Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 399694 |
| ensemblid | ENSG00000185634.12 |
| hgncid | 16743 |
| symbol | SHC4 |
| name | SHC adaptor protein 4 |
| refseq_nuc | NM_203349.4 |
| refseq_prot | NP_976224.3 |
| ensembl_nuc | ENST00000332408.9 |
| ensembl_prot | ENSP00000329668.4 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 48823741 |
| end | 48963919 |
| strand | - |
| ver | v1.2 |
| region | chr15:48823741-48963919 |
| region5000 | chr15:48818741-48968919 |
| regionname0 | SHC4_chr15_48823741_48963919 |
| regionname5000 | SHC4_chr15_48818741_48968919 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 630 | 361 | 84 | 63 | 152 | 16 | 44 | 116 | SHC4_chr15_48818741_48968919 | SHC4 | MRERG others(625): Show |
chr15 | 48818741 | 48968919 |
| a0002 | 0/0 | 630 | 16 | 0 | 1 | 15 | 0 | 0 | 9 | SHC4_chr15_48818741_48968919 | SHC4 | MRERG others(625): Show |
chr15 | 48818741 | 48968919 |
| a0003 | 0/0 | 630 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SHC4_chr15_48818741_48968919 | SHC4 | MRERG others(625): Show |
chr15 | 48818741 | 48968919 |
| a0004 | 0/0 | 630 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SHC4_chr15_48818741_48968919 | SHC4 | MRERG others(625): Show |
chr15 | 48818741 | 48968919 |
| a0005 | 0/0 | 630 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | MRERG others(625): Show |
chr15 | 48818741 | 48968919 |
| a0006 | 0/0 | 211 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | MRERG others(206): Show |
chr15 | 48818741 | 48968919 |
| a0007 | 0/0 | 630 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | MRERG others(625): Show |
chr15 | 48818741 | 48968919 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1890 | 316 | 78 | 56 | 127 | 16 | 37 | SHC4_chr15_48818741_48968919 | SHC4 | ATGCG others(1885): Show |
chr15 | 48818741 | 48968919 | ||
| a0001c0002 | 0/0 | 1890 | 37 | 2 | 6 | 22 | 0 | 7 | SHC4_chr15_48818741_48968919 | SHC4 | ATGCG others(1885): Show |
chr15 | 48818741 | 48968919 | ||
| a0001c0004 | 0/0 | 1890 | 4 | 4 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATGCG others(1885): Show |
chr15 | 48818741 | 48968919 | ||
| a0001c0006 | 0/0 | 1890 | 2 | 0 | 0 | 2 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATGCG others(1885): Show |
chr15 | 48818741 | 48968919 | ||
| a0001c0007 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATGCG others(1885): Show |
chr15 | 48818741 | 48968919 | ||
| a0001c0012 | 0/0 | 1890 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATGCG others(1885): Show |
chr15 | 48818741 | 48968919 | ||
| a0002c0003 | 0/0 | 1890 | 16 | 0 | 1 | 15 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATGCG others(1885): Show |
chr15 | 48818741 | 48968919 | ||
| a0003c0010 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATGCG others(1885): Show |
chr15 | 48818741 | 48968919 | ||
| a0003c0011 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATGCG others(1885): Show |
chr15 | 48818741 | 48968919 | ||
| a0004c0005 | 0/0 | 1890 | 2 | 0 | 0 | 2 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATGCG others(1885): Show |
chr15 | 48818741 | 48968919 | ||
| a0005c0009 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATGCG others(1885): Show |
chr15 | 48818741 | 48968919 | ||
| a0006c0013 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATGCG others(1885): Show |
chr15 | 48818741 | 48968919 | ||
| a0007c0008 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATGCG others(1885): Show |
chr15 | 48818741 | 48968919 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5028 | 147 | 32 | 31 | 62 | 6 | 15 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5023): Show |
chr15 | 48818741 | 48968919 |
| a0001c0001t0002 | 0/0 | 5028 | 81 | 10 | 14 | 44 | 5 | 8 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5023): Show |
chr15 | 48818741 | 48968919 |
| a0001c0001t0003 | 0/0 | 5027 | 28 | 5 | 5 | 18 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5022): Show |
chr15 | 48818741 | 48968919 |
| a0001c0001t0004 | 0/0 | 5029 | 7 | 1 | 1 | 1 | 1 | 3 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5024): Show |
chr15 | 48818741 | 48968919 |
| a0001c0001t0005 | 0/0 | 5027 | 21 | 7 | 5 | 0 | 4 | 5 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5022): Show |
chr15 | 48818741 | 48968919 |
| a0001c0001t0006 | 0/0 | 5028 | 6 | 6 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5023): Show |
chr15 | 48818741 | 48968919 |
| a0001c0001t0008 | 0/0 | 5028 | 3 | 3 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5023): Show |
chr15 | 48818741 | 48968919 |
| a0001c0001t0009 | 0/0 | 5028 | 3 | 3 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5023): Show |
chr15 | 48818741 | 48968919 |
| a0001c0001t0010 | 0/0 | 5028 | 3 | 3 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5023): Show |
chr15 | 48818741 | 48968919 |
| a0001c0001t0011 | 0/0 | 5028 | 2 | 0 | 0 | 0 | 0 | 2 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5023): Show |
chr15 | 48818741 | 48968919 |
| a0001c0001t0012 | 1/0 | 5027 | 2 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5022): Show |
chr15 | 48818741 | 48968919 |
| a0001c0001t0013 | 0/0 | 5027 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5022): Show |
chr15 | 48818741 | 48968919 |
| a0001c0001t0014 | 0/0 | 5028 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5023): Show |
chr15 | 48818741 | 48968919 |
| a0001c0001t0015 | 0/0 | 5028 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5023): Show |
chr15 | 48818741 | 48968919 |
| a0001c0001t0016 | 0/0 | 5028 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5023): Show |
chr15 | 48818741 | 48968919 |
| a0001c0001t0017 | 0/0 | 5028 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5023): Show |
chr15 | 48818741 | 48968919 |
| a0001c0001t0019 | 0/0 | 5028 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5023): Show |
chr15 | 48818741 | 48968919 |
| a0001c0001t0020 | 0/0 | 5027 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5022): Show |
chr15 | 48818741 | 48968919 |
| a0001c0001t0021 | 0/0 | 5028 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5023): Show |
chr15 | 48818741 | 48968919 |
| a0001c0001t0022 | 0/0 | 5028 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5023): Show |
chr15 | 48818741 | 48968919 |
| a0001c0001t0023 | 0/0 | 5028 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5023): Show |
chr15 | 48818741 | 48968919 |
| a0001c0001t0024 | 0/0 | 5027 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5022): Show |
chr15 | 48818741 | 48968919 |
| a0001c0001t0025 | 0/0 | 5027 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5022): Show |
chr15 | 48818741 | 48968919 |
| a0001c0001t0026 | 0/0 | 5028 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5023): Show |
chr15 | 48818741 | 48968919 |
| a0001c0002t0004 | 0/0 | 5029 | 33 | 2 | 6 | 19 | 0 | 6 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5024): Show |
chr15 | 48818741 | 48968919 |
| a0001c0002t0007 | 0/0 | 5028 | 3 | 0 | 0 | 3 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5023): Show |
chr15 | 48818741 | 48968919 |
| a0001c0002t0018 | 0/0 | 5029 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5024): Show |
chr15 | 48818741 | 48968919 |
| a0001c0004t0001 | 0/0 | 5028 | 2 | 2 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5023): Show |
chr15 | 48818741 | 48968919 |
| a0001c0004t0003 | 0/0 | 5027 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5022): Show |
chr15 | 48818741 | 48968919 |
| a0001c0004t0005 | 0/0 | 5027 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5022): Show |
chr15 | 48818741 | 48968919 |
| a0001c0006t0001 | 0/0 | 5028 | 2 | 0 | 0 | 2 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5023): Show |
chr15 | 48818741 | 48968919 |
| a0001c0007t0002 | 0/0 | 5028 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5023): Show |
chr15 | 48818741 | 48968919 |
| a0001c0012t0003 | 0/0 | 5027 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5022): Show |
chr15 | 48818741 | 48968919 |
| a0002c0003t0001 | 0/0 | 5028 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5023): Show |
chr15 | 48818741 | 48968919 |
| a0002c0003t0003 | 0/0 | 5027 | 13 | 0 | 1 | 12 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5022): Show |
chr15 | 48818741 | 48968919 |
| a0002c0003t0013 | 0/0 | 5027 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5022): Show |
chr15 | 48818741 | 48968919 |
| a0002c0003t0027 | 0/0 | 5029 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5024): Show |
chr15 | 48818741 | 48968919 |
| a0003c0010t0002 | 0/0 | 5028 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5023): Show |
chr15 | 48818741 | 48968919 |
| a0003c0011t0007 | 0/0 | 5028 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5023): Show |
chr15 | 48818741 | 48968919 |
| a0004c0005t0001 | 0/0 | 5028 | 2 | 0 | 0 | 2 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5023): Show |
chr15 | 48818741 | 48968919 |
| a0005c0009t0001 | 0/0 | 5028 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5023): Show |
chr15 | 48818741 | 48968919 |
| a0006c0013t0003 | 0/0 | 5027 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5022): Show |
chr15 | 48818741 | 48968919 |
| a0007c0008t0004 | 0/0 | 5029 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | ATTCA others(5024): Show |
chr15 | 48818741 | 48968919 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0067 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0002g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0003g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0003g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0003g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0003g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0003g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0005g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0005g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0005g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0005g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0005g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0005g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0005g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0005g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0005g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0005g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0005g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0006g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0006g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0006g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0008g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0008g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0008g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0009g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0009g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0009g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0010g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0010g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0010g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0011g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0011g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0012g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0012g0020 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0013g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0014g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0015g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0016g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0017g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0019g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0020g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0021g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0022g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0023g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0024g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0025g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0001t0026g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0004g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0004g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0004g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0004g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0004g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0004g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0004g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0004g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0004g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0004g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0004g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0004g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0004g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0007g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0007g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0007g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0002t0018g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0004t0001g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0004t0001g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0004t0003g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0004t0005g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0006t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0006t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0007t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0001c0012t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0002c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0002c0003t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0002c0003t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0002c0003t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0002c0003t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0002c0003t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0002c0003t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0002c0003t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0002c0003t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0002c0003t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0002c0003t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0002c0003t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0002c0003t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0002c0003t0003g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0002c0003t0013g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0002c0003t0027g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0003c0010t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0003c0011t0007g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0004c0005t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0004c0005t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0005c0009t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0006c0013t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| a0007c0008t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0208 | EUR | GBR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0172 | EUR | GBR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG00140 | hp1 | a0001 | c0001 | t0005 | g0114 | EUR | GBR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0369 | EUR | GBR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0267 | EUR | FIN | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0058 | EUR | FIN | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG00408 | hp1 | a0002 | c0003 | t0001 | g0095 | EAS | CHS | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0344 | EAS | CHS | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | CHS | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | CHS | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0373 | EAS | CHS | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | CHS | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | CHS | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | CHS | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG00558 | hp1 | a0002 | c0003 | t0003 | g0264 | EAS | CHS | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0340 | EAS | CHS | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG00597 | hp2 | a0002 | c0003 | t0003 | g0357 | EAS | CHS | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | CHS | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | CHS | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG00621 | hp2 | a0001 | c0007 | t0002 | g0022 | EAS | CHS | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | PUR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0345 | EAS | CHS | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | CHS | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0246 | AMR | PUR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG00741 | hp1 | a0001 | c0002 | t0004 | g0178 | AMR | PUR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG00741 | hp2 | a0001 | c0002 | t0004 | g0288 | AMR | PUR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0186 | AMR | PUR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0173 | AMR | PUR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | PUR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | PUR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0123 | AMR | PUR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | PUR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01175 | hp2 | a0001 | c0002 | t0004 | g0132 | AMR | PUR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0277 | AMR | PUR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0213 | AMR | PUR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01255 | hp1 | a0002 | c0003 | t0003 | g0046 | AMR | CLM | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | CLM | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01258 | hp2 | a0001 | c0002 | t0004 | g0047 | AMR | CLM | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01361 | hp1 | a0001 | c0001 | t0005 | g0274 | AMR | CLM | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0260 | AMR | CLM | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0091 | AMR | CLM | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01496 | hp2 | a0001 | c0012 | t0003 | g0040 | AMR | CLM | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0289 | EUR | IBS | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0190 | EUR | IBS | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01516 | hp1 | a0001 | c0001 | t0005 | g0121 | EUR | IBS | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0099 | EUR | IBS | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0120 | EUR | IBS | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0290 | EUR | IBS | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0360 | AMR | PEL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0348 | AMR | PEL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0338 | AMR | PEL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0339 | AMR | PEL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01978 | hp2 | a0001 | c0002 | t0004 | g0131 | AMR | PEL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0151 | AMR | PEL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01993 | hp2 | a0001 | c0002 | t0004 | g0157 | AMR | PEL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0253 | AMR | PEL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0355 | EAS | KHV | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | KHV | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0334 | EAS | KHV | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0037 | AFR | ACB | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | KHV | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02056 | hp2 | a0002 | c0003 | t0003 | g0240 | EAS | KHV | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0358 | EAS | KHV | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0365 | EAS | KHV | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02129 | hp1 | a0001 | c0002 | t0004 | g0342 | EAS | KHV | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | KHV | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02132 | hp1 | a0002 | c0003 | t0003 | g0294 | EAS | KHV | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0371 | EAS | KHV | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02135 | hp2 | a0001 | c0002 | t0004 | g0372 | EAS | KHV | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | CDX | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | CDX | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0364 | EAS | CDX | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CDX | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | ACB | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0061 | AFR | ACB | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02258 | hp2 | a0001 | c0001 | t0024 | g0025 | AFR | ACB | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0180 | AMR | PEL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02293 | hp2 | a0001 | c0001 | t0005 | g0057 | AMR | PEL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0343 | AMR | PEL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PEL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0038 | AFR | ACB | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02451 | hp2 | a0001 | c0001 | t0019 | g0021 | AFR | ACB | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02572 | hp1 | a0001 | c0004 | t0005 | g0376 | AFR | GWD | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0367 | SAS | PJL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0062 | AFR | GWD | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02622 | hp2 | a0001 | c0001 | t0012 | g0017 | AFR | GWD | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0088 | AFR | GWD | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02630 | hp2 | a0001 | c0001 | t0008 | g0013 | AFR | GWD | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02647 | hp1 | a0001 | c0001 | t0026 | g0258 | AFR | GWD | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02647 | hp2 | a0001 | c0001 | t0014 | g0005 | AFR | GWD | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02683 | hp1 | a0001 | c0001 | t0011 | g0009 | SAS | PJL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02683 | hp2 | a0001 | c0001 | t0025 | g0347 | SAS | PJL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02698 | hp1 | a0001 | c0002 | t0018 | g0010 | SAS | PJL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0206 | SAS | PJL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02717 | hp2 | a0001 | c0001 | t0009 | g0019 | AFR | GWD | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02723 | hp2 | a0001 | c0001 | t0010 | g0112 | AFR | GWD | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02738 | hp1 | a0001 | c0001 | t0017 | g0011 | SAS | PJL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0060 | AFR | GWD | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0278 | AFR | GWD | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02897 | hp1 | a0005 | c0009 | t0001 | g0103 | AFR | GWD | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0109 | AFR | ESN | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02922 | hp2 | a0001 | c0004 | t0001 | g0377 | AFR | ESN | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02965 | hp2 | a0001 | c0001 | t0010 | g0066 | AFR | ESN | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | ESN | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0142 | AFR | ESN | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0036 | AFR | GWD | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03041 | hp2 | a0001 | c0001 | t0022 | g0254 | AFR | GWD | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03098 | hp1 | a0001 | c0001 | t0021 | g0028 | AFR | MSL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03098 | hp2 | a0001 | c0001 | t0020 | g0014 | AFR | MSL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | ESN | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03130 | hp2 | a0001 | c0001 | t0010 | g0193 | AFR | ESN | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0086 | AFR | ESN | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0016 | AFR | MSL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | MSL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0301 | SAS | PJL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0039 | AFR | MSL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | MSL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03486 | hp2 | a0001 | c0004 | t0001 | g0375 | AFR | MSL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03490 | hp1 | a0001 | c0002 | t0004 | g0048 | SAS | PJL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03491 | hp1 | a0001 | c0001 | t0005 | g0135 | SAS | PJL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03492 | hp1 | a0001 | c0001 | t0005 | g0134 | SAS | PJL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03492 | hp2 | a0001 | c0002 | t0004 | g0049 | SAS | PJL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03516 | hp2 | a0001 | c0001 | t0009 | g0012 | AFR | ESN | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0195 | AFR | GWD | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0032 | AFR | MSL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03654 | hp2 | a0001 | c0001 | t0011 | g0008 | SAS | PJL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0168 | SAS | PJL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0136 | SAS | PJL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03710 | hp2 | a0001 | c0001 | t0016 | g0007 | SAS | PJL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03831 | hp1 | a0001 | c0002 | t0004 | g0325 | SAS | BEB | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0072 | SAS | BEB | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03834 | hp2 | a0001 | c0002 | t0004 | g0130 | SAS | BEB | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | BEB | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0203 | SAS | BEB | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | BEB | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0078 | SAS | BEB | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG04184 | hp1 | a0001 | c0002 | t0004 | g0235 | SAS | BEB | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG04184 | hp2 | a0001 | c0001 | t0005 | g0349 | SAS | BEB | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | STU | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0155 | SAS | STU | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | STU | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG04204 | hp2 | a0001 | c0001 | t0015 | g0006 | SAS | STU | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | STU | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | STU | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | CHB | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18612 | hp2 | a0002 | c0003 | t0003 | g0187 | EAS | CHB | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | CHB | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0184 | EAS | CHB | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0138 | AFR | YRI | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0015 | AFR | YRI | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18939 | hp2 | a0001 | c0002 | t0004 | g0105 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18941 | hp1 | a0001 | c0006 | t0001 | g0319 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18945 | hp2 | a0001 | c0002 | t0004 | g0248 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18946 | hp1 | a0001 | c0002 | t0004 | g0249 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0362 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18949 | hp1 | a0002 | c0003 | t0013 | g0380 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18954 | hp2 | a0001 | c0006 | t0001 | g0228 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18960 | hp2 | a0001 | c0002 | t0004 | g0234 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18962 | hp1 | a0001 | c0002 | t0004 | g0222 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18966 | hp1 | a0002 | c0003 | t0003 | g0185 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18966 | hp2 | a0001 | c0002 | t0004 | g0149 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18968 | hp1 | a0001 | c0002 | t0004 | g0218 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18968 | hp2 | a0002 | c0003 | t0003 | g0171 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0363 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0271 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18978 | hp1 | a0001 | c0002 | t0004 | g0265 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18979 | hp2 | a0006 | c0013 | t0003 | g0127 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0350 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18980 | hp2 | a0001 | c0002 | t0007 | g0356 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18981 | hp2 | a0001 | c0002 | t0004 | g0221 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18983 | hp1 | a0002 | c0003 | t0003 | g0304 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18986 | hp2 | a0003 | c0010 | t0002 | g0242 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18989 | hp2 | a0001 | c0002 | t0007 | g0270 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0368 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18994 | hp1 | a0001 | c0002 | t0004 | g0250 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18999 | hp2 | a0001 | c0002 | t0004 | g0251 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19000 | hp2 | a0002 | c0003 | t0003 | g0111 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19007 | hp2 | a0001 | c0002 | t0004 | g0233 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19010 | hp1 | a0001 | c0002 | t0007 | g0226 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19010 | hp2 | a0001 | c0001 | t0023 | g0150 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19030 | hp1 | a0007 | c0008 | t0004 | g0104 | AFR | LWK | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | LWK | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | LWK | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0336 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19054 | hp2 | a0001 | c0001 | t0013 | g0379 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19058 | hp1 | a0004 | c0005 | t0001 | g0219 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19058 | hp2 | a0002 | c0003 | t0003 | g0170 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0320 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0354 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19066 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0346 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19068 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19076 | hp1 | a0004 | c0005 | t0001 | g0298 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19076 | hp2 | a0001 | c0002 | t0004 | g0118 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19078 | hp1 | a0002 | c0003 | t0003 | g0214 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19079 | hp1 | a0003 | c0011 | t0007 | g0110 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19080 | hp1 | a0002 | c0003 | t0003 | g0311 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19082 | hp1 | a0002 | c0003 | t0027 | g0378 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19082 | hp2 | a0001 | c0002 | t0004 | g0352 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19086 | hp2 | a0001 | c0002 | t0004 | g0317 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0370 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | YRI | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | YRI | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | ASW | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA20129 | hp2 | a0001 | c0001 | t0009 | g0018 | AFR | ASW | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0286 | EUR | TSI | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | TSI | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | TSI | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0276 | EUR | TSI | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0079 | SAS | GIH | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA20905 | hp2 | a0001 | c0002 | t0004 | g0366 | SAS | GIH | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | CLM | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0024 | AFR | ACB | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02109 | hp2 | a0001 | c0002 | t0004 | g0083 | AFR | ACB | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02486 | hp1 | a0001 | c0002 | t0004 | g0129 | AFR | ACB | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0031 | AFR | ACB | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | ACB | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0281 | AFR | MSL | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | USA | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | USA | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | USA | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0279 | AFR | USA | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA21309 | hp1 | a0001 | c0004 | t0003 | g0374 | AFR | LWK | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | LWK | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0067 | REF | REF | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0012 | g0020 | REF | REF | SHC4_chr15_48818741_48968919 | SHC4 | chr15 | 48818741 | 48968919 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:48826054 | T | C | 1 | a0003 | 2 | NA18986.hp2 NA19079.hp1 |
missense_variant | MODERATE | c.1810A>G | p.Ile604Val | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 12/12 | 2714/5027 | 1810/1893 | 604/630 | chr15 | 48826054 | |||
| chr15:48826092 | C | T | 1 | a0005 | 1 | HG02897.hp1 | missense_variant | MODERATE | c.1772G>A | p.Gly591Asp | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 12/12 | 2676/5027 | 1772/1893 | 591/630 | chr15 | 48826092 | |||
| chr15:48855995 | T | G | 1 | a0002 | 16 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(13): Show |
missense_variant | MODERATE | c.1200A>C | p.Gln400His | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/12 | 2104/5027 | 1200/1893 | 400/630 | chr15 | 48855995 | |||
| chr15:48857740 | C | T | 1 | a0004 | 2 | NA19058.hp1 NA19076.hp1 |
missense_variant | MODERATE | c.1022G>A | p.Arg341Gln | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 7/12 | 1926/5027 | 1022/1893 | 341/630 | chr15 | 48857740 | |||
| chr15:48890774 | C | T | 1 | a0007 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.694G>A | p.Ala232Thr | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/12 | 1598/5027 | 694/1893 | 232/630 | chr15 | 48890774 | |||
| chr15:48924901 | C | A | 1 | a0006 | 1 | NA18979.hp2 | stop_gained | HIGH | c.634G>T | p.Gly212* | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/12 | 1538/5027 | 634/1893 | 212/630 | chr15 | 48924901 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:48834937 | G | A | 2 | a0001c0002 a0003c0011 |
38 | HG00741.hp1 HG00741.hp2 HG01175.hp2 others(35): Show |
synonymous_variant | LOW | c.1569C>T | p.Ser523Ser | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/12 | 2473/5027 | 1569/1893 | 523/630 | chr15 | 48834937 | |||
| chr15:48843437 | T | C | 1 | a0001c0012 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.1455A>G | p.Gln485Gln | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/12 | 2359/5027 | 1455/1893 | 485/630 | chr15 | 48843437 | |||
| chr15:48857739 | C | G | 1 | a0001c0006 | 2 | NA18941.hp1 NA18954.hp2 |
synonymous_variant | LOW | c.1023G>C | p.Arg341Arg | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 7/12 | 1927/5027 | 1023/1893 | 341/630 | chr15 | 48857739 | |||
| chr15:48962578 | C | T | 1 | a0001c0007 | 1 | HG00621.hp2 | synonymous_variant | LOW | c.438G>A | p.Pro146Pro | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/12 | 1342/5027 | 438/1893 | 146/630 | chr15 | 48962578 | |||
| chr15:48962770 | T | C | 1 | a0001c0004 | 4 | HG02572.hp1 HG02922.hp2 HG03486.hp2 others(1): Show |
synonymous_variant | LOW | c.246A>G | p.Pro82Pro | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/12 | 1150/5027 | 246/1893 | 82/630 | chr15 | 48962770 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:48823776 | C | T | 1 | a0001c0001t0023 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2195G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 12/12 | 2195 | chr15 | 48823776 | ||||||
| chr15:48823920 | C | T | 1 | a0001c0001t0022 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2051G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 12/12 | 2051 | chr15 | 48823920 | ||||||
| chr15:48823942 | T | G | 1 | a0001c0001t0019 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2029A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 12/12 | 2029 | chr15 | 48823942 | ||||||
| chr15:48824196 | A | G | 9 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0011 others(6): Show |
92 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*1775T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 12/12 | 1775 | chr15 | 48824196 | ||||||
| chr15:48824414 | T | TA | 7 | a0001c0001t0004 a0001c0002t0004 a0001c0002t0007 others(4): Show |
47 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1556dupT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 12/12 | 1556 | chr15 | 48824414 | ||||||
| chr15:48824424 | A | C | 1 | a0001c0001t0021 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1547T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 12/12 | 1547 | chr15 | 48824424 | ||||||
| chr15:48824530 | T | C | 1 | a0001c0001t0024 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1441A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 12/12 | 1441 | chr15 | 48824530 | ||||||
| chr15:48824928 | G | GT | 37 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(34): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(351): Show |
3_prime_UTR_variant | MODIFIER | c.*1042dupA | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 12/12 | 1042 | chr15 | 48824928 | ||||||
| chr15:48825035 | A | C | 39 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(36): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(355): Show |
3_prime_UTR_variant | MODIFIER | c.*936T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 12/12 | 936 | chr15 | 48825035 | ||||||
| chr15:48825098 | G | T | 1 | a0001c0001t0010 | 3 | HG02723.hp2 HG02965.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*873C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 12/12 | 873 | chr15 | 48825098 | ||||||
| chr15:48825156 | GT | G | 9 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0020 others(6): Show |
48 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*814delA | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 12/12 | 814 | chr15 | 48825156 | ||||||
| chr15:48825229 | A | C | 10 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(7): Show |
98 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*742T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 12/12 | 742 | chr15 | 48825229 | ||||||
| chr15:48825352 | A | G | 10 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(7): Show |
98 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*619T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 12/12 | 619 | chr15 | 48825352 | ||||||
| chr15:48825498 | T | C | 1 | a0001c0001t0025 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*473A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 12/12 | 473 | chr15 | 48825498 | ||||||
| chr15:48825846 | G | A | 1 | a0001c0001t0026 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*125C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 12/12 | 125 | chr15 | 48825846 | ||||||
| chr15:48825890 | C | T | 9 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0011 others(6): Show |
92 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*81G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 12/12 | 81 | chr15 | 48825890 | ||||||
| chr15:48963225 | T | C | 38 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(35): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
5_prime_UTR_variant | MODIFIER | c.-210A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/12 | 210 | chr15 | 48963225 | ||||||
| chr15:48963366 | C | A | 3 | a0001c0001t0013 a0002c0003t0013 a0002c0003t0027 |
3 | NA18949.hp1 NA19054.hp2 NA19082.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-351G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/12 | chr15 | 48963366 | |||||||
| chr15:48963443 | C | T | 2 | a0001c0001t0017 a0001c0002t0018 |
2 | HG02698.hp1 HG02738.hp1 |
5_prime_UTR_variant | MODIFIER | c.-428G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/12 | 428 | chr15 | 48963443 | ||||||
| chr15:48963485 | A | T | 2 | a0001c0001t0011 a0001c0001t0016 |
3 | HG02683.hp1 HG03654.hp2 HG03710.hp2 |
5_prime_UTR_variant | MODIFIER | c.-470T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/12 | 470 | chr15 | 48963485 | ||||||
| chr15:48963726 | G | T | 1 | a0001c0001t0015 | 1 | HG04204.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-711C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/12 | chr15 | 48963726 | |||||||
| chr15:48963751 | C | G | 1 | a0001c0001t0014 | 1 | HG02647.hp2 | 5_prime_UTR_variant | MODIFIER | c.-736G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/12 | 736 | chr15 | 48963751 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:48826253 | CT | C | 63 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0052 others(60): Show |
65 | HG00099.hp2 HG00642.hp1 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.1738-128delA | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48826253 | |||||||
| chr15:48826395 | C | T | 2 | a0001c0006t0001g0228 a0001c0006t0001g0319 |
2 | NA18941.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.1738-269G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48826395 | |||||||
| chr15:48826625 | C | T | 4 | a0001c0002t0004g0129 a0001c0002t0004g0131 a0001c0002t0004g0132 others(1): Show |
4 | HG00741.hp2 HG01175.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-499G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48826625 | |||||||
| chr15:48826697 | C | A | 25 | a0001c0001t0003g0063 a0001c0001t0003g0080 a0001c0001t0003g0096 others(22): Show |
25 | HG00673.hp2 HG00735.hp2 HG01981.hp2 others(22): Show |
intron_variant | MODIFIER | c.1738-571G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48826697 | |||||||
| chr15:48826868 | T | A | 1 | a0001c0001t0001g0166 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1738-742A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48826868 | |||||||
| chr15:48826909 | C | T | 7 | a0001c0001t0002g0085 a0001c0001t0002g0117 a0001c0001t0002g0211 others(4): Show |
7 | HG02630.hp2 HG03098.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1738-783G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48826909 | |||||||
| chr15:48827054 | T | C | 1 | a0001c0001t0002g0065 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1738-928A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48827054 | |||||||
| chr15:48827260 | A | C | 95 | a0001c0001t0002g0002 a0001c0001t0002g0033 a0001c0001t0002g0034 others(92): Show |
96 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1738-1134T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48827260 | |||||||
| chr15:48827452 | A | T | 93 | a0001c0001t0002g0002 a0001c0001t0002g0033 a0001c0001t0002g0043 others(90): Show |
94 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1738-1326T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48827452 | |||||||
| chr15:48827550 | C | CTTCTGCC others(4): Show |
351 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0023 others(348): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(352): Show |
intron_variant | MODIFIER | c.1738-1425_1738-142 others(15): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48827550 | |||||||
| chr15:48827707 | C | T | 1 | a0001c0001t0005g0024 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1738-1581G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48827707 | |||||||
| chr15:48828086 | T | C | 1 | a0001c0001t0026g0258 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1738-1960A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48828086 | |||||||
| chr15:48828093 | ATG | A | 24 | a0001c0001t0001g0089 a0001c0001t0001g0119 a0001c0001t0001g0152 others(21): Show |
24 | HG00408.hp1 HG01109.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.1738-1969_1738-196 others(6): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48828093 | |||||||
| chr15:48828113 | GTGTA | G | 4 | a0001c0001t0001g0137 a0001c0001t0001g0192 a0001c0001t0009g0012 others(1): Show |
4 | HG00741.hp2 HG02258.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1738-1991_1738-198 others(8): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48828113 | |||||||
| chr15:48828113 | GTGTATA | G | 58 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0052 others(55): Show |
60 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.1738-1993_1738-198 others(10): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48828113 | |||||||
| chr15:48828115 | GTA | G | 49 | a0001c0001t0001g0183 a0001c0001t0001g0364 a0001c0001t0002g0027 others(46): Show |
49 | HG00558.hp1 HG00597.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.1738-1991_1738-199 others(6): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48828115 | |||||||
| chr15:48828115 | GTATA | G | 97 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(94): Show |
97 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.1738-1993_1738-199 others(8): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48828115 | |||||||
| chr15:48828117 | A | G | 95 | a0001c0001t0002g0002 a0001c0001t0002g0033 a0001c0001t0002g0034 others(92): Show |
96 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1738-1991T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48828117 | |||||||
| chr15:48828119 | A | G | 5 | a0001c0001t0001g0183 a0001c0001t0001g0364 a0001c0001t0002g0099 others(2): Show |
5 | HG01516.hp2 HG02165.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-1993T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48828119 | |||||||
| chr15:48828121 | A | G | 93 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(90): Show |
93 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.1738-1995T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48828121 | |||||||
| chr15:48828123 | A | G | 2 | a0001c0001t0001g0159 a0001c0001t0001g0327 |
2 | HG03017.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1738-1997T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48828123 | |||||||
| chr15:48828132 | TATAC | T | 86 | a0001c0001t0002g0002 a0001c0001t0002g0034 a0001c0001t0002g0043 others(83): Show |
87 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1738-2010_1738-200 others(8): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48828132 | |||||||
| chr15:48828134 | TAC | T | 9 | a0001c0001t0002g0033 a0001c0001t0002g0244 a0001c0001t0002g0262 others(6): Show |
9 | HG02451.hp1 HG02486.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1738-2010_1738-200 others(6): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48828134 | |||||||
| chr15:48828222 | C | T | 3 | a0001c0001t0003g0241 a0001c0001t0003g0271 a0001c0001t0013g0379 |
3 | NA18977.hp1 NA19009.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1738-2096G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48828222 | |||||||
| chr15:48828325 | C | T | 3 | a0001c0001t0010g0066 a0001c0001t0010g0112 a0001c0001t0010g0193 |
3 | HG02723.hp2 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1738-2199G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48828325 | |||||||
| chr15:48828503 | T | C | 3 | a0001c0001t0010g0066 a0001c0001t0010g0112 a0001c0001t0010g0193 |
