Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2888 |
| ensemblid | ENSG00000115290.11 |
| hgncid | 4565 |
| symbol | GRB14 |
| name | growth factor receptor bound protein 14 |
| refseq_nuc | NM_004490.3 |
| refseq_prot | NP_004481.2 |
| ensembl_nuc | ENST00000263915.8 |
| ensembl_prot | ENSP00000263915.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 164492417 |
| end | 164621482 |
| strand | - |
| ver | v1.2 |
| region | chr2:164492417-164621482 |
| region5000 | chr2:164487417-164626482 |
| regionname0 | GRB14_chr2_164492417_164621482 |
| regionname5000 | GRB14_chr2_164487417_164626482 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 540 | 154 | 72 | 21 | 48 | 4 | 7 | 34 | GRB14_chr2_164487417_164626482 | GRB14 | MTTSL others(535): Show |
chr2 | 164487417 | 164626482 |
| a0002 | 0/0 | 540 | 132 | 8 | 38 | 57 | 7 | 22 | 43 | GRB14_chr2_164487417_164626482 | GRB14 | MTTSL others(535): Show |
chr2 | 164487417 | 164626482 |
| a0003 | 0/0 | 540 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | MTTSL others(535): Show |
chr2 | 164487417 | 164626482 |
| a0004 | 0/0 | 540 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | MTTSL others(535): Show |
chr2 | 164487417 | 164626482 |
| a0005 | 0/0 | 540 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | MTTSL others(535): Show |
chr2 | 164487417 | 164626482 |
| a0006 | 0/0 | 540 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | MTTSL others(535): Show |
chr2 | 164487417 | 164626482 |
| a0007 | 0/0 | 540 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | MTTSL others(535): Show |
chr2 | 164487417 | 164626482 |
| a0008 | 0/0 | 540 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | MTTSL others(535): Show |
chr2 | 164487417 | 164626482 |
| a0009 | 0/0 | 540 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | MTTSL others(535): Show |
chr2 | 164487417 | 164626482 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1620 | 149 | 72 | 20 | 46 | 3 | 6 | GRB14_chr2_164487417_164626482 | GRB14 | ATGAC others(1615): Show |
chr2 | 164487417 | 164626482 | ||
| a0001c0003 | 0/0 | 1620 | 2 | 0 | 0 | 1 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | ATGAC others(1615): Show |
chr2 | 164487417 | 164626482 | ||
| a0001c0005 | 0/0 | 1620 | 2 | 0 | 1 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | ATGAC others(1615): Show |
chr2 | 164487417 | 164626482 | ||
| a0001c0012 | 0/0 | 1620 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | ATGAC others(1615): Show |
chr2 | 164487417 | 164626482 | ||
| a0002c0002 | 0/0 | 1620 | 132 | 8 | 38 | 57 | 7 | 22 | GRB14_chr2_164487417_164626482 | GRB14 | ATGAC others(1615): Show |
chr2 | 164487417 | 164626482 | ||
| a0003c0004 | 0/0 | 1620 | 2 | 0 | 1 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | ATGAC others(1615): Show |
chr2 | 164487417 | 164626482 | ||
| a0004c0008 | 0/0 | 1620 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | ATGAC others(1615): Show |
chr2 | 164487417 | 164626482 | ||
| a0005c0010 | 0/0 | 1620 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | ATGAC others(1615): Show |
chr2 | 164487417 | 164626482 | ||
| a0006c0007 | 0/0 | 1620 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | ATGAC others(1615): Show |
chr2 | 164487417 | 164626482 | ||
| a0007c0011 | 0/0 | 1620 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | ATGAC others(1615): Show |
chr2 | 164487417 | 164626482 | ||
| a0008c0009 | 0/0 | 1620 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | ATGAC others(1615): Show |
chr2 | 164487417 | 164626482 | ||
| a0009c0006 | 0/0 | 1620 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | ATGAC others(1615): Show |
chr2 | 164487417 | 164626482 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2415 | 89 | 42 | 10 | 32 | 0 | 3 | GRB14_chr2_164487417_164626482 | GRB14 | GCAGA others(2410): Show |
chr2 | 164487417 | 164626482 |
| a0001c0001t0004 | 0/0 | 2412 | 29 | 11 | 4 | 9 | 2 | 3 | GRB14_chr2_164487417_164626482 | GRB14 | GCAGA others(2407): Show |
chr2 | 164487417 | 164626482 |
| a0001c0001t0006 | 0/0 | 2415 | 14 | 7 | 2 | 4 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | GCAGA others(2410): Show |
chr2 | 164487417 | 164626482 |
| a0001c0001t0007 | 0/0 | 2415 | 6 | 6 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | GCAGA others(2410): Show |
chr2 | 164487417 | 164626482 |
| a0001c0001t0008 | 0/0 | 2415 | 3 | 2 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | GCAGA others(2410): Show |
chr2 | 164487417 | 164626482 |
| a0001c0001t0009 | 0/0 | 2412 | 3 | 3 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | GCAGA others(2407): Show |
chr2 | 164487417 | 164626482 |
| a0001c0001t0010 | 0/0 | 2412 | 3 | 0 | 2 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | GCAGA others(2407): Show |
chr2 | 164487417 | 164626482 |
| a0001c0001t0011 | 0/0 | 2412 | 2 | 1 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | GCAGA others(2407): Show |
chr2 | 164487417 | 164626482 |
| a0001c0003t0001 | 0/0 | 2415 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | GCAGA others(2410): Show |
chr2 | 164487417 | 164626482 |
| a0001c0003t0007 | 0/0 | 2415 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | GCAGA others(2410): Show |
chr2 | 164487417 | 164626482 |
| a0001c0005t0001 | 0/0 | 2415 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | GCAGA others(2410): Show |
chr2 | 164487417 | 164626482 |
| a0001c0005t0007 | 0/0 | 2415 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | GCAGA others(2410): Show |
chr2 | 164487417 | 164626482 |
| a0001c0012t0001 | 0/0 | 2415 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | GCAGA others(2410): Show |
chr2 | 164487417 | 164626482 |
| a0002c0002t0002 | 0/0 | 2412 | 68 | 0 | 19 | 34 | 4 | 11 | GRB14_chr2_164487417_164626482 | GRB14 | GCAGA others(2407): Show |
chr2 | 164487417 | 164626482 |
| a0002c0002t0003 | 0/0 | 2415 | 47 | 5 | 10 | 23 | 1 | 8 | GRB14_chr2_164487417_164626482 | GRB14 | GCAGA others(2410): Show |
chr2 | 164487417 | 164626482 |
| a0002c0002t0005 | 0/0 | 2415 | 17 | 3 | 9 | 0 | 2 | 3 | GRB14_chr2_164487417_164626482 | GRB14 | GCAGA others(2410): Show |
chr2 | 164487417 | 164626482 |
| a0003c0004t0008 | 0/0 | 2415 | 2 | 0 | 1 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | GCAGA others(2410): Show |
chr2 | 164487417 | 164626482 |
| a0004c0008t0013 | 0/0 | 2412 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | GCAGA others(2407): Show |
chr2 | 164487417 | 164626482 |
| a0005c0010t0012 | 0/0 | 2415 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | GCAGA others(2410): Show |
chr2 | 164487417 | 164626482 |
| a0006c0007t0003 | 0/0 | 2415 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | GCAGA others(2410): Show |
chr2 | 164487417 | 164626482 |
| a0007c0011t0007 | 0/0 | 2415 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | GCAGA others(2410): Show |
chr2 | 164487417 | 164626482 |
| a0008c0009t0005 | 0/0 | 2415 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | GCAGA others(2410): Show |
chr2 | 164487417 | 164626482 |
| a0009c0006t0001 | 0/0 | 2415 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | GCAGA others(2410): Show |
chr2 | 164487417 | 164626482 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0056 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0086 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0006g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0006g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0006g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0006g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0006g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0006g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0006g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0007g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0007g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0007g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0007g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0007g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0007g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0008g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0008g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0008g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0009g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0009g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0009g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0010g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0010g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0010g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0011g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0001t0011g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0003t0007g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0005t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0005t0007g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0001c0012t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0002c0002t0005g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0003c0004t0008g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0003c0004t0008g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0004c0008t0013g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0005c0010t0012g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0006c0007t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0007c0011t0007g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0008c0009t0005g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| a0009c0006t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0168 | EUR | GBR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0076 | EUR | GBR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0011 | EUR | GBR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0252 | EUR | GBR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | CHS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00423 | hp1 | a0002 | c0002 | t0003 | g0173 | EAS | CHS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0175 | EAS | CHS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0167 | EAS | CHS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0213 | EAS | CHS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00609 | hp1 | a0001 | c0003 | t0007 | g0067 | EAS | CHS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0171 | EAS | CHS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00639 | hp1 | a0001 | c0005 | t0007 | g0072 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0195 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00642 | hp1 | a0002 | c0002 | t0003 | g0257 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00642 | hp2 | a0002 | c0002 | t0005 | g0266 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0260 | EAS | CHS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00733 | hp2 | a0001 | c0001 | t0008 | g0153 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00735 | hp1 | a0001 | c0001 | t0011 | g0091 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0237 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00738 | hp1 | a0002 | c0002 | t0003 | g0186 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0194 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01069 | hp1 | a0001 | c0001 | t0006 | g0001 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01069 | hp2 | a0002 | c0002 | t0002 | g0191 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0065 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01071 | hp1 | a0001 | c0001 | t0006 | g0001 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0254 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01099 | hp1 | a0003 | c0004 | t0008 | g0152 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0215 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01169 | hp2 | a0002 | c0002 | t0005 | g0193 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01175 | hp1 | a0001 | c0001 | t0010 | g0140 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0119 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0288 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01255 | hp1 | a0002 | c0002 | t0003 | g0241 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0162 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01256 | hp1 | a0002 | c0002 | t0003 | g0199 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0225 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01257 | hp1 | a0002 | c0002 | t0005 | g0163 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01257 | hp2 | a0002 | c0002 | t0003 | g0002 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01258 | hp1 | a0002 | c0002 | t0003 | g0002 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0203 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0181 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01346 | hp1 | a0002 | c0002 | t0005 | g0268 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0059 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0275 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01433 | hp2 | a0001 | c0001 | t0010 | g0154 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01515 | hp1 | a0001 | c0001 | t0006 | g0148 | EUR | IBS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0238 | EUR | IBS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01516 | hp1 | a0002 | c0002 | t0005 | g0269 | EUR | IBS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01516 | hp2 | a0002 | c0002 | t0003 | g0200 | EUR | IBS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0204 | EUR | IBS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01517 | hp2 | a0002 | c0002 | t0005 | g0222 | EUR | IBS | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01884 | hp2 | a0002 | c0002 | t0005 | g0197 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01928 | hp1 | a0002 | c0002 | t0005 | g0218 | AMR | PEL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0243 | AMR | PEL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01934 | hp1 | a0002 | c0002 | t0003 | g0248 | AMR | PEL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0246 | AMR | PEL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01975 | hp1 | a0002 | c0002 | t0002 | g0198 | AMR | PEL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01975 | hp2 | a0002 | c0002 | t0005 | g0217 | AMR | PEL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0247 | AMR | PEL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01993 | hp2 | a0002 | c0002 | t0005 | g0267 | AMR | PEL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02027 | hp1 | a0002 | c0002 | t0003 | g0245 | EAS | KHV | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0109 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02056 | hp1 | a0002 | c0002 | t0003 | g0236 | EAS | KHV | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0046 | EAS | KHV | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02071 | hp2 | a0002 | c0002 | t0003 | g0176 | EAS | KHV | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0272 | EAS | KHV | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02080 | hp2 | a0002 | c0002 | t0003 | g0259 | EAS | KHV | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0169 | EAS | KHV | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02083 | hp2 | a0002 | c0002 | t0003 | g0205 | EAS | KHV | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02148 | hp1 | a0002 | c0002 | t0003 | g0270 | AMR | PEL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02148 | hp2 | a0002 | c0002 | t0005 | g0265 | AMR | PEL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0190 | EAS | CDX | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | CDX | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0150 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02273 | hp1 | a0002 | c0002 | t0005 | g0233 | AMR | PEL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02273 | hp2 | a0002 | c0002 | t0003 | g0234 | AMR | PEL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0111 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0089 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02293 | hp1 | a0002 | c0002 | t0003 | g0271 | AMR | PEL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0251 | AMR | PEL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02451 | hp1 | a0001 | c0001 | t0011 | g0087 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0123 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0158 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02572 | hp2 | a0001 | c0001 | t0007 | g0114 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0286 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0099 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02630 | hp2 | a0002 | c0002 | t0003 | g0292 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02647 | hp1 | a0004 | c0008 | t0013 | g0229 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0043 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02723 | hp1 | a0001 | c0001 | t0008 | g0141 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0107 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02738 | hp1 | a0002 | c0002 | t0003 | g0184 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0235 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0136 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0098 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0159 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02896 | hp2 | a0002 | c0002 | t0003 | g0177 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02897 | hp1 | a0001 | c0001 | t0006 | g0151 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02922 | hp1 | a0002 | c0002 | t0005 | g0180 | AFR | ESN | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02970 | hp1 | a0002 | c0002 | t0003 | g0183 | AFR | ESN | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03017 | hp1 | a0002 | c0002 | t0005 | g0196 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03017 | hp2 | a0002 | c0002 | t0003 | g0182 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03130 | hp2 | a0001 | c0001 | t0009 | g0102 | AFR | ESN | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0149 | AFR | ESN | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0088 | AFR | ESN | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0104 | AFR | ESN | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0142 | AFR | MSL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0029 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0015 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0216 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03490 | hp2 | a0002 | c0002 | t0003 | g0192 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03491 | hp1 | a0005 | c0010 | t0012 | g0014 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0291 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0256 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03492 | hp2 | a0002 | c0002 | t0002 | g0281 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03516 | hp1 | a0001 | c0001 | t0009 | g0116 | AFR | ESN | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03654 | hp1 | a0002 | c0002 | t0003 | g0223 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03654 | hp2 | a0003 | c0004 | t0008 | g0155 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0253 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03704 | hp1 | a0002 | c0002 | t0002 | g0166 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03704 | hp2 | a0002 | c0002 | t0003 | g0206 | SAS | PJL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0274 | SAS | BEB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03831 | hp2 | a0002 | c0002 | t0005 | g0164 | SAS | BEB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0249 | SAS | BEB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03834 | hp2 | a0002 | c0002 | t0003 | g0160 | SAS | BEB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG04184 | hp1 | a0002 | c0002 | t0003 | g0283 | SAS | BEB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0060 | SAS | BEB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | STU | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0202 | SAS | STU | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG04228 | hp1 | a0001 | c0003 | t0001 | g0049 | SAS | STU | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG04228 | hp2 | a0002 | c0002 | t0003 | g0258 | SAS | STU | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | YRI | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | YRI | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | YRI | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18940 | hp2 | a0006 | c0007 | t0003 | g0239 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18941 | hp2 | a0002 | c0002 | t0003 | g0220 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18944 | hp1 | a0002 | c0002 | t0003 | g0289 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0290 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0058 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18945 | hp2 | a0002 | c0002 | t0003 | g0187 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18951 | hp1 | a0001 | c0012 | t0001 | g0139 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0279 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18954 | hp2 | a0002 | c0002 | t0003 | g0240 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18963 | hp1 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18966 | hp1 | a0001 | c0001 | t0006 | g0145 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18966 | hp2 | a0002 | c0002 | t0002 | g0278 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18970 | hp2 | a0002 | c0002 | t0003 | g0261 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18972 | hp2 | a0002 | c0002 | t0002 | g0262 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18974 | hp1 | a0002 | c0002 | t0002 | g0230 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18974 | hp2 | a0001 | c0001 | t0006 | g0143 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18975 | hp1 | a0002 | c0002 | t0003 | g0244 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0227 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0287 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0211 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18982 | hp1 | a0002 | c0002 | t0003 | g0210 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0221 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18985 | hp2 | a0001 | c0001 | t0004 | g0074 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0172 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18988 | hp2 | a0002 | c0002 | t0002 | g0263 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0277 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18991 | hp2 | a0001 | c0001 | t0006 | g0156 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18998 | hp1 | a0002 | c0002 | t0003 | g0209 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19001 | hp1 | a0002 | c0002 | t0003 | g0161 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19001 | hp2 | a0002 | c0002 | t0002 | g0282 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19003 | hp2 | a0002 | c0002 | t0003 | g0242 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0170 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19006 | hp1 | a0001 | c0001 | t0004 | g0062 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0188 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19007 | hp2 | a0002 | c0002 | t0003 | g0201 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0280 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19030 | hp2 | a0007 | c0011 | t0007 | g0128 | AFR | LWK | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0147 | AFR | LWK | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19043 | hp2 | a0002 | c0002 | t0003 | g0179 | AFR | LWK | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19056 | hp1 | a0002 | c0002 | t0002 | g0207 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0264 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19065 | hp1 | a0002 | c0002 | t0003 | g0214 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0219 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0231 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19068 | hp2 | a0002 | c0002 | t0003 | g0165 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0189 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0224 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19079 | hp1 | a0002 | c0002 | t0003 | g0285 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19079 | hp2 | a0001 | c0001 | t0010 | g0157 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19081 | hp1 | a0002 | c0002 | t0003 | g0226 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0228 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19084 | hp1 | a0001 | c0001 | t0006 | g0144 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19084 | hp2 | a0002 | c0002 | t0003 | g0232 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19087 | hp2 | a0002 | c0002 | t0003 | g0276 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0212 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19089 | hp1 | a0002 | c0002 | t0002 | g0208 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0108 | AFR | YRI | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0146 | AFR | ASW | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA20129 | hp2 | a0001 | c0001 | t0007 | g0112 | AFR | ASW | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA20805 | hp1 | a0008 | c0009 | t0005 | g0250 | EUR | TSI | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA20805 | hp2 | a0001 | c0005 | t0001 | g0035 | EUR | TSI | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA20905 | hp1 | a0002 | c0002 | t0005 | g0255 | SAS | GIH | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA20905 | hp2 | a0009 | c0006 | t0001 | g0003 | SAS | GIH | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0273 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0284 | AMR | CLM | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02486 | hp1 | a0001 | c0001 | t0009 | g0125 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0073 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0110 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0133 | AFR | ACB | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03471 | hp1 | a0002 | c0002 | t0003 | g0185 | AFR | MSL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | USA | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | USA | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0174 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA21309 | hp1 | a0002 | c0002 | t0005 | g0178 | AFR | LWK | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0086 | REF | REF | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0056 | REF | REF | GRB14_chr2_164487417_164626482 | GRB14 | chr2 | 164487417 | 164626482 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:164497473 | A | T | 1 | a0004 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.1122T>A | p.Asn374Lys | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 10/14 | 1295/2415 | 1122/1623 | 374/540 | chr2 | 164497473 | |||
| chr2:164525008 | A | G | 1 | a0006 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.674T>C | p.Leu225Ser | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/14 | 847/2415 | 674/1623 | 225/540 | chr2 | 164525008 | |||
| chr2:164525032 | C | A | 2 | a0003 a0008 |
3 | HG01099.hp1 HG03654.hp2 NA20805.hp1 |
missense_variant | MODERATE | c.650G>T | p.Gly217Val | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/14 | 823/2415 | 650/1623 | 217/540 | chr2 | 164525032 | |||
| chr2:164547710 | A | G | 1 | a0007 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.431T>C | p.Ile144Thr | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/14 | 604/2415 | 431/1623 | 144/540 | chr2 | 164547710 | |||
| chr2:164547749 | C | T | 1 | a0005 | 1 | HG03491.hp1 | missense_variant | MODERATE | c.392G>A | p.Arg131Gln | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/14 | 565/2415 | 392/1623 | 131/540 | chr2 | 164547749 | |||
| chr2:164619743 | A | T | 4 | a0002 a0004 a0006 others(1): Show |
135 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(132): Show |
missense_variant | MODERATE | c.268T>A | p.Phe90Ile | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/14 | 441/2415 | 268/1623 | 90/540 | chr2 | 164619743 | |||
| chr2:164621134 | C | T | 1 | a0009 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.176G>A | p.Gly59Asp | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/14 | 349/2415 | 176/1623 | 59/540 | chr2 | 164621134 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:164527056 | A | G | 1 | a0001c0003 | 2 | HG00609.hp1 HG04228.hp1 |
synonymous_variant | LOW | c.561T>C | p.Phe187Phe | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/14 | 734/2415 | 561/1623 | 187/540 | chr2 | 164527056 | |||
| chr2:164527116 | G | A | 1 | a0001c0005 | 2 | HG00639.hp1 NA20805.hp2 |
synonymous_variant | LOW | c.501C>T | p.His167His | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/14 | 674/2415 | 501/1623 | 167/540 | chr2 | 164527116 | |||
| chr2:164621238 | G | A | 1 | a0001c0012 | 1 | NA18951.hp1 | synonymous_variant | LOW | c.72C>T | p.Ala24Ala | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/14 | 245/2415 | 72/1623 | 24/540 | chr2 | 164621238 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:164492493 | G | A | 2 | a0001c0001t0009 a0004c0008t0013 |
4 | HG02486.hp1 HG02647.hp1 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*543C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 14/14 | 543 | chr2 | 164492493 | ||||||
| chr2:164492538 | C | T | 14 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 others(11): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*498G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 14/14 | 498 | chr2 | 164492538 | ||||||
| chr2:164492539 | G | A | 1 | a0005c0010t0012 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*497C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 14/14 | 497 | chr2 | 164492539 | ||||||
| chr2:164492609 | GTTA | G | 6 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0010 others(3): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*424_*426delTAA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 14/14 | 424 | chr2 | 164492609 | ||||||
| chr2:164492630 | A | G | 1 | a0001c0001t0011 | 2 | HG00735.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*406T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 14/14 | 406 | chr2 | 164492630 | ||||||
| chr2:164492712 | T | C | 14 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 others(11): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*324A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 14/14 | 324 | chr2 | 164492712 | ||||||
| chr2:164492724 | T | C | 1 | a0001c0001t0011 | 2 | HG00735.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*312A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 14/14 | 312 | chr2 | 164492724 | ||||||
| chr2:164492949 | G | A | 14 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 others(11): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*87C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 14/14 | 87 | chr2 | 164492949 | ||||||
| chr2:164492953 | T | C | 8 | a0001c0001t0007 a0001c0001t0008 a0001c0003t0007 others(5): Show |
32 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*83A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 14/14 | 83 | chr2 | 164492953 | ||||||
| chr2:164621326 | G | A | 4 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0010 others(1): Show |
22 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(19): Show |
