g0045 a0001c0003t0001g0060 a0001c0003t0001g0063 others(30): Show |
34 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.1175-1272T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426503 | |||||||
| chr19:426503 | AGGCAGAG others(98): Show |
A | 34 | a0001c0002t0001g0004 a0001c0002t0001g0079 a0001c0002t0001g0080 others(31): Show |
35 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.1175-1377_1175-127 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426503 | |||||||
| chr19:426538 | A | AGGCAGAG others(28): Show |
1 | a0001c0001t0001g0163 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1175-1342_1175-130 others(39): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426538 | |||||||
| chr19:426538 | A | AGGCAGAG others(63): Show |
1 | a0001c0001t0001g0133 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1175-1377_1175-130 others(74): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426538 | |||||||
| chr19:426538 | A | G | 4 | a0001c0002t0004g0176 a0001c0002t0004g0177 a0001c0003t0004g0110 others(1): Show |
4 | NA18612.hp2 NA18947.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.1175-1307T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426538 | |||||||
| chr19:426538 | AGGCAGAG others(28): Show |
A | 7 | a0001c0001t0001g0142 a0001c0001t0001g0178 a0001c0001t0004g0031 others(4): Show |
7 | HG00639.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1175-1342_1175-130 others(39): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426538 | |||||||
| chr19:426538 | AGGCAGAG others(63): Show |
A | 24 | a0001c0001t0002g0035 a0001c0001t0002g0056 a0001c0001t0002g0101 others(21): Show |
25 | HG01891.hp2 HG01978.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1175-1377_1175-130 others(74): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426538 | |||||||
| chr19:426538 | AGGCAGAG others(133): Show |
A | 8 | a0001c0007t0002g0077 a0001c0007t0006g0033 a0001c0007t0006g0054 others(5): Show |
8 | HG01109.hp2 HG01884.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1175-1447_1175-130 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426538 | |||||||
| chr19:426566 | C | G | 33 | a0001c0002t0002g0045 a0001c0003t0001g0060 a0001c0003t0001g0063 others(30): Show |
34 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.1175-1335G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426566 | |||||||
| chr19:426568 | G | A | 33 | a0001c0002t0002g0045 a0001c0003t0001g0060 a0001c0003t0001g0063 others(30): Show |
34 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.1175-1337C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426568 | |||||||
| chr19:426569 | A | C | 33 | a0001c0002t0002g0045 a0001c0003t0001g0060 a0001c0003t0001g0063 others(30): Show |
34 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.1175-1338T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426569 | |||||||
| chr19:426573 | G | A | 33 | a0001c0002t0002g0045 a0001c0003t0001g0060 a0001c0003t0001g0063 others(30): Show |
34 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.1175-1342C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426573 | |||||||
| chr19:426585 | G | A | 1 | a0001c0003t0002g0112 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1175-1354C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426585 | |||||||
| chr19:426608 | G | A | 27 | a0001c0002t0002g0045 a0001c0003t0001g0060 a0001c0003t0001g0063 others(24): Show |
28 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.1175-1377C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426608 | |||||||
| chr19:426670 | ACCGAGAG others(134): Show |
A | 1 | a0003c0008t0005g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1175-1580_1175-144 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426670 | |||||||
| chr19:426671 | C | G | 1 | a0001c0005t0001g0011 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1175-1440G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426671 | |||||||
| chr19:426672 | C | T | 1 | a0001c0005t0001g0011 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1175-1441G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426672 | |||||||
| chr19:426674 | A | C | 1 | a0001c0005t0001g0011 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1175-1443T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426674 | |||||||
| chr19:426800 | G | GGAGGACG others(63): Show |
2 | a0001c0001t0001g0099 a0001c0001t0001g0103 |
2 | NA18999.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1175-1570_1175-156 others(74): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426800 | |||||||
| chr19:426810 | AC | A | 70 | a0001c0001t0002g0051 a0001c0002t0001g0004 a0001c0002t0001g0079 others(67): Show |
72 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.1175-1580delG | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426810 | |||||||
| chr19:426811 | C | G | 4 | a0001c0001t0004g0162 a0001c0001t0004g0164 a0002c0004t0001g0192 others(1): Show |
4 | HG01358.hp2 HG01981.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175-1580G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426811 | |||||||
| chr19:426812 | C | T | 4 | a0001c0001t0004g0162 a0001c0001t0004g0164 a0002c0004t0001g0192 others(1): Show |
4 | HG01358.hp2 HG01981.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175-1581G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426812 | |||||||
| chr19:426814 | A | C | 4 | a0001c0001t0004g0162 a0001c0001t0004g0164 a0002c0004t0001g0192 others(1): Show |
4 | HG01358.hp2 HG01981.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175-1583T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426814 | |||||||
| chr19:426814 | AGAGGGGC others(28): Show |
A | 2 | a0001c0007t0003g0039 a0001c0007t0006g0041 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1175-1618_1175-158 others(39): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426814 | |||||||
| chr19:426853 | G | T | 68 | a0001c0002t0001g0004 a0001c0002t0001g0079 a0001c0002t0001g0080 others(65): Show |
70 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1175-1622C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426853 | |||||||
| chr19:426974 | C | T | 76 | a0001c0001t0002g0051 a0001c0001t0002g0076 a0001c0001t0003g0032 others(73): Show |
78 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.1175-1743G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 426974 | |||||||
| chr19:427009 | C | T | 1 | a0001c0002t0001g0088 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1175-1778G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427009 | |||||||
| chr19:427455 | GGGGGAAT others(18): Show |
G | 1 | a0002c0004t0001g0206 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1175-2249_1175-222 others(29): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427455 | |||||||
| chr19:427466 | ACACGGCA others(43): Show |
A | 1 | a0001c0001t0004g0002 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1175-2285_1175-223 others(54): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427466 | |||||||
| chr19:427476 | G | A | 7 | a0001c0001t0002g0101 a0001c0001t0007g0038 a0001c0001t0011g0034 others(4): Show |
7 | HG02486.hp1 HG02572.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1175-2245C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427476 | |||||||
| chr19:427491 | A | ACACGGCA others(18): Show |
8 | a0001c0007t0002g0077 a0001c0007t0006g0033 a0001c0007t0006g0054 others(5): Show |
8 | HG01109.hp2 HG01884.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1175-2285_1175-226 others(29): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427491 | |||||||
| chr19:427491 | A | G | 1 | a0002c0004t0001g0193 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1175-2260T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427491 | |||||||
| chr19:427516 | G | A | 1 | a0001c0003t0002g0152 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1175-2285C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427516 | |||||||
| chr19:427548 | ACAGGGAA others(143): Show |
A | 35 | a0001c0001t0002g0051 a0001c0001t0005g0046 a0001c0002t0002g0045 others(32): Show |
36 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.1175-2467_1175-231 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427548 | |||||||
| chr19:427573 | ACAGGGAA others(19): Show |
A | 1 | a0001c0001t0004g0124 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1175-2368_1175-234 others(30): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427573 | |||||||
| chr19:427573 | ACAGGGAA others(118): Show |
A | 40 | a0001c0001t0002g0076 a0001c0001t0003g0032 a0001c0001t0003g0070 others(37): Show |
41 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.1175-2467_1175-234 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427573 | |||||||
| chr19:427580 | AGGGGGAA others(93): Show |
A | 2 | a0001c0002t0001g0146 a0001c0002t0003g0174 |
2 | NA18960.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1175-2449_1175-235 others(104): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427580 | |||||||
| chr19:427645 | GGCGCACA others(61): Show |
G | 1 | a0003c0008t0005g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1175-2482_1175-241 others(72): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427645 | |||||||
| chr19:427687 | C | T | 2 | a0001c0002t0001g0146 a0001c0002t0003g0174 |
2 | NA18960.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1175-2456G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427687 | |||||||
| chr19:427691 | A | G | 2 | a0001c0002t0001g0146 a0001c0002t0003g0174 |
2 | NA18960.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1175-2460T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427691 | |||||||
| chr19:427698 | G | A | 2 | a0001c0002t0001g0146 a0001c0002t0003g0174 |
2 | NA18960.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1175-2467C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427698 | |||||||
| chr19:427727 | GGAAGGGG others(144): Show |
G | 1 | a0001c0001t0001g0165 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1175-2647_1175-249 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427727 | |||||||
| chr19:427852 | GGAAGGGG others(19): Show |
G | 4 | a0001c0001t0016g0069 a0001c0013t0005g0006 a0001c0017t0005g0055 others(1): Show |
4 | HG02622.hp1 HG02622.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175-2647_1175-262 others(30): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427852 | |||||||
| chr19:427989 | C | G | 1 | a0001c0002t0003g0044 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1174+2695G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 427989 | |||||||
| chr19:428066 | A | T | 1 | a0003c0008t0005g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1174+2618T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 428066 | |||||||
| chr19:428077 | G | T | 71 | a0001c0001t0002g0051 a0001c0001t0002g0076 a0001c0001t0003g0032 others(68): Show |
73 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.1174+2607C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 428077 | |||||||
| chr19:428463 | C | T | 1 | a0001c0005t0001g0012 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1174+2221G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 428463 | |||||||
| chr19:428527 | G | A | 1 | a0001c0001t0005g0102 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1174+2157C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 428527 | |||||||
| chr19:428530 | T | G | 6 | a0001c0003t0001g0060 a0001c0003t0001g0064 a0001c0003t0002g0001 others(3): Show |
7 | HG00544.hp2 HG00621.hp1 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.1174+2154A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 428530 | |||||||
| chr19:428605 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1174+2079T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 428605 | |||||||
| chr19:428608 | A | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1174+2076T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 428608 | |||||||
| chr19:428792 | GAC | G | 74 | a0001c0001t0002g0101 a0001c0001t0003g0070 a0001c0001t0007g0038 others(71): Show |
76 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.1174+1890_1174+189 others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 428792 | |||||||
| chr19:428832 | T | C | 1 | a0005c0009t0014g0036 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1174+1852A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 428832 | |||||||
| chr19:428907 | C | T | 1 | a0003c0008t0005g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1174+1777G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 428907 | |||||||
| chr19:428955 | C | G | 21 | a0001c0001t0002g0035 a0001c0001t0002g0056 a0001c0001t0003g0005 others(18): Show |
22 | HG01891.hp2 HG01978.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1174+1729G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 428955 | |||||||
| chr19:429109 | GTGCACGG others(581): Show |
G | 2 | a0001c0001t0001g0163 a0001c0016t0001g0159 |
2 | HG00733.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1174+987_1174+1574 others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429109 | |||||||
| chr19:429128 | TGTGTGGA others(42): Show |
T | 3 | a0001c0006t0001g0013 a0001c0006t0001g0016 a0001c0006t0001g0017 |
3 | HG03209.hp2 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1174+1507_1174+155 others(53): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429128 | |||||||
| chr19:429139 | T | C | 80 | a0001c0001t0002g0051 a0001c0001t0002g0076 a0001c0001t0002g0101 others(77): Show |
82 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.1174+1545A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429139 | |||||||
| chr19:429227 | G | A | 4 | a0001c0001t0002g0076 a0001c0001t0003g0032 a0001c0001t0013g0072 others(1): Show |
4 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174+1457C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429227 | |||||||
| chr19:429304 | C | T | 1 | a0003c0008t0005g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1174+1380G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429304 | |||||||
| chr19:429306 | T | C | 1 | a0005c0009t0005g0047 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1174+1378A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429306 | |||||||
| chr19:429404 | T | G | 26 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0004g0002 others(23): Show |
27 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.1174+1280A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429404 | |||||||
| chr19:429410 | G | T | 1 | a0001c0001t0007g0038 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1174+1274C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429410 | |||||||
| chr19:429533 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1174+1151G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429533 | |||||||
| chr19:429553 | C | T | 1 | a0001c0002t0002g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1174+1131G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429553 | |||||||
| chr19:429560 | A | T | 33 | a0001c0003t0001g0060 a0001c0003t0001g0063 a0001c0003t0001g0064 others(30): Show |
34 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.1174+1124T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429560 | |||||||
| chr19:429575 | G | A | 1 | a0002c0004t0001g0206 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1174+1109C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429575 | |||||||
| chr19:429581 | GCAGTACC others(42): Show |
G | 4 | a0001c0001t0002g0076 a0001c0001t0003g0032 a0001c0001t0013g0072 others(1): Show |
4 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174+1054_1174+110 others(53): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429581 | |||||||
| chr19:429599 | A | G | 4 | a0001c0001t0011g0034 a0005c0009t0005g0047 a0005c0009t0014g0036 others(1): Show |
4 | HG02486.hp1 NA18522.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174+1085T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429599 | |||||||
| chr19:429604 | G | C | 1 | a0001c0001t0011g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1174+1080C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429604 | |||||||
| chr19:429613 | AATACCGT others(42): Show |
A | 4 | a0001c0001t0003g0070 a0005c0009t0005g0047 a0005c0009t0014g0036 others(1): Show |
4 | NA18522.hp2 NA19240.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174+1022_1174+107 others(53): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429613 | |||||||
| chr19:429615 | T | C | 1 | a0001c0001t0011g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1174+1069A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429615 | |||||||
| chr19:429630 | A | G | 2 | a0001c0001t0011g0034 a0001c0006t0002g0023 |
2 | HG01943.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1174+1054T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429630 | |||||||
| chr19:429653 | C | G | 1 | a0001c0001t0011g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1174+1031G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429653 | |||||||
| chr19:429654 | G | A | 1 | a0001c0001t0011g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1174+1030C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429654 | |||||||
| chr19:429659 | T | C | 1 | a0001c0001t0011g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1174+1025A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429659 | |||||||
| chr19:429662 | C | A | 1 | a0001c0001t0011g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1174+1022G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429662 | |||||||
| chr19:429664 | TACCGTGT others(42): Show |
T | 1 | a0002c0004t0001g0206 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1174+971_1174+1019 others(52): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429664 | |||||||
| chr19:429679 | G | A | 1 | a0001c0001t0011g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1174+1005C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429679 | |||||||
| chr19:429721 | G | A | 1 | a0003c0008t0005g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1174+963C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429721 | |||||||
| chr19:429725 | G | A | 3 | a0001c0002t0001g0108 a0001c0002t0001g0153 a0001c0002t0001g0154 |
3 | HG02015.hp1 HG02080.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1174+959C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429725 | |||||||
| chr19:429746 | A | G | 33 | a0001c0003t0001g0060 a0001c0003t0001g0063 a0001c0003t0001g0064 others(30): Show |
34 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.1174+938T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429746 | |||||||
| chr19:429751 | C | T | 2 | a0001c0003t0004g0110 a0001c0003t0004g0111 |
2 | NA18612.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1174+933G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429751 | |||||||
| chr19:429776 | C | T | 1 | a0001c0002t0002g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1174+908G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429776 | |||||||
| chr19:429815 | G | A | 3 | a0001c0003t0002g0001 a0001c0003t0002g0112 a0001c0003t0002g0152 |
4 | HG00544.hp2 NA18954.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174+869C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429815 | |||||||
| chr19:429850 | A | G | 2 | a0001c0001t0004g0162 a0001c0005t0006g0008 |
2 | HG02148.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1174+834T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429850 | |||||||
| chr19:429891 | A | G | 1 | a0002c0004t0001g0193 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1174+793T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429891 | |||||||
| chr19:429930 | T | C | 1 | a0001c0001t0002g0051 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1174+754A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429930 | |||||||
| chr19:429962 | A | G | 94 | a0001c0001t0002g0051 a0001c0001t0002g0076 a0001c0001t0002g0101 others(91): Show |
97 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.1174+722T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429962 | |||||||
| chr19:429976 | G | A | 1 | a0001c0001t0011g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1174+708C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429976 | |||||||
| chr19:429991 | A | G | 3 | a0001c0001t0002g0101 a0001c0001t0007g0038 a0009c0021t0002g0028 |
3 | HG02572.hp2 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1174+693T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 429991 | |||||||
| chr19:430029 | C | T | 2 | a0001c0001t0003g0172 a0003c0008t0003g0184 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1174+655G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430029 | |||||||
| chr19:430034 | CCCCAACG others(43): Show |
C | 1 | a0005c0009t0014g0036 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1174+600_1174+649d others(52): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430034 | |||||||
| chr19:430097 | G | A | 1 | a0001c0018t0006g0180 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1174+587C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430097 | |||||||
| chr19:430105 | A | G | 1 | a0005c0009t0014g0036 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1174+579T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430105 | |||||||
| chr19:430141 | A | G | 36 | a0001c0001t0003g0005 a0001c0001t0003g0181 a0001c0002t0002g0045 others(33): Show |
38 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1174+543T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430141 | |||||||
| chr19:430148 | GA | G | 33 | a0001c0003t0001g0060 a0001c0003t0001g0063 a0001c0003t0001g0064 others(30): Show |
34 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.1174+535delT | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430148 | |||||||
| chr19:430178 | C | T | 3 | a0001c0003t0002g0001 a0001c0003t0002g0112 a0001c0003t0002g0152 |
4 | HG00544.hp2 NA18954.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174+506G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430178 | |||||||
| chr19:430184 | C | A | 2 | a0001c0014t0001g0014 a0001c0020t0001g0105 |
2 | HG00735.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1174+500G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430184 | |||||||
| chr19:430205 | A | G | 2 | a0001c0001t0003g0005 a0001c0001t0003g0181 |
3 | HG01978.hp1 HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1174+479T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430205 | |||||||
| chr19:430211 | G | A | 2 | a0001c0001t0002g0076 a0001c0001t0013g0072 |
2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1174+473C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430211 | |||||||
| chr19:430246 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1174+438C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430246 | |||||||
| chr19:430271 | G | A | 19 | a0001c0001t0002g0035 a0001c0001t0002g0056 a0001c0001t0003g0005 others(16): Show |
20 | HG01891.hp2 HG01978.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1174+413C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430271 | |||||||
| chr19:430301 | C | G | 5 | a0001c0001t0002g0051 a0001c0001t0002g0076 a0001c0001t0003g0032 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174+383G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430301 | |||||||
| chr19:430310 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1174+374C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430310 | |||||||
| chr19:430323 | G | A | 2 | a0001c0001t0003g0005 a0001c0001t0003g0181 |
3 | HG01978.hp1 HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1174+361C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430323 | |||||||
| chr19:430370 | C | T | 39 | a0001c0001t0002g0101 a0001c0001t0007g0038 a0001c0002t0001g0004 others(36): Show |
40 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.1174+314G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430370 | |||||||
| chr19:430380 | A | G | 11 | a0001c0001t0004g0002 a0001c0001t0004g0162 a0001c0001t0004g0164 others(8): Show |
12 | HG00323.hp2 HG01258.hp1 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.1174+304T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430380 | |||||||
| chr19:430450 | C | G | 2 | a0001c0001t0002g0076 a0001c0001t0013g0072 |
2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1174+234G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430450 | |||||||
| chr19:430458 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1174+226C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430458 | |||||||
| chr19:430559 | G | A | 5 | a0001c0001t0001g0120 a0001c0001t0001g0127 a0001c0005t0001g0018 others(2): Show |
5 | HG00639.hp2 HG01071.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174+125C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430559 | |||||||
| chr19:430613 | G | A | 4 | a0001c0001t0002g0076 a0001c0001t0003g0032 a0001c0001t0013g0072 others(1): Show |
4 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174+71C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 9/12 | chr19 | 430613 | |||||||
| chr19:430807 | ACCCCCAG others(3): Show |
A | 1 | a0001c0001t0001g0128 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1111-70_1111-61del others(10): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 430807 | |||||||
| chr19:430822 | G | A | 1 | a0001c0001t0006g0030 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1111-75C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 430822 | |||||||
| chr19:430847 | A | C | 2 | a0001c0001t0002g0076 a0001c0001t0013g0072 |
2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1111-100T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 430847 | |||||||
| chr19:430934 | G | A | 5 | a0001c0001t0002g0051 a0001c0001t0002g0076 a0001c0001t0003g0032 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111-187C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 430934 | |||||||
| chr19:431029 | T | A | 141 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0145 others(138): Show |
145 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.1111-282A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431029 | |||||||
| chr19:431033 | C | T | 2 | a0001c0007t0003g0039 a0001c0007t0006g0041 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1111-286G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431033 | |||||||
| chr19:431097 | C | T | 1 | a0001c0001t0011g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1111-350G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431097 | |||||||
| chr19:431104 | AC | A | 38 | a0001c0001t0001g0145 a0001c0001t0003g0070 a0001c0003t0001g0060 others(35): Show |
39 | HG00544.hp2 HG00558.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.1111-358delG | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431104 | |||||||
| chr19:431123 | G | A | 1 | a0002c0004t0001g0190 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1111-376C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431123 | |||||||
| chr19:431187 | G | A | 37 | a0001c0001t0003g0070 a0001c0003t0001g0060 a0001c0003t0001g0063 others(34): Show |
38 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1111-440C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431187 | |||||||
| chr19:431239 | T | G | 4 | a0001c0001t0002g0076 a0001c0001t0003g0032 a0001c0001t0013g0072 others(1): Show |
4 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111-492A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431239 | |||||||
| chr19:431248 | C | CAGAGGAG others(51): Show |
69 | a0001c0001t0001g0130 a0001c0002t0001g0004 a0001c0002t0001g0079 others(66): Show |
71 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.1111-559_1111-502d others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431248 | |||||||
| chr19:431248 | C | CAGAGGAG others(167): Show |
2 | a0005c0009t0005g0047 a0005c0009t0014g0036 |
2 | NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1111-502_1111-501i others(176): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431248 | |||||||
| chr19:431248 | C | CAGAGGAG others(279): Show |
1 | a0001c0002t0002g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1111-502_1111-501i others(288): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431248 | |||||||
| chr19:431248 | C | CAGAGGAG others(283): Show |
2 | a0001c0001t0002g0076 a0001c0001t0013g0072 |
2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1111-502_1111-501i others(292): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431248 | |||||||
| chr19:431266 | T | TAGATGGC others(395): Show |
1 | a0001c0007t0002g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1111-520_1111-519i others(404): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431266 | |||||||
| chr19:431281 | CGTGA | C | 4 | a0001c0001t0002g0056 a0001c0001t0003g0049 a0001c0001t0006g0030 others(1): Show |
4 | HG02486.hp2 HG02970.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111-538_1111-535d others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431281 | |||||||
| chr19:431305 | T | A | 1 | a0001c0007t0002g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1111-558A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431305 | |||||||
| chr19:431316 | C | CGGGCAGA others(391): Show |
1 | a0001c0006t0006g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1111-570_1111-569i others(400): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431316 | |||||||
| chr19:431316 | CGGGCAGA others(329): Show |
C | 1 | a0002c0004t0005g0189 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1111-905_1111-570d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431316 | |||||||
| chr19:431332 | G | GCTTCATC others(167): Show |
6 | a0001c0007t0006g0033 a0001c0007t0006g0054 a0001c0023t0007g0187 others(3): Show |
6 | HG01109.hp2 HG01884.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1111-586_1111-585i others(176): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431332 | |||||||
| chr19:431363 | A | T | 15 | a0001c0001t0002g0051 a0001c0001t0002g0101 a0001c0001t0003g0032 others(12): Show |
15 | HG00639.hp1 HG01943.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1111-616T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431363 | |||||||
| chr19:431375 | A | G | 26 | a0001c0001t0001g0130 a0001c0001t0002g0035 a0001c0001t0002g0051 others(23): Show |
26 | HG00639.hp1 HG01109.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.1111-628T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431375 | |||||||
| chr19:431390 | A | G | 24 | a0001c0001t0001g0130 a0001c0001t0002g0035 a0001c0001t0002g0051 others(21): Show |
24 | HG00639.hp1 HG01109.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.1111-643T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431390 | |||||||
| chr19:431421 | T | A | 6 | a0001c0001t0002g0035 a0001c0001t0003g0070 a0001c0006t0002g0023 others(3): Show |
6 | HG00639.hp1 HG01943.hp2 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1111-674A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431421 | |||||||
| chr19:431421 | TTAGAGGA others(47): Show |
T | 2 | a0001c0001t0003g0005 a0001c0001t0003g0181 |
3 | HG01978.hp1 HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1111-728_1111-675d others(56): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431421 | |||||||
| chr19:431421 | TTAGAGGA others(155): Show |
T | 1 | a0001c0001t0006g0052 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1111-836_1111-675d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431421 | |||||||
| chr19:431432 | CGGGCAGA others(557): Show |
C | 1 | a0001c0001t0011g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1111-1249_1111-686 others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431432 | |||||||
| chr19:431433 | G | A | 1 | a0001c0006t0002g0023 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1111-686C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431433 | |||||||
| chr19:431436 | C | CAGAT | 15 | a0001c0001t0001g0130 a0001c0001t0003g0070 a0001c0006t0002g0023 others(12): Show |
15 | HG00639.hp1 HG01109.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.1111-693_1111-690d others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431436 | |||||||
| chr19:431436 | C | CAGATAGA others(453): Show |
2 | a0001c0001t0003g0032 a0001c0005t0006g0009 |
2 | HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1111-690_1111-689i others(462): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431436 | |||||||
| chr19:431436 | C | CAGATAGA others(55): Show |
1 | a0003c0008t0005g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1111-690_1111-689i others(64): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431436 | |||||||
| chr19:431440 | TGGCGCTT others(43): Show |
T | 1 | a0001c0001t0002g0051 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1111-743_1111-694d others(52): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431440 | |||||||
| chr19:431444 | G | A | 1 | a0001c0006t0002g0023 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1111-697C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431444 | |||||||
| chr19:431452 | G | A | 2 | a0001c0001t0002g0076 a0001c0001t0013g0072 |
2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1111-705C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431452 | |||||||
| chr19:431474 | G | A | 1 | a0001c0003t0001g0140 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1111-727C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431474 | |||||||
| chr19:431475 | A | T | 6 | a0001c0001t0003g0070 a0001c0006t0002g0023 a0002c0004t0001g0190 others(3): Show |
6 | HG00639.hp1 HG01943.hp2 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1111-728T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431475 | |||||||
| chr19:431486 | C | T | 1 | a0001c0001t0002g0035 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1111-739G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431486 | |||||||
| chr19:431487 | G | A | 2 | a0001c0001t0001g0130 a0001c0002t0004g0096 |
2 | HG01123.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.1111-740C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431487 | |||||||
| chr19:431490 | C | CAGAT | 20 | a0001c0001t0001g0130 a0001c0001t0002g0035 a0001c0001t0002g0101 others(17): Show |
20 | HG00639.hp1 HG01109.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.1111-747_1111-744d others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431490 | |||||||
| chr19:431490 | C | CAGATAGA others(55): Show |
1 | a0001c0002t0004g0096 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1111-744_1111-743i others(64): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431490 | |||||||
| chr19:431490 | C | CAGATGGC others(167): Show |
1 | a0002c0012t0004g0195 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1111-744_1111-743i others(176): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431490 | |||||||
| chr19:431490 | CAGATGGC others(163): Show |
C | 12 | a0001c0001t0003g0172 a0001c0001t0005g0102 a0001c0001t0006g0042 others(9): Show |
12 | HG01891.hp2 HG02145.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1111-913_1111-744d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431490 | |||||||
| chr19:431498 | G | A | 4 | a0001c0001t0001g0130 a0001c0001t0003g0032 a0001c0005t0006g0009 others(1): Show |
4 | HG01123.hp1 HG02055.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111-751C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431498 | |||||||
| chr19:431529 | A | ATAGAGGA others(109): Show |
1 | a0001c0003t0002g0074 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1111-783_1111-782i others(118): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431529 | |||||||
| chr19:431529 | A | ATAGAGGA others(167): Show |
4 | a0001c0003t0002g0071 a0001c0003t0002g0182 a0001c0003t0004g0109 others(1): Show |
4 | HG01952.hp1 HG02132.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111-783_1111-782i others(176): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431529 | |||||||
| chr19:431529 | A | T | 8 | a0001c0001t0001g0130 a0001c0001t0002g0051 a0001c0001t0003g0070 others(5): Show |
8 | HG01123.hp1 HG02559.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1111-782T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431529 | |||||||
| chr19:431529 | ATAGAGGA others(221): Show |
A | 1 | a0001c0005t0006g0008 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1111-1010_1111-783 others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431529 | |||||||
| chr19:431540 | C | G | 3 | a0001c0001t0002g0101 a0001c0001t0007g0038 a0009c0021t0002g0028 |
3 | HG02572.hp2 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1111-793G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431540 | |||||||
| chr19:431540 | CGGGCAGA others(105): Show |
C | 20 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0004g0002 others(17): Show |
21 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.1111-905_1111-794d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431540 | |||||||
| chr19:431541 | G | A | 6 | a0001c0001t0002g0035 a0001c0001t0003g0070 a0001c0002t0002g0045 others(3): Show |
6 | HG00639.hp1 HG03942.hp1 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.1111-794C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431541 | |||||||
| chr19:431544 | C | CAGAT | 32 | a0001c0001t0002g0035 a0001c0001t0002g0056 a0001c0001t0002g0076 others(29): Show |
32 | HG00099.hp1 HG00639.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.1111-801_1111-798d others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431544 | |||||||
| chr19:431544 | C | CAGATAGA others(229): Show |
1 | a0001c0001t0004g0029 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1111-798_1111-797i others(238): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431544 | |||||||
| chr19:431544 | C | CAGATAGA others(573): Show |
1 | a0001c0017t0005g0055 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1111-798_1111-797i others(582): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431544 | |||||||
| chr19:431544 | C | CAGATAGA others(399): Show |
1 | a0005c0009t0005g0047 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1111-798_1111-797i others(408): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431544 | |||||||
| chr19:431544 | C | CAGATAGA others(457): Show |
1 | a0005c0009t0014g0036 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1111-798_1111-797i others(466): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431544 | |||||||
| chr19:431544 | C | CAGATAGA others(225): Show |
7 | a0001c0003t0001g0060 a0001c0003t0001g0063 a0001c0003t0001g0064 others(4): Show |
8 | HG00544.hp2 HG00621.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1111-798_1111-797i others(234): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431544 | |||||||
| chr19:431544 | C | CAGATAGA others(283): Show |
2 | a0001c0003t0002g0062 a0002c0012t0002g0205 |
2 | NA18960.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1111-798_1111-797i others(292): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431544 | |||||||
| chr19:431544 | C | CAGATAGA others(341): Show |
11 | a0001c0003t0001g0114 a0001c0003t0002g0065 a0001c0003t0002g0068 others(8): Show |
11 | HG00558.hp1 HG00621.hp2 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.1111-798_1111-797i others(350): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431544 | |||||||
| chr19:431544 | C | CAGATAGA others(689): Show |
1 | a0001c0003t0001g0140 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1111-798_1111-797i others(698): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431544 | |||||||
| chr19:431544 | C | CAGATAGA others(55): Show |
2 | a0001c0002t0001g0146 a0001c0002t0003g0174 |
2 | NA18960.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1111-798_1111-797i others(64): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431544 | |||||||
| chr19:431544 | C | CAGATAGA others(113): Show |
31 | a0001c0002t0001g0004 a0001c0002t0001g0079 a0001c0002t0001g0080 others(28): Show |
32 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.1111-798_1111-797i others(122): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431544 | |||||||
| chr19:431549 | G | A | 5 | a0001c0001t0002g0056 a0001c0001t0003g0049 a0001c0001t0006g0030 others(2): Show |
5 | HG00099.hp1 HG02486.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111-802C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431549 | |||||||
| chr19:431551 | C | T | 1 | a0001c0002t0001g0093 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1111-804G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431551 | |||||||
| chr19:431552 | G | A | 6 | a0001c0001t0002g0035 a0001c0001t0003g0070 a0001c0002t0002g0045 others(3): Show |
6 | HG00639.hp1 HG03942.hp1 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.1111-805C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431552 | |||||||
| chr19:431583 | A | T | 51 | a0001c0001t0002g0035 a0001c0001t0002g0056 a0001c0001t0002g0076 others(48): Show |
52 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.1111-836T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431583 | |||||||
| chr19:431583 | ATAGAGGA others(283): Show |
A | 1 | a0001c0001t0001g0122 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1111-1126_1111-837 others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431583 | |||||||
| chr19:431594 | C | G | 25 | a0001c0001t0002g0101 a0001c0001t0003g0070 a0001c0001t0004g0029 others(22): Show |
26 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.1111-847G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431594 | |||||||
| chr19:431595 | G | A | 8 | a0001c0001t0002g0051 a0001c0003t0002g0071 a0001c0003t0002g0074 others(5): Show |
8 | HG01952.hp1 HG02132.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1111-848C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431595 | |||||||
| chr19:431598 | CAGAT | C | 7 | a0001c0001t0001g0130 a0001c0001t0002g0035 a0002c0004t0001g0190 others(4): Show |
7 | HG00639.hp1 HG01123.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1111-855_1111-852d others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431598 | |||||||
| chr19:431602 | T | TAGATGGC others(47): Show |
1 | a0001c0007t0002g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1111-856_1111-855i others(56): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431602 | |||||||
| chr19:431604 | G | C | 1 | a0001c0017t0005g0055 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1111-857C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431604 | |||||||
| chr19:431607 | G | A | 2 | a0001c0001t0003g0005 a0001c0001t0003g0181 |
3 | HG01978.hp1 HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1111-860C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431607 | |||||||
| chr19:431607 | GGCGCTTC others(109): Show |
G | 1 | a0001c0005t0001g0015 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1111-976_1111-861d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431607 | |||||||
| chr19:431610 | G | A | 1 | a0001c0001t0004g0029 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1111-863C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431610 | |||||||
| chr19:431629 | C | T | 1 | a0005c0009t0005g0047 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1111-882G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431629 | |||||||
| chr19:431641 | A | T | 57 | a0001c0001t0001g0129 a0001c0001t0002g0056 a0001c0001t0003g0005 others(54): Show |
59 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.1111-894T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431641 | |||||||
| chr19:431652 | G | C | 89 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0002g0035 others(86): Show |
92 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.1111-905C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431652 | |||||||
| chr19:431653 | G | A | 6 | a0001c0002t0002g0045 a0001c0007t0006g0033 a0001c0023t0007g0187 others(3): Show |
6 | HG01109.hp2 HG01884.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1111-906C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431653 | |||||||
| chr19:431656 | CAGAT | C | 7 | a0001c0001t0001g0130 a0001c0001t0002g0035 a0001c0001t0006g0052 others(4): Show |
7 | HG00639.hp1 HG01123.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.1111-913_1111-910d others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431656 | |||||||
| chr19:431660 | T | TAGATGGC others(47): Show |
2 | a0001c0001t0002g0076 a0001c0001t0013g0072 |
2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1111-914_1111-913i others(56): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431660 | |||||||
| chr19:431660 | T | TAGATGGC others(47): Show |
1 | a0001c0001t0007g0038 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1111-914_1111-913i others(56): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431660 | |||||||
| chr19:431660 | T | TAGATGGC others(101): Show |
1 | a0009c0021t0002g0028 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1111-914_1111-913i others(110): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431660 | |||||||
| chr19:431660 | T | TAGATGGC others(101): Show |
1 | a0001c0001t0002g0101 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1111-914_1111-913i others(110): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431660 | |||||||
| chr19:431660 | T | TAGATGGC others(47): Show |
2 | a0001c0001t0003g0032 a0001c0005t0006g0009 |
2 | HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1111-914_1111-913i others(56): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431660 | |||||||
| chr19:431660 | T | TAGATGGC others(441): Show |
1 | a0001c0006t0002g0022 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1111-914_1111-913i others(450): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431660 | |||||||
| chr19:431665 | G | A | 20 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0004g0002 others(17): Show |
21 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.1111-918C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431665 | |||||||
| chr19:431668 | G | A | 37 | a0001c0002t0001g0004 a0001c0002t0001g0079 a0001c0002t0001g0080 others(34): Show |
38 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.1111-921C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431668 | |||||||
| chr19:431699 | A | ATAGAGGA others(51): Show |
2 | a0001c0001t0002g0101 a0009c0021t0002g0028 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1111-953_1111-952i others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431699 | |||||||
| chr19:431699 | A | T | 76 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0129 others(73): Show |
80 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.1111-952T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431699 | |||||||
| chr19:431708 | G | A | 1 | a0011c0022t0002g0185 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1111-961C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431708 | |||||||
| chr19:431710 | C | G | 19 | a0001c0003t0001g0060 a0001c0003t0001g0063 a0001c0003t0001g0064 others(16): Show |
20 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.1111-963G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431710 | |||||||
| chr19:431711 | G | A | 5 | a0001c0002t0002g0045 a0001c0006t0001g0013 a0001c0006t0001g0016 others(2): Show |
5 | HG03098.hp2 HG03209.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111-964C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431711 | |||||||
| chr19:431714 | CAGAT | C | 9 | a0001c0001t0001g0129 a0001c0001t0002g0056 a0001c0001t0003g0049 others(6): Show |
9 | HG00639.hp1 HG02015.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1111-971_1111-968d others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431714 | |||||||
| chr19:431720 | G | C | 4 | a0001c0001t0004g0162 a0001c0001t0004g0164 a0002c0004t0001g0192 others(1): Show |
4 | HG01358.hp2 HG01981.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111-973C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431720 | |||||||
| chr19:431723 | A | G | 130 | a0001c0001t0001g0043 a0001c0001t0001g0090 a0001c0001t0001g0097 others(127): Show |
134 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.1111-976T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431723 | |||||||
| chr19:431725 | C | CGCTTCAT others(109): Show |
1 | a0001c0002t0003g0175 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1111-979_1111-978i others(118): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431725 | |||||||
| chr19:431725 | C | CGCTTCAT others(109): Show |
1 | a0001c0002t0001g0093 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1111-979_1111-978i others(118): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431725 | |||||||
| chr19:431725 | C | T | 32 | a0001c0002t0001g0004 a0001c0002t0001g0079 a0001c0002t0001g0080 others(29): Show |
33 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1111-978G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431725 | |||||||
| chr19:431726 | G | A | 3 | a0001c0001t0001g0139 a0004c0011t0005g0057 a0004c0011t0005g0061 |
3 | HG01109.hp2 HG02040.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1111-979C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431726 | |||||||
| chr19:431726 | G | ACTTCATC others(51): Show |
1 | a0001c0002t0003g0174 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1111-979_1111-978i others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431726 | |||||||