3 | HG02723.hp2 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1738-2377A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48828503 | |||||||
| chr15:48828511 | T | C | 93 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(90): Show |
93 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.1738-2385A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48828511 | |||||||
| chr15:48828558 | T | C | 59 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0052 others(56): Show |
61 | HG00099.hp2 HG00642.hp1 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.1738-2432A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48828558 | |||||||
| chr15:48828585 | C | T | 3 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0002g0033 |
3 | HG03704.hp1 NA18999.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1738-2459G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48828585 | |||||||
| chr15:48829026 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1738-2900A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48829026 | |||||||
| chr15:48829108 | T | G | 92 | a0001c0001t0002g0002 a0001c0001t0002g0027 a0001c0001t0002g0033 others(89): Show |
93 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.1738-2982A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48829108 | |||||||
| chr15:48829144 | C | T | 89 | a0001c0001t0002g0002 a0001c0001t0002g0033 a0001c0001t0002g0034 others(86): Show |
90 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1738-3018G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48829144 | |||||||
| chr15:48829577 | A | C | 5 | a0001c0001t0002g0117 a0001c0001t0008g0013 a0001c0001t0008g0015 others(2): Show |
5 | HG02630.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-3451T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48829577 | |||||||
| chr15:48829629 | G | C | 49 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0063 others(46): Show |
49 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1738-3503C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48829629 | |||||||
| chr15:48829692 | G | A | 1 | a0001c0001t0001g0330 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1738-3566C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48829692 | |||||||
| chr15:48829850 | C | T | 1 | a0006c0013t0003g0127 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1738-3724G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48829850 | |||||||
| chr15:48829934 | T | C | 2 | a0001c0001t0005g0213 a0001c0001t0005g0278 |
2 | HG01243.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1738-3808A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48829934 | |||||||
| chr15:48830034 | T | A | 1 | a0001c0001t0001g0044 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1738-3908A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48830034 | |||||||
| chr15:48830091 | T | A | 1 | a0001c0001t0002g0370 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1738-3965A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48830091 | |||||||
| chr15:48830145 | T | C | 1 | a0001c0001t0026g0258 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1738-4019A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48830145 | |||||||
| chr15:48830201 | T | C | 6 | a0001c0001t0006g0031 a0001c0001t0006g0032 a0001c0001t0006g0038 others(3): Show |
6 | HG02451.hp1 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-4075A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48830201 | |||||||
| chr15:48830405 | T | C | 7 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0281 others(4): Show |
7 | HG01496.hp2 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1738-4279A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48830405 | |||||||
| chr15:48830467 | T | C | 97 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(94): Show |
97 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.1737+4302A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48830467 | |||||||
| chr15:48830802 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0009g0012 |
2 | HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1737+3967C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48830802 | |||||||
| chr15:48830874 | G | A | 48 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(45): Show |
48 | HG00140.hp2 HG00408.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.1737+3895C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48830874 | |||||||
| chr15:48831012 | T | C | 7 | a0001c0001t0001g0044 a0001c0001t0006g0031 a0001c0001t0006g0032 others(4): Show |
7 | HG02451.hp1 HG02486.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1737+3757A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48831012 | |||||||
| chr15:48831037 | C | CA | 6 | a0001c0001t0004g0037 a0001c0001t0004g0123 a0001c0001t0004g0136 others(3): Show |
6 | HG00099.hp1 HG01106.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1737+3731dupT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48831037 | |||||||
| chr15:48831260 | T | TA | 48 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0026 others(45): Show |
49 | HG00408.hp1 HG01109.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.1737+3508dupT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48831260 | |||||||
| chr15:48831567 | G | A | 86 | a0001c0001t0002g0002 a0001c0001t0002g0033 a0001c0001t0002g0043 others(83): Show |
87 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1737+3202C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48831567 | |||||||
| chr15:48832009 | G | A | 38 | a0001c0001t0002g0002 a0001c0001t0002g0064 a0001c0001t0002g0090 others(35): Show |
39 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.1737+2760C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48832009 | |||||||
| chr15:48832052 | A | C | 351 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0023 others(348): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(352): Show |
intron_variant | MODIFIER | c.1737+2717T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48832052 | |||||||
| chr15:48832207 | G | A | 38 | a0001c0001t0004g0168 a0001c0001t0004g0184 a0001c0002t0004g0003 others(35): Show |
39 | HG00741.hp1 HG00741.hp2 HG01175.hp2 others(36): Show |
intron_variant | MODIFIER | c.1737+2562C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48832207 | |||||||
| chr15:48832251 | G | A | 1 | a0001c0001t0002g0075 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1737+2518C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48832251 | |||||||
| chr15:48832385 | G | A | 1 | a0001c0001t0002g0293 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1737+2384C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48832385 | |||||||
| chr15:48832408 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1737+2361A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48832408 | |||||||
| chr15:48832472 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1737+2297A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48832472 | |||||||
| chr15:48832524 | C | A | 2 | a0001c0001t0005g0134 a0001c0001t0005g0135 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1737+2245G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48832524 | |||||||
| chr15:48832525 | A | T | 2 | a0001c0001t0005g0134 a0001c0001t0005g0135 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1737+2244T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48832525 | |||||||
| chr15:48832527 | A | G | 2 | a0001c0001t0005g0134 a0001c0001t0005g0135 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1737+2242T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48832527 | |||||||
| chr15:48832559 | G | A | 2 | a0001c0002t0004g0248 a0001c0002t0004g0249 |
2 | NA18945.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.1737+2210C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48832559 | |||||||
| chr15:48832572 | A | C | 335 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(332): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.1737+2197T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48832572 | |||||||
| chr15:48832733 | A | G | 1 | a0001c0012t0003g0040 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1737+2036T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48832733 | |||||||
| chr15:48832759 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1737+2010A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48832759 | |||||||
| chr15:48833038 | G | C | 1 | a0001c0001t0001g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1737+1731C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48833038 | |||||||
| chr15:48833062 | T | C | 1 | a0001c0007t0002g0022 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1737+1707A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48833062 | |||||||
| chr15:48833127 | T | C | 8 | a0001c0001t0001g0068 a0001c0001t0001g0147 a0001c0001t0001g0172 others(5): Show |
8 | HG00099.hp2 HG00642.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.1737+1642A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48833127 | |||||||
| chr15:48833193 | C | T | 1 | a0001c0001t0002g0286 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1737+1576G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48833193 | |||||||
| chr15:48833242 | G | A | 85 | a0001c0001t0002g0002 a0001c0001t0002g0033 a0001c0001t0002g0043 others(82): Show |
86 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1737+1527C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48833242 | |||||||
| chr15:48833289 | G | A | 46 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0063 others(43): Show |
46 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.1737+1480C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48833289 | |||||||
| chr15:48833363 | C | G | 2 | a0001c0001t0001g0137 a0001c0001t0009g0012 |
2 | HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1737+1406G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48833363 | |||||||
| chr15:48833403 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1737+1366C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48833403 | |||||||
| chr15:48833546 | G | A | 88 | a0001c0001t0002g0002 a0001c0001t0002g0033 a0001c0001t0002g0043 others(85): Show |
89 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1737+1223C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48833546 | |||||||
| chr15:48833574 | G | A | 2 | a0001c0006t0001g0228 a0001c0006t0001g0319 |
2 | NA18941.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.1737+1195C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48833574 | |||||||
| chr15:48833729 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1737+1040G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48833729 | |||||||
| chr15:48833898 | A | C | 375 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0023 others(372): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.1737+871T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48833898 | |||||||
| chr15:48834080 | T | C | 2 | a0001c0001t0006g0195 a0001c0001t0009g0018 |
2 | HG03540.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1737+689A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48834080 | |||||||
| chr15:48834085 | G | A | 47 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0063 others(44): Show |
47 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.1737+684C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48834085 | |||||||
| chr15:48834233 | C | A | 1 | a0002c0003t0003g0111 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1737+536G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48834233 | |||||||
| chr15:48834498 | C | T | 1 | a0001c0012t0003g0040 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1737+271G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48834498 | |||||||
| chr15:48834543 | T | C | 1 | a0001c0012t0003g0040 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1737+226A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48834543 | |||||||
| chr15:48834626 | G | C | 1 | a0001c0001t0002g0336 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1737+143C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48834626 | |||||||
| chr15:48834659 | A | C | 43 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0026 others(40): Show |
44 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.1737+110T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 11/11 | chr15 | 48834659 | |||||||
| chr15:48835300 | G | A | 3 | a0001c0001t0010g0066 a0001c0001t0010g0112 a0001c0001t0010g0193 |
3 | HG02723.hp2 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1484-278C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48835300 | |||||||
| chr15:48835417 | A | G | 351 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0023 others(348): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(352): Show |
intron_variant | MODIFIER | c.1484-395T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48835417 | |||||||
| chr15:48835671 | C | T | 1 | a0001c0002t0007g0356 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1484-649G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48835671 | |||||||
| chr15:48835975 | C | T | 2 | a0001c0001t0019g0021 a0001c0012t0003g0040 |
2 | HG01496.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1484-953G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48835975 | |||||||
| chr15:48835995 | T | C | 2 | a0001c0001t0019g0021 a0001c0012t0003g0040 |
2 | HG01496.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1484-973A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48835995 | |||||||
| chr15:48836014 | C | CA | 102 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(99): Show |
102 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1484-993dupT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48836014 | |||||||
| chr15:48836021 | T | A | 84 | a0001c0001t0001g0224 a0001c0001t0001g0364 a0001c0001t0002g0002 others(81): Show |
85 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1484-999A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48836021 | |||||||
| chr15:48836022 | C | T | 84 | a0001c0001t0001g0224 a0001c0001t0001g0364 a0001c0001t0002g0002 others(81): Show |
85 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1484-1000G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48836022 | |||||||
| chr15:48836023 | C | CA | 111 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0023 others(108): Show |
114 | HG00099.hp2 HG00642.hp1 HG00738.hp1 others(111): Show |
intron_variant | MODIFIER | c.1484-1002dupT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48836023 | |||||||
| chr15:48836023 | C | CAA | 15 | a0001c0001t0001g0045 a0001c0001t0001g0059 a0001c0001t0001g0140 others(12): Show |
15 | HG00741.hp2 HG02145.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.1484-1003_1484-100 others(6): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48836023 | |||||||
| chr15:48836024 | A | C | 84 | a0001c0001t0001g0224 a0001c0001t0001g0364 a0001c0001t0002g0002 others(81): Show |
85 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1484-1002T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48836024 | |||||||
| chr15:48836052 | G | A | 1 | a0001c0007t0002g0022 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1484-1030C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48836052 | |||||||
| chr15:48836148 | G | A | 2 | a0001c0001t0005g0036 a0001c0001t0012g0017 |
2 | HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1484-1126C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48836148 | |||||||
| chr15:48836368 | T | G | 1 | a0001c0001t0005g0024 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1484-1346A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48836368 | |||||||
| chr15:48836380 | A | C | 1 | a0001c0012t0003g0040 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1484-1358T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48836380 | |||||||
| chr15:48836406 | T | C | 1 | a0001c0001t0017g0011 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1484-1384A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48836406 | |||||||
| chr15:48836480 | G | A | 351 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0023 others(348): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(352): Show |
intron_variant | MODIFIER | c.1484-1458C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48836480 | |||||||
| chr15:48836540 | C | G | 2 | a0001c0001t0005g0062 a0001c0001t0005g0109 |
2 | HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1484-1518G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48836540 | |||||||
| chr15:48836775 | C | T | 1 | a0001c0001t0003g0153 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1484-1753G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48836775 | |||||||
| chr15:48836982 | C | G | 1 | a0007c0008t0004g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1484-1960G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48836982 | |||||||
| chr15:48837090 | G | T | 1 | a0001c0001t0001g0367 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1484-2068C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48837090 | |||||||
| chr15:48837091 | G | T | 1 | a0001c0001t0001g0044 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1484-2069C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48837091 | |||||||
| chr15:48837105 | A | T | 4 | a0001c0001t0004g0123 a0001c0001t0004g0136 a0001c0001t0004g0155 others(1): Show |
4 | HG00099.hp1 HG01106.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1484-2083T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48837105 | |||||||
| chr15:48837126 | A | G | 40 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0026 others(37): Show |
41 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.1484-2104T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48837126 | |||||||
| chr15:48837281 | A | T | 1 | a0001c0001t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1484-2259T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48837281 | |||||||
| chr15:48837302 | C | T | 1 | a0001c0012t0003g0040 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1484-2280G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48837302 | |||||||
| chr15:48837405 | A | G | 1 | a0001c0001t0004g0184 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1484-2383T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48837405 | |||||||
| chr15:48837459 | G | A | 2 | a0001c0001t0003g0086 a0001c0001t0003g0279 |
2 | HG03195.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1484-2437C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48837459 | |||||||
| chr15:48837747 | A | T | 47 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0063 others(44): Show |
47 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.1484-2725T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48837747 | |||||||
| chr15:48837766 | C | T | 5 | a0001c0001t0004g0037 a0001c0001t0004g0136 a0001c0001t0004g0155 others(2): Show |
5 | HG00099.hp1 HG02055.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.1484-2744G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48837766 | |||||||
| chr15:48837821 | C | T | 1 | a0003c0011t0007g0110 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1484-2799G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48837821 | |||||||
| chr15:48838163 | A | G | 7 | a0001c0001t0002g0027 a0001c0001t0004g0037 a0001c0001t0004g0123 others(4): Show |
7 | HG00099.hp1 HG01106.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1484-3141T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48838163 | |||||||
| chr15:48838235 | C | T | 335 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(332): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.1484-3213G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48838235 | |||||||
| chr15:48838456 | T | C | 351 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0023 others(348): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(352): Show |
intron_variant | MODIFIER | c.1484-3434A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48838456 | |||||||
| chr15:48838605 | A | T | 1 | a0001c0002t0004g0178 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1484-3583T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48838605 | |||||||
| chr15:48838714 | CA | C | 3 | a0001c0001t0005g0114 a0001c0001t0005g0260 a0001c0001t0005g0267 |
3 | HG00140.hp1 HG00280.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1484-3693delT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48838714 | |||||||
| chr15:48839080 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1484-4058A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48839080 | |||||||
| chr15:48839114 | C | G | 1 | a0001c0001t0002g0091 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1484-4092G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48839114 | |||||||
| chr15:48839215 | C | G | 1 | a0002c0003t0003g0264 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1484-4193G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48839215 | |||||||
| chr15:48839222 | C | T | 1 | a0001c0001t0019g0021 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1483+4187G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48839222 | |||||||
| chr15:48839268 | A | C | 1 | a0002c0003t0003g0294 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1483+4141T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48839268 | |||||||
| chr15:48839414 | A | G | 89 | a0001c0001t0002g0002 a0001c0001t0002g0033 a0001c0001t0002g0043 others(86): Show |
90 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1483+3995T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48839414 | |||||||
| chr15:48839485 | G | T | 61 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0052 others(58): Show |
63 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1483+3924C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48839485 | |||||||
| chr15:48839488 | GA | G | 61 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0052 others(58): Show |
63 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1483+3920delT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48839488 | |||||||
| chr15:48839519 | A | T | 1 | a0001c0001t0019g0021 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1483+3890T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48839519 | |||||||
| chr15:48839625 | T | G | 1 | a0001c0001t0001g0162 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1483+3784A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48839625 | |||||||
| chr15:48839710 | G | A | 1 | a0001c0001t0002g0190 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1483+3699C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48839710 | |||||||
| chr15:48839807 | T | G | 7 | a0001c0002t0004g0047 a0001c0002t0004g0048 a0001c0002t0004g0049 others(4): Show |
7 | HG00741.hp2 HG01175.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1483+3602A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48839807 | |||||||
| chr15:48839877 | C | T | 56 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0052 others(53): Show |
58 | HG00099.hp2 HG00642.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.1483+3532G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48839877 | |||||||
| chr15:48840135 | C | T | 1 | a0001c0001t0002g0043 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1483+3274G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48840135 | |||||||
| chr15:48840741 | T | C | 1 | a0001c0001t0009g0012 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1483+2668A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48840741 | |||||||
| chr15:48840838 | C | T | 1 | a0007c0008t0004g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1483+2571G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48840838 | |||||||
| chr15:48840856 | GGAGATC | G | 7 | a0001c0001t0006g0031 a0001c0001t0006g0032 a0001c0001t0006g0038 others(4): Show |
7 | HG02451.hp1 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1483+2547_1483+255 others(10): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48840856 | |||||||
| chr15:48840863 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1483+2546C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48840863 | |||||||
| chr15:48840997 | C | T | 47 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0063 others(44): Show |
47 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.1483+2412G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48840997 | |||||||
| chr15:48841045 | TATTGA | T | 93 | a0001c0001t0002g0002 a0001c0001t0002g0033 a0001c0001t0002g0043 others(90): Show |
94 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1483+2359_1483+236 others(9): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48841045 | |||||||
| chr15:48841332 | T | C | 36 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0089 others(33): Show |
36 | HG01109.hp1 HG01884.hp1 HG01928.hp2 others(33): Show |
intron_variant | MODIFIER | c.1483+2077A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48841332 | |||||||
| chr15:48841596 | G | C | 2 | a0001c0001t0005g0036 a0001c0001t0012g0017 |
2 | HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1483+1813C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48841596 | |||||||
| chr15:48842251 | C | A | 1 | a0001c0001t0003g0271 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1483+1158G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48842251 | |||||||
| chr15:48842447 | T | C | 1 | a0001c0001t0001g0296 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1483+962A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48842447 | |||||||
| chr15:48842516 | C | T | 88 | a0001c0001t0002g0002 a0001c0001t0002g0033 a0001c0001t0002g0043 others(85): Show |
89 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1483+893G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48842516 | |||||||
| chr15:48842655 | G | A | 1 | a0001c0012t0003g0040 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1483+754C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48842655 | |||||||
| chr15:48842923 | C | A | 2 | a0001c0001t0001g0137 a0001c0001t0009g0012 |
2 | HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1483+486G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48842923 | |||||||
| chr15:48842939 | A | C | 1 | a0001c0001t0001g0291 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1483+470T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48842939 | |||||||
| chr15:48842992 | C | G | 1 | a0001c0001t0003g0153 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1483+417G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48842992 | |||||||
| chr15:48843209 | A | G | 2 | a0001c0001t0002g0321 a0001c0001t0002g0322 |
2 | NA18960.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1483+200T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 10/11 | chr15 | 48843209 | |||||||
| chr15:48843695 | C | T | 88 | a0001c0001t0002g0002 a0001c0001t0002g0033 a0001c0001t0002g0043 others(85): Show |
89 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1304-107G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48843695 | |||||||
| chr15:48843829 | G | A | 57 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0052 others(54): Show |
59 | HG00099.hp2 HG00642.hp1 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.1304-241C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48843829 | |||||||
| chr15:48843898 | G | GA | 99 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(96): Show |
99 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.1304-311dupT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48843898 | |||||||
| chr15:48844148 | A | G | 1 | a0001c0001t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1304-560T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48844148 | |||||||
| chr15:48844391 | T | G | 48 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0026 others(45): Show |
49 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.1304-803A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48844391 | |||||||
| chr15:48844403 | T | A | 7 | a0001c0002t0004g0047 a0001c0002t0004g0048 a0001c0002t0004g0049 others(4): Show |
7 | HG00741.hp2 HG01175.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1304-815A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48844403 | |||||||
| chr15:48844684 | T | C | 5 | a0001c0001t0004g0037 a0001c0001t0004g0136 a0001c0001t0004g0155 others(2): Show |
5 | HG00099.hp1 HG02055.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.1304-1096A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48844684 | |||||||
| chr15:48844964 | C | T | 10 | a0001c0001t0001g0169 a0001c0001t0001g0179 a0001c0001t0001g0223 others(7): Show |
10 | HG01928.hp1 HG01952.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.1304-1376G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48844964 | |||||||
| chr15:48844982 | A | G | 44 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0026 others(41): Show |
45 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.1304-1394T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48844982 | |||||||
| chr15:48845085 | T | C | 355 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0023 others(352): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(356): Show |
intron_variant | MODIFIER | c.1304-1497A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48845085 | |||||||
| chr15:48845198 | A | G | 6 | a0001c0001t0004g0037 a0001c0001t0004g0123 a0001c0001t0004g0136 others(3): Show |
6 | HG00099.hp1 HG01106.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1304-1610T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48845198 | |||||||
| chr15:48845398 | T | C | 2 | a0001c0001t0001g0087 a0001c0001t0001g0183 |
2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1304-1810A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48845398 | |||||||
| chr15:48845591 | C | A | 1 | a0001c0012t0003g0040 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1304-2003G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48845591 | |||||||
| chr15:48845764 | T | G | 38 | a0001c0001t0002g0002 a0001c0001t0002g0064 a0001c0001t0002g0090 others(35): Show |
39 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.1304-2176A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48845764 | |||||||
| chr15:48845769 | T | C | 1 | a0001c0001t0011g0009 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1304-2181A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48845769 | |||||||
| chr15:48845868 | C | T | 197 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0044 others(194): Show |
200 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.1304-2280G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48845868 | |||||||
| chr15:48845895 | G | C | 47 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0063 others(44): Show |
47 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.1304-2307C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48845895 | |||||||
| chr15:48846123 | G | A | 1 | a0001c0001t0004g0168 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1304-2535C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48846123 | |||||||
| chr15:48846196 | G | T | 1 | a0001c0001t0017g0011 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1304-2608C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48846196 | |||||||
| chr15:48846266 | A | C | 1 | a0001c0001t0001g0044 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1304-2678T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48846266 | |||||||
| chr15:48846304 | A | G | 6 | a0001c0001t0001g0225 a0001c0001t0001g0299 a0001c0001t0001g0308 others(3): Show |
6 | NA18949.hp2 NA18957.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.1304-2716T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48846304 | |||||||
| chr15:48846423 | T | C | 1 | a0001c0001t0004g0168 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1304-2835A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48846423 | |||||||
| chr15:48846523 | C | T | 3 | a0001c0001t0010g0066 a0001c0001t0010g0112 a0001c0001t0010g0193 |
3 | HG02723.hp2 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1304-2935G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48846523 | |||||||
| chr15:48846526 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1304-2938A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48846526 | |||||||
| chr15:48846647 | G | A | 3 | a0001c0001t0010g0066 a0001c0001t0010g0112 a0001c0001t0010g0193 |
3 | HG02723.hp2 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1304-3059C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48846647 | |||||||
| chr15:48846757 | A | T | 47 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0063 others(44): Show |
47 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.1304-3169T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48846757 | |||||||
| chr15:48847022 | CT | C | 11 | a0001c0001t0001g0175 a0001c0001t0001g0196 a0001c0001t0001g0209 others(8): Show |
11 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1304-3435delA | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48847022 | |||||||
| chr15:48847023 | T | C | 1 | a0001c0002t0004g0235 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1304-3435A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48847023 | |||||||
| chr15:48847144 | G | A | 1 | a0001c0001t0002g0332 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1304-3556C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48847144 | |||||||
| chr15:48847436 | A | G | 7 | a0001c0001t0006g0031 a0001c0001t0006g0032 a0001c0001t0006g0038 others(4): Show |
7 | HG02451.hp1 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1303+3752T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48847436 | |||||||
| chr15:48847570 | C | T | 47 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0063 others(44): Show |
47 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.1303+3618G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48847570 | |||||||
| chr15:48847692 | G | A | 2 | a0001c0001t0002g0236 a0001c0001t0002g0295 |
2 | NA18964.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.1303+3496C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48847692 | |||||||
| chr15:48847727 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1303+3461C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48847727 | |||||||
| chr15:48847728 | C | T | 2 | a0001c0001t0002g0156 a0001c0001t0011g0008 |
2 | HG02976.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1303+3460G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48847728 | |||||||
| chr15:48847800 | C | T | 1 | a0001c0001t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1303+3388G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48847800 | |||||||
| chr15:48847871 | G | A | 1 | a0001c0001t0003g0232 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1303+3317C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48847871 | |||||||
| chr15:48847927 | G | A | 1 | a0001c0001t0002g0125 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1303+3261C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48847927 | |||||||
| chr15:48847951 | G | A | 7 | a0001c0001t0002g0090 a0001c0001t0002g0145 a0001c0001t0002g0227 others(4): Show |
7 | HG02056.hp1 NA18950.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.1303+3237C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48847951 | |||||||
| chr15:48848001 | T | TA | 101 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(98): Show |
101 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.1303+3186dupT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48848001 | |||||||
| chr15:48848009 | A | C | 1 | a0001c0002t0004g0118 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1303+3179T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48848009 | |||||||
| chr15:48848010 | A | C | 3 | a0001c0001t0010g0066 a0001c0001t0010g0112 a0001c0001t0010g0193 |
3 | HG02723.hp2 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1303+3178T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48848010 | |||||||
| chr15:48848011 | A | C | 1 | a0001c0001t0005g0278 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1303+3177T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48848011 | |||||||
| chr15:48848014 | AAAACAAA others(6): Show |
A | 13 | a0002c0003t0001g0095 a0002c0003t0003g0111 a0002c0003t0003g0170 others(10): Show |
13 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(10): Show |
intron_variant | MODIFIER | c.1303+3161_1303+317 others(17): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48848014 | |||||||
| chr15:48848015 | A | C | 1 | a0001c0001t0001g0283 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1303+3173T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48848015 | |||||||
| chr15:48848015 | AAACAAAA others(5): Show |
A | 1 | a0002c0003t0003g0214 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1303+3161_1303+317 others(16): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48848015 | |||||||
| chr15:48848018 | C | A | 2 | a0001c0001t0002g0034 a0001c0007t0002g0022 |
2 | HG00621.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1303+3170G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48848018 | |||||||
| chr15:48848027 | C | A | 1 | a0001c0001t0006g0031 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1303+3161G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48848027 | |||||||
| chr15:48848031 | C | CA | 7 | a0001c0001t0006g0031 a0001c0001t0006g0032 a0001c0001t0006g0038 others(4): Show |
7 | HG02451.hp1 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1303+3156dupT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48848031 | |||||||
| chr15:48848378 | T | C | 47 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0063 others(44): Show |
47 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.1303+2810A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48848378 | |||||||
| chr15:48848504 | C | A | 1 | a0001c0001t0020g0014 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1303+2684G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48848504 | |||||||
| chr15:48848599 | C | T | 1 | a0001c0001t0002g0197 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1303+2589G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48848599 | |||||||
| chr15:48848630 | C | G | 1 | a0001c0002t0018g0010 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1303+2558G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48848630 | |||||||
| chr15:48848645 | T | C | 25 | a0001c0001t0003g0063 a0001c0001t0003g0080 a0001c0001t0003g0096 others(22): Show |
25 | HG00673.hp2 HG00735.hp2 HG01981.hp2 others(22): Show |
intron_variant | MODIFIER | c.1303+2543A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48848645 | |||||||
| chr15:48848711 | A | G | 2 | a0001c0001t0001g0318 a0001c0001t0001g0359 |
2 | HG02155.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1303+2477T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48848711 | |||||||
| chr15:48848938 | TC | T | 47 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0063 others(44): Show |
47 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.1303+2249delG | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48848938 | |||||||
| chr15:48849187 | T | C | 351 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0023 others(348): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(352): Show |
intron_variant | MODIFIER | c.1303+2001A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48849187 | |||||||
| chr15:48849226 | T | C | 2 | a0001c0001t0001g0137 a0001c0001t0009g0012 |
2 | HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1303+1962A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48849226 | |||||||
| chr15:48849941 | G | A | 1 | a0001c0002t0004g0235 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1303+1247C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48849941 | |||||||
| chr15:48849984 | C | G | 1 | a0001c0001t0009g0012 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1303+1204G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48849984 | |||||||
| chr15:48850070 | G | C | 1 | a0001c0001t0001g0162 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1303+1118C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48850070 | |||||||
| chr15:48850072 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1303+1116C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48850072 | |||||||
| chr15:48850220 | T | TATAA | 6 | a0001c0001t0004g0037 a0001c0001t0004g0123 a0001c0001t0004g0136 others(3): Show |
6 | HG00099.hp1 HG01106.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1303+964_1303+967d others(6): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48850220 | |||||||
| chr15:48850233 | ATAAAC | A | 98 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(95): Show |
98 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1303+950_1303+954d others(7): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48850233 | |||||||
| chr15:48850268 | AG | A | 47 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0063 others(44): Show |
47 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.1303+919delC | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48850268 | |||||||
| chr15:48850388 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1303+800C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48850388 | |||||||
| chr15:48850791 | A | G | 16 | a0002c0003t0001g0095 a0002c0003t0003g0046 a0002c0003t0003g0111 others(13): Show |
16 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(13): Show |
intron_variant | MODIFIER | c.1303+397T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48850791 | |||||||
| chr15:48850853 | C | A | 57 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0052 others(54): Show |
59 | HG00099.hp2 HG00642.hp1 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.1303+335G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48850853 | |||||||
| chr15:48851001 | A | G | 1 | a0001c0002t0004g0218 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1303+187T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48851001 | |||||||
| chr15:48851035 | G | T | 96 | a0001c0001t0002g0002 a0001c0001t0002g0033 a0001c0001t0002g0043 others(93): Show |
97 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1303+153C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48851035 | |||||||
| chr15:48851051 | C | G | 1 | a0001c0001t0004g0168 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1303+137G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 9/11 | chr15 | 48851051 | |||||||
| chr15:48851331 | G | A | 57 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0052 others(54): Show |
59 | HG00099.hp2 HG00642.hp1 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.1243-83C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48851331 | |||||||
| chr15:48851384 | A | G | 36 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0056 others(33): Show |
36 | HG00140.hp2 HG00408.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.1243-136T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48851384 | |||||||
| chr15:48851495 | T | C | 16 | a0002c0003t0001g0095 a0002c0003t0003g0046 a0002c0003t0003g0111 others(13): Show |
16 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(13): Show |
intron_variant | MODIFIER | c.1243-247A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48851495 | |||||||
| chr15:48851690 | C | G | 1 | a0001c0001t0001g0044 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1243-442G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48851690 | |||||||
| chr15:48851732 | G | A | 1 | a0001c0012t0003g0040 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1243-484C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48851732 | |||||||
| chr15:48851748 | G | A | 1 | a0001c0001t0024g0025 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1243-500C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48851748 | |||||||
| chr15:48851749 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1243-501C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48851749 | |||||||
| chr15:48851763 | T | C | 1 | a0001c0012t0003g0040 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1243-515A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48851763 | |||||||
| chr15:48851915 | G | A | 7 | a0001c0001t0006g0031 a0001c0001t0006g0032 a0001c0001t0006g0038 others(4): Show |
7 | HG02451.hp1 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1243-667C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48851915 | |||||||
| chr15:48852117 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1243-869T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48852117 | |||||||
| chr15:48852174 | A | C | 1 | a0001c0001t0001g0044 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1243-926T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48852174 | |||||||
| chr15:48852197 | G | A | 41 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0026 others(38): Show |
42 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.1243-949C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48852197 | |||||||
| chr15:48852310 | T | C | 10 | a0001c0001t0001g0030 a0001c0001t0001g0082 a0001c0001t0001g0087 others(7): Show |
10 | HG02145.hp2 HG02723.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1243-1062A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48852310 | |||||||
| chr15:48852632 | C | T | 89 | a0001c0001t0002g0002 a0001c0001t0002g0033 a0001c0001t0002g0043 others(86): Show |
90 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1243-1384G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48852632 | |||||||
| chr15:48852635 | C | T | 1 | a0001c0012t0003g0040 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1243-1387G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48852635 | |||||||
| chr15:48852692 | A | G | 1 | a0001c0001t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1243-1444T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48852692 | |||||||
| chr15:48852710 | T | G | 1 | a0001c0001t0001g0368 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1243-1462A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48852710 | |||||||
| chr15:48852915 | A | AAAAT | 181 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0023 others(178): Show |
185 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1243-1671_1243-166 others(8): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48852915 | |||||||
| chr15:48852915 | A | AAAATAAA others(1): Show |
7 | a0001c0001t0001g0140 a0001c0001t0001g0198 a0001c0001t0002g0043 others(4): Show |
7 | HG00544.hp2 HG00597.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1243-1675_1243-166 others(12): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48852915 | |||||||
| chr15:48853060 | T | C | 2 | a0001c0001t0005g0138 a0001c0001t0005g0142 |
2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1243-1812A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48853060 | |||||||
| chr15:48853598 | G | A | 5 | a0001c0001t0004g0037 a0001c0001t0004g0136 a0001c0001t0004g0155 others(2): Show |
5 | HG00099.hp1 HG02055.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.1243-2350C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48853598 | |||||||
| chr15:48853635 | T | G | 3 | a0001c0002t0004g0047 a0001c0002t0004g0048 a0001c0002t0004g0049 |
3 | HG01258.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1242+2318A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48853635 | |||||||
| chr15:48853843 | T | C | 1 | a0001c0001t0002g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1242+2110A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48853843 | |||||||
| chr15:48853849 | C | T | 1 | a0001c0001t0002g0331 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1242+2104G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48853849 | |||||||