5_prime_UTR_variant | MODIFIER | c.-17C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/14 | 17 | chr2 | 164621326 | ||||||
| chr2:164621393 | G | C | 6 | a0002c0002t0002 a0002c0002t0003 a0002c0002t0005 others(3): Show |
135 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(132): Show |
5_prime_UTR_variant | MODIFIER | c.-84C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/14 | 84 | chr2 | 164621393 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:164493258 | T | C | 1 | a0002c0002t0003g0177 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1477-76A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 13/13 | chr2 | 164493258 | |||||||
| chr2:164493330 | GT | G | 133 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(130): Show |
135 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1477-149delA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 13/13 | chr2 | 164493330 | |||||||
| chr2:164493352 | T | C | 27 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(24): Show |
27 | HG01261.hp2 HG01891.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1477-170A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 13/13 | chr2 | 164493352 | |||||||
| chr2:164493392 | C | T | 145 | a0001c0001t0001g0090 a0001c0001t0001g0106 a0001c0001t0001g0113 others(142): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.1477-210G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 13/13 | chr2 | 164493392 | |||||||
| chr2:164493424 | TTC | T | 21 | a0001c0001t0007g0073 a0001c0001t0007g0088 a0001c0001t0007g0136 others(18): Show |
21 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.1477-244_1477-243d others(4): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 13/13 | chr2 | 164493424 | |||||||
| chr2:164493492 | T | C | 28 | a0001c0001t0007g0073 a0001c0001t0007g0088 a0001c0001t0007g0104 others(25): Show |
28 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.1477-310A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 13/13 | chr2 | 164493492 | |||||||
| chr2:164493783 | G | A | 4 | a0001c0001t0009g0102 a0001c0001t0009g0116 a0001c0001t0009g0125 others(1): Show |
4 | HG02486.hp1 HG02647.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1477-601C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 13/13 | chr2 | 164493783 | |||||||
| chr2:164493791 | A | AATT | 21 | a0001c0001t0007g0073 a0001c0001t0007g0088 a0001c0001t0007g0136 others(18): Show |
21 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.1477-612_1477-610d others(5): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 13/13 | chr2 | 164493791 | |||||||
| chr2:164493915 | G | A | 4 | a0001c0001t0001g0040 a0002c0002t0003g0220 a0002c0002t0003g0232 others(1): Show |
4 | NA18941.hp2 NA18954.hp2 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.1476+516C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 13/13 | chr2 | 164493915 | |||||||
| chr2:164494050 | C | T | 32 | a0001c0001t0007g0073 a0001c0001t0007g0088 a0001c0001t0007g0104 others(29): Show |
32 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.1476+381G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 13/13 | chr2 | 164494050 | |||||||
| chr2:164494174 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1476+257G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 13/13 | chr2 | 164494174 | |||||||
| chr2:164494401 | T | C | 7 | a0001c0001t0007g0104 a0001c0001t0008g0141 a0001c0001t0008g0142 others(4): Show |
7 | HG01169.hp2 HG01516.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.1476+30A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 13/13 | chr2 | 164494401 | |||||||
| chr2:164494678 | A | G | 1 | a0001c0001t0001g0022 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1383-154T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164494678 | |||||||
| chr2:164494698 | C | T | 142 | a0001c0001t0001g0106 a0001c0001t0001g0113 a0001c0001t0001g0131 others(139): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.1383-174G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164494698 | |||||||
| chr2:164494720 | C | T | 1 | a0004c0008t0013g0229 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1383-196G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164494720 | |||||||
| chr2:164494953 | AT | A | 133 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(130): Show |
135 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1383-430delA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164494953 | |||||||
| chr2:164495028 | G | A | 1 | a0001c0001t0011g0087 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1383-504C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164495028 | |||||||
| chr2:164495230 | C | T | 3 | a0001c0001t0001g0090 a0001c0001t0001g0117 a0001c0001t0001g0137 |
3 | HG02257.hp2 HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1383-706G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164495230 | |||||||
| chr2:164495386 | G | A | 133 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(130): Show |
135 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1383-862C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164495386 | |||||||
| chr2:164495401 | TA | T | 133 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(130): Show |
135 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1383-878delT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164495401 | |||||||
| chr2:164495445 | G | T | 9 | a0001c0001t0001g0008 a0001c0001t0001g0082 a0001c0001t0001g0084 others(6): Show |
9 | HG01891.hp1 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1383-921C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164495445 | |||||||
| chr2:164495591 | C | T | 133 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(130): Show |
135 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1383-1067G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164495591 | |||||||
| chr2:164495655 | C | T | 133 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(130): Show |
135 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1383-1131G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164495655 | |||||||
| chr2:164495895 | G | A | 131 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(128): Show |
133 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.1382+1113C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164495895 | |||||||
| chr2:164496017 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1382+991G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164496017 | |||||||
| chr2:164496030 | T | A | 1 | a0001c0001t0004g0011 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1382+978A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164496030 | |||||||
| chr2:164496035 | T | A | 275 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(272): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.1382+973A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164496035 | |||||||
| chr2:164496066 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1382+942G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164496066 | |||||||
| chr2:164496157 | T | C | 62 | a0001c0001t0001g0134 a0001c0001t0004g0004 a0001c0001t0004g0015 others(59): Show |
62 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.1382+851A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164496157 | |||||||
| chr2:164496198 | T | C | 4 | a0001c0001t0009g0102 a0001c0001t0009g0116 a0001c0001t0009g0125 others(1): Show |
4 | HG02486.hp1 HG02647.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1382+810A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164496198 | |||||||
| chr2:164496621 | CAT | C | 61 | a0001c0001t0004g0004 a0001c0001t0004g0015 a0001c0001t0004g0020 others(58): Show |
61 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1382+385_1382+386d others(4): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164496621 | |||||||
| chr2:164496648 | C | T | 136 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(133): Show |
138 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.1382+360G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164496648 | |||||||
| chr2:164496779 | C | T | 284 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(281): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1382+229G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164496779 | |||||||
| chr2:164496813 | A | G | 33 | a0001c0001t0001g0106 a0001c0001t0001g0113 a0001c0001t0007g0073 others(30): Show |
33 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1382+195T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 12/13 | chr2 | 164496813 | |||||||
| chr2:164497202 | C | T | 170 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(167): Show |
171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1294+9G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 11/13 | chr2 | 164497202 | |||||||
| chr2:164497608 | T | G | 6 | a0001c0001t0001g0083 a0001c0001t0004g0098 a0001c0001t0004g0099 others(3): Show |
6 | HG01516.hp1 HG01517.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1105-118A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164497608 | |||||||
| chr2:164497999 | T | C | 19 | a0001c0001t0007g0073 a0001c0001t0007g0136 a0001c0003t0007g0067 others(16): Show |
19 | HG00609.hp1 HG00639.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1105-509A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164497999 | |||||||
| chr2:164498473 | C | A | 1 | a0006c0007t0003g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1105-983G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164498473 | |||||||
| chr2:164498499 | A | G | 4 | a0001c0001t0001g0084 a0001c0001t0001g0105 a0001c0001t0006g0151 others(1): Show |
4 | HG02258.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1105-1009T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164498499 | |||||||
| chr2:164498597 | A | C | 1 | a0001c0001t0008g0141 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1105-1107T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164498597 | |||||||
| chr2:164498659 | C | T | 14 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(11): Show |
14 | HG01255.hp2 HG01261.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1105-1169G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164498659 | |||||||
| chr2:164498694 | T | C | 1 | a0001c0001t0004g0099 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1105-1204A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164498694 | |||||||
| chr2:164498955 | G | C | 1 | a0001c0001t0001g0022 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1105-1465C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164498955 | |||||||
| chr2:164499035 | C | G | 1 | a0001c0001t0004g0065 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1105-1545G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164499035 | |||||||
| chr2:164499236 | T | G | 2 | a0001c0001t0004g0107 a0006c0007t0003g0239 |
2 | HG02723.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.1105-1746A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164499236 | |||||||
| chr2:164499361 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1105-1871G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164499361 | |||||||
| chr2:164499434 | T | C | 68 | a0001c0001t0001g0022 a0001c0001t0001g0038 a0001c0001t0001g0050 others(65): Show |
68 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.1105-1944A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164499434 | |||||||
| chr2:164499609 | C | G | 1 | a0001c0001t0001g0137 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1105-2119G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164499609 | |||||||
| chr2:164499833 | A | G | 194 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(191): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1105-2343T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164499833 | |||||||
| chr2:164499842 | C | A | 4 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0115 others(1): Show |
4 | HG02109.hp1 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1105-2352G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164499842 | |||||||
| chr2:164499956 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1104+2299C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164499956 | |||||||
| chr2:164500293 | C | T | 1 | a0001c0001t0006g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1104+1962G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164500293 | |||||||
| chr2:164500394 | A | G | 1 | a0001c0001t0004g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1104+1861T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164500394 | |||||||
| chr2:164500450 | A | G | 14 | a0001c0001t0001g0100 a0001c0001t0001g0106 a0001c0001t0001g0113 others(11): Show |
14 | HG01175.hp2 HG02258.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1104+1805T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164500450 | |||||||
| chr2:164500525 | C | A | 2 | a0001c0001t0006g0143 a0001c0001t0006g0144 |
2 | NA18974.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1104+1730G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164500525 | |||||||
| chr2:164500626 | A | G | 29 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0105 others(26): Show |
30 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.1104+1629T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164500626 | |||||||
| chr2:164500837 | C | A | 4 | a0002c0002t0002g0227 a0002c0002t0002g0228 a0002c0002t0002g0279 others(1): Show |
4 | NA18951.hp2 NA18975.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.1104+1418G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164500837 | |||||||
| chr2:164500843 | A | G | 7 | a0001c0001t0004g0108 a0001c0001t0004g0109 a0001c0001t0004g0110 others(4): Show |
7 | HG02055.hp2 HG02280.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1104+1412T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164500843 | |||||||
| chr2:164501053 | T | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0048 |
2 | NA18979.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1104+1202A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164501053 | |||||||
| chr2:164501126 | T | A | 4 | a0002c0002t0002g0227 a0002c0002t0002g0228 a0002c0002t0002g0279 others(1): Show |
4 | NA18951.hp2 NA18975.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.1104+1129A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164501126 | |||||||
| chr2:164501184 | T | C | 1 | a0001c0001t0004g0076 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1104+1071A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164501184 | |||||||
| chr2:164502127 | G | C | 1 | a0001c0001t0001g0005 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1104+128C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164502127 | |||||||
| chr2:164502145 | T | A | 30 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0105 others(27): Show |
31 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.1104+110A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164502145 | |||||||
| chr2:164502162 | A | G | 194 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(191): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1104+93T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 9/13 | chr2 | 164502162 | |||||||
| chr2:164502516 | A | C | 1 | a0006c0007t0003g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1024-181T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164502516 | |||||||
| chr2:164502532 | T | C | 29 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0105 others(26): Show |
30 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.1024-197A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164502532 | |||||||
| chr2:164502651 | T | TA | 69 | a0001c0001t0001g0022 a0001c0001t0001g0038 a0001c0001t0001g0050 others(66): Show |