| chr19:431726 | G | ACTTCATC others(51): Show |
1 | a0001c0002t0001g0146 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1111-979_1111-978i others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431726 | |||||||
| chr19:431745 | C | A | 6 | a0001c0003t0001g0060 a0001c0003t0001g0064 a0001c0003t0002g0001 others(3): Show |
7 | HG00544.hp2 HG00621.hp1 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.1111-998G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431745 | |||||||
| chr19:431757 | T | A | 45 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0002g0051 others(42): Show |
46 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.1111-1010A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431757 | |||||||
| chr19:431757 | T | TTAGAGGA others(51): Show |
2 | a0001c0001t0003g0032 a0001c0005t0006g0009 |
2 | HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1111-1011_1111-101 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431757 | |||||||
| chr19:431768 | C | A | 1 | a0001c0001t0002g0051 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1111-1021G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431768 | |||||||
| chr19:431768 | C | G | 11 | a0001c0003t0001g0140 a0001c0003t0002g0062 a0001c0003t0002g0071 others(8): Show |
11 | HG01952.hp1 HG02132.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1111-1021G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431768 | |||||||
| chr19:431769 | G | A | 6 | a0001c0001t0001g0129 a0001c0001t0002g0056 a0001c0001t0003g0049 others(3): Show |
6 | HG02015.hp2 HG02486.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1111-1022C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431769 | |||||||
| chr19:431772 | CAGAT | C | 3 | a0001c0001t0003g0005 a0001c0001t0003g0070 a0001c0001t0003g0181 |
4 | HG01978.hp1 HG02055.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111-1029_1111-102 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431772 | |||||||
| chr19:431772 | CAGATAGA others(341): Show |
C | 4 | a0001c0001t0004g0162 a0001c0001t0004g0164 a0002c0004t0001g0192 others(1): Show |
4 | HG01358.hp2 HG01981.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111-1373_1111-102 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431772 | |||||||
| chr19:431781 | G | A | 1 | a0001c0005t0006g0008 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1111-1034C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431781 | |||||||
| chr19:431804 | G | A | 2 | a0001c0001t0003g0032 a0001c0005t0006g0009 |
2 | HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1111-1057C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431804 | |||||||
| chr19:431804 | G | GTGAGTGA others(561): Show |
1 | a0001c0002t0002g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1111-1058_1111-105 others(572): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431804 | |||||||
| chr19:431815 | T | A | 26 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0002g0056 others(23): Show |
28 | HG00544.hp2 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1111-1068A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431815 | |||||||
| chr19:431815 | T | TTAGAGGA others(449): Show |
3 | a0001c0007t0006g0033 a0001c0007t0006g0054 a0002c0024t0003g0200 |
3 | HG02451.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1111-1069_1111-106 others(460): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431815 | |||||||
| chr19:431826 | C | CGGGCAGA others(109): Show |
1 | a0001c0001t0004g0029 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1111-1080_1111-107 others(120): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431826 | |||||||
| chr19:431826 | C | G | 14 | a0001c0001t0001g0129 a0001c0003t0001g0114 a0001c0003t0002g0065 others(11): Show |
14 | HG00558.hp1 HG00621.hp2 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.1111-1079G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431826 | |||||||
| chr19:431827 | G | A | 9 | a0001c0001t0001g0130 a0001c0001t0003g0070 a0001c0006t0001g0013 others(6): Show |
9 | HG00639.hp1 HG01123.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1111-1080C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431827 | |||||||
| chr19:431827 | GGGCAGAT others(105): Show |
G | 1 | a0001c0001t0002g0051 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1111-1192_1111-108 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431827 | |||||||
| chr19:431830 | CAGAT | C | 3 | a0001c0001t0001g0130 a0002c0004t0001g0193 a0011c0022t0002g0185 |
3 | HG00639.hp1 HG01123.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1111-1087_1111-108 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431830 | |||||||
| chr19:431834 | T | TGGCGCTT others(719): Show |
1 | a0001c0023t0007g0187 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1111-1088_1111-108 others(730): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431834 | |||||||
| chr19:431861 | C | A | 11 | a0001c0003t0001g0114 a0001c0003t0002g0065 a0001c0003t0002g0068 others(8): Show |
11 | HG00558.hp1 HG00621.hp2 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.1111-1114G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431861 | |||||||
| chr19:431873 | T | A | 34 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0003g0070 others(31): Show |
35 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.1111-1126A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431873 | |||||||
| chr19:431874 | T | C | 1 | a0001c0001t0004g0029 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1111-1127A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431874 | |||||||
| chr19:431884 | C | G | 20 | a0001c0001t0002g0056 a0001c0001t0003g0049 a0001c0001t0003g0070 others(17): Show |
21 | HG00544.hp2 HG00621.hp1 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.1111-1137G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431884 | |||||||
| chr19:431885 | G | A | 6 | a0001c0001t0007g0038 a0001c0007t0006g0033 a0001c0007t0006g0054 others(3): Show |
6 | HG02451.hp2 HG02818.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1111-1138C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431885 | |||||||
| chr19:431888 | C | CAGAT | 39 | a0001c0001t0001g0129 a0001c0001t0002g0056 a0001c0001t0003g0005 others(36): Show |
41 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.1111-1145_1111-114 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431888 | |||||||
| chr19:431888 | C | CAGATAGA others(217): Show |
1 | a0005c0009t0014g0036 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1111-1142_1111-114 others(228): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431888 | |||||||
| chr19:431888 | C | CAGATAGA others(171): Show |
1 | a0001c0003t0002g0182 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1111-1142_1111-114 others(182): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431888 | |||||||
| chr19:431888 | C | CAGATAGA others(171): Show |
1 | a0001c0003t0002g0074 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1111-1142_1111-114 others(182): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431888 | |||||||
| chr19:431888 | C | CAGATAGA others(275): Show |
1 | a0005c0009t0005g0047 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1111-1142_1111-114 others(286): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431888 | |||||||
| chr19:431888 | C | CAGATGGC others(225): Show |
1 | a0001c0001t0001g0078 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1111-1142_1111-114 others(236): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431888 | |||||||
| chr19:431888 | CAGATGGC others(457): Show |
C | 2 | a0001c0001t0003g0172 a0003c0008t0003g0184 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1111-1605_1111-114 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431888 | |||||||
| chr19:431895 | C | T | 2 | a0004c0011t0005g0057 a0004c0011t0005g0061 |
2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1111-1148G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431895 | |||||||
| chr19:431915 | C | A | 2 | a0001c0003t0002g0062 a0002c0012t0002g0205 |
2 | NA18960.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1111-1168G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431915 | |||||||
| chr19:431927 | A | T | 14 | a0001c0003t0001g0060 a0001c0003t0001g0064 a0001c0003t0002g0001 others(11): Show |
15 | HG00544.hp2 HG00621.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1111-1180T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431927 | |||||||
| chr19:431938 | C | G | 6 | a0001c0001t0002g0056 a0001c0001t0003g0049 a0001c0001t0006g0030 others(3): Show |
6 | HG01109.hp2 HG02486.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1111-1191G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431938 | |||||||
| chr19:431938 | C | T | 2 | a0005c0009t0005g0047 a0005c0009t0014g0036 |
2 | NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1111-1191G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431938 | |||||||
| chr19:431939 | A | G | 51 | a0001c0001t0001g0122 a0001c0001t0001g0129 a0001c0001t0001g0130 others(48): Show |
52 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1111-1192T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431939 | |||||||
| chr19:431939 | A | GGGCAGAT others(109): Show |
1 | a0001c0001t0001g0144 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1111-1192_1111-119 others(120): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431939 | |||||||
| chr19:431942 | CAGAT | C | 4 | a0001c0001t0001g0122 a0001c0001t0001g0130 a0002c0004t0001g0190 others(1): Show |
4 | HG01123.hp1 HG03239.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111-1199_1111-119 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431942 | |||||||
| chr19:431942 | CAGATAGA others(55): Show |
C | 1 | a0002c0004t0001g0193 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1111-1257_1111-119 others(66): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431942 | |||||||
| chr19:431948 | G | C | 1 | a0001c0001t0007g0038 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1111-1201C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431948 | |||||||
| chr19:431954 | G | A | 2 | a0001c0001t0003g0005 a0001c0001t0003g0181 |
3 | HG01978.hp1 HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1111-1207C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431954 | |||||||
| chr19:431985 | A | T | 15 | a0001c0001t0001g0144 a0001c0001t0002g0076 a0001c0001t0003g0005 others(12): Show |
16 | HG01074.hp2 HG01109.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1111-1238T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431985 | |||||||
| chr19:431996 | G | C | 19 | a0001c0001t0001g0122 a0001c0001t0001g0129 a0001c0001t0001g0144 others(16): Show |
20 | HG01884.hp1 HG01884.hp2 HG01978.hp1 others(17): Show |
intron_variant | MODIFIER | c.1111-1249C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431996 | |||||||
| chr19:431996 | G | GGGGCAGA others(51): Show |
2 | a0001c0001t0003g0032 a0001c0005t0006g0009 |
2 | HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1111-1250_1111-124 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431996 | |||||||
| chr19:431996 | G | GGGGCAGA others(51): Show |
1 | a0001c0003t0001g0140 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1111-1250_1111-124 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431996 | |||||||
| chr19:431996 | GGGGCAGA others(109): Show |
G | 1 | a0001c0001t0006g0052 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1111-1365_1111-125 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431996 | |||||||
| chr19:431997 | G | A | 2 | a0001c0001t0002g0076 a0001c0001t0013g0072 |
2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1111-1250C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 431997 | |||||||
| chr19:432000 | CAGAT | C | 4 | a0001c0001t0003g0005 a0001c0001t0003g0181 a0002c0004t0001g0190 others(1): Show |
5 | HG01978.hp1 HG02055.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1111-1257_1111-125 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432000 | |||||||
| chr19:432006 | G | C | 1 | a0001c0001t0001g0129 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1111-1259C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432006 | |||||||
| chr19:432012 | G | ACTTCATC others(109): Show |
1 | a0001c0002t0002g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1111-1265_1111-126 others(120): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432012 | |||||||
| chr19:432020 | G | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1111-1273C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432020 | |||||||
| chr19:432031 | C | A | 5 | a0001c0003t0001g0063 a0001c0003t0002g0071 a0001c0003t0004g0109 others(2): Show |
5 | HG01074.hp2 HG01952.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.1111-1284G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432031 | |||||||
| chr19:432031 | C | CGTGAGTG others(167): Show |
1 | a0001c0006t0002g0023 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1111-1285_1111-128 others(178): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432031 | |||||||
| chr19:432043 | A | ATAGAGGA others(105): Show |
1 | a0001c0023t0007g0187 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1111-1297_1111-129 others(116): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432043 | |||||||
| chr19:432043 | A | T | 29 | a0001c0001t0001g0129 a0001c0001t0002g0051 a0001c0001t0003g0070 others(26): Show |
30 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.1111-1296T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432043 | |||||||
| chr19:432054 | C | CGGGCAGA others(151): Show |
1 | a0001c0001t0004g0029 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1111-1308_1111-130 others(162): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432054 | |||||||
| chr19:432054 | C | G | 1 | a0001c0001t0001g0122 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1111-1307G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432054 | |||||||
| chr19:432055 | G | A | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG00609.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.1111-1308C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432055 | |||||||
| chr19:432058 | CAGAT | C | 3 | a0001c0001t0003g0005 a0001c0001t0003g0181 a0001c0001t0011g0034 |
4 | HG01978.hp1 HG02055.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111-1315_1111-131 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432058 | |||||||
| chr19:432062 | T | TAGATGGC others(47): Show |
3 | a0001c0003t0002g0001 a0001c0003t0010g0059 a0001c0017t0005g0055 |
4 | HG00621.hp1 HG02622.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111-1316_1111-131 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432062 | |||||||
| chr19:432067 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1111-1320C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432067 | |||||||
| chr19:432089 | C | CGTGAGTG others(333): Show |
1 | a0001c0003t0004g0111 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1111-1343_1111-134 others(344): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432089 | |||||||
| chr19:432089 | C | CGTGAGTG others(333): Show |
9 | a0001c0003t0002g0065 a0001c0003t0002g0074 a0001c0003t0002g0075 others(6): Show |
9 | HG00558.hp1 HG00621.hp2 HG03688.hp1 others(6): Show |
intron_variant | MODIFIER | c.1111-1343_1111-134 others(344): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432089 | |||||||
| chr19:432089 | C | CGTGAGTG others(109): Show |
1 | a0001c0006t0002g0022 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1111-1343_1111-134 others(120): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432089 | |||||||
| chr19:432089 | C | T | 1 | a0011c0022t0002g0185 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1111-1342G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432089 | |||||||
| chr19:432101 | A | ATAGAGGA others(109): Show |
2 | a0001c0003t0001g0063 a0002c0012t0004g0195 |
2 | HG01074.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1111-1355_1111-135 others(120): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432101 | |||||||
| chr19:432101 | A | ATAGAGGA others(51): Show |
2 | a0001c0002t0001g0079 a0001c0002t0001g0080 |
2 | HG00558.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1111-1355_1111-135 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432101 | |||||||
| chr19:432101 | A | T | 14 | a0001c0001t0001g0130 a0001c0001t0002g0101 a0001c0001t0004g0029 others(11): Show |
14 | HG00544.hp2 HG01109.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.1111-1354T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432101 | |||||||
| chr19:432112 | C | G | 55 | a0001c0001t0001g0129 a0001c0001t0001g0144 a0001c0001t0001g0145 others(52): Show |
56 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.1111-1365G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432112 | |||||||
| chr19:432113 | G | A | 15 | a0001c0001t0002g0056 a0001c0001t0003g0049 a0001c0001t0005g0102 others(12): Show |
15 | HG01891.hp2 HG02486.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1111-1366C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432113 | |||||||
| chr19:432120 | T | TAGATGGC others(619): Show |
1 | a0001c0001t0001g0145 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1111-1374_1111-137 others(630): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432120 | |||||||
| chr19:432120 | T | TAGATGGC others(279): Show |
1 | a0001c0006t0006g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1111-1374_1111-137 others(290): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432120 | |||||||
| chr19:432120 | T | TAGATGGC others(275): Show |
2 | a0004c0011t0005g0057 a0004c0011t0005g0061 |
2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1111-1374_1111-137 others(286): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432120 | |||||||
| chr19:432120 | T | TGGCGCTT others(159): Show |
4 | a0001c0003t0001g0060 a0001c0003t0001g0064 a0001c0003t0002g0112 others(1): Show |
4 | HG00544.hp2 NA18940.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111-1374_1111-137 others(170): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432120 | |||||||
| chr19:432125 | G | A | 3 | a0001c0001t0001g0122 a0001c0001t0003g0005 a0001c0001t0003g0181 |
4 | HG01978.hp1 HG02055.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111-1378C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432125 | |||||||
| chr19:432128 | G | A | 1 | a0001c0002t0002g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1111-1381C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432128 | |||||||
| chr19:432144 | G | C | 3 | a0001c0007t0006g0033 a0001c0007t0006g0054 a0002c0024t0003g0200 |
3 | HG02451.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1111-1397C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432144 | |||||||
| chr19:432147 | C | A | 4 | a0001c0003t0001g0060 a0001c0003t0001g0064 a0001c0003t0002g0112 others(1): Show |
4 | HG00544.hp2 NA18940.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111-1400G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432147 | |||||||
| chr19:432147 | C | CGTGAGTG others(275): Show |
4 | a0001c0003t0002g0062 a0001c0003t0002g0068 a0001c0003t0002g0073 others(1): Show |
4 | NA18954.hp2 NA18960.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111-1401_1111-140 others(286): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432147 | |||||||
| chr19:432147 | C | CGTGAGTG others(271): Show |
1 | a0001c0002t0001g0173 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1111-1401_1111-140 others(282): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432147 | |||||||
| chr19:432148 | G | A | 1 | a0001c0001t0011g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1111-1401C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432148 | |||||||
| chr19:432150 | G | GAGTGAGA others(101): Show |
1 | a0001c0003t0010g0059 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1111-1404_1111-140 others(112): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432150 | |||||||
| chr19:432159 | A | ATAGAGGA others(329): Show |
1 | a0001c0002t0003g0151 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1111-1413_1111-141 others(340): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432159 | |||||||
| chr19:432159 | A | T | 70 | a0001c0001t0001g0122 a0001c0001t0001g0130 a0001c0001t0002g0051 others(67): Show |
73 | HG00423.hp2 HG00558.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.1111-1412T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432159 | |||||||
| chr19:432170 | C | CGGGCAGA others(109): Show |
1 | a0001c0005t0006g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1111-1424_1111-142 others(120): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432170 | |||||||
| chr19:432170 | C | G | 8 | a0001c0001t0001g0097 a0001c0001t0002g0101 a0001c0003t0001g0063 others(5): Show |
8 | HG01074.hp2 HG01952.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.1111-1423G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432170 | |||||||
| chr19:432171 | G | A | 5 | a0001c0001t0002g0035 a0001c0007t0006g0033 a0001c0007t0006g0054 others(2): Show |
5 | HG01884.hp2 HG02451.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111-1424C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432171 | |||||||
| chr19:432171 | G | GGGCAGAT others(109): Show |
1 | a0001c0001t0001g0145 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1111-1425_1111-142 others(120): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432171 | |||||||
| chr19:432176 | GATAC | G | 3 | a0001c0007t0006g0033 a0001c0007t0006g0054 a0002c0024t0003g0200 |
3 | HG02451.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1111-1433_1111-143 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432176 | |||||||
| chr19:432178 | T | TAGATGGC others(47): Show |
1 | a0001c0007t0002g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1111-1432_1111-143 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432178 | |||||||
| chr19:432180 | C | G | 107 | a0001c0001t0001g0090 a0001c0001t0001g0097 a0001c0001t0001g0122 others(104): Show |
110 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.1111-1433G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432180 | |||||||
| chr19:432183 | G | A | 5 | a0001c0001t0001g0129 a0001c0001t0011g0034 a0002c0004t0001g0190 others(2): Show |
5 | HG00639.hp1 HG02015.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111-1436C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432183 | |||||||
| chr19:432186 | G | A | 2 | a0005c0009t0005g0047 a0005c0009t0014g0036 |
2 | NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1111-1439C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432186 | |||||||
| chr19:432194 | G | A | 1 | a0001c0001t0016g0069 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1111-1447C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432194 | |||||||
| chr19:432205 | C | CGTGAGTG others(387): Show |
1 | a0001c0002t0001g0088 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1111-1459_1111-145 others(398): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432205 | |||||||
| chr19:432205 | C | CGTGAGTG others(167): Show |
2 | a0001c0006t0001g0013 a0001c0006t0001g0016 |
2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1111-1459_1111-145 others(178): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432205 | |||||||
| chr19:432205 | C | CGTGAGTG others(225): Show |
1 | a0001c0006t0001g0017 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1111-1459_1111-145 others(236): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432205 | |||||||
| chr19:432211 | T | G | 1 | a0001c0001t0003g0032 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1111-1464A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432211 | |||||||
| chr19:432217 | T | A | 63 | a0001c0001t0001g0144 a0001c0001t0002g0035 a0001c0001t0002g0101 others(60): Show |
65 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.1111-1470A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432217 | |||||||
| chr19:432218 | T | C | 1 | a0001c0005t0006g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1111-1471A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432218 | |||||||
| chr19:432228 | C | CGGGCAGA others(449): Show |
1 | a0001c0003t0001g0114 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1111-1482_1111-148 others(460): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432228 | |||||||
| chr19:432228 | C | G | 5 | a0001c0002t0001g0079 a0001c0002t0001g0080 a0001c0006t0006g0010 others(2): Show |
5 | HG00558.hp2 HG02622.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1111-1481G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432228 | |||||||
| chr19:432232 | CAGAT | C | 3 | a0001c0001t0001g0130 a0001c0001t0003g0070 a0003c0008t0005g0183 |
3 | HG01123.hp1 HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1111-1489_1111-148 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432232 | |||||||
| chr19:432232 | CAGATAGA others(287): Show |
C | 1 | a0001c0001t0002g0051 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1111-1779_1111-148 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432232 | |||||||
| chr19:432244 | G | A | 1 | a0001c0003t0001g0140 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1111-1497C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432244 | |||||||
| chr19:432263 | C | CGTGAGTG others(329): Show |
3 | a0001c0002t0001g0092 a0001c0002t0004g0176 a0001c0002t0004g0177 |
3 | HG01993.hp2 NA18947.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1111-1517_1111-151 others(340): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432263 | |||||||
| chr19:432275 | T | A | 70 | a0001c0001t0001g0130 a0001c0001t0001g0144 a0001c0001t0001g0145 others(67): Show |
72 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.1111-1528A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432275 | |||||||
| chr19:432276 | T | C | 1 | a0001c0001t0003g0032 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1111-1529A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432276 | |||||||
| chr19:432286 | C | CGGGCAGA others(51): Show |
5 | a0001c0003t0001g0060 a0001c0003t0001g0064 a0001c0003t0002g0112 others(2): Show |
5 | HG00544.hp2 HG00621.hp1 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.1111-1597_1111-154 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432286 | |||||||
| chr19:432286 | C | CGGGCAGA others(221): Show |
1 | a0001c0003t0001g0140 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1111-1540_1111-153 others(232): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432286 | |||||||
| chr19:432286 | C | G | 50 | a0001c0001t0003g0032 a0001c0002t0001g0004 a0001c0002t0001g0079 others(47): Show |
52 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.1111-1539G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432286 | |||||||
| chr19:432287 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0145 |
2 | HG00609.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.1111-1540C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432287 | |||||||
| chr19:432287 | G | GGGCAGAT others(47): Show |
1 | a0001c0023t0007g0187 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1111-1541_1111-154 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432287 | |||||||
| chr19:432290 | CAGAT | C | 6 | a0001c0001t0002g0076 a0001c0001t0007g0038 a0001c0001t0013g0072 others(3): Show |
6 | HG01074.hp2 HG01361.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.1111-1547_1111-154 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432290 | |||||||
| chr19:432290 | CAGATAGA others(55): Show |
C | 3 | a0001c0001t0001g0122 a0001c0001t0003g0005 a0001c0001t0003g0181 |
4 | HG01978.hp1 HG02055.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111-1605_1111-154 others(66): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432290 | |||||||
| chr19:432290 | CAGATAGA others(403): Show |
C | 1 | a0007c0025t0001g0207 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1111-1953_1111-154 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432290 | |||||||
| chr19:432290 | CAGATAGA others(689): Show |
C | 1 | a0001c0001t0001g0097 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1110+1723_1111-154 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432290 | |||||||
| chr19:432296 | G | C | 1 | a0001c0001t0001g0144 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1111-1549C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432296 | |||||||
| chr19:432302 | G | A | 1 | a0001c0007t0002g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1111-1555C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432302 | |||||||
| chr19:432318 | G | GATCGTGA others(383): Show |
1 | a0001c0001t0003g0032 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1111-1572_1111-157 others(394): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432318 | |||||||
| chr19:432321 | C | A | 2 | a0001c0001t0011g0034 a0001c0006t0002g0023 |
2 | HG01943.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1111-1574G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432321 | |||||||
| chr19:432321 | C | CGTGAGTG others(275): Show |
1 | a0008c0015t0012g0026 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1111-1575_1111-157 others(286): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432321 | |||||||
| chr19:432333 | A | T | 55 | a0001c0001t0001g0129 a0001c0001t0001g0144 a0001c0001t0004g0162 others(52): Show |
56 | HG00423.hp2 HG00558.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.1111-1586T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432333 | |||||||
| chr19:432344 | G | C | 34 | a0001c0001t0001g0129 a0001c0001t0001g0144 a0001c0001t0002g0035 others(31): Show |
34 | HG00639.hp1 HG01074.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.1111-1597C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432344 | |||||||
| chr19:432344 | G | GGGGCAGA others(93): Show |
1 | a0001c0005t0006g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1111-1598_1111-159 others(104): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432344 | |||||||
| chr19:432344 | GGGGCAGA others(51): Show |
G | 1 | a0001c0001t0011g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1111-1655_1111-159 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432344 | |||||||
| chr19:432344 | GGGGCAGA others(457): Show |
G | 28 | a0001c0001t0001g0003 a0001c0001t0001g0081 a0001c0001t0001g0083 others(25): Show |
29 | HG00609.hp1 HG00639.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.1110+1901_1111-159 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432344 | |||||||
| chr19:432345 | G | A | 6 | a0001c0001t0002g0035 a0001c0001t0003g0070 a0001c0001t0007g0038 others(3): Show |
6 | HG02451.hp2 HG02818.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1111-1598C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432345 | |||||||
| chr19:432348 | CAGAT | C | 8 | a0001c0001t0001g0129 a0001c0001t0004g0162 a0001c0001t0004g0164 others(5): Show |
8 | HG00639.hp1 HG01358.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.1111-1605_1111-160 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432348 | |||||||
| chr19:432352 | T | TAGATGGC others(47): Show |
1 | a0004c0011t0005g0061 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1111-1606_1111-160 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432352 | |||||||
| chr19:432352 | T | TAGATGGC others(47): Show |
1 | a0004c0011t0005g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1111-1606_1111-160 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432352 | |||||||
| chr19:432352 | T | TGGCGCTT others(214): Show |
1 | a0001c0007t0002g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1111-1606_1111-160 others(225): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432352 | |||||||
| chr19:432376 | G | GATCGTGA others(39): Show |
3 | a0001c0002t0001g0079 a0001c0002t0001g0080 a0001c0002t0001g0173 |
3 | HG00558.hp2 HG03942.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1111-1630_1111-162 others(50): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432376 | |||||||
| chr19:432379 | C | A | 1 | a0001c0006t0002g0022 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1111-1632G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432379 | |||||||
| chr19:432379 | C | CGTGAGTG others(101): Show |
1 | a0001c0002t0001g0086 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1111-1633_1111-163 others(112): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432379 | |||||||
| chr19:432379 | C | CGTGAGTG others(271): Show |
1 | a0001c0002t0001g0157 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1111-1633_1111-163 others(282): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432379 | |||||||
| chr19:432379 | C | CGTGAGTG others(213): Show |
1 | a0001c0002t0001g0094 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1111-1633_1111-163 others(224): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432379 | |||||||
| chr19:432391 | T | A | 29 | a0001c0001t0001g0122 a0001c0001t0001g0129 a0001c0001t0001g0130 others(26): Show |
30 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.1111-1644A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432391 | |||||||
| chr19:432391 | T | TTAGAGGA others(275): Show |
1 | a0001c0006t0006g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1111-1645_1111-164 others(286): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432391 | |||||||
| chr19:432391 | T | TTAGAGGA others(43): Show |
1 | a0001c0002t0003g0149 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1111-1645_1111-164 others(54): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432391 | |||||||
| chr19:432391 | T | TTAGAGGA others(491): Show |
22 | a0001c0002t0001g0004 a0001c0002t0001g0082 a0001c0002t0001g0093 others(19): Show |
23 | HG00423.hp2 HG01952.hp2 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.1111-1645_1111-164 others(502): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432391 | |||||||
| chr19:432391 | T | TTAGAGGA others(565): Show |
2 | a0001c0003t0002g0071 a0001c0003t0004g0109 |
2 | HG02132.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1111-1645_1111-164 others(576): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432391 | |||||||
| chr19:432391 | T | TTAGAGGA others(105): Show |
2 | a0001c0007t0006g0054 a0002c0024t0003g0200 |
2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1111-1645_1111-164 others(116): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432391 | |||||||
| chr19:432402 | C | CGGGCAGA others(773): Show |
2 | a0001c0002t0003g0091 a0001c0002t0003g0174 |
2 | NA18960.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1111-1656_1111-165 others(784): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432402 | |||||||
| chr19:432402 | C | G | 6 | a0001c0001t0003g0070 a0001c0001t0007g0038 a0001c0002t0001g0088 others(3): Show |
6 | HG01361.hp1 HG02293.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1111-1655G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432402 | |||||||
| chr19:432403 | G | A | 15 | a0001c0001t0001g0122 a0001c0001t0001g0129 a0001c0001t0002g0076 others(12): Show |
16 | HG00639.hp1 HG01358.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1111-1656C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432403 | |||||||
| chr19:432403 | G | GGGCAGAT others(213): Show |
1 | a0011c0022t0002g0185 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1111-1657_1111-165 others(224): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432403 | |||||||
| chr19:432403 | G | GGGCAGAT others(163): Show |
1 | a0001c0014t0001g0014 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1111-1657_1111-165 others(174): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432403 | |||||||
| chr19:432410 | T | TAGATGGC others(47): Show |
19 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0078 others(16): Show |
19 | HG00423.hp1 HG00544.hp1 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.1111-1664_1111-166 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432410 | |||||||
| chr19:432412 | G | C | 1 | a0001c0001t0002g0035 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1111-1665C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432412 | |||||||
| chr19:432418 | G | A | 3 | a0001c0003t0001g0063 a0001c0007t0002g0077 a0002c0012t0004g0195 |
3 | HG01074.hp2 HG03017.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1111-1671C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432418 | |||||||
| chr19:432422 | CATCGTGA others(5): Show |
C | 1 | a0001c0002t0003g0151 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1111-1687_1111-167 others(16): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432422 | |||||||
| chr19:432425 | C | T | 1 | a0001c0013t0005g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1111-1678G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432425 | |||||||
| chr19:432437 | C | A | 1 | a0001c0003t0001g0114 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1111-1690G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432437 | |||||||
| chr19:432437 | C | CGTGAGTG others(971): Show |
1 | a0001c0006t0001g0017 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1111-1691_1111-169 others(982): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432437 | |||||||
| chr19:432437 | C | CGTGAGTG others(47): Show |
2 | a0001c0003t0001g0063 a0002c0012t0004g0195 |
2 | HG01074.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1111-1691_1111-169 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432437 | |||||||
| chr19:432437 | C | T | 1 | a0001c0002t0003g0149 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1111-1690G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432437 | |||||||
| chr19:432449 | A | ATAGAGGA others(391): Show |
2 | a0001c0006t0001g0013 a0001c0006t0001g0016 |
2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1111-1703_1111-170 others(402): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432449 | |||||||
| chr19:432449 | A | T | 64 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0103 others(61): Show |
65 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.1111-1702T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432449 | |||||||
| chr19:432460 | C | G | 21 | a0001c0001t0001g0122 a0001c0001t0001g0129 a0001c0001t0001g0144 others(18): Show |
22 | HG00639.hp1 HG00735.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.1111-1713G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432460 | |||||||
| chr19:432460 | C | T | 3 | a0001c0001t0003g0032 a0001c0005t0006g0009 a0011c0022t0002g0185 |
3 | HG02055.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1111-1713G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432460 | |||||||
| chr19:432461 | G | A | 5 | a0001c0001t0002g0056 a0001c0001t0003g0049 a0001c0001t0006g0030 others(2): Show |
5 | HG02486.hp2 HG02622.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111-1714C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432461 | |||||||
| chr19:432464 | CAGAT | C | 24 | a0001c0001t0001g0099 a0001c0001t0001g0103 a0001c0001t0001g0104 others(21): Show |
24 | HG00323.hp1 HG01071.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1111-1721_1111-171 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432464 | |||||||
| chr19:432464 | CAGATAGA others(55): Show |
C | 1 | a0001c0001t0016g0069 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1111-1779_1111-171 others(66): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432464 | |||||||
| chr19:432464 | CAGATAGA others(113): Show |
C | 1 | a0001c0005t0015g0007 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1111-1837_1111-171 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432464 | |||||||
| chr19:432464 | CAGATAGA others(515): Show |
C | 20 | a0001c0001t0001g0098 a0001c0001t0004g0002 a0001c0001t0004g0031 others(17): Show |
21 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.1110+1723_1111-171 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432464 | |||||||
| chr19:432468 | T | TAGATGGC others(205): Show |
1 | a0001c0002t0001g0088 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1111-1722_1111-172 others(216): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432468 | |||||||
| chr19:432468 | T | TAGATGGC others(163): Show |
1 | a0004c0011t0005g0061 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1111-1722_1111-172 others(174): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432468 | |||||||
| chr19:432468 | T | TAGATGGC others(105): Show |
1 | a0001c0023t0007g0187 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1111-1722_1111-172 others(116): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432468 | |||||||
| chr19:432484 | G | A | 27 | a0001c0002t0001g0004 a0001c0002t0001g0079 a0001c0002t0001g0080 others(24): Show |
28 | HG00423.hp2 HG00558.hp2 HG01952.hp2 others(25): Show |
intron_variant | MODIFIER | c.1111-1737C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432484 | |||||||
| chr19:432495 | C | A | 1 | a0001c0002t0001g0086 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1111-1748G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432495 | |||||||
| chr19:432507 | A | T | 33 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0078 others(30): Show |
33 | HG00423.hp1 HG00544.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1111-1760T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432507 | |||||||
| chr19:432516 | G | A | 1 | a0011c0022t0002g0185 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1111-1769C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432516 | |||||||
| chr19:432518 | C | A | 1 | a0001c0006t0002g0023 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1111-1771G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432518 | |||||||
| chr19:432518 | C | G | 30 | a0001c0001t0002g0056 a0001c0001t0002g0101 a0001c0001t0003g0049 others(27): Show |
31 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.1111-1771G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432518 | |||||||
| chr19:432519 | G | A | 16 | a0001c0001t0005g0102 a0001c0001t0006g0042 a0001c0001t0006g0048 others(13): Show |
16 | HG01109.hp2 HG01358.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1111-1772C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432519 | |||||||
| chr19:432522 | CAGAT | C | 3 | a0001c0001t0003g0070 a0001c0002t0003g0149 a0001c0020t0001g0105 |
3 | HG01071.hp2 HG01361.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1111-1779_1111-177 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432522 | |||||||
| chr19:432526 | T | TAGATGGC others(259): Show |
3 | a0001c0002t0001g0092 a0001c0002t0004g0176 a0001c0002t0004g0177 |
3 | HG01993.hp2 NA18947.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1111-1780_1111-177 others(270): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432526 | |||||||
| chr19:432526 | T | TAGATGGC others(43): Show |
23 | a0001c0002t0001g0004 a0001c0002t0001g0079 a0001c0002t0001g0080 others(20): Show |
24 | HG00423.hp2 HG00558.hp2 HG01952.hp2 others(21): Show |
intron_variant | MODIFIER | c.1111-1780_1111-177 others(54): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432526 | |||||||
| chr19:432526 | T | TAGATGGC others(47): Show |
4 | a0001c0001t0001g0133 a0001c0001t0001g0144 a0001c0006t0002g0022 others(1): Show |
4 | HG00544.hp1 HG01943.hp2 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111-1780_1111-177 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432526 | |||||||
| chr19:432528 | G | C | 1 | a0001c0001t0001g0130 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1111-1781C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432528 | |||||||
| chr19:432528 | G | CATGGCGC others(279): Show |
1 | a0001c0001t0001g0145 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1111-1781_1111-178 others(290): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432528 | |||||||
| chr19:432542 | G | A | 1 | a0001c0002t0003g0151 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1111-1795C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432542 | |||||||
| chr19:432553 | C | A | 1 | a0001c0002t0003g0149 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1111-1806G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432553 | |||||||
| chr19:432553 | C | CGTGAGTG others(105): Show |
1 | a0003c0008t0005g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1111-1807_1111-180 others(116): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432553 | |||||||
| chr19:432558 | G | GTGAGAGA others(43): Show |
2 | a0001c0002t0001g0146 a0001c0002t0003g0175 |
2 | HG04228.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1111-1812_1111-181 others(54): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432558 | |||||||
| chr19:432565 | A | AGGAGGCC others(43): Show |
2 | a0001c0002t0003g0091 a0001c0002t0003g0174 |
2 | NA18960.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1111-1819_1111-181 others(54): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432565 | |||||||
| chr19:432565 | A | ATAGAGGA others(51): Show |
1 | a0001c0001t0003g0032 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1111-1819_1111-181 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432565 | |||||||
| chr19:432565 | A | T | 24 | a0001c0001t0001g0099 a0001c0001t0001g0103 a0001c0001t0001g0120 others(21): Show |
24 | HG01071.hp1 HG01071.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1111-1818T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432565 | |||||||
| chr19:432566 | T | C | 1 | a0001c0007t0006g0033 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1111-1819A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432566 | |||||||
| chr19:432576 | C | G | 40 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0078 others(37): Show |
40 | HG00423.hp1 HG01358.hp1 HG01891.hp2 others(37): Show |
intron_variant | MODIFIER | c.1111-1829G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432576 | |||||||
| chr19:432577 | G | A | 32 | a0001c0001t0001g0104 a0001c0001t0001g0131 a0001c0001t0016g0069 others(29): Show |
33 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.1111-1830C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432577 | |||||||
| chr19:432584 | T | TAGATGGC others(43): Show |
1 | a0005c0009t0005g0047 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1111-1838_1111-183 others(54): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432584 | |||||||
| chr19:432584 | T | TAGATGGC others(333): Show |
1 | a0001c0001t0004g0029 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1111-1838_1111-183 others(344): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432584 | |||||||
| chr19:432584 | T | TAGATGGC others(1122): Show |
2 | a0001c0007t0006g0054 a0002c0024t0003g0200 |
2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1111-1838_1111-183 others(1133): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432584 | |||||||
| chr19:432584 | T | TGGCGCTT others(275): Show |
1 | a0004c0011t0005g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1111-1838_1111-183 others(286): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432584 | |||||||
| chr19:432584 | TAGATGGC others(337): Show |
T | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1110+1781_1111-183 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432584 | |||||||
| chr19:432586 | G | C | 2 | a0001c0001t0011g0034 a0003c0008t0005g0183 |
2 | HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1111-1839C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432586 | |||||||
| chr19:432591 | C | T | 3 | a0001c0002t0001g0092 a0001c0002t0004g0176 a0001c0002t0004g0177 |
3 | HG01993.hp2 NA18947.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1111-1844G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432591 | |||||||
| chr19:432623 | A | AGGAGGCC others(101): Show |
1 | a0001c0002t0003g0151 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1111-1877_1111-187 others(112): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432623 | |||||||
| chr19:432623 | A | T | 69 | a0001c0001t0001g0133 a0001c0001t0001g0144 a0001c0001t0001g0145 others(66): Show |
71 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.1111-1876T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432623 | |||||||
| chr19:432631 | G | A | 1 | a0005c0009t0014g0036 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1111-1884C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432631 | |||||||
| chr19:432634 | C | CGGGCAGA others(321): Show |
1 | a0001c0002t0001g0094 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1111-1888_1111-188 others(332): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432634 | |||||||
| chr19:432634 | C | G | 56 | a0001c0001t0001g0099 a0001c0001t0001g0103 a0001c0001t0001g0104 others(53): Show |
57 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.1111-1887G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432634 | |||||||
| chr19:432635 | G | A | 18 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0078 others(15): Show |
19 | HG00423.hp1 HG01109.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.1111-1888C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432635 | |||||||
| chr19:432642 | T | TAGATGGC others(329): Show |
1 | a0001c0007t0002g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1111-1896_1111-189 others(340): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432642 | |||||||