| chr15:48853850 | G | A | 57 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0052 others(54): Show |
59 | HG00099.hp2 HG00642.hp1 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.1242+2103C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48853850 | |||||||
| chr15:48854073 | C | A | 38 | a0001c0001t0004g0168 a0001c0002t0004g0003 a0001c0002t0004g0047 others(35): Show |
39 | HG00741.hp1 HG00741.hp2 HG01175.hp2 others(36): Show |
intron_variant | MODIFIER | c.1242+1880G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48854073 | |||||||
| chr15:48854237 | T | C | 1 | a0001c0001t0003g0365 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1242+1716A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48854237 | |||||||
| chr15:48854274 | CATATCAT | C | 3 | a0001c0001t0010g0066 a0001c0001t0010g0112 a0001c0001t0010g0193 |
3 | HG02723.hp2 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1242+1672_1242+167 others(11): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48854274 | |||||||
| chr15:48854281 | T | C | 370 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0023 others(367): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.1242+1672A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48854281 | |||||||
| chr15:48854298 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1242+1655A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48854298 | |||||||
| chr15:48854547 | G | A | 1 | a0001c0012t0003g0040 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1242+1406C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48854547 | |||||||
| chr15:48854586 | G | C | 1 | a0001c0004t0005g0376 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1242+1367C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48854586 | |||||||
| chr15:48854749 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1242+1204A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48854749 | |||||||
| chr15:48854782 | G | A | 32 | a0001c0001t0001g0070 a0001c0001t0001g0084 a0001c0001t0001g0093 others(29): Show |
32 | HG00438.hp1 HG01069.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.1242+1171C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48854782 | |||||||
| chr15:48854811 | C | T | 1 | a0001c0001t0002g0125 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1242+1142G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48854811 | |||||||
| chr15:48854814 | C | T | 47 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0063 others(44): Show |
47 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.1242+1139G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48854814 | |||||||
| chr15:48854918 | C | T | 57 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0052 others(54): Show |
59 | HG00099.hp2 HG00642.hp1 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.1242+1035G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48854918 | |||||||
| chr15:48854992 | C | T | 98 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(95): Show |
98 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1242+961G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48854992 | |||||||
| chr15:48855030 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1242+923C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48855030 | |||||||
| chr15:48855302 | T | A | 1 | a0001c0001t0001g0146 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1242+651A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48855302 | |||||||
| chr15:48855373 | A | C | 1 | a0001c0001t0022g0254 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1242+580T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48855373 | |||||||
| chr15:48855373 | A | G | 5 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0035 others(2): Show |
6 | HG01167.hp1 HG01169.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1242+580T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48855373 | |||||||
| chr15:48855414 | A | G | 1 | a0001c0001t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1242+539T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 8/11 | chr15 | 48855414 | |||||||
| chr15:48856159 | C | A | 98 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(95): Show |
98 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1071-35G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 7/11 | chr15 | 48856159 | |||||||
| chr15:48856159 | C | T | 1 | a0001c0001t0005g0277 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1071-35G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 7/11 | chr15 | 48856159 | |||||||
| chr15:48856280 | G | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0023 others(145): Show |
151 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.1071-156C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 7/11 | chr15 | 48856280 | |||||||
| chr15:48856299 | T | C | 2 | a0001c0001t0001g0137 a0001c0001t0009g0012 |
2 | HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1071-175A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 7/11 | chr15 | 48856299 | |||||||
| chr15:48856323 | C | A | 1 | a0002c0003t0001g0095 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1071-199G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 7/11 | chr15 | 48856323 | |||||||
| chr15:48856390 | T | C | 1 | a0001c0001t0005g0349 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1071-266A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 7/11 | chr15 | 48856390 | |||||||
| chr15:48856433 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1071-309T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 7/11 | chr15 | 48856433 | |||||||
| chr15:48856773 | T | TA | 52 | a0001c0001t0001g0029 a0001c0001t0001g0044 a0001c0001t0001g0098 others(49): Show |
52 | HG00741.hp1 HG00741.hp2 HG01175.hp2 others(49): Show |
intron_variant | MODIFIER | c.1071-650dupT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 7/11 | chr15 | 48856773 | |||||||
| chr15:48856773 | T | TAA | 39 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0026 others(36): Show |
41 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(38): Show |
intron_variant | MODIFIER | c.1071-651_1071-650d others(4): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 7/11 | chr15 | 48856773 | |||||||
| chr15:48856773 | TA | T | 8 | a0001c0001t0002g0236 a0001c0001t0002g0262 a0001c0001t0002g0303 others(5): Show |
8 | HG00099.hp1 HG02055.hp1 HG03710.hp1 others(5): Show |
intron_variant | MODIFIER | c.1071-650delT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 7/11 | chr15 | 48856773 | |||||||
| chr15:48856851 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1071-727A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 7/11 | chr15 | 48856851 | |||||||
| chr15:48856954 | C | T | 1 | a0001c0001t0003g0253 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1070+738G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 7/11 | chr15 | 48856954 | |||||||
| chr15:48856980 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1070+712G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 7/11 | chr15 | 48856980 | |||||||
| chr15:48857062 | C | T | 51 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0063 others(48): Show |
51 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.1070+630G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 7/11 | chr15 | 48857062 | |||||||
| chr15:48857445 | T | C | 1 | a0001c0001t0002g0055 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1070+247A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 7/11 | chr15 | 48857445 | |||||||
| chr15:48857631 | C | T | 335 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(332): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.1070+61G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 7/11 | chr15 | 48857631 | |||||||
| chr15:48857881 | C | T | 6 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0281 others(3): Show |
6 | HG02257.hp2 HG02258.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.947-66G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48857881 | |||||||
| chr15:48857979 | C | G | 1 | a0001c0001t0001g0327 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.947-164G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48857979 | |||||||
| chr15:48858189 | G | C | 1 | a0001c0001t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.947-374C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48858189 | |||||||
| chr15:48858298 | T | G | 1 | a0001c0001t0001g0215 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.947-483A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48858298 | |||||||
| chr15:48858481 | T | C | 2 | a0001c0006t0001g0228 a0001c0006t0001g0319 |
2 | NA18941.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.947-666A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48858481 | |||||||
| chr15:48858544 | G | A | 1 | a0001c0002t0004g0234 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.947-729C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48858544 | |||||||
| chr15:48858695 | T | C | 5 | a0001c0001t0001g0044 a0001c0001t0010g0066 a0001c0001t0010g0112 others(2): Show |
5 | HG01496.hp2 HG02602.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.947-880A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48858695 | |||||||
| chr15:48858759 | C | A | 1 | a0001c0001t0001g0216 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.947-944G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48858759 | |||||||
| chr15:48858808 | A | G | 1 | a0001c0001t0005g0062 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.947-993T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48858808 | |||||||
| chr15:48858852 | C | G | 1 | a0007c0008t0004g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.947-1037G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48858852 | |||||||
| chr15:48858891 | A | G | 25 | a0001c0001t0001g0045 a0001c0001t0001g0089 a0001c0001t0001g0119 others(22): Show |
25 | HG01109.hp1 HG01884.hp1 HG01928.hp2 others(22): Show |
intron_variant | MODIFIER | c.947-1076T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48858891 | |||||||
| chr15:48859108 | T | A | 1 | a0001c0001t0012g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.947-1293A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48859108 | |||||||
| chr15:48859206 | C | T | 337 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(334): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.947-1391G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48859206 | |||||||
| chr15:48859304 | GGGGT | G | 5 | a0001c0001t0001g0225 a0001c0001t0001g0299 a0001c0001t0001g0308 others(2): Show |
5 | NA18949.hp2 NA18957.hp2 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.947-1493_947-1490d others(6): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48859304 | |||||||
| chr15:48859306 | G | GGT | 33 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0045 others(30): Show |
34 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.947-1493_947-1492d others(4): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48859306 | |||||||
| chr15:48859306 | G | GGTGT | 39 | a0001c0001t0001g0029 a0001c0001t0001g0089 a0001c0001t0001g0097 others(36): Show |
40 | HG00741.hp1 HG01175.hp2 HG01361.hp2 others(37): Show |
intron_variant | MODIFIER | c.947-1495_947-1492d others(6): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48859306 | |||||||
| chr15:48859306 | G | GGTGTGT | 10 | a0001c0002t0004g0047 a0001c0002t0004g0048 a0001c0002t0004g0049 others(7): Show |
10 | HG00741.hp2 HG01258.hp2 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.947-1497_947-1492d others(8): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48859306 | |||||||
| chr15:48859306 | G | GGTGTGTG others(7): Show |
1 | a0001c0001t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.947-1505_947-1492d others(16): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48859306 | |||||||
| chr15:48859306 | G | T | 1 | a0001c0001t0001g0323 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.947-1491C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48859306 | |||||||
| chr15:48859306 | GGT | G | 123 | a0001c0001t0001g0068 a0001c0001t0001g0076 a0001c0001t0001g0087 others(120): Show |
124 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.947-1493_947-1492d others(4): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48859306 | |||||||
| chr15:48859306 | GGTGT | G | 89 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(86): Show |
89 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.947-1495_947-1492d others(6): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48859306 | |||||||
| chr15:48859306 | GGTGTGT | G | 20 | a0001c0001t0003g0063 a0001c0001t0003g0080 a0001c0001t0003g0096 others(17): Show |
20 | HG00735.hp2 HG01981.hp2 HG02004.hp1 others(17): Show |
intron_variant | MODIFIER | c.947-1497_947-1492d others(8): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48859306 | |||||||
| chr15:48859310 | T | G | 3 | a0001c0001t0010g0066 a0001c0001t0010g0112 a0001c0001t0010g0193 |
3 | HG02723.hp2 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.947-1495A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48859310 | |||||||
| chr15:48859453 | G | A | 3 | a0001c0002t0004g0129 a0001c0002t0004g0131 a0001c0002t0004g0132 |
3 | HG01175.hp2 HG01978.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.947-1638C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48859453 | |||||||
| chr15:48859515 | G | A | 6 | a0001c0001t0002g0064 a0001c0001t0002g0164 a0001c0001t0002g0315 others(3): Show |
6 | HG00423.hp2 HG00609.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.947-1700C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48859515 | |||||||
| chr15:48859601 | A | G | 1 | a0001c0001t0003g0271 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.947-1786T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48859601 | |||||||
| chr15:48859800 | C | T | 7 | a0001c0001t0006g0031 a0001c0001t0006g0032 a0001c0001t0006g0038 others(4): Show |
7 | HG02451.hp1 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.947-1985G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48859800 | |||||||
| chr15:48859810 | C | G | 102 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(99): Show |
102 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.947-1995G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48859810 | |||||||
| chr15:48859912 | A | G | 1 | a0007c0008t0004g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.947-2097T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48859912 | |||||||
| chr15:48859940 | G | T | 88 | a0001c0001t0002g0002 a0001c0001t0002g0033 a0001c0001t0002g0043 others(85): Show |
89 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.947-2125C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48859940 | |||||||
| chr15:48860157 | C | CT | 159 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0052 others(156): Show |
162 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.947-2343dupA | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48860157 | |||||||
| chr15:48860188 | T | C | 47 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0063 others(44): Show |
47 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.947-2373A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48860188 | |||||||
| chr15:48860198 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.947-2383G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48860198 | |||||||
| chr15:48860341 | T | C | 212 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0044 others(209): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.947-2526A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48860341 | |||||||
| chr15:48860356 | A | T | 159 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0052 others(156): Show |
162 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.947-2541T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48860356 | |||||||
| chr15:48860615 | G | A | 1 | a0001c0001t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.947-2800C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48860615 | |||||||
| chr15:48860922 | T | C | 6 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0281 others(3): Show |
6 | HG02257.hp2 HG02258.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.947-3107A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48860922 | |||||||
| chr15:48861166 | G | C | 1 | a0001c0001t0001g0162 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.947-3351C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48861166 | |||||||
| chr15:48861307 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.947-3492A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48861307 | |||||||
| chr15:48861396 | T | G | 6 | a0001c0001t0004g0037 a0001c0001t0004g0123 a0001c0001t0004g0136 others(3): Show |
6 | HG00099.hp1 HG01106.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.947-3581A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48861396 | |||||||
| chr15:48861446 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.947-3631A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48861446 | |||||||
| chr15:48861549 | T | G | 25 | a0001c0001t0003g0063 a0001c0001t0003g0080 a0001c0001t0003g0096 others(22): Show |
25 | HG00673.hp2 HG00735.hp2 HG01981.hp2 others(22): Show |
intron_variant | MODIFIER | c.947-3734A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48861549 | |||||||
| chr15:48861785 | A | G | 3 | a0001c0001t0003g0151 a0001c0001t0003g0246 a0001c0001t0003g0253 |
3 | HG00735.hp2 HG01981.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.947-3970T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48861785 | |||||||
| chr15:48861886 | A | G | 1 | a0001c0001t0001g0284 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.947-4071T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48861886 | |||||||
| chr15:48862022 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.947-4207A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48862022 | |||||||
| chr15:48862052 | T | C | 40 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0026 others(37): Show |
41 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.947-4237A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48862052 | |||||||
| chr15:48862192 | TG | T | 6 | a0001c0001t0001g0076 a0001c0001t0001g0269 a0001c0001t0001g0327 others(3): Show |
6 | HG00544.hp1 HG00558.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.947-4378delC | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48862192 | |||||||
| chr15:48862196 | G | GT | 16 | a0001c0001t0001g0175 a0001c0001t0002g0322 a0001c0001t0005g0057 others(13): Show |
16 | HG00140.hp1 HG00280.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.947-4382dupA | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48862196 | |||||||
| chr15:48862196 | G | T | 95 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(92): Show |
95 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.947-4381C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48862196 | |||||||
| chr15:48862244 | T | C | 1 | a0001c0001t0001g0337 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.947-4429A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48862244 | |||||||
| chr15:48862361 | C | A | 1 | a0001c0001t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.947-4546G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48862361 | |||||||
| chr15:48862521 | A | T | 5 | a0001c0001t0001g0029 a0001c0001t0001g0097 a0001c0001t0001g0098 others(2): Show |
5 | HG01361.hp2 HG02922.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.947-4706T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48862521 | |||||||
| chr15:48862626 | T | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0026 others(38): Show |
42 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.947-4811A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48862626 | |||||||
| chr15:48862808 | C | T | 1 | a0001c0001t0005g0036 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.947-4993G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48862808 | |||||||
| chr15:48862810 | C | T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0026 others(38): Show |
42 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.947-4995G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48862810 | |||||||
| chr15:48863003 | C | A | 7 | a0001c0002t0004g0047 a0001c0002t0004g0048 a0001c0002t0004g0049 others(4): Show |
7 | HG00741.hp2 HG01175.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.946+4815G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48863003 | |||||||
| chr15:48863065 | A | AACTTGCT others(317): Show |
1 | a0001c0001t0001g0158 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.946+4752_946+4753i others(326): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48863065 | |||||||
| chr15:48863065 | A | AACTTGCT others(319): Show |
1 | a0001c0001t0001g0159 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.946+4752_946+4753i others(328): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48863065 | |||||||
| chr15:48863065 | A | AACTTGCT others(318): Show |
3 | a0001c0001t0001g0162 a0001c0006t0001g0319 a0005c0009t0001g0103 |
3 | HG02897.hp1 HG03017.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.946+4752_946+4753i others(327): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48863065 | |||||||
| chr15:48863065 | A | AACTTGCT others(319): Show |
9 | a0001c0001t0001g0056 a0001c0001t0001g0148 a0001c0001t0001g0268 others(6): Show |
9 | HG00140.hp2 HG01099.hp2 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.946+4752_946+4753i others(328): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48863065 | |||||||
| chr15:48863065 | A | AACTTGCT others(321): Show |
4 | a0001c0001t0001g0069 a0001c0001t0001g0137 a0001c0001t0001g0166 others(1): Show |
4 | HG01496.hp1 HG02602.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.946+4752_946+4753i others(330): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48863065 | |||||||
| chr15:48863065 | A | AACTTGCT others(320): Show |
16 | a0001c0001t0001g0082 a0001c0001t0001g0087 a0001c0001t0001g0100 others(13): Show |
16 | HG00408.hp2 HG00621.hp1 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.946+4752_946+4753i others(329): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48863065 | |||||||
| chr15:48863065 | A | AACTTGCT others(322): Show |
23 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0084 others(20): Show |
23 | HG00544.hp1 HG00558.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.946+4752_946+4753i others(331): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48863065 | |||||||
| chr15:48863065 | A | AACTTGCT others(321): Show |
14 | a0001c0001t0001g0030 a0001c0001t0001g0042 a0001c0001t0001g0126 others(11): Show |
14 | HG01167.hp2 HG01952.hp2 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.946+4752_946+4753i others(330): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48863065 | |||||||
| chr15:48863065 | A | AACTTGCT others(323): Show |
11 | a0001c0001t0001g0070 a0001c0001t0001g0076 a0001c0001t0001g0093 others(8): Show |
11 | HG00438.hp1 HG01243.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.946+4752_946+4753i others(332): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48863065 | |||||||
| chr15:48863065 | A | AACTTGCT others(322): Show |
2 | a0001c0001t0001g0041 a0001c0001t0001g0255 |
2 | HG03927.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.946+4752_946+4753i others(331): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48863065 | |||||||
| chr15:48863065 | A | AACTTGCT others(324): Show |
10 | a0001c0001t0001g0108 a0001c0001t0001g0146 a0001c0001t0001g0216 others(7): Show |
10 | HG01257.hp2 HG02155.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.946+4752_946+4753i others(333): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48863065 | |||||||
| chr15:48863065 | A | AACTTGCT others(323): Show |
1 | a0001c0001t0001g0194 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.946+4752_946+4753i others(332): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48863065 | |||||||
| chr15:48863065 | A | AACTTGCT others(324): Show |
1 | a0001c0001t0001g0154 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.946+4752_946+4753i others(333): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48863065 | |||||||
| chr15:48863065 | A | AACTTGCT others(327): Show |
1 | a0001c0001t0017g0011 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.946+4752_946+4753i others(336): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48863065 | |||||||
| chr15:48863065 | A | AACTTGCT others(326): Show |
1 | a0001c0001t0002g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.946+4752_946+4753i others(335): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48863065 | |||||||
| chr15:48863134 | T | C | 48 | a0001c0001t0001g0044 a0001c0001t0003g0060 a0001c0001t0003g0061 others(45): Show |
48 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.946+4684A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48863134 | |||||||
| chr15:48863293 | C | T | 351 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0023 others(348): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(352): Show |
intron_variant | MODIFIER | c.946+4525G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48863293 | |||||||
| chr15:48863449 | G | T | 1 | a0001c0001t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.946+4369C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48863449 | |||||||
| chr15:48863480 | A | AAATT | 353 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0023 others(350): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(354): Show |
intron_variant | MODIFIER | c.946+4334_946+4337d others(6): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48863480 | |||||||
| chr15:48863602 | T | C | 1 | a0001c0001t0003g0232 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.946+4216A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48863602 | |||||||
| chr15:48863682 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.946+4136T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48863682 | |||||||
| chr15:48863705 | T | C | 1 | a0001c0001t0003g0063 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.946+4113A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48863705 | |||||||
| chr15:48863753 | T | C | 1 | a0001c0001t0002g0055 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.946+4065A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48863753 | |||||||
| chr15:48863817 | A | T | 98 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(95): Show |
98 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.946+4001T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48863817 | |||||||
| chr15:48863967 | G | A | 47 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0063 others(44): Show |
47 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.946+3851C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48863967 | |||||||
| chr15:48864010 | G | A | 1 | a0001c0001t0002g0197 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.946+3808C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48864010 | |||||||
| chr15:48864066 | T | C | 351 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0023 others(348): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(352): Show |
intron_variant | MODIFIER | c.946+3752A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48864066 | |||||||
| chr15:48864436 | C | CT | 19 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0035 others(16): Show |
20 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.946+3381dupA | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48864436 | |||||||
| chr15:48864436 | CT | C | 195 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0041 others(192): Show |
198 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.946+3381delA | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48864436 | |||||||
| chr15:48864436 | CTT | C | 84 | a0001c0001t0001g0030 a0001c0001t0001g0042 a0001c0001t0001g0056 others(81): Show |
84 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.946+3380_946+3381d others(4): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48864436 | |||||||
| chr15:48864436 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0019g0021 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.946+3371_946+3381d others(13): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48864436 | |||||||
| chr15:48864436 | CTTTTTTT others(6): Show |
C | 1 | a0007c0008t0004g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.946+3369_946+3381d others(15): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48864436 | |||||||
| chr15:48864471 | A | G | 5 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0281 others(2): Show |
5 | HG02257.hp2 HG02809.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.946+3347T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48864471 | |||||||
| chr15:48864508 | C | T | 5 | a0001c0001t0004g0037 a0001c0001t0004g0136 a0001c0001t0004g0155 others(2): Show |
5 | HG00099.hp1 HG02055.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.946+3310G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48864508 | |||||||
| chr15:48864540 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.946+3278G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48864540 | |||||||
| chr15:48864610 | G | A | 47 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0063 others(44): Show |
47 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.946+3208C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48864610 | |||||||
| chr15:48865040 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.946+2778A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48865040 | |||||||
| chr15:48865203 | T | A | 47 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(44): Show |
47 | HG00140.hp2 HG00408.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.946+2615A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48865203 | |||||||
| chr15:48865259 | G | A | 1 | a0001c0012t0003g0040 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.946+2559C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48865259 | |||||||
| chr15:48865407 | T | A | 24 | a0001c0001t0001g0045 a0001c0001t0001g0089 a0001c0001t0001g0119 others(21): Show |
24 | HG01109.hp1 HG01884.hp1 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.946+2411A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48865407 | |||||||
| chr15:48865409 | T | G | 49 | a0001c0001t0001g0044 a0001c0001t0003g0060 a0001c0001t0003g0061 others(46): Show |
49 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.946+2409A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48865409 | |||||||
| chr15:48865595 | C | T | 1 | a0001c0001t0019g0021 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.946+2223G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48865595 | |||||||
| chr15:48865766 | A | T | 337 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(334): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.946+2052T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48865766 | |||||||
| chr15:48866444 | G | C | 1 | a0001c0001t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.946+1374C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48866444 | |||||||
| chr15:48866486 | A | G | 1 | a0001c0001t0001g0045 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.946+1332T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48866486 | |||||||
| chr15:48866506 | C | G | 1 | a0001c0012t0003g0040 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.946+1312G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48866506 | |||||||
| chr15:48866508 | C | A | 43 | a0001c0001t0001g0029 a0001c0001t0001g0097 a0001c0001t0001g0098 others(40): Show |
44 | HG00741.hp1 HG00741.hp2 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.946+1310G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48866508 | |||||||
| chr15:48866744 | T | C | 1 | a0001c0012t0003g0040 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.946+1074A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48866744 | |||||||
| chr15:48866809 | A | C | 351 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0023 others(348): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(352): Show |
intron_variant | MODIFIER | c.946+1009T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48866809 | |||||||
| chr15:48866859 | G | A | 1 | a0001c0001t0001g0367 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.946+959C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48866859 | |||||||
| chr15:48866901 | G | A | 156 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0044 others(153): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.946+917C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48866901 | |||||||
| chr15:48867083 | C | G | 149 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0052 others(146): Show |
152 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.946+735G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48867083 | |||||||
| chr15:48867191 | C | T | 1 | a0001c0012t0003g0040 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.946+627G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48867191 | |||||||
| chr15:48867402 | T | C | 1 | a0002c0003t0013g0380 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.946+416A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48867402 | |||||||
| chr15:48867422 | GACACACA others(5): Show |
G | 25 | a0001c0001t0003g0063 a0001c0001t0003g0080 a0001c0001t0003g0096 others(22): Show |
25 | HG00673.hp2 HG00735.hp2 HG01981.hp2 others(22): Show |
intron_variant | MODIFIER | c.946+384_946+395del others(12): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48867422 | |||||||
| chr15:48867593 | G | A | 1 | a0001c0001t0006g0088 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.946+225C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48867593 | |||||||
| chr15:48867632 | T | C | 1 | a0001c0002t0004g0218 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.946+186A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48867632 | |||||||
| chr15:48867817 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG02273.hp2 | splice_donor_variant&intron_variant | HIGH | c.946+1G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 6/11 | chr15 | 48867817 | |||||||
| chr15:48867892 | G | C | 6 | a0001c0001t0002g0064 a0001c0001t0002g0164 a0001c0001t0002g0315 others(3): Show |
6 | HG00423.hp2 HG00609.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.895-23C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48867892 | |||||||
| chr15:48868037 | A | C | 1 | a0001c0001t0004g0037 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.895-168T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48868037 | |||||||
| chr15:48868124 | T | C | 1 | a0001c0001t0004g0123 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.895-255A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48868124 | |||||||
| chr15:48868139 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.895-270T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48868139 | |||||||
| chr15:48868161 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.895-292A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48868161 | |||||||
| chr15:48868415 | A | G | 1 | a0001c0001t0002g0167 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.895-546T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48868415 | |||||||
| chr15:48868501 | G | A | 3 | a0001c0001t0005g0114 a0001c0001t0005g0260 a0001c0001t0005g0267 |
3 | HG00140.hp1 HG00280.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.895-632C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48868501 | |||||||
| chr15:48868624 | T | C | 2 | a0001c0001t0002g0227 a0001c0001t0002g0370 |
2 | NA18950.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.895-755A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48868624 | |||||||
| chr15:48868821 | T | C | 7 | a0001c0001t0001g0068 a0001c0001t0001g0147 a0001c0001t0001g0172 others(4): Show |
7 | HG00099.hp2 HG00642.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.895-952A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48868821 | |||||||
| chr15:48868839 | G | A | 8 | a0001c0001t0006g0031 a0001c0001t0006g0032 a0001c0001t0006g0038 others(5): Show |
8 | HG02451.hp1 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.895-970C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48868839 | |||||||
| chr15:48868842 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.895-973T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48868842 | |||||||
| chr15:48869093 | T | C | 47 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0063 others(44): Show |
47 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.895-1224A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48869093 | |||||||
| chr15:48869194 | T | A | 1 | a0001c0001t0019g0021 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.895-1325A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48869194 | |||||||
| chr15:48869318 | A | G | 47 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0063 others(44): Show |
47 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.895-1449T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48869318 | |||||||
| chr15:48869347 | G | T | 1 | a0001c0001t0002g0197 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.895-1478C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48869347 | |||||||
| chr15:48869365 | T | C | 20 | a0001c0001t0001g0045 a0001c0001t0001g0089 a0001c0001t0001g0152 others(17): Show |
20 | HG01109.hp1 HG01928.hp2 HG02273.hp1 others(17): Show |
intron_variant | MODIFIER | c.895-1496A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48869365 | |||||||
| chr15:48869522 | G | C | 1 | a0001c0001t0001g0275 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.895-1653C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48869522 | |||||||
| chr15:48869550 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.895-1681G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48869550 | |||||||
| chr15:48869737 | A | C | 119 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(116): Show |
120 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.895-1868T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48869737 | |||||||
| chr15:48869740 | G | A | 1 | a0001c0001t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.895-1871C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48869740 | |||||||
| chr15:48869804 | C | T | 178 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0045 others(175): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.895-1935G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48869804 | |||||||
| chr15:48869805 | G | A | 48 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0063 others(45): Show |
48 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.895-1936C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48869805 | |||||||
| chr15:48869920 | TTAA | T | 4 | a0001c0001t0001g0122 a0001c0001t0001g0144 a0001c0001t0001g0189 others(1): Show |
4 | HG00738.hp1 HG01081.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.895-2054_895-2052d others(5): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48869920 | |||||||
| chr15:48870037 | A | C | 2 | a0001c0001t0004g0037 a0007c0008t0004g0104 |
2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.894+2052T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48870037 | |||||||
| chr15:48870057 | C | T | 1 | a0001c0004t0005g0376 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.894+2032G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48870057 | |||||||
| chr15:48870083 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.894+2006G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48870083 | |||||||
| chr15:48870229 | G | T | 1 | a0001c0001t0005g0057 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.894+1860C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48870229 | |||||||
| chr15:48870320 | C | T | 1 | a0001c0001t0002g0190 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.894+1769G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48870320 | |||||||
| chr15:48870506 | C | A | 1 | a0002c0003t0003g0264 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.894+1583G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48870506 | |||||||
| chr15:48870592 | A | C | 1 | a0001c0001t0019g0021 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.894+1497T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48870592 | |||||||
| chr15:48870669 | C | A | 1 | a0002c0003t0001g0095 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.894+1420G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48870669 | |||||||
| chr15:48870677 | C | CA | 12 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0082 others(9): Show |
12 | HG02109.hp1 HG02145.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.894+1411dupT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48870677 | |||||||
| chr15:48870686 | A | G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0209 |
2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.894+1403T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48870686 | |||||||
| chr15:48870723 | A | G | 336 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(333): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.894+1366T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48870723 | |||||||
| chr15:48870736 | C | T | 1 | a0001c0001t0002g0033 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.894+1353G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48870736 | |||||||
| chr15:48870756 | T | C | 182 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0044 others(179): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.894+1333A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48870756 | |||||||
| chr15:48870849 | G | A | 336 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(333): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.894+1240C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48870849 | |||||||
| chr15:48870905 | C | T | 1 | a0001c0001t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.894+1184G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48870905 | |||||||
| chr15:48870974 | A | G | 1 | a0002c0003t0003g0264 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.894+1115T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48870974 | |||||||
| chr15:48870987 | C | T | 48 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0063 others(45): Show |
48 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.894+1102G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48870987 | |||||||
| chr15:48871144 | G | A | 2 | a0001c0001t0001g0243 a0001c0001t0001g0373 |
2 | HG00438.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.894+945C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48871144 | |||||||
| chr15:48871197 | A | T | 47 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0063 others(44): Show |
47 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.894+892T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48871197 | |||||||
| chr15:48871563 | G | A | 1 | a0001c0001t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.894+526C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48871563 | |||||||
| chr15:48871642 | T | C | 2 | a0001c0001t0001g0137 a0001c0001t0009g0012 |
2 | HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.894+447A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48871642 | |||||||
| chr15:48871666 | T | C | 25 | a0001c0001t0003g0063 a0001c0001t0003g0080 a0001c0001t0003g0096 others(22): Show |
25 | HG00673.hp2 HG00735.hp2 HG01981.hp2 others(22): Show |
intron_variant | MODIFIER | c.894+423A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48871666 | |||||||
| chr15:48871852 | T | C | 8 | a0001c0001t0002g0085 a0001c0001t0006g0031 a0001c0001t0006g0032 others(5): Show |
8 | HG02451.hp1 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.894+237A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48871852 | |||||||
| chr15:48872000 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.894+89T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 5/11 | chr15 | 48872000 | |||||||
| chr15:48872304 | C | T | 47 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0063 others(44): Show |
47 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.841-162G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48872304 | |||||||
| chr15:48872330 | C | T | 1 | a0002c0003t0003g0187 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.841-188G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48872330 | |||||||
| chr15:48872721 | T | G | 1 | a0001c0012t0003g0040 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.841-579A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48872721 | |||||||
| chr15:48872814 | T | A | 8 | a0001c0001t0001g0084 a0001c0001t0001g0177 a0001c0001t0001g0261 others(5): Show |
8 | HG02155.hp1 NA18957.hp1 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.841-672A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48872814 | |||||||
| chr15:48872922 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.841-780A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48872922 | |||||||
| chr15:48872995 | A | C | 1 | a0001c0002t0004g0325 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.841-853T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48872995 | |||||||
| chr15:48873020 | T | C | 15 | a0001c0001t0001g0175 a0001c0001t0005g0057 a0001c0001t0005g0072 others(12): Show |
15 | HG00140.hp1 HG00280.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.841-878A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48873020 | |||||||
| chr15:48873084 | C | A | 1 | a0001c0001t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.841-942G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48873084 | |||||||
| chr15:48873126 | C | CA | 336 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(333): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.841-985dupT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48873126 | |||||||
| chr15:48873181 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.841-1039T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48873181 | |||||||
| chr15:48873235 | T | C | 20 | a0001c0001t0002g0033 a0001c0001t0002g0043 a0001c0001t0002g0051 others(17): Show |
20 | HG00280.hp2 HG00609.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.841-1093A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48873235 | |||||||
| chr15:48873413 | C | T | 2 | a0001c0001t0004g0037 a0007c0008t0004g0104 |
2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.841-1271G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48873413 | |||||||
| chr15:48873419 | C | T | 100 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(97): Show |
100 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.841-1277G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48873419 | |||||||
| chr15:48873511 | G | A | 102 | a0001c0001t0001g0137 a0001c0001t0002g0002 a0001c0001t0002g0033 others(99): Show |
103 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.841-1369C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48873511 | |||||||
| chr15:48873520 | G | A | 2 | a0001c0001t0001g0224 a0001c0001t0001g0268 |
2 | HG02165.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.841-1378C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48873520 | |||||||
| chr15:48873537 | G | A | 3 | a0001c0001t0010g0066 a0001c0001t0010g0112 a0001c0001t0010g0193 |
3 | HG02723.hp2 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.841-1395C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48873537 | |||||||