69 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1024-317dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164502651 | |||||||
| chr2:164502749 | T | A | 1 | a0002c0002t0002g0262 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1024-414A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164502749 | |||||||
| chr2:164503051 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1024-716A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503051 | |||||||
| chr2:164503169 | T | TA | 32 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0013 others(29): Show |
32 | HG00735.hp1 HG01123.hp2 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.1024-835dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503169 | |||||||
| chr2:164503169 | T | TAA | 63 | a0001c0001t0001g0038 a0001c0001t0001g0050 a0001c0001t0004g0004 others(60): Show |
63 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.1024-836_1024-835d others(4): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503169 | |||||||
| chr2:164503169 | TA | T | 37 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0030 others(34): Show |
38 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1024-835delT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503169 | |||||||
| chr2:164503183 | A | AG | 4 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0150 others(1): Show |
4 | HG02257.hp1 HG02886.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024-849_1024-848i others(3): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503183 | |||||||
| chr2:164503183 | A | G | 20 | a0001c0001t0006g0001 a0001c0001t0007g0073 a0001c0001t0010g0154 others(17): Show |
21 | HG00639.hp1 HG00642.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.1024-848T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503183 | |||||||
| chr2:164503184 | A | G | 2 | a0002c0002t0002g0216 a0002c0002t0002g0281 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1024-849T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503184 | |||||||
| chr2:164503375 | C | T | 5 | a0002c0002t0003g0161 a0002c0002t0003g0173 a0002c0002t0003g0244 others(2): Show |
5 | HG00423.hp1 NA18970.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1024-1040G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503375 | |||||||
| chr2:164503442 | C | CA | 39 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0025 others(36): Show |
39 | HG00423.hp2 HG00738.hp1 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.1024-1108dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503442 | |||||||
| chr2:164503442 | C | CAA | 10 | a0001c0001t0001g0026 a0001c0001t0001g0044 a0001c0001t0001g0051 others(7): Show |
10 | HG00423.hp1 HG01070.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.1024-1109_1024-110 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503442 | |||||||
| chr2:164503442 | CA | C | 22 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01070.hp2 HG01071.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.1024-1108delT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503442 | |||||||
| chr2:164503442 | CAA | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0113 a0001c0001t0004g0004 others(3): Show |
6 | HG01433.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1024-1109_1024-110 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503442 | |||||||
| chr2:164503442 | CAAA | C | 38 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0126 others(35): Show |
38 | HG00544.hp1 HG00673.hp2 HG01175.hp1 others(35): Show |
intron_variant | MODIFIER | c.1024-1110_1024-110 others(7): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503442 | |||||||
| chr2:164503442 | CAAAA | C | 59 | a0001c0001t0001g0022 a0001c0001t0001g0050 a0001c0001t0001g0100 others(56): Show |
59 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.1024-1111_1024-110 others(8): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503442 | |||||||
| chr2:164503442 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0004g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1024-1118_1024-110 others(15): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503442 | |||||||
| chr2:164503442 | CAAAAAAA others(7): Show |
C | 28 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0105 others(25): Show |
29 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1024-1121_1024-110 others(18): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503442 | |||||||
| chr2:164503442 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0131 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1024-1122_1024-110 others(19): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503442 | |||||||
| chr2:164503442 | CAAAAAAA others(10): Show |
C | 27 | a0001c0001t0004g0011 a0001c0001t0004g0029 a0001c0001t0008g0153 others(24): Show |
28 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(25): Show |
intron_variant | MODIFIER | c.1024-1124_1024-110 others(21): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503442 | |||||||
| chr2:164503442 | CAAAAAAA others(16): Show |
C | 1 | a0001c0001t0001g0090 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1024-1130_1024-110 others(27): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503442 | |||||||
| chr2:164503765 | A | G | 1 | a0001c0001t0001g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1024-1430T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164503765 | |||||||
| chr2:164504314 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1024-1979C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164504314 | |||||||
| chr2:164504326 | G | A | 2 | a0001c0001t0008g0141 a0001c0001t0008g0142 |
2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1024-1991C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164504326 | |||||||
| chr2:164504371 | T | C | 2 | a0002c0002t0002g0170 a0002c0002t0003g0205 |
2 | HG02083.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1024-2036A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164504371 | |||||||
| chr2:164504669 | C | T | 1 | a0004c0008t0013g0229 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1024-2334G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164504669 | |||||||
| chr2:164505113 | A | G | 2 | a0002c0002t0003g0179 a0002c0002t0003g0185 |
2 | HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1024-2778T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164505113 | |||||||
| chr2:164505318 | AGT | A | 13 | a0001c0001t0001g0106 a0001c0001t0001g0113 a0001c0001t0001g0120 others(10): Show |
13 | HG01175.hp2 HG02258.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1024-2985_1024-298 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164505318 | |||||||
| chr2:164505435 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1023+3020G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164505435 | |||||||
| chr2:164505891 | G | A | 1 | a0002c0002t0003g0176 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1023+2564C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164505891 | |||||||
| chr2:164506331 | G | T | 28 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0105 others(25): Show |
29 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1023+2124C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164506331 | |||||||
| chr2:164506471 | T | C | 13 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(10): Show |
13 | HG01255.hp2 HG01261.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1023+1984A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164506471 | |||||||
| chr2:164506643 | A | C | 1 | a0001c0001t0001g0124 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1023+1812T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164506643 | |||||||
| chr2:164506706 | T | C | 1 | a0001c0001t0001g0022 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1023+1749A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164506706 | |||||||
| chr2:164506840 | C | T | 6 | a0002c0002t0002g0256 a0002c0002t0002g0291 a0002c0002t0003g0002 others(3): Show |
7 | HG01256.hp1 HG01257.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1023+1615G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164506840 | |||||||
| chr2:164506853 | T | G | 1 | a0004c0008t0013g0229 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1023+1602A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164506853 | |||||||
| chr2:164506895 | T | C | 1 | a0002c0002t0003g0292 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1023+1560A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164506895 | |||||||
| chr2:164506932 | CACAG | C | 5 | a0001c0001t0001g0042 a0001c0001t0001g0124 a0001c0001t0009g0102 others(2): Show |
5 | HG01106.hp2 HG02486.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1023+1519_1023+152 others(8): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164506932 | |||||||
| chr2:164507403 | C | G | 29 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0105 others(26): Show |
30 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.1023+1052G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164507403 | |||||||
| chr2:164507498 | A | G | 1 | a0001c0001t0001g0005 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1023+957T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164507498 | |||||||
| chr2:164507661 | G | A | 3 | a0001c0001t0001g0090 a0001c0001t0011g0087 a0001c0001t0011g0091 |
3 | HG00735.hp1 HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1023+794C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164507661 | |||||||
| chr2:164507663 | G | A | 2 | a0001c0005t0001g0035 a0001c0005t0007g0072 |
2 | HG00639.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1023+792C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164507663 | |||||||
| chr2:164507758 | G | GATAATTG others(2): Show |
145 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(142): Show |
146 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.1023+696_1023+697i others(11): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164507758 | |||||||
| chr2:164508068 | C | T | 1 | a0002c0002t0003g0177 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1023+387G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164508068 | |||||||
| chr2:164508106 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1023+349G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164508106 | |||||||
| chr2:164508128 | C | T | 1 | a0001c0001t0001g0007 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1023+327G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164508128 | |||||||
| chr2:164508352 | A | G | 1 | a0002c0002t0003g0183 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1023+103T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164508352 | |||||||
| chr2:164508370 | A | C | 4 | a0001c0001t0004g0043 a0001c0001t0004g0089 a0001c0001t0004g0133 others(1): Show |
4 | HG02280.hp2 HG02559.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1023+85T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164508370 | |||||||
| chr2:164508377 | G | A | 26 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0105 others(23): Show |
26 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.1023+78C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 8/13 | chr2 | 164508377 | |||||||
| chr2:164508587 | T | C | 2 | a0001c0001t0004g0020 a0001c0001t0004g0031 |
2 | NA18963.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.928-37A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 7/13 | chr2 | 164508587 | |||||||
| chr2:164508958 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0135 |
2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.817-106C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164508958 | |||||||
| chr2:164509007 | C | T | 4 | a0001c0001t0001g0084 a0001c0001t0001g0105 a0001c0001t0006g0151 others(1): Show |
4 | HG02258.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.817-155G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164509007 | |||||||
| chr2:164509106 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.817-254C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164509106 | |||||||
| chr2:164509176 | G | A | 1 | a0001c0001t0004g0015 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.817-324C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164509176 | |||||||
| chr2:164509399 | C | T | 2 | a0002c0002t0002g0252 a0002c0002t0002g0284 |
2 | HG00140.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.817-547G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164509399 | |||||||
| chr2:164509419 | A | G | 14 | a0001c0001t0001g0017 a0001c0001t0001g0030 a0001c0001t0001g0032 others(11): Show |
14 | HG00408.hp1 HG00621.hp1 HG02523.hp2 others(11): Show |
intron_variant | MODIFIER | c.817-567T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164509419 | |||||||
| chr2:164509792 | G | GA | 87 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(84): Show |
89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.817-941dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164509792 | |||||||
| chr2:164509792 | G | GAA | 10 | a0001c0001t0001g0010 a0001c0001t0006g0158 a0001c0001t0007g0114 others(7): Show |
10 | HG00733.hp2 HG01243.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.817-942_817-941dup others(2): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164509792 | |||||||
| chr2:164509804 | A | C | 1 | a0001c0001t0001g0057 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.817-952T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164509804 | |||||||
| chr2:164509897 | G | A | 3 | a0001c0001t0001g0084 a0001c0001t0006g0151 a0001c0001t0006g0159 |
3 | HG02258.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.817-1045C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164509897 | |||||||
| chr2:164510082 | A | C | 193 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(190): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.817-1230T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164510082 | |||||||
| chr2:164510309 | T | C | 1 | a0001c0001t0001g0131 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.817-1457A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164510309 | |||||||
| chr2:164510413 | G | A | 1 | a0006c0007t0003g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.817-1561C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164510413 | |||||||
| chr2:164510460 | C | T | 64 | a0001c0001t0001g0022 a0001c0001t0001g0038 a0001c0001t0001g0050 others(61): Show |
64 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.817-1608G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164510460 | |||||||
| chr2:164510634 | C | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0037 |
2 | NA18972.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.817-1782G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164510634 | |||||||
| chr2:164510775 | A | G | 1 | a0001c0001t0004g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.817-1923T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164510775 | |||||||
| chr2:164510896 | G | A | 1 | a0001c0012t0001g0139 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.817-2044C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164510896 | |||||||
| chr2:164511040 | CTACCCAT others(11): Show |
C | 4 | a0001c0001t0001g0006 a0001c0001t0001g0061 a0001c0001t0001g0064 others(1): Show |
4 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-2206_817-2189d others(20): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164511040 | |||||||
| chr2:164511305 | T | G | 1 | a0009c0006t0001g0003 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.817-2453A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164511305 | |||||||
| chr2:164511331 | C | T | 1 | a0006c0007t0003g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.817-2479G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164511331 | |||||||