| chr19:432644 | G | C | 13 | a0001c0001t0001g0122 a0001c0001t0001g0129 a0001c0001t0003g0172 others(10): Show |
13 | HG00639.hp1 HG00735.hp1 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.1111-1897C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432644 | |||||||
| chr19:432649 | C | CGCTTCAT others(379): Show |
1 | a0001c0002t0001g0157 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1111-1903_1111-190 others(390): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432649 | |||||||
| chr19:432649 | C | T | 3 | a0001c0002t0001g0088 a0001c0002t0003g0091 a0001c0002t0003g0174 |
3 | NA18960.hp2 NA19009.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1111-1902G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432649 | |||||||
| chr19:432650 | G | A | 2 | a0001c0001t0002g0051 a0003c0008t0005g0183 |
2 | HG02559.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1111-1903C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432650 | |||||||
| chr19:432669 | C | A | 2 | a0001c0003t0002g0071 a0001c0003t0004g0109 |
2 | HG02132.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1111-1922G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432669 | |||||||
| chr19:432669 | C | CGTGAGTG others(51): Show |
21 | a0001c0003t0001g0060 a0001c0003t0001g0064 a0001c0003t0001g0114 others(18): Show |
22 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.1111-1923_1111-192 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432669 | |||||||
| chr19:432681 | A | ATAGAGGA others(51): Show |
2 | a0001c0003t0001g0063 a0002c0012t0004g0195 |
2 | HG01074.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1111-1935_1111-193 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432681 | |||||||
| chr19:432681 | A | T | 35 | a0001c0001t0001g0122 a0001c0001t0001g0129 a0001c0001t0001g0130 others(32): Show |
35 | HG00639.hp1 HG00735.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.1111-1934T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432681 | |||||||
| chr19:432682 | T | C | 2 | a0001c0001t0002g0076 a0001c0001t0013g0072 |
2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1111-1935A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432682 | |||||||
| chr19:432692 | C | A | 1 | a0001c0016t0001g0159 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1111-1945G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432692 | |||||||
| chr19:432692 | C | CGGGCAGA others(51): Show |
1 | a0001c0005t0006g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1111-1946_1111-194 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432692 | |||||||
| chr19:432692 | C | CGGGCAGA others(47): Show |
2 | a0001c0006t0002g0022 a0001c0006t0002g0023 |
2 | HG01943.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1111-1946_1111-194 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432692 | |||||||
| chr19:432692 | C | G | 39 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0078 others(36): Show |
40 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.1111-1945G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432692 | |||||||
| chr19:432693 | G | A | 8 | a0001c0001t0001g0099 a0001c0001t0001g0103 a0001c0001t0001g0135 others(5): Show |
8 | HG02040.hp2 HG02132.hp1 NA18999.hp2 others(5): Show |
intron_variant | MODIFIER | c.1111-1946C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432693 | |||||||
| chr19:432696 | CAGAT | C | 5 | a0001c0001t0002g0035 a0001c0001t0002g0051 a0001c0013t0005g0006 others(2): Show |
5 | HG02559.hp1 HG02622.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1111-1953_1111-195 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432696 | |||||||
| chr19:432700 | T | TAGATGGC others(155): Show |
1 | a0005c0009t0014g0036 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1111-1954_1111-195 others(166): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432700 | |||||||
| chr19:432700 | T | TAGATGGC others(47): Show |
1 | a0001c0014t0001g0014 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1111-1954_1111-195 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432700 | |||||||
| chr19:432702 | G | C | 1 | a0001c0002t0002g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1111-1955C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432702 | |||||||
| chr19:432707 | C | T | 30 | a0001c0002t0001g0004 a0001c0002t0001g0079 a0001c0002t0001g0080 others(27): Show |
31 | HG00423.hp2 HG00558.hp2 HG01952.hp2 others(28): Show |
intron_variant | MODIFIER | c.1111-1960G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432707 | |||||||
| chr19:432724 | G | GATCGTGA others(151): Show |
2 | a0001c0001t0002g0076 a0001c0001t0013g0072 |
2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1111-1978_1111-197 others(162): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432724 | |||||||
| chr19:432727 | C | A | 1 | a0001c0006t0001g0017 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1111-1980G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432727 | |||||||
| chr19:432727 | C | CGTGAGTG others(51): Show |
2 | a0001c0003t0002g0100 a0008c0015t0012g0026 |
2 | HG00621.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1110+1981_1111-198 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432727 | |||||||
| chr19:432739 | A | T | 53 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0078 others(50): Show |
53 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.1110+1970T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432739 | |||||||
| chr19:432750 | C | A | 3 | a0001c0001t0001g0104 a0001c0001t0001g0131 a0002c0004t0001g0206 |
3 | HG00323.hp1 HG02735.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1110+1959G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432750 | |||||||
| chr19:432750 | C | CGGGCAGA others(321): Show |
1 | a0001c0002t0001g0086 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1110+1958_1110+195 others(332): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432750 | |||||||
| chr19:432750 | C | G | 14 | a0001c0001t0001g0099 a0001c0001t0001g0103 a0001c0001t0001g0135 others(11): Show |
14 | HG01071.hp2 HG02040.hp2 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.1110+1959G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432750 | |||||||
| chr19:432750 | C | T | 1 | a0001c0007t0002g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1110+1959G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432750 | |||||||
| chr19:432751 | G | A | 6 | a0001c0001t0001g0133 a0001c0001t0001g0144 a0001c0001t0001g0145 others(3): Show |
6 | HG00544.hp1 HG00609.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.1110+1958C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432751 | |||||||
| chr19:432758 | T | TAGATGGC others(47): Show |
2 | a0001c0007t0006g0033 a0004c0011t0005g0061 |
2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1110+1950_1110+195 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432758 | |||||||
| chr19:432758 | T | TAGATGGC others(105): Show |
4 | a0001c0001t0002g0056 a0001c0001t0003g0049 a0001c0001t0006g0030 others(1): Show |
4 | HG02486.hp2 HG02970.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1110+1950_1110+195 others(116): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432758 | |||||||
| chr19:432758 | TAGATGGC others(163): Show |
T | 1 | a0001c0001t0002g0035 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1110+1781_1110+195 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432758 | |||||||
| chr19:432785 | C | A | 1 | a0001c0001t0002g0051 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1110+1924G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432785 | |||||||
| chr19:432797 | A | T | 61 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0078 others(58): Show |
62 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.1110+1912T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432797 | |||||||
| chr19:432808 | C | A | 1 | a0001c0020t0001g0105 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1110+1901G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432808 | |||||||
| chr19:432808 | C | G | 46 | a0001c0001t0001g0122 a0001c0001t0001g0129 a0001c0001t0001g0130 others(43): Show |
47 | HG00544.hp1 HG00609.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.1110+1901G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432808 | |||||||
| chr19:432809 | G | A | 1 | a0001c0023t0007g0187 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1110+1900C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432809 | |||||||
| chr19:432812 | CAGAT | C | 13 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0078 others(10): Show |
13 | HG00423.hp1 HG02027.hp1 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.1110+1893_1110+189 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432812 | |||||||
| chr19:432818 | G | C | 1 | a0001c0001t0002g0051 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1110+1891C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432818 | |||||||
| chr19:432823 | C | A | 1 | a0001c0005t0015g0007 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1110+1886G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432823 | |||||||
| chr19:432823 | C | T | 1 | a0001c0002t0001g0086 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1110+1886G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432823 | |||||||
| chr19:432824 | G | A | 5 | a0001c0001t0004g0029 a0001c0002t0001g0088 a0001c0002t0001g0157 others(2): Show |
5 | HG02698.hp2 HG03098.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+1885C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432824 | |||||||
| chr19:432824 | G | GCTTCATC others(51): Show |
30 | a0001c0002t0001g0004 a0001c0002t0001g0079 a0001c0002t0001g0080 others(27): Show |
31 | HG00423.hp2 HG00558.hp2 HG01952.hp2 others(28): Show |
intron_variant | MODIFIER | c.1110+1884_1110+188 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432824 | |||||||
| chr19:432828 | CATCGTGA others(5): Show |
C | 1 | a0001c0002t0003g0149 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1110+1869_1110+188 others(16): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432828 | |||||||
| chr19:432840 | G | C | 2 | a0001c0007t0006g0054 a0002c0024t0003g0200 |
2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1110+1869C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432840 | |||||||
| chr19:432855 | T | A | 34 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0078 others(31): Show |
34 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.1110+1854A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432855 | |||||||
| chr19:432855 | T | TTAGAGGA others(47): Show |
8 | a0001c0001t0001g0099 a0001c0001t0001g0103 a0001c0001t0001g0135 others(5): Show |
8 | HG02040.hp2 HG02132.hp1 NA18999.hp2 others(5): Show |
intron_variant | MODIFIER | c.1110+1853_1110+185 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432855 | |||||||
| chr19:432866 | C | CGGGCAGA others(105): Show |
1 | a0001c0003t0001g0114 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1110+1842_1110+184 others(116): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432866 | |||||||
| chr19:432866 | C | G | 7 | a0001c0001t0001g0104 a0001c0001t0001g0131 a0001c0001t0002g0101 others(4): Show |
7 | HG00323.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1110+1843G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432866 | |||||||
| chr19:432866 | CGGGCAGA others(221): Show |
C | 2 | a0001c0001t0003g0005 a0001c0001t0003g0181 |
3 | HG01978.hp1 HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1110+1615_1110+184 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432866 | |||||||
| chr19:432866 | CGGGCAGA others(337): Show |
C | 1 | a0001c0020t0001g0105 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1110+1499_1110+184 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432866 | |||||||
| chr19:432867 | G | A | 2 | a0001c0007t0006g0054 a0002c0024t0003g0200 |
2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1110+1842C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432867 | |||||||
| chr19:432870 | CAGAT | C | 2 | a0001c0007t0006g0054 a0002c0024t0003g0200 |
2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1110+1835_1110+183 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432870 | |||||||
| chr19:432874 | TAGATGGC others(47): Show |
T | 1 | a0001c0001t0016g0069 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1110+1781_1110+183 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432874 | |||||||
| chr19:432882 | G | A | 8 | a0001c0001t0002g0056 a0001c0001t0003g0049 a0001c0001t0006g0030 others(5): Show |
8 | HG01109.hp2 HG01884.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1110+1827C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432882 | |||||||
| chr19:432882 | G | GCTTCATC others(333): Show |
1 | a0001c0002t0002g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1110+1826_1110+182 others(344): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432882 | |||||||
| chr19:432889 | CGTGA | C | 2 | a0001c0006t0002g0022 a0001c0006t0002g0023 |
2 | HG01943.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1110+1816_1110+181 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432889 | |||||||
| chr19:432898 | G | C | 1 | a0001c0007t0002g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1110+1811C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432898 | |||||||
| chr19:432913 | T | A | 6 | a0001c0002t0002g0045 a0001c0002t0003g0149 a0001c0003t0001g0114 others(3): Show |
6 | HG01071.hp2 HG01884.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+1796A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432913 | |||||||
| chr19:432913 | T | TTAGAGGA others(743): Show |
3 | a0001c0006t0001g0013 a0001c0006t0001g0016 a0001c0006t0006g0010 |
3 | HG03098.hp2 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1110+1795_1110+179 others(754): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432913 | |||||||
| chr19:432924 | C | G | 24 | a0001c0001t0007g0038 a0001c0003t0001g0060 a0001c0003t0001g0064 others(21): Show |
25 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.1110+1785G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432924 | |||||||
| chr19:432924 | CGGGCAGA others(163): Show |
C | 2 | a0001c0013t0005g0006 a0001c0018t0006g0180 |
2 | HG02622.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1110+1615_1110+178 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432924 | |||||||
| chr19:432924 | CGGGCAGA others(395): Show |
C | 2 | a0001c0001t0001g0104 a0001c0001t0001g0131 |
2 | HG00323.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1110+1383_1110+178 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432924 | |||||||
| chr19:432925 | G | A | 1 | a0001c0007t0002g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1110+1784C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432925 | |||||||
| chr19:432928 | C | CAGAT | 63 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0078 others(60): Show |
64 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1110+1777_1110+178 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432928 | |||||||
| chr19:432928 | C | CAGATAGA others(163): Show |
1 | a0003c0008t0005g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1110+1780_1110+178 others(174): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432928 | |||||||
| chr19:432928 | C | CAGATGGC others(51): Show |
1 | a0001c0001t0006g0030 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1110+1780_1110+178 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432928 | |||||||
| chr19:432928 | CAGATGGC others(51): Show |
C | 5 | a0001c0001t0004g0162 a0001c0001t0004g0164 a0001c0001t0011g0034 others(2): Show |
5 | HG01358.hp2 HG01981.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+1723_1110+178 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432928 | |||||||
| chr19:432936 | G | A | 2 | a0005c0009t0005g0047 a0005c0009t0014g0036 |
2 | NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1110+1773C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432936 | |||||||
| chr19:432944 | G | A | 1 | a0001c0002t0003g0149 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1110+1765C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432944 | |||||||
| chr19:432955 | C | A | 28 | a0001c0001t0002g0056 a0001c0001t0003g0049 a0001c0001t0006g0030 others(25): Show |
29 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1110+1754G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432955 | |||||||
| chr19:432955 | C | T | 2 | a0001c0006t0002g0022 a0001c0006t0002g0023 |
2 | HG01943.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1110+1754G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432955 | |||||||
| chr19:432956 | G | A | 1 | a0011c0022t0002g0185 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1110+1753C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432956 | |||||||
| chr19:432967 | A | T | 11 | a0001c0001t0002g0051 a0001c0001t0005g0053 a0001c0003t0001g0063 others(8): Show |
11 | HG00621.hp2 HG01074.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1110+1742T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432967 | |||||||
| chr19:432978 | C | CGGGCAGA others(109): Show |
1 | a0001c0001t0001g0133 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1110+1730_1110+173 others(120): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432978 | |||||||
| chr19:432978 | C | G | 32 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0078 others(29): Show |
32 | HG00423.hp1 HG00621.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.1110+1731G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432978 | |||||||
| chr19:432978 | CGGGCAGA others(341): Show |
C | 1 | a0001c0001t0005g0102 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1110+1383_1110+173 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432978 | |||||||
| chr19:432979 | G | A | 9 | a0001c0001t0001g0168 a0001c0003t0001g0060 a0001c0003t0001g0064 others(6): Show |
10 | HG00544.hp2 HG00621.hp1 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.1110+1730C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432979 | |||||||
| chr19:432979 | GGGCAGAT others(51): Show |
G | 1 | a0001c0005t0015g0007 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1110+1672_1110+172 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432979 | |||||||
| chr19:432982 | CAGAT | C | 2 | a0001c0001t0004g0029 a0002c0004t0001g0206 |
2 | HG03098.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1110+1723_1110+172 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432982 | |||||||
| chr19:432986 | T | TAGATGGC others(105): Show |
1 | a0001c0002t0001g0086 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1110+1722_1110+172 others(116): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432986 | |||||||
| chr19:432986 | T | TAGATGGC others(221): Show |
1 | a0008c0015t0012g0026 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1110+1722_1110+172 others(232): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432986 | |||||||
| chr19:432986 | T | TAGATGGC others(163): Show |
1 | a0001c0003t0001g0063 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1110+1722_1110+172 others(174): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432986 | |||||||
| chr19:432986 | T | TAGATGGC others(43): Show |
1 | a0001c0002t0003g0149 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1110+1722_1110+172 others(54): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432986 | |||||||
| chr19:432986 | T | TAGATGGC others(163): Show |
10 | a0001c0003t0002g0001 a0001c0003t0002g0062 a0001c0003t0002g0065 others(7): Show |
11 | HG02132.hp2 HG03688.hp1 NA18612.hp2 others(8): Show |
intron_variant | MODIFIER | c.1110+1722_1110+172 others(174): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432986 | |||||||
| chr19:432986 | T | TAGATGGC others(453): Show |
1 | a0002c0012t0004g0195 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1110+1722_1110+172 others(464): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432986 | |||||||
| chr19:432986 | T | TAGATGGC others(221): Show |
1 | a0001c0007t0002g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1110+1722_1110+172 others(232): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432986 | |||||||
| chr19:432986 | T | TAGATGGC others(723): Show |
1 | a0001c0002t0001g0088 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1110+1722_1110+172 others(734): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432986 | |||||||
| chr19:432986 | T | TAGATGGC others(163): Show |
2 | a0001c0001t0002g0076 a0001c0001t0013g0072 |
2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1110+1722_1110+172 others(174): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432986 | |||||||
| chr19:432986 | T | TAGATGGC others(782): Show |
1 | a0001c0007t0006g0033 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1110+1722_1110+172 others(793): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 432986 | |||||||
| chr19:433002 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1110+1707C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433002 | |||||||
| chr19:433002 | G | GTGAGTGA others(109): Show |
2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG00609.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.1110+1706_1110+170 others(120): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433002 | |||||||
| chr19:433013 | C | A | 4 | a0001c0001t0002g0056 a0001c0001t0003g0049 a0001c0001t0006g0050 others(1): Show |
4 | HG00621.hp2 HG02970.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1110+1696G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433013 | |||||||
| chr19:433025 | A | T | 29 | a0001c0001t0002g0076 a0001c0001t0003g0032 a0001c0001t0003g0070 others(26): Show |
29 | HG01109.hp2 HG01358.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.1110+1684T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433025 | |||||||
| chr19:433034 | G | A | 2 | a0005c0009t0005g0047 a0005c0009t0014g0036 |
2 | NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1110+1675C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433034 | |||||||
| chr19:433036 | C | G | 37 | a0001c0001t0002g0101 a0001c0002t0001g0004 a0001c0002t0001g0079 others(34): Show |
38 | HG00423.hp2 HG00558.hp2 HG01952.hp2 others(35): Show |
intron_variant | MODIFIER | c.1110+1673G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433036 | |||||||
| chr19:433037 | A | G | 90 | a0001c0001t0002g0035 a0001c0001t0002g0051 a0001c0001t0002g0056 others(87): Show |
91 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.1110+1672T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433037 | |||||||
| chr19:433040 | CAGAT | C | 5 | a0001c0001t0003g0172 a0001c0006t0002g0022 a0001c0006t0002g0023 others(2): Show |
5 | HG01358.hp1 HG01943.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110+1665_1110+166 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433040 | |||||||
| chr19:433044 | T | TAGATGGC others(47): Show |
1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1664_1110+166 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433044 | |||||||
| chr19:433044 | T | TAGATGGC others(217): Show |
1 | a0011c0022t0002g0185 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1110+1664_1110+166 others(228): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433044 | |||||||
| chr19:433044 | T | TAGATGGC others(217): Show |
2 | a0001c0001t0003g0032 a0001c0005t0006g0009 |
2 | HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1110+1664_1110+166 others(228): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433044 | |||||||
| chr19:433044 | T | TAGATGGC others(727): Show |
1 | a0001c0003t0002g0100 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1110+1664_1110+166 others(738): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433044 | |||||||
| chr19:433044 | T | TAGATGGC others(105): Show |
4 | a0001c0001t0002g0056 a0001c0001t0003g0049 a0001c0001t0006g0050 others(1): Show |
4 | HG02622.hp1 HG02970.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1110+1664_1110+166 others(116): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433044 | |||||||
| chr19:433044 | T | TAGATGGC others(669): Show |
12 | a0001c0003t0001g0060 a0001c0003t0001g0064 a0001c0003t0001g0140 others(9): Show |
12 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.1110+1664_1110+166 others(680): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433044 | |||||||
| chr19:433044 | T | TAGATGGC others(271): Show |
1 | a0001c0003t0001g0114 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1110+1664_1110+166 others(282): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433044 | |||||||
| chr19:433044 | T | TAGATGGC others(47): Show |
1 | a0001c0001t0006g0030 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1110+1664_1110+166 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433044 | |||||||
| chr19:433052 | G | A | 8 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(5): Show |
8 | HG01109.hp2 HG02572.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1110+1657C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433052 | |||||||
| chr19:433057 | A | G | 2 | a0001c0002t0001g0079 a0001c0002t0001g0080 |
2 | HG00558.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1110+1652T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433057 | |||||||
| chr19:433071 | C | A | 3 | a0001c0001t0003g0070 a0001c0016t0001g0159 a0011c0022t0002g0185 |
3 | HG01358.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1110+1638G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433071 | |||||||
| chr19:433083 | A | T | 18 | a0001c0001t0002g0101 a0001c0001t0004g0029 a0001c0001t0006g0042 others(15): Show |
18 | HG01071.hp2 HG02015.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.1110+1626T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433083 | |||||||
| chr19:433094 | G | C | 58 | a0001c0001t0002g0051 a0001c0001t0003g0032 a0001c0001t0003g0070 others(55): Show |
59 | HG00423.hp2 HG00558.hp2 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.1110+1615C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433094 | |||||||
| chr19:433095 | G | A | 1 | a0004c0011t0005g0061 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1110+1614C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433095 | |||||||
| chr19:433098 | CAGAT | C | 10 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(7): Show |
10 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.1110+1607_1110+161 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433098 | |||||||
| chr19:433102 | T | TAGATGGC others(47): Show |
2 | a0001c0007t0006g0054 a0002c0024t0003g0200 |
2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1110+1606_1110+160 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433102 | |||||||
| chr19:433102 | T | TGGCGCTT others(214): Show |
1 | a0004c0011t0005g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1110+1606_1110+160 others(225): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433102 | |||||||
| chr19:433102 | T | TGGCGCTT others(97): Show |
1 | a0003c0008t0005g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1110+1606_1110+160 others(108): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433102 | |||||||
| chr19:433110 | G | GCTTCATC others(105): Show |
1 | a0004c0011t0005g0061 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1110+1598_1110+159 others(116): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433110 | |||||||
| chr19:433121 | A | AGTGAGAT others(43): Show |
2 | a0001c0001t0002g0101 a0009c0021t0002g0028 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1110+1587_1110+158 others(54): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433121 | |||||||
| chr19:433129 | C | A | 11 | a0001c0001t0002g0051 a0001c0001t0003g0070 a0001c0001t0006g0042 others(8): Show |
11 | HG01358.hp1 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1110+1580G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433129 | |||||||
| chr19:433141 | A | ATAGAGGA others(51): Show |
2 | a0001c0001t0002g0076 a0001c0001t0013g0072 |
2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1110+1567_1110+156 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433141 | |||||||
| chr19:433141 | A | ATAGAGGA others(47): Show |
31 | a0001c0002t0001g0004 a0001c0002t0001g0079 a0001c0002t0001g0082 others(28): Show |
32 | HG00423.hp2 HG00558.hp2 HG01952.hp2 others(29): Show |
intron_variant | MODIFIER | c.1110+1567_1110+156 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433141 | |||||||
| chr19:433141 | A | T | 11 | a0001c0001t0002g0035 a0001c0001t0003g0172 a0001c0001t0016g0069 others(8): Show |
11 | HG01109.hp2 HG02145.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1110+1568T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433141 | |||||||
| chr19:433152 | C | G | 11 | a0001c0001t0002g0056 a0001c0001t0003g0005 a0001c0001t0003g0049 others(8): Show |
12 | HG01978.hp1 HG02015.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1110+1557G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433152 | |||||||
| chr19:433152 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | NA19005.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1110+1557G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433152 | |||||||
| chr19:433153 | G | A | 4 | a0001c0001t0003g0172 a0001c0007t0006g0054 a0002c0024t0003g0200 others(1): Show |
4 | HG02145.hp1 HG03195.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1110+1556C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433153 | |||||||
| chr19:433153 | G | GGGCAGAT others(449): Show |
1 | a0001c0007t0006g0033 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1110+1555_1110+155 others(460): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433153 | |||||||
| chr19:433156 | CAGAT | C | 13 | a0001c0003t0001g0063 a0001c0003t0002g0001 a0001c0003t0002g0062 others(10): Show |
14 | HG01074.hp2 HG01952.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.1110+1549_1110+155 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433156 | |||||||
| chr19:433160 | T | TGGCGCTT others(43): Show |
1 | a0001c0002t0002g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1110+1548_1110+154 others(54): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433160 | |||||||
| chr19:433160 | T | TGGCGCTT others(159): Show |
1 | a0001c0001t0004g0029 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1110+1548_1110+154 others(170): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433160 | |||||||
| chr19:433162 | G | C | 3 | a0001c0001t0002g0051 a0001c0002t0001g0080 a0001c0002t0001g0154 |
3 | HG02015.hp1 HG02559.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1110+1547C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433162 | |||||||
| chr19:433167 | C | T | 2 | a0001c0002t0001g0088 a0001c0002t0003g0149 |
2 | HG01071.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1110+1542G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433167 | |||||||
| chr19:433168 | G | A | 1 | a0004c0011t0005g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1110+1541C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433168 | |||||||
| chr19:433187 | C | A | 8 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(5): Show |
8 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1110+1522G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433187 | |||||||
| chr19:433187 | C | T | 2 | a0001c0001t0002g0101 a0009c0021t0002g0028 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1110+1522G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433187 | |||||||
| chr19:433188 | G | GTGAGAGT others(217): Show |
2 | a0001c0002t0001g0080 a0001c0002t0001g0154 |
2 | HG02015.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1110+1520_1110+152 others(228): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433188 | |||||||
| chr19:433199 | A | ATAGAGGA others(109): Show |
1 | a0001c0001t0007g0038 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1110+1509_1110+151 others(120): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433199 | |||||||
| chr19:433199 | A | T | 32 | a0001c0001t0002g0051 a0001c0001t0002g0101 a0001c0001t0003g0005 others(29): Show |
33 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.1110+1510T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433199 | |||||||
| chr19:433210 | A | C | 39 | a0001c0001t0002g0035 a0001c0001t0002g0051 a0001c0001t0002g0056 others(36): Show |
40 | HG01071.hp2 HG01109.hp2 HG01358.hp1 others(37): Show |
intron_variant | MODIFIER | c.1110+1499T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433210 | |||||||
| chr19:433210 | A | G | 103 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0002g0076 others(100): Show |
106 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.1110+1499T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433210 | |||||||
| chr19:433211 | G | A | 1 | a0001c0002t0002g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1110+1498C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433211 | |||||||
| chr19:433214 | CAGAT | C | 4 | a0001c0001t0002g0035 a0001c0001t0016g0069 a0002c0004t0001g0190 others(1): Show |
4 | HG03831.hp1 HG04204.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1110+1491_1110+149 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433214 | |||||||
| chr19:433220 | G | C | 1 | a0001c0002t0001g0086 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1110+1489C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433220 | |||||||
| chr19:433226 | G | A | 1 | a0001c0023t0007g0187 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1110+1483C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433226 | |||||||
| chr19:433229 | T | A | 1 | a0001c0001t0002g0051 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1110+1480A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433229 | |||||||
| chr19:433234 | G | A | 27 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0004g0002 others(24): Show |
28 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1110+1475C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433234 | |||||||
| chr19:433245 | C | A | 2 | a0001c0001t0002g0035 a0002c0004t0001g0190 |
2 | HG04204.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1110+1464G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433245 | |||||||
| chr19:433245 | CGTGAGTG others(391): Show |
C | 2 | a0001c0001t0003g0172 a0003c0008t0003g0184 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1110+1066_1110+146 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433245 | |||||||
| chr19:433246 | G | A | 1 | a0001c0002t0002g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1110+1463C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433246 | |||||||
| chr19:433257 | T | A | 19 | a0001c0001t0002g0035 a0001c0001t0004g0029 a0001c0001t0006g0042 others(16): Show |
19 | HG01358.hp1 HG01884.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1110+1452A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433257 | |||||||
| chr19:433268 | C | G | 6 | a0001c0001t0002g0056 a0001c0001t0003g0049 a0001c0001t0003g0070 others(3): Show |
6 | HG02486.hp2 HG02970.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1110+1441G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433268 | |||||||
| chr19:433269 | G | A | 1 | a0002c0004t0001g0206 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1110+1440C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433269 | |||||||
| chr19:433272 | CAGAT | C | 11 | a0001c0001t0002g0051 a0001c0001t0002g0101 a0001c0001t0003g0005 others(8): Show |
12 | HG01978.hp1 HG02015.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1110+1433_1110+143 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433272 | |||||||
| chr19:433276 | T | TAGATGGC others(159): Show |
28 | a0001c0002t0001g0004 a0001c0002t0001g0079 a0001c0002t0001g0092 others(25): Show |
29 | HG00423.hp2 HG00558.hp2 HG01952.hp2 others(26): Show |
intron_variant | MODIFIER | c.1110+1432_1110+143 others(170): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433276 | |||||||
| chr19:433276 | T | TAGATGGC others(159): Show |
1 | a0001c0002t0001g0157 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1110+1432_1110+143 others(170): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433276 | |||||||
| chr19:433276 | T | TGGCGCTT others(43): Show |
1 | a0001c0016t0001g0159 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1110+1432_1110+143 others(54): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433276 | |||||||
| chr19:433278 | G | GATGGCAC others(840): Show |
1 | a0001c0007t0002g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1110+1430_1110+143 others(851): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433278 | |||||||
| chr19:433278 | G | GATGGCGC others(159): Show |
1 | a0004c0011t0005g0061 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1110+1430_1110+143 others(170): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433278 | |||||||
| chr19:433278 | G | GATGGCGC others(217): Show |
1 | a0004c0011t0005g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1110+1430_1110+143 others(228): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433278 | |||||||
| chr19:433284 | G | A | 1 | a0001c0001t0011g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1110+1425C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433284 | |||||||
| chr19:433295 | A | AGTGAGAT others(3909): Show |
1 | a0001c0023t0007g0187 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1110+1413_1110+141 others(3920): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433295 | |||||||
| chr19:433303 | C | A | 4 | a0001c0001t0002g0051 a0001c0001t0002g0101 a0002c0004t0001g0190 others(1): Show |
4 | HG02559.hp1 HG02572.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1110+1406G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433303 | |||||||
| chr19:433303 | CGTGAGTG others(333): Show |
C | 2 | a0001c0007t0003g0039 a0001c0007t0006g0041 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1110+1066_1110+140 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433303 | |||||||
| chr19:433315 | A | T | 13 | a0001c0001t0003g0032 a0001c0001t0006g0042 a0001c0001t0006g0048 others(10): Show |
13 | HG01978.hp2 HG02055.hp2 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.1110+1394T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433315 | |||||||
| chr19:433326 | G | C | 65 | a0001c0001t0002g0035 a0001c0001t0002g0051 a0001c0001t0002g0056 others(62): Show |
67 | HG00423.hp2 HG00558.hp2 HG01109.hp2 others(64): Show |
intron_variant | MODIFIER | c.1110+1383C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433326 | |||||||
| chr19:433336 | G | C | 1 | a0001c0001t0002g0051 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1110+1373C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433336 | |||||||
| chr19:433342 | G | A | 5 | a0001c0001t0003g0032 a0001c0001t0016g0069 a0001c0002t0001g0088 others(2): Show |
5 | HG01071.hp2 HG02055.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110+1367C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433342 | |||||||
| chr19:433372 | G | C | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1337C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433372 | |||||||
| chr19:433373 | T | A | 40 | a0001c0001t0001g0104 a0001c0001t0001g0131 a0001c0001t0002g0076 others(37): Show |
41 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.1110+1336A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433373 | |||||||
| chr19:433373 | T | TTAGAGGA others(51): Show |
3 | a0001c0001t0002g0056 a0001c0001t0003g0049 a0001c0001t0006g0050 |
3 | HG02970.hp1 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1110+1335_1110+133 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433373 | |||||||
| chr19:433373 | TTAGAGGA others(217): Show |
T | 1 | a0002c0004t0001g0190 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1110+1112_1110+133 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433373 | |||||||
| chr19:433374 | T | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1335A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433374 | |||||||
| chr19:433375 | A | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1334T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433375 | |||||||
| chr19:433378 | G | GTCTGTGA others(499): Show |
1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1330_1110+133 others(510): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433378 | |||||||
| chr19:433382 | G | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1327C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433382 | |||||||
| chr19:433383 | C | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1326G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433383 | |||||||
| chr19:433384 | C | G | 9 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(6): Show |
9 | HG01978.hp2 HG02083.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1110+1325G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433384 | |||||||
| chr19:433386 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1323C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433386 | |||||||
| chr19:433388 | CAGAT | C | 3 | a0001c0001t0004g0029 a0001c0001t0016g0069 a0001c0016t0001g0159 |
3 | HG01358.hp1 HG03098.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1110+1317_1110+132 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433388 | |||||||
| chr19:433391 | A | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1318T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433391 | |||||||
| chr19:433392 | T | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1317A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433392 | |||||||
| chr19:433397 | G | C | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1312C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433397 | |||||||
| chr19:433398 | G | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1311C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433398 | |||||||
| chr19:433399 | C | A | 26 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0004g0002 others(23): Show |
27 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.1110+1310G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433399 | |||||||
| chr19:433400 | G | A | 10 | a0001c0001t0002g0035 a0001c0001t0002g0051 a0001c0001t0003g0005 others(7): Show |
11 | HG01891.hp2 HG01978.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1110+1309C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433400 | |||||||
| chr19:433401 | C | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1308G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433401 | |||||||
| chr19:433402 | T | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1307A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433402 | |||||||
| chr19:433404 | C | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1305G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433404 | |||||||
| chr19:433407 | CGTGA | C | 13 | a0001c0003t0001g0063 a0001c0003t0002g0001 a0001c0003t0002g0062 others(10): Show |
14 | HG01074.hp2 HG01952.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.1110+1298_1110+130 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433407 | |||||||
| chr19:433419 | C | A | 1 | a0001c0001t0016g0069 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1110+1290G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433419 | |||||||
| chr19:433427 | A | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1282T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433427 | |||||||
| chr19:433431 | T | A | 12 | a0001c0001t0002g0051 a0001c0001t0006g0030 a0001c0001t0006g0042 others(9): Show |
12 | HG01358.hp1 HG01978.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1110+1278A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433431 | |||||||
| chr19:433432 | T | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1277A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433432 | |||||||
| chr19:433436 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1273C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433436 | |||||||
| chr19:433440 | G | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1269C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433440 | |||||||
| chr19:433442 | C | G | 6 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+1267G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433442 | |||||||
| chr19:433442 | C | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1267G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433442 | |||||||
| chr19:433444 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1265C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433444 | |||||||
| chr19:433446 | C | CAGAT | 11 | a0001c0001t0002g0101 a0001c0001t0004g0029 a0001c0001t0006g0042 others(8): Show |
11 | HG02572.hp1 HG02572.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1110+1259_1110+126 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433446 | |||||||
| chr19:433446 | C | CAGATAGA others(557): Show |
1 | a0001c0002t0001g0082 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1110+1262_1110+126 others(568): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433446 | |||||||
| chr19:433446 | C | CAGATAGA others(1693): Show |
1 | a0001c0002t0003g0084 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1110+1262_1110+126 others(1704): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433446 | |||||||
| chr19:433446 | C | CAGATAGA others(677): Show |
2 | a0001c0001t0003g0032 a0001c0005t0006g0009 |
2 | HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1110+1262_1110+126 others(688): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433446 | |||||||
| chr19:433446 | C | CAGATAGA others(113): Show |
1 | a0003c0008t0005g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1110+1262_1110+126 others(124): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433446 | |||||||
| chr19:433446 | C | CAGATAGA others(55): Show |
2 | a0001c0001t0002g0076 a0001c0001t0013g0072 |
2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1110+1262_1110+126 others(66): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433446 | |||||||
| chr19:433446 | C | CAGATAGA others(109): Show |
1 | a0001c0001t0006g0030 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1110+1262_1110+126 others(120): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433446 | |||||||
| chr19:433446 | C | CAGATGGC others(561): Show |
1 | a0001c0002t0001g0086 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1110+1262_1110+126 others(572): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433446 | |||||||
| chr19:433446 | C | CAGATGGC others(47): Show |
1 | a0001c0001t0007g0038 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1110+1262_1110+126 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433446 | |||||||
| chr19:433448 | G | GATAGATG others(3271): Show |
1 | a0001c0002t0002g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1110+1260_1110+126 others(3282): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433448 | |||||||
| chr19:433450 | TGGCGCTT others(101): Show |
T | 2 | a0001c0001t0002g0051 a0001c0001t0016g0069 |
2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1110+1151_1110+125 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433450 | |||||||
| chr19:433451 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1258C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433451 | |||||||
| chr19:433453 | C | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1256G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433453 | |||||||
| chr19:433454 | G | A | 5 | a0001c0001t0003g0032 a0001c0001t0004g0029 a0001c0002t0001g0082 others(2): Show |
5 | HG01978.hp2 HG02055.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+1255C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433454 | |||||||
| chr19:433455 | C | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1254G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433455 | |||||||
| chr19:433456 | T | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1253A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433456 | |||||||
| chr19:433458 | C | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1251G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433458 | |||||||
| chr19:433462 | G | A | 1 | a0002c0004t0001g0206 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1110+1247C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433462 | |||||||
| chr19:433473 | C | A | 8 | a0001c0001t0001g0104 a0001c0001t0001g0131 a0001c0001t0002g0035 others(5): Show |
9 | HG00323.hp1 HG01891.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.1110+1236G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433473 | |||||||
| chr19:433473 | C | T | 14 | a0001c0001t0007g0038 a0001c0003t0001g0063 a0001c0003t0002g0001 others(11): Show |
15 | HG01074.hp2 HG01952.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.1110+1236G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433473 | |||||||
| chr19:433473 | CGTGAGTG others(163): Show |
C | 1 | a0001c0001t0005g0053 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1110+1066_1110+123 others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433473 | |||||||
| chr19:433474 | G | A | 4 | a0001c0001t0003g0070 a0005c0009t0005g0047 a0005c0009t0014g0036 others(1): Show |