| chr15:48873728 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.841-1586C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48873728 | |||||||
| chr15:48873740 | C | CA | 51 | a0001c0001t0001g0139 a0001c0001t0001g0215 a0001c0001t0002g0027 others(48): Show |
51 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.841-1599dupT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48873740 | |||||||
| chr15:48873761 | A | G | 1 | a0001c0001t0002g0211 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.841-1619T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48873761 | |||||||
| chr15:48873920 | G | T | 1 | a0001c0001t0002g0321 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.841-1778C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48873920 | |||||||
| chr15:48873997 | T | G | 1 | a0001c0001t0001g0192 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.841-1855A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48873997 | |||||||
| chr15:48874220 | A | G | 235 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0044 others(232): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.841-2078T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48874220 | |||||||
| chr15:48874258 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.841-2116A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48874258 | |||||||
| chr15:48874406 | G | A | 1 | a0001c0001t0003g0312 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.841-2264C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48874406 | |||||||
| chr15:48874406 | G | C | 16 | a0002c0003t0001g0095 a0002c0003t0003g0046 a0002c0003t0003g0111 others(13): Show |
16 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(13): Show |
intron_variant | MODIFIER | c.841-2264C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48874406 | |||||||
| chr15:48874484 | ACTGT | A | 102 | a0001c0001t0001g0137 a0001c0001t0002g0002 a0001c0001t0002g0033 others(99): Show |
103 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.841-2346_841-2343d others(6): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48874484 | |||||||
| chr15:48874485 | C | T | 1 | a0001c0002t0004g0288 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.841-2343G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48874485 | |||||||
| chr15:48874537 | G | C | 5 | a0001c0001t0001g0030 a0001c0001t0001g0126 a0001c0001t0001g0194 others(2): Show |
5 | HG02723.hp1 HG02818.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.841-2395C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48874537 | |||||||
| chr15:48874539 | G | C | 100 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(97): Show |
100 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.841-2397C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48874539 | |||||||
| chr15:48874545 | A | G | 2 | a0001c0001t0004g0037 a0007c0008t0004g0104 |
2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.841-2403T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48874545 | |||||||
| chr15:48874610 | G | C | 47 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0063 others(44): Show |
47 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.841-2468C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48874610 | |||||||
| chr15:48874643 | A | C | 1 | a0001c0001t0001g0192 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.841-2501T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48874643 | |||||||
| chr15:48874665 | T | C | 1 | a0001c0002t0018g0010 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.841-2523A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48874665 | |||||||
| chr15:48874678 | T | C | 2 | a0001c0001t0004g0037 a0007c0008t0004g0104 |
2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.841-2536A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48874678 | |||||||
| chr15:48874885 | A | G | 336 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(333): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.841-2743T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48874885 | |||||||
| chr15:48874927 | T | G | 1 | a0001c0001t0002g0203 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.841-2785A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48874927 | |||||||
| chr15:48875023 | T | C | 103 | a0001c0001t0001g0044 a0001c0001t0001g0137 a0001c0001t0002g0002 others(100): Show |
104 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.841-2881A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48875023 | |||||||
| chr15:48875192 | GCTAT | G | 103 | a0001c0001t0001g0044 a0001c0001t0001g0137 a0001c0001t0002g0002 others(100): Show |
104 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.841-3054_841-3051d others(6): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48875192 | |||||||
| chr15:48875275 | G | C | 103 | a0001c0001t0001g0044 a0001c0001t0001g0137 a0001c0001t0002g0002 others(100): Show |
104 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.841-3133C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48875275 | |||||||
| chr15:48875708 | G | C | 100 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(97): Show |
100 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.841-3566C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48875708 | |||||||
| chr15:48875725 | T | C | 1 | a0001c0001t0005g0349 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.841-3583A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48875725 | |||||||
| chr15:48875783 | T | A | 1 | a0001c0012t0003g0040 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.841-3641A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48875783 | |||||||
| chr15:48875799 | G | A | 100 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(97): Show |
100 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.841-3657C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48875799 | |||||||
| chr15:48875932 | C | T | 1 | a0001c0001t0002g0286 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.841-3790G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48875932 | |||||||
| chr15:48876047 | A | C | 2 | a0001c0001t0002g0203 a0001c0001t0002g0204 |
2 | HG01099.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.841-3905T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48876047 | |||||||
| chr15:48876095 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.841-3953G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48876095 | |||||||
| chr15:48876197 | A | C | 1 | a0001c0001t0004g0168 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.841-4055T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48876197 | |||||||
| chr15:48876450 | TATAC | T | 20 | a0001c0001t0001g0045 a0001c0001t0001g0089 a0001c0001t0001g0152 others(17): Show |
20 | HG01109.hp1 HG01928.hp2 HG02273.hp1 others(17): Show |
intron_variant | MODIFIER | c.841-4312_841-4309d others(6): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48876450 | |||||||
| chr15:48876452 | TAC | T | 213 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0044 others(210): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.841-4312_841-4311d others(4): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48876452 | |||||||
| chr15:48876454 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.841-4312G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48876454 | |||||||
| chr15:48876644 | G | A | 103 | a0001c0001t0001g0137 a0001c0001t0002g0002 a0001c0001t0002g0033 others(100): Show |
104 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.841-4502C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48876644 | |||||||
| chr15:48876734 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.841-4592A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48876734 | |||||||
| chr15:48876903 | A | G | 1 | a0001c0001t0005g0277 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.841-4761T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48876903 | |||||||
| chr15:48877063 | G | A | 1 | a0001c0001t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.841-4921C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48877063 | |||||||
| chr15:48877286 | G | A | 1 | a0001c0012t0003g0040 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.841-5144C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48877286 | |||||||
| chr15:48877549 | G | T | 1 | a0001c0001t0002g0090 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.841-5407C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48877549 | |||||||
| chr15:48877617 | C | T | 1 | a0001c0001t0003g0246 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.841-5475G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48877617 | |||||||
| chr15:48877638 | T | TA | 18 | a0001c0001t0001g0045 a0001c0001t0001g0089 a0001c0001t0001g0152 others(15): Show |
18 | HG01109.hp1 HG01928.hp2 HG02273.hp1 others(15): Show |
intron_variant | MODIFIER | c.841-5497dupT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48877638 | |||||||
| chr15:48877640 | A | C | 3 | a0001c0001t0002g0050 a0001c0001t0002g0173 a0001c0001t0002g0186 |
3 | HG01071.hp1 HG01081.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.841-5498T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48877640 | |||||||
| chr15:48877656 | A | T | 1 | a0001c0001t0001g0338 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.841-5514T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48877656 | |||||||
| chr15:48877657 | A | G | 1 | a0001c0001t0001g0338 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.841-5515T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48877657 | |||||||
| chr15:48877801 | T | C | 1 | a0002c0003t0001g0095 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.841-5659A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48877801 | |||||||
| chr15:48877821 | G | A | 14 | a0001c0001t0003g0096 a0001c0001t0003g0106 a0001c0001t0003g0107 others(11): Show |
14 | HG00673.hp2 HG00735.hp2 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.841-5679C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48877821 | |||||||
| chr15:48877836 | T | C | 1 | a0001c0001t0003g0165 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.841-5694A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48877836 | |||||||
| chr15:48878473 | C | T | 2 | a0001c0001t0002g0064 a0001c0001t0002g0164 |
2 | HG00423.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.840+5775G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48878473 | |||||||
| chr15:48878503 | C | T | 1 | a0001c0002t0004g0083 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.840+5745G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48878503 | |||||||
| chr15:48878576 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.840+5672T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48878576 | |||||||
| chr15:48878780 | G | A | 8 | a0001c0001t0002g0074 a0001c0001t0002g0075 a0001c0001t0002g0113 others(5): Show |
8 | HG02027.hp2 HG02155.hp2 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.840+5468C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48878780 | |||||||
| chr15:48879201 | A | C | 8 | a0001c0001t0002g0085 a0001c0001t0006g0031 a0001c0001t0006g0032 others(5): Show |
8 | HG02451.hp1 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.840+5047T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48879201 | |||||||
| chr15:48879423 | T | A | 1 | a0001c0001t0001g0192 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.840+4825A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48879423 | |||||||
| chr15:48880120 | T | G | 101 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(98): Show |
101 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.840+4128A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48880120 | |||||||
| chr15:48880192 | T | A | 1 | a0001c0001t0014g0005 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.840+4056A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48880192 | |||||||
| chr15:48880308 | A | G | 1 | a0001c0001t0003g0350 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.840+3940T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48880308 | |||||||
| chr15:48880369 | G | A | 1 | a0001c0001t0004g0168 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.840+3879C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48880369 | |||||||
| chr15:48880619 | G | C | 14 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0068 others(11): Show |
15 | HG00099.hp2 HG00642.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.840+3629C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48880619 | |||||||
| chr15:48880895 | TTAATCTC others(9): Show |
T | 1 | a0001c0012t0003g0040 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.840+3337_840+3352d others(18): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48880895 | |||||||
| chr15:48880981 | T | TGA | 28 | a0001c0001t0001g0029 a0001c0001t0001g0097 a0001c0001t0001g0098 others(25): Show |
29 | HG00741.hp1 HG01361.hp2 HG01993.hp2 others(26): Show |
intron_variant | MODIFIER | c.840+3265_840+3266d others(4): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48880981 | |||||||
| chr15:48880983 | AGAGTGTG others(3): Show |
A | 1 | a0001c0001t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.840+3255_840+3264d others(12): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48880983 | |||||||
| chr15:48880985 | A | AGAGT | 5 | a0001c0002t0004g0129 a0001c0002t0004g0132 a0001c0002t0004g0233 others(2): Show |
5 | HG00741.hp2 HG01175.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.840+3262_840+3263i others(6): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48880985 | |||||||
| chr15:48880985 | A | AGT | 36 | a0001c0001t0002g0043 a0001c0001t0002g0050 a0001c0001t0002g0074 others(33): Show |
36 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.840+3261_840+3262d others(4): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48880985 | |||||||
| chr15:48880985 | A | AGTGT | 13 | a0001c0001t0002g0117 a0001c0001t0002g0124 a0001c0001t0002g0133 others(10): Show |
13 | HG02630.hp2 HG03041.hp1 HG03041.hp2 others(10): Show |
intron_variant | MODIFIER | c.840+3259_840+3262d others(6): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48880985 | |||||||
| chr15:48880985 | A | AGTGTGTG others(1): Show |
4 | a0001c0001t0002g0145 a0001c0001t0002g0313 a0001c0001t0002g0321 others(1): Show |
4 | NA18960.hp1 NA18965.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.840+3255_840+3262d others(10): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48880985 | |||||||
| chr15:48880985 | AGT | A | 49 | a0001c0001t0001g0137 a0001c0001t0001g0175 a0001c0001t0001g0257 others(46): Show |
49 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.840+3261_840+3262d others(4): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48880985 | |||||||
| chr15:48880985 | AGTGT | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0026 others(97): Show |
102 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.840+3259_840+3262d others(6): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48880985 | |||||||
| chr15:48880985 | AGTGTGT | A | 51 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0068 others(48): Show |
51 | HG00673.hp2 HG00735.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.840+3257_840+3262d others(8): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48880985 | |||||||
| chr15:48880985 | AGTGTGTG others(1): Show |
A | 19 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0119 others(16): Show |
20 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.840+3255_840+3262d others(10): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48880985 | |||||||
| chr15:48880985 | AGTGTGTG others(3): Show |
A | 32 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0056 others(29): Show |
32 | HG00140.hp2 HG00621.hp1 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.840+3253_840+3262d others(12): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48880985 | |||||||
| chr15:48880985 | AGTGTGTG others(9): Show |
A | 8 | a0001c0001t0002g0065 a0001c0001t0002g0197 a0001c0001t0003g0060 others(5): Show |
8 | HG01255.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.840+3247_840+3262d others(18): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48880985 | |||||||
| chr15:48880987 | T | A | 7 | a0001c0002t0004g0047 a0001c0002t0004g0248 a0001c0002t0004g0265 others(4): Show |
7 | HG01258.hp2 NA18945.hp2 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.840+3261A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48880987 | |||||||
| chr15:48880989 | T | A | 2 | a0001c0002t0004g0235 a0001c0002t0004g0352 |
2 | HG04184.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.840+3259A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48880989 | |||||||
| chr15:48881096 | A | C | 376 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0023 others(373): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.840+3152T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48881096 | |||||||
| chr15:48881137 | T | A | 8 | a0001c0001t0002g0085 a0001c0001t0006g0031 a0001c0001t0006g0032 others(5): Show |
8 | HG02451.hp1 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.840+3111A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48881137 | |||||||
| chr15:48881160 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.840+3088G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48881160 | |||||||
| chr15:48881176 | C | T | 2 | a0001c0001t0004g0037 a0007c0008t0004g0104 |
2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.840+3072G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48881176 | |||||||
| chr15:48881178 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.840+3070G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48881178 | |||||||
| chr15:48881375 | C | CA | 77 | a0001c0001t0001g0029 a0001c0001t0001g0045 a0001c0001t0001g0089 others(74): Show |
78 | HG00438.hp1 HG00558.hp2 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.840+2872dupT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48881375 | |||||||
| chr15:48881375 | C | CAA | 47 | a0001c0001t0001g0198 a0001c0001t0001g0316 a0001c0001t0002g0197 others(44): Show |
47 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.840+2871_840+2872d others(4): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48881375 | |||||||
| chr15:48881520 | G | A | 1 | a0001c0001t0003g0232 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.840+2728C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48881520 | |||||||
| chr15:48881727 | A | G | 2 | a0001c0001t0004g0037 a0007c0008t0004g0104 |
2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.840+2521T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48881727 | |||||||
| chr15:48882036 | G | T | 1 | a0001c0001t0001g0100 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.840+2212C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48882036 | |||||||
| chr15:48882038 | G | A | 3 | a0001c0002t0004g0129 a0001c0002t0004g0131 a0001c0002t0004g0132 |
3 | HG01175.hp2 HG01978.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.840+2210C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48882038 | |||||||
| chr15:48882114 | C | T | 7 | a0001c0001t0001g0068 a0001c0001t0001g0147 a0001c0001t0001g0172 others(4): Show |
7 | HG00099.hp2 HG00642.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.840+2134G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48882114 | |||||||
| chr15:48882123 | G | A | 46 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0063 others(43): Show |
46 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.840+2125C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48882123 | |||||||
| chr15:48882157 | C | T | 22 | a0001c0001t0001g0045 a0001c0001t0001g0089 a0001c0001t0001g0152 others(19): Show |
22 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.840+2091G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48882157 | |||||||
| chr15:48882205 | T | G | 1 | a0001c0001t0001g0285 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.840+2043A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48882205 | |||||||
| chr15:48882223 | A | G | 20 | a0001c0001t0001g0045 a0001c0001t0001g0089 a0001c0001t0001g0152 others(17): Show |
20 | HG01109.hp1 HG01928.hp2 HG02273.hp1 others(17): Show |
intron_variant | MODIFIER | c.840+2025T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48882223 | |||||||
| chr15:48882464 | C | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0369 |
2 | HG00140.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.840+1784G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48882464 | |||||||
| chr15:48882522 | G | C | 1 | a0001c0001t0002g0065 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.840+1726C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48882522 | |||||||
| chr15:48882643 | A | T | 1 | a0001c0001t0001g0093 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.840+1605T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48882643 | |||||||
| chr15:48882726 | C | A | 1 | a0001c0002t0004g0157 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.840+1522G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48882726 | |||||||
| chr15:48883197 | G | A | 1 | a0001c0004t0005g0376 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.840+1051C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48883197 | |||||||
| chr15:48883503 | G | A | 1 | a0001c0001t0015g0006 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.840+745C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48883503 | |||||||
| chr15:48883651 | A | G | 2 | a0001c0001t0002g0065 a0001c0001t0002g0197 |
2 | HG01255.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.840+597T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48883651 | |||||||
| chr15:48883853 | T | C | 3 | a0001c0001t0010g0066 a0001c0001t0010g0112 a0001c0001t0010g0193 |
3 | HG02723.hp2 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.840+395A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48883853 | |||||||
| chr15:48883866 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.840+382G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48883866 | |||||||
| chr15:48883938 | T | A | 1 | a0001c0001t0004g0037 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.840+310A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48883938 | |||||||
| chr15:48884006 | A | T | 170 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(167): Show |
170 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.840+242T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48884006 | |||||||
| chr15:48884078 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.840+170T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48884078 | |||||||
| chr15:48884085 | C | T | 2 | a0001c0001t0003g0060 a0001c0004t0003g0374 |
2 | HG02809.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.840+163G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48884085 | |||||||
| chr15:48884194 | C | T | 2 | a0001c0001t0001g0137 a0001c0001t0009g0012 |
2 | HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.840+54G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48884194 | |||||||
| chr15:48884195 | G | A | 1 | a0001c0001t0005g0138 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.840+53C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 4/11 | chr15 | 48884195 | |||||||
| chr15:48884529 | C | CT | 97 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(94): Show |
97 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.721-163dupA | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48884529 | |||||||
| chr15:48884537 | T | TA | 3 | a0001c0001t0001g0087 a0001c0001t0001g0183 a0001c0001t0005g0024 |
3 | HG02109.hp1 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.721-171dupT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48884537 | |||||||
| chr15:48884539 | A | G | 4 | a0001c0001t0004g0123 a0001c0001t0004g0136 a0001c0001t0004g0155 others(1): Show |
4 | HG00099.hp1 HG01106.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-172T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48884539 | |||||||
| chr15:48884553 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0001g0073 |
2 | HG02132.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.721-186C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48884553 | |||||||
| chr15:48884621 | C | T | 2 | a0001c0001t0003g0151 a0001c0001t0003g0253 |
2 | HG01981.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.721-254G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48884621 | |||||||
| chr15:48884672 | C | T | 1 | a0001c0001t0003g0165 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.721-305G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48884672 | |||||||
| chr15:48884833 | C | A | 1 | a0001c0001t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.721-466G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48884833 | |||||||
| chr15:48884835 | A | C | 1 | a0001c0001t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.721-468T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48884835 | |||||||
| chr15:48884932 | G | A | 1 | a0001c0001t0019g0021 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.721-565C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48884932 | |||||||
| chr15:48884965 | A | G | 100 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(97): Show |
100 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.721-598T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48884965 | |||||||
| chr15:48884977 | A | G | 21 | a0001c0001t0001g0045 a0001c0001t0001g0089 a0001c0001t0001g0152 others(18): Show |
21 | HG01109.hp1 HG01496.hp2 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.721-610T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48884977 | |||||||
| chr15:48885051 | C | A | 172 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(169): Show |
172 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.721-684G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48885051 | |||||||
| chr15:48885053 | G | C | 19 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0052 others(16): Show |
20 | HG00099.hp2 HG00642.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.721-686C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48885053 | |||||||
| chr15:48885117 | G | C | 8 | a0001c0001t0002g0085 a0001c0001t0006g0031 a0001c0001t0006g0032 others(5): Show |
8 | HG02451.hp1 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.721-750C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48885117 | |||||||
| chr15:48885219 | G | C | 15 | a0002c0003t0001g0095 a0002c0003t0003g0046 a0002c0003t0003g0111 others(12): Show |
15 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(12): Show |
intron_variant | MODIFIER | c.721-852C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48885219 | |||||||
| chr15:48885329 | TG | T | 70 | a0001c0001t0001g0045 a0001c0001t0001g0089 a0001c0001t0001g0152 others(67): Show |
70 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.721-963delC | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48885329 | |||||||
| chr15:48885848 | A | G | 172 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(169): Show |
172 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.721-1481T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48885848 | |||||||
| chr15:48885937 | G | T | 20 | a0001c0001t0001g0045 a0001c0001t0001g0089 a0001c0001t0001g0152 others(17): Show |
20 | HG01109.hp1 HG01928.hp2 HG02273.hp1 others(17): Show |
intron_variant | MODIFIER | c.721-1570C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48885937 | |||||||
| chr15:48885987 | G | A | 20 | a0001c0001t0002g0033 a0001c0001t0002g0043 a0001c0001t0002g0051 others(17): Show |
20 | HG00280.hp2 HG00609.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.721-1620C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48885987 | |||||||
| chr15:48886054 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.721-1687G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48886054 | |||||||
| chr15:48886055 | G | A | 1 | a0001c0001t0003g0355 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.721-1688C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48886055 | |||||||
| chr15:48886146 | ACT | A | 41 | a0001c0001t0004g0168 a0001c0001t0010g0066 a0001c0001t0010g0112 others(38): Show |
42 | HG00741.hp1 HG00741.hp2 HG01175.hp2 others(39): Show |
intron_variant | MODIFIER | c.721-1781_721-1780d others(4): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48886146 | |||||||
| chr15:48886296 | T | A | 1 | a0001c0001t0002g0197 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.721-1929A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48886296 | |||||||
| chr15:48886340 | G | C | 3 | a0001c0001t0001g0292 a0001c0001t0001g0302 a0001c0001t0001g0361 |
3 | NA18943.hp2 NA18979.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.721-1973C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48886340 | |||||||
| chr15:48886375 | C | T | 60 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0052 others(57): Show |
62 | HG00099.hp2 HG00642.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.721-2008G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48886375 | |||||||
| chr15:48886489 | G | A | 20 | a0001c0001t0001g0045 a0001c0001t0001g0089 a0001c0001t0001g0152 others(17): Show |
20 | HG01109.hp1 HG01928.hp2 HG02273.hp1 others(17): Show |
intron_variant | MODIFIER | c.721-2122C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48886489 | |||||||
| chr15:48886583 | A | G | 1 | a0001c0001t0002g0197 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.721-2216T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48886583 | |||||||
| chr15:48886598 | T | C | 2 | a0001c0001t0001g0137 a0001c0001t0009g0012 |
2 | HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.721-2231A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48886598 | |||||||
| chr15:48886709 | T | C | 49 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(46): Show |
49 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.721-2342A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48886709 | |||||||
| chr15:48886741 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.721-2374C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48886741 | |||||||
| chr15:48886919 | G | C | 3 | a0001c0001t0002g0055 a0001c0001t0002g0078 a0001c0001t0002g0079 |
3 | HG00609.hp2 HG03942.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.721-2552C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48886919 | |||||||
| chr15:48887001 | G | T | 1 | a0001c0001t0005g0274 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.721-2634C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48887001 | |||||||
| chr15:48887003 | C | G | 100 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(97): Show |
100 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.721-2636G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48887003 | |||||||
| chr15:48887035 | C | A | 1 | a0001c0001t0019g0021 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.721-2668G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48887035 | |||||||
| chr15:48887054 | A | G | 6 | a0001c0001t0001g0166 a0001c0001t0001g0239 a0001c0001t0001g0243 others(3): Show |
6 | HG00438.hp1 HG01496.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.721-2687T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48887054 | |||||||
| chr15:48887166 | TA | T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0035 others(2): Show |
6 | HG01167.hp1 HG01169.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.721-2800delT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48887166 | |||||||
| chr15:48887170 | G | A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0035 others(2): Show |
6 | HG01167.hp1 HG01169.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.721-2803C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48887170 | |||||||
| chr15:48887928 | C | T | 1 | a0001c0001t0003g0107 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.720+2820G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48887928 | |||||||
| chr15:48888357 | A | G | 1 | a0001c0001t0005g0278 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.720+2391T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48888357 | |||||||
| chr15:48888387 | C | T | 14 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0068 others(11): Show |
15 | HG00099.hp2 HG00642.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.720+2361G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48888387 | |||||||
| chr15:48888649 | T | C | 100 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(97): Show |
100 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.720+2099A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48888649 | |||||||
| chr15:48888882 | C | CA | 176 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0069 others(173): Show |
177 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.720+1865dupT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48888882 | |||||||
| chr15:48888882 | C | CAA | 6 | a0001c0001t0001g0071 a0001c0001t0001g0108 a0001c0001t0002g0287 others(3): Show |
6 | HG02683.hp1 HG03130.hp2 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.720+1864_720+1865d others(4): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48888882 | |||||||
| chr15:48888882 | CA | C | 58 | a0001c0001t0001g0023 a0001c0001t0001g0059 a0001c0001t0001g0081 others(55): Show |
58 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.720+1865delT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48888882 | |||||||
| chr15:48888882 | CAA | C | 22 | a0001c0001t0001g0045 a0001c0001t0001g0089 a0001c0001t0001g0152 others(19): Show |
22 | HG01109.hp1 HG01255.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.720+1864_720+1865d others(4): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48888882 | |||||||
| chr15:48889129 | C | T | 40 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0056 others(37): Show |
40 | HG00140.hp2 HG00408.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.720+1619G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48889129 | |||||||
| chr15:48889176 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.720+1572C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48889176 | |||||||
| chr15:48889198 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.720+1550A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48889198 | |||||||
| chr15:48889494 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.720+1254G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48889494 | |||||||
| chr15:48889502 | C | G | 100 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(97): Show |
100 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.720+1246G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48889502 | |||||||
| chr15:48889741 | G | A | 45 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0063 others(42): Show |
45 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.720+1007C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48889741 | |||||||
| chr15:48889791 | C | T | 100 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(97): Show |
100 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.720+957G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48889791 | |||||||
| chr15:48889881 | C | T | 1 | a0001c0001t0001g0338 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.720+867G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48889881 | |||||||
| chr15:48890208 | G | A | 4 | a0001c0002t0004g0105 a0001c0002t0004g0221 a0001c0002t0004g0250 others(1): Show |
4 | NA18939.hp2 NA18981.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+540C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48890208 | |||||||
| chr15:48890339 | A | C | 1 | a0001c0012t0003g0040 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.720+409T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48890339 | |||||||
| chr15:48890408 | G | C | 12 | a0001c0001t0001g0029 a0001c0001t0001g0097 a0001c0001t0001g0098 others(9): Show |
12 | HG00741.hp2 HG01175.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.720+340C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48890408 | |||||||
| chr15:48890719 | A | T | 2 | a0001c0001t0004g0037 a0007c0008t0004g0104 |
2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.720+29T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 3/11 | chr15 | 48890719 | |||||||
| chr15:48891002 | A | C | 2 | a0001c0001t0004g0037 a0007c0008t0004g0104 |
2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.657-191T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48891002 | |||||||
| chr15:48891093 | TTG | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0126 a0001c0001t0001g0194 others(2): Show |
5 | HG02723.hp1 HG02818.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.657-284_657-283del others(2): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48891093 | |||||||
| chr15:48891253 | C | CTA | 77 | a0001c0001t0001g0045 a0001c0001t0001g0089 a0001c0001t0001g0152 others(74): Show |
77 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.657-443_657-442ins others(2): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48891253 | |||||||
| chr15:48891384 | A | T | 1 | a0001c0001t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.657-573T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48891384 | |||||||
| chr15:48891412 | C | G | 4 | a0001c0001t0002g0117 a0001c0001t0008g0013 a0001c0001t0008g0015 others(1): Show |
4 | HG02630.hp2 HG03130.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.657-601G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48891412 | |||||||
| chr15:48891448 | G | A | 1 | a0002c0003t0003g0185 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.657-637C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48891448 | |||||||
| chr15:48891495 | G | A | 1 | a0001c0001t0002g0293 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.657-684C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48891495 | |||||||
| chr15:48892077 | G | A | 1 | a0001c0001t0002g0303 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.657-1266C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48892077 | |||||||
| chr15:48892077 | G | C | 11 | a0001c0002t0004g0105 a0001c0002t0004g0218 a0001c0002t0004g0221 others(8): Show |
11 | NA18939.hp2 NA18945.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.657-1266C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48892077 | |||||||
| chr15:48892091 | G | A | 11 | a0001c0002t0004g0105 a0001c0002t0004g0218 a0001c0002t0004g0221 others(8): Show |
11 | NA18939.hp2 NA18945.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.657-1280C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48892091 | |||||||
| chr15:48892093 | T | G | 12 | a0001c0001t0001g0284 a0001c0002t0004g0105 a0001c0002t0004g0218 others(9): Show |
12 | HG03942.hp1 NA18939.hp2 NA18945.hp2 others(9): Show |
intron_variant | MODIFIER | c.657-1282A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48892093 | |||||||
| chr15:48892097 | C | T | 11 | a0001c0002t0004g0105 a0001c0002t0004g0218 a0001c0002t0004g0221 others(8): Show |
11 | NA18939.hp2 NA18945.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.657-1286G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48892097 | |||||||
| chr15:48892114 | T | C | 11 | a0001c0002t0004g0105 a0001c0002t0004g0218 a0001c0002t0004g0221 others(8): Show |
11 | NA18939.hp2 NA18945.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.657-1303A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48892114 | |||||||
| chr15:48892116 | A | C | 11 | a0001c0002t0004g0105 a0001c0002t0004g0218 a0001c0002t0004g0221 others(8): Show |
11 | NA18939.hp2 NA18945.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.657-1305T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48892116 | |||||||
| chr15:48892121 | T | C | 11 | a0001c0002t0004g0105 a0001c0002t0004g0218 a0001c0002t0004g0221 others(8): Show |
11 | NA18939.hp2 NA18945.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.657-1310A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48892121 | |||||||
| chr15:48892127 | C | T | 11 | a0001c0002t0004g0105 a0001c0002t0004g0218 a0001c0002t0004g0221 others(8): Show |
11 | NA18939.hp2 NA18945.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.657-1316G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48892127 | |||||||
| chr15:48892129 | ACAGGCGT others(3536): Show |
A | 11 | a0001c0002t0004g0105 a0001c0002t0004g0218 a0001c0002t0004g0221 others(8): Show |
11 | NA18939.hp2 NA18945.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.657-4861_657-1319d others(2): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48892129 | |||||||
| chr15:48892276 | A | G | 1 | a0001c0001t0004g0136 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.657-1465T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48892276 | |||||||
| chr15:48892461 | C | G | 1 | a0001c0001t0002g0362 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.657-1650G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48892461 | |||||||
| chr15:48892484 | G | A | 39 | a0001c0001t0002g0033 a0001c0001t0002g0043 a0001c0001t0002g0050 others(36): Show |
39 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.657-1673C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48892484 | |||||||
| chr15:48892502 | G | C | 1 | a0001c0001t0001g0328 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.657-1691C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48892502 | |||||||
| chr15:48892519 | T | C | 1 | a0001c0001t0002g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.657-1708A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48892519 | |||||||
| chr15:48892861 | CT | C | 45 | a0001c0001t0001g0152 a0001c0001t0001g0198 a0001c0001t0001g0284 others(42): Show |
45 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.657-2051delA | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48892861 | |||||||
| chr15:48892862 | T | A | 1 | a0001c0001t0001g0192 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.657-2051A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48892862 | |||||||
| chr15:48892862 | T | C | 7 | a0001c0001t0002g0065 a0001c0001t0002g0197 a0001c0001t0003g0320 others(4): Show |
7 | HG00597.hp2 HG01255.hp2 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.657-2051A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48892862 | |||||||
| chr15:48892863 | C | A | 8 | a0001c0001t0001g0192 a0001c0001t0002g0065 a0001c0001t0002g0197 others(5): Show |
8 | HG00597.hp2 HG01255.hp2 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.657-2052G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48892863 | |||||||
| chr15:48892863 | C | CA | 117 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(114): Show |
117 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.657-2053dupT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48892863 | |||||||
| chr15:48892900 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.657-2089C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48892900 | |||||||
| chr15:48893138 | T | A | 1 | a0001c0001t0001g0139 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.657-2327A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48893138 | |||||||
| chr15:48893265 | T | C | 1 | a0001c0001t0001g0373 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.657-2454A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48893265 | |||||||
| chr15:48893369 | A | C | 116 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(113): Show |
116 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.657-2558T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48893369 | |||||||
| chr15:48893396 | T | G | 6 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0281 others(3): Show |
6 | HG02257.hp2 HG02258.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.657-2585A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48893396 | |||||||
| chr15:48893425 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.657-2614T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48893425 | |||||||
| chr15:48893431 | G | C | 1 | a0001c0001t0001g0192 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.657-2620C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48893431 | |||||||
| chr15:48893446 | T | A | 2 | a0001c0001t0004g0037 a0007c0008t0004g0104 |
2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.657-2635A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48893446 | |||||||
| chr15:48893643 | A | T | 1 | a0001c0001t0001g0044 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.657-2832T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48893643 | |||||||
| chr15:48893918 | C | G | 1 | a0001c0001t0002g0091 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.657-3107G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48893918 | |||||||
| chr15:48894039 | A | C | 1 | a0001c0001t0001g0296 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.657-3228T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48894039 | |||||||
| chr15:48894318 | A | G | 1 | a0001c0001t0001g0348 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.657-3507T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48894318 | |||||||
| chr15:48894367 | G | A | 100 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0041 others(97): Show |
101 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.657-3556C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48894367 | |||||||
| chr15:48894409 | G | T | 1 | a0001c0001t0003g0061 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.657-3598C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48894409 | |||||||
| chr15:48894498 | A | T | 1 | a0001c0001t0004g0136 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.657-3687T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48894498 | |||||||
| chr15:48894539 | A | T | 47 | a0001c0001t0002g0065 a0001c0001t0002g0197 a0001c0001t0003g0060 others(44): Show |
47 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.657-3728T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48894539 | |||||||
| chr15:48894578 | C | T | 1 | a0001c0001t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.657-3767G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48894578 | |||||||
| chr15:48894682 | A | C | 1 | a0001c0001t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.657-3871T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48894682 | |||||||
| chr15:48894685 | C | T | 2 | a0001c0001t0002g0065 a0001c0001t0002g0197 |
2 | HG01255.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.657-3874G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48894685 | |||||||
| chr15:48894729 | G | A | 2 | a0001c0001t0002g0065 a0001c0001t0002g0197 |
2 | HG01255.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.657-3918C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48894729 | |||||||
| chr15:48894822 | T | C | 92 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0002g0002 others(89): Show |
93 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.657-4011A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48894822 | |||||||
| chr15:48894884 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.657-4073A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48894884 | |||||||
| chr15:48894987 | T | A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0035 others(2): Show |
6 | HG01167.hp1 HG01169.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.657-4176A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48894987 | |||||||
| chr15:48895001 | C | T | 4 | a0001c0001t0003g0241 a0001c0001t0003g0271 a0001c0001t0013g0379 others(1): Show |
4 | HG02132.hp1 NA18977.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.657-4190G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48895001 | |||||||