| chr2:164511836 | T | C | 24 | a0001c0001t0001g0082 a0001c0001t0001g0121 a0001c0001t0007g0073 others(21): Show |
24 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.817-2984A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164511836 | |||||||
| chr2:164512060 | G | C | 1 | a0001c0001t0001g0113 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.817-3208C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164512060 | |||||||
| chr2:164512070 | T | C | 10 | a0001c0001t0001g0017 a0001c0001t0001g0030 a0001c0001t0001g0033 others(7): Show |
10 | HG00621.hp1 NA18941.hp1 NA18972.hp1 others(7): Show |
intron_variant | MODIFIER | c.817-3218A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164512070 | |||||||
| chr2:164512078 | C | A | 212 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(209): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.817-3226G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164512078 | |||||||
| chr2:164512111 | A | G | 1 | a0001c0001t0001g0131 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.817-3259T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164512111 | |||||||
| chr2:164512467 | G | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0106 |
2 | HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.817-3615C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164512467 | |||||||
| chr2:164512539 | A | G | 12 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0137 others(9): Show |
12 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.817-3687T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164512539 | |||||||
| chr2:164512878 | C | T | 1 | a0005c0010t0012g0014 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.817-4026G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164512878 | |||||||
| chr2:164513117 | T | C | 1 | a0002c0002t0002g0195 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.817-4265A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164513117 | |||||||
| chr2:164513300 | GC | G | 12 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0137 others(9): Show |
12 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.817-4449delG | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164513300 | |||||||
| chr2:164513444 | T | C | 25 | a0001c0001t0001g0082 a0001c0001t0001g0121 a0001c0001t0007g0073 others(22): Show |
25 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.817-4592A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164513444 | |||||||
| chr2:164513551 | A | C | 45 | a0001c0001t0001g0006 a0001c0001t0001g0061 a0001c0001t0001g0064 others(42): Show |
47 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(44): Show |
intron_variant | MODIFIER | c.817-4699T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164513551 | |||||||
| chr2:164513776 | A | C | 1 | a0001c0001t0001g0083 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.817-4924T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164513776 | |||||||
| chr2:164513833 | A | C | 25 | a0001c0001t0001g0082 a0001c0001t0001g0121 a0001c0001t0007g0073 others(22): Show |
25 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.817-4981T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164513833 | |||||||
| chr2:164513948 | GGACATAG others(4): Show |
G | 1 | a0001c0001t0001g0113 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.817-5107_817-5097d others(13): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164513948 | |||||||
| chr2:164514148 | T | A | 24 | a0001c0001t0001g0082 a0001c0001t0001g0121 a0001c0001t0007g0073 others(21): Show |
24 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.817-5296A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164514148 | |||||||
| chr2:164514176 | A | T | 1 | a0002c0002t0002g0171 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.817-5324T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164514176 | |||||||
| chr2:164514255 | T | C | 2 | a0001c0001t0001g0038 a0001c0001t0001g0050 |
2 | HG02027.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.817-5403A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164514255 | |||||||
| chr2:164514374 | T | A | 1 | a0002c0002t0003g0206 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.817-5522A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164514374 | |||||||
| chr2:164514916 | C | T | 1 | a0001c0001t0001g0005 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.817-6064G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164514916 | |||||||
| chr2:164514923 | C | T | 24 | a0001c0001t0001g0082 a0001c0001t0001g0121 a0001c0001t0007g0073 others(21): Show |
24 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.817-6071G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164514923 | |||||||
| chr2:164514925 | T | C | 1 | a0006c0007t0003g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.817-6073A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164514925 | |||||||
| chr2:164515230 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.817-6378G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164515230 | |||||||
| chr2:164515255 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.817-6403G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164515255 | |||||||
| chr2:164515287 | T | C | 1 | a0007c0011t0007g0128 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.817-6435A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164515287 | |||||||
| chr2:164515511 | G | A | 1 | a0006c0007t0003g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.816+6469C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164515511 | |||||||
| chr2:164515518 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.816+6462G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164515518 | |||||||
| chr2:164515748 | T | G | 4 | a0001c0001t0001g0013 a0001c0001t0001g0095 a0001c0001t0001g0097 others(1): Show |
4 | HG01261.hp2 HG02818.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+6232A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164515748 | |||||||
| chr2:164515803 | G | GA | 159 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(156): Show |
160 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.816+6176dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164515803 | |||||||
| chr2:164515803 | G | GAA | 23 | a0001c0001t0001g0022 a0001c0001t0001g0085 a0001c0001t0001g0100 others(20): Show |
24 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.816+6175_816+6176d others(4): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164515803 | |||||||
| chr2:164515879 | A | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0019 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.816+6101T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164515879 | |||||||
| chr2:164516007 | A | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0019 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.816+5973T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164516007 | |||||||
| chr2:164516026 | T | A | 1 | a0001c0001t0004g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.816+5954A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164516026 | |||||||
| chr2:164516076 | G | T | 12 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0137 others(9): Show |
12 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.816+5904C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164516076 | |||||||
| chr2:164516435 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0135 a0001c0001t0004g0043 others(3): Show |
6 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.816+5545G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164516435 | |||||||
| chr2:164516795 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0006g0143 a0001c0001t0006g0144 |
3 | NA18954.hp1 NA18974.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.816+5185C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164516795 | |||||||
| chr2:164516883 | G | C | 2 | a0002c0002t0005g0222 a0002c0002t0005g0269 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.816+5097C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164516883 | |||||||
| chr2:164516900 | T | C | 4 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0150 others(1): Show |
4 | HG02257.hp1 HG02886.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+5080A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164516900 | |||||||
| chr2:164516948 | C | A | 7 | a0001c0001t0004g0108 a0001c0001t0004g0109 a0001c0001t0004g0110 others(4): Show |
7 | HG02055.hp2 HG02280.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+5032G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164516948 | |||||||
| chr2:164517041 | C | T | 1 | a0002c0002t0003g0245 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.816+4939G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164517041 | |||||||
| chr2:164517091 | G | T | 65 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0038 others(62): Show |
65 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.816+4889C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164517091 | |||||||
| chr2:164517253 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0048 |
2 | NA18979.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.816+4727C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164517253 | |||||||
| chr2:164517442 | A | T | 1 | a0001c0001t0001g0130 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.816+4538T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164517442 | |||||||
| chr2:164517450 | A | C | 89 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(86): Show |
89 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.816+4530T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164517450 | |||||||
| chr2:164517529 | A | G | 1 | a0002c0002t0002g0166 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.816+4451T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164517529 | |||||||
| chr2:164518152 | G | C | 3 | a0001c0001t0004g0098 a0001c0001t0004g0099 a0001c0001t0007g0104 |
3 | HG02622.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.816+3828C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164518152 | |||||||
| chr2:164518186 | T | G | 1 | a0006c0007t0003g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.816+3794A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164518186 | |||||||
| chr2:164518734 | A | G | 1 | a0001c0001t0001g0131 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.816+3246T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164518734 | |||||||
| chr2:164519019 | T | C | 2 | a0001c0001t0001g0037 a0002c0002t0002g0262 |
2 | NA18972.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.816+2961A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164519019 | |||||||
| chr2:164519270 | T | C | 25 | a0001c0001t0001g0082 a0001c0001t0001g0121 a0001c0001t0007g0073 others(22): Show |
25 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.816+2710A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164519270 | |||||||
| chr2:164519841 | A | G | 1 | a0001c0001t0006g0001 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.816+2139T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164519841 | |||||||
| chr2:164519869 | C | A | 1 | a0004c0008t0013g0229 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.816+2111G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164519869 | |||||||
| chr2:164520101 | C | T | 1 | a0006c0007t0003g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.816+1879G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164520101 | |||||||
| chr2:164520298 | G | A | 24 | a0001c0001t0001g0082 a0001c0001t0001g0121 a0001c0001t0007g0073 others(21): Show |
24 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.816+1682C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164520298 | |||||||
| chr2:164520304 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.816+1676A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164520304 | |||||||
| chr2:164520358 | A | C | 1 | a0001c0001t0001g0075 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.816+1622T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164520358 | |||||||
| chr2:164520536 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.816+1444G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164520536 | |||||||
| chr2:164520593 | T | C | 22 | a0001c0001t0004g0011 a0001c0001t0004g0029 a0001c0001t0008g0153 others(19): Show |
23 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.816+1387A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164520593 | |||||||
| chr2:164520650 | A | G | 1 | a0002c0002t0003g0289 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.816+1330T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164520650 | |||||||
| chr2:164520771 | C | A | 1 | a0004c0008t0013g0229 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.816+1209G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164520771 | |||||||
| chr2:164521030 | A | C | 1 | a0001c0001t0004g0065 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.816+950T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164521030 | |||||||
| chr2:164521049 | T | C | 1 | a0006c0007t0003g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.816+931A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164521049 | |||||||
| chr2:164521101 | A | T | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.816+879T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164521101 | |||||||
| chr2:164521396 | T | G | 3 | a0001c0001t0004g0004 a0002c0002t0002g0207 a0002c0002t0002g0260 |
3 | HG00673.hp2 HG01433.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.816+584A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164521396 | |||||||
| chr2:164521412 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.816+568A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164521412 | |||||||
| chr2:164521623 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.816+357C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164521623 | |||||||
| chr2:164521670 | A | G | 11 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0137 others(8): Show |
11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.816+310T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164521670 | |||||||
| chr2:164521820 | T | C | 8 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0078 others(5): Show |
8 | HG01891.hp2 HG02630.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.816+160A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164521820 | |||||||
| chr2:164521917 | C | A | 25 | a0001c0001t0001g0082 a0001c0001t0001g0121 a0001c0001t0007g0073 others(22): Show |
25 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.816+63G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 6/13 | chr2 | 164521917 | |||||||
| chr2:164522324 | T | A | 1 | a0002c0002t0002g0175 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.679-207A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164522324 | |||||||
| chr2:164522444 | G | A | 1 | a0002c0002t0003g0165 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.679-327C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164522444 | |||||||
| chr2:164522454 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.679-337A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164522454 | |||||||
| chr2:164522635 | G | A | 2 | a0001c0003t0001g0049 a0001c0003t0007g0067 |
2 | HG00609.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.679-518C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164522635 | |||||||
| chr2:164522659 | G | A | 13 | a0001c0001t0001g0100 a0001c0001t0001g0106 a0001c0001t0001g0120 others(10): Show |
13 | HG01175.hp2 HG02258.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.679-542C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164522659 | |||||||
| chr2:164522840 | C | T | 9 | a0001c0001t0001g0118 a0002c0002t0003g0186 a0002c0002t0003g0187 others(6): Show |