4 | NA18522.hp2 NA19240.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1110+1235C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433474 | |||||||
| chr19:433483 | A | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1226T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433483 | |||||||
| chr19:433485 | A | T | 11 | a0001c0001t0002g0101 a0001c0001t0006g0030 a0001c0001t0007g0038 others(8): Show |
11 | HG01978.hp2 HG02083.hp2 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.1110+1224T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433485 | |||||||
| chr19:433485 | ATAGAGGA others(221): Show |
A | 26 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0004g0002 others(23): Show |
27 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.1110+996_1110+1223 others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433485 | |||||||
| chr19:433486 | T | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1223A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433486 | |||||||
| chr19:433488 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1221C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433488 | |||||||
| chr19:433489 | A | C | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1220T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433489 | |||||||
| chr19:433494 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1215C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433494 | |||||||
| chr19:433496 | C | G | 3 | a0001c0001t0002g0101 a0001c0006t0001g0017 a0009c0021t0002g0028 |
3 | HG02572.hp2 HG02922.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1110+1213G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433496 | |||||||
| chr19:433496 | C | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1213G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433496 | |||||||
| chr19:433498 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1211C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433498 | |||||||
| chr19:433503 | A | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1206T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433503 | |||||||
| chr19:433504 | T | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1205A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433504 | |||||||
| chr19:433504 | TAGATGGC others(47): Show |
T | 6 | a0001c0001t0002g0035 a0001c0001t0003g0005 a0001c0001t0003g0181 others(3): Show |
7 | HG01891.hp2 HG01978.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1110+1151_1110+120 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433504 | |||||||
| chr19:433512 | G | A | 3 | a0001c0001t0006g0030 a0001c0002t0001g0086 a0001c0002t0003g0084 |
3 | HG02083.hp2 HG02135.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1110+1197C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433512 | |||||||
| chr19:433512 | G | GCTTCATC others(1017): Show |
1 | a0001c0002t0001g0088 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1110+1196_1110+119 others(1028): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433512 | |||||||
| chr19:433512 | G | GCTTCATC others(51): Show |
22 | a0001c0001t0002g0056 a0001c0001t0003g0049 a0001c0001t0006g0050 others(19): Show |
22 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.1110+1196_1110+119 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433512 | |||||||
| chr19:433512 | G | GCTTCATC others(279): Show |
1 | a0001c0002t0003g0160 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1110+1196_1110+119 others(290): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433512 | |||||||
| chr19:433512 | G | GCTTCATC others(7223): Show |
1 | a0001c0002t0003g0175 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1110+1196_1110+119 others(7234): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433512 | |||||||
| chr19:433519 | C | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1190G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433519 | |||||||
| chr19:433531 | C | A | 1 | a0001c0005t0015g0007 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1110+1178G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433531 | |||||||
| chr19:433542 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1167C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433542 | |||||||
| chr19:433543 | T | A | 11 | a0001c0001t0002g0101 a0001c0001t0006g0042 a0001c0001t0006g0048 others(8): Show |
11 | HG01071.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1110+1166A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433543 | |||||||
| chr19:433543 | T | C | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1166A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433543 | |||||||
| chr19:433544 | T | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1165A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433544 | |||||||
| chr19:433545 | A | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1164T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433545 | |||||||
| chr19:433549 | G | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1160C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433549 | |||||||
| chr19:433550 | A | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1159T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433550 | |||||||
| chr19:433551 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1158C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433551 | |||||||
| chr19:433553 | C | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1156G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433553 | |||||||
| chr19:433554 | C | G | 4 | a0001c0001t0003g0070 a0001c0002t0003g0149 a0001c0016t0001g0159 others(1): Show |
4 | HG01071.hp2 HG01358.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1110+1155G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433554 | |||||||
| chr19:433555 | G | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1154C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433555 | |||||||
| chr19:433557 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1152C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433557 | |||||||
| chr19:433558 | C | CAGAT | 18 | a0001c0001t0002g0101 a0001c0001t0003g0032 a0001c0001t0004g0029 others(15): Show |
18 | HG01071.hp2 HG01358.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1110+1147_1110+115 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433558 | |||||||
| chr19:433558 | C | CAGATAGA others(337): Show |
1 | a0005c0009t0014g0036 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1110+1150_1110+115 others(348): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433558 | |||||||
| chr19:433558 | C | CAGATAGA others(1419): Show |
2 | a0001c0001t0002g0076 a0001c0001t0013g0072 |
2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1110+1150_1110+115 others(1430): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433558 | |||||||
| chr19:433558 | C | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1151G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433558 | |||||||
| chr19:433560 | G | GATAGATG others(1014): Show |
3 | a0001c0007t0006g0033 a0001c0007t0006g0054 a0002c0024t0003g0200 |
3 | HG02451.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1110+1148_1110+114 others(1025): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433560 | |||||||
| chr19:433560 | G | GATAGATG others(279): Show |
1 | a0001c0023t0007g0187 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1110+1148_1110+114 others(290): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433560 | |||||||
| chr19:433563 | G | C | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1146C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433563 | |||||||
| chr19:433565 | C | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1144G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433565 | |||||||
| chr19:433566 | G | A | 3 | a0001c0006t0001g0013 a0001c0006t0001g0016 a0001c0006t0006g0010 |
3 | HG03098.hp2 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1110+1143C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433566 | |||||||
| chr19:433567 | C | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1142G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433567 | |||||||
| chr19:433568 | T | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1141A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433568 | |||||||
| chr19:433573 | C | T | 2 | a0001c0001t0003g0070 a0001c0002t0001g0093 |
2 | NA18940.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1110+1136G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433573 | |||||||
| chr19:433574 | G | A | 3 | a0001c0006t0001g0013 a0001c0006t0001g0016 a0001c0006t0006g0010 |
3 | HG03098.hp2 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1110+1135C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433574 | |||||||
| chr19:433585 | A | C | 70 | a0001c0001t0002g0051 a0001c0001t0002g0076 a0001c0001t0002g0101 others(67): Show |
72 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(69): Show |
intron_variant | MODIFIER | c.1110+1124T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433585 | |||||||
| chr19:433586 | G | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1123C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433586 | |||||||
| chr19:433595 | A | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1114T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433595 | |||||||
| chr19:433597 | A | ATAGAGGA others(51): Show |
3 | a0001c0007t0002g0077 a0004c0011t0005g0057 a0004c0011t0005g0061 |
3 | HG01109.hp2 HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1110+1111_1110+111 others(62): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433597 | |||||||
| chr19:433597 | A | T | 39 | a0001c0002t0001g0004 a0001c0002t0001g0079 a0001c0002t0001g0080 others(36): Show |
40 | HG00423.hp2 HG00558.hp2 HG01358.hp1 others(37): Show |
intron_variant | MODIFIER | c.1110+1112T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433597 | |||||||
| chr19:433598 | T | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1111A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433598 | |||||||
| chr19:433600 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1109C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433600 | |||||||
| chr19:433601 | A | C | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1108T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433601 | |||||||
| chr19:433606 | G | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1103C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433606 | |||||||
| chr19:433607 | C | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1102G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433607 | |||||||
| chr19:433608 | C | G | 14 | a0001c0003t0001g0063 a0001c0003t0002g0001 a0001c0003t0002g0062 others(11): Show |
15 | HG01074.hp2 HG01358.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.1110+1101G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433608 | |||||||
| chr19:433608 | C | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1101G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433608 | |||||||
| chr19:433610 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1099C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433610 | |||||||
| chr19:433612 | CAGAT | C | 3 | a0001c0006t0001g0013 a0001c0006t0001g0016 a0001c0006t0006g0010 |
3 | HG03098.hp2 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1110+1093_1110+109 others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433612 | |||||||
| chr19:433615 | A | T | 2 | a0001c0001t0003g0070 a0001c0003t0004g0111 |
2 | NA19066.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1110+1094T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433615 | |||||||
| chr19:433616 | T | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1093A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433616 | |||||||
| chr19:433616 | T | TGGCGCTT others(159): Show |
1 | a0001c0006t0001g0017 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1110+1092_1110+109 others(170): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433616 | |||||||
| chr19:433618 | G | C | 1 | a0001c0002t0002g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1110+1091C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433618 | |||||||
| chr19:433623 | C | A | 1 | a0002c0004t0001g0206 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1110+1086G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433623 | |||||||
| chr19:433624 | G | A | 3 | a0001c0001t0003g0032 a0001c0001t0004g0029 a0001c0005t0006g0009 |
3 | HG02055.hp2 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1110+1085C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433624 | |||||||
| chr19:433625 | C | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1084G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433625 | |||||||
| chr19:433626 | T | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1083A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433626 | |||||||
| chr19:433627 | T | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1082A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433627 | |||||||
| chr19:433628 | C | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1081G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433628 | |||||||
| chr19:433631 | C | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1078G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433631 | |||||||
| chr19:433632 | G | A | 1 | a0001c0007t0006g0033 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1110+1077C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433632 | |||||||
| chr19:433643 | A | C | 112 | a0001c0001t0001g0043 a0001c0001t0001g0078 a0001c0001t0001g0090 others(109): Show |
115 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.1110+1066T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433643 | |||||||
| chr19:433643 | A | T | 1 | a0002c0004t0001g0190 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1110+1066T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433643 | |||||||
| chr19:433651 | A | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1058T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433651 | |||||||
| chr19:433655 | A | ATAGAGGA others(47): Show |
1 | a0001c0002t0003g0149 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1110+1053_1110+105 others(58): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433655 | |||||||
| chr19:433655 | A | T | 37 | a0001c0001t0002g0051 a0001c0001t0002g0076 a0001c0001t0003g0032 others(34): Show |
37 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1110+1054T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433655 | |||||||
| chr19:433660 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1049C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433660 | |||||||
| chr19:433664 | G | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1045C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433664 | |||||||
| chr19:433666 | C | G | 2 | a0001c0001t0002g0035 a0001c0002t0001g0082 |
2 | HG01978.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1110+1043G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433666 | |||||||
| chr19:433668 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1041C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433668 | |||||||
| chr19:433676 | G | C | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1033C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433676 | |||||||
| chr19:433680 | G | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1029C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433680 | |||||||
| chr19:433681 | C | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1028G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433681 | |||||||
| chr19:433682 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1027C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433682 | |||||||
| chr19:433684 | T | TGTGAGTG others(3): Show |
1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1024_1110+102 others(14): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433684 | |||||||
| chr19:433689 | C | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+1020G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433689 | |||||||
| chr19:433701 | C | T | 1 | a0002c0004t0001g0190 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1110+1008G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433701 | |||||||
| chr19:433702 | G | A | 2 | a0001c0003t0004g0110 a0001c0003t0004g0111 |
2 | NA18612.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1110+1007C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433702 | |||||||
| chr19:433713 | T | A | 43 | a0001c0001t0002g0056 a0001c0001t0002g0101 a0001c0001t0003g0049 others(40): Show |
44 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.1110+996A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433713 | |||||||
| chr19:433714 | T | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+995A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433714 | |||||||
| chr19:433718 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+991C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433718 | |||||||
| chr19:433719 | G | C | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+990C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433719 | |||||||
| chr19:433721 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+988C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433721 | |||||||
| chr19:433724 | C | CGGGCAGA others(47): Show |
1 | a0005c0009t0005g0047 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1110+984_1110+985i others(56): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433724 | |||||||
| chr19:433724 | C | G | 14 | a0001c0002t0003g0149 a0001c0003t0001g0063 a0001c0003t0002g0001 others(11): Show |
15 | HG01071.hp2 HG01074.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.1110+985G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433724 | |||||||
| chr19:433728 | CAGAT | C | 6 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+977_1110+980d others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433728 | |||||||
| chr19:433731 | A | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+978T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433731 | |||||||
| chr19:433732 | T | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+977A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433732 | |||||||
| chr19:433732 | T | TAGATGGC others(43): Show |
2 | a0001c0001t0002g0101 a0009c0021t0002g0028 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1110+976_1110+977i others(52): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433732 | |||||||
| chr19:433734 | G | GATGGCGC others(1187): Show |
1 | a0001c0002t0001g0082 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1110+974_1110+975i others(1196): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433734 | |||||||
| chr19:433737 | G | C | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+972C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433737 | |||||||
| chr19:433739 | C | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+970G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433739 | |||||||
| chr19:433740 | G | A | 1 | a0001c0001t0005g0053 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1110+969C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433740 | |||||||
| chr19:433741 | C | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+968G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433741 | |||||||
| chr19:433742 | T | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+967A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433742 | |||||||
| chr19:433744 | C | CTGTGAGA others(47): Show |
1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+964_1110+965i others(56): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433744 | |||||||
| chr19:433759 | C | A | 6 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+950G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433759 | |||||||
| chr19:433759 | C | CGTGAGTG others(221): Show |
1 | a0003c0008t0005g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1110+949_1110+950i others(230): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433759 | |||||||
| chr19:433771 | T | A | 11 | a0001c0001t0002g0101 a0001c0001t0006g0042 a0001c0001t0006g0048 others(8): Show |
11 | HG01978.hp2 HG02559.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1110+938A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433771 | |||||||
| chr19:433771 | T | TTAGAGGA others(337): Show |
27 | a0001c0002t0001g0004 a0001c0002t0001g0079 a0001c0002t0001g0080 others(24): Show |
28 | HG00558.hp2 HG01952.hp2 HG01993.hp2 others(25): Show |
intron_variant | MODIFIER | c.1110+937_1110+938i others(346): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433771 | |||||||
| chr19:433771 | T | TTAGAGGA others(2841): Show |
1 | a0001c0002t0001g0155 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1110+937_1110+938i others(2850): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433771 | |||||||
| chr19:433771 | T | TTAGAGGA others(337): Show |
1 | a0001c0002t0003g0148 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1110+937_1110+938i others(346): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433771 | |||||||
| chr19:433771 | T | TTAGAGGA others(333): Show |
1 | a0001c0001t0007g0038 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1110+937_1110+938i others(342): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433771 | |||||||
| chr19:433772 | T | C | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+937A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433772 | |||||||
| chr19:433773 | A | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+936T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433773 | |||||||
| chr19:433775 | A | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+934T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433775 | |||||||
| chr19:433777 | G | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+932C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433777 | |||||||
| chr19:433779 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+930C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433779 | |||||||
| chr19:433782 | C | G | 34 | a0001c0001t0002g0035 a0001c0001t0002g0051 a0001c0001t0003g0005 others(31): Show |
35 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.1110+927G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433782 | |||||||
| chr19:433783 | G | A | 1 | a0001c0001t0007g0038 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1110+926C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433783 | |||||||
| chr19:433792 | G | A | 3 | a0001c0002t0003g0084 a0001c0002t0003g0160 a0001c0002t0003g0175 |
3 | HG02083.hp2 HG04228.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.1110+917C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433792 | |||||||
| chr19:433792 | G | AATGGCGC others(51): Show |
2 | a0001c0002t0001g0086 a0001c0002t0001g0088 |
2 | HG02135.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1110+917_1110+918i others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433792 | |||||||
| chr19:433792 | G | C | 7 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(4): Show |
7 | HG02559.hp2 HG02572.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1110+917C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433792 | |||||||
| chr19:433794 | T | C | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+915A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433794 | |||||||
| chr19:433798 | G | A | 27 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0004g0002 others(24): Show |
28 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1110+911C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433798 | |||||||
| chr19:433800 | T | C | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+909A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433800 | |||||||
| chr19:433801 | T | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+908A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433801 | |||||||
| chr19:433801 | T | C | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+908A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433801 | |||||||
| chr19:433802 | C | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+907G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433802 | |||||||
| chr19:433802 | C | CATTGTGA others(541): Show |
5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+906_1110+907i others(550): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433802 | |||||||
| chr19:433806 | G | A | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+903C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433806 | |||||||
| chr19:433810 | G | T | 1 | a0001c0001t0001g0134 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1110+899C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433810 | |||||||
| chr19:433817 | C | A | 1 | a0001c0001t0005g0053 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1110+892G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433817 | |||||||
| chr19:433825 | A | AGTCTGT | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+883_1110+884i others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433825 | |||||||
| chr19:433828 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+881C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433828 | |||||||
| chr19:433829 | T | A | 69 | a0001c0001t0001g0113 a0001c0001t0002g0035 a0001c0001t0002g0051 others(66): Show |
72 | HG00423.hp2 HG00558.hp2 HG01074.hp2 others(69): Show |
intron_variant | MODIFIER | c.1110+880A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433829 | |||||||
| chr19:433829 | T | C | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+880A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433829 | |||||||
| chr19:433829 | T | TTAGAGGA others(387): Show |
1 | a0005c0009t0014g0036 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1110+879_1110+880i others(396): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433829 | |||||||
| chr19:433830 | T | G | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+879A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433830 | |||||||
| chr19:433831 | A | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+878T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433831 | |||||||
| chr19:433833 | A | ATC | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+875_1110+876i others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433833 | |||||||
| chr19:433835 | G | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+874C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433835 | |||||||
| chr19:433837 | G | A | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+872C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433837 | |||||||
| chr19:433838 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+871C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433838 | |||||||
| chr19:433839 | C | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+870G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433839 | |||||||
| chr19:433840 | G | C | 73 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0002g0051 others(70): Show |
75 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.1110+869C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433840 | |||||||
| chr19:433840 | G | GGGGCAGA others(51): Show |
2 | a0001c0002t0002g0045 a0005c0009t0014g0036 |
2 | NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1110+868_1110+869i others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433840 | |||||||
| chr19:433841 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+868C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433841 | |||||||
| chr19:433842 | G | A | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+867C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433842 | |||||||
| chr19:433843 | G | A | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+866C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433843 | |||||||
| chr19:433843 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+866C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433843 | |||||||
| chr19:433844 | C | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+865G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433844 | |||||||
| chr19:433844 | C | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+865G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433844 | |||||||
| chr19:433844 | CAGAT | C | 28 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0004g0002 others(25): Show |
29 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.1110+861_1110+864d others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433844 | |||||||
| chr19:433847 | A | T | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+862T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433847 | |||||||
| chr19:433848 | T | G | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+861A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433848 | |||||||
| chr19:433848 | T | TAGATGGC others(2559): Show |
1 | a0001c0003t0002g0075 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1110+860_1110+861i others(2568): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433848 | |||||||
| chr19:433848 | T | TAGATGGC others(163): Show |
17 | a0001c0003t0001g0060 a0001c0003t0001g0064 a0001c0003t0001g0114 others(14): Show |
17 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.1110+860_1110+861i others(172): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433848 | |||||||
| chr19:433848 | T | TAGATGGC others(735): Show |
1 | a0001c0003t0002g0071 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1110+860_1110+861i others(744): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433848 | |||||||
| chr19:433848 | T | TAGATGGC others(735): Show |
11 | a0001c0003t0001g0063 a0001c0003t0002g0001 a0001c0003t0002g0062 others(8): Show |
12 | HG01074.hp2 HG01952.hp1 HG03017.hp1 others(9): Show |
intron_variant | MODIFIER | c.1110+860_1110+861i others(744): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433848 | |||||||
| chr19:433848 | T | TAGATGGC others(221): Show |
3 | a0001c0006t0001g0013 a0001c0006t0001g0016 a0001c0006t0001g0017 |
3 | HG03209.hp2 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1110+860_1110+861i others(230): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433848 | |||||||
| chr19:433853 | G | C | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+856C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433853 | |||||||
| chr19:433855 | C | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+854G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433855 | |||||||
| chr19:433856 | G | A | 2 | a0001c0001t0003g0070 a0001c0002t0003g0149 |
2 | HG01071.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1110+853C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433856 | |||||||
| chr19:433857 | C | A | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+852G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433857 | |||||||
| chr19:433857 | C | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+852G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433857 | |||||||
| chr19:433858 | T | G | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+851A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433858 | |||||||
| chr19:433859 | T | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+850A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433859 | |||||||
| chr19:433860 | C | CTGTGAG | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+848_1110+849i others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433860 | |||||||
| chr19:433860 | C | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+849G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433860 | |||||||
| chr19:433864 | G | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+845C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433864 | |||||||
| chr19:433872 | G | A | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+837C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433872 | |||||||
| chr19:433875 | C | A | 28 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0004g0002 others(25): Show |
29 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.1110+834G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433875 | |||||||
| chr19:433876 | G | A | 1 | a0001c0002t0003g0149 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1110+833C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433876 | |||||||
| chr19:433881 | T | TTATATC | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+827_1110+828i others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433881 | |||||||
| chr19:433883 | A | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+826T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433883 | |||||||
| chr19:433885 | A | AGATAGAG others(51): Show |
1 | a0001c0023t0007g0187 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1110+823_1110+824i others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433885 | |||||||
| chr19:433886 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+823C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433886 | |||||||
| chr19:433887 | A | C | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+822T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433887 | |||||||
| chr19:433887 | A | T | 6 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(3): Show |
6 | HG02559.hp2 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1110+822T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433887 | |||||||
| chr19:433888 | T | G | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+821A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433888 | |||||||
| chr19:433889 | A | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+820T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433889 | |||||||
| chr19:433891 | A | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+818T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433891 | |||||||
| chr19:433893 | G | A | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+816C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433893 | |||||||
| chr19:433893 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+816C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433893 | |||||||
| chr19:433894 | A | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+815T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433894 | |||||||
| chr19:433895 | G | A | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+814C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433895 | |||||||
| chr19:433896 | G | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+813C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433896 | |||||||
| chr19:433897 | C | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+812G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433897 | |||||||
| chr19:433898 | G | C | 128 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0113 others(125): Show |
132 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1110+811C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433898 | |||||||
| chr19:433898 | G | GGGGCAGA others(51): Show |
5 | a0001c0001t0002g0056 a0001c0001t0003g0049 a0001c0001t0006g0030 others(2): Show |
5 | HG02486.hp2 HG02622.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110+753_1110+810d others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433898 | |||||||
| chr19:433898 | G | GGGGCAGA others(109): Show |
1 | a0003c0008t0005g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1110+695_1110+810d others(118): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433898 | |||||||
| chr19:433899 | G | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+810C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433899 | |||||||
| chr19:433899 | G | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+810C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433899 | |||||||
| chr19:433901 | G | A | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+808C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433901 | |||||||
| chr19:433901 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+808C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433901 | |||||||
| chr19:433902 | C | G | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+807G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433902 | |||||||
| chr19:433903 | A | T | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+806T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433903 | |||||||
| chr19:433905 | A | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+804T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433905 | |||||||
| chr19:433906 | T | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+803A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433906 | |||||||
| chr19:433908 | G | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+801C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433908 | |||||||
| chr19:433909 | A | C | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+800T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433909 | |||||||
| chr19:433909 | A | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+800T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433909 | |||||||
| chr19:433910 | T | A | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+799A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433910 | |||||||
| chr19:433910 | T | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+799A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433910 | |||||||
| chr19:433911 | G | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+798C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433911 | |||||||
| chr19:433911 | G | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+798C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433911 | |||||||
| chr19:433913 | C | A | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+796G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433913 | |||||||
| chr19:433913 | C | T | 1 | a0001c0002t0001g0157 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1110+796G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433913 | |||||||
| chr19:433914 | G | C | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+795C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433914 | |||||||
| chr19:433915 | C | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+794G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433915 | |||||||
| chr19:433916 | T | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+793A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433916 | |||||||
| chr19:433916 | T | G | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+793A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433916 | |||||||
| chr19:433917 | T | A | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+792A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433917 | |||||||
| chr19:433918 | C | G | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+791G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433918 | |||||||
| chr19:433922 | G | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+787C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433922 | |||||||
| chr19:433924 | G | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+785C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433924 | |||||||
| chr19:433926 | G | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+783C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433926 | |||||||
| chr19:433933 | C | A | 30 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0004g0002 others(27): Show |
31 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.1110+776G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433933 | |||||||
| chr19:433933 | C | CGTGAGTG others(51): Show |
1 | a0001c0002t0003g0160 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1110+775_1110+776i others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433933 | |||||||
| chr19:433934 | G | A | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+775C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433934 | |||||||
| chr19:433940 | G | C | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+769C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433940 | |||||||
| chr19:433943 | A | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+766T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433943 | |||||||
| chr19:433944 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+765C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433944 | |||||||
| chr19:433945 | A | AGATCATG others(417): Show |
5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+763_1110+764i others(426): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433945 | |||||||
| chr19:433945 | A | ATAGAGGA others(51): Show |
2 | a0001c0001t0002g0101 a0009c0021t0002g0028 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1110+763_1110+764i others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433945 | |||||||
| chr19:433945 | A | C | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+764T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433945 | |||||||
| chr19:433945 | A | T | 1 | a0001c0002t0003g0149 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1110+764T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433945 | |||||||
| chr19:433946 | T | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+763A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433946 | |||||||
| chr19:433947 | A | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+762T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433947 | |||||||
| chr19:433948 | G | A | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+761C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433948 | |||||||
| chr19:433950 | G | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+759C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433950 | |||||||
| chr19:433954 | G | A | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+755C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433954 | |||||||
| chr19:433954 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+755C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433954 | |||||||
| chr19:433955 | C | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+754G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433955 | |||||||
| chr19:433956 | C | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+753G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433956 | |||||||
| chr19:433958 | G | T | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+751C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433958 | |||||||
| chr19:433959 | GC | G | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+749delG | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433959 | |||||||
| chr19:433963 | A | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+746T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433963 | |||||||
| chr19:433964 | T | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+745A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433964 | |||||||
| chr19:433965 | A | C | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+744T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433965 | |||||||
| chr19:433967 | A | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+742T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433967 | |||||||
| chr19:433968 | T | G | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+741A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433968 | |||||||
| chr19:433969 | G | A | 6 | a0001c0001t0005g0053 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+740C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433969 | |||||||
| chr19:433970 | G | C | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+739C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433970 | |||||||
| chr19:433971 | C | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+738G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433971 | |||||||
| chr19:433972 | G | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+737C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433972 | |||||||
| chr19:433973 | C | A | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+736G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433973 | |||||||
| chr19:433973 | C | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+736G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433973 | |||||||
| chr19:433974 | T | G | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+735A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433974 | |||||||
| chr19:433975 | T | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+734A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433975 | |||||||
| chr19:433976 | C | CT | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+732_1110+733i others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433976 | |||||||
| chr19:433976 | C | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+733G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433976 | |||||||
| chr19:433978 | T | TG | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+730_1110+731i others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433978 | |||||||
| chr19:433979 | C | A | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+730G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433979 | |||||||
| chr19:433980 | G | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+729C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433980 | |||||||
| chr19:433982 | G | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+727C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433982 | |||||||
| chr19:433984 | G | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+725C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433984 | |||||||
| chr19:433991 | C | CGTGAGTG others(445): Show |
1 | a0005c0009t0005g0047 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1110+717_1110+718i others(454): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433991 | |||||||
| chr19:433992 | G | A | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+717C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433992 | |||||||
| chr19:433997 | T | G | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+712A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 433997 | |||||||
| chr19:434001 | A | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+708T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434001 | |||||||
| chr19:434003 | A | T | 1 | a0001c0001t0007g0038 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1110+706T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434003 | |||||||
| chr19:434004 | T | G | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+705A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434004 | |||||||
| chr19:434005 | A | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+704T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434005 | |||||||
| chr19:434006 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+703C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434006 | |||||||
| chr19:434007 | A | C | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+702T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434007 | |||||||
| chr19:434010 | A | G | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+699T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434010 | |||||||
| chr19:434011 | G | A | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+698C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434011 | |||||||
| chr19:434012 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+697C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434012 | |||||||
| chr19:434013 | C | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+696G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434013 | |||||||
| chr19:434013 | C | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+696G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434013 | |||||||
| chr19:434014 | C | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+695G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434014 | |||||||
| chr19:434014 | C | CGGGCAGA others(51): Show |
5 | a0001c0007t0002g0077 a0001c0007t0006g0054 a0002c0024t0003g0200 others(2): Show |
5 | HG01109.hp2 HG03225.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110+694_1110+695i others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434014 | |||||||
| chr19:434014 | C | G | 1 | a0001c0023t0007g0187 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1110+695G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434014 | |||||||
| chr19:434015 | G | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+694C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434015 | |||||||
| chr19:434016 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+693C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434016 | |||||||
| chr19:434017 | G | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+692C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434017 | |||||||