| chr15:48895053 | C | A | 5 | a0001c0001t0001g0152 a0001c0001t0001g0198 a0001c0001t0001g0284 others(2): Show |
5 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.657-4242G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48895053 | |||||||
| chr15:48895369 | G | C | 1 | a0001c0001t0001g0098 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.657-4558C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48895369 | |||||||
| chr15:48895431 | C | T | 4 | a0001c0001t0001g0152 a0001c0001t0001g0198 a0001c0001t0001g0284 others(1): Show |
4 | HG01109.hp1 HG01496.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-4620G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48895431 | |||||||
| chr15:48895477 | G | A | 116 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(113): Show |
116 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.657-4666C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48895477 | |||||||
| chr15:48895542 | C | T | 1 | a0001c0002t0004g0083 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.657-4731G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48895542 | |||||||
| chr15:48895543 | G | A | 1 | a0007c0008t0004g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.657-4732C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48895543 | |||||||
| chr15:48895564 | G | T | 1 | a0001c0002t0007g0270 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.657-4753C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48895564 | |||||||
| chr15:48895694 | T | A | 1 | a0002c0003t0003g0311 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.657-4883A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48895694 | |||||||
| chr15:48895746 | A | G | 4 | a0001c0001t0001g0119 a0001c0001t0001g0257 a0001c0001t0001g0259 others(1): Show |
4 | HG01884.hp1 HG02647.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-4935T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48895746 | |||||||
| chr15:48895922 | A | AT | 11 | a0001c0002t0004g0105 a0001c0002t0004g0218 a0001c0002t0004g0221 others(8): Show |
11 | NA18939.hp2 NA18945.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.657-5112_657-5111i others(3): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48895922 | |||||||
| chr15:48896159 | A | C | 1 | a0001c0001t0001g0068 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.657-5348T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48896159 | |||||||
| chr15:48896223 | TCTCC | T | 3 | a0001c0001t0002g0117 a0001c0001t0008g0015 a0001c0001t0008g0016 |
3 | HG03130.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.657-5416_657-5413d others(6): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48896223 | |||||||
| chr15:48896261 | CCTCCCTC others(19): Show |
C | 1 | a0001c0001t0001g0243 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.657-5476_657-5451d others(28): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48896261 | |||||||
| chr15:48896325 | CT | C | 116 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(113): Show |
116 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.657-5515delA | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48896325 | |||||||
| chr15:48896343 | C | T | 1 | a0001c0001t0001g0364 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.657-5532G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48896343 | |||||||
| chr15:48896360 | G | C | 11 | a0001c0001t0001g0148 a0001c0001t0001g0169 a0001c0001t0001g0179 others(8): Show |
11 | HG01928.hp1 HG01952.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.657-5549C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48896360 | |||||||
| chr15:48896448 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.657-5637C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48896448 | |||||||
| chr15:48896544 | C | T | 1 | a0001c0002t0018g0010 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.657-5733G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48896544 | |||||||
| chr15:48896646 | G | A | 61 | a0001c0001t0001g0152 a0001c0001t0001g0192 a0001c0001t0001g0198 others(58): Show |
61 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.657-5835C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48896646 | |||||||
| chr15:48896813 | T | C | 1 | a0001c0001t0002g0065 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.657-6002A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48896813 | |||||||
| chr15:48897290 | G | C | 1 | a0001c0001t0004g0123 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.657-6479C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48897290 | |||||||
| chr15:48897508 | C | CCA | 9 | a0001c0001t0001g0141 a0001c0001t0001g0154 a0001c0001t0002g0065 others(6): Show |
9 | HG00597.hp1 HG01255.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.657-6699_657-6698d others(4): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48897508 | |||||||
| chr15:48897508 | CCA | C | 187 | a0001c0001t0001g0030 a0001c0001t0001g0042 a0001c0001t0001g0069 others(184): Show |
188 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(185): Show |
intron_variant | MODIFIER | c.657-6699_657-6698d others(4): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48897508 | |||||||
| chr15:48897530 | A | G | 48 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(45): Show |
48 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.657-6719T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48897530 | |||||||
| chr15:48897541 | CT | C | 38 | a0001c0001t0003g0063 a0001c0001t0003g0080 a0001c0001t0003g0096 others(35): Show |
38 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.657-6731delA | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48897541 | |||||||
| chr15:48897640 | T | C | 1 | a0001c0001t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.657-6829A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48897640 | |||||||
| chr15:48897756 | G | GAC | 90 | a0001c0001t0001g0044 a0001c0001t0001g0137 a0001c0001t0002g0002 others(87): Show |
91 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.657-6947_657-6946d others(4): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48897756 | |||||||
| chr15:48897756 | G | GACAC | 23 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0068 others(20): Show |
24 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.657-6949_657-6946d others(6): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48897756 | |||||||
| chr15:48897756 | G | GACACAC | 10 | a0001c0001t0001g0052 a0001c0001t0001g0069 a0001c0001t0001g0141 others(7): Show |
10 | HG01496.hp1 HG01496.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.657-6951_657-6946d others(8): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48897756 | |||||||
| chr15:48897756 | G | GACACACA others(1): Show |
56 | a0001c0001t0001g0045 a0001c0001t0001g0070 a0001c0001t0001g0076 others(53): Show |
56 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.657-6953_657-6946d others(10): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48897756 | |||||||
| chr15:48897756 | G | GACACACA others(3): Show |
6 | a0001c0001t0001g0073 a0001c0001t0001g0263 a0001c0001t0001g0275 others(3): Show |
6 | HG02071.hp2 HG02132.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.657-6955_657-6946d others(12): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48897756 | |||||||
| chr15:48897756 | G | GACACACA others(5): Show |
14 | a0001c0001t0001g0071 a0001c0001t0001g0344 a0001c0001t0003g0060 others(11): Show |
14 | HG00408.hp2 HG00741.hp2 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.657-6957_657-6946d others(14): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48897756 | |||||||
| chr15:48897756 | G | GACACACA others(7): Show |
15 | a0001c0001t0001g0087 a0001c0001t0001g0152 a0001c0001t0001g0154 others(12): Show |
15 | HG00673.hp2 HG01109.hp1 HG02074.hp1 others(12): Show |
intron_variant | MODIFIER | c.657-6959_657-6946d others(16): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48897756 | |||||||
| chr15:48897756 | G | GACACACA others(9): Show |
45 | a0001c0001t0001g0056 a0001c0001t0001g0116 a0001c0001t0001g0148 others(42): Show |
46 | HG00741.hp1 HG01099.hp2 HG01928.hp1 others(43): Show |
intron_variant | MODIFIER | c.657-6961_657-6946d others(18): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48897756 | |||||||
| chr15:48897756 | G | GACACACA others(11): Show |
29 | a0001c0001t0001g0030 a0001c0001t0001g0042 a0001c0001t0001g0082 others(26): Show |
29 | HG00140.hp2 HG00558.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.657-6963_657-6946d others(20): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48897756 | |||||||
| chr15:48897756 | G | GACACACA others(13): Show |
28 | a0001c0001t0001g0041 a0001c0001t0001g0100 a0001c0001t0001g0176 others(25): Show |
28 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.657-6965_657-6946d others(22): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48897756 | |||||||
| chr15:48897756 | G | GACACACA others(15): Show |
12 | a0001c0001t0001g0139 a0001c0001t0001g0194 a0001c0001t0003g0063 others(9): Show |
12 | HG01167.hp2 HG02015.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.657-6967_657-6946d others(24): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48897756 | |||||||
| chr15:48897756 | G | GACACACA others(17): Show |
3 | a0001c0002t0004g0235 a0002c0003t0003g0111 a0002c0003t0013g0380 |
3 | HG04184.hp1 NA18949.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.657-6969_657-6946d others(26): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48897756 | |||||||
| chr15:48897756 | G | GACACACA others(19): Show |
1 | a0001c0001t0001g0310 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.657-6971_657-6946d others(28): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48897756 | |||||||
| chr15:48897770 | C | CACACACA others(5): Show |
1 | a0001c0002t0004g0083 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.657-6960_657-6959i others(14): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48897770 | |||||||
| chr15:48897786 | T | C | 25 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0052 others(22): Show |
26 | HG00099.hp2 HG00642.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.657-6975A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48897786 | |||||||
| chr15:48897846 | G | C | 1 | a0001c0002t0004g0129 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.657-7035C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48897846 | |||||||
| chr15:48897904 | C | G | 1 | a0001c0001t0002g0295 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.657-7093G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48897904 | |||||||
| chr15:48897960 | C | T | 1 | a0001c0001t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.657-7149G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48897960 | |||||||
| chr15:48898175 | A | G | 5 | a0001c0001t0001g0030 a0001c0001t0001g0126 a0001c0001t0001g0194 others(2): Show |
5 | HG02723.hp1 HG02818.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.657-7364T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48898175 | |||||||
| chr15:48898214 | T | G | 1 | a0001c0001t0001g0192 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.657-7403A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48898214 | |||||||
| chr15:48898363 | T | G | 87 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(84): Show |
87 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.657-7552A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48898363 | |||||||
| chr15:48898543 | A | G | 94 | a0001c0001t0001g0137 a0001c0001t0002g0002 a0001c0001t0002g0033 others(91): Show |
95 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.657-7732T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48898543 | |||||||
| chr15:48898688 | C | A | 4 | a0001c0001t0002g0117 a0001c0001t0008g0013 a0001c0001t0008g0015 others(1): Show |
4 | HG02630.hp2 HG03130.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.657-7877G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48898688 | |||||||
| chr15:48899044 | G | GA | 90 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0073 others(87): Show |
90 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.657-8234dupT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48899044 | |||||||
| chr15:48899044 | G | GAA | 6 | a0001c0001t0001g0071 a0001c0001t0001g0108 a0001c0001t0003g0096 others(3): Show |
6 | HG02027.hp1 HG02074.hp1 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.657-8235_657-8234d others(4): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48899044 | |||||||
| chr15:48899044 | GA | G | 8 | a0001c0001t0001g0068 a0001c0001t0001g0174 a0001c0001t0001g0192 others(5): Show |
8 | HG01123.hp2 HG01192.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.657-8234delT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48899044 | |||||||
| chr15:48899056 | A | AC | 72 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(69): Show |
72 | HG00140.hp2 HG00621.hp1 HG01099.hp2 others(69): Show |
intron_variant | MODIFIER | c.657-8246_657-8245i others(3): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48899056 | |||||||
| chr15:48899056 | A | C | 39 | a0001c0001t0001g0344 a0001c0001t0004g0168 a0001c0002t0004g0003 others(36): Show |
40 | HG00408.hp2 HG00741.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.657-8245T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48899056 | |||||||
| chr15:48899058 | A | C | 8 | a0001c0001t0002g0074 a0001c0001t0002g0075 a0001c0001t0002g0113 others(5): Show |
8 | HG02027.hp2 HG02155.hp2 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.657-8247T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48899058 | |||||||
| chr15:48899064 | C | T | 2 | a0001c0001t0001g0082 a0001c0001t0001g0188 |
2 | HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.657-8253G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48899064 | |||||||
| chr15:48899087 | C | CCCA | 6 | a0001c0001t0001g0192 a0001c0001t0002g0027 a0001c0001t0002g0117 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.657-8279_657-8277d others(5): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48899087 | |||||||
| chr15:48899332 | T | G | 1 | a0001c0001t0003g0297 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.657-8521A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48899332 | |||||||
| chr15:48899353 | G | T | 3 | a0001c0001t0001g0152 a0001c0001t0001g0198 a0001c0001t0001g0284 |
3 | HG01109.hp1 HG02559.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.657-8542C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48899353 | |||||||
| chr15:48899434 | A | C | 72 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(69): Show |
72 | HG00140.hp2 HG00621.hp1 HG01099.hp2 others(69): Show |
intron_variant | MODIFIER | c.657-8623T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48899434 | |||||||
| chr15:48899803 | G | A | 39 | a0001c0001t0001g0344 a0001c0001t0004g0168 a0001c0002t0004g0003 others(36): Show |
40 | HG00408.hp2 HG00741.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.657-8992C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48899803 | |||||||
| chr15:48899969 | G | A | 1 | a0001c0001t0023g0150 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.657-9158C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48899969 | |||||||
| chr15:48899977 | G | C | 1 | a0007c0008t0004g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.657-9166C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48899977 | |||||||
| chr15:48899990 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.657-9179A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48899990 | |||||||
| chr15:48900129 | T | C | 165 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(162): Show |
165 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.657-9318A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48900129 | |||||||
| chr15:48900214 | G | A | 1 | a0001c0001t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.657-9403C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48900214 | |||||||
| chr15:48900317 | G | C | 25 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0052 others(22): Show |
26 | HG00099.hp2 HG00642.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.657-9506C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48900317 | |||||||
| chr15:48900379 | C | T | 72 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(69): Show |
72 | HG00140.hp2 HG00621.hp1 HG01099.hp2 others(69): Show |
intron_variant | MODIFIER | c.657-9568G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48900379 | |||||||
| chr15:48900506 | C | CA | 7 | a0001c0001t0001g0004 a0001c0001t0001g0364 a0001c0001t0002g0345 others(4): Show |
8 | HG00673.hp1 HG01257.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.657-9696dupT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48900506 | |||||||
| chr15:48900594 | T | C | 72 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(69): Show |
72 | HG00140.hp2 HG00621.hp1 HG01099.hp2 others(69): Show |
intron_variant | MODIFIER | c.657-9783A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48900594 | |||||||
| chr15:48900694 | A | C | 374 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0023 others(371): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.657-9883T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48900694 | |||||||
| chr15:48900819 | C | T | 1 | a0007c0008t0004g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.657-10008G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48900819 | |||||||
| chr15:48900885 | A | G | 6 | a0001c0001t0001g0192 a0001c0001t0002g0027 a0001c0001t0002g0117 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.657-10074T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48900885 | |||||||
| chr15:48900961 | T | G | 1 | a0007c0008t0004g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.657-10150A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48900961 | |||||||
| chr15:48901316 | T | C | 1 | a0001c0001t0002g0204 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.657-10505A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48901316 | |||||||
| chr15:48901383 | T | A | 1 | a0001c0001t0001g0044 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.657-10572A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48901383 | |||||||
| chr15:48901417 | T | C | 1 | a0001c0002t0004g0235 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.657-10606A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48901417 | |||||||
| chr15:48901429 | T | C | 1 | a0007c0008t0004g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.657-10618A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48901429 | |||||||
| chr15:48901506 | G | A | 1 | a0001c0001t0005g0109 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.657-10695C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48901506 | |||||||
| chr15:48901559 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.657-10748C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48901559 | |||||||
| chr15:48901601 | C | A | 48 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(45): Show |
48 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.657-10790G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48901601 | |||||||
| chr15:48901607 | A | G | 1 | a0001c0001t0001g0348 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.657-10796T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48901607 | |||||||
| chr15:48901678 | A | T | 166 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(163): Show |
166 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.657-10867T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48901678 | |||||||
| chr15:48901821 | T | A | 2 | a0001c0001t0002g0065 a0001c0001t0002g0197 |
2 | HG01255.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.657-11010A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48901821 | |||||||
| chr15:48901844 | A | G | 72 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(69): Show |
72 | HG00140.hp2 HG00621.hp1 HG01099.hp2 others(69): Show |
intron_variant | MODIFIER | c.657-11033T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48901844 | |||||||
| chr15:48902202 | C | CA | 30 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0052 others(27): Show |
31 | HG00099.hp2 HG00642.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.657-11392dupT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48902202 | |||||||
| chr15:48902305 | T | G | 3 | a0001c0001t0001g0166 a0001c0001t0001g0266 a0001c0001t0001g0360 |
3 | HG01496.hp1 HG01943.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.657-11494A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48902305 | |||||||
| chr15:48902394 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.657-11583G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48902394 | |||||||
| chr15:48902436 | T | C | 4 | a0001c0001t0001g0119 a0001c0001t0001g0257 a0001c0001t0001g0259 others(1): Show |
4 | HG01884.hp1 HG02647.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-11625A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48902436 | |||||||
| chr15:48902544 | C | T | 70 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(67): Show |
70 | HG00140.hp2 HG00621.hp1 HG01099.hp2 others(67): Show |
intron_variant | MODIFIER | c.657-11733G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48902544 | |||||||
| chr15:48902708 | G | A | 1 | a0001c0001t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.657-11897C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48902708 | |||||||
| chr15:48902720 | G | A | 1 | a0001c0001t0010g0066 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.657-11909C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48902720 | |||||||
| chr15:48902769 | G | T | 39 | a0001c0001t0003g0063 a0001c0001t0003g0080 a0001c0001t0003g0096 others(36): Show |
39 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.657-11958C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48902769 | |||||||
| chr15:48902855 | A | G | 7 | a0001c0001t0001g0210 a0001c0001t0001g0215 a0001c0001t0001g0216 others(4): Show |
7 | NA18954.hp1 NA18964.hp2 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.657-12044T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48902855 | |||||||
| chr15:48902914 | C | T | 48 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(45): Show |
48 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.657-12103G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48902914 | |||||||
| chr15:48903328 | C | A | 1 | a0001c0001t0001g0044 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.657-12517G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48903328 | |||||||
| chr15:48903369 | C | T | 1 | a0001c0001t0005g0277 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.657-12558G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48903369 | |||||||
| chr15:48903378 | C | T | 4 | a0001c0001t0004g0123 a0001c0001t0004g0136 a0001c0001t0004g0155 others(1): Show |
4 | HG00099.hp1 HG01106.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.657-12567G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48903378 | |||||||
| chr15:48903423 | G | A | 7 | a0001c0001t0002g0050 a0001c0001t0002g0173 a0001c0001t0002g0186 others(4): Show |
7 | HG00642.hp2 HG01071.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.657-12612C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48903423 | |||||||
| chr15:48903681 | G | A | 1 | a0001c0002t0004g0130 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.657-12870C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48903681 | |||||||
| chr15:48903758 | T | C | 70 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(67): Show |
70 | HG00140.hp2 HG00621.hp1 HG01099.hp2 others(67): Show |
intron_variant | MODIFIER | c.657-12947A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48903758 | |||||||
| chr15:48903759 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.657-12948A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48903759 | |||||||
| chr15:48903880 | C | T | 1 | a0001c0001t0002g0206 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.657-13069G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48903880 | |||||||
| chr15:48903924 | C | A | 1 | a0001c0001t0005g0267 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.657-13113G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48903924 | |||||||
| chr15:48903926 | C | A | 1 | a0001c0001t0005g0267 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.657-13115G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48903926 | |||||||
| chr15:48903991 | T | C | 1 | a0001c0001t0006g0088 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.657-13180A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48903991 | |||||||
| chr15:48904040 | A | G | 39 | a0001c0001t0003g0063 a0001c0001t0003g0080 a0001c0001t0003g0096 others(36): Show |
39 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.657-13229T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48904040 | |||||||
| chr15:48904095 | A | T | 3 | a0001c0001t0001g0139 a0001c0001t0002g0065 a0001c0001t0002g0197 |
3 | HG01167.hp2 HG01255.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.657-13284T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48904095 | |||||||
| chr15:48904380 | G | A | 1 | a0001c0001t0001g0324 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.657-13569C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48904380 | |||||||
| chr15:48904411 | C | T | 2 | a0001c0001t0002g0065 a0001c0001t0002g0197 |
2 | HG01255.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.657-13600G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48904411 | |||||||
| chr15:48904595 | T | C | 2 | a0001c0001t0002g0065 a0001c0001t0002g0197 |
2 | HG01255.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.657-13784A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48904595 | |||||||
| chr15:48904724 | C | A | 40 | a0001c0001t0001g0152 a0001c0001t0001g0344 a0001c0001t0004g0168 others(37): Show |
41 | HG00408.hp2 HG00741.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.657-13913G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48904724 | |||||||
| chr15:48904725 | A | C | 2 | a0001c0001t0001g0172 a0001c0001t0001g0200 |
2 | HG00099.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.657-13914T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48904725 | |||||||
| chr15:48904726 | A | C | 3 | a0001c0001t0001g0137 a0001c0001t0009g0012 a0007c0008t0004g0104 |
3 | HG02717.hp1 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.657-13915T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48904726 | |||||||
| chr15:48904933 | C | G | 1 | a0001c0002t0004g0083 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.657-14122G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48904933 | |||||||
| chr15:48904935 | G | C | 2 | a0001c0001t0003g0365 a0001c0002t0004g0083 |
2 | HG02074.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.657-14124C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48904935 | |||||||
| chr15:48904937 | C | G | 1 | a0001c0001t0003g0365 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.657-14126G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48904937 | |||||||
| chr15:48904939 | C | A | 1 | a0001c0002t0004g0083 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.657-14128G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48904939 | |||||||
| chr15:48904940 | A | AAC | 62 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0068 others(59): Show |
64 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.657-14131_657-1413 others(6): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48904940 | |||||||
| chr15:48904940 | A | AACAC | 63 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0045 others(60): Show |
63 | HG00140.hp2 HG00621.hp1 HG01099.hp2 others(60): Show |
intron_variant | MODIFIER | c.657-14133_657-1413 others(8): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48904940 | |||||||
| chr15:48904940 | A | AACACAC | 5 | a0001c0001t0001g0126 a0001c0001t0001g0196 a0001c0001t0001g0209 others(2): Show |
5 | HG02055.hp2 HG02723.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.657-14135_657-1413 others(10): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48904940 | |||||||
| chr15:48904940 | A | C | 1 | a0001c0002t0004g0083 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.657-14129T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48904940 | |||||||
| chr15:48904940 | AAC | A | 39 | a0001c0001t0001g0154 a0001c0001t0001g0192 a0001c0001t0001g0210 others(36): Show |
39 | HG01255.hp2 HG01496.hp2 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.657-14131_657-1413 others(6): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48904940 | |||||||
| chr15:48904940 | AACAC | A | 61 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(58): Show |
61 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.657-14133_657-1413 others(8): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48904940 | |||||||
| chr15:48904940 | AACACACA others(5): Show |
A | 1 | a0001c0002t0004g0178 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.657-14141_657-1413 others(16): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48904940 | |||||||
| chr15:48904941 | A | C | 1 | a0001c0001t0003g0365 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.657-14130T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48904941 | |||||||
| chr15:48904942 | C | A | 1 | a0001c0001t0003g0365 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.657-14131G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48904942 | |||||||
| chr15:48905069 | C | T | 2 | a0001c0001t0001g0196 a0001c0001t0001g0209 |
2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.657-14258G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48905069 | |||||||
| chr15:48905285 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.657-14474A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48905285 | |||||||
| chr15:48905436 | G | C | 1 | a0007c0008t0004g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.657-14625C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48905436 | |||||||
| chr15:48905464 | A | C | 1 | a0001c0001t0006g0088 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.657-14653T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48905464 | |||||||
| chr15:48906155 | G | C | 6 | a0001c0001t0001g0084 a0001c0001t0001g0177 a0001c0001t0001g0261 others(3): Show |
6 | NA18957.hp1 NA18977.hp2 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.657-15344C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48906155 | |||||||
| chr15:48906171 | T | A | 6 | a0001c0001t0001g0192 a0001c0001t0002g0027 a0001c0001t0002g0117 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.657-15360A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48906171 | |||||||
| chr15:48906228 | T | C | 1 | a0001c0001t0022g0254 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.657-15417A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48906228 | |||||||
| chr15:48906314 | G | A | 1 | a0001c0001t0010g0193 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.657-15503C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48906314 | |||||||
| chr15:48906517 | C | T | 1 | a0001c0001t0002g0033 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.657-15706G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48906517 | |||||||
| chr15:48906609 | C | T | 34 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0056 others(31): Show |
34 | HG00140.hp2 HG00621.hp1 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.657-15798G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48906609 | |||||||
| chr15:48906734 | C | T | 70 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(67): Show |
70 | HG00140.hp2 HG00621.hp1 HG01099.hp2 others(67): Show |
intron_variant | MODIFIER | c.657-15923G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48906734 | |||||||
| chr15:48906781 | T | C | 73 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(70): Show |
73 | HG00140.hp2 HG00621.hp1 HG01099.hp2 others(70): Show |
intron_variant | MODIFIER | c.657-15970A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48906781 | |||||||
| chr15:48906833 | A | G | 2 | a0001c0001t0002g0065 a0001c0001t0002g0197 |
2 | HG01255.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.657-16022T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48906833 | |||||||
| chr15:48906875 | ATCTT | A | 4 | a0001c0001t0001g0119 a0001c0001t0001g0257 a0001c0001t0001g0259 others(1): Show |
4 | HG01884.hp1 HG02647.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-16068_657-1606 others(8): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48906875 | |||||||
| chr15:48907058 | T | G | 22 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0002g0033 others(19): Show |
22 | HG00280.hp2 HG00609.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.657-16247A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48907058 | |||||||
| chr15:48907133 | A | C | 17 | a0001c0001t0001g0045 a0001c0001t0001g0089 a0001c0001t0001g0160 others(14): Show |
17 | HG01928.hp2 HG02273.hp1 HG03710.hp2 others(14): Show |
intron_variant | MODIFIER | c.657-16322T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48907133 | |||||||
| chr15:48907180 | A | G | 38 | a0001c0001t0001g0344 a0001c0001t0004g0168 a0001c0002t0004g0003 others(35): Show |
39 | HG00408.hp2 HG00741.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.657-16369T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48907180 | |||||||
| chr15:48907195 | G | A | 68 | a0001c0001t0001g0137 a0001c0001t0002g0002 a0001c0001t0002g0033 others(65): Show |
69 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.657-16384C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48907195 | |||||||
| chr15:48907294 | G | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0052 others(14): Show |
18 | HG00099.hp2 HG00642.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.657-16483C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48907294 | |||||||
| chr15:48907354 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.657-16543G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48907354 | |||||||
| chr15:48907416 | T | G | 1 | a0001c0001t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.657-16605A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48907416 | |||||||
| chr15:48907454 | T | C | 5 | a0001c0001t0001g0192 a0001c0001t0002g0117 a0001c0001t0008g0013 others(2): Show |
5 | HG02258.hp1 HG02630.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.657-16643A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48907454 | |||||||
| chr15:48907462 | C | T | 21 | a0001c0001t0003g0080 a0001c0001t0003g0096 a0001c0001t0003g0106 others(18): Show |
21 | HG00673.hp2 HG01981.hp2 HG02004.hp1 others(18): Show |
intron_variant | MODIFIER | c.657-16651G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48907462 | |||||||
| chr15:48907655 | C | T | 5 | a0001c0001t0001g0192 a0001c0001t0002g0117 a0001c0001t0008g0013 others(2): Show |
5 | HG02258.hp1 HG02630.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.657-16844G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48907655 | |||||||
| chr15:48907771 | CAT | C | 187 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(184): Show |
187 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.657-16962_657-1696 others(6): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48907771 | |||||||
| chr15:48907814 | A | ATG | 3 | a0001c0001t0001g0102 a0001c0001t0002g0027 a0001c0001t0002g0287 |
3 | HG01884.hp2 HG02970.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.657-17005_657-1700 others(6): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48907814 | |||||||
| chr15:48907814 | ATG | A | 72 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(69): Show |
72 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.657-17005_657-1700 others(6): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48907814 | |||||||
| chr15:48907840 | G | A | 79 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(76): Show |
79 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.657-17029C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48907840 | |||||||
| chr15:48907840 | G | GTGTA | 16 | a0001c0001t0003g0320 a0002c0003t0001g0095 a0002c0003t0003g0046 others(13): Show |
16 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(13): Show |
intron_variant | MODIFIER | c.657-17030_657-1702 others(8): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48907840 | |||||||
| chr15:48907840 | G | GTGTATA | 22 | a0001c0001t0003g0063 a0001c0001t0003g0080 a0001c0001t0003g0096 others(19): Show |
22 | HG00673.hp2 HG01981.hp2 HG02004.hp1 others(19): Show |
intron_variant | MODIFIER | c.657-17030_657-1702 others(10): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48907840 | |||||||
| chr15:48907840 | G | GTGTGTAT others(27): Show |
2 | a0001c0001t0001g0176 a0001c0001t0001g0268 |
2 | HG00621.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.657-17030_657-1702 others(38): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48907840 | |||||||
| chr15:48907840 | G | GTGTGTGT others(33): Show |
1 | a0001c0001t0001g0284 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.657-17030_657-1702 others(44): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48907840 | |||||||
| chr15:48907840 | G | GTGTGTGT others(29): Show |
7 | a0001c0001t0001g0030 a0001c0001t0001g0045 a0001c0001t0001g0126 others(4): Show |
7 | HG02723.hp1 HG02818.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.657-17030_657-1702 others(40): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48907840 | |||||||
| chr15:48907840 | G | GTGTGTGT others(33): Show |
1 | a0001c0001t0001g0152 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.657-17030_657-1702 others(44): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48907840 | |||||||
| chr15:48907840 | G | GTGTGTGT others(31): Show |
40 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0044 others(37): Show |
40 | HG00140.hp2 HG01099.hp2 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.657-17030_657-1702 others(42): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48907840 | |||||||
| chr15:48907840 | G | GTGTGTGT others(31): Show |
6 | a0001c0001t0001g0225 a0001c0001t0001g0299 a0001c0001t0001g0308 others(3): Show |
6 | NA18949.hp2 NA18957.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.657-17030_657-1702 others(42): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48907840 | |||||||
| chr15:48907840 | G | GTGTGTGT others(29): Show |
5 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0281 others(2): Show |
5 | HG02257.hp2 HG02809.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.657-17030_657-1702 others(40): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48907840 | |||||||
| chr15:48907840 | G | GTGTGTGT others(35): Show |
3 | a0001c0001t0001g0087 a0001c0001t0001g0183 a0001c0001t0005g0024 |
3 | HG02109.hp1 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.657-17030_657-1702 others(46): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48907840 | |||||||
| chr15:48907840 | G | GTGTGTGT others(33): Show |
1 | a0001c0001t0001g0198 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.657-17030_657-1702 others(44): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48907840 | |||||||
| chr15:48907840 | G | GTGTGTGT others(35): Show |
1 | a0001c0001t0001g0116 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.657-17030_657-1702 others(46): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48907840 | |||||||
| chr15:48907840 | G | GTGTGTGT others(31): Show |
4 | a0001c0001t0001g0161 a0001c0001t0001g0179 a0001c0001t0001g0182 others(1): Show |
4 | HG02165.hp2 HG02273.hp2 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.657-17030_657-1702 others(42): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48907840 | |||||||
| chr15:48907842 | A | G | 7 | a0001c0001t0001g0141 a0001c0001t0001g0154 a0001c0001t0004g0123 others(4): Show |
7 | HG01106.hp2 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.657-17031T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48907842 | |||||||
| chr15:48907844 | A | G | 1 | a0001c0001t0010g0112 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.657-17033T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48907844 | |||||||
| chr15:48908043 | T | C | 1 | a0001c0001t0025g0347 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.656+16836A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48908043 | |||||||
| chr15:48908351 | T | C | 1 | a0001c0001t0002g0335 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.656+16528A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48908351 | |||||||
| chr15:48908595 | T | G | 1 | a0001c0001t0004g0208 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.656+16284A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48908595 | |||||||
| chr15:48908625 | T | C | 39 | a0001c0001t0003g0063 a0001c0001t0003g0080 a0001c0001t0003g0096 others(36): Show |
39 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.656+16254A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48908625 | |||||||
| chr15:48908633 | A | T | 188 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(185): Show |
188 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.656+16246T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48908633 | |||||||
| chr15:48908690 | G | A | 1 | a0001c0001t0002g0197 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.656+16189C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48908690 | |||||||
| chr15:48908761 | C | T | 1 | a0001c0001t0002g0167 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.656+16118G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48908761 | |||||||
| chr15:48909079 | G | T | 1 | a0007c0008t0004g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.656+15800C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48909079 | |||||||
| chr15:48909289 | A | AT | 330 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0023 others(327): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.656+15589dupA | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48909289 | |||||||
| chr15:48909289 | A | ATT | 44 | a0001c0001t0001g0071 a0001c0001t0001g0093 a0001c0001t0002g0203 others(41): Show |
44 | HG00408.hp1 HG00558.hp1 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.656+15588_656+1558 others(6): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48909289 | |||||||
| chr15:48909387 | A | C | 1 | a0001c0001t0006g0088 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.656+15492T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48909387 | |||||||
| chr15:48909422 | T | C | 3 | a0001c0001t0001g0166 a0001c0001t0001g0266 a0001c0001t0001g0360 |
3 | HG01496.hp1 HG01943.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.656+15457A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48909422 | |||||||
| chr15:48909757 | A | G | 1 | a0001c0001t0003g0106 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.656+15122T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48909757 | |||||||
| chr15:48909767 | G | A | 1 | a0001c0002t0004g0178 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.656+15112C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48909767 | |||||||
| chr15:48909856 | T | A | 1 | a0001c0001t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.656+15023A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48909856 | |||||||
| chr15:48909923 | T | A | 73 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(70): Show |
73 | HG00140.hp2 HG00621.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.656+14956A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48909923 | |||||||
| chr15:48909924 | A | T | 73 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(70): Show |
73 | HG00140.hp2 HG00621.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.656+14955T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48909924 | |||||||
| chr15:48910016 | C | A | 1 | a0001c0001t0001g0191 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.656+14863G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48910016 | |||||||
| chr15:48910083 | A | AAGGTATG others(2): Show |
39 | a0001c0001t0003g0063 a0001c0001t0003g0080 a0001c0001t0003g0096 others(36): Show |
39 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.656+14787_656+1479 others(13): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48910083 | |||||||
| chr15:48910192 | T | C | 5 | a0001c0001t0001g0192 a0001c0001t0002g0117 a0001c0001t0008g0013 others(2): Show |
5 | HG02258.hp1 HG02630.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.656+14687A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48910192 | |||||||
| chr15:48910346 | G | A | 1 | a0001c0002t0004g0157 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.656+14533C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48910346 | |||||||
| chr15:48910647 | G | A | 1 | a0001c0002t0004g0342 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.656+14232C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48910647 | |||||||
| chr15:48910698 | T | C | 2 | a0001c0001t0005g0138 a0001c0001t0005g0142 |
2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.656+14181A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48910698 | |||||||
| chr15:48910716 | C | G | 2 | a0001c0001t0001g0056 a0001c0001t0001g0369 |
2 | HG00140.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.656+14163G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48910716 | |||||||
| chr15:48910766 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.656+14113A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48910766 | |||||||
| chr15:48910835 | C | A | 1 | a0001c0012t0003g0040 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.656+14044G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48910835 | |||||||
| chr15:48911102 | T | TAA | 39 | a0001c0001t0003g0063 a0001c0001t0003g0080 a0001c0001t0003g0096 others(36): Show |
39 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.656+13776_656+1377 others(6): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48911102 | |||||||
| chr15:48911341 | A | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0128 a0001c0001t0003g0063 others(38): Show |
42 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.656+13538T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48911341 | |||||||
| chr15:48911370 | A | G | 74 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(71): Show |
74 | HG00140.hp2 HG00621.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.656+13509T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48911370 | |||||||
| chr15:48911446 | A | C | 4 | a0001c0001t0002g0145 a0001c0001t0002g0313 a0001c0001t0002g0321 others(1): Show |
4 | NA18960.hp1 NA18965.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.656+13433T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48911446 | |||||||
| chr15:48911527 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.656+13352C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48911527 | |||||||
| chr15:48911608 | C | T | 74 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(71): Show |
74 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.656+13271G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48911608 | |||||||
| chr15:48912082 | A | G | 6 | a0001c0001t0003g0080 a0001c0001t0003g0231 a0001c0001t0003g0312 others(3): Show |
6 | NA18939.hp1 NA18950.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.656+12797T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48912082 | |||||||
| chr15:48912100 | C | A | 51 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(48): Show |
51 | HG00140.hp2 HG00621.hp1 HG01099.hp2 others(48): Show |