9 | HG00738.hp1 HG01106.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.679-723G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164522840 | |||||||
| chr2:164523054 | G | C | 1 | a0001c0001t0004g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.679-937C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164523054 | |||||||
| chr2:164523068 | G | A | 1 | a0001c0001t0001g0016 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.679-951C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164523068 | |||||||
| chr2:164523107 | G | C | 1 | a0002c0002t0005g0178 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.679-990C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164523107 | |||||||
| chr2:164523188 | G | A | 2 | a0002c0002t0002g0168 a0002c0002t0002g0254 |
2 | HG00099.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.679-1071C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164523188 | |||||||
| chr2:164523211 | C | G | 6 | a0001c0001t0001g0117 a0001c0001t0001g0131 a0001c0001t0001g0134 others(3): Show |
6 | HG02109.hp2 HG02257.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.679-1094G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164523211 | |||||||
| chr2:164523251 | A | C | 25 | a0001c0001t0001g0082 a0001c0001t0001g0121 a0001c0001t0007g0073 others(22): Show |
25 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.679-1134T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164523251 | |||||||
| chr2:164523412 | C | T | 1 | a0002c0002t0003g0205 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.679-1295G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164523412 | |||||||
| chr2:164523417 | A | T | 2 | a0001c0001t0004g0024 a0002c0002t0002g0174 |
2 | NA18955.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.679-1300T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164523417 | |||||||
| chr2:164523908 | G | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0135 a0001c0001t0004g0043 others(3): Show |
6 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.678+1096C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164523908 | |||||||
| chr2:164524066 | A | G | 1 | a0002c0002t0003g0271 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.678+938T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164524066 | |||||||
| chr2:164524323 | A | G | 3 | a0001c0001t0007g0112 a0001c0001t0007g0114 a0002c0002t0005g0180 |
3 | HG02572.hp2 HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.678+681T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164524323 | |||||||
| chr2:164524342 | A | G | 4 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0004g0021 others(1): Show |
4 | HG02080.hp2 HG02165.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.678+662T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164524342 | |||||||
| chr2:164524396 | T | C | 24 | a0001c0001t0001g0082 a0001c0001t0001g0121 a0001c0001t0007g0073 others(21): Show |
24 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.678+608A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164524396 | |||||||
| chr2:164524517 | T | C | 1 | a0001c0001t0001g0025 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.678+487A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164524517 | |||||||
| chr2:164524844 | T | C | 2 | a0001c0001t0001g0009 a0002c0002t0002g0162 |
2 | HG01255.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.678+160A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164524844 | |||||||
| chr2:164524959 | T | C | 11 | a0001c0001t0001g0100 a0001c0001t0001g0106 a0001c0001t0001g0120 others(8): Show |
11 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.678+45A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 5/13 | chr2 | 164524959 | |||||||
| chr2:164525105 | C | T | 3 | a0001c0001t0001g0090 a0001c0001t0011g0087 a0001c0001t0011g0091 |
3 | HG00735.hp1 HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.604-27G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/13 | chr2 | 164525105 | |||||||
| chr2:164525107 | C | T | 11 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0137 others(8): Show |
11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.604-29G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/13 | chr2 | 164525107 | |||||||
| chr2:164525375 | A | C | 1 | a0006c0007t0003g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.604-297T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/13 | chr2 | 164525375 | |||||||
| chr2:164525411 | G | C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0019 |
2 | HG03195.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.604-333C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/13 | chr2 | 164525411 | |||||||
| chr2:164525438 | C | A | 1 | a0006c0007t0003g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.604-360G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/13 | chr2 | 164525438 | |||||||
| chr2:164525790 | C | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0019 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.604-712G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/13 | chr2 | 164525790 | |||||||
| chr2:164526032 | T | C | 1 | a0006c0007t0003g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.604-954A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/13 | chr2 | 164526032 | |||||||
| chr2:164526062 | A | C | 12 | a0001c0001t0001g0100 a0001c0001t0001g0106 a0001c0001t0001g0120 others(9): Show |
12 | HG01175.hp2 HG02258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.603+952T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/13 | chr2 | 164526062 | |||||||
| chr2:164526237 | A | G | 2 | a0001c0001t0004g0046 a0002c0002t0003g0236 |
2 | HG02056.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.603+777T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/13 | chr2 | 164526237 | |||||||
| chr2:164526274 | C | T | 9 | a0001c0001t0001g0118 a0002c0002t0003g0186 a0002c0002t0003g0187 others(6): Show |
9 | HG00738.hp1 HG01106.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.603+740G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/13 | chr2 | 164526274 | |||||||
| chr2:164526294 | T | C | 3 | a0002c0002t0003g0160 a0002c0002t0003g0182 a0002c0002t0003g0184 |
3 | HG02738.hp1 HG03017.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.603+720A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/13 | chr2 | 164526294 | |||||||
| chr2:164526528 | C | T | 13 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(10): Show |
13 | HG01255.hp2 HG01261.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.603+486G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/13 | chr2 | 164526528 | |||||||
| chr2:164526574 | C | A | 13 | a0001c0001t0001g0117 a0001c0001t0001g0131 a0001c0001t0001g0134 others(10): Show |
13 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.603+440G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/13 | chr2 | 164526574 | |||||||
| chr2:164526613 | T | C | 3 | a0001c0001t0001g0090 a0001c0001t0011g0087 a0001c0001t0011g0091 |
3 | HG00735.hp1 HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.603+401A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/13 | chr2 | 164526613 | |||||||
| chr2:164526667 | G | C | 1 | a0002c0002t0005g0267 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.603+347C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 4/13 | chr2 | 164526667 | |||||||
| chr2:164527151 | C | T | 3 | a0001c0001t0010g0140 a0002c0002t0002g0273 a0002c0002t0002g0275 |
3 | HG01123.hp1 HG01175.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.482-16G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527151 | |||||||
| chr2:164527174 | CAAATATA others(1): Show |
C | 3 | a0001c0001t0004g0011 a0002c0002t0002g0252 a0002c0002t0003g0214 |
3 | HG00140.hp1 HG00140.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.482-47_482-40delAT others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527174 | |||||||
| chr2:164527175 | AAATATAT others(4): Show |
A | 1 | a0002c0002t0003g0283 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.482-51_482-41delAT others(9): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527175 | |||||||
| chr2:164527176 | A | AAT | 9 | a0001c0001t0001g0016 a0001c0001t0001g0038 a0001c0001t0001g0051 others(6): Show |
9 | HG01175.hp1 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.482-43_482-42dupAT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | |||||||
| chr2:164527176 | A | AATAT | 4 | a0001c0001t0001g0039 a0001c0001t0001g0053 a0001c0001t0008g0142 others(1): Show |
4 | HG00733.hp1 HG01099.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.482-45_482-42dupAT others(2): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | |||||||
| chr2:164527176 | A | AATATAT | 6 | a0001c0001t0001g0040 a0001c0001t0001g0075 a0001c0001t0008g0141 others(3): Show |
6 | HG00408.hp1 HG00438.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.482-47_482-42dupAT others(4): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | |||||||
| chr2:164527176 | A | AATATATA others(5): Show |
1 | a0001c0001t0001g0032 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.482-53_482-42dupAT others(10): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | |||||||
| chr2:164527176 | A | T | 1 | a0001c0001t0001g0063 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.482-41T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | |||||||
| chr2:164527176 | AAT | A | 29 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0066 others(26): Show |
29 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.482-43_482-42delAT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | |||||||
| chr2:164527176 | AATAT | A | 36 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0044 others(33): Show |
36 | HG00408.hp2 HG00738.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.482-45_482-42delAT others(2): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | |||||||
| chr2:164527176 | AATATAT | A | 36 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0037 others(33): Show |
37 | HG00609.hp2 HG00673.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.482-47_482-42delAT others(4): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | |||||||
| chr2:164527176 | AATATATA others(1): Show |
A | 30 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0028 others(27): Show |
30 | HG00639.hp2 HG00735.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.482-49_482-42delAT others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | |||||||
| chr2:164527176 | AATATATA others(3): Show |
A | 25 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0061 others(22): Show |
25 | HG00642.hp1 HG00733.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.482-51_482-42delAT others(8): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | |||||||
| chr2:164527176 | AATATATA others(5): Show |
A | 31 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0085 others(28): Show |
32 | HG00544.hp1 HG01069.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.482-53_482-42delAT others(10): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | |||||||
| chr2:164527176 | AATATATA others(7): Show |
A | 20 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0092 others(17): Show |
20 | HG01123.hp2 HG02055.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.482-55_482-42delAT others(12): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | |||||||
| chr2:164527176 | AATATATA others(9): Show |
A | 25 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0082 others(22): Show |
25 | HG00639.hp1 HG00642.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.482-57_482-42delAT others(14): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | |||||||
| chr2:164527176 | AATATATA others(11): Show |
A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0135 a0001c0001t0004g0043 others(5): Show |
8 | HG00099.hp1 HG00609.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.482-59_482-42delAT others(16): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | |||||||
| chr2:164527176 | AATATATA others(13): Show |
A | 1 | a0001c0003t0001g0049 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.482-61_482-42delAT others(18): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | |||||||
| chr2:164527176 | AATATATA others(15): Show |
A | 1 | a0002c0002t0002g0254 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.482-63_482-42delAT others(20): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | |||||||
| chr2:164527176 | AATATATA others(19): Show |
A | 1 | a0001c0001t0004g0076 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.482-67_482-42delAT others(24): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | |||||||
| chr2:164527176 | AATATATA others(23): Show |
A | 1 | a0001c0001t0001g0113 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.482-71_482-42delAT others(28): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527176 | |||||||
| chr2:164527218 | T | C | 1 | a0001c0001t0009g0102 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.482-83A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527218 | |||||||
| chr2:164527220 | T | C | 36 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0028 others(33): Show |
36 | HG00639.hp2 HG00738.hp2 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.482-85A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527220 | |||||||
| chr2:164527259 | G | A | 1 | a0001c0001t0004g0062 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.482-124C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527259 | |||||||
| chr2:164527522 | A | C | 1 | a0001c0001t0001g0113 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.482-387T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164527522 | |||||||
| chr2:164528027 | C | T | 1 | a0006c0007t0003g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.482-892G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164528027 | |||||||
| chr2:164528177 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.482-1042C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164528177 | |||||||
| chr2:164528304 | C | T | 1 | a0001c0001t0006g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.482-1169G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164528304 | |||||||
| chr2:164528548 | T | G | 195 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(192): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.482-1413A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164528548 | |||||||
| chr2:164528600 | T | C | 3 | a0003c0004t0008g0152 a0003c0004t0008g0155 a0008c0009t0005g0250 |
3 | HG01099.hp1 HG03654.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.482-1465A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164528600 | |||||||
| chr2:164528740 | C | G | 1 | a0001c0001t0001g0129 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.482-1605G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164528740 | |||||||
| chr2:164528742 | A | C | 1 | a0006c0007t0003g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.482-1607T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164528742 | |||||||
| chr2:164528747 | G | A | 5 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0009g0102 others(2): Show |
5 | HG02258.hp1 HG02486.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.482-1612C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164528747 | |||||||
| chr2:164528932 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.482-1797C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164528932 | |||||||
| chr2:164529241 | T | C | 4 | a0001c0001t0001g0085 a0001c0001t0006g0001 a0002c0002t0003g0289 others(1): Show |
5 | HG01069.hp1 HG01071.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.482-2106A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164529241 | |||||||