| chr19:434018 | C | G | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+691G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434018 | |||||||
| chr19:434020 | G | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+689C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434020 | |||||||
| chr19:434020 | G | GATAGATG others(51): Show |
1 | a0001c0002t0003g0084 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1110+688_1110+689i others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434020 | |||||||
| chr19:434023 | A | C | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+686T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434023 | |||||||
| chr19:434024 | GA | G | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+684delT | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434024 | |||||||
| chr19:434027 | G | GAGTCTGT others(48): Show |
5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+681_1110+682i others(57): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434027 | |||||||
| chr19:434027 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+682C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434027 | |||||||
| chr19:434029 | C | A | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+680G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434029 | |||||||
| chr19:434031 | C | A | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+678G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434031 | |||||||
| chr19:434031 | C | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+678G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434031 | |||||||
| chr19:434032 | T | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+677A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434032 | |||||||
| chr19:434033 | T | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+676A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434033 | |||||||
| chr19:434033 | T | C | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+676A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434033 | |||||||
| chr19:434034 | C | G | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+675G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434034 | |||||||
| chr19:434037 | C | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+672G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434037 | |||||||
| chr19:434038 | G | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+671C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434038 | |||||||
| chr19:434053 | A | AGTCT | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+655_1110+656i others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434053 | |||||||
| chr19:434060 | G | C | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+649C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434060 | |||||||
| chr19:434061 | T | A | 3 | a0001c0001t0003g0070 a0001c0002t0003g0149 a0001c0007t0006g0033 |
3 | HG01071.hp2 HG02451.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1110+648A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434061 | |||||||
| chr19:434062 | T | G | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+647A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434062 | |||||||
| chr19:434063 | A | C | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+646T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434063 | |||||||
| chr19:434063 | A | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+646T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434063 | |||||||
| chr19:434066 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+643C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434066 | |||||||
| chr19:434067 | G | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+642C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434067 | |||||||
| chr19:434068 | A | C | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+641T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434068 | |||||||
| chr19:434069 | G | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+640C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434069 | |||||||
| chr19:434070 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+639C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434070 | |||||||
| chr19:434071 | C | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+638G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434071 | |||||||
| chr19:434072 | C | G | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+637G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434072 | |||||||
| chr19:434072 | C | GGGGCAGA others(51): Show |
1 | a0001c0007t0006g0033 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1110+637_1110+638i others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434072 | |||||||
| chr19:434072 | C | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+637G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434072 | |||||||
| chr19:434073 | G | A | 6 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+636C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434073 | |||||||
| chr19:434074 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+635C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434074 | |||||||
| chr19:434075 | G | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+634C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434075 | |||||||
| chr19:434076 | C | G | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+633G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434076 | |||||||
| chr19:434079 | A | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+630T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434079 | |||||||
| chr19:434080 | T | C | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+629A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434080 | |||||||
| chr19:434080 | T | G | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+629A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434080 | |||||||
| chr19:434082 | G | A | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+627C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434082 | |||||||
| chr19:434082 | GATGGCGC others(3): Show |
G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+617_1110+626d others(12): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434082 | |||||||
| chr19:434084 | T | TCG | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+624_1110+625i others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434084 | |||||||
| chr19:434085 | G | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+624C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434085 | |||||||
| chr19:434087 | C | A | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+622G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434087 | |||||||
| chr19:434089 | C | A | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+620G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434089 | |||||||
| chr19:434091 | T | C | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+618A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434091 | |||||||
| chr19:434092 | C | G | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+617G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434092 | |||||||
| chr19:434101 | T | A | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+608A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434101 | |||||||
| chr19:434108 | G | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+601C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434108 | |||||||
| chr19:434112 | G | GTC | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+596_1110+597i others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434112 | |||||||
| chr19:434115 | A | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+594T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434115 | |||||||
| chr19:434119 | T | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+590A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434119 | |||||||
| chr19:434120 | T | G | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+589A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434120 | |||||||
| chr19:434121 | A | C | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+588T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434121 | |||||||
| chr19:434123 | A | T | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+586T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434123 | |||||||
| chr19:434125 | G | A | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+584C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434125 | |||||||
| chr19:434126 | A | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+583T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434126 | |||||||
| chr19:434127 | G | A | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+582C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434127 | |||||||
| chr19:434128 | G | T | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+581C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434128 | |||||||
| chr19:434130 | C | A | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+579G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434130 | |||||||
| chr19:434130 | C | T | 2 | a0001c0001t0003g0172 a0003c0008t0003g0184 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1110+579G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434130 | |||||||
| chr19:434131 | G | T | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+578C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434131 | |||||||
| chr19:434132 | GGC | G | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+575_1110+576d others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434132 | |||||||
| chr19:434133 | G | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+576C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434133 | |||||||
| chr19:434134 | C | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+575G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434134 | |||||||
| chr19:434135 | A | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+574T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434135 | |||||||
| chr19:434138 | T | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+571A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434138 | |||||||
| chr19:434139 | G | C | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+570C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434139 | |||||||
| chr19:434139 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+570C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434139 | |||||||
| chr19:434141 | C | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+568G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434141 | |||||||
| chr19:434141 | C | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+568G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434141 | |||||||
| chr19:434143 | C | A | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+566G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434143 | |||||||
| chr19:434144 | T | G | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+565A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434144 | |||||||
| chr19:434146 | CA | C | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+562delT | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434146 | |||||||
| chr19:434149 | C | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+560G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434149 | |||||||
| chr19:434159 | A | G | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+550T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434159 | |||||||
| chr19:434161 | A | C | 43 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(40): Show |
44 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.1110+548T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434161 | |||||||
| chr19:434162 | G | A | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+547C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434162 | |||||||
| chr19:434168 | G | C | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+541C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434168 | |||||||
| chr19:434169 | A | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+540T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434169 | |||||||
| chr19:434171 | A | T | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+538T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434171 | |||||||
| chr19:434174 | T | G | 7 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(4): Show |
7 | HG01361.hp1 HG02572.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1110+535A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434174 | |||||||
| chr19:434175 | A | T | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+534T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434175 | |||||||
| chr19:434178 | G | GT | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+530_1110+531i others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434178 | |||||||
| chr19:434181 | G | A | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+528C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434181 | |||||||
| chr19:434182 | G | A | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+527C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434182 | |||||||
| chr19:434183 | C | T | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+526G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434183 | |||||||
| chr19:434185 | G | GTGA | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+523_1110+524i others(5): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434185 | |||||||
| chr19:434187 | G | T | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+522C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434187 | |||||||
| chr19:434188 | C | G | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+521G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434188 | |||||||
| chr19:434192 | TA | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+516delT | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434192 | |||||||
| chr19:434195 | AC | A | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+513delG | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434195 | |||||||
| chr19:434197 | G | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+512C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434197 | |||||||
| chr19:434199 | C | A | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+510G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434199 | |||||||
| chr19:434201 | C | T | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+508G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434201 | |||||||
| chr19:434202 | C | G | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+507G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434202 | |||||||
| chr19:434203 | C | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+506G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434203 | |||||||
| chr19:434203 | C | G | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+506G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434203 | |||||||
| chr19:434204 | C | G | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+505G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434204 | |||||||
| chr19:434207 | T | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+502A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434207 | |||||||
| chr19:434207 | T | C | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+502A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434207 | |||||||
| chr19:434208 | G | C | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+501C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434208 | |||||||
| chr19:434213 | C | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+496G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434213 | |||||||
| chr19:434213 | C | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+496G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434213 | |||||||
| chr19:434214 | C | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+495G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434214 | |||||||
| chr19:434215 | T | C | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+494A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434215 | |||||||
| chr19:434220 | T | G | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+489A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434220 | |||||||
| chr19:434222 | G | C | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+487C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434222 | |||||||
| chr19:434227 | A | AAATCGTG others(421): Show |
5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+481_1110+482i others(430): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434227 | |||||||
| chr19:434239 | C | CATAAGTG others(96): Show |
1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+469_1110+470i others(105): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434239 | |||||||
| chr19:434240 | C | CTGAGTGA others(85): Show |
5 | a0001c0001t0002g0076 a0001c0001t0003g0032 a0001c0001t0004g0029 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110+377_1110+468d others(94): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434240 | |||||||
| chr19:434240 | C | G | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+469G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434240 | |||||||
| chr19:434243 | A | AATGAGAC others(1): Show |
5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+465_1110+466i others(10): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434243 | |||||||
| chr19:434256 | GTGAGTGA others(5): Show |
G | 6 | a0001c0001t0002g0035 a0001c0001t0002g0056 a0001c0001t0003g0049 others(3): Show |
6 | HG02486.hp2 HG02970.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+441_1110+452d others(14): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434256 | |||||||
| chr19:434259 | A | AGTCAGTG others(337): Show |
1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+449_1110+450i others(346): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434259 | |||||||
| chr19:434267 | C | CGTGAGTC others(1): Show |
5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+441_1110+442i others(10): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434267 | |||||||
| chr19:434268 | A | G | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+441T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434268 | |||||||
| chr19:434277 | A | C | 36 | a0001c0002t0001g0004 a0001c0002t0001g0079 a0001c0002t0001g0080 others(33): Show |
37 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1110+432T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434277 | |||||||
| chr19:434280 | A | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+429T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434280 | |||||||
| chr19:434296 | A | G | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+413T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434296 | |||||||
| chr19:434303 | A | AGATC | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+405_1110+406i others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434303 | |||||||
| chr19:434311 | C | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+398G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434311 | |||||||
| chr19:434316 | C | G | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+393G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434316 | |||||||
| chr19:434324 | A | G | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+385T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434324 | |||||||
| chr19:434343 | C | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+366G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434343 | |||||||
| chr19:434344 | A | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+365T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434344 | |||||||
| chr19:434354 | G | C | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+355C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434354 | |||||||
| chr19:434355 | A | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+354T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434355 | |||||||
| chr19:434357 | A | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+352T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434357 | |||||||
| chr19:434358 | T | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+351A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434358 | |||||||
| chr19:434359 | C | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+350G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434359 | |||||||
| chr19:434359 | CATGAGAT others(13): Show |
C | 1 | a0001c0007t0002g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1110+330_1110+349d others(22): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434359 | |||||||
| chr19:434360 | A | G | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+349T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434360 | |||||||
| chr19:434367 | C | T | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+342G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434367 | |||||||
| chr19:434379 | G | C | 95 | a0001c0001t0002g0051 a0001c0001t0002g0076 a0001c0001t0002g0101 others(92): Show |
97 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.1110+330C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434379 | |||||||
| chr19:434380 | A | G | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+329T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434380 | |||||||
| chr19:434384 | G | GAT | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+324_1110+325i others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434384 | |||||||
| chr19:434386 | C | G | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+323G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434386 | |||||||
| chr19:434389 | A | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+320T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434389 | |||||||
| chr19:434390 | G | GAGTGTGA others(3): Show |
1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+318_1110+319i others(12): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434390 | |||||||
| chr19:434405 | T | TGTGAGAT others(615): Show |
5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+303_1110+304i others(624): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434405 | |||||||
| chr19:434416 | T | TCATA | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+292_1110+293i others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434416 | |||||||
| chr19:434417 | A | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+292T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434417 | |||||||
| chr19:434425 | A | AGGT | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+283_1110+284i others(5): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434425 | |||||||
| chr19:434428 | C | G | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+281G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434428 | |||||||
| chr19:434436 | G | A | 1 | a0001c0005t0001g0015 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1110+273C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434436 | |||||||
| chr19:434440 | A | G | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+269T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434440 | |||||||
| chr19:434446 | C | G | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+263G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434446 | |||||||
| chr19:434447 | T | A | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+262A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434447 | |||||||
| chr19:434452 | G | C | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+257C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434452 | |||||||
| chr19:434454 | T | TCGTGAGT others(88): Show |
1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+254_1110+255i others(97): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434454 | |||||||
| chr19:434455 | A | C | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+254T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434455 | |||||||
| chr19:434461 | C | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+248G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434461 | |||||||
| chr19:434461 | C | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+248G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434461 | |||||||
| chr19:434462 | A | C | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+247T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434462 | |||||||
| chr19:434462 | A | T | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+247T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434462 | |||||||
| chr19:434463 | A | C | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+246T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434463 | |||||||
| chr19:434463 | A | T | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+246T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434463 | |||||||
| chr19:434476 | G | A | 1 | a0001c0001t0005g0102 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1110+233C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434476 | |||||||
| chr19:434483 | TGTGA | T | 3 | a0001c0001t0002g0101 a0001c0001t0007g0038 a0009c0021t0002g0028 |
3 | HG02572.hp2 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1110+222_1110+225d others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434483 | |||||||
| chr19:434485 | T | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+224A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434485 | |||||||
| chr19:434487 | A | AGATG | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+221_1110+222i others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434487 | |||||||
| chr19:434488 | G | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+221C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434488 | |||||||
| chr19:434488 | GTGAGTGA others(5): Show |
G | 1 | a0001c0001t0002g0051 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1110+209_1110+220d others(14): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434488 | |||||||
| chr19:434496 | A | G | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+213T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434496 | |||||||
| chr19:434499 | C | CGTGAGTC others(319): Show |
1 | a0001c0001t0006g0048 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1110+209_1110+210i others(328): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434499 | |||||||
| chr19:434499 | C | CGTGAGTC others(319): Show |
4 | a0001c0001t0006g0042 a0001c0001t0006g0052 a0001c0005t0006g0008 others(1): Show |
4 | HG02818.hp1 HG02922.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1110+209_1110+210i others(328): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434499 | |||||||
| chr19:434500 | A | G | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+209T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434500 | |||||||
| chr19:434501 | T | C | 36 | a0001c0003t0001g0060 a0001c0003t0001g0063 a0001c0003t0001g0064 others(33): Show |
37 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1110+208A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434501 | |||||||
| chr19:434511 | C | A | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+198G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434511 | |||||||
| chr19:434511 | C | CGTGATTG others(371): Show |
1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+197_1110+198i others(380): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434511 | |||||||
| chr19:434517 | C | T | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+192G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434517 | |||||||
| chr19:434519 | T | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+190A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434519 | |||||||
| chr19:434527 | T | C | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+182A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434527 | |||||||
| chr19:434539 | T | C | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+170A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434539 | |||||||
| chr19:434547 | TGTGA | T | 7 | a0001c0007t0002g0077 a0001c0007t0006g0033 a0001c0007t0006g0054 others(4): Show |
7 | HG01109.hp2 HG02451.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.1110+158_1110+161d others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434547 | |||||||
| chr19:434552 | G | GATCA | 5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+156_1110+157i others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434552 | |||||||
| chr19:434554 | A | G | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+155T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434554 | |||||||
| chr19:434556 | G | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+153C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434556 | |||||||
| chr19:434560 | A | G | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+149T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434560 | |||||||
| chr19:434564 | A | G | 6 | a0001c0001t0003g0070 a0001c0001t0006g0042 a0001c0001t0006g0048 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+145T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434564 | |||||||
| chr19:434567 | A | AGTGAGAT others(832): Show |
5 | a0001c0001t0006g0042 a0001c0001t0006g0048 a0001c0001t0006g0052 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+141_1110+142i others(841): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTC others(39): Show |
1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1110+141_1110+142i others(48): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3713): Show |
1 | a0001c0001t0001g0106 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1110+141_1110+142i others(3722): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3693): Show |
1 | a0002c0012t0002g0205 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1110+141_1110+142i others(3702): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3713): Show |
6 | a0001c0001t0002g0035 a0001c0001t0002g0056 a0001c0001t0003g0049 others(3): Show |
6 | HG02486.hp2 HG02970.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3722): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3713): Show |
2 | a0001c0001t0003g0005 a0001c0001t0003g0181 |
3 | HG01978.hp1 HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3722): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3713): Show |
4 | a0001c0001t0016g0069 a0001c0013t0005g0006 a0001c0017t0005g0055 others(1): Show |
4 | HG02622.hp1 HG02622.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3722): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3681): Show |
1 | a0001c0002t0003g0044 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1110+141_1110+142i others(3690): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3669): Show |
3 | a0001c0001t0002g0101 a0001c0001t0007g0038 a0009c0021t0002g0028 |
3 | HG02572.hp2 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3678): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3685): Show |
28 | a0001c0002t0001g0004 a0001c0002t0001g0082 a0001c0002t0001g0086 others(25): Show |
29 | HG00423.hp2 HG01978.hp2 HG01993.hp2 others(26): Show |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3694): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3685): Show |
4 | a0001c0002t0001g0079 a0001c0002t0001g0080 a0001c0002t0001g0093 others(1): Show |
4 | HG00558.hp2 HG02027.hp2 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3694): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3673): Show |
2 | a0001c0002t0003g0149 a0001c0002t0003g0150 |
2 | HG01071.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3682): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3685): Show |
1 | a0001c0002t0001g0095 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1110+141_1110+142i others(3694): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3691): Show |
5 | a0001c0003t0002g0065 a0001c0003t0002g0068 a0001c0003t0002g0073 others(2): Show |
5 | NA18954.hp2 NA18999.hp1 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3700): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3693): Show |
23 | a0001c0003t0001g0060 a0001c0003t0001g0063 a0001c0003t0001g0064 others(20): Show |
24 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3702): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3713): Show |
2 | a0001c0007t0003g0039 a0001c0007t0006g0041 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3722): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3711): Show |
1 | a0001c0001t0005g0102 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1110+141_1110+142i others(3720): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3712): Show |
1 | a0001c0001t0001g0119 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1110+141_1110+142i others(3721): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3711): Show |
2 | a0001c0001t0003g0172 a0003c0008t0003g0184 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3720): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3709): Show |
1 | a0001c0001t0011g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1110+141_1110+142i others(3718): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3710): Show |
1 | a0001c0014t0001g0014 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1110+141_1110+142i others(3719): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3713): Show |
60 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0078 others(57): Show |
60 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3722): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3713): Show |
1 | a0005c0009t0014g0036 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1110+141_1110+142i others(3722): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3713): Show |
2 | a0005c0009t0005g0047 a0011c0022t0002g0185 |
2 | NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3722): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3729): Show |
1 | a0001c0001t0001g0003 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3738): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3707): Show |
1 | a0001c0005t0001g0025 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1110+141_1110+142i others(3716): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3707): Show |
15 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0004g0031 others(12): Show |
15 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3716): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3707): Show |
9 | a0001c0001t0004g0002 a0001c0001t0004g0162 a0001c0001t0005g0046 others(6): Show |
10 | HG01258.hp1 HG01358.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3716): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3707): Show |
1 | a0002c0004t0005g0204 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1110+141_1110+142i others(3716): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3755): Show |
1 | a0001c0001t0004g0164 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1110+141_1110+142i others(3764): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3657): Show |
2 | a0004c0011t0005g0057 a0004c0011t0005g0061 |
2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3666): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3657): Show |
5 | a0001c0007t0002g0077 a0001c0007t0006g0033 a0001c0007t0006g0054 others(2): Show |
5 | HG01884.hp2 HG02451.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3666): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3643): Show |
3 | a0001c0001t0003g0032 a0001c0001t0004g0029 a0001c0005t0006g0009 |
3 | HG02055.hp2 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3652): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3601): Show |
1 | a0001c0001t0002g0051 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1110+141_1110+142i others(3610): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3643): Show |
2 | a0001c0001t0002g0076 a0001c0001t0013g0072 |
2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3652): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3671): Show |
1 | a0003c0008t0005g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1110+141_1110+142i others(3680): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434567 | A | AGTGAGTG others(3693): Show |
4 | a0001c0006t0001g0013 a0001c0006t0001g0016 a0001c0006t0001g0017 others(1): Show |
4 | HG03098.hp2 HG03209.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1110+141_1110+142i others(3702): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434567 | |||||||
| chr19:434576 | G | GATCATGA others(3639): Show |
1 | a0001c0002t0002g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1110+132_1110+133i others(3648): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 8/12 | chr19 | 434576 | |||||||
| chr19:434970 | CA | C | 33 | a0001c0003t0001g0060 a0001c0003t0001g0063 a0001c0003t0001g0064 others(30): Show |
34 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.954-106delT | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 434970 | |||||||
| chr19:434986 | A | C | 1 | a0003c0008t0005g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.954-121T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 434986 | |||||||
| chr19:435076 | G | A | 1 | a0001c0001t0002g0051 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.954-211C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 435076 | |||||||
| chr19:435080 | T | G | 5 | a0001c0002t0001g0079 a0001c0002t0001g0080 a0001c0002t0001g0093 others(2): Show |
5 | HG00558.hp2 HG02027.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.954-215A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 435080 | |||||||
| chr19:435138 | C | T | 2 | a0001c0001t0002g0051 a0001c0001t0011g0034 |
2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.954-273G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 435138 | |||||||
| chr19:435141 | C | G | 40 | a0001c0001t0002g0051 a0001c0001t0002g0101 a0001c0001t0007g0038 others(37): Show |
41 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.954-276G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 435141 | |||||||
| chr19:435178 | C | A | 5 | a0001c0003t0002g0065 a0001c0003t0002g0068 a0001c0003t0002g0073 others(2): Show |
5 | NA18954.hp2 NA18999.hp1 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.954-313G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 435178 | |||||||
| chr19:435307 | C | T | 5 | a0001c0001t0002g0076 a0001c0001t0003g0032 a0001c0001t0004g0029 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.954-442G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 435307 | |||||||
| chr19:435337 | C | T | 1 | a0001c0002t0002g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.954-472G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 435337 | |||||||
| chr19:435386 | T | C | 1 | a0001c0001t0001g0098 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.954-521A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 435386 | |||||||
| chr19:435493 | C | T | 34 | a0001c0001t0007g0038 a0001c0002t0001g0004 a0001c0002t0001g0079 others(31): Show |
35 | HG00423.hp2 HG00558.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.954-628G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 435493 | |||||||
| chr19:435495 | C | T | 1 | a0002c0004t0001g0198 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.954-630G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 435495 | |||||||
| chr19:435551 | T | C | 7 | a0001c0007t0002g0077 a0001c0007t0006g0033 a0001c0007t0006g0054 others(4): Show |
7 | HG01109.hp2 HG01884.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.953+614A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 435551 | |||||||
| chr19:435691 | A | G | 1 | a0001c0001t0001g0103 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.953+474T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 435691 | |||||||
| chr19:435753 | G | A | 2 | a0004c0011t0005g0057 a0004c0011t0005g0061 |
2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.953+412C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 435753 | |||||||
| chr19:435875 | G | A | 1 | a0001c0023t0007g0187 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.953+290C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 435875 | |||||||
| chr19:436004 | C | T | 1 | a0001c0003t0002g0074 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.953+161G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 436004 | |||||||
| chr19:436015 | G | C | 1 | a0003c0008t0003g0184 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.953+150C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 436015 | |||||||
| chr19:436053 | G | A | 1 | a0003c0008t0003g0184 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.953+112C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 7/12 | chr19 | 436053 | |||||||
| chr19:436369 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.826+11C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 6/12 | chr19 | 436369 | |||||||
| chr19:436541 | C | T | 1 | a0001c0001t0004g0164 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.774+89G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 5/12 | chr19 | 436541 | |||||||
| chr19:436690 | C | T | 36 | a0001c0001t0003g0032 a0001c0003t0001g0060 a0001c0003t0001g0063 others(33): Show |
37 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(34): Show |
splice_region_variant&intron_variant | LOW | c.721-7G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 436690 | |||||||
| chr19:436727 | G | A | 1 | a0003c0008t0003g0184 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.721-44C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 436727 | |||||||
| chr19:436741 | C | T | 3 | a0001c0001t0003g0172 a0005c0009t0005g0047 a0005c0009t0014g0036 |
3 | HG03195.hp2 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.721-58G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 436741 | |||||||
| chr19:436770 | G | C | 1 | a0001c0001t0002g0051 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.721-87C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 436770 | |||||||
| chr19:436975 | T | C | 4 | a0001c0001t0002g0076 a0001c0001t0004g0029 a0001c0001t0013g0072 others(1): Show |
4 | HG01884.hp1 HG02258.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-292A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 436975 | |||||||
| chr19:437100 | G | A | 1 | a0011c0022t0002g0185 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.721-417C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 437100 | |||||||
| chr19:437165 | T | C | 3 | a0001c0001t0004g0029 a0001c0005t0006g0009 a0003c0008t0006g0186 |
3 | HG02818.hp1 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.721-482A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 437165 | |||||||
| chr19:437206 | G | A | 1 | a0003c0008t0003g0184 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.721-523C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 437206 | |||||||
| chr19:437217 | C | CATCTGCG others(17): Show |
1 | a0001c0001t0002g0051 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.721-535_721-534ins others(24): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 437217 | |||||||
| chr19:437242 | A | G | 1 | a0001c0001t0002g0051 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.721-559T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 437242 | |||||||
| chr19:437253 | C | T | 1 | a0001c0003t0001g0140 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.721-570G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 437253 | |||||||
| chr19:437256 | T | C | 92 | a0001c0001t0001g0147 a0001c0001t0001g0178 a0001c0001t0002g0035 others(89): Show |
95 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.721-573A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 437256 | |||||||
| chr19:437266 | G | A | 1 | a0009c0021t0002g0028 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.721-583C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 437266 | |||||||
| chr19:437266 | GTCTGCGT others(17): Show |
G | 4 | a0001c0007t0002g0077 a0001c0007t0006g0033 a0002c0024t0003g0200 others(1): Show |
4 | HG02451.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.721-607_721-584del others(24): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 437266 | |||||||
| chr19:437320 | ATGCTCAT others(5): Show |
A | 1 | a0001c0003t0002g0062 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.721-649_721-638del others(12): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 437320 | |||||||
| chr19:437368 | G | A | 1 | a0001c0002t0001g0157 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.721-685C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 437368 | |||||||
| chr19:437607 | G | A | 1 | a0001c0002t0001g0086 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.721-924C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 437607 | |||||||
| chr19:437784 | G | A | 1 | a0003c0008t0005g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.720+934C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 437784 | |||||||
| chr19:437846 | CCCT | C | 3 | a0001c0001t0003g0172 a0005c0009t0005g0047 a0005c0009t0014g0036 |
3 | HG03195.hp2 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.720+869_720+871del others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 437846 | |||||||
| chr19:437958 | T | C | 3 | a0001c0001t0003g0172 a0005c0009t0005g0047 a0005c0009t0014g0036 |
3 | HG03195.hp2 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.720+760A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 437958 | |||||||
| chr19:438248 | G | C | 1 | a0001c0001t0011g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.720+470C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 438248 | |||||||
| chr19:438357 | T | C | 70 | a0001c0001t0002g0035 a0001c0001t0002g0056 a0001c0001t0002g0076 others(67): Show |
72 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.720+361A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 438357 | |||||||
| chr19:438358 | T | C | 1 | a0001c0023t0007g0187 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.720+360A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 438358 | |||||||
| chr19:438417 | G | A | 4 | a0001c0002t0001g0082 a0001c0002t0001g0086 a0001c0002t0001g0088 others(1): Show |
4 | HG01978.hp2 HG02083.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+301C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 438417 | |||||||
| chr19:438421 | C | T | 44 | a0001c0001t0002g0076 a0001c0001t0002g0101 a0001c0001t0003g0172 others(41): Show |
45 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.720+297G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 438421 | |||||||
| chr19:438430 | G | C | 3 | a0001c0001t0003g0172 a0005c0009t0005g0047 a0005c0009t0014g0036 |
3 | HG03195.hp2 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.720+288C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 438430 | |||||||
| chr19:438436 | GGCGTCCT others(22): Show |
G | 2 | a0001c0001t0003g0172 a0005c0009t0005g0047 |
2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.720+253_720+281del others(29): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 438436 | |||||||
| chr19:438438 | C | T | 1 | a0001c0005t0001g0011 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.720+280G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 438438 | |||||||
| chr19:438468 | G | A | 1 | a0001c0001t0004g0029 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.720+250C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 438468 | |||||||
| chr19:438475 | C | G | 1 | a0001c0003t0001g0140 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.720+243G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 438475 | |||||||
| chr19:438584 | C | G | 5 | a0001c0001t0004g0031 a0001c0001t0005g0027 a0001c0001t0005g0037 others(2): Show |
5 | HG01891.hp1 HG02145.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.720+134G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 4/12 | chr19 | 438584 | |||||||
| chr19:438868 | G | A | 17 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0004g0002 others(14): Show |
18 | HG00099.hp1 HG00323.hp2 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.601-31C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 3/12 | chr19 | 438868 | |||||||
| chr19:438911 | C | T | 20 | a0001c0001t0001g0163 a0001c0001t0001g0167 a0001c0001t0005g0102 others(17): Show |
20 | HG00733.hp1 HG01358.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.600+59G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 3/12 | chr19 | 438911 | |||||||
| chr19:438915 | C | T | 20 | a0001c0001t0001g0163 a0001c0001t0002g0076 a0001c0001t0004g0162 others(17): Show |
20 | HG00733.hp1 HG01358.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.600+55G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 3/12 | chr19 | 438915 | |||||||
| chr19:438916 | C | T | 1 | a0011c0022t0002g0185 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.600+54G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 3/12 | chr19 | 438916 | |||||||