intron_variant | MODIFIER | c.656+12779G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48912100 | |||||||
| chr15:48912235 | G | C | 1 | a0001c0001t0001g0339 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.656+12644C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48912235 | |||||||
| chr15:48912461 | A | G | 6 | a0001c0001t0001g0093 a0001c0001t0001g0108 a0001c0001t0001g0146 others(3): Show |
6 | HG01069.hp2 HG01243.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.656+12418T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48912461 | |||||||
| chr15:48912492 | T | G | 5 | a0001c0001t0001g0030 a0001c0001t0001g0126 a0001c0001t0001g0194 others(2): Show |
5 | HG02723.hp1 HG02818.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.656+12387A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48912492 | |||||||
| chr15:48912558 | T | G | 1 | a0001c0001t0001g0148 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.656+12321A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48912558 | |||||||
| chr15:48912684 | G | A | 1 | a0001c0002t0004g0118 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.656+12195C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48912684 | |||||||
| chr15:48912744 | C | T | 1 | a0001c0001t0002g0190 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.656+12135G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48912744 | |||||||
| chr15:48912893 | T | G | 1 | a0001c0001t0004g0184 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.656+11986A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48912893 | |||||||
| chr15:48912914 | G | A | 1 | a0001c0001t0002g0217 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.656+11965C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48912914 | |||||||
| chr15:48912931 | C | T | 3 | a0001c0001t0010g0066 a0001c0001t0010g0112 a0001c0001t0010g0193 |
3 | HG02723.hp2 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.656+11948G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48912931 | |||||||
| chr15:48913014 | G | C | 1 | a0001c0001t0001g0371 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.656+11865C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48913014 | |||||||
| chr15:48913025 | G | C | 15 | a0002c0003t0001g0095 a0002c0003t0003g0046 a0002c0003t0003g0111 others(12): Show |
15 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(12): Show |
intron_variant | MODIFIER | c.656+11854C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48913025 | |||||||
| chr15:48913057 | A | ATTT | 331 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(328): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.656+11821_656+1182 others(7): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48913057 | |||||||
| chr15:48913119 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.656+11760T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48913119 | |||||||
| chr15:48913494 | C | T | 41 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0002g0033 others(38): Show |
41 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.656+11385G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48913494 | |||||||
| chr15:48913510 | A | G | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | HG00642.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.656+11369T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48913510 | |||||||
| chr15:48913630 | C | T | 1 | a0002c0003t0003g0046 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.656+11249G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48913630 | |||||||
| chr15:48913760 | G | A | 1 | a0001c0001t0003g0320 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.656+11119C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48913760 | |||||||
| chr15:48914010 | G | A | 1 | a0001c0001t0004g0184 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.656+10869C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48914010 | |||||||
| chr15:48914127 | T | A | 29 | a0001c0001t0001g0045 a0001c0001t0001g0089 a0001c0001t0001g0159 others(26): Show |
29 | HG01255.hp2 HG01496.hp2 HG01928.hp2 others(26): Show |
intron_variant | MODIFIER | c.656+10752A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48914127 | |||||||
| chr15:48914162 | G | A | 4 | a0001c0001t0002g0262 a0001c0001t0002g0287 a0001c0001t0002g0303 others(1): Show |
4 | NA18992.hp1 NA18994.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.656+10717C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48914162 | |||||||
| chr15:48914248 | T | C | 4 | a0001c0001t0002g0117 a0001c0001t0008g0013 a0001c0001t0008g0015 others(1): Show |
4 | HG02630.hp2 HG03130.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.656+10631A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48914248 | |||||||
| chr15:48914413 | G | A | 1 | a0001c0001t0005g0349 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.656+10466C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48914413 | |||||||
| chr15:48914431 | C | T | 3 | a0001c0002t0004g0047 a0001c0002t0004g0048 a0001c0002t0004g0049 |
3 | HG01258.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.656+10448G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48914431 | |||||||
| chr15:48914517 | T | C | 21 | a0001c0001t0001g0348 a0001c0001t0002g0186 a0001c0001t0002g0202 others(18): Show |
21 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.656+10362A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48914517 | |||||||
| chr15:48914600 | A | G | 247 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0045 others(244): Show |
248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.656+10279T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48914600 | |||||||
| chr15:48914653 | C | T | 4 | a0001c0001t0002g0027 a0001c0001t0010g0066 a0001c0001t0010g0112 others(1): Show |
4 | HG01884.hp2 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.656+10226G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48914653 | |||||||
| chr15:48914705 | A | G | 229 | a0001c0001t0001g0030 a0001c0001t0001g0042 a0001c0001t0001g0045 others(226): Show |
230 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.656+10174T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48914705 | |||||||
| chr15:48914789 | A | C | 61 | a0001c0001t0001g0041 a0001c0001t0001g0044 a0001c0001t0001g0070 others(58): Show |
61 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.656+10090T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48914789 | |||||||
| chr15:48914799 | C | T | 62 | a0001c0001t0001g0041 a0001c0001t0001g0044 a0001c0001t0001g0070 others(59): Show |
62 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.656+10080G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48914799 | |||||||
| chr15:48914940 | C | T | 4 | a0001c0001t0001g0068 a0001c0001t0001g0147 a0001c0001t0001g0172 others(1): Show |
4 | HG00099.hp2 HG01123.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.656+9939G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48914940 | |||||||
| chr15:48915033 | C | T | 32 | a0001c0001t0001g0139 a0001c0001t0001g0148 a0001c0001t0001g0308 others(29): Show |
33 | HG00408.hp2 HG01167.hp2 HG01496.hp2 others(30): Show |
intron_variant | MODIFIER | c.656+9846G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48915033 | |||||||
| chr15:48915195 | T | C | 153 | a0001c0001t0001g0030 a0001c0001t0001g0042 a0001c0001t0001g0045 others(150): Show |
153 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.656+9684A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48915195 | |||||||
| chr15:48915213 | G | T | 3 | a0001c0001t0001g0126 a0001c0001t0001g0212 a0001c0001t0001g0255 |
3 | HG02723.hp1 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.656+9666C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48915213 | |||||||
| chr15:48915275 | G | A | 3 | a0001c0001t0002g0065 a0001c0001t0005g0062 a0001c0001t0005g0109 |
3 | HG02622.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.656+9604C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48915275 | |||||||
| chr15:48915477 | A | T | 1 | a0001c0001t0001g0209 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.656+9402T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48915477 | |||||||
| chr15:48915576 | AC | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0128 a0001c0001t0001g0256 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.656+9302delG | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48915576 | |||||||
| chr15:48915720 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.656+9159T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48915720 | |||||||
| chr15:48915822 | C | G | 26 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0029 others(23): Show |
27 | HG00099.hp2 HG00738.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.656+9057G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48915822 | |||||||
| chr15:48915831 | T | A | 1 | a0001c0001t0001g0144 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.656+9048A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48915831 | |||||||
| chr15:48915843 | G | A | 2 | a0001c0001t0002g0050 a0001c0001t0002g0173 |
2 | HG01081.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.656+9036C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48915843 | |||||||
| chr15:48915885 | G | A | 3 | a0001c0001t0002g0065 a0001c0001t0005g0062 a0001c0001t0005g0109 |
3 | HG02622.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.656+8994C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48915885 | |||||||
| chr15:48916105 | C | T | 4 | a0001c0001t0001g0154 a0001c0001t0002g0065 a0001c0001t0005g0062 others(1): Show |
4 | HG02622.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.656+8774G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48916105 | |||||||
| chr15:48916178 | T | TC | 14 | a0001c0001t0001g0030 a0001c0001t0001g0126 a0001c0001t0001g0188 others(11): Show |
14 | HG01255.hp2 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.656+8700dupG | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48916178 | |||||||
| chr15:48916271 | GCT | G | 5 | a0001c0001t0001g0119 a0001c0001t0001g0257 a0001c0001t0001g0259 others(2): Show |
5 | HG01884.hp1 HG02647.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.656+8606_656+8607d others(4): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48916271 | |||||||
| chr15:48916271 | GCTCA | G | 13 | a0001c0001t0001g0082 a0001c0001t0001g0089 a0001c0001t0001g0160 others(10): Show |
13 | HG02273.hp1 HG02559.hp2 HG03471.hp1 others(10): Show |
intron_variant | MODIFIER | c.656+8604_656+8607d others(6): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48916271 | |||||||
| chr15:48916271 | GCTCACA | G | 4 | a0001c0001t0001g0237 a0001c0001t0002g0303 a0001c0001t0005g0213 others(1): Show |
4 | HG01243.hp1 NA18994.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.656+8602_656+8607d others(8): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48916271 | |||||||
| chr15:48916271 | GCTCACAC others(1): Show |
G | 5 | a0001c0001t0001g0045 a0001c0001t0001g0087 a0001c0001t0001g0161 others(2): Show |
5 | HG02109.hp1 HG03139.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.656+8600_656+8607d others(10): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48916271 | |||||||
| chr15:48916271 | GCTCACAC others(3): Show |
G | 1 | a0001c0001t0001g0330 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.656+8598_656+8607d others(12): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48916271 | |||||||
| chr15:48916273 | T | TCA | 3 | a0001c0001t0001g0108 a0001c0001t0002g0145 a0001c0002t0018g0010 |
3 | HG02698.hp1 NA18965.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.656+8604_656+8605d others(4): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48916273 | |||||||
| chr15:48916273 | TCA | T | 59 | a0001c0001t0001g0026 a0001c0001t0001g0084 a0001c0001t0001g0137 others(56): Show |
59 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.656+8604_656+8605d others(4): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48916273 | |||||||
| chr15:48916273 | TCACA | T | 52 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0029 others(49): Show |
53 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.656+8602_656+8605d others(6): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48916273 | |||||||
| chr15:48916273 | TCACACA | T | 62 | a0001c0001t0001g0059 a0001c0001t0001g0101 a0001c0001t0001g0126 others(59): Show |
63 | HG00735.hp1 HG00738.hp2 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.656+8600_656+8605d others(8): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48916273 | |||||||
| chr15:48916273 | TCACACAC others(1): Show |
T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0042 a0001c0001t0001g0071 others(85): Show |
89 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.656+8598_656+8605d others(10): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48916273 | |||||||
| chr15:48916273 | TCACACAC others(3): Show |
T | 7 | a0001c0001t0001g0146 a0001c0001t0001g0181 a0001c0001t0001g0308 others(4): Show |
7 | HG00140.hp2 HG01257.hp2 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.656+8596_656+8605d others(12): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48916273 | |||||||
| chr15:48916273 | TCACACAC others(5): Show |
T | 5 | a0001c0001t0001g0139 a0001c0001t0002g0164 a0001c0001t0002g0340 others(2): Show |
5 | HG00597.hp1 HG01167.hp2 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.656+8594_656+8605d others(14): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48916273 | |||||||
| chr15:48916273 | TCACACAC others(7): Show |
T | 30 | a0001c0001t0001g0070 a0001c0001t0001g0148 a0001c0001t0001g0225 others(27): Show |
31 | HG00408.hp2 HG01496.hp2 HG01993.hp2 others(28): Show |
intron_variant | MODIFIER | c.656+8592_656+8605d others(16): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48916273 | |||||||
| chr15:48916273 | TCACACAC others(9): Show |
T | 4 | a0001c0001t0001g0154 a0001c0001t0002g0065 a0001c0001t0005g0062 others(1): Show |
4 | HG02622.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.656+8590_656+8605d others(18): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48916273 | |||||||
| chr15:48916273 | TCACACAC others(11): Show |
T | 1 | a0001c0002t0004g0221 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.656+8588_656+8605d others(20): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48916273 | |||||||
| chr15:48916311 | ACACACAC | A | 4 | a0001c0001t0001g0263 a0001c0001t0001g0282 a0001c0001t0002g0358 others(1): Show |
4 | HG00597.hp2 HG02071.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.656+8561_656+8567d others(9): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48916311 | |||||||
| chr15:48916317 | AC | A | 6 | a0001c0001t0001g0035 a0001c0001t0001g0100 a0001c0001t0002g0054 others(3): Show |
6 | HG01169.hp1 HG02056.hp2 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.656+8561delG | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48916317 | |||||||
| chr15:48916437 | A | G | 1 | a0001c0001t0001g0330 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.656+8442T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48916437 | |||||||
| chr15:48916485 | G | T | 1 | a0001c0001t0002g0092 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.656+8394C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48916485 | |||||||
| chr15:48916559 | C | CA | 320 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0026 others(317): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.656+8319dupT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48916559 | |||||||
| chr15:48916559 | C | CAA | 22 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0192 others(19): Show |
22 | HG01106.hp1 HG01981.hp2 HG02004.hp1 others(19): Show |
intron_variant | MODIFIER | c.656+8318_656+8319d others(4): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48916559 | |||||||
| chr15:48916559 | C | CAAA | 11 | a0001c0001t0001g0275 a0001c0001t0001g0280 a0001c0001t0001g0292 others(8): Show |
11 | HG00673.hp2 HG02071.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.656+8317_656+8319d others(5): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48916559 | |||||||
| chr15:48916596 | A | T | 362 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0029 others(359): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.656+8283T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48916596 | |||||||
| chr15:48916625 | C | T | 17 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0068 others(14): Show |
18 | HG00099.hp2 HG00738.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.656+8254G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48916625 | |||||||
| chr15:48916637 | A | G | 1 | a0001c0002t0004g0248 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.656+8242T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48916637 | |||||||
| chr15:48916681 | C | T | 1 | a0001c0001t0002g0303 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.656+8198G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48916681 | |||||||
| chr15:48916768 | C | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0175 |
2 | HG03490.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.656+8111G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48916768 | |||||||
| chr15:48916795 | A | T | 336 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0029 others(333): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.656+8084T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48916795 | |||||||
| chr15:48917195 | T | C | 2 | a0001c0001t0001g0045 a0001c0001t0002g0113 |
2 | NA18946.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.656+7684A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48917195 | |||||||
| chr15:48917243 | T | TTG | 3 | a0001c0001t0001g0044 a0001c0001t0001g0285 a0001c0001t0005g0138 |
3 | HG02602.hp1 HG03491.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.656+7634_656+7635d others(4): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48917243 | |||||||
| chr15:48917243 | T | TTGTG | 3 | a0001c0001t0001g0209 a0001c0001t0002g0117 a0001c0001t0008g0013 |
3 | HG02630.hp2 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.656+7632_656+7635d others(6): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48917243 | |||||||
| chr15:48917243 | T | TTGTGTG | 3 | a0001c0001t0001g0256 a0001c0001t0001g0280 a0001c0001t0008g0016 |
3 | HG02809.hp1 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.656+7630_656+7635d others(8): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48917243 | |||||||
| chr15:48917243 | TTG | T | 32 | a0001c0001t0001g0056 a0001c0001t0001g0089 a0001c0001t0001g0108 others(29): Show |
32 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.656+7634_656+7635d others(4): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48917243 | |||||||
| chr15:48917243 | TTGTG | T | 131 | a0001c0001t0001g0029 a0001c0001t0001g0041 a0001c0001t0001g0042 others(128): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.656+7632_656+7635d others(6): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48917243 | |||||||
| chr15:48917243 | TTGTGTG | T | 89 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0093 others(86): Show |
90 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.656+7630_656+7635d others(8): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48917243 | |||||||
| chr15:48917243 | TTGTGTGT others(1): Show |
T | 45 | a0001c0001t0001g0026 a0001c0001t0001g0035 a0001c0001t0001g0070 others(42): Show |
45 | HG01081.hp2 HG01123.hp2 HG01496.hp2 others(42): Show |
intron_variant | MODIFIER | c.656+7628_656+7635d others(10): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48917243 | |||||||
| chr15:48917243 | TTGTGTGT others(3): Show |
T | 20 | a0001c0001t0001g0023 a0001c0001t0001g0159 a0001c0001t0001g0179 others(17): Show |
20 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(17): Show |
intron_variant | MODIFIER | c.656+7626_656+7635d others(12): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48917243 | |||||||
| chr15:48917243 | TTGTGTGT others(5): Show |
T | 13 | a0001c0001t0001g0087 a0001c0001t0001g0183 a0001c0001t0001g0299 others(10): Show |
13 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.656+7624_656+7635d others(14): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48917243 | |||||||
| chr15:48917243 | TTGTGTGT others(7): Show |
T | 1 | a0001c0001t0002g0197 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.656+7622_656+7635d others(16): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48917243 | |||||||
| chr15:48917243 | TTGTGTGT others(9): Show |
T | 15 | a0001c0001t0001g0030 a0001c0001t0001g0126 a0001c0001t0001g0188 others(12): Show |
15 | HG01243.hp1 HG02145.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.656+7620_656+7635d others(18): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48917243 | |||||||
| chr15:48917243 | TTGTGTGT others(11): Show |
T | 2 | a0001c0001t0003g0279 a0001c0004t0005g0376 |
2 | HG02572.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.656+7618_656+7635d others(20): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48917243 | |||||||
| chr15:48917243 | TTGTGTGT others(15): Show |
T | 1 | a0007c0008t0004g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.656+7614_656+7635d others(24): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48917243 | |||||||
| chr15:48917392 | T | A | 4 | a0001c0001t0001g0154 a0001c0001t0001g0181 a0001c0001t0005g0062 others(1): Show |
4 | HG02622.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.656+7487A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48917392 | |||||||
| chr15:48917415 | G | A | 2 | a0001c0001t0002g0207 a0001c0001t0004g0208 |
2 | HG00099.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.656+7464C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48917415 | |||||||
| chr15:48917431 | CTCTCTTC others(3): Show |
C | 1 | a0001c0001t0001g0215 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.656+7438_656+7447d others(12): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48917431 | |||||||
| chr15:48917435 | C | T | 114 | a0001c0001t0001g0041 a0001c0001t0001g0044 a0001c0001t0001g0045 others(111): Show |
115 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.656+7444G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48917435 | |||||||
| chr15:48917463 | C | T | 5 | a0001c0001t0001g0280 a0001c0001t0002g0117 a0001c0001t0008g0013 others(2): Show |
5 | HG02630.hp2 HG02809.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.656+7416G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48917463 | |||||||
| chr15:48917484 | C | T | 3 | a0001c0001t0003g0153 a0001c0001t0003g0232 a0006c0013t0003g0127 |
3 | NA18965.hp1 NA18979.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.656+7395G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48917484 | |||||||
| chr15:48917789 | C | CT | 371 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(368): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.656+7089dupA | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48917789 | |||||||
| chr15:48918035 | G | A | 9 | a0001c0001t0001g0108 a0001c0001t0002g0074 a0001c0001t0002g0145 others(6): Show |
9 | HG02155.hp2 NA18960.hp1 NA18965.hp2 others(6): Show |
intron_variant | MODIFIER | c.656+6844C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48918035 | |||||||
| chr15:48918115 | T | TA | 24 | a0001c0001t0001g0026 a0001c0001t0001g0035 a0001c0001t0001g0140 others(21): Show |
24 | HG00423.hp2 HG00673.hp2 HG02004.hp1 others(21): Show |
intron_variant | MODIFIER | c.656+6763dupT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48918115 | |||||||
| chr15:48918131 | A | G | 3 | a0001c0001t0001g0087 a0001c0001t0001g0183 a0001c0001t0005g0024 |
3 | HG02109.hp1 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.656+6748T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48918131 | |||||||
| chr15:48918232 | A | G | 1 | a0001c0001t0001g0071 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.656+6647T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48918232 | |||||||
| chr15:48918411 | C | T | 4 | a0001c0001t0001g0082 a0001c0001t0001g0188 a0001c0001t0001g0198 others(1): Show |
4 | HG02145.hp2 HG02559.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.656+6468G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48918411 | |||||||
| chr15:48918579 | AT | A | 110 | a0001c0001t0001g0041 a0001c0001t0001g0044 a0001c0001t0001g0056 others(107): Show |
111 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.656+6299delA | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48918579 | |||||||
| chr15:48918670 | C | T | 1 | a0001c0001t0004g0037 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.656+6209G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48918670 | |||||||
| chr15:48919018 | G | T | 1 | a0001c0001t0002g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.656+5861C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919018 | |||||||
| chr15:48919096 | T | TC | 341 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(338): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.656+5782dupG | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919096 | |||||||
| chr15:48919240 | C | A | 3 | a0001c0001t0001g0100 a0001c0001t0004g0136 a0001c0001t0005g0072 |
3 | HG03710.hp1 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.656+5639G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919240 | |||||||
| chr15:48919295 | A | AT | 9 | a0001c0001t0001g0179 a0001c0001t0001g0191 a0001c0001t0001g0192 others(6): Show |
9 | HG01192.hp2 HG01943.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.656+5583dupA | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919295 | |||||||
| chr15:48919295 | A | ATT | 96 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0084 others(93): Show |
97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.656+5582_656+5583d others(4): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919295 | |||||||
| chr15:48919295 | A | ATTT | 9 | a0001c0001t0001g0239 a0001c0001t0001g0263 a0001c0001t0001g0272 others(6): Show |
9 | HG01981.hp2 HG02109.hp2 HG03490.hp1 others(6): Show |
intron_variant | MODIFIER | c.656+5581_656+5583d others(5): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919295 | |||||||
| chr15:48919295 | A | ATTTTTTT others(1): Show |
8 | a0001c0001t0001g0344 a0001c0001t0002g0117 a0001c0001t0002g0164 others(5): Show |
8 | HG00408.hp2 HG02559.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.656+5576_656+5583d others(10): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919295 | |||||||
| chr15:48919295 | A | ATTTTTTT others(2): Show |
37 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0068 others(34): Show |
38 | HG00099.hp2 HG00738.hp1 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.656+5575_656+5583d others(11): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919295 | |||||||
| chr15:48919295 | A | ATTTTTTT others(3): Show |
19 | a0001c0001t0001g0052 a0001c0001t0001g0139 a0001c0001t0001g0174 others(16): Show |
19 | HG00280.hp2 HG01123.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.656+5574_656+5583d others(12): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919295 | |||||||
| chr15:48919295 | A | ATTTTTTT others(4): Show |
9 | a0001c0001t0001g0081 a0001c0001t0001g0101 a0001c0001t0001g0196 others(6): Show |
9 | HG01109.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.656+5573_656+5583d others(13): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919295 | |||||||
| chr15:48919295 | A | ATTTTTTT others(5): Show |
2 | a0001c0001t0001g0059 a0001c0002t0004g0265 |
2 | HG03516.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.656+5572_656+5583d others(14): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919295 | |||||||
| chr15:48919295 | A | ATTTTTTT others(6): Show |
2 | a0001c0001t0002g0002 a0001c0001t0002g0143 |
3 | HG00738.hp2 HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.656+5571_656+5583d others(15): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919295 | |||||||
| chr15:48919295 | A | ATTTTTTT others(9): Show |
3 | a0001c0001t0001g0119 a0001c0001t0002g0027 a0001c0001t0026g0258 |
3 | HG01884.hp1 HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.656+5568_656+5583d others(18): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919295 | |||||||
| chr15:48919295 | A | ATTTTTTT others(10): Show |
4 | a0001c0001t0001g0181 a0001c0001t0001g0257 a0001c0001t0001g0259 others(1): Show |
4 | HG02155.hp2 HG02897.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.656+5567_656+5583d others(19): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919295 | |||||||
| chr15:48919295 | A | ATTTTTTT others(11): Show |
4 | a0001c0001t0005g0109 a0001c0001t0005g0301 a0001c0001t0010g0066 others(1): Show |
4 | HG02922.hp1 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.656+5566_656+5583d others(20): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919295 | |||||||
| chr15:48919295 | A | ATTTTTTT others(12): Show |
1 | a0001c0001t0005g0062 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.656+5565_656+5583d others(21): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919295 | |||||||
| chr15:48919295 | A | ATTTTTTT others(13): Show |
2 | a0001c0001t0002g0091 a0001c0001t0002g0340 |
2 | HG00597.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.656+5564_656+5583d others(22): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919295 | |||||||
| chr15:48919295 | A | ATTTTTTT others(14): Show |
4 | a0001c0001t0001g0041 a0001c0001t0001g0337 a0001c0001t0001g0338 others(1): Show |
4 | HG01952.hp2 HG03927.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.656+5583_656+5584i others(23): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919295 | |||||||
| chr15:48919295 | A | ATTTTTTT others(15): Show |
23 | a0001c0001t0001g0044 a0001c0001t0001g0089 a0001c0001t0001g0141 others(20): Show |
23 | HG00609.hp1 HG00621.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.656+5583_656+5584i others(24): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919295 | |||||||
| chr15:48919295 | A | ATTTTTTT others(16): Show |
7 | a0001c0001t0001g0160 a0001c0001t0001g0163 a0001c0001t0001g0316 others(4): Show |
7 | HG00597.hp2 HG02273.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.656+5583_656+5584i others(25): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919295 | |||||||
| chr15:48919295 | A | ATTTTTTT others(17): Show |
16 | a0001c0001t0001g0056 a0001c0001t0001g0201 a0001c0001t0001g0268 others(13): Show |
16 | HG01081.hp1 HG01099.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.656+5583_656+5584i others(26): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919295 | |||||||
| chr15:48919295 | A | ATTTTTTT others(18): Show |
9 | a0001c0001t0001g0225 a0001c0001t0001g0306 a0001c0001t0001g0318 others(6): Show |
9 | HG00423.hp1 HG00609.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.656+5583_656+5584i others(27): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919295 | |||||||
| chr15:48919295 | A | ATTTTTTT others(19): Show |
8 | a0001c0001t0001g0098 a0001c0001t0001g0152 a0001c0001t0001g0361 others(5): Show |
8 | HG00438.hp1 HG01109.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.656+5583_656+5584i others(28): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919295 | |||||||
| chr15:48919295 | A | ATTTTTTT others(20): Show |
6 | a0001c0001t0001g0071 a0001c0001t0001g0137 a0001c0001t0001g0162 others(3): Show |
6 | HG02647.hp2 HG02717.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.656+5583_656+5584i others(29): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919295 | |||||||
| chr15:48919295 | A | ATTTTTTT others(21): Show |
9 | a0001c0001t0002g0033 a0001c0001t0002g0053 a0001c0001t0002g0085 others(6): Show |
9 | HG00735.hp1 HG03098.hp1 HG03492.hp1 others(6): Show |
intron_variant | MODIFIER | c.656+5583_656+5584i others(30): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919295 | |||||||
| chr15:48919295 | A | ATTTTTTT others(22): Show |
6 | a0001c0001t0001g0200 a0001c0001t0002g0145 a0001c0001t0005g0036 others(3): Show |
6 | HG00642.hp1 HG03041.hp1 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.656+5583_656+5584i others(31): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919295 | |||||||
| chr15:48919295 | A | ATTTTTTT others(23): Show |
6 | a0001c0001t0001g0023 a0001c0001t0001g0108 a0001c0001t0004g0184 others(3): Show |
6 | HG02622.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.656+5583_656+5584i others(32): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919295 | |||||||
| chr15:48919295 | A | ATTTTTTT others(24): Show |
1 | a0001c0001t0015g0006 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.656+5583_656+5584i others(33): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919295 | |||||||
| chr15:48919295 | A | ATTTTTTT others(26): Show |
1 | a0001c0001t0001g0175 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.656+5583_656+5584i others(35): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919295 | |||||||
| chr15:48919295 | A | ATTTTTTT others(28): Show |
1 | a0001c0001t0002g0370 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.656+5583_656+5584i others(37): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919295 | |||||||
| chr15:48919295 | AT | A | 18 | a0001c0001t0001g0030 a0001c0001t0001g0126 a0001c0001t0001g0154 others(15): Show |
18 | HG01243.hp1 HG02257.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.656+5583delA | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919295 | |||||||
| chr15:48919316 | G | T | 1 | a0001c0001t0002g0262 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.656+5563C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919316 | |||||||
| chr15:48919467 | T | C | 1 | a0001c0001t0002g0065 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.656+5412A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919467 | |||||||
| chr15:48919652 | G | A | 9 | a0001c0001t0001g0023 a0001c0001t0002g0085 a0001c0001t0005g0036 others(6): Show |
9 | HG02486.hp2 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.656+5227C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919652 | |||||||
| chr15:48919796 | C | G | 1 | a0001c0001t0002g0115 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.656+5083G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919796 | |||||||
| chr15:48919851 | A | G | 145 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0029 others(142): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.656+5028T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48919851 | |||||||
| chr15:48920015 | G | GT | 19 | a0001c0001t0001g0052 a0001c0001t0001g0100 a0001c0001t0001g0177 others(16): Show |
19 | HG01884.hp2 HG01981.hp2 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.656+4863dupA | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48920015 | |||||||
| chr15:48920015 | GT | G | 33 | a0001c0001t0001g0026 a0001c0001t0001g0035 a0001c0001t0001g0082 others(30): Show |
33 | HG00423.hp2 HG00673.hp2 HG02004.hp1 others(30): Show |
intron_variant | MODIFIER | c.656+4863delA | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48920015 | |||||||
| chr15:48920022 | T | G | 1 | a0001c0001t0001g0166 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.656+4857A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48920022 | |||||||
| chr15:48920096 | G | T | 22 | a0001c0001t0001g0026 a0001c0001t0001g0035 a0001c0001t0001g0087 others(19): Show |
22 | HG00423.hp2 HG00673.hp2 HG02004.hp1 others(19): Show |
intron_variant | MODIFIER | c.656+4783C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48920096 | |||||||
| chr15:48920181 | A | AT | 136 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0042 others(133): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.656+4697dupA | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48920181 | |||||||
| chr15:48920181 | A | ATT | 29 | a0001c0001t0001g0026 a0001c0001t0001g0035 a0001c0001t0001g0087 others(26): Show |
29 | HG00423.hp2 HG00673.hp2 HG02004.hp1 others(26): Show |
intron_variant | MODIFIER | c.656+4696_656+4697d others(4): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48920181 | |||||||
| chr15:48920204 | G | A | 2 | a0001c0001t0005g0062 a0001c0001t0005g0109 |
2 | HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.656+4675C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48920204 | |||||||
| chr15:48920242 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.656+4637G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48920242 | |||||||
| chr15:48920243 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.656+4636C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48920243 | |||||||
| chr15:48920408 | C | T | 5 | a0001c0001t0001g0280 a0001c0001t0002g0117 a0001c0001t0008g0013 others(2): Show |
5 | HG02630.hp2 HG02809.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.656+4471G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48920408 | |||||||
| chr15:48920410 | G | A | 138 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0029 others(135): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.656+4469C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48920410 | |||||||
| chr15:48920521 | T | C | 357 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(354): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.656+4358A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48920521 | |||||||
| chr15:48920550 | C | T | 3 | a0001c0001t0001g0001 a0001c0001t0001g0128 a0001c0001t0001g0256 |
4 | HG01167.hp1 HG01169.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.656+4329G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48920550 | |||||||
| chr15:48920566 | C | T | 35 | a0001c0001t0001g0026 a0001c0001t0001g0035 a0001c0001t0001g0082 others(32): Show |
35 | HG00423.hp2 HG00673.hp2 HG02004.hp1 others(32): Show |
intron_variant | MODIFIER | c.656+4313G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48920566 | |||||||
| chr15:48920567 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.656+4312C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48920567 | |||||||
| chr15:48920570 | C | T | 2 | a0001c0001t0002g0341 a0001c0001t0002g0362 |
2 | NA18948.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.656+4309G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48920570 | |||||||
| chr15:48920572 | G | A | 7 | a0001c0001t0001g0082 a0001c0001t0001g0154 a0001c0001t0001g0188 others(4): Show |
7 | HG02145.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.656+4307C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48920572 | |||||||
| chr15:48920619 | A | AG | 8 | a0001c0001t0001g0042 a0001c0001t0001g0196 a0001c0001t0001g0280 others(5): Show |
8 | HG00423.hp1 HG01255.hp2 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.656+4259dupC | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48920619 | |||||||
| chr15:48920628 | C | A | 1 | a0001c0002t0004g0047 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.656+4251G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48920628 | |||||||
| chr15:48920783 | A | T | 1 | a0001c0001t0001g0215 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.656+4096T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48920783 | |||||||
| chr15:48920843 | G | T | 1 | a0001c0002t0004g0372 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.656+4036C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48920843 | |||||||
| chr15:48920870 | G | A | 1 | a0001c0001t0005g0109 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.656+4009C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48920870 | |||||||
| chr15:48920889 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.656+3990G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48920889 | |||||||
| chr15:48920899 | A | T | 1 | a0001c0001t0001g0215 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.656+3980T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48920899 | |||||||
| chr15:48920910 | CT | C | 173 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(170): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.656+3968delA | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48920910 | |||||||
| chr15:48921229 | T | C | 11 | a0001c0001t0001g0082 a0001c0001t0001g0100 a0001c0001t0001g0154 others(8): Show |
11 | HG02145.hp2 HG02258.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.656+3650A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48921229 | |||||||
| chr15:48921259 | C | G | 1 | a0001c0001t0001g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.656+3620G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48921259 | |||||||
| chr15:48921331 | G | GT | 92 | a0001c0001t0001g0041 a0001c0001t0001g0059 a0001c0001t0001g0069 others(89): Show |
93 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.656+3547dupA | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48921331 | |||||||
| chr15:48921331 | G | GTT | 6 | a0001c0001t0001g0044 a0001c0001t0001g0339 a0001c0001t0001g0361 others(3): Show |
6 | HG01433.hp2 HG01978.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.656+3546_656+3547d others(4): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48921331 | |||||||
| chr15:48921331 | G | T | 1 | a0001c0001t0002g0064 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.656+3548C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48921331 | |||||||
| chr15:48921331 | GT | G | 9 | a0001c0001t0001g0082 a0001c0001t0001g0100 a0001c0001t0001g0188 others(6): Show |
9 | HG02145.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.656+3547delA | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48921331 | |||||||
| chr15:48921387 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.656+3492A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48921387 | |||||||
| chr15:48921420 | C | T | 1 | a0001c0001t0001g0326 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.656+3459G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48921420 | |||||||
| chr15:48921576 | C | A | 1 | a0001c0001t0001g0339 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.656+3303G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48921576 | |||||||
| chr15:48921625 | G | A | 2 | a0001c0001t0002g0002 a0001c0001t0002g0143 |
3 | HG00738.hp2 HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.656+3254C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48921625 | |||||||
| chr15:48921656 | A | G | 1 | a0001c0012t0003g0040 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.656+3223T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48921656 | |||||||
| chr15:48921667 | C | T | 126 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0042 others(123): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.656+3212G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48921667 | |||||||
| chr15:48921729 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.656+3150G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48921729 | |||||||
| chr15:48921752 | T | C | 2 | a0001c0004t0005g0376 a0007c0008t0004g0104 |
2 | HG02572.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.656+3127A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48921752 | |||||||
| chr15:48921765 | T | C | 104 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0084 others(101): Show |
105 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.656+3114A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48921765 | |||||||
| chr15:48921859 | G | A | 249 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(246): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.656+3020C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48921859 | |||||||
| chr15:48921862 | T | G | 1 | a0001c0001t0017g0011 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.656+3017A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48921862 | |||||||
| chr15:48921878 | T | A | 1 | a0001c0001t0001g0215 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.656+3001A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48921878 | |||||||
| chr15:48921879 | A | T | 1 | a0001c0001t0001g0215 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.656+3000T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48921879 | |||||||
| chr15:48921959 | T | G | 1 | a0001c0001t0002g0085 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.656+2920A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48921959 | |||||||
| chr15:48922046 | G | A | 72 | a0001c0001t0001g0041 a0001c0001t0001g0044 a0001c0001t0001g0069 others(69): Show |
73 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.656+2833C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48922046 | |||||||
| chr15:48922051 | A | T | 1 | a0001c0001t0001g0215 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.656+2828T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48922051 | |||||||
| chr15:48922088 | C | T | 5 | a0001c0001t0003g0350 a0001c0002t0004g0233 a0001c0002t0004g0234 others(2): Show |
5 | NA18945.hp2 NA18946.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.656+2791G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48922088 | |||||||
| chr15:48922210 | C | G | 10 | a0001c0001t0001g0082 a0001c0001t0001g0100 a0001c0001t0001g0154 others(7): Show |
10 | HG02145.hp2 HG02559.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.656+2669G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48922210 | |||||||
| chr15:48922392 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.656+2487G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48922392 | |||||||
| chr15:48922434 | C | T | 247 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(244): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.656+2445G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48922434 | |||||||
| chr15:48922481 | G | C | 247 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(244): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.656+2398C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48922481 | |||||||
| chr15:48922504 | C | T | 247 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(244): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.656+2375G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48922504 | |||||||
| chr15:48922821 | G | A | 1 | a0002c0003t0003g0046 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.656+2058C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48922821 | |||||||
| chr15:48922871 | G | GTC | 247 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(244): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.656+2007_656+2008i others(4): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48922871 | |||||||
| chr15:48923001 | G | A | 345 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(342): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.656+1878C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48923001 | |||||||
| chr15:48923012 | G | C | 249 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(246): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.656+1867C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48923012 | |||||||
| chr15:48923076 | A | G | 22 | a0001c0001t0001g0179 a0001c0001t0001g0348 a0001c0001t0002g0050 others(19): Show |
22 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(19): Show |
intron_variant | MODIFIER | c.656+1803T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48923076 | |||||||
| chr15:48923112 | C | T | 112 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0035 others(109): Show |
113 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.656+1767G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48923112 | |||||||
| chr15:48923328 | A | G | 1 | a0001c0001t0003g0363 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.656+1551T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48923328 | |||||||
| chr15:48923544 | CA | C | 150 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0042 others(147): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.656+1334delT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48923544 | |||||||