| chr2:164529337 | C | T | 1 | a0001c0001t0001g0030 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-2202G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164529337 | |||||||
| chr2:164529350 | T | G | 1 | a0007c0011t0007g0128 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.482-2215A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164529350 | |||||||
| chr2:164529375 | C | T | 1 | a0006c0007t0003g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.482-2240G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164529375 | |||||||
| chr2:164529398 | A | G | 1 | a0006c0007t0003g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.482-2263T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164529398 | |||||||
| chr2:164529438 | C | T | 8 | a0001c0001t0001g0007 a0001c0001t0001g0092 a0001c0001t0001g0093 others(5): Show |
8 | HG02109.hp1 HG02572.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.482-2303G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164529438 | |||||||
| chr2:164529528 | G | A | 1 | a0002c0002t0003g0206 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.482-2393C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164529528 | |||||||
| chr2:164529571 | C | T | 3 | a0001c0001t0001g0090 a0001c0001t0011g0087 a0001c0001t0011g0091 |
3 | HG00735.hp1 HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.482-2436G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164529571 | |||||||
| chr2:164529747 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.482-2612A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164529747 | |||||||
| chr2:164529800 | G | C | 3 | a0001c0001t0001g0090 a0001c0001t0011g0087 a0001c0001t0011g0091 |
3 | HG00735.hp1 HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.482-2665C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164529800 | |||||||
| chr2:164529803 | T | C | 3 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0001g0122 |
3 | HG02109.hp1 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.482-2668A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164529803 | |||||||
| chr2:164529998 | T | C | 213 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(210): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.482-2863A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164529998 | |||||||
| chr2:164530085 | G | A | 1 | a0006c0007t0003g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.482-2950C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164530085 | |||||||
| chr2:164530184 | G | A | 8 | a0001c0001t0001g0120 a0001c0001t0001g0124 a0001c0001t0001g0126 others(5): Show |
8 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.482-3049C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164530184 | |||||||
| chr2:164530273 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.482-3138A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164530273 | |||||||
| chr2:164530292 | G | A | 2 | a0001c0001t0006g0151 a0001c0001t0006g0159 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.482-3157C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164530292 | |||||||
| chr2:164530361 | C | T | 1 | a0001c0001t0004g0029 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.482-3226G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164530361 | |||||||
| chr2:164530436 | G | C | 3 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0006g0145 |
3 | NA18940.hp1 NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.482-3301C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164530436 | |||||||
| chr2:164530552 | A | C | 1 | a0001c0001t0006g0148 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.482-3417T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164530552 | |||||||
| chr2:164530606 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.482-3471C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164530606 | |||||||
| chr2:164530807 | G | C | 1 | a0001c0001t0001g0041 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.482-3672C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164530807 | |||||||
| chr2:164530886 | T | G | 1 | a0002c0002t0003g0258 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.482-3751A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164530886 | |||||||
| chr2:164531003 | G | T | 1 | a0001c0001t0001g0131 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.482-3868C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164531003 | |||||||
| chr2:164531117 | C | A | 1 | a0001c0003t0001g0049 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.482-3982G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164531117 | |||||||
| chr2:164531370 | T | C | 101 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(98): Show |
101 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.482-4235A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164531370 | |||||||
| chr2:164531467 | T | G | 48 | a0001c0001t0001g0006 a0001c0001t0001g0061 a0001c0001t0001g0064 others(45): Show |
50 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(47): Show |
intron_variant | MODIFIER | c.482-4332A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164531467 | |||||||
| chr2:164531478 | C | T | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.482-4343G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164531478 | |||||||
| chr2:164531596 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.482-4461G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164531596 | |||||||
| chr2:164531859 | C | T | 1 | a0001c0001t0001g0005 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.482-4724G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164531859 | |||||||
| chr2:164531903 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.482-4768T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164531903 | |||||||
| chr2:164531963 | C | T | 8 | a0001c0001t0001g0007 a0001c0001t0001g0092 a0001c0001t0001g0093 others(5): Show |
8 | HG02109.hp1 HG02572.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.482-4828G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164531963 | |||||||
| chr2:164532108 | G | C | 1 | a0002c0002t0003g0176 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.482-4973C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164532108 | |||||||
| chr2:164532148 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.482-5013A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164532148 | |||||||
| chr2:164532196 | T | C | 1 | a0001c0001t0004g0015 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.482-5061A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164532196 | |||||||
| chr2:164532226 | A | C | 1 | a0001c0001t0001g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.482-5091T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164532226 | |||||||
| chr2:164532390 | A | G | 195 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(192): Show |
197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.482-5255T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164532390 | |||||||
| chr2:164532577 | T | C | 2 | a0001c0001t0008g0141 a0001c0001t0008g0142 |
2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.482-5442A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164532577 | |||||||
| chr2:164532585 | G | C | 1 | a0006c0007t0003g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.482-5450C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164532585 | |||||||
| chr2:164532914 | G | A | 24 | a0001c0001t0001g0082 a0001c0001t0001g0121 a0001c0001t0007g0073 others(21): Show |
24 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.482-5779C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164532914 | |||||||
| chr2:164533053 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.482-5918T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164533053 | |||||||
| chr2:164533124 | C | T | 1 | a0002c0002t0002g0190 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.482-5989G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164533124 | |||||||
| chr2:164533224 | C | CT | 28 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0084 others(25): Show |
28 | HG00438.hp1 HG00642.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.482-6090dupA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164533224 | |||||||
| chr2:164533224 | CT | C | 98 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(95): Show |
98 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.482-6090delA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164533224 | |||||||
| chr2:164533224 | CTT | C | 10 | a0001c0001t0001g0008 a0001c0001t0001g0054 a0001c0001t0001g0135 others(7): Show |
10 | HG01255.hp1 HG01891.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.482-6091_482-6090d others(4): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164533224 | |||||||
| chr2:164533224 | CTTTTTTT others(3): Show |
C | 11 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0137 others(8): Show |
11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.482-6099_482-6090d others(12): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164533224 | |||||||
| chr2:164533279 | G | A | 2 | a0001c0003t0001g0049 a0001c0003t0007g0067 |
2 | HG00609.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.482-6144C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164533279 | |||||||
| chr2:164533408 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.482-6273T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164533408 | |||||||
| chr2:164533474 | C | A | 5 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0009g0102 others(2): Show |
5 | HG02258.hp1 HG02486.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.482-6339G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164533474 | |||||||
| chr2:164533734 | T | C | 1 | a0007c0011t0007g0128 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.482-6599A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164533734 | |||||||
| chr2:164533818 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.482-6683G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164533818 | |||||||
| chr2:164533931 | G | T | 1 | a0001c0001t0001g0131 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.482-6796C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164533931 | |||||||
| chr2:164534024 | C | T | 1 | a0001c0001t0010g0154 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.482-6889G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164534024 | |||||||
| chr2:164534055 | T | G | 11 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0137 others(8): Show |
11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.482-6920A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164534055 | |||||||
| chr2:164534108 | A | G | 3 | a0001c0001t0001g0090 a0001c0001t0011g0087 a0001c0001t0011g0091 |
3 | HG00735.hp1 HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.482-6973T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164534108 | |||||||
| chr2:164534276 | A | G | 1 | a0002c0002t0003g0206 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.482-7141T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164534276 | |||||||
| chr2:164534417 | T | G | 1 | a0001c0001t0007g0073 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.482-7282A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164534417 | |||||||
| chr2:164534480 | A | G | 1 | a0002c0002t0002g0235 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.482-7345T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164534480 | |||||||
| chr2:164534541 | G | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0135 a0001c0001t0004g0043 others(3): Show |
6 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.482-7406C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164534541 | |||||||
| chr2:164534710 | C | A | 1 | a0006c0007t0003g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.482-7575G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164534710 | |||||||
| chr2:164535262 | T | C | 1 | a0006c0007t0003g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.482-8127A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164535262 | |||||||
| chr2:164535512 | C | T | 3 | a0001c0001t0007g0073 a0002c0002t0002g0215 a0002c0002t0002g0237 |
3 | HG00735.hp2 HG01169.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.482-8377G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164535512 | |||||||
| chr2:164535520 | G | A | 1 | a0001c0001t0007g0136 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.482-8385C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164535520 | |||||||
| chr2:164535821 | G | A | 1 | a0001c0001t0004g0058 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.482-8686C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164535821 | |||||||
| chr2:164535826 | T | C | 2 | a0001c0001t0001g0009 a0002c0002t0002g0162 |
2 | HG01255.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.482-8691A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164535826 | |||||||
| chr2:164535877 | G | A | 1 | a0001c0001t0006g0150 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.482-8742C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164535877 | |||||||
| chr2:164536135 | A | G | 68 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0038 others(65): Show |
68 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.482-9000T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164536135 | |||||||
| chr2:164536415 | GTTTA | G | 12 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0137 others(9): Show |
12 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.482-9284_482-9281d others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164536415 | |||||||
| chr2:164536442 | A | G | 1 | a0001c0001t0008g0153 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.482-9307T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164536442 | |||||||
| chr2:164536559 | G | A | 1 | a0006c0007t0003g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.482-9424C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164536559 | |||||||
| chr2:164536644 | A | G | 1 | a0001c0001t0010g0157 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.482-9509T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164536644 | |||||||
| chr2:164536645 | A | G | 1 | a0001c0001t0004g0059 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.482-9510T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164536645 | |||||||
| chr2:164536742 | A | G | 96 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0038 others(93): Show |
96 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.482-9607T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164536742 | |||||||
| chr2:164536788 | T | C | 1 | a0001c0001t0001g0068 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.482-9653A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164536788 | |||||||
| chr2:164536847 | G | T | 194 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(191): Show |
196 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.482-9712C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164536847 | |||||||
| chr2:164537168 | T | A | 3 | a0001c0001t0001g0026 a0001c0001t0006g0143 a0001c0001t0006g0144 |
3 | NA18954.hp1 NA18974.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.482-10033A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164537168 | |||||||
| chr2:164537272 | G | T | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.482-10137C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164537272 | |||||||
| chr2:164537536 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.481+10124C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164537536 | |||||||
| chr2:164537693 | G | A | 1 | a0001c0001t0006g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.481+9967C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164537693 | |||||||