| chr19:439055 | G | A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0104 a0001c0001t0001g0113 others(10): Show |
14 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.540-25C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439055 | |||||||
| chr19:439112 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.540-82C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439112 | |||||||
| chr19:439193 | A | G | 80 | a0001c0001t0001g0043 a0001c0001t0001g0083 a0001c0001t0001g0085 others(77): Show |
81 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.540-163T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439193 | |||||||
| chr19:439214 | A | G | 11 | a0001c0001t0002g0051 a0001c0001t0003g0005 a0001c0001t0003g0172 others(8): Show |
12 | HG01978.hp1 HG02055.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.540-184T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439214 | |||||||
| chr19:439393 | C | T | 11 | a0001c0001t0003g0005 a0001c0001t0003g0172 a0001c0001t0003g0181 others(8): Show |
12 | HG01884.hp2 HG01891.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.540-363G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439393 | |||||||
| chr19:439431 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.540-401G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439431 | |||||||
| chr19:439457 | C | A | 2 | a0001c0001t0003g0049 a0001c0001t0006g0050 |
2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.540-427G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439457 | |||||||
| chr19:439463 | C | CCTGTCTG others(21): Show |
5 | a0001c0001t0011g0034 a0001c0005t0006g0009 a0001c0007t0002g0077 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.540-461_540-434dup others(28): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439463 | |||||||
| chr19:439510 | G | A | 2 | a0001c0002t0001g0004 a0001c0002t0004g0096 |
3 | NA18939.hp1 NA18988.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.540-480C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439510 | |||||||
| chr19:439547 | T | C | 2 | a0001c0003t0002g0068 a0001c0003t0002g0073 |
2 | NA18954.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.540-517A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439547 | |||||||
| chr19:439566 | C | T | 4 | a0001c0001t0005g0102 a0001c0001t0006g0030 a0003c0008t0003g0184 others(1): Show |
4 | HG01891.hp2 HG02145.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.540-536G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439566 | |||||||
| chr19:439580 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.540-550G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439580 | |||||||
| chr19:439601 | C | T | 3 | a0001c0003t0001g0114 a0001c0003t0002g0001 a0008c0015t0012g0026 |
4 | HG01952.hp1 HG02293.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.540-571G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439601 | |||||||
| chr19:439727 | C | G | 1 | a0001c0005t0001g0024 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.540-697G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439727 | |||||||
| chr19:439752 | G | A | 1 | a0001c0005t0001g0021 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.540-722C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439752 | |||||||
| chr19:439801 | G | A | 1 | a0001c0001t0016g0069 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.540-771C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439801 | |||||||
| chr19:439841 | C | T | 3 | a0001c0001t0003g0172 a0001c0017t0005g0055 a0005c0009t0005g0047 |
3 | HG02622.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.540-811G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439841 | |||||||
| chr19:439855 | G | A | 1 | a0003c0008t0005g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.540-825C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439855 | |||||||
| chr19:439868 | A | T | 1 | a0003c0008t0005g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.540-838T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 439868 | |||||||
| chr19:440005 | A | G | 90 | a0001c0001t0001g0058 a0001c0001t0001g0147 a0001c0001t0001g0179 others(87): Show |
93 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.539+857T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 440005 | |||||||
| chr19:440025 | C | CA | 11 | a0001c0001t0001g0132 a0001c0001t0001g0171 a0001c0001t0003g0172 others(8): Show |
11 | HG00544.hp2 HG01928.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.539+836dupT | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 440025 | |||||||
| chr19:440025 | C | CAA | 42 | a0001c0001t0001g0058 a0001c0001t0002g0035 a0001c0001t0002g0051 others(39): Show |
43 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.539+835_539+836dup others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 440025 | |||||||
| chr19:440088 | A | AACGCCAT others(12): Show |
77 | a0001c0001t0001g0058 a0001c0001t0001g0147 a0001c0001t0001g0179 others(74): Show |
80 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.539+755_539+773dup others(19): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 440088 | |||||||
| chr19:440114 | G | C | 1 | a0001c0016t0001g0159 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.539+748C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 440114 | |||||||
| chr19:440128 | C | T | 1 | a0001c0002t0002g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.539+734G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 440128 | |||||||
| chr19:440282 | A | G | 4 | a0001c0001t0003g0172 a0001c0001t0007g0038 a0001c0017t0005g0055 others(1): Show |
4 | HG02622.hp1 HG02818.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.539+580T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 440282 | |||||||
| chr19:440314 | C | T | 1 | a0001c0023t0007g0187 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.539+548G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 440314 | |||||||
| chr19:440316 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.539+546A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 440316 | |||||||
| chr19:440478 | G | C | 87 | a0001c0001t0001g0058 a0001c0001t0001g0147 a0001c0001t0001g0178 others(84): Show |
90 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.539+384C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 440478 | |||||||
| chr19:440598 | C | T | 4 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0002t0004g0176 others(1): Show |
4 | HG00423.hp1 NA18947.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.539+264G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 440598 | |||||||
| chr19:440655 | C | T | 6 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0002t0004g0176 others(3): Show |
6 | HG00423.hp1 HG02976.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.539+207G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 440655 | |||||||
| chr19:440701 | C | T | 2 | a0001c0003t0002g0062 a0002c0012t0002g0205 |
2 | NA18960.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.539+161G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 440701 | |||||||
| chr19:440785 | CGCTGCCG others(9): Show |
C | 4 | a0001c0001t0011g0034 a0001c0007t0002g0077 a0001c0007t0006g0033 others(1): Show |
4 | HG02451.hp2 HG02486.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.539+61_539+76delAC others(14): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 440785 | |||||||
| chr19:440817 | T | C | 50 | a0001c0001t0001g0147 a0001c0001t0001g0178 a0001c0001t0001g0179 others(47): Show |
52 | HG00423.hp1 HG00423.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.539+45A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 440817 | |||||||
| chr19:440846 | A | G | 1 | a0003c0008t0005g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.539+16T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 2/12 | chr19 | 440846 | |||||||
| chr19:441027 | T | A | 16 | a0001c0001t0002g0035 a0001c0001t0002g0051 a0001c0001t0002g0056 others(13): Show |
16 | HG02559.hp1 HG02572.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.469-95A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441027 | |||||||
| chr19:441069 | G | T | 35 | a0001c0001t0001g0147 a0001c0001t0001g0178 a0001c0001t0001g0179 others(32): Show |
37 | HG00423.hp1 HG00423.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.469-137C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441069 | |||||||
| chr19:441100 | T | C | 35 | a0001c0001t0001g0147 a0001c0001t0001g0178 a0001c0001t0001g0179 others(32): Show |
37 | HG00423.hp1 HG00423.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.469-168A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441100 | |||||||
| chr19:441111 | T | C | 51 | a0001c0001t0001g0147 a0001c0001t0001g0178 a0001c0001t0001g0179 others(48): Show |
53 | HG00423.hp1 HG00423.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.469-179A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441111 | |||||||
| chr19:441114 | G | A | 4 | a0001c0001t0009g0166 a0001c0014t0001g0014 a0001c0020t0001g0105 others(1): Show |
4 | HG00735.hp1 HG01099.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.469-182C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441114 | |||||||
| chr19:441130 | C | T | 1 | a0001c0001t0004g0029 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.469-198G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441130 | |||||||
| chr19:441148 | G | C | 35 | a0001c0001t0001g0147 a0001c0001t0001g0178 a0001c0001t0001g0179 others(32): Show |
37 | HG00423.hp1 HG00423.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.469-216C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441148 | |||||||
| chr19:441163 | A | G | 35 | a0001c0001t0001g0147 a0001c0001t0001g0178 a0001c0001t0001g0179 others(32): Show |
37 | HG00423.hp1 HG00423.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.469-231T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441163 | |||||||
| chr19:441186 | C | A | 1 | a0001c0002t0001g0146 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.469-254G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441186 | |||||||
| chr19:441195 | C | G | 35 | a0001c0001t0001g0147 a0001c0001t0001g0178 a0001c0001t0001g0179 others(32): Show |
37 | HG00423.hp1 HG00423.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.469-263G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441195 | |||||||
| chr19:441226 | C | T | 7 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0002t0004g0176 others(4): Show |
7 | HG00423.hp1 HG02559.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.469-294G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441226 | |||||||
| chr19:441243 | A | G | 35 | a0001c0001t0001g0147 a0001c0001t0001g0178 a0001c0001t0001g0179 others(32): Show |
37 | HG00423.hp1 HG00423.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.469-311T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441243 | |||||||
| chr19:441252 | G | A | 1 | a0001c0002t0003g0151 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.469-320C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441252 | |||||||
| chr19:441257 | C | T | 15 | a0001c0001t0002g0035 a0001c0001t0002g0051 a0001c0001t0002g0056 others(12): Show |
15 | HG02559.hp1 HG02572.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.469-325G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441257 | |||||||
| chr19:441354 | C | T | 1 | a0001c0005t0001g0020 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.469-422G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441354 | |||||||
| chr19:441373 | C | G | 6 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0002t0004g0176 others(3): Show |
6 | HG00423.hp1 HG02976.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-441G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441373 | |||||||
| chr19:441376 | C | T | 5 | a0001c0003t0002g0065 a0001c0003t0002g0068 a0001c0003t0002g0073 others(2): Show |
5 | NA18954.hp2 NA18999.hp1 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.469-444G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441376 | |||||||
| chr19:441448 | A | G | 8 | a0001c0001t0001g0058 a0001c0003t0001g0060 a0001c0003t0001g0064 others(5): Show |
9 | HG00544.hp2 HG00621.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.469-516T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441448 | |||||||
| chr19:441456 | T | A | 7 | a0001c0001t0004g0031 a0001c0001t0005g0027 a0001c0001t0005g0037 others(4): Show |
7 | HG00733.hp2 HG01256.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.469-524A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441456 | |||||||
| chr19:441457 | A | G | 93 | a0001c0001t0001g0058 a0001c0001t0001g0147 a0001c0001t0001g0178 others(90): Show |
96 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.469-525T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441457 | |||||||
| chr19:441686 | C | T | 1 | a0003c0008t0005g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.469-754G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441686 | |||||||
| chr19:441718 | T | C | 4 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0002t0004g0176 others(1): Show |
4 | HG00423.hp1 NA18947.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.469-786A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441718 | |||||||
| chr19:441730 | C | T | 1 | a0003c0008t0005g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.469-798G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441730 | |||||||
| chr19:441764 | G | A | 33 | a0001c0001t0001g0058 a0001c0001t0003g0032 a0001c0003t0001g0060 others(30): Show |
34 | HG00544.hp2 HG00621.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.469-832C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441764 | |||||||
| chr19:441813 | G | A | 1 | a0001c0023t0007g0187 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.469-881C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 441813 | |||||||
| chr19:442378 | G | A | 1 | a0003c0008t0005g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.469-1446C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442378 | |||||||
| chr19:442437 | G | A | 1 | a0003c0008t0005g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.469-1505C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442437 | |||||||
| chr19:442475 | GTGGGTGG others(1): Show |
G | 28 | a0001c0001t0001g0147 a0001c0001t0002g0076 a0001c0001t0003g0005 others(25): Show |
30 | HG00423.hp2 HG00621.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.469-1551_469-1544d others(10): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442475 | |||||||
| chr19:442511 | ATGGATGG others(9): Show |
A | 4 | a0001c0001t0011g0034 a0001c0007t0002g0077 a0001c0007t0006g0033 others(1): Show |
4 | HG02451.hp2 HG02486.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.469-1595_469-1580d others(18): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442511 | |||||||
| chr19:442531 | ATGGATGG others(9): Show |
A | 32 | a0001c0001t0001g0147 a0001c0001t0002g0076 a0001c0001t0003g0005 others(29): Show |
34 | HG00423.hp2 HG00621.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.469-1615_469-1600d others(18): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442531 | |||||||
| chr19:442535 | A | ATGGGTGG others(13): Show |
3 | a0001c0003t0001g0114 a0001c0003t0002g0001 a0008c0015t0012g0026 |
4 | HG01952.hp1 HG02293.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.469-1604_469-1603i others(22): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442535 | |||||||
| chr19:442547 | G | A | 56 | a0001c0001t0001g0058 a0001c0001t0001g0178 a0001c0001t0001g0179 others(53): Show |
57 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.469-1615C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442547 | |||||||
| chr19:442557 | G | A | 1 | a0001c0001t0003g0032 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.469-1625C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442557 | |||||||
| chr19:442568 | C | T | 1 | a0001c0005t0006g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.469-1636G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442568 | |||||||
| chr19:442569 | G | A | 5 | a0001c0001t0001g0099 a0001c0001t0001g0103 a0001c0001t0001g0106 others(2): Show |
5 | HG00544.hp1 HG02559.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.469-1637C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442569 | |||||||
| chr19:442623 | GTGAATGG others(9): Show |
G | 4 | a0001c0001t0011g0034 a0001c0007t0002g0077 a0001c0007t0006g0033 others(1): Show |
4 | HG02451.hp2 HG02486.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.469-1707_469-1692d others(18): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442623 | |||||||
| chr19:442626 | A | G | 112 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0081 others(109): Show |
115 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.469-1694T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442626 | |||||||
| chr19:442631 | G | GTGGA | 88 | a0001c0001t0001g0058 a0001c0001t0001g0147 a0001c0001t0001g0178 others(85): Show |
91 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.469-1703_469-1700d others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442631 | |||||||
| chr19:442662 | G | GGTGGATG others(1): Show |
6 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0002t0004g0176 others(3): Show |
6 | HG00423.hp1 HG02976.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-1738_469-1731d others(10): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442662 | |||||||
| chr19:442696 | C | T | 26 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0035 others(23): Show |
26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-1764G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442696 | |||||||
| chr19:442704 | C | T | 4 | a0001c0001t0003g0172 a0001c0001t0004g0029 a0001c0017t0005g0055 others(1): Show |
4 | HG02622.hp1 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.469-1772G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442704 | |||||||
| chr19:442707 | A | G | 26 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0035 others(23): Show |
26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-1775T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442707 | |||||||
| chr19:442711 | C | A | 26 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0035 others(23): Show |
26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-1779G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442711 | |||||||
| chr19:442712 | T | C | 26 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0035 others(23): Show |
26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-1780A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442712 | |||||||
| chr19:442731 | A | G | 16 | a0001c0001t0002g0035 a0001c0001t0002g0051 a0001c0001t0002g0056 others(13): Show |
16 | HG02559.hp1 HG02572.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.469-1799T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442731 | |||||||
| chr19:442733 | G | A | 26 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0035 others(23): Show |
26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-1801C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442733 | |||||||
| chr19:442736 | C | T | 26 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0035 others(23): Show |
26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-1804G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442736 | |||||||
| chr19:442738 | G | A | 26 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0035 others(23): Show |
26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-1806C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442738 | |||||||
| chr19:442743 | G | A | 26 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0035 others(23): Show |
26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-1811C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442743 | |||||||
| chr19:442750 | G | T | 2 | a0001c0007t0003g0039 a0001c0007t0006g0041 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.469-1818C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442750 | |||||||
| chr19:442759 | G | A | 26 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0035 others(23): Show |
26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-1827C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442759 | |||||||
| chr19:442767 | G | A | 26 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0035 others(23): Show |
26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-1835C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442767 | |||||||
| chr19:442772 | T | C | 26 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0035 others(23): Show |
26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-1840A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442772 | |||||||
| chr19:442775 | A | G | 26 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0035 others(23): Show |
26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-1843T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442775 | |||||||
| chr19:442779 | A | G | 26 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0035 others(23): Show |
26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-1847T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442779 | |||||||
| chr19:442808 | TGAGTGGA others(97): Show |
T | 26 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0035 others(23): Show |
26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-1980_469-1877d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442808 | |||||||
| chr19:442895 | A | G | 12 | a0001c0001t0001g0117 a0001c0001t0001g0125 a0001c0001t0001g0128 others(9): Show |
12 | HG00558.hp1 HG01074.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.469-1963T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442895 | |||||||
| chr19:442898 | A | G | 12 | a0001c0001t0001g0117 a0001c0001t0001g0125 a0001c0001t0001g0128 others(9): Show |
12 | HG00558.hp1 HG01074.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.469-1966T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442898 | |||||||
| chr19:442910 | G | C | 1 | a0001c0005t0006g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.469-1978C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442910 | |||||||
| chr19:442913 | G | A | 27 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0035 others(24): Show |
27 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(24): Show |
intron_variant | MODIFIER | c.469-1981C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442913 | |||||||
| chr19:442915 | G | A | 26 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0035 others(23): Show |
26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-1983C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442915 | |||||||
| chr19:442918 | G | A | 26 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0035 others(23): Show |
26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-1986C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442918 | |||||||
| chr19:442932 | T | C | 26 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0035 others(23): Show |
26 | HG00423.hp1 HG02559.hp1 HG02572.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-2000A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442932 | |||||||
| chr19:442932 | T | TGGATGGG others(29): Show |
155 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0058 others(152): Show |
159 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.469-2001_469-2000i others(38): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442932 | |||||||
| chr19:442932 | T | TGGATGGG others(32): Show |
1 | a0001c0001t0001g0089 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.469-2001_469-2000i others(41): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 442932 | |||||||
| chr19:443029 | G | A | 2 | a0001c0001t0003g0070 a0001c0001t0016g0069 |
2 | NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.469-2097C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443029 | |||||||
| chr19:443162 | ATGGATGG others(21): Show |
A | 1 | a0001c0003t0002g0152 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.469-2258_469-2231d others(30): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443162 | |||||||
| chr19:443309 | A | G | 28 | a0001c0001t0001g0147 a0001c0001t0002g0076 a0001c0001t0003g0005 others(25): Show |
30 | HG00423.hp2 HG00621.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.469-2377T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443309 | |||||||
| chr19:443318 | G | A | 28 | a0001c0001t0001g0147 a0001c0001t0002g0076 a0001c0001t0003g0005 others(25): Show |
30 | HG00423.hp2 HG00621.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.469-2386C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443318 | |||||||
| chr19:443320 | G | GGACA | 28 | a0001c0001t0001g0147 a0001c0001t0002g0076 a0001c0001t0003g0005 others(25): Show |
30 | HG00423.hp2 HG00621.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.469-2389_469-2388i others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443320 | |||||||
| chr19:443320 | G | GGATGGAT others(5): Show |
27 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0035 others(24): Show |
27 | HG00423.hp1 HG02559.hp1 HG02559.hp2 others(24): Show |
intron_variant | MODIFIER | c.469-2389_469-2388i others(14): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443320 | |||||||
| chr19:443379 | TGGGTGGG others(189): Show |
T | 2 | a0001c0001t0001g0163 a0001c0001t0004g0162 |
2 | HG00733.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.469-2643_469-2448d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443379 | |||||||
| chr19:443388 | G | A | 1 | a0001c0023t0007g0187 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.469-2456C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443388 | |||||||
| chr19:443527 | CAGAT | C | 5 | a0001c0001t0006g0048 a0001c0001t0006g0052 a0001c0005t0015g0007 others(2): Show |
5 | HG02572.hp1 HG02922.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.469-2599_469-2596d others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443527 | |||||||
| chr19:443575 | CGGGTGGG others(105): Show |
C | 1 | a0001c0017t0005g0055 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.469-2755_469-2644d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443575 | |||||||
| chr19:443636 | AGATGGAT others(105): Show |
A | 1 | a0001c0001t0001g0137 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.469-2816_469-2705d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443636 | |||||||
| chr19:443782 | ATGGATGG others(21): Show |
A | 4 | a0001c0001t0001g0099 a0001c0001t0001g0103 a0001c0001t0001g0106 others(1): Show |
4 | HG00544.hp1 NA18999.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.469-2878_469-2851d others(30): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443782 | |||||||
| chr19:443843 | T | C | 1 | a0001c0003t0002g0182 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.469-2911A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443843 | |||||||
| chr19:443859 | T | A | 3 | a0001c0002t0001g0108 a0001c0002t0001g0153 a0001c0002t0001g0154 |
3 | HG02015.hp1 HG02080.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.469-2927A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443859 | |||||||
| chr19:443879 | T | C | 1 | a0001c0001t0002g0101 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.469-2947A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443879 | |||||||
| chr19:443882 | GTGGATGG others(13): Show |
G | 1 | a0011c0022t0002g0185 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.469-2970_469-2951d others(22): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443882 | |||||||
| chr19:443906 | A | ATGGG | 11 | a0001c0001t0001g0058 a0001c0001t0003g0032 a0001c0003t0001g0060 others(8): Show |
12 | HG00544.hp2 HG00621.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.469-2978_469-2975d others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443906 | |||||||
| chr19:443918 | A | G | 22 | a0001c0003t0001g0063 a0001c0003t0001g0140 a0001c0003t0002g0062 others(19): Show |
22 | HG01074.hp2 HG01943.hp2 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.469-2986T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443918 | |||||||
| chr19:443930 | ATGGACGG others(100): Show |
A | 22 | a0001c0003t0001g0063 a0001c0003t0001g0140 a0001c0003t0002g0062 others(19): Show |
22 | HG01074.hp2 HG01943.hp2 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.469-3105_469-2999d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443930 | |||||||
| chr19:443936 | G | A | 28 | a0001c0001t0001g0147 a0001c0001t0002g0076 a0001c0001t0003g0005 others(25): Show |
30 | HG00423.hp2 HG00621.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.469-3004C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443936 | |||||||
| chr19:443951 | T | TGGGTGGA others(4): Show |
1 | a0001c0002t0001g0108 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.469-3030_469-3020d others(13): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 443951 | |||||||
| chr19:444049 | A | G | 22 | a0001c0003t0001g0063 a0001c0003t0001g0140 a0001c0003t0002g0062 others(19): Show |
22 | HG01074.hp2 HG01943.hp2 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.469-3117T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 444049 | |||||||
| chr19:444052 | G | A | 22 | a0001c0003t0001g0063 a0001c0003t0001g0140 a0001c0003t0002g0062 others(19): Show |
22 | HG01074.hp2 HG01943.hp2 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.469-3120C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 444052 | |||||||
| chr19:444054 | T | G | 4 | a0001c0001t0011g0034 a0001c0007t0002g0077 a0001c0007t0006g0033 others(1): Show |
4 | HG02451.hp2 HG02486.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.469-3122A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 444054 | |||||||
| chr19:444373 | G | A | 1 | a0001c0023t0007g0187 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.469-3441C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 444373 | |||||||
| chr19:444386 | G | A | 1 | a0011c0022t0002g0185 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.469-3454C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 444386 | |||||||
| chr19:444417 | T | C | 33 | a0001c0001t0001g0058 a0001c0001t0003g0032 a0001c0003t0001g0060 others(30): Show |
34 | HG00544.hp2 HG00621.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.469-3485A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 444417 | |||||||
| chr19:444489 | A | G | 1 | a0001c0003t0002g0071 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.469-3557T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 444489 | |||||||
| chr19:444567 | C | T | 1 | a0001c0002t0003g0148 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.469-3635G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 444567 | |||||||
| chr19:444737 | C | A | 28 | a0001c0001t0001g0147 a0001c0001t0002g0076 a0001c0001t0003g0005 others(25): Show |
30 | HG00423.hp2 HG00621.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.469-3805G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 444737 | |||||||
| chr19:444797 | G | A | 1 | a0001c0002t0002g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.469-3865C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 444797 | |||||||
| chr19:444866 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.469-3934T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 444866 | |||||||
| chr19:444872 | C | T | 1 | a0001c0005t0006g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.469-3940G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 444872 | |||||||
| chr19:444918 | C | A | 32 | a0001c0001t0001g0058 a0001c0001t0003g0032 a0001c0003t0001g0060 others(29): Show |
33 | HG00544.hp2 HG00621.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.469-3986G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 444918 | |||||||
| chr19:445070 | C | T | 1 | a0001c0002t0003g0091 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.469-4138G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 445070 | |||||||
| chr19:445406 | G | C | 1 | a0011c0022t0002g0185 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.469-4474C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 445406 | |||||||
| chr19:445425 | T | A | 1 | a0002c0004t0004g0203 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.469-4493A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 445425 | |||||||
| chr19:445434 | G | A | 1 | a0001c0005t0006g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.469-4502C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 445434 | |||||||
| chr19:445699 | C | T | 1 | a0001c0023t0007g0187 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.469-4767G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 445699 | |||||||
| chr19:445746 | C | A | 1 | a0001c0018t0006g0180 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.469-4814G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 445746 | |||||||
| chr19:446131 | C | T | 3 | a0001c0006t0001g0013 a0001c0006t0001g0016 a0001c0006t0001g0017 |
3 | HG03209.hp2 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.469-5199G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 446131 | |||||||
| chr19:446243 | G | A | 32 | a0001c0001t0001g0058 a0001c0001t0003g0032 a0001c0003t0001g0060 others(29): Show |
33 | HG00544.hp2 HG00621.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.469-5311C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 446243 | |||||||
| chr19:446378 | A | T | 31 | a0001c0001t0001g0115 a0001c0001t0001g0147 a0001c0001t0002g0076 others(28): Show |
33 | HG00423.hp2 HG00621.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.469-5446T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 446378 | |||||||
| chr19:446380 | G | A | 1 | a0001c0001t0005g0053 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.469-5448C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 446380 | |||||||
| chr19:446405 | G | T | 1 | a0001c0005t0006g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.469-5473C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 446405 | |||||||
| chr19:446450 | A | G | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | NA18747.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.469-5518T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 446450 | |||||||
| chr19:446455 | C | T | 14 | a0001c0001t0002g0035 a0001c0001t0002g0056 a0001c0001t0002g0101 others(11): Show |
14 | HG02572.hp1 HG02572.hp2 HG02818.hp2 others(11): Show |
intron_variant | MODIFIER | c.469-5523G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 446455 | |||||||
| chr19:446460 | A | G | 1 | a0001c0002t0003g0175 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.469-5528T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 446460 | |||||||
| chr19:446462 | T | C | 1 | a0001c0002t0003g0175 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.469-5530A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 446462 | |||||||
| chr19:446472 | G | A | 1 | a0001c0016t0001g0159 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.469-5540C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 446472 | |||||||
| chr19:446552 | G | A | 2 | a0001c0001t0002g0076 a0001c0001t0013g0072 |
2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.469-5620C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 446552 | |||||||
| chr19:446601 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.469-5669C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 446601 | |||||||
| chr19:446821 | G | A | 2 | a0001c0002t0001g0094 a0001c0002t0001g0095 |
2 | HG03831.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.469-5889C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 446821 | |||||||
| chr19:446827 | A | T | 82 | a0001c0001t0001g0058 a0001c0001t0001g0147 a0001c0001t0001g0178 others(79): Show |
85 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.469-5895T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 446827 | |||||||
| chr19:446840 | G | A | 1 | a0001c0005t0005g0019 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.469-5908C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 446840 | |||||||
| chr19:446887 | A | G | 86 | a0001c0001t0001g0058 a0001c0001t0001g0147 a0001c0001t0001g0178 others(83): Show |
89 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.469-5955T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 446887 | |||||||
| chr19:447078 | A | G | 1 | a0003c0008t0005g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.469-6146T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447078 | |||||||
| chr19:447089 | C | T | 1 | a0001c0017t0005g0055 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.469-6157G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447089 | |||||||
| chr19:447105 | T | C | 1 | a0001c0001t0016g0069 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.469-6173A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447105 | |||||||
| chr19:447262 | T | C | 3 | a0001c0001t0006g0042 a0001c0007t0003g0039 a0001c0007t0006g0041 |
3 | HG02976.hp1 HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.469-6330A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447262 | |||||||
| chr19:447286 | G | A | 4 | a0001c0001t0011g0034 a0001c0007t0002g0077 a0001c0007t0006g0033 others(1): Show |
4 | HG02451.hp2 HG02486.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.469-6354C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447286 | |||||||
| chr19:447307 | G | C | 1 | a0001c0023t0007g0187 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.469-6375C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447307 | |||||||
| chr19:447314 | A | G | 1 | a0001c0002t0001g0082 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.469-6382T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447314 | |||||||
| chr19:447320 | G | C | 30 | a0001c0001t0001g0147 a0001c0001t0002g0076 a0001c0001t0003g0005 others(27): Show |
32 | HG00423.hp2 HG00621.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.469-6388C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447320 | |||||||
| chr19:447402 | C | A | 2 | a0001c0001t0002g0101 a0009c0021t0002g0028 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.469-6470G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447402 | |||||||
| chr19:447550 | G | A | 15 | a0001c0001t0002g0035 a0001c0001t0002g0051 a0001c0001t0002g0056 others(12): Show |
15 | HG02559.hp1 HG02572.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.469-6618C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447550 | |||||||
| chr19:447570 | G | A | 1 | a0002c0004t0005g0204 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.469-6638C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447570 | |||||||
| chr19:447641 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.469-6709C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447641 | |||||||
| chr19:447710 | G | A | 1 | a0011c0022t0002g0185 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.469-6778C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447710 | |||||||
| chr19:447727 | G | A | 2 | a0001c0001t0002g0076 a0001c0001t0013g0072 |
2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.469-6795C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447727 | |||||||
| chr19:447777 | T | TA | 40 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(37): Show |
42 | HG00423.hp1 HG00423.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.469-6846dupT | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447777 | |||||||
| chr19:447785 | A | T | 2 | a0001c0005t0006g0008 a0001c0007t0006g0054 |
2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.469-6853T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447785 | |||||||
| chr19:447848 | C | A | 2 | a0001c0002t0001g0094 a0001c0002t0001g0095 |
2 | HG03831.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.469-6916G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447848 | |||||||
| chr19:447964 | C | G | 5 | a0001c0001t0003g0172 a0001c0001t0006g0030 a0001c0017t0005g0055 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.469-7032G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 447964 | |||||||
| chr19:448041 | C | T | 60 | a0001c0001t0001g0058 a0001c0001t0001g0147 a0001c0001t0002g0076 others(57): Show |
64 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.469-7109G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448041 | |||||||
| chr19:448064 | G | A | 26 | a0001c0001t0001g0147 a0001c0001t0002g0076 a0001c0001t0003g0005 others(23): Show |
28 | HG00423.hp2 HG00621.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.469-7132C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448064 | |||||||
| chr19:448093 | G | A | 1 | a0001c0002t0001g0093 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.469-7161C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448093 | |||||||
| chr19:448106 | C | T | 1 | a0005c0009t0014g0036 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.469-7174G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448106 | |||||||
| chr19:448109 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.469-7177G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448109 | |||||||
| chr19:448123 | C | T | 7 | a0001c0001t0003g0172 a0001c0001t0004g0029 a0001c0001t0006g0030 others(4): Show |
7 | HG01884.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.469-7191G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448123 | |||||||
| chr19:448173 | T | C | 91 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0081 others(88): Show |
93 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.469-7241A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448173 | |||||||
| chr19:448177 | C | A | 91 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0081 others(88): Show |
93 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.469-7245G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448177 | |||||||
| chr19:448253 | C | G | 3 | a0001c0001t0001g0089 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | HG00609.hp1 NA18985.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.469-7321G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448253 | |||||||
| chr19:448271 | G | A | 2 | a0001c0001t0001g0099 a0001c0002t0001g0169 |
2 | HG02027.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.469-7339C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448271 | |||||||
| chr19:448289 | A | G | 139 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0081 others(136): Show |
143 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.469-7357T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448289 | |||||||
| chr19:448292 | G | A | 2 | a0001c0001t0002g0035 a0001c0001t0007g0038 |
2 | HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.469-7360C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448292 | |||||||
| chr19:448342 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.469-7410G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448342 | |||||||
| chr19:448395 | C | T | 61 | a0001c0001t0001g0043 a0001c0001t0001g0081 a0001c0001t0001g0083 others(58): Show |
61 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.469-7463G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448395 | |||||||
| chr19:448408 | G | A | 1 | a0001c0001t0005g0053 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.469-7476C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448408 | |||||||
| chr19:448463 | CTCT | C | 15 | a0001c0001t0002g0035 a0001c0001t0002g0051 a0001c0001t0002g0056 others(12): Show |
15 | HG02559.hp1 HG02572.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.469-7534_469-7532d others(5): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448463 | |||||||
| chr19:448598 | C | T | 4 | a0001c0001t0003g0172 a0001c0001t0006g0030 a0001c0017t0005g0055 others(1): Show |
4 | HG01884.hp2 HG02486.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.469-7666G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448598 | |||||||
| chr19:448696 | C | T | 23 | a0001c0001t0002g0035 a0001c0001t0002g0051 a0001c0001t0002g0056 others(20): Show |
23 | HG02145.hp1 HG02451.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.469-7764G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448696 | |||||||
| chr19:448700 | T | A | 23 | a0001c0001t0002g0035 a0001c0001t0002g0051 a0001c0001t0002g0056 others(20): Show |
23 | HG02145.hp1 HG02451.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.469-7768A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448700 | |||||||
| chr19:448773 | G | A | 1 | a0001c0001t0004g0029 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.469-7841C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448773 | |||||||
| chr19:448874 | C | T | 2 | a0001c0001t0003g0172 a0002c0004t0001g0193 |
2 | HG00639.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.469-7942G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448874 | |||||||
| chr19:448932 | G | A | 1 | a0005c0009t0014g0036 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.469-8000C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448932 | |||||||
| chr19:448940 | T | C | 143 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0081 others(140): Show |
147 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.469-8008A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448940 | |||||||
| chr19:448970 | T | C | 1 | a0001c0006t0006g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.469-8038A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448970 | |||||||
| chr19:448997 | AAAAAATA others(1): Show |
A | 12 | a0001c0001t0002g0035 a0001c0001t0002g0051 a0001c0001t0002g0056 others(9): Show |
12 | HG02559.hp1 HG02572.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.469-8073_469-8066d others(10): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 448997 | |||||||
| chr19:449146 | C | T | 2 | a0001c0001t0001g0058 a0001c0003t0001g0064 |
2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.469-8214G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 449146 | |||||||
| chr19:449175 | T | A | 139 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0081 others(136): Show |
143 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.469-8243A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 449175 | |||||||
| chr19:449252 | A | G | 147 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0081 others(144): Show |
151 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.469-8320T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 449252 | |||||||
| chr19:449289 | C | T | 1 | a0001c0005t0001g0011 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.469-8357G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 449289 | |||||||
| chr19:449357 | C | A | 1 | a0001c0002t0001g0086 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.469-8425G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 449357 | |||||||
| chr19:449367 | G | C | 1 | a0001c0002t0001g0086 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.469-8435C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 449367 | |||||||
| chr19:449459 | G | A | 10 | a0001c0001t0002g0035 a0001c0001t0002g0056 a0001c0001t0002g0101 others(7): Show |
10 | HG02572.hp1 HG02572.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-8527C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 449459 | |||||||
| chr19:449483 | T | C | 2 | a0001c0002t0001g0153 a0001c0002t0001g0154 |
2 | HG02015.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.469-8551A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 449483 | |||||||
| chr19:449591 | G | A | 1 | a0001c0017t0005g0055 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.469-8659C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 449591 | |||||||
| chr19:449627 | G | A | 2 | a0001c0002t0001g0108 a0001c0003t0002g0112 |
2 | HG00544.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.469-8695C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 449627 | |||||||
| chr19:449659 | C | G | 150 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0081 others(147): Show |
154 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.469-8727G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 449659 | |||||||
| chr19:449822 | G | A | 3 | a0003c0008t0003g0184 a0003c0008t0005g0183 a0003c0008t0006g0186 |
3 | HG02145.hp1 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.469-8890C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 449822 | |||||||
| chr19:449920 | G | A | 1 | a0001c0005t0006g0008 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.469-8988C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 449920 | |||||||
| chr19:449982 | C | A | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-9050G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 449982 | |||||||
| chr19:450013 | A | G | 26 | a0001c0001t0001g0099 a0001c0001t0003g0172 a0001c0001t0004g0029 others(23): Show |
26 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.469-9081T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450013 | |||||||
| chr19:450051 | C | T | 3 | a0001c0001t0001g0081 a0001c0002t0001g0082 a0001c0002t0001g0088 |
3 | HG01978.hp2 HG02004.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.469-9119G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450051 | |||||||