| chr15:48923544 | CAA | C | 154 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0056 others(151): Show |
155 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.656+1333_656+1334d others(4): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48923544 | |||||||
| chr15:48923547 | A | G | 2 | a0001c0001t0002g0203 a0001c0001t0002g0204 |
2 | HG01099.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.656+1332T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48923547 | |||||||
| chr15:48923560 | A | AG | 4 | a0001c0001t0001g0119 a0001c0001t0001g0257 a0001c0001t0001g0259 others(1): Show |
4 | HG01884.hp1 HG02647.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.656+1318_656+1319i others(3): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48923560 | |||||||
| chr15:48923560 | AC | A | 25 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0035 others(22): Show |
25 | HG00673.hp2 HG02004.hp1 HG02004.hp2 others(22): Show |
intron_variant | MODIFIER | c.656+1318delG | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48923560 | |||||||
| chr15:48923561 | C | A | 6 | a0001c0001t0001g0140 a0001c0001t0001g0181 a0001c0001t0002g0064 others(3): Show |
6 | HG00423.hp2 HG02027.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.656+1318G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48923561 | |||||||
| chr15:48923561 | C | G | 1 | a0001c0001t0002g0054 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.656+1318G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48923561 | |||||||
| chr15:48923582 | A | T | 1 | a0001c0001t0001g0215 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.656+1297T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48923582 | |||||||
| chr15:48923586 | T | A | 1 | a0001c0001t0001g0215 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.656+1293A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48923586 | |||||||
| chr15:48923606 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.656+1273A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48923606 | |||||||
| chr15:48923635 | C | CT | 103 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0044 others(100): Show |
104 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.656+1243dupA | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48923635 | |||||||
| chr15:48923635 | C | CTT | 34 | a0001c0001t0001g0026 a0001c0001t0001g0035 a0001c0001t0001g0087 others(31): Show |
34 | HG00423.hp2 HG00673.hp2 HG01928.hp1 others(31): Show |
intron_variant | MODIFIER | c.656+1242_656+1243d others(4): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48923635 | |||||||
| chr15:48923635 | C | CTTT | 9 | a0001c0001t0001g0023 a0001c0001t0001g0292 a0001c0001t0003g0096 others(6): Show |
9 | HG02027.hp1 HG02486.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.656+1241_656+1243d others(5): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48923635 | |||||||
| chr15:48923635 | CT | C | 26 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0052 others(23): Show |
27 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.656+1243delA | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48923635 | |||||||
| chr15:48923757 | A | T | 1 | a0001c0001t0001g0215 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.656+1122T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48923757 | |||||||
| chr15:48923852 | G | A | 73 | a0001c0001t0001g0041 a0001c0001t0001g0044 a0001c0001t0001g0069 others(70): Show |
74 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.656+1027C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48923852 | |||||||
| chr15:48924133 | T | C | 339 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(336): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.656+746A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48924133 | |||||||
| chr15:48924362 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.656+517C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48924362 | |||||||
| chr15:48924481 | C | T | 9 | a0001c0001t0001g0116 a0001c0001t0001g0291 a0002c0003t0003g0111 others(6): Show |
9 | HG00558.hp1 HG02056.hp2 NA18612.hp2 others(6): Show |
intron_variant | MODIFIER | c.656+398G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48924481 | |||||||
| chr15:48924482 | G | A | 1 | a0001c0001t0001g0369 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.656+397C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48924482 | |||||||
| chr15:48924526 | G | T | 78 | a0001c0001t0001g0056 a0001c0001t0001g0070 a0001c0001t0001g0073 others(75): Show |
78 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.656+353C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48924526 | |||||||
| chr15:48924749 | C | A | 1 | a0001c0001t0002g0064 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.656+130G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48924749 | |||||||
| chr15:48924765 | C | T | 1 | a0001c0001t0002g0077 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.656+114G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 2/11 | chr15 | 48924765 | |||||||
| chr15:48925015 | C | A | 4 | a0001c0001t0001g0119 a0001c0001t0001g0257 a0001c0001t0001g0259 others(1): Show |
4 | HG01884.hp1 HG02647.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.586-66G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48925015 | |||||||
| chr15:48925107 | G | A | 3 | a0001c0002t0004g0047 a0001c0002t0004g0048 a0001c0002t0004g0049 |
3 | HG01258.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.586-158C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48925107 | |||||||
| chr15:48925277 | C | A | 1 | a0001c0001t0001g0212 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.586-328G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48925277 | |||||||
| chr15:48925399 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.586-450G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48925399 | |||||||
| chr15:48925409 | A | G | 173 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0026 others(170): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.586-460T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48925409 | |||||||
| chr15:48925417 | G | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0026 others(168): Show |
173 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.586-468C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48925417 | |||||||
| chr15:48925662 | T | C | 133 | a0001c0001t0001g0030 a0001c0001t0001g0042 a0001c0001t0001g0044 others(130): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.586-713A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48925662 | |||||||
| chr15:48925717 | C | A | 2 | a0001c0001t0005g0062 a0001c0001t0005g0109 |
2 | HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.586-768G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48925717 | |||||||
| chr15:48925739 | T | A | 1 | a0001c0001t0001g0192 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.586-790A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48925739 | |||||||
| chr15:48925770 | G | A | 116 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0045 others(113): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.586-821C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48925770 | |||||||
| chr15:48925976 | C | T | 2 | a0001c0001t0002g0091 a0001c0002t0004g0288 |
2 | HG00741.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.586-1027G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48925976 | |||||||
| chr15:48925998 | C | G | 15 | a0001c0001t0001g0030 a0001c0001t0001g0212 a0001c0001t0001g0255 others(12): Show |
15 | HG01243.hp1 HG01255.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.586-1049G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48925998 | |||||||
| chr15:48926157 | G | A | 4 | a0001c0001t0001g0100 a0001c0001t0004g0136 a0001c0001t0005g0072 others(1): Show |
4 | HG02647.hp2 HG03710.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.586-1208C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48926157 | |||||||
| chr15:48926267 | A | G | 1 | a0001c0004t0005g0376 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.586-1318T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48926267 | |||||||
| chr15:48926310 | G | A | 24 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0052 others(21): Show |
25 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.586-1361C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48926310 | |||||||
| chr15:48926349 | T | C | 3 | a0001c0001t0002g0027 a0001c0001t0010g0066 a0001c0001t0010g0193 |
3 | HG01884.hp2 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.586-1400A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48926349 | |||||||
| chr15:48926433 | C | T | 1 | a0001c0001t0001g0371 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.586-1484G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48926433 | |||||||
| chr15:48926461 | CT | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0026 others(147): Show |
152 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.586-1513delA | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48926461 | |||||||
| chr15:48926461 | CTT | C | 19 | a0001c0001t0001g0030 a0001c0001t0001g0100 a0001c0001t0001g0212 others(16): Show |
19 | HG01243.hp1 HG01255.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.586-1514_586-1513d others(4): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48926461 | |||||||
| chr15:48926478 | T | G | 1 | a0001c0001t0001g0318 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.586-1529A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48926478 | |||||||
| chr15:48926513 | T | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0026 others(165): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.586-1564A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48926513 | |||||||
| chr15:48926526 | G | C | 1 | a0001c0001t0017g0011 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.586-1577C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48926526 | |||||||
| chr15:48926539 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.586-1590A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48926539 | |||||||
| chr15:48926545 | C | T | 24 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0052 others(21): Show |
25 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.586-1596G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48926545 | |||||||
| chr15:48926638 | T | A | 5 | a0001c0001t0001g0280 a0001c0001t0002g0117 a0001c0001t0008g0013 others(2): Show |
5 | HG02630.hp2 HG02809.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.586-1689A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48926638 | |||||||
| chr15:48926701 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.586-1752C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48926701 | |||||||
| chr15:48926714 | T | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0026 others(167): Show |
172 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.586-1765A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48926714 | |||||||
| chr15:48926753 | G | A | 1 | a0001c0001t0002g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.586-1804C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48926753 | |||||||
| chr15:48926856 | G | A | 2 | a0001c0001t0005g0062 a0001c0001t0005g0109 |
2 | HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.586-1907C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48926856 | |||||||
| chr15:48926865 | A | T | 1 | a0001c0001t0001g0158 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.586-1916T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48926865 | |||||||
| chr15:48926919 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.586-1970C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48926919 | |||||||
| chr15:48927239 | C | T | 69 | a0001c0001t0001g0041 a0001c0001t0001g0069 a0001c0001t0001g0071 others(66): Show |
70 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.586-2290G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48927239 | |||||||
| chr15:48927243 | C | T | 15 | a0001c0001t0001g0030 a0001c0001t0001g0212 a0001c0001t0001g0255 others(12): Show |
15 | HG01243.hp1 HG01255.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.586-2294G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48927243 | |||||||
| chr15:48927270 | C | A | 9 | a0001c0001t0001g0056 a0001c0001t0002g0033 a0001c0001t0002g0055 others(6): Show |
9 | HG00609.hp2 HG01099.hp2 HG03491.hp1 others(6): Show |
intron_variant | MODIFIER | c.586-2321G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48927270 | |||||||
| chr15:48927278 | T | C | 2 | a0001c0001t0019g0021 a0001c0001t0026g0258 |
2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.586-2329A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48927278 | |||||||
| chr15:48927434 | T | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0026 others(167): Show |
172 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.586-2485A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48927434 | |||||||
| chr15:48927475 | A | T | 1 | a0001c0001t0003g0151 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.586-2526T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48927475 | |||||||
| chr15:48927578 | T | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0026 others(167): Show |
172 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.586-2629A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48927578 | |||||||
| chr15:48927755 | A | T | 170 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0026 others(167): Show |
172 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.586-2806T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48927755 | |||||||
| chr15:48927903 | T | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0026 others(167): Show |
172 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.586-2954A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48927903 | |||||||
| chr15:48927955 | C | A | 109 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0045 others(106): Show |
110 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.586-3006G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48927955 | |||||||
| chr15:48928074 | C | T | 109 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0045 others(106): Show |
110 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.586-3125G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48928074 | |||||||
| chr15:48928087 | G | A | 72 | a0001c0001t0001g0041 a0001c0001t0001g0069 a0001c0001t0001g0071 others(69): Show |
73 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.586-3138C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48928087 | |||||||
| chr15:48928168 | G | GAAC | 251 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0026 others(248): Show |
253 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.586-3222_586-3220d others(5): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48928168 | |||||||
| chr15:48928174 | C | T | 1 | a0001c0001t0001g0338 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.586-3225G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48928174 | |||||||
| chr15:48928260 | A | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0026 others(247): Show |
252 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.586-3311T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48928260 | |||||||
| chr15:48928271 | G | A | 1 | a0001c0001t0017g0011 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.586-3322C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48928271 | |||||||
| chr15:48928420 | A | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0026 others(242): Show |
247 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.586-3471T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48928420 | |||||||
| chr15:48928468 | G | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0026 others(167): Show |
172 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.586-3519C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48928468 | |||||||
| chr15:48928518 | T | C | 3 | a0001c0001t0001g0137 a0001c0001t0005g0062 a0001c0001t0005g0109 |
3 | HG02622.hp1 HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.586-3569A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48928518 | |||||||
| chr15:48928618 | G | A | 76 | a0001c0001t0001g0030 a0001c0001t0001g0070 a0001c0001t0001g0073 others(73): Show |
76 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.586-3669C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48928618 | |||||||
| chr15:48928638 | C | T | 1 | a0001c0001t0001g0296 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.586-3689G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48928638 | |||||||
| chr15:48928642 | G | T | 360 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0023 others(357): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.586-3693C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48928642 | |||||||
| chr15:48928665 | G | T | 1 | a0001c0001t0005g0278 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.586-3716C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48928665 | |||||||
| chr15:48928914 | T | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0026 others(247): Show |
252 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.586-3965A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48928914 | |||||||
| chr15:48929056 | T | C | 354 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0023 others(351): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.586-4107A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48929056 | |||||||
| chr15:48929088 | G | A | 4 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0369 others(1): Show |
4 | HG00140.hp2 HG00741.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.586-4139C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48929088 | |||||||
| chr15:48929115 | G | A | 1 | a0001c0001t0002g0335 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.586-4166C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48929115 | |||||||
| chr15:48929170 | G | A | 1 | a0001c0001t0002g0202 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.586-4221C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48929170 | |||||||
| chr15:48929394 | G | T | 67 | a0001c0001t0001g0044 a0001c0001t0001g0084 a0001c0001t0001g0093 others(64): Show |
67 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.586-4445C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48929394 | |||||||
| chr15:48929563 | A | G | 1 | a0001c0001t0001g0181 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.586-4614T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48929563 | |||||||
| chr15:48929628 | A | T | 73 | a0001c0001t0001g0044 a0001c0001t0001g0084 a0001c0001t0001g0093 others(70): Show |
73 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.586-4679T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48929628 | |||||||
| chr15:48929653 | C | T | 4 | a0001c0001t0001g0169 a0001c0001t0001g0300 a0001c0001t0001g0338 others(1): Show |
4 | HG01243.hp2 HG01928.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.586-4704G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48929653 | |||||||
| chr15:48929684 | G | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0026 others(84): Show |
88 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.586-4735C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48929684 | |||||||
| chr15:48929732 | T | C | 1 | a0001c0001t0001g0259 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.586-4783A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48929732 | |||||||
| chr15:48929808 | C | T | 1 | a0001c0001t0002g0115 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.586-4859G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48929808 | |||||||
| chr15:48930030 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.586-5081T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48930030 | |||||||
| chr15:48930049 | A | C | 141 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0070 others(138): Show |
142 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.586-5100T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48930049 | |||||||
| chr15:48930069 | T | A | 1 | a0001c0001t0001g0154 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.586-5120A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48930069 | |||||||
| chr15:48930246 | A | T | 8 | a0001c0001t0001g0023 a0001c0001t0002g0085 a0001c0001t0005g0036 others(5): Show |
8 | HG02486.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.586-5297T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48930246 | |||||||
| chr15:48930379 | A | G | 141 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0070 others(138): Show |
142 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.586-5430T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48930379 | |||||||
| chr15:48930379 | A | T | 1 | a0001c0002t0004g0130 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.586-5430T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48930379 | |||||||
| chr15:48930554 | T | C | 75 | a0001c0001t0001g0044 a0001c0001t0001g0084 a0001c0001t0001g0093 others(72): Show |
75 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.586-5605A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48930554 | |||||||
| chr15:48930611 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.586-5662A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48930611 | |||||||
| chr15:48930757 | A | C | 2 | a0001c0001t0002g0211 a0001c0001t0021g0028 |
2 | HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.586-5808T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48930757 | |||||||
| chr15:48930806 | T | C | 3 | a0001c0001t0001g0373 a0001c0001t0003g0151 a0001c0001t0023g0150 |
3 | HG00438.hp1 HG01981.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.586-5857A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48930806 | |||||||
| chr15:48930821 | A | T | 140 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0070 others(137): Show |
141 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.586-5872T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48930821 | |||||||
| chr15:48930830 | G | T | 1 | a0001c0002t0007g0356 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.586-5881C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48930830 | |||||||
| chr15:48930993 | C | T | 7 | a0001c0001t0001g0188 a0001c0001t0001g0198 a0001c0001t0001g0289 others(4): Show |
7 | HG00140.hp2 HG00741.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.586-6044G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48930993 | |||||||
| chr15:48931039 | G | A | 1 | a0001c0001t0002g0077 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.586-6090C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48931039 | |||||||
| chr15:48931185 | C | T | 1 | a0001c0001t0002g0055 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.586-6236G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48931185 | |||||||
| chr15:48931237 | A | T | 16 | a0001c0001t0001g0030 a0001c0001t0001g0212 a0001c0001t0001g0255 others(13): Show |
16 | HG01243.hp1 HG01255.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.586-6288T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48931237 | |||||||
| chr15:48931293 | G | A | 19 | a0001c0001t0001g0108 a0001c0001t0001g0223 a0001c0001t0001g0224 others(16): Show |
19 | HG00423.hp2 HG00673.hp2 HG02004.hp1 others(16): Show |
intron_variant | MODIFIER | c.586-6344C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48931293 | |||||||
| chr15:48931535 | A | T | 7 | a0001c0001t0001g0188 a0001c0001t0001g0198 a0001c0001t0001g0289 others(4): Show |
7 | HG00140.hp2 HG00741.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.586-6586T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48931535 | |||||||
| chr15:48931549 | C | T | 9 | a0001c0001t0001g0108 a0001c0001t0001g0223 a0001c0001t0001g0292 others(6): Show |
9 | HG02004.hp1 HG02004.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.586-6600G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48931549 | |||||||
| chr15:48931700 | T | A | 72 | a0001c0001t0001g0044 a0001c0001t0001g0084 a0001c0001t0001g0093 others(69): Show |
72 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.586-6751A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48931700 | |||||||
| chr15:48931775 | C | T | 1 | a0001c0001t0002g0065 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.586-6826G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48931775 | |||||||
| chr15:48931916 | G | T | 3 | a0001c0001t0001g0068 a0001c0001t0001g0147 a0001c0001t0001g0172 |
3 | HG00099.hp2 HG01192.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.586-6967C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48931916 | |||||||
| chr15:48931985 | A | G | 147 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0070 others(144): Show |
148 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.586-7036T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48931985 | |||||||
| chr15:48932175 | G | A | 91 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0001g0082 others(88): Show |
91 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.586-7226C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48932175 | |||||||
| chr15:48932286 | G | T | 16 | a0001c0001t0001g0030 a0001c0001t0001g0212 a0001c0001t0001g0255 others(13): Show |
16 | HG01243.hp1 HG01255.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.586-7337C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48932286 | |||||||
| chr15:48932455 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.586-7506C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48932455 | |||||||
| chr15:48932692 | C | T | 344 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(341): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.586-7743G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48932692 | |||||||
| chr15:48932926 | C | A | 8 | a0001c0001t0001g0188 a0001c0001t0001g0198 a0001c0001t0001g0289 others(5): Show |
8 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.586-7977G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48932926 | |||||||
| chr15:48933031 | A | G | 24 | a0001c0001t0001g0108 a0001c0001t0001g0223 a0001c0001t0001g0224 others(21): Show |
24 | HG00423.hp2 HG00673.hp2 HG02004.hp1 others(21): Show |
intron_variant | MODIFIER | c.586-8082T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48933031 | |||||||
| chr15:48933186 | G | A | 1 | a0001c0001t0001g0323 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.586-8237C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48933186 | |||||||
| chr15:48933194 | C | T | 272 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0041 others(269): Show |
275 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.586-8245G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48933194 | |||||||
| chr15:48933487 | T | C | 2 | a0001c0001t0001g0126 a0001c0001t0001g0181 |
2 | HG02723.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.586-8538A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48933487 | |||||||
| chr15:48933731 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.586-8782C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48933731 | |||||||
| chr15:48934233 | C | G | 1 | a0001c0001t0001g0230 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.586-9284G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48934233 | |||||||
| chr15:48934506 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.586-9557T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48934506 | |||||||
| chr15:48934581 | A | G | 7 | a0001c0001t0001g0059 a0001c0001t0001g0101 a0001c0001t0002g0197 others(4): Show |
7 | HG01255.hp2 HG02622.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.586-9632T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48934581 | |||||||
| chr15:48934638 | T | G | 6 | a0001c0001t0001g0082 a0001c0001t0002g0117 a0001c0001t0008g0013 others(3): Show |
6 | HG02630.hp2 HG03098.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.586-9689A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48934638 | |||||||
| chr15:48934666 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.586-9717A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48934666 | |||||||
| chr15:48934730 | G | T | 1 | a0001c0001t0001g0191 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.586-9781C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48934730 | |||||||
| chr15:48934854 | T | G | 4 | a0001c0001t0001g0087 a0001c0001t0001g0183 a0001c0001t0002g0085 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.586-9905A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48934854 | |||||||
| chr15:48934994 | A | G | 1 | a0001c0001t0003g0343 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.586-10045T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48934994 | |||||||
| chr15:48935035 | C | A | 1 | a0001c0001t0001g0029 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.586-10086G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48935035 | |||||||
| chr15:48935244 | T | G | 1 | a0001c0001t0010g0066 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.586-10295A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48935244 | |||||||
| chr15:48935282 | G | T | 1 | a0001c0002t0004g0366 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.586-10333C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48935282 | |||||||
| chr15:48935298 | C | A | 6 | a0001c0001t0001g0082 a0001c0001t0002g0117 a0001c0001t0008g0013 others(3): Show |
6 | HG02630.hp2 HG03098.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.586-10349G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48935298 | |||||||
| chr15:48935381 | T | A | 2 | a0001c0001t0001g0154 a0001c0004t0005g0376 |
2 | HG02572.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.586-10432A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48935381 | |||||||
| chr15:48935486 | A | G | 2 | a0001c0001t0001g0154 a0001c0004t0005g0376 |
2 | HG02572.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.586-10537T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48935486 | |||||||
| chr15:48935558 | G | T | 8 | a0001c0001t0001g0023 a0001c0001t0001g0126 a0001c0001t0005g0036 others(5): Show |
8 | HG02486.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.586-10609C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48935558 | |||||||
| chr15:48935624 | C | T | 332 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0029 others(329): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.586-10675G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48935624 | |||||||
| chr15:48935869 | A | T | 1 | a0001c0001t0010g0112 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.586-10920T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48935869 | |||||||
| chr15:48936026 | A | C | 1 | a0001c0001t0002g0336 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.586-11077T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48936026 | |||||||
| chr15:48936198 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.586-11249G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48936198 | |||||||
| chr15:48936289 | G | C | 1 | a0001c0001t0010g0066 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.586-11340C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48936289 | |||||||
| chr15:48936322 | T | C | 2 | a0001c0001t0001g0154 a0001c0004t0005g0376 |
2 | HG02572.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.586-11373A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48936322 | |||||||
| chr15:48936401 | G | T | 1 | a0001c0001t0001g0337 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.586-11452C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48936401 | |||||||
| chr15:48936418 | A | G | 123 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0069 others(120): Show |
124 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.586-11469T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48936418 | |||||||
| chr15:48936534 | C | G | 109 | a0001c0001t0001g0029 a0001c0001t0001g0044 a0001c0001t0001g0056 others(106): Show |
109 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.586-11585G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48936534 | |||||||
| chr15:48936570 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0140 |
2 | HG02145.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.586-11621G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48936570 | |||||||
| chr15:48936574 | T | G | 2 | a0001c0001t0002g0354 a0001c0001t0003g0355 |
2 | HG02015.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.586-11625A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48936574 | |||||||
| chr15:48936587 | A | G | 7 | a0001c0001t0001g0188 a0001c0001t0001g0198 a0001c0001t0001g0289 others(4): Show |
7 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.586-11638T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48936587 | |||||||
| chr15:48936915 | A | G | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.586-11966T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48936915 | |||||||
| chr15:48937255 | G | A | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | NA19056.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.586-12306C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48937255 | |||||||
| chr15:48937275 | T | A | 1 | a0001c0001t0002g0245 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.586-12326A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48937275 | |||||||
| chr15:48937494 | C | T | 1 | a0002c0003t0003g0214 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.586-12545G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48937494 | |||||||
| chr15:48937583 | C | CATAG | 105 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0059 others(102): Show |
105 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.586-12638_586-1263 others(8): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48937583 | |||||||
| chr15:48937583 | C | CATAGATA others(1): Show |
18 | a0001c0001t0001g0068 a0001c0001t0001g0100 a0001c0001t0001g0147 others(15): Show |
18 | HG00673.hp2 HG00741.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.586-12642_586-1263 others(12): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48937583 | |||||||
| chr15:48937583 | C | CATAGATA others(5): Show |
2 | a0001c0001t0001g0302 a0001c0001t0002g0053 |
2 | HG00735.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.586-12646_586-1263 others(16): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48937583 | |||||||
| chr15:48937583 | CATAG | C | 79 | a0001c0001t0001g0026 a0001c0001t0001g0035 a0001c0001t0001g0042 others(76): Show |
81 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.586-12638_586-1263 others(8): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48937583 | |||||||
| chr15:48937583 | CATAGATA others(1): Show |
C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0189 others(8): Show |
12 | HG01071.hp1 HG01175.hp1 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.586-12642_586-1263 others(12): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48937583 | |||||||
| chr15:48937583 | CATAGATA others(9): Show |
C | 1 | a0001c0001t0016g0007 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.586-12650_586-1263 others(20): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48937583 | |||||||
| chr15:48937629 | G | T | 1 | a0001c0001t0001g0056 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.586-12680C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48937629 | |||||||
| chr15:48937631 | T | G | 1 | a0001c0001t0001g0056 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.586-12682A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48937631 | |||||||
| chr15:48937656 | T | C | 2 | a0001c0001t0001g0154 a0001c0004t0005g0376 |
2 | HG02572.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.586-12707A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48937656 | |||||||
| chr15:48937908 | C | A | 2 | a0001c0001t0001g0154 a0001c0004t0005g0376 |
2 | HG02572.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.586-12959G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48937908 | |||||||
| chr15:48937913 | G | A | 16 | a0001c0001t0001g0076 a0001c0001t0001g0116 a0001c0001t0001g0291 others(13): Show |
16 | HG00408.hp2 HG01255.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.586-12964C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48937913 | |||||||
| chr15:48937915 | C | G | 332 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0029 others(329): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.586-12966G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48937915 | |||||||
| chr15:48938015 | A | G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0128 |
3 | HG01167.hp1 HG01169.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.586-13066T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48938015 | |||||||
| chr15:48938035 | G | A | 1 | a0001c0001t0002g0335 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.586-13086C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48938035 | |||||||
| chr15:48938257 | T | G | 1 | a0001c0001t0001g0275 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.586-13308A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48938257 | |||||||
| chr15:48938260 | C | T | 5 | a0001c0001t0002g0117 a0001c0001t0008g0013 a0001c0001t0008g0015 others(2): Show |
5 | HG02630.hp2 HG03098.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.586-13311G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48938260 | |||||||
| chr15:48938288 | A | G | 1 | a0001c0001t0002g0085 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.586-13339T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48938288 | |||||||
| chr15:48938309 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.586-13360G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48938309 | |||||||
| chr15:48938366 | T | A | 1 | a0001c0001t0002g0190 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.586-13417A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48938366 | |||||||
| chr15:48938468 | G | A | 130 | a0001c0001t0001g0023 a0001c0001t0001g0042 a0001c0001t0001g0045 others(127): Show |
131 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.586-13519C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48938468 | |||||||
| chr15:48938701 | G | GC | 130 | a0001c0001t0001g0023 a0001c0001t0001g0042 a0001c0001t0001g0045 others(127): Show |
131 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.586-13753dupG | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48938701 | |||||||
| chr15:48938752 | G | C | 121 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0069 others(118): Show |
122 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.586-13803C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48938752 | |||||||
| chr15:48938835 | G | C | 2 | a0001c0001t0002g0354 a0001c0001t0003g0355 |
2 | HG02015.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.586-13886C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48938835 | |||||||
| chr15:48938842 | A | G | 1 | a0001c0001t0001g0291 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.586-13893T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48938842 | |||||||
| chr15:48938853 | C | G | 121 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0069 others(118): Show |
122 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.586-13904G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48938853 | |||||||
| chr15:48938872 | T | C | 1 | a0001c0001t0001g0280 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.586-13923A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48938872 | |||||||
| chr15:48938914 | G | A | 76 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0081 others(73): Show |
76 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.586-13965C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48938914 | |||||||
| chr15:48938933 | G | A | 9 | a0001c0001t0001g0023 a0001c0001t0001g0126 a0001c0001t0001g0181 others(6): Show |
9 | HG02486.hp2 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.586-13984C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48938933 | |||||||
| chr15:48939065 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.586-14116C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48939065 | |||||||
| chr15:48939134 | T | C | 1 | a0001c0001t0002g0206 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.586-14185A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48939134 | |||||||
| chr15:48939212 | C | T | 1 | a0001c0001t0002g0051 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.586-14263G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48939212 | |||||||
| chr15:48939317 | G | A | 271 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0023 others(268): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.586-14368C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48939317 | |||||||
| chr15:48939383 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.586-14434G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48939383 | |||||||
| chr15:48939468 | C | A | 320 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0035 others(317): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.586-14519G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48939468 | |||||||
| chr15:48939493 | T | A | 11 | a0001c0001t0001g0023 a0001c0001t0001g0126 a0001c0001t0001g0154 others(8): Show |
11 | HG02486.hp2 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.586-14544A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48939493 | |||||||
| chr15:48939645 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0009g0018 |
2 | HG02818.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.586-14696A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48939645 | |||||||
| chr15:48939682 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.586-14733G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48939682 | |||||||
| chr15:48939861 | C | T | 11 | a0001c0001t0001g0023 a0001c0001t0001g0126 a0001c0001t0001g0154 others(8): Show |
11 | HG02486.hp2 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.586-14912G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48939861 | |||||||
| chr15:48939993 | T | C | 11 | a0001c0001t0001g0023 a0001c0001t0001g0126 a0001c0001t0001g0154 others(8): Show |
11 | HG02486.hp2 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.586-15044A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48939993 | |||||||
| chr15:48940067 | G | A | 15 | a0001c0001t0001g0076 a0001c0001t0001g0116 a0001c0001t0001g0291 others(12): Show |
15 | HG00408.hp2 HG01255.hp1 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.586-15118C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48940067 | |||||||
| chr15:48940120 | A | G | 11 | a0001c0001t0001g0023 a0001c0001t0001g0126 a0001c0001t0001g0154 others(8): Show |
11 | HG02486.hp2 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.586-15171T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48940120 | |||||||
| chr15:48940197 | C | G | 1 | a0001c0001t0001g0097 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.586-15248G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48940197 | |||||||
| chr15:48940351 | A | C | 4 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0189 others(1): Show |
5 | HG01071.hp1 HG01175.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.586-15402T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48940351 | |||||||
| chr15:48940400 | C | G | 11 | a0001c0001t0001g0023 a0001c0001t0001g0126 a0001c0001t0001g0154 others(8): Show |
11 | HG02486.hp2 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.586-15451G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48940400 | |||||||
| chr15:48940422 | G | T | 11 | a0001c0001t0001g0023 a0001c0001t0001g0126 a0001c0001t0001g0154 others(8): Show |
11 | HG02486.hp2 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.586-15473C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48940422 | |||||||
| chr15:48940433 | G | A | 11 | a0001c0001t0001g0023 a0001c0001t0001g0126 a0001c0001t0001g0154 others(8): Show |
11 | HG02486.hp2 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.586-15484C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48940433 | |||||||
| chr15:48940461 | C | T | 5 | a0001c0001t0002g0117 a0001c0001t0008g0013 a0001c0001t0008g0015 others(2): Show |
5 | HG02630.hp2 HG03098.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.586-15512G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48940461 | |||||||
| chr15:48940528 | A | ACT | 11 | a0001c0001t0001g0023 a0001c0001t0001g0126 a0001c0001t0001g0154 others(8): Show |
11 | HG02486.hp2 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.586-15581_586-1558 others(6): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48940528 | |||||||
| chr15:48940611 | T | C | 1 | a0007c0008t0004g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.586-15662A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48940611 | |||||||
| chr15:48940618 | C | A | 1 | a0001c0001t0002g0307 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.586-15669G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48940618 | |||||||
| chr15:48940702 | G | A | 1 | a0001c0001t0002g0051 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.586-15753C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48940702 | |||||||
| chr15:48940735 | A | G | 15 | a0001c0001t0001g0119 a0001c0001t0001g0191 a0001c0001t0001g0212 others(12): Show |
15 | HG01243.hp1 HG01884.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.586-15786T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48940735 | |||||||
| chr15:48940905 | G | A | 36 | a0001c0001t0001g0044 a0001c0001t0001g0084 a0001c0001t0001g0093 others(33): Show |
36 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.586-15956C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48940905 | |||||||
| chr15:48940970 | A | T | 1 | a0001c0001t0001g0280 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.586-16021T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48940970 | |||||||
| chr15:48940989 | A | G | 9 | a0001c0001t0001g0023 a0001c0001t0001g0126 a0001c0001t0001g0181 others(6): Show |
9 | HG02486.hp2 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.586-16040T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48940989 | |||||||
| chr15:48940997 | A | G | 5 | a0001c0001t0001g0035 a0001c0001t0002g0197 a0001c0001t0003g0086 others(2): Show |
5 | HG01255.hp2 HG02622.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.586-16048T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48940997 | |||||||
| chr15:48941038 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.586-16089G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48941038 | |||||||
| chr15:48941048 | T | C | 2 | a0001c0001t0001g0154 a0001c0004t0005g0376 |
2 | HG02572.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.586-16099A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48941048 | |||||||
| chr15:48941053 | G | A | 6 | a0001c0001t0001g0116 a0001c0001t0001g0291 a0002c0003t0003g0171 others(3): Show |
6 | NA18612.hp2 NA18942.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.586-16104C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48941053 | |||||||
| chr15:48941181 | C | T | 62 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0081 others(59): Show |
62 | HG00408.hp1 HG00438.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.586-16232G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48941181 | |||||||