| chr19:450055 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.469-9123G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450055 | |||||||
| chr19:450056 | G | A | 5 | a0001c0002t0001g0155 a0001c0002t0001g0156 a0003c0008t0003g0184 others(2): Show |
5 | HG00423.hp2 HG02145.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.469-9124C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450056 | |||||||
| chr19:450067 | T | C | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-9135A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450067 | |||||||
| chr19:450068 | G | A | 3 | a0003c0008t0003g0184 a0003c0008t0005g0183 a0003c0008t0006g0186 |
3 | HG02145.hp1 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.469-9136C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450068 | |||||||
| chr19:450117 | C | T | 2 | a0001c0001t0002g0101 a0009c0021t0002g0028 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.469-9185G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450117 | |||||||
| chr19:450120 | G | A | 20 | a0001c0001t0001g0099 a0001c0001t0003g0172 a0001c0001t0004g0164 others(17): Show |
20 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.469-9188C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450120 | |||||||
| chr19:450149 | G | A | 1 | a0001c0002t0001g0157 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.469-9217C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450149 | |||||||
| chr19:450165 | G | A | 3 | a0003c0008t0003g0184 a0003c0008t0005g0183 a0003c0008t0006g0186 |
3 | HG02145.hp1 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.469-9233C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450165 | |||||||
| chr19:450168 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.469-9236C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450168 | |||||||
| chr19:450180 | G | A | 20 | a0001c0001t0001g0099 a0001c0001t0003g0172 a0001c0001t0004g0164 others(17): Show |
20 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.469-9248C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450180 | |||||||
| chr19:450219 | G | A | 1 | a0001c0001t0005g0053 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.469-9287C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450219 | |||||||
| chr19:450231 | A | G | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-9299T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450231 | |||||||
| chr19:450238 | T | G | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-9306A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450238 | |||||||
| chr19:450282 | C | T | 19 | a0001c0001t0001g0099 a0001c0001t0003g0172 a0001c0001t0004g0164 others(16): Show |
19 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.469-9350G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450282 | |||||||
| chr19:450294 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.469-9362G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450294 | |||||||
| chr19:450302 | A | G | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-9370T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450302 | |||||||
| chr19:450393 | C | T | 1 | a0002c0012t0002g0205 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.469-9461G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450393 | |||||||
| chr19:450489 | A | G | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-9557T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450489 | |||||||
| chr19:450493 | CACTT | C | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-9565_469-9562d others(6): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450493 | |||||||
| chr19:450507 | C | T | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-9575G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450507 | |||||||
| chr19:450515 | C | T | 19 | a0001c0001t0001g0099 a0001c0001t0003g0172 a0001c0001t0004g0164 others(16): Show |
19 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.469-9583G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450515 | |||||||
| chr19:450626 | C | T | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-9694G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450626 | |||||||
| chr19:450627 | A | G | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-9695T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450627 | |||||||
| chr19:450643 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.469-9711G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450643 | |||||||
| chr19:450644 | G | A | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-9712C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450644 | |||||||
| chr19:450715 | C | T | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-9783G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450715 | |||||||
| chr19:450813 | C | T | 7 | a0001c0001t0003g0181 a0001c0001t0004g0031 a0001c0001t0005g0027 others(4): Show |
7 | HG01891.hp1 HG02145.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.468+9716G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450813 | |||||||
| chr19:450814 | G | A | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+9715C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450814 | |||||||
| chr19:450817 | ATATTTCA others(31): Show |
A | 2 | a0001c0002t0001g0094 a0001c0002t0001g0095 |
2 | HG03831.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.468+9674_468+9711d others(40): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450817 | |||||||
| chr19:450882 | G | A | 3 | a0003c0008t0003g0184 a0003c0008t0005g0183 a0003c0008t0006g0186 |
3 | HG02145.hp1 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.468+9647C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450882 | |||||||
| chr19:450916 | T | C | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+9613A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450916 | |||||||
| chr19:450927 | T | C | 25 | a0001c0001t0001g0043 a0001c0001t0001g0099 a0001c0001t0003g0172 others(22): Show |
25 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.468+9602A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450927 | |||||||
| chr19:450931 | A | G | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+9598T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450931 | |||||||
| chr19:450941 | G | A | 1 | a0001c0001t0003g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.468+9588C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 450941 | |||||||
| chr19:451005 | C | A | 1 | a0001c0002t0004g0158 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.468+9524G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451005 | |||||||
| chr19:451007 | G | A | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+9522C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451007 | |||||||
| chr19:451033 | C | T | 1 | a0001c0001t0002g0051 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.468+9496G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451033 | |||||||
| chr19:451055 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.468+9474C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451055 | |||||||
| chr19:451069 | G | A | 2 | a0001c0001t0005g0046 a0002c0004t0005g0188 |
2 | HG03017.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.468+9460C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451069 | |||||||
| chr19:451072 | G | A | 8 | a0001c0001t0001g0043 a0001c0001t0003g0181 a0001c0001t0004g0031 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.468+9457C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451072 | |||||||
| chr19:451079 | C | T | 3 | a0003c0008t0003g0184 a0003c0008t0005g0183 a0003c0008t0006g0186 |
3 | HG02145.hp1 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.468+9450G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451079 | |||||||
| chr19:451083 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.468+9446C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451083 | |||||||
| chr19:451089 | T | C | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+9440A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451089 | |||||||
| chr19:451093 | G | GTGTGGAT others(69): Show |
6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+9435_468+9436i others(78): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451093 | |||||||
| chr19:451158 | T | C | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+9371A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451158 | |||||||
| chr19:451206 | CGTGTGGA others(31): Show |
C | 18 | a0001c0001t0001g0099 a0001c0001t0003g0172 a0001c0001t0004g0164 others(15): Show |
18 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.468+9285_468+9322d others(40): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451206 | |||||||
| chr19:451259 | G | A | 18 | a0001c0001t0001g0099 a0001c0001t0003g0172 a0001c0001t0004g0164 others(15): Show |
18 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.468+9270C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451259 | |||||||
| chr19:451261 | C | T | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+9268G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451261 | |||||||
| chr19:451264 | G | T | 1 | a0001c0001t0001g0043 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.468+9265C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451264 | |||||||
| chr19:451320 | C | G | 43 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0085 others(40): Show |
43 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.468+9209G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451320 | |||||||
| chr19:451335 | G | A | 7 | a0001c0001t0004g0029 a0001c0003t0010g0059 a0001c0005t0015g0007 others(4): Show |
7 | HG00621.hp1 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.468+9194C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451335 | |||||||
| chr19:451339 | TGGCTGTG others(32): Show |
T | 1 | a0001c0002t0001g0004 | 2 | NA18939.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.468+9151_468+9189d others(41): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451339 | |||||||
| chr19:451377 | TG | T | 147 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0081 others(144): Show |
150 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.468+9151delC | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451377 | |||||||
| chr19:451388 | G | A | 6 | a0001c0003t0002g0065 a0001c0003t0002g0068 a0001c0003t0002g0073 others(3): Show |
6 | HG03225.hp1 NA18954.hp2 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+9141C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451388 | |||||||
| chr19:451465 | G | A | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+9064C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451465 | |||||||
| chr19:451583 | C | G | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+8946G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451583 | |||||||
| chr19:451666 | C | T | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+8863G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451666 | |||||||
| chr19:451746 | C | T | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+8783G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451746 | |||||||
| chr19:451814 | G | C | 9 | a0001c0001t0004g0029 a0001c0002t0002g0045 a0001c0005t0015g0007 others(6): Show |
9 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.468+8715C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451814 | |||||||
| chr19:451849 | T | A | 147 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0081 others(144): Show |
151 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.468+8680A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451849 | |||||||
| chr19:451876 | A | C | 147 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0081 others(144): Show |
151 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.468+8653T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451876 | |||||||
| chr19:451908 | A | G | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+8621T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451908 | |||||||
| chr19:451959 | G | A | 3 | a0001c0002t0002g0045 a0001c0007t0002g0077 a0002c0024t0003g0200 |
3 | NA18906.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.468+8570C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451959 | |||||||
| chr19:451981 | G | A | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+8548C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 451981 | |||||||
| chr19:452062 | C | T | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+8467G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452062 | |||||||
| chr19:452105 | T | C | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+8424A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452105 | |||||||
| chr19:452197 | G | A | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+8332C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452197 | |||||||
| chr19:452226 | C | T | 1 | a0001c0001t0003g0032 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.468+8303G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452226 | |||||||
| chr19:452244 | G | A | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+8285C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452244 | |||||||
| chr19:452252 | G | A | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+8277C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452252 | |||||||
| chr19:452270 | G | A | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+8259C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452270 | |||||||
| chr19:452270 | GTTTCATT others(188): Show |
G | 1 | a0001c0001t0001g0043 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.468+8064_468+8258d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452270 | |||||||
| chr19:452296 | T | C | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+8233A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452296 | |||||||
| chr19:452309 | G | GTTCCTGC others(58): Show |
1 | a0001c0001t0001g0098 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.468+8155_468+8219d others(67): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452309 | |||||||
| chr19:452309 | GTTCCTGC others(58): Show |
G | 19 | a0001c0001t0001g0099 a0001c0001t0003g0172 a0001c0001t0004g0164 others(16): Show |
19 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.468+8155_468+8219d others(67): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452309 | |||||||
| chr19:452320 | G | A | 16 | a0001c0001t0001g0147 a0001c0001t0003g0005 a0001c0001t0005g0102 others(13): Show |
17 | HG00423.hp2 HG01071.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+8209C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452320 | |||||||
| chr19:452335 | GTTTCATT others(123): Show |
G | 5 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(2): Show |
5 | HG02145.hp1 HG02818.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+8064_468+8193d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452335 | |||||||
| chr19:452374 | A | G | 5 | a0001c0001t0005g0053 a0001c0007t0002g0077 a0002c0024t0003g0200 others(2): Show |
5 | HG02559.hp2 NA18522.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+8155T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452374 | |||||||
| chr19:452381 | C | T | 41 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0085 others(38): Show |
42 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.468+8148G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452381 | |||||||
| chr19:452382 | G | A | 1 | a0003c0008t0005g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.468+8147C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452382 | |||||||
| chr19:452385 | G | A | 1 | a0001c0002t0003g0160 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.468+8144C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452385 | |||||||
| chr19:452422 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.468+8107C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452422 | |||||||
| chr19:452447 | A | G | 2 | a0001c0001t0001g0003 a0001c0003t0001g0064 |
3 | HG01256.hp1 HG01258.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.468+8082T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452447 | |||||||
| chr19:452449 | A | G | 18 | a0001c0001t0001g0099 a0001c0001t0003g0172 a0001c0001t0004g0164 others(15): Show |
18 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.468+8080T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452449 | |||||||
| chr19:452478 | T | C | 2 | a0001c0001t0001g0058 a0001c0003t0001g0064 |
2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.468+8051A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452478 | |||||||
| chr19:452486 | C | T | 17 | a0001c0001t0001g0099 a0001c0001t0003g0172 a0001c0001t0004g0164 others(14): Show |
17 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.468+8043G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452486 | |||||||
| chr19:452512 | G | A | 5 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(2): Show |
5 | HG02145.hp1 HG02818.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+8017C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452512 | |||||||
| chr19:452595 | G | A | 18 | a0001c0001t0001g0099 a0001c0001t0003g0172 a0001c0001t0004g0164 others(15): Show |
18 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.468+7934C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452595 | |||||||
| chr19:452745 | G | T | 7 | a0001c0001t0001g0043 a0001c0001t0004g0029 a0001c0005t0015g0007 others(4): Show |
7 | HG02145.hp1 HG02165.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.468+7784C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452745 | |||||||
| chr19:452803 | C | T | 2 | a0001c0001t0002g0101 a0009c0021t0002g0028 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.468+7726G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452803 | |||||||
| chr19:452975 | C | T | 1 | a0002c0012t0004g0195 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.468+7554G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452975 | |||||||
| chr19:452976 | G | A | 3 | a0003c0008t0003g0184 a0003c0008t0005g0183 a0003c0008t0006g0186 |
3 | HG02145.hp1 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.468+7553C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 452976 | |||||||
| chr19:453105 | A | G | 182 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0058 others(179): Show |
187 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.468+7424T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 453105 | |||||||
| chr19:453127 | T | C | 188 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0058 others(185): Show |
193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.468+7402A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 453127 | |||||||
| chr19:453160 | A | G | 187 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0058 others(184): Show |
192 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.468+7369T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 453160 | |||||||
| chr19:453389 | T | C | 188 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0058 others(185): Show |
193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.468+7140A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 453389 | |||||||
| chr19:453397 | A | G | 187 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0058 others(184): Show |
192 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.468+7132T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 453397 | |||||||
| chr19:453439 | T | G | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+7090A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 453439 | |||||||
| chr19:453478 | C | T | 1 | a0001c0001t0004g0164 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.468+7051G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 453478 | |||||||
| chr19:453687 | G | T | 185 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0058 others(182): Show |
190 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.468+6842C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 453687 | |||||||
| chr19:453731 | C | T | 1 | a0002c0004t0005g0189 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.468+6798G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 453731 | |||||||
| chr19:453750 | T | G | 190 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0058 others(187): Show |
195 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.468+6779A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 453750 | |||||||
| chr19:453782 | C | A | 24 | a0001c0001t0001g0058 a0001c0001t0004g0002 a0001c0003t0001g0060 others(21): Show |
26 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.468+6747G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 453782 | |||||||
| chr19:453794 | G | A | 7 | a0001c0001t0003g0181 a0001c0001t0004g0031 a0001c0001t0005g0027 others(4): Show |
7 | HG01891.hp1 HG02145.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.468+6735C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 453794 | |||||||
| chr19:453826 | A | G | 190 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0058 others(187): Show |
195 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.468+6703T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 453826 | |||||||
| chr19:453898 | G | A | 6 | a0001c0001t0004g0029 a0001c0005t0015g0007 a0003c0008t0003g0184 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+6631C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 453898 | |||||||
| chr19:454015 | A | G | 1 | a0001c0001t0002g0051 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.468+6514T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 454015 | |||||||
| chr19:454351 | C | A | 3 | a0003c0008t0003g0184 a0003c0008t0005g0183 a0003c0008t0006g0186 |
3 | HG02145.hp1 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.468+6178G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 454351 | |||||||
| chr19:454430 | G | A | 56 | a0001c0001t0001g0003 a0001c0001t0001g0078 a0001c0001t0001g0089 others(53): Show |
57 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.468+6099C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 454430 | |||||||
| chr19:454524 | C | T | 8 | a0001c0001t0003g0181 a0001c0001t0004g0031 a0001c0001t0005g0027 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+6005G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 454524 | |||||||
| chr19:454605 | G | A | 1 | a0001c0001t0004g0031 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.468+5924C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 454605 | |||||||
| chr19:454658 | C | T | 1 | a0001c0002t0002g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.468+5871G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 454658 | |||||||
| chr19:454668 | T | C | 1 | a0001c0002t0002g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.468+5861A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 454668 | |||||||
| chr19:454738 | C | T | 3 | a0001c0001t0002g0056 a0001c0001t0003g0049 a0001c0001t0006g0050 |
3 | HG02970.hp1 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.468+5791G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 454738 | |||||||
| chr19:454751 | C | T | 1 | a0007c0025t0001g0207 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.468+5778G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 454751 | |||||||
| chr19:454790 | CA | C | 86 | a0001c0001t0001g0003 a0001c0001t0001g0078 a0001c0001t0001g0089 others(83): Show |
87 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.468+5738delT | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 454790 | |||||||
| chr19:454821 | C | T | 45 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0103 others(42): Show |
46 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.468+5708G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 454821 | |||||||
| chr19:454849 | G | A | 1 | a0001c0001t0004g0164 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.468+5680C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 454849 | |||||||
| chr19:454943 | C | T | 9 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0002t0001g0173 others(6): Show |
9 | HG00423.hp1 HG00544.hp2 HG03942.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+5586G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 454943 | |||||||
| chr19:454955 | C | G | 24 | a0001c0001t0001g0058 a0001c0001t0004g0002 a0001c0002t0001g0108 others(21): Show |
26 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.468+5574G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 454955 | |||||||
| chr19:455148 | G | A | 1 | a0001c0001t0006g0048 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.468+5381C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 455148 | |||||||
| chr19:455200 | G | A | 3 | a0001c0001t0003g0049 a0001c0001t0006g0050 a0001c0005t0015g0007 |
3 | HG02970.hp1 HG02976.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.468+5329C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 455200 | |||||||
| chr19:455256 | C | T | 1 | a0001c0023t0007g0187 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.468+5273G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 455256 | |||||||
| chr19:455285 | G | A | 3 | a0001c0001t0001g0163 a0001c0001t0004g0162 a0001c0001t0004g0164 |
3 | HG00733.hp1 HG01981.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.468+5244C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 455285 | |||||||
| chr19:455488 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.468+5041G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 455488 | |||||||
| chr19:455661 | A | G | 39 | a0001c0001t0001g0058 a0001c0001t0002g0051 a0001c0001t0003g0070 others(36): Show |
41 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.468+4868T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 455661 | |||||||
| chr19:455663 | G | A | 2 | a0001c0005t0005g0019 a0001c0005t0006g0009 |
2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.468+4866C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 455663 | |||||||
| chr19:455664 | C | T | 1 | a0001c0023t0007g0187 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.468+4865G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 455664 | |||||||
| chr19:455757 | G | C | 22 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0085 others(19): Show |
23 | HG00558.hp2 HG00621.hp2 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.468+4772C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 455757 | |||||||
| chr19:455878 | C | A | 19 | a0001c0001t0003g0172 a0001c0005t0001g0011 a0001c0005t0001g0012 others(16): Show |
19 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.468+4651G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 455878 | |||||||
| chr19:455957 | G | C | 1 | a0009c0021t0002g0028 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.468+4572C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 455957 | |||||||
| chr19:455957 | G | GC | 77 | a0001c0001t0001g0058 a0001c0001t0001g0178 a0001c0001t0001g0179 others(74): Show |
79 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.468+4571_468+4572i others(3): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 455957 | |||||||
| chr19:455993 | C | A | 2 | a0001c0001t0001g0043 a0001c0002t0003g0044 |
2 | HG02165.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.468+4536G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 455993 | |||||||
| chr19:456054 | A | G | 10 | a0001c0001t0002g0035 a0001c0001t0005g0027 a0001c0001t0005g0037 others(7): Show |
10 | HG01891.hp1 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.468+4475T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456054 | |||||||
| chr19:456118 | T | C | 1 | a0001c0001t0001g0165 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.468+4411A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456118 | |||||||
| chr19:456165 | C | T | 3 | a0001c0003t0010g0059 a0001c0020t0001g0105 a0007c0025t0001g0207 |
3 | HG00621.hp1 HG01099.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.468+4364G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456165 | |||||||
| chr19:456177 | G | A | 7 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(4): Show |
7 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.468+4352C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456177 | |||||||
| chr19:456180 | G | A | 18 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(15): Show |
18 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.468+4349C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456180 | |||||||
| chr19:456286 | T | C | 56 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0178 others(53): Show |
58 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.468+4243A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456286 | |||||||
| chr19:456302 | T | C | 80 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0178 others(77): Show |
82 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.468+4227A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456302 | |||||||
| chr19:456358 | G | C | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+4171C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456358 | |||||||
| chr19:456440 | C | T | 48 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0178 others(45): Show |
50 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.468+4089G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456440 | |||||||
| chr19:456441 | G | A | 1 | a0001c0001t0009g0166 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.468+4088C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456441 | |||||||
| chr19:456516 | C | T | 8 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0002t0001g0173 others(5): Show |
8 | HG00423.hp1 HG03942.hp2 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.468+4013G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456516 | |||||||
| chr19:456655 | C | T | 2 | a0001c0001t0006g0042 a0001c0007t0006g0041 |
2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.468+3874G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456655 | |||||||
| chr19:456682 | G | A | 1 | a0001c0002t0002g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.468+3847C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456682 | |||||||
| chr19:456736 | C | T | 20 | a0001c0001t0001g0058 a0001c0001t0003g0070 a0001c0001t0004g0002 others(17): Show |
22 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.468+3793G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456736 | |||||||
| chr19:456738 | C | G | 1 | a0001c0001t0001g0104 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.468+3791G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456738 | |||||||
| chr19:456739 | G | A | 16 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(13): Show |
16 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.468+3790C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456739 | |||||||
| chr19:456768 | C | A | 4 | a0001c0001t0002g0035 a0001c0001t0011g0034 a0001c0007t0006g0033 others(1): Show |
4 | HG02451.hp2 HG02486.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.468+3761G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456768 | |||||||
| chr19:456776 | A | AGAACTCT others(51): Show |
4 | a0002c0004t0001g0190 a0002c0004t0001g0192 a0002c0004t0001g0193 others(1): Show |
4 | HG00639.hp1 HG01358.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.468+3695_468+3752d others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456776 | |||||||
| chr19:456776 | AGAACTCT others(51): Show |
A | 16 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0003g0032 others(13): Show |
16 | HG00423.hp1 HG01258.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.468+3695_468+3752d others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456776 | |||||||
| chr19:456828 | CTGCCTGG others(52): Show |
C | 4 | a0001c0001t0002g0035 a0001c0001t0011g0034 a0001c0007t0006g0033 others(1): Show |
4 | HG02451.hp2 HG02486.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.468+3642_468+3700d others(61): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456828 | |||||||
| chr19:456834 | G | A | 26 | a0001c0001t0001g0058 a0001c0001t0002g0076 a0001c0001t0003g0070 others(23): Show |
28 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.468+3695C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456834 | |||||||
| chr19:456834 | G | GGAACTCT others(482): Show |
16 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(13): Show |
16 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.468+3694_468+3695i others(491): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456834 | |||||||
| chr19:456834 | G | GGAACTCT others(482): Show |
1 | a0001c0005t0006g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.468+3694_468+3695i others(491): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456834 | |||||||
| chr19:456847 | C | T | 33 | a0001c0001t0002g0076 a0001c0001t0003g0070 a0001c0001t0004g0002 others(30): Show |
35 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.468+3682G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456847 | |||||||
| chr19:456849 | AT | A | 33 | a0001c0001t0002g0076 a0001c0001t0003g0070 a0001c0001t0004g0002 others(30): Show |
35 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.468+3679delA | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456849 | |||||||
| chr19:456850 | T | A | 1 | a0001c0001t0001g0058 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.468+3679A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456850 | |||||||
| chr19:456851 | C | A | 33 | a0001c0001t0002g0076 a0001c0001t0003g0070 a0001c0001t0004g0002 others(30): Show |
35 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.468+3678G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456851 | |||||||
| chr19:456858 | A | G | 33 | a0001c0001t0002g0076 a0001c0001t0003g0070 a0001c0001t0004g0002 others(30): Show |
35 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.468+3671T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456858 | |||||||
| chr19:456860 | G | A | 1 | a0001c0001t0001g0058 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.468+3669C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456860 | |||||||
| chr19:456862 | G | C | 1 | a0001c0001t0001g0058 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.468+3667C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456862 | |||||||
| chr19:456863 | G | A | 1 | a0001c0001t0001g0058 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.468+3666C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456863 | |||||||
| chr19:456875 | CTGCTGTG others(44): Show |
C | 1 | a0001c0001t0001g0058 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.468+3603_468+3653d others(53): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456875 | |||||||
| chr19:456883 | C | CCCCGCCC others(55): Show |
25 | a0001c0001t0002g0076 a0001c0001t0003g0070 a0001c0001t0004g0002 others(22): Show |
27 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.468+3645_468+3646i others(64): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456883 | |||||||
| chr19:456886 | CT | C | 8 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+3642delA | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456886 | |||||||
| chr19:456887 | T | C | 25 | a0001c0001t0002g0076 a0001c0001t0003g0070 a0001c0001t0004g0002 others(22): Show |
27 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.468+3642A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456887 | |||||||
| chr19:456905 | T | C | 8 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+3624A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456905 | |||||||
| chr19:456911 | CACTGCGT others(48): Show |
C | 8 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+3563_468+3617d others(57): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456911 | |||||||
| chr19:456914 | T | C | 45 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0035 others(42): Show |
47 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.468+3615A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456914 | |||||||
| chr19:456917 | G | A | 4 | a0001c0001t0005g0053 a0001c0001t0006g0052 a0001c0007t0006g0054 others(1): Show |
4 | HG02622.hp1 HG02922.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.468+3612C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456917 | |||||||
| chr19:456944 | GCC | G | 25 | a0001c0001t0001g0058 a0001c0001t0003g0070 a0001c0001t0004g0002 others(22): Show |
27 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.468+3583_468+3584d others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456944 | |||||||
| chr19:456946 | C | CTAGAACT others(83): Show |
1 | a0001c0001t0002g0076 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.468+3582_468+3583i others(92): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456946 | |||||||
| chr19:456947 | C | A | 2 | a0001c0001t0001g0058 a0001c0001t0002g0076 |
2 | HG01884.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.468+3582G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456947 | |||||||
| chr19:456963 | T | C | 26 | a0001c0001t0001g0058 a0001c0001t0002g0076 a0001c0001t0003g0070 others(23): Show |
28 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.468+3566A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456963 | |||||||
| chr19:456968 | T | A | 8 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+3561A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456968 | |||||||
| chr19:456968 | T | C | 26 | a0001c0001t0001g0058 a0001c0001t0002g0076 a0001c0001t0003g0070 others(23): Show |
28 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.468+3561A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456968 | |||||||
| chr19:456972 | C | CCA | 26 | a0001c0001t0001g0058 a0001c0001t0002g0076 a0001c0001t0003g0070 others(23): Show |
28 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.468+3556_468+3557i others(4): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456972 | |||||||
| chr19:456973 | A | C | 25 | a0001c0001t0002g0076 a0001c0001t0003g0070 a0001c0001t0004g0002 others(22): Show |
27 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.468+3556T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456973 | |||||||
| chr19:456973 | A | T | 1 | a0001c0001t0001g0058 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.468+3556T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456973 | |||||||
| chr19:456973 | AG | A | 8 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+3555delC | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456973 | |||||||
| chr19:456974 | G | A | 26 | a0001c0001t0001g0058 a0001c0001t0002g0076 a0001c0001t0003g0070 others(23): Show |
28 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.468+3555C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456974 | |||||||
| chr19:456994 | G | C | 34 | a0001c0001t0001g0058 a0001c0001t0002g0076 a0001c0001t0003g0070 others(31): Show |
36 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.468+3535C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 456994 | |||||||
| chr19:457002 | G | A | 9 | a0001c0001t0001g0058 a0001c0001t0005g0027 a0001c0001t0005g0037 others(6): Show |
9 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+3527C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457002 | |||||||
| chr19:457007 | G | C | 8 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+3522C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457007 | |||||||
| chr19:457008 | C | A | 25 | a0001c0001t0002g0076 a0001c0001t0003g0070 a0001c0001t0004g0002 others(22): Show |
27 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.468+3521G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457008 | |||||||
| chr19:457014 | A | T | 9 | a0001c0001t0001g0058 a0001c0001t0005g0027 a0001c0001t0005g0037 others(6): Show |
9 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+3515T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457014 | |||||||
| chr19:457024 | T | C | 34 | a0001c0001t0001g0058 a0001c0001t0002g0076 a0001c0001t0003g0070 others(31): Show |
36 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.468+3505A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457024 | |||||||
| chr19:457027 | A | AC | 25 | a0001c0001t0002g0076 a0001c0001t0003g0070 a0001c0001t0004g0002 others(22): Show |
27 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.468+3501dupG | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457027 | |||||||
| chr19:457034 | G | A | 34 | a0001c0001t0001g0058 a0001c0001t0002g0076 a0001c0001t0003g0070 others(31): Show |
36 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.468+3495C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457034 | |||||||
| chr19:457035 | C | T | 12 | a0001c0001t0001g0058 a0001c0001t0002g0076 a0001c0001t0005g0027 others(9): Show |
12 | HG01884.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.468+3494G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457035 | |||||||
| chr19:457036 | G | A | 26 | a0001c0001t0001g0058 a0001c0001t0002g0076 a0001c0001t0003g0070 others(23): Show |
28 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.468+3493C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457036 | |||||||
| chr19:457038 | G | C | 34 | a0001c0001t0001g0058 a0001c0001t0002g0076 a0001c0001t0003g0070 others(31): Show |
36 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.468+3491C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457038 | |||||||
| chr19:457039 | G | A | 34 | a0001c0001t0001g0058 a0001c0001t0002g0076 a0001c0001t0003g0070 others(31): Show |
36 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.468+3490C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457039 | |||||||
| chr19:457045 | T | TTGCACC | 13 | a0001c0001t0001g0058 a0001c0001t0002g0076 a0001c0001t0005g0027 others(10): Show |
13 | HG01884.hp1 HG01891.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.468+3478_468+3483d others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457045 | |||||||
| chr19:457046 | T | TGCACCA | 21 | a0001c0001t0003g0070 a0001c0001t0004g0002 a0001c0001t0013g0072 others(18): Show |
23 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.468+3482_468+3483i others(8): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457046 | |||||||
| chr19:457058 | G | A | 3 | a0001c0001t0002g0076 a0001c0001t0005g0046 a0002c0004t0005g0188 |
3 | HG01884.hp1 HG03017.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.468+3471C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457058 | |||||||
| chr19:457063 | G | C | 2 | a0001c0001t0005g0046 a0002c0004t0005g0188 |
2 | HG03017.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.468+3466C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457063 | |||||||
| chr19:457064 | C | A | 22 | a0001c0001t0003g0070 a0001c0001t0004g0002 a0001c0001t0013g0072 others(19): Show |
24 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.468+3465G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457064 | |||||||
| chr19:457064 | C | T | 9 | a0001c0001t0001g0058 a0001c0001t0005g0027 a0001c0001t0005g0037 others(6): Show |
9 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+3465G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457064 | |||||||
| chr19:457064 | CCTAGAAC others(119): Show |
C | 6 | a0001c0001t0002g0056 a0001c0023t0007g0187 a0003c0008t0003g0184 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.468+3339_468+3464d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457064 | |||||||
| chr19:457070 | A | T | 3 | a0001c0001t0002g0076 a0001c0001t0005g0046 a0002c0004t0005g0188 |
3 | HG01884.hp1 HG03017.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.468+3459T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457070 | |||||||
| chr19:457073 | C | A | 1 | a0001c0001t0001g0058 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.468+3456G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457073 | |||||||
| chr19:457083 | AC | A | 3 | a0001c0001t0002g0076 a0001c0001t0005g0046 a0002c0004t0005g0188 |
3 | HG01884.hp1 HG03017.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.468+3445delG | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457083 | |||||||
| chr19:457084 | C | CCCCACCA others(55): Show |
1 | a0001c0002t0002g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.468+3444_468+3445i others(64): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457084 | |||||||
| chr19:457085 | C | T | 8 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+3444G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457085 | |||||||
| chr19:457091 | A | G | 1 | a0001c0001t0001g0058 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.468+3438T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457091 | |||||||
| chr19:457092 | C | CATCAGGC others(54): Show |
1 | a0001c0003t0002g0073 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.468+3436_468+3437i others(63): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457092 | |||||||
| chr19:457092 | C | T | 4 | a0001c0001t0002g0076 a0001c0001t0005g0046 a0001c0002t0002g0045 others(1): Show |
4 | HG01884.hp1 HG03017.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.468+3437G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457092 | |||||||
| chr19:457093 | A | ATCAGGCC others(55): Show |
17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+3435_468+3436i others(64): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457093 | |||||||
| chr19:457096 | A | G | 1 | a0001c0001t0001g0058 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.468+3433T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457096 | |||||||
| chr19:457127 | A | T | 23 | a0001c0001t0001g0058 a0001c0001t0002g0076 a0001c0001t0005g0046 others(20): Show |
23 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.468+3402T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457127 | |||||||
| chr19:457136 | C | A | 5 | a0001c0001t0002g0076 a0001c0001t0005g0046 a0001c0002t0002g0045 others(2): Show |
5 | HG01884.hp1 HG03017.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+3393G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457136 | |||||||
| chr19:457148 | C | T | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+3381G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457148 | |||||||
| chr19:457154 | A | ATATCAGG others(117): Show |
20 | a0001c0001t0003g0070 a0001c0001t0004g0002 a0001c0001t0013g0072 others(17): Show |
22 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.468+3374_468+3375i others(126): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457154 | |||||||
| chr19:457154 | A | G | 5 | a0001c0001t0002g0076 a0001c0001t0005g0046 a0001c0002t0002g0045 others(2): Show |
5 | HG01884.hp1 HG03017.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+3375T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457154 | |||||||
| chr19:457159 | A | G | 25 | a0001c0001t0002g0076 a0001c0001t0003g0070 a0001c0001t0004g0002 others(22): Show |
27 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.468+3370T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457159 | |||||||
| chr19:457172 | A | T | 51 | a0001c0001t0001g0058 a0001c0001t0002g0076 a0001c0001t0003g0070 others(48): Show |
53 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.468+3357T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457172 | |||||||
| chr19:457189 | G | A | 1 | a0001c0007t0002g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.468+3340C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457189 | |||||||
| chr19:457190 | A | T | 25 | a0001c0001t0002g0076 a0001c0001t0003g0070 a0001c0001t0004g0002 others(22): Show |
27 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.468+3339T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457190 | |||||||
| chr19:457196 | A | T | 1 | a0001c0001t0006g0042 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.468+3333T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457196 | |||||||
| chr19:457218 | C | T | 2 | a0001c0001t0001g0058 a0001c0001t0006g0042 |
2 | HG03540.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.468+3311G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457218 | |||||||
| chr19:457247 | G | A | 9 | a0001c0001t0001g0058 a0001c0001t0005g0027 a0001c0001t0005g0037 others(6): Show |
9 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+3282C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457247 | |||||||
| chr19:457252 | G | C | 9 | a0001c0001t0001g0058 a0001c0001t0005g0027 a0001c0001t0005g0037 others(6): Show |
9 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+3277C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457252 | |||||||
| chr19:457253 | A | C | 9 | a0001c0001t0001g0058 a0001c0001t0005g0027 a0001c0001t0005g0037 others(6): Show |
9 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+3276T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457253 | |||||||
| chr19:457253 | A | T | 1 | a0001c0001t0006g0042 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.468+3276T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457253 | |||||||
| chr19:457259 | A | ACTCTGTC others(56): Show |
1 | a0001c0002t0001g0088 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.468+3207_468+3269d others(65): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457259 | |||||||
| chr19:457259 | A | T | 9 | a0001c0001t0001g0058 a0001c0001t0005g0027 a0001c0001t0005g0037 others(6): Show |