| chr15:48941557 | A | G | 11 | a0001c0001t0001g0023 a0001c0001t0001g0126 a0001c0001t0001g0154 others(8): Show |
11 | HG02486.hp2 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.586-16608T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48941557 | |||||||
| chr15:48941581 | A | G | 5 | a0001c0001t0001g0035 a0001c0001t0002g0197 a0001c0001t0003g0086 others(2): Show |
5 | HG01255.hp2 HG02622.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.586-16632T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48941581 | |||||||
| chr15:48941602 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.586-16653C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48941602 | |||||||
| chr15:48941666 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.586-16717G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48941666 | |||||||
| chr15:48941720 | T | C | 2 | a0001c0001t0001g0154 a0001c0004t0005g0376 |
2 | HG02572.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.586-16771A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48941720 | |||||||
| chr15:48941979 | T | C | 1 | a0001c0001t0010g0193 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.586-17030A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48941979 | |||||||
| chr15:48942148 | G | T | 17 | a0001c0001t0001g0108 a0001c0001t0001g0223 a0001c0001t0001g0224 others(14): Show |
17 | HG00423.hp2 HG00673.hp2 HG02004.hp2 others(14): Show |
intron_variant | MODIFIER | c.586-17199C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48942148 | |||||||
| chr15:48942179 | T | TA | 89 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0045 others(86): Show |
90 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.586-17231dupT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48942179 | |||||||
| chr15:48942180 | A | T | 2 | a0001c0001t0001g0154 a0001c0004t0005g0376 |
2 | HG02572.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.586-17231T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48942180 | |||||||
| chr15:48942196 | T | C | 22 | a0001c0001t0001g0108 a0001c0001t0001g0223 a0001c0001t0001g0224 others(19): Show |
22 | HG00423.hp2 HG00673.hp2 HG02004.hp2 others(19): Show |
intron_variant | MODIFIER | c.586-17247A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48942196 | |||||||
| chr15:48942319 | G | T | 4 | a0001c0001t0002g0124 a0001c0001t0002g0333 a0001c0001t0002g0334 others(1): Show |
4 | HG02027.hp2 NA18971.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.586-17370C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48942319 | |||||||
| chr15:48942381 | A | T | 5 | a0001c0001t0002g0117 a0001c0001t0008g0013 a0001c0001t0008g0015 others(2): Show |
5 | HG02630.hp2 HG03098.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.586-17432T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48942381 | |||||||
| chr15:48942628 | C | G | 11 | a0001c0001t0001g0023 a0001c0001t0001g0126 a0001c0001t0001g0154 others(8): Show |
11 | HG02486.hp2 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.586-17679G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48942628 | |||||||
| chr15:48942930 | C | A | 1 | a0001c0001t0001g0243 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.586-17981G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48942930 | |||||||
| chr15:48942983 | T | C | 1 | a0002c0003t0003g0294 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.586-18034A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48942983 | |||||||
| chr15:48943054 | G | C | 64 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0081 others(61): Show |
64 | HG00408.hp1 HG00438.hp1 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.586-18105C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48943054 | |||||||
| chr15:48943168 | C | T | 1 | a0001c0001t0001g0348 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.586-18219G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48943168 | |||||||
| chr15:48943173 | G | C | 5 | a0001c0001t0001g0035 a0001c0001t0002g0197 a0001c0001t0003g0086 others(2): Show |
5 | HG01255.hp2 HG02622.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.586-18224C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48943173 | |||||||
| chr15:48943337 | A | C | 53 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0071 others(50): Show |
55 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.586-18388T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48943337 | |||||||
| chr15:48943344 | T | C | 1 | a0001c0002t0004g0366 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.586-18395A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48943344 | |||||||
| chr15:48943362 | T | C | 1 | a0001c0001t0005g0349 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.586-18413A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48943362 | |||||||
| chr15:48943421 | A | G | 1 | a0001c0001t0001g0280 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.586-18472T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48943421 | |||||||
| chr15:48943452 | A | G | 15 | a0001c0001t0001g0119 a0001c0001t0001g0191 a0001c0001t0001g0212 others(12): Show |
15 | HG01243.hp1 HG01884.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.586-18503T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48943452 | |||||||
| chr15:48943526 | T | C | 22 | a0001c0001t0001g0076 a0001c0001t0001g0116 a0001c0001t0001g0291 others(19): Show |
22 | HG00408.hp2 HG01255.hp1 HG02074.hp2 others(19): Show |
intron_variant | MODIFIER | c.586-18577A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48943526 | |||||||
| chr15:48943560 | A | G | 53 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0071 others(50): Show |
55 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.586-18611T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48943560 | |||||||
| chr15:48943561 | C | T | 18 | a0001c0001t0001g0071 a0001c0001t0001g0089 a0001c0001t0001g0160 others(15): Show |
18 | HG00609.hp1 HG02273.hp1 HG03710.hp2 others(15): Show |
intron_variant | MODIFIER | c.586-18612G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48943561 | |||||||
| chr15:48943670 | C | A | 37 | a0001c0001t0001g0044 a0001c0001t0001g0084 a0001c0001t0001g0093 others(34): Show |
37 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.586-18721G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48943670 | |||||||
| chr15:48943675 | A | T | 55 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0071 others(52): Show |
57 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.586-18726T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48943675 | |||||||
| chr15:48943943 | C | T | 1 | a0001c0001t0003g0153 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.585+18488G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48943943 | |||||||
| chr15:48944117 | A | G | 2 | a0001c0001t0002g0034 a0001c0001t0005g0138 |
2 | NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.585+18314T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48944117 | |||||||
| chr15:48944284 | C | G | 1 | a0001c0004t0005g0376 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.585+18147G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48944284 | |||||||
| chr15:48944369 | T | A | 1 | a0001c0001t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.585+18062A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48944369 | |||||||
| chr15:48944413 | G | C | 31 | a0001c0001t0001g0023 a0001c0001t0001g0082 a0001c0001t0001g0108 others(28): Show |
31 | HG00673.hp2 HG02004.hp2 HG02015.hp2 others(28): Show |
intron_variant | MODIFIER | c.585+18018C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48944413 | |||||||
| chr15:48944416 | T | A | 2 | a0001c0001t0001g0269 a0001c0001t0001g0371 |
2 | HG00558.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.585+18015A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48944416 | |||||||
| chr15:48944754 | C | A | 3 | a0001c0001t0002g0092 a0001c0001t0002g0229 a0001c0001t0002g0295 |
3 | NA18747.hp1 NA18955.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.585+17677G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48944754 | |||||||
| chr15:48944951 | A | G | 1 | a0001c0001t0019g0021 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.585+17480T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48944951 | |||||||
| chr15:48945000 | C | T | 1 | a0001c0001t0002g0262 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.585+17431G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48945000 | |||||||
| chr15:48945084 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.585+17347A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48945084 | |||||||
| chr15:48945146 | G | C | 1 | a0001c0001t0001g0367 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.585+17285C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48945146 | |||||||
| chr15:48945166 | C | G | 1 | a0001c0001t0001g0159 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.585+17265G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48945166 | |||||||
| chr15:48945279 | T | C | 24 | a0001c0001t0001g0056 a0001c0001t0001g0098 a0001c0001t0001g0174 others(21): Show |
24 | HG00609.hp2 HG00642.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.585+17152A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48945279 | |||||||
| chr15:48945321 | G | GA | 9 | a0001c0001t0001g0023 a0001c0001t0001g0126 a0001c0001t0001g0181 others(6): Show |
9 | HG02486.hp2 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.585+17109dupT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48945321 | |||||||
| chr15:48945351 | TC | T | 9 | a0001c0001t0001g0188 a0001c0001t0001g0192 a0001c0001t0001g0198 others(6): Show |
9 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.585+17079delG | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48945351 | |||||||
| chr15:48945361 | C | T | 52 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0071 others(49): Show |
54 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(51): Show |
intron_variant | MODIFIER | c.585+17070G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48945361 | |||||||
| chr15:48945438 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.585+16993A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48945438 | |||||||
| chr15:48945512 | G | A | 134 | a0001c0001t0001g0026 a0001c0001t0001g0041 a0001c0001t0001g0056 others(131): Show |
134 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.585+16919C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48945512 | |||||||
| chr15:48945686 | T | C | 1 | a0005c0009t0001g0103 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.585+16745A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48945686 | |||||||
| chr15:48945715 | G | A | 9 | a0001c0001t0001g0035 a0001c0001t0001g0087 a0001c0001t0001g0183 others(6): Show |
9 | HG01255.hp2 HG02109.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.585+16716C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48945715 | |||||||
| chr15:48945729 | G | GGCT | 352 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(349): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.585+16699_585+1670 others(7): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48945729 | |||||||
| chr15:48945883 | G | C | 1 | a0002c0003t0001g0095 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.585+16548C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48945883 | |||||||
| chr15:48945887 | T | C | 1 | a0001c0001t0010g0066 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.585+16544A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48945887 | |||||||
| chr15:48946100 | A | T | 1 | a0001c0001t0001g0201 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.585+16331T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48946100 | |||||||
| chr15:48946184 | T | C | 1 | a0001c0001t0002g0064 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.585+16247A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48946184 | |||||||
| chr15:48946233 | C | T | 181 | a0001c0001t0001g0029 a0001c0001t0001g0041 a0001c0001t0001g0042 others(178): Show |
182 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.585+16198G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48946233 | |||||||
| chr15:48946324 | T | C | 1 | a0002c0003t0003g0304 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.585+16107A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48946324 | |||||||
| chr15:48946587 | G | A | 344 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(341): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.585+15844C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48946587 | |||||||
| chr15:48946594 | A | T | 1 | a0001c0001t0025g0347 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.585+15837T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48946594 | |||||||
| chr15:48946641 | C | T | 45 | a0001c0001t0001g0035 a0001c0001t0001g0044 a0001c0001t0001g0084 others(42): Show |
45 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.585+15790G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48946641 | |||||||
| chr15:48946805 | A | T | 1 | a0001c0001t0001g0166 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.585+15626T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48946805 | |||||||
| chr15:48946828 | T | A | 1 | a0001c0001t0001g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.585+15603A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48946828 | |||||||
| chr15:48946932 | C | CA | 9 | a0001c0001t0001g0035 a0001c0001t0001g0087 a0001c0001t0001g0183 others(6): Show |
9 | HG01255.hp2 HG02109.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.585+15498dupT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48946932 | |||||||
| chr15:48947106 | T | C | 54 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0071 others(51): Show |
56 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(53): Show |
intron_variant | MODIFIER | c.585+15325A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48947106 | |||||||
| chr15:48947215 | T | C | 54 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0071 others(51): Show |
56 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(53): Show |
intron_variant | MODIFIER | c.585+15216A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48947215 | |||||||
| chr15:48947242 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.585+15189G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48947242 | |||||||
| chr15:48947344 | G | A | 1 | a0005c0009t0001g0103 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.585+15087C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48947344 | |||||||
| chr15:48947451 | C | T | 1 | a0001c0006t0001g0319 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.585+14980G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48947451 | |||||||
| chr15:48947597 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.585+14834G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48947597 | |||||||
| chr15:48947627 | A | C | 54 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0071 others(51): Show |
56 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(53): Show |
intron_variant | MODIFIER | c.585+14804T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48947627 | |||||||
| chr15:48947961 | T | A | 15 | a0001c0001t0001g0026 a0001c0001t0001g0119 a0001c0001t0001g0212 others(12): Show |
15 | HG01243.hp1 HG01884.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.585+14470A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48947961 | |||||||
| chr15:48948079 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.585+14352T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48948079 | |||||||
| chr15:48948156 | C | G | 1 | a0001c0001t0002g0247 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.585+14275G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48948156 | |||||||
| chr15:48948174 | C | T | 1 | a0001c0001t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.585+14257G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48948174 | |||||||
| chr15:48948571 | C | T | 1 | a0001c0001t0010g0066 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.585+13860G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48948571 | |||||||
| chr15:48948615 | A | T | 9 | a0001c0001t0001g0035 a0001c0001t0001g0087 a0001c0001t0001g0183 others(6): Show |
9 | HG01255.hp2 HG02109.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.585+13816T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48948615 | |||||||
| chr15:48948653 | C | T | 53 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0071 others(50): Show |
55 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(52): Show |
intron_variant | MODIFIER | c.585+13778G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48948653 | |||||||
| chr15:48949040 | A | G | 1 | a0005c0009t0001g0103 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.585+13391T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48949040 | |||||||
| chr15:48949046 | C | T | 20 | a0001c0001t0001g0026 a0001c0001t0001g0119 a0001c0001t0001g0212 others(17): Show |
20 | HG01243.hp1 HG01884.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.585+13385G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48949046 | |||||||
| chr15:48949320 | T | A | 2 | a0001c0001t0003g0246 a0001c0001t0003g0343 |
2 | HG00735.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.585+13111A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48949320 | |||||||
| chr15:48949370 | C | CA | 16 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0001g0126 others(13): Show |
16 | HG01433.hp2 HG01515.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.585+13060dupT | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48949370 | |||||||
| chr15:48949427 | A | G | 1 | a0007c0008t0004g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.585+13004T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48949427 | |||||||
| chr15:48949461 | C | G | 18 | a0001c0001t0001g0108 a0001c0001t0001g0223 a0001c0001t0001g0224 others(15): Show |
18 | HG00423.hp2 HG00673.hp2 HG02004.hp2 others(15): Show |
intron_variant | MODIFIER | c.585+12970G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48949461 | |||||||
| chr15:48949614 | T | G | 1 | a0001c0001t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.585+12817A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48949614 | |||||||
| chr15:48949753 | C | T | 308 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0029 others(305): Show |
309 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.585+12678G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48949753 | |||||||
| chr15:48949820 | A | AAT | 2 | a0001c0001t0002g0002 a0001c0001t0002g0143 |
3 | HG00738.hp2 HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.585+12609_585+1261 others(6): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48949820 | |||||||
| chr15:48949921 | A | G | 1 | a0001c0001t0010g0066 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.585+12510T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48949921 | |||||||
| chr15:48949937 | G | T | 1 | a0001c0001t0001g0139 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.585+12494C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48949937 | |||||||
| chr15:48949951 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.585+12480A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48949951 | |||||||
| chr15:48949988 | A | G | 25 | a0001c0001t0001g0030 a0001c0001t0001g0070 a0001c0001t0001g0097 others(22): Show |
25 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.585+12443T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48949988 | |||||||
| chr15:48950087 | AT | A | 53 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0071 others(50): Show |
55 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(52): Show |
intron_variant | MODIFIER | c.585+12343delA | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48950087 | |||||||
| chr15:48950099 | T | C | 1 | a0001c0001t0006g0032 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.585+12332A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48950099 | |||||||
| chr15:48950285 | A | G | 54 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0071 others(51): Show |
56 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(53): Show |
intron_variant | MODIFIER | c.585+12146T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48950285 | |||||||
| chr15:48950292 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.585+12139G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48950292 | |||||||
| chr15:48950312 | C | G | 1 | a0001c0001t0002g0065 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.585+12119G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48950312 | |||||||
| chr15:48950322 | G | A | 7 | a0001c0001t0001g0198 a0001c0001t0001g0289 a0001c0001t0001g0290 others(4): Show |
7 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.585+12109C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48950322 | |||||||
| chr15:48950427 | A | T | 65 | a0001c0001t0001g0041 a0001c0001t0001g0069 a0001c0001t0001g0073 others(62): Show |
65 | HG00408.hp1 HG00438.hp1 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.585+12004T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48950427 | |||||||
| chr15:48950608 | G | A | 54 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0071 others(51): Show |
56 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(53): Show |
intron_variant | MODIFIER | c.585+11823C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48950608 | |||||||
| chr15:48950739 | G | A | 1 | a0001c0006t0001g0228 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.585+11692C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48950739 | |||||||
| chr15:48950817 | C | G | 1 | a0001c0001t0002g0197 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.585+11614G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48950817 | |||||||
| chr15:48951032 | C | G | 1 | a0001c0002t0004g0130 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.585+11399G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48951032 | |||||||
| chr15:48951240 | A | C | 361 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(358): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.585+11191T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48951240 | |||||||
| chr15:48951269 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.585+11162G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48951269 | |||||||
| chr15:48951357 | C | A | 10 | a0001c0001t0001g0081 a0001c0001t0001g0087 a0001c0001t0001g0183 others(7): Show |
10 | HG01496.hp2 HG02109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.585+11074G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48951357 | |||||||
| chr15:48951387 | C | T | 15 | a0001c0001t0001g0026 a0001c0001t0001g0119 a0001c0001t0001g0212 others(12): Show |
15 | HG01243.hp1 HG01884.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.585+11044G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48951387 | |||||||
| chr15:48951454 | A | T | 1 | a0001c0001t0001g0283 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.585+10977T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48951454 | |||||||
| chr15:48951507 | G | C | 15 | a0001c0001t0001g0026 a0001c0001t0001g0119 a0001c0001t0001g0212 others(12): Show |
15 | HG01243.hp1 HG01884.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.585+10924C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48951507 | |||||||
| chr15:48951622 | G | T | 1 | a0001c0001t0005g0062 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.585+10809C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48951622 | |||||||
| chr15:48951656 | A | G | 26 | a0001c0001t0001g0029 a0001c0001t0001g0059 a0001c0001t0001g0068 others(23): Show |
26 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.585+10775T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48951656 | |||||||
| chr15:48951766 | T | C | 361 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(358): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.585+10665A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48951766 | |||||||
| chr15:48951858 | A | G | 1 | a0001c0001t0001g0181 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.585+10573T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48951858 | |||||||
| chr15:48951891 | C | T | 3 | a0001c0001t0005g0120 a0001c0001t0005g0121 a0001c0001t0005g0274 |
3 | HG01361.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.585+10540G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48951891 | |||||||
| chr15:48952137 | A | G | 2 | a0001c0002t0004g0118 a0004c0005t0001g0298 |
2 | NA19076.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.585+10294T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48952137 | |||||||
| chr15:48952468 | A | G | 1 | a0001c0001t0005g0057 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.585+9963T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48952468 | |||||||
| chr15:48952527 | C | T | 1 | a0001c0001t0022g0254 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.585+9904G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48952527 | |||||||
| chr15:48952528 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.585+9903A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48952528 | |||||||
| chr15:48952582 | T | C | 1 | a0001c0001t0002g0065 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.585+9849A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48952582 | |||||||
| chr15:48952599 | A | G | 3 | a0001c0001t0002g0092 a0001c0001t0002g0229 a0001c0001t0002g0295 |
3 | NA18747.hp1 NA18955.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.585+9832T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48952599 | |||||||
| chr15:48952751 | A | C | 124 | a0001c0001t0001g0035 a0001c0001t0001g0042 a0001c0001t0001g0044 others(121): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.585+9680T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48952751 | |||||||
| chr15:48952804 | C | T | 301 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0029 others(298): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.585+9627G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48952804 | |||||||
| chr15:48952979 | C | T | 1 | a0001c0001t0010g0066 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.585+9452G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48952979 | |||||||
| chr15:48952986 | A | G | 24 | a0001c0001t0001g0076 a0001c0001t0001g0116 a0001c0001t0001g0230 others(21): Show |
24 | HG00408.hp2 HG01255.hp1 HG02074.hp2 others(21): Show |
intron_variant | MODIFIER | c.585+9445T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48952986 | |||||||
| chr15:48953076 | C | T | 5 | a0001c0001t0002g0117 a0001c0001t0008g0013 a0001c0001t0008g0015 others(2): Show |
5 | HG02630.hp2 HG03098.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.585+9355G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48953076 | |||||||
| chr15:48953231 | A | T | 112 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0045 others(109): Show |
113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.585+9200T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48953231 | |||||||
| chr15:48953363 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.585+9068G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48953363 | |||||||
| chr15:48953394 | C | T | 2 | a0001c0001t0001g0243 a0003c0010t0002g0242 |
2 | HG02015.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.585+9037G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48953394 | |||||||
| chr15:48953432 | C | G | 8 | a0001c0001t0001g0035 a0001c0001t0001g0081 a0001c0001t0001g0087 others(5): Show |
8 | HG01496.hp2 HG02109.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.585+8999G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48953432 | |||||||
| chr15:48953447 | T | C | 10 | a0001c0001t0001g0023 a0001c0001t0001g0126 a0001c0001t0001g0181 others(7): Show |
10 | HG02486.hp2 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.585+8984A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48953447 | |||||||
| chr15:48953504 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.585+8927A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48953504 | |||||||
| chr15:48953523 | A | G | 1 | a0002c0003t0003g0185 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.585+8908T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48953523 | |||||||
| chr15:48953525 | G | C | 1 | a0001c0001t0001g0216 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.585+8906C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48953525 | |||||||
| chr15:48953780 | G | C | 1 | a0001c0001t0004g0155 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.585+8651C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48953780 | |||||||
| chr15:48953945 | T | C | 89 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0071 others(86): Show |
91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.585+8486A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48953945 | |||||||
| chr15:48953982 | A | C | 1 | a0001c0001t0001g0139 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.585+8449T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48953982 | |||||||
| chr15:48954041 | A | G | 28 | a0001c0001t0001g0029 a0001c0001t0001g0059 a0001c0001t0001g0068 others(25): Show |
28 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.585+8390T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48954041 | |||||||
| chr15:48954672 | G | T | 26 | a0001c0001t0001g0108 a0001c0001t0001g0210 a0001c0001t0001g0220 others(23): Show |
26 | HG00423.hp2 HG00673.hp2 HG02004.hp2 others(23): Show |
intron_variant | MODIFIER | c.585+7759C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48954672 | |||||||
| chr15:48954701 | C | T | 11 | a0001c0001t0001g0059 a0001c0001t0001g0101 a0001c0001t0001g0137 others(8): Show |
11 | HG01109.hp2 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.585+7730G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48954701 | |||||||
| chr15:48954702 | G | A | 1 | a0001c0001t0003g0096 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.585+7729C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48954702 | |||||||
| chr15:48954928 | T | C | 3 | a0001c0001t0001g0174 a0001c0001t0002g0207 a0001c0001t0004g0208 |
3 | HG00099.hp1 HG00642.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.585+7503A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48954928 | |||||||
| chr15:48954950 | A | C | 10 | a0001c0001t0001g0081 a0001c0001t0001g0087 a0001c0001t0001g0183 others(7): Show |
10 | HG01496.hp2 HG02109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.585+7481T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48954950 | |||||||
| chr15:48954976 | C | T | 1 | a0001c0002t0018g0010 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.585+7455G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48954976 | |||||||
| chr15:48955016 | T | C | 1 | a0001c0001t0001g0351 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.585+7415A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48955016 | |||||||
| chr15:48955203 | A | C | 1 | a0001c0001t0002g0358 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.585+7228T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48955203 | |||||||
| chr15:48955323 | T | C | 147 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0069 others(144): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.585+7108A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48955323 | |||||||
| chr15:48955333 | C | G | 31 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0071 others(28): Show |
33 | HG00609.hp1 HG00738.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.585+7098G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48955333 | |||||||
| chr15:48955429 | A | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0071 others(51): Show |
57 | HG00609.hp1 HG00738.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.585+7002T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48955429 | |||||||
| chr15:48955463 | T | C | 10 | a0001c0001t0001g0023 a0001c0001t0001g0126 a0001c0001t0001g0181 others(7): Show |
10 | HG02486.hp2 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.585+6968A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48955463 | |||||||
| chr15:48955484 | T | G | 28 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0097 others(25): Show |
28 | HG00609.hp2 HG00642.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.585+6947A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48955484 | |||||||
| chr15:48955489 | G | C | 25 | a0001c0001t0001g0026 a0001c0001t0001g0059 a0001c0001t0001g0101 others(22): Show |
25 | HG01109.hp2 HG01167.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.585+6942C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48955489 | |||||||
| chr15:48955713 | A | G | 1 | a0001c0001t0002g0313 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.585+6718T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48955713 | |||||||
| chr15:48955770 | G | A | 1 | a0001c0007t0002g0022 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.585+6661C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48955770 | |||||||
| chr15:48955804 | G | A | 125 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0035 others(122): Show |
125 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.585+6627C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48955804 | |||||||
| chr15:48955930 | G | A | 16 | a0001c0001t0001g0087 a0001c0001t0001g0367 a0001c0001t0001g0369 others(13): Show |
16 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(13): Show |
intron_variant | MODIFIER | c.585+6501C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48955930 | |||||||
| chr15:48956033 | G | A | 3 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0002t0004g0288 |
3 | HG00741.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.585+6398C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48956033 | |||||||
| chr15:48956037 | A | G | 1 | a0001c0001t0003g0312 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.585+6394T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48956037 | |||||||
| chr15:48956069 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.585+6362C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48956069 | |||||||
| chr15:48956127 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.585+6304G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48956127 | |||||||
| chr15:48956271 | T | C | 17 | a0001c0001t0001g0023 a0001c0001t0001g0029 a0001c0001t0001g0030 others(14): Show |
17 | HG00642.hp1 HG02258.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.585+6160A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48956271 | |||||||
| chr15:48956411 | C | G | 2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | NA19081.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.585+6020G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48956411 | |||||||
| chr15:48956525 | G | C | 6 | a0001c0001t0001g0188 a0001c0001t0001g0194 a0001c0001t0001g0196 others(3): Show |
6 | HG01255.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.585+5906C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48956525 | |||||||
| chr15:48956930 | ACTT | A | 12 | a0001c0001t0001g0023 a0001c0001t0001g0126 a0001c0001t0001g0137 others(9): Show |
12 | HG02486.hp2 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.585+5498_585+5500d others(5): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48956930 | |||||||
| chr15:48956950 | TTTTC | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0068 others(86): Show |
91 | HG00438.hp1 HG00673.hp2 HG00738.hp1 others(88): Show |
intron_variant | MODIFIER | c.585+5477_585+5480d others(6): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48956950 | |||||||
| chr15:48956970 | CTTTCT | C | 213 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0044 others(210): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.585+5456_585+5460d others(7): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48956970 | |||||||
| chr15:48956970 | CTTTCTT | C | 61 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(58): Show |
62 | HG00642.hp1 HG01123.hp1 HG01175.hp1 others(59): Show |
intron_variant | MODIFIER | c.585+5455_585+5460d others(8): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48956970 | |||||||
| chr15:48956974 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.585+5457G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48956974 | |||||||
| chr15:48957001 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.585+5430T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48957001 | |||||||
| chr15:48957138 | C | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0198 |
2 | HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.585+5293G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48957138 | |||||||
| chr15:48957257 | C | T | 1 | a0001c0001t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.585+5174G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48957257 | |||||||
| chr15:48957441 | T | C | 1 | a0001c0001t0001g0368 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.585+4990A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48957441 | |||||||
| chr15:48957484 | A | G | 1 | a0001c0001t0002g0078 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.585+4947T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48957484 | |||||||
| chr15:48957620 | G | A | 4 | a0001c0001t0001g0137 a0001c0001t0003g0279 a0001c0001t0005g0138 others(1): Show |
4 | HG02717.hp1 HG02886.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.585+4811C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48957620 | |||||||
| chr15:48957995 | T | G | 155 | a0001c0001t0001g0004 a0001c0001t0001g0116 a0001c0001t0001g0158 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.585+4436A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48957995 | |||||||
| chr15:48958004 | G | A | 1 | a0001c0002t0004g0372 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.585+4427C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48958004 | |||||||
| chr15:48958028 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.585+4403G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48958028 | |||||||
| chr15:48958068 | A | G | 22 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(19): Show |
22 | HG00642.hp1 HG01243.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.585+4363T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48958068 | |||||||
| chr15:48958097 | C | G | 3 | a0001c0001t0001g0302 a0001c0001t0002g0303 a0002c0003t0003g0304 |
3 | NA18983.hp1 NA18994.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.585+4334G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48958097 | |||||||
| chr15:48958192 | T | C | 4 | a0001c0001t0001g0137 a0001c0001t0003g0279 a0001c0001t0005g0138 others(1): Show |
4 | HG02717.hp1 HG02886.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.585+4239A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48958192 | |||||||
| chr15:48958435 | A | G | 29 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0059 others(26): Show |
30 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.585+3996T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48958435 | |||||||
| chr15:48959110 | G | A | 1 | a0001c0002t0004g0157 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.585+3321C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48959110 | |||||||
| chr15:48959170 | G | A | 168 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0101 others(165): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.585+3261C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48959170 | |||||||
| chr15:48959345 | A | T | 2 | a0001c0001t0001g0158 a0001c0001t0001g0282 |
2 | HG03654.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.585+3086T>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48959345 | |||||||
| chr15:48959451 | T | G | 3 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0002g0085 |
3 | HG02572.hp2 HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.585+2980A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48959451 | |||||||
| chr15:48959888 | A | C | 1 | a0001c0001t0003g0086 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.585+2543T>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48959888 | |||||||
| chr15:48959976 | A | G | 1 | a0001c0001t0002g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.585+2455T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48959976 | |||||||
| chr15:48960003 | C | G | 3 | a0001c0001t0001g0001 a0001c0001t0001g0128 a0001c0001t0001g0140 |
4 | HG01167.hp1 HG01169.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.585+2428G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48960003 | |||||||
| chr15:48960072 | G | A | 1 | a0001c0001t0002g0276 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.585+2359C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48960072 | |||||||
| chr15:48960087 | G | A | 3 | a0001c0001t0001g0179 a0001c0001t0005g0277 a0001c0002t0004g0178 |
3 | HG00741.hp1 HG01192.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.585+2344C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48960087 | |||||||
| chr15:48960175 | C | G | 1 | a0001c0001t0001g0300 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.585+2256G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48960175 | |||||||
| chr15:48960176 | A | G | 247 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0023 others(244): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.585+2255T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48960176 | |||||||
| chr15:48960233 | C | A | 2 | a0001c0001t0003g0279 a0001c0001t0005g0278 |
2 | HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.585+2198G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48960233 | |||||||
| chr15:48960243 | C | T | 4 | a0001c0001t0001g0137 a0001c0001t0003g0279 a0001c0001t0005g0138 others(1): Show |
4 | HG02717.hp1 HG02886.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.585+2188G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48960243 | |||||||
| chr15:48960314 | G | A | 1 | a0001c0001t0003g0180 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.585+2117C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48960314 | |||||||
| chr15:48960323 | A | G | 4 | a0001c0001t0001g0137 a0001c0001t0003g0279 a0001c0001t0005g0138 others(1): Show |
4 | HG02717.hp1 HG02886.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.585+2108T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48960323 | |||||||
| chr15:48960376 | T | C | 172 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0101 others(169): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.585+2055A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48960376 | |||||||
| chr15:48960381 | C | T | 3 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0002g0085 |
3 | HG02572.hp2 HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.585+2050G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48960381 | |||||||
| chr15:48960382 | G | A | 4 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0369 others(1): Show |
4 | HG00140.hp2 HG00741.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.585+2049C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48960382 | |||||||
| chr15:48960447 | G | A | 1 | a0001c0001t0002g0370 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.585+1984C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48960447 | |||||||
| chr15:48960485 | C | G | 1 | a0001c0001t0005g0062 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.585+1946G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48960485 | |||||||
| chr15:48960624 | A | G | 1 | a0001c0001t0001g0210 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.585+1807T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48960624 | |||||||
| chr15:48960654 | TTGTC | T | 6 | a0001c0001t0001g0102 a0001c0001t0001g0183 a0001c0001t0001g0192 others(3): Show |
6 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.585+1773_585+1776d others(6): Show |
SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48960654 | |||||||
| chr15:48961043 | G | C | 1 | a0001c0001t0001g0371 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.585+1388C>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48961043 | |||||||
| chr15:48961103 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.585+1328G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48961103 | |||||||
| chr15:48961105 | T | G | 1 | a0001c0001t0001g0182 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.585+1326A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48961105 | |||||||
| chr15:48961278 | T | C | 12 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0126 others(9): Show |
12 | HG02109.hp2 HG02486.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.585+1153A>G | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48961278 | |||||||
| chr15:48961280 | A | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0035 others(83): Show |
87 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.585+1151T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48961280 | |||||||
| chr15:48961321 | T | A | 1 | a0001c0001t0001g0182 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.585+1110A>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48961321 | |||||||
| chr15:48961333 | C | T | 1 | a0001c0001t0002g0033 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.585+1098G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48961333 | |||||||
| chr15:48961379 | A | G | 1 | a0006c0013t0003g0127 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.585+1052T>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48961379 | |||||||
| chr15:48961404 | C | G | 22 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0029 others(19): Show |
22 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.585+1027G>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48961404 | |||||||
| chr15:48961430 | T | G | 25 | a0001c0001t0001g0004 a0001c0001t0001g0084 a0001c0001t0001g0119 others(22): Show |
26 | HG01071.hp1 HG01175.hp1 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.585+1001A>C | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48961430 | |||||||
| chr15:48961449 | C | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0023 others(151): Show |
158 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.585+982G>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48961449 | |||||||
| chr15:48961696 | G | A | 90 | a0001c0001t0001g0122 a0001c0001t0001g0289 a0001c0001t0001g0290 others(87): Show |
90 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.585+735C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48961696 | |||||||
| chr15:48961764 | C | A | 268 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0126 others(265): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.585+667G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48961764 | |||||||
| chr15:48961797 | G | T | 1 | a0001c0001t0009g0012 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.585+634C>A | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48961797 | |||||||
| chr15:48961919 | G | A | 1 | a0001c0002t0004g0372 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.585+512C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48961919 | |||||||
| chr15:48962053 | C | A | 1 | a0001c0001t0001g0373 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.585+378G>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48962053 | |||||||
| chr15:48962180 | G | A | 1 | a0001c0007t0002g0022 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.585+251C>T | SHC4 | ENSG00000185634.12 | transcript | ENST00000332408.9 | protein_coding | 1/11 | chr15 | 48962180 |