9 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+3270T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457259 | |||||||
| chr19:457262 | C | A | 1 | a0001c0001t0006g0042 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.468+3267G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457262 | |||||||
| chr19:457262 | CTGTCTGC others(118): Show |
C | 1 | a0001c0001t0001g0103 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.468+3142_468+3266d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457262 | |||||||
| chr19:457272 | AC | A | 9 | a0001c0001t0001g0058 a0001c0001t0005g0027 a0001c0001t0005g0037 others(6): Show |
9 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+3256delG | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457272 | |||||||
| chr19:457280 | A | G | 1 | a0001c0001t0006g0042 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.468+3249T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457280 | |||||||
| chr19:457281 | C | T | 53 | a0001c0001t0001g0058 a0001c0001t0001g0178 a0001c0001t0001g0179 others(50): Show |
55 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.468+3248G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457281 | |||||||
| chr19:457281 | CATCAGGC others(55): Show |
C | 1 | a0001c0001t0006g0042 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.468+3186_468+3247d others(64): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457281 | |||||||
| chr19:457282 | A | G | 8 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+3247T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457282 | |||||||
| chr19:457310 | A | G | 9 | a0001c0001t0001g0058 a0001c0001t0005g0027 a0001c0001t0005g0037 others(6): Show |
9 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+3219T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457310 | |||||||
| chr19:457315 | C | A | 3 | a0001c0001t0005g0053 a0001c0001t0006g0052 a0001c0007t0006g0054 |
3 | HG02922.hp2 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.468+3214G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457315 | |||||||
| chr19:457315 | C | G | 9 | a0001c0001t0001g0058 a0001c0001t0005g0027 a0001c0001t0005g0037 others(6): Show |
9 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+3214G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457315 | |||||||
| chr19:457316 | C | T | 9 | a0001c0001t0001g0058 a0001c0001t0005g0027 a0001c0001t0005g0037 others(6): Show |
9 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+3213G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457316 | |||||||
| chr19:457317 | CT | C | 4 | a0001c0001t0003g0049 a0001c0001t0006g0048 a0001c0001t0006g0050 others(1): Show |
4 | HG02572.hp1 HG02970.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.468+3211delA | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457317 | |||||||
| chr19:457322 | T | A | 26 | a0001c0001t0001g0058 a0001c0001t0005g0027 a0001c0001t0005g0037 others(23): Show |
26 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.468+3207A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457322 | |||||||
| chr19:457325 | C | A | 9 | a0001c0001t0001g0058 a0001c0001t0005g0027 a0001c0001t0005g0037 others(6): Show |
9 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+3204G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457325 | |||||||
| chr19:457335 | A | AC | 9 | a0001c0001t0001g0058 a0001c0001t0005g0027 a0001c0001t0005g0037 others(6): Show |
9 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+3193dupG | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457335 | |||||||
| chr19:457342 | A | G | 9 | a0001c0001t0001g0058 a0001c0001t0005g0027 a0001c0001t0005g0037 others(6): Show |
9 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+3187T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457342 | |||||||
| chr19:457343 | T | C | 26 | a0001c0001t0001g0058 a0001c0001t0005g0027 a0001c0001t0005g0037 others(23): Show |
26 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.468+3186A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457343 | |||||||
| chr19:457344 | A | G | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+3185T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457344 | |||||||
| chr19:457347 | A | AGGCCTTT others(56): Show |
30 | a0001c0001t0002g0035 a0001c0001t0002g0076 a0001c0001t0003g0070 others(27): Show |
32 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.468+3181_468+3182i others(65): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457347 | |||||||
| chr19:457347 | A | AGGCCTTT others(307): Show |
13 | a0001c0001t0001g0178 a0001c0001t0003g0032 a0001c0001t0003g0172 others(10): Show |
13 | HG01258.hp1 HG02055.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.468+3181_468+3182i others(316): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457347 | |||||||
| chr19:457347 | A | AGGCCTTT others(306): Show |
1 | a0001c0001t0001g0179 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.468+3181_468+3182i others(315): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457347 | |||||||
| chr19:457347 | A | G | 10 | a0001c0001t0001g0058 a0001c0001t0005g0027 a0001c0001t0005g0037 others(7): Show |
10 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.468+3182T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457347 | |||||||
| chr19:457363 | A | ACCTGCTG others(56): Show |
17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+3165_468+3166i others(65): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457363 | |||||||
| chr19:457407 | C | T | 3 | a0001c0001t0002g0101 a0001c0001t0003g0005 a0001c0001t0005g0102 |
4 | HG01891.hp2 HG01978.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.468+3122G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457407 | |||||||
| chr19:457423 | C | T | 44 | a0001c0001t0001g0058 a0001c0001t0001g0178 a0001c0001t0001g0179 others(41): Show |
46 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.468+3106G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457423 | |||||||
| chr19:457720 | T | A | 1 | a0001c0001t0001g0167 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.468+2809A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457720 | |||||||
| chr19:457732 | A | G | 21 | a0001c0001t0002g0035 a0001c0001t0011g0034 a0001c0005t0001g0011 others(18): Show |
21 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.468+2797T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457732 | |||||||
| chr19:457742 | C | T | 8 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+2787G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457742 | |||||||
| chr19:457789 | G | T | 2 | a0001c0001t0001g0043 a0001c0002t0003g0044 |
2 | HG02165.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.468+2740C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457789 | |||||||
| chr19:457801 | C | A | 8 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+2728G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457801 | |||||||
| chr19:457805 | C | T | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2724G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457805 | |||||||
| chr19:457844 | T | C | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2685A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457844 | |||||||
| chr19:457881 | C | G | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2648G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457881 | |||||||
| chr19:457954 | CGGGGAGG others(14): Show |
C | 8 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+2554_468+2574d others(23): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 457954 | |||||||
| chr19:458010 | A | G | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2519T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458010 | |||||||
| chr19:458032 | A | G | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2497T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458032 | |||||||
| chr19:458038 | CGGGGAGG others(14): Show |
C | 1 | a0001c0003t0002g0074 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.468+2470_468+2490d others(23): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458038 | |||||||
| chr19:458045 | G | A | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2484C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458045 | |||||||
| chr19:458047 | G | A | 1 | a0001c0003t0002g0065 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.468+2482C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458047 | |||||||
| chr19:458047 | GGAAGCGG others(56): Show |
G | 1 | a0001c0001t0003g0172 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.468+2419_468+2481d others(65): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458047 | |||||||
| chr19:458052 | C | T | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2477G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458052 | |||||||
| chr19:458057 | C | T | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2472G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458057 | |||||||
| chr19:458058 | T | C | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2471A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458058 | |||||||
| chr19:458059 | T | C | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2470A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458059 | |||||||
| chr19:458067 | C | G | 3 | a0001c0001t0001g0043 a0001c0002t0003g0044 a0002c0004t0001g0206 |
3 | HG02165.hp1 HG03831.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.468+2462G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458067 | |||||||
| chr19:458068 | G | A | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2461C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458068 | |||||||
| chr19:458071 | A | C | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2458T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458071 | |||||||
| chr19:458073 | CGGGTCTT others(14): Show |
C | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2435_468+2455d others(23): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458073 | |||||||
| chr19:458099 | C | T | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2430G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458099 | |||||||
| chr19:458100 | C | T | 1 | a0001c0001t0006g0042 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.468+2429G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458100 | |||||||
| chr19:458101 | CGGGGAGG others(14): Show |
C | 1 | a0001c0001t0005g0046 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.468+2407_468+2427d others(23): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458101 | |||||||
| chr19:458110 | A | G | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2419T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458110 | |||||||
| chr19:458116 | G | T | 11 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0003g0032 others(8): Show |
11 | HG00423.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.468+2413C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458116 | |||||||
| chr19:458121 | T | C | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2408A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458121 | |||||||
| chr19:458122 | T | C | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2407A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458122 | |||||||
| chr19:458144 | G | A | 18 | a0001c0001t0001g0168 a0001c0005t0001g0011 a0001c0005t0001g0012 others(15): Show |
18 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.468+2385C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458144 | |||||||
| chr19:458150 | A | G | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2379T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458150 | |||||||
| chr19:458162 | T | C | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2367A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458162 | |||||||
| chr19:458173 | A | G | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2356T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458173 | |||||||
| chr19:458176 | C | A | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2353G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458176 | |||||||
| chr19:458179 | A | G | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2350T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458179 | |||||||
| chr19:458180 | T | G | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2349A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458180 | |||||||
| chr19:458181 | G | A | 76 | a0001c0001t0001g0003 a0001c0001t0001g0078 a0001c0001t0001g0103 others(73): Show |
78 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.468+2348C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458181 | |||||||
| chr19:458186 | G | A | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2343C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458186 | |||||||
| chr19:458188 | G | A | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2341C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458188 | |||||||
| chr19:458192 | C | G | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2337G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458192 | |||||||
| chr19:458192 | CGGGGAAG others(36): Show |
C | 2 | a0001c0001t0006g0042 a0001c0007t0006g0041 |
2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.468+2294_468+2336d others(45): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458192 | |||||||
| chr19:458231 | C | G | 76 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0178 others(73): Show |
78 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.468+2298G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458231 | |||||||
| chr19:458235 | G | C | 11 | a0001c0005t0001g0015 a0001c0005t0001g0018 a0001c0005t0001g0024 others(8): Show |
11 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.468+2294C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458235 | |||||||
| chr19:458235 | G | T | 6 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0020 others(3): Show |
6 | HG00099.hp2 HG00735.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.468+2294C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458235 | |||||||
| chr19:458250 | C | T | 8 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+2279G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458250 | |||||||
| chr19:458270 | T | C | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2259A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458270 | |||||||
| chr19:458278 | GCGGAAGT others(56): Show |
G | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2188_468+2250d others(65): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458278 | |||||||
| chr19:458285 | TGGGTCCC others(56): Show |
T | 1 | a0001c0003t0002g0075 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.468+2181_468+2243d others(65): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458285 | |||||||
| chr19:458287 | G | A | 37 | a0001c0001t0001g0058 a0001c0001t0001g0178 a0001c0001t0001g0179 others(34): Show |
39 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.468+2242C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458287 | |||||||
| chr19:458322 | GGAAGCGG others(14): Show |
G | 22 | a0001c0001t0001g0058 a0001c0001t0002g0076 a0001c0001t0003g0070 others(19): Show |
24 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.468+2186_468+2206d others(23): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458322 | |||||||
| chr19:458327 | C | T | 148 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0078 others(145): Show |
151 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.468+2202G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458327 | |||||||
| chr19:458341 | A | G | 19 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0035 others(16): Show |
19 | HG00423.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.468+2188T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458341 | |||||||
| chr19:458343 | A | G | 19 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0035 others(16): Show |
19 | HG00423.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.468+2186T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458343 | |||||||
| chr19:458348 | C | T | 22 | a0001c0001t0001g0058 a0001c0001t0002g0076 a0001c0001t0003g0070 others(19): Show |
24 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.468+2181G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458348 | |||||||
| chr19:458355 | C | CG | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2173dupC | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458355 | |||||||
| chr19:458363 | C | G | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2166G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458363 | |||||||
| chr19:458376 | C | T | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2153G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458376 | |||||||
| chr19:458385 | G | A | 12 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0003g0032 others(9): Show |
12 | HG00423.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.468+2144C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458385 | |||||||
| chr19:458389 | T | G | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2140A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458389 | |||||||
| chr19:458397 | C | CG | 16 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(13): Show |
16 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.468+2131dupC | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458397 | |||||||
| chr19:458402 | A | G | 1 | a0001c0006t0006g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.468+2127T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458402 | |||||||
| chr19:458405 | C | G | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2124G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458405 | |||||||
| chr19:458412 | G | A | 1 | a0009c0021t0002g0028 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.468+2117C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458412 | |||||||
| chr19:458414 | G | A | 1 | a0001c0002t0001g0169 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.468+2115C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458414 | |||||||
| chr19:458416 | C | T | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2113G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458416 | |||||||
| chr19:458427 | A | G | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2102T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458427 | |||||||
| chr19:458458 | T | C | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+2071A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458458 | |||||||
| chr19:458469 | AGACGCAT others(78): Show |
A | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1975_468+2059d others(87): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458469 | |||||||
| chr19:458497 | A | G | 52 | a0001c0001t0001g0058 a0001c0001t0001g0178 a0001c0001t0001g0179 others(49): Show |
54 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.468+2032T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458497 | |||||||
| chr19:458498 | G | T | 4 | a0001c0001t0002g0035 a0001c0001t0011g0034 a0001c0007t0006g0033 others(1): Show |
4 | HG02451.hp2 HG02486.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.468+2031C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458498 | |||||||
| chr19:458524 | T | C | 8 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+2005A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458524 | |||||||
| chr19:458545 | CGGGGAGG others(14): Show |
C | 1 | a0009c0021t0002g0028 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.468+1963_468+1983d others(23): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458545 | |||||||
| chr19:458553 | TGGAAGCG others(121): Show |
T | 1 | a0002c0024t0003g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.468+1848_468+1975d others(2): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458553 | |||||||
| chr19:458565 | C | T | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1964G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458565 | |||||||
| chr19:458570 | G | T | 8 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+1959C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458570 | |||||||
| chr19:458574 | C | T | 8 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+1955G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458574 | |||||||
| chr19:458575 | G | A | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1954C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458575 | |||||||
| chr19:458580 | C | T | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1949G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458580 | |||||||
| chr19:458587 | C | T | 3 | a0001c0001t0001g0043 a0001c0002t0003g0044 a0002c0004t0001g0206 |
3 | HG02165.hp1 HG03831.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.468+1942G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458587 | |||||||
| chr19:458594 | C | A | 3 | a0001c0001t0001g0043 a0001c0002t0003g0044 a0002c0004t0001g0206 |
3 | HG02165.hp1 HG03831.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.468+1935G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458594 | |||||||
| chr19:458594 | C | T | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1935G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458594 | |||||||
| chr19:458609 | C | CGGGGAGG others(98): Show |
6 | a0001c0001t0005g0027 a0001c0001t0005g0040 a0001c0001t0007g0038 others(3): Show |
6 | HG01891.hp1 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.468+1919_468+1920i others(107): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458609 | |||||||
| chr19:458609 | C | CGGGGAGG others(99): Show |
1 | a0001c0001t0005g0037 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.468+1919_468+1920i others(108): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458609 | |||||||
| chr19:458610 | A | G | 8 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+1919T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458610 | |||||||
| chr19:458613 | G | GAGGCGGA others(98): Show |
1 | a0001c0005t0006g0008 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.468+1915_468+1916i others(107): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458613 | |||||||
| chr19:458621 | C | A | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1908G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458621 | |||||||
| chr19:458628 | T | C | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1901A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458628 | |||||||
| chr19:458630 | C | T | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1899G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458630 | |||||||
| chr19:458631 | G | A | 8 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0002t0001g0173 others(5): Show |
8 | HG00423.hp1 HG03942.hp2 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.468+1898C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458631 | |||||||
| chr19:458642 | A | G | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1887T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458642 | |||||||
| chr19:458645 | C | G | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1884G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458645 | |||||||
| chr19:458646 | G | A | 8 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+1883C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458646 | |||||||
| chr19:458649 | C | T | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1880G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458649 | |||||||
| chr19:458650 | T | C | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1879A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458650 | |||||||
| chr19:458651 | T | C | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1878A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458651 | |||||||
| chr19:458665 | T | C | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1864A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458665 | |||||||
| chr19:458668 | GT | G | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1860delA | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458668 | |||||||
| chr19:458673 | G | T | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1856C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458673 | |||||||
| chr19:458678 | A | AG | 6 | a0001c0001t0002g0056 a0001c0001t0005g0037 a0001c0002t0001g0088 others(3): Show |
6 | HG01099.hp1 HG01109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.468+1850dupC | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458678 | |||||||
| chr19:458681 | G | C | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1848C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458681 | |||||||
| chr19:458729 | T | C | 1 | a0009c0021t0002g0028 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.468+1800A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458729 | |||||||
| chr19:458736 | C | CG | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1792dupC | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458736 | |||||||
| chr19:458742 | G | C | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1787C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458742 | |||||||
| chr19:458744 | C | G | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1785G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458744 | |||||||
| chr19:458748 | A | G | 7 | a0001c0001t0002g0056 a0001c0017t0005g0055 a0001c0023t0007g0187 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.468+1781T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458748 | |||||||
| chr19:458750 | C | T | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1779G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458750 | |||||||
| chr19:458755 | C | T | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1774G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458755 | |||||||
| chr19:458755 | CCCGGGGA others(14): Show |
C | 3 | a0001c0001t0005g0053 a0001c0001t0006g0052 a0001c0007t0006g0054 |
3 | HG02922.hp2 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.468+1753_468+1773d others(23): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458755 | |||||||
| chr19:458757 | CGGGGAGG others(35): Show |
C | 1 | a0001c0002t0001g0170 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.468+1730_468+1771d others(44): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458757 | |||||||
| chr19:458765 | C | T | 1 | a0002c0004t0001g0193 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.468+1764G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458765 | |||||||
| chr19:458769 | G | A | 7 | a0001c0001t0002g0056 a0001c0017t0005g0055 a0001c0023t0007g0187 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.468+1760C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458769 | |||||||
| chr19:458769 | G | GGCGGGTT others(14): Show |
1 | a0001c0001t0005g0102 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.468+1739_468+1759d others(23): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458769 | |||||||
| chr19:458771 | C | CGGGTTCC others(56): Show |
1 | a0001c0003t0002g0073 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.468+1695_468+1757d others(65): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458771 | |||||||
| chr19:458778 | C | T | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1751G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458778 | |||||||
| chr19:458778 | CGGGGAGG others(14): Show |
C | 2 | a0001c0001t0006g0042 a0001c0002t0003g0174 |
2 | HG03540.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.468+1730_468+1750d others(23): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458778 | |||||||
| chr19:458798 | CTGGGGAG others(14): Show |
C | 1 | a0001c0003t0002g0062 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.468+1710_468+1730d others(23): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458798 | |||||||
| chr19:458829 | G | A | 19 | a0001c0001t0006g0042 a0001c0005t0001g0011 a0001c0005t0001g0012 others(16): Show |
19 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.468+1700C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458829 | |||||||
| chr19:458832 | A | G | 8 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+1697T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458832 | |||||||
| chr19:458841 | C | T | 7 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0085 others(4): Show |
7 | HG01978.hp2 HG02004.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.468+1688G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458841 | |||||||
| chr19:458846 | A | G | 1 | a0001c0001t0002g0076 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.468+1683T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458846 | |||||||
| chr19:458849 | C | G | 1 | a0001c0001t0002g0076 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.468+1680G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458849 | |||||||
| chr19:458852 | A | AGGGGCGG others(28): Show |
1 | a0001c0001t0002g0076 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.468+1676_468+1677i others(37): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458852 | |||||||
| chr19:458853 | A | G | 1 | a0001c0001t0002g0076 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.468+1676T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458853 | |||||||
| chr19:458855 | C | G | 1 | a0001c0001t0002g0076 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.468+1674G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458855 | |||||||
| chr19:458856 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.468+1673C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458856 | |||||||
| chr19:458859 | T | G | 1 | a0001c0001t0002g0076 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.468+1670A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458859 | |||||||
| chr19:458860 | C | A | 1 | a0001c0001t0002g0076 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.468+1669G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458860 | |||||||
| chr19:458861 | C | G | 1 | a0001c0001t0002g0076 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.468+1668G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458861 | |||||||
| chr19:458862 | T | G | 1 | a0001c0001t0002g0076 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.468+1667A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458862 | |||||||
| chr19:458867 | A | G | 1 | a0001c0001t0002g0076 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.468+1662T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458867 | |||||||
| chr19:458882 | G | A | 7 | a0001c0001t0003g0049 a0001c0001t0005g0053 a0001c0001t0006g0048 others(4): Show |
7 | HG02572.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.468+1647C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458882 | |||||||
| chr19:458919 | G | A | 1 | a0002c0012t0002g0205 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.468+1610C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458919 | |||||||
| chr19:458935 | A | G | 87 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0178 others(84): Show |
89 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.468+1594T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458935 | |||||||
| chr19:458993 | C | T | 4 | a0001c0001t0002g0035 a0001c0001t0011g0034 a0001c0007t0006g0033 others(1): Show |
4 | HG02451.hp2 HG02486.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.468+1536G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 458993 | |||||||
| chr19:459074 | T | C | 87 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0178 others(84): Show |
89 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.468+1455A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459074 | |||||||
| chr19:459087 | G | A | 87 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0178 others(84): Show |
89 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.468+1442C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459087 | |||||||
| chr19:459093 | G | A | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1436C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459093 | |||||||
| chr19:459110 | C | T | 8 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0002t0001g0173 others(5): Show |
8 | HG00423.hp1 HG03942.hp2 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.468+1419G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459110 | |||||||
| chr19:459112 | T | C | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1417A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459112 | |||||||
| chr19:459119 | AATATAAG others(2): Show |
A | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1401_468+1409d others(11): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459119 | |||||||
| chr19:459184 | TGTAGGGG others(22): Show |
T | 8 | a0001c0001t0002g0051 a0001c0001t0003g0049 a0001c0001t0005g0053 others(5): Show |
8 | HG02559.hp1 HG02572.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+1316_468+1344d others(31): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459184 | |||||||
| chr19:459208 | C | G | 2 | a0001c0005t0001g0024 a0001c0005t0001g0025 |
2 | HG01109.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.468+1321G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459208 | |||||||
| chr19:459237 | CCCAGCGT others(51): Show |
C | 8 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+1234_468+1291d others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459237 | |||||||
| chr19:459260 | T | A | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1269A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459260 | |||||||
| chr19:459263 | C | G | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1266G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459263 | |||||||
| chr19:459267 | T | C | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1262A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459267 | |||||||
| chr19:459269 | G | A | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1260C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459269 | |||||||
| chr19:459270 | G | A | 2 | a0001c0001t0002g0056 a0001c0023t0007g0187 |
2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.468+1259C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459270 | |||||||
| chr19:459271 | T | C | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1258A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459271 | |||||||
| chr19:459275 | G | GGGGGAAG others(109): Show |
1 | a0001c0005t0001g0025 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.468+1253_468+1254i others(118): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459275 | |||||||
| chr19:459295 | G | C | 1 | a0001c0005t0001g0025 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.468+1234C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459295 | |||||||
| chr19:459295 | G | GCCAGCGT others(109): Show |
1 | a0001c0005t0001g0024 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.468+1233_468+1234i others(118): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459295 | |||||||
| chr19:459324 | C | T | 1 | a0001c0001t0003g0172 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.468+1205G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459324 | |||||||
| chr19:459324 | CCCAGCGT others(22): Show |
C | 5 | a0001c0001t0001g0078 a0001c0001t0002g0035 a0001c0001t0011g0034 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.468+1176_468+1204d others(31): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459324 | |||||||
| chr19:459325 | C | CCAGCGTA others(167): Show |
14 | a0001c0005t0001g0011 a0001c0005t0001g0015 a0001c0005t0001g0018 others(11): Show |
14 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.468+1203_468+1204i others(176): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459325 | |||||||
| chr19:459325 | C | CCAGCGTA others(167): Show |
1 | a0001c0005t0001g0012 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.468+1203_468+1204i others(176): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459325 | |||||||
| chr19:459347 | A | T | 8 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+1182T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459347 | |||||||
| chr19:459350 | G | C | 8 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+1179C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459350 | |||||||
| chr19:459353 | G | C | 27 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(24): Show |
27 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.468+1176C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459353 | |||||||
| chr19:459353 | G | GCCAGCGT others(22): Show |
2 | a0001c0002t0001g0079 a0001c0002t0001g0080 |
2 | HG00558.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.468+1175_468+1176i others(31): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459353 | |||||||
| chr19:459354 | C | T | 23 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(20): Show |
23 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.468+1175G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459354 | |||||||
| chr19:459356 | A | G | 8 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+1173T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459356 | |||||||
| chr19:459358 | C | A | 2 | a0001c0005t0001g0024 a0001c0005t0001g0025 |
2 | HG01109.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.468+1171G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459358 | |||||||
| chr19:459358 | C | T | 23 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(20): Show |
23 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.468+1171G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459358 | |||||||
| chr19:459362 | G | A | 15 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(12): Show |
15 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.468+1167C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459362 | |||||||
| chr19:459362 | G | GGGGGAAG others(51): Show |
2 | a0001c0005t0001g0024 a0001c0005t0001g0025 |
2 | HG01109.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.468+1166_468+1167i others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459362 | |||||||
| chr19:459382 | G | C | 158 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0081 others(155): Show |
162 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.468+1147C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459382 | |||||||
| chr19:459382 | G | GCCAGCGT others(22): Show |
2 | a0001c0002t0001g0079 a0001c0002t0001g0080 |
2 | HG00558.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.468+1118_468+1146d others(31): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459382 | |||||||
| chr19:459410 | A | ACCCAGCG others(51): Show |
10 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(7): Show |
10 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.468+1118_468+1119i others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459410 | |||||||
| chr19:459411 | C | G | 8 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+1118G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459411 | |||||||
| chr19:459431 | C | A | 2 | a0001c0001t0006g0042 a0001c0007t0006g0041 |
2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.468+1098G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459431 | |||||||
| chr19:459441 | CCAGCGTA others(22): Show |
C | 4 | a0001c0001t0002g0035 a0001c0001t0011g0034 a0001c0007t0006g0033 others(1): Show |
4 | HG02451.hp2 HG02486.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.468+1059_468+1087d others(31): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459441 | |||||||
| chr19:459463 | T | A | 25 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(22): Show |
25 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.468+1066A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459463 | |||||||
| chr19:459466 | C | G | 25 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(22): Show |
25 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.468+1063G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459466 | |||||||
| chr19:459468 | A | G | 7 | a0001c0005t0001g0020 a0001c0005t0001g0021 a0001c0005t0001g0024 others(4): Show |
7 | HG00099.hp2 HG00735.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.468+1061T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459468 | |||||||
| chr19:459469 | C | CCCAGCGT others(51): Show |
7 | a0001c0005t0001g0020 a0001c0005t0001g0021 a0001c0005t0001g0024 others(4): Show |
7 | HG00099.hp2 HG00735.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.468+1059_468+1060i others(60): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459469 | |||||||
| chr19:459469 | C | G | 11 | a0001c0003t0001g0063 a0001c0005t0001g0011 a0001c0005t0001g0012 others(8): Show |
11 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.468+1060G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459469 | |||||||
| chr19:459470 | T | C | 25 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(22): Show |
25 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.468+1059A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459470 | |||||||
| chr19:459472 | A | C | 1 | a0001c0007t0006g0041 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.468+1057T>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459472 | |||||||
| chr19:459515 | G | A | 2 | a0001c0001t0002g0076 a0001c0007t0002g0077 |
2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.468+1014C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459515 | |||||||
| chr19:459520 | T | C | 25 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(22): Show |
25 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.468+1009A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459520 | |||||||
| chr19:459521 | T | A | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1008A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459521 | |||||||
| chr19:459524 | C | G | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1005G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459524 | |||||||
| chr19:459524 | CAACTCAG others(22): Show |
C | 8 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+976_468+1004de others(30): Show |
SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459524 | |||||||
| chr19:459527 | C | G | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1002G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459527 | |||||||
| chr19:459528 | T | C | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+1001A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459528 | |||||||
| chr19:459532 | T | C | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+997A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459532 | |||||||
| chr19:459537 | A | G | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+992T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459537 | |||||||
| chr19:459549 | T | C | 21 | a0001c0001t0002g0035 a0001c0001t0011g0034 a0001c0005t0001g0011 others(18): Show |
21 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.468+980A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459549 | |||||||
| chr19:459557 | T | C | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+972A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459557 | |||||||
| chr19:459579 | A | T | 8 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+950T>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459579 | |||||||
| chr19:459582 | G | C | 8 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+947C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459582 | |||||||
| chr19:459615 | T | C | 8 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+914A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459615 | |||||||
| chr19:459619 | T | C | 8 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+910A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459619 | |||||||
| chr19:459623 | A | G | 8 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+906T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459623 | |||||||
| chr19:459707 | T | C | 8 | a0001c0001t0005g0027 a0001c0001t0005g0037 a0001c0001t0005g0040 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+822A>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459707 | |||||||
| chr19:459740 | C | T | 4 | a0001c0001t0003g0049 a0001c0001t0006g0048 a0001c0001t0006g0050 others(1): Show |
4 | HG02572.hp1 HG02970.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.468+789G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459740 | |||||||
| chr19:459922 | C | T | 1 | a0001c0002t0002g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.468+607G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459922 | |||||||
| chr19:459949 | C | A | 2 | a0001c0001t0006g0042 a0001c0007t0006g0041 |
2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.468+580G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459949 | |||||||
| chr19:459976 | C | T | 2 | a0001c0001t0001g0043 a0001c0002t0003g0044 |
2 | HG02165.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.468+553G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 459976 | |||||||
| chr19:460025 | A | G | 44 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0002g0076 others(41): Show |
46 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.468+504T>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460025 | |||||||
| chr19:460027 | G | A | 44 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0002g0076 others(41): Show |
46 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.468+502C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460027 | |||||||
| chr19:460049 | C | T | 44 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0002g0076 others(41): Show |
46 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.468+480G>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460049 | |||||||
| chr19:460073 | T | A | 44 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0002g0076 others(41): Show |
46 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.468+456A>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460073 | |||||||
| chr19:460190 | G | C | 1 | a0001c0003t0002g0182 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.468+339C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460190 | |||||||
| chr19:460222 | G | A | 2 | a0001c0001t0002g0056 a0001c0023t0007g0187 |
2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.468+307C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460222 | |||||||
| chr19:460260 | T | TG | 9 | a0001c0001t0002g0051 a0001c0001t0003g0049 a0001c0001t0005g0053 others(6): Show |
9 | HG02559.hp1 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.468+268dupC | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460260 | |||||||
| chr19:460274 | C | A | 1 | a0001c0001t0002g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.468+255G>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460274 | |||||||
| chr19:460274 | C | G | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+255G>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460274 | |||||||
| chr19:460292 | TC | T | 17 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(14): Show |
17 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.468+236delG | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460292 | |||||||
| chr19:460343 | G | A | 23 | a0001c0001t0001g0058 a0001c0001t0002g0076 a0001c0001t0003g0070 others(20): Show |
25 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.468+186C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460343 | |||||||
| chr19:460382 | G | A | 16 | a0001c0005t0001g0011 a0001c0005t0001g0012 a0001c0005t0001g0015 others(13): Show |
16 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.468+147C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460382 | |||||||
| chr19:460403 | G | A | 2 | a0003c0008t0006g0186 a0011c0022t0002g0185 |
2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.468+126C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460403 | |||||||
| chr19:460475 | G | C | 116 | a0001c0001t0001g0003 a0001c0001t0001g0078 a0001c0001t0001g0081 others(113): Show |
119 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.468+54C>G | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460475 | |||||||
| chr19:460507 | G | A | 11 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0003g0172 others(8): Show |
11 | HG00423.hp1 HG02258.hp2 HG03195.hp2 others(8): Show |
intron_variant | MODIFIER | c.468+22C>T | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460507 | |||||||
| chr19:460515 | T | G | 1 | a0002c0004t0001g0190 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.468+14A>C | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460515 | |||||||
| chr19:460515 | TG | T | 6 | a0001c0001t0005g0037 a0001c0001t0005g0040 a0001c0005t0006g0008 others(3): Show |
6 | HG02145.hp2 HG02622.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.468+13delC | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460515 | |||||||
| chr19:460516 | G | T | 1 | a0001c0001t0005g0027 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.468+13C>A | SHC2 | ENSG00000129946.11 | transcript | ENST00000264554.11 | protein_coding | 1/12 | chr19 | 460516 |