| chr2:164537760 | A | G | 10 | a0001c0001t0001g0118 a0002c0002t0002g0243 a0002c0002t0003g0186 others(7): Show |
10 | HG00738.hp1 HG01106.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.481+9900T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164537760 | |||||||
| chr2:164537773 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.481+9887C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164537773 | |||||||
| chr2:164537981 | A | C | 1 | a0002c0002t0003g0002 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.481+9679T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164537981 | |||||||
| chr2:164538001 | T | TA | 9 | a0002c0002t0005g0163 a0002c0002t0005g0197 a0002c0002t0005g0217 others(6): Show |
9 | HG00642.hp2 HG01257.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.481+9658dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164538001 | |||||||
| chr2:164538070 | T | G | 46 | a0001c0001t0001g0006 a0001c0001t0001g0061 a0001c0001t0001g0064 others(43): Show |
48 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(45): Show |
intron_variant | MODIFIER | c.481+9590A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164538070 | |||||||
| chr2:164538176 | A | G | 1 | a0002c0002t0002g0273 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.481+9484T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164538176 | |||||||
| chr2:164538670 | A | C | 2 | a0001c0001t0006g0147 a0001c0001t0007g0136 |
2 | HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.481+8990T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164538670 | |||||||
| chr2:164538857 | T | C | 4 | a0001c0001t0004g0043 a0001c0001t0004g0089 a0001c0001t0004g0133 others(1): Show |
4 | HG02280.hp2 HG02559.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.481+8803A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164538857 | |||||||
| chr2:164538874 | A | G | 1 | a0006c0007t0003g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.481+8786T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164538874 | |||||||
| chr2:164538927 | C | T | 194 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(191): Show |
196 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.481+8733G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164538927 | |||||||
| chr2:164538996 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.481+8664C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164538996 | |||||||
| chr2:164539447 | C | G | 3 | a0002c0002t0002g0211 a0002c0002t0002g0212 a0002c0002t0003g0214 |
3 | NA18979.hp2 NA19065.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.481+8213G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164539447 | |||||||
| chr2:164539475 | G | GA | 195 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(192): Show |
197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.481+8184dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164539475 | |||||||
| chr2:164539503 | T | A | 4 | a0001c0001t0001g0084 a0001c0001t0001g0105 a0001c0001t0006g0151 others(1): Show |
4 | HG02258.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.481+8157A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164539503 | |||||||
| chr2:164539753 | A | C | 2 | a0002c0002t0002g0170 a0002c0002t0003g0205 |
2 | HG02083.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.481+7907T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164539753 | |||||||
| chr2:164539902 | T | C | 1 | a0001c0005t0007g0072 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.481+7758A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164539902 | |||||||
| chr2:164540440 | C | G | 4 | a0001c0001t0001g0094 a0001c0001t0001g0096 a0001c0001t0001g0101 others(1): Show |
4 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.481+7220G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164540440 | |||||||
| chr2:164540682 | T | C | 1 | a0002c0002t0003g0232 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.481+6978A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164540682 | |||||||
| chr2:164540719 | A | G | 1 | a0006c0007t0003g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.481+6941T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164540719 | |||||||
| chr2:164541132 | G | A | 1 | a0001c0001t0006g0150 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.481+6528C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164541132 | |||||||
| chr2:164541233 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.481+6427G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164541233 | |||||||
| chr2:164541428 | C | T | 1 | a0004c0008t0013g0229 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.481+6232G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164541428 | |||||||
| chr2:164541579 | C | T | 11 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0137 others(8): Show |
11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.481+6081G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164541579 | |||||||
| chr2:164541749 | G | T | 67 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0038 others(64): Show |
67 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.481+5911C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164541749 | |||||||
| chr2:164541795 | C | T | 5 | a0002c0002t0002g0216 a0002c0002t0002g0281 a0002c0002t0003g0160 others(2): Show |
5 | HG02738.hp1 HG03017.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.481+5865G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164541795 | |||||||
| chr2:164541873 | G | A | 18 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(15): Show |
18 | HG01255.hp2 HG01261.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.481+5787C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164541873 | |||||||
| chr2:164541890 | T | C | 3 | a0001c0001t0001g0090 a0001c0001t0011g0087 a0001c0001t0011g0091 |
3 | HG00735.hp1 HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.481+5770A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164541890 | |||||||
| chr2:164542665 | G | C | 3 | a0002c0002t0003g0160 a0002c0002t0003g0182 a0002c0002t0003g0184 |
3 | HG02738.hp1 HG03017.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.481+4995C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164542665 | |||||||
| chr2:164542822 | A | G | 1 | a0002c0002t0003g0206 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.481+4838T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164542822 | |||||||
| chr2:164542831 | G | A | 1 | a0001c0001t0004g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.481+4829C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164542831 | |||||||
| chr2:164543117 | A | G | 1 | a0002c0002t0003g0241 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.481+4543T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164543117 | |||||||
| chr2:164543126 | C | G | 1 | a0001c0001t0001g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.481+4534G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164543126 | |||||||
| chr2:164543142 | T | TA | 12 | a0001c0001t0001g0083 a0001c0001t0001g0124 a0001c0001t0001g0126 others(9): Show |
12 | HG01516.hp1 HG01517.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.481+4517dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164543142 | |||||||
| chr2:164543143 | A | T | 1 | a0001c0001t0001g0113 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.481+4517T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164543143 | |||||||
| chr2:164543186 | A | T | 1 | a0001c0001t0006g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.481+4474T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164543186 | |||||||
| chr2:164543232 | C | T | 2 | a0001c0001t0001g0105 a0002c0002t0003g0177 |
2 | HG02896.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.481+4428G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164543232 | |||||||
| chr2:164543721 | T | C | 1 | a0001c0001t0004g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.481+3939A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164543721 | |||||||
| chr2:164543928 | G | A | 1 | a0002c0002t0003g0201 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.481+3732C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164543928 | |||||||
| chr2:164544180 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.481+3480G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164544180 | |||||||
| chr2:164544241 | G | C | 1 | a0001c0001t0001g0131 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.481+3419C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164544241 | |||||||
| chr2:164544414 | T | G | 1 | a0002c0002t0003g0177 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.481+3246A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164544414 | |||||||
| chr2:164544619 | C | A | 3 | a0002c0002t0002g0219 a0002c0002t0002g0224 a0002c0002t0002g0230 |
3 | NA18974.hp1 NA19065.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.481+3041G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164544619 | |||||||
| chr2:164544691 | A | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0079 |
2 | NA19006.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.481+2969T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164544691 | |||||||
| chr2:164544746 | A | C | 1 | a0001c0001t0001g0054 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.481+2914T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164544746 | |||||||
| chr2:164544977 | A | G | 44 | a0001c0001t0001g0006 a0001c0001t0001g0061 a0001c0001t0001g0064 others(41): Show |
46 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(43): Show |
intron_variant | MODIFIER | c.481+2683T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164544977 | |||||||
| chr2:164545136 | A | C | 1 | a0006c0007t0003g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.481+2524T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164545136 | |||||||
| chr2:164545217 | A | G | 1 | a0001c0001t0006g0149 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.481+2443T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164545217 | |||||||
| chr2:164545240 | G | A | 2 | a0002c0002t0002g0216 a0002c0002t0002g0281 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.481+2420C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164545240 | |||||||
| chr2:164545291 | T | C | 110 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(107): Show |
110 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.481+2369A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164545291 | |||||||
| chr2:164545714 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.481+1946T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164545714 | |||||||
| chr2:164545944 | A | G | 1 | a0001c0001t0001g0071 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.481+1716T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164545944 | |||||||
| chr2:164546028 | A | G | 46 | a0001c0001t0001g0006 a0001c0001t0001g0061 a0001c0001t0001g0064 others(43): Show |
48 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(45): Show |
intron_variant | MODIFIER | c.481+1632T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164546028 | |||||||
| chr2:164546783 | C | G | 1 | a0001c0001t0001g0131 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.481+877G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164546783 | |||||||
| chr2:164547118 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.481+542C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164547118 | |||||||
| chr2:164547433 | T | C | 2 | a0002c0002t0002g0256 a0002c0002t0002g0291 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.481+227A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 3/13 | chr2 | 164547433 | |||||||
| chr2:164548076 | C | A | 1 | a0001c0001t0001g0134 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.325-260G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164548076 | |||||||
| chr2:164548284 | C | A | 1 | a0001c0001t0001g0070 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.325-468G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164548284 | |||||||
| chr2:164548396 | G | T | 2 | a0001c0001t0001g0022 a0001c0001t0004g0074 |
2 | NA18985.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.325-580C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164548396 | |||||||
| chr2:164548492 | T | G | 2 | a0002c0002t0002g0202 a0002c0002t0002g0274 |
2 | HG03831.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.325-676A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164548492 | |||||||
| chr2:164548520 | G | T | 1 | a0001c0001t0001g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.325-704C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164548520 | |||||||
| chr2:164548581 | G | C | 1 | a0001c0001t0001g0113 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.325-765C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164548581 | |||||||
| chr2:164548733 | T | G | 1 | a0001c0001t0004g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.325-917A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164548733 | |||||||
| chr2:164548946 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.325-1130G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164548946 | |||||||
| chr2:164549026 | C | A | 3 | a0002c0002t0002g0198 a0002c0002t0002g0231 a0002c0002t0005g0233 |
3 | HG01975.hp1 HG02273.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.325-1210G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549026 | |||||||
| chr2:164549051 | A | AT | 47 | a0001c0001t0001g0006 a0001c0001t0001g0061 a0001c0001t0001g0064 others(44): Show |
49 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(46): Show |
intron_variant | MODIFIER | c.325-1236dupA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549051 | |||||||
| chr2:164549424 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.325-1608C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549424 | |||||||
| chr2:164549558 | T | C | 2 | a0002c0002t0002g0202 a0002c0002t0002g0274 |
2 | HG03831.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.325-1742A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549558 | |||||||
| chr2:164549563 | A | C | 1 | a0001c0001t0001g0025 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.325-1747T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549563 | |||||||
| chr2:164549566 | T | C | 3 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0001g0122 |
3 | HG02109.hp1 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.325-1750A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549566 | |||||||
| chr2:164549674 | C | T | 3 | a0001c0001t0004g0098 a0001c0001t0004g0099 a0001c0001t0007g0104 |
3 | HG02622.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.325-1858G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549674 | |||||||
| chr2:164549770 | A | C | 1 | a0006c0007t0003g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.325-1954T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549770 | |||||||
| chr2:164549863 | A | AAAAAT | 3 | a0001c0001t0001g0096 a0002c0002t0002g0166 a0002c0002t0002g0284 |
3 | HG01123.hp2 HG02630.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.325-2052_325-2048d others(7): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549863 | |||||||
| chr2:164549863 | A | AAAAATAA others(3): Show |
5 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0013 others(2): Show |
5 | HG01255.hp2 HG01261.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.325-2057_325-2048d others(12): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549863 | |||||||
| chr2:164549863 | A | AAAAATAA others(8): Show |
1 | a0001c0001t0001g0097 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.325-2062_325-2048d others(17): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549863 | |||||||
| chr2:164549863 | A | AAAAATAA others(13): Show |
3 | a0001c0001t0001g0009 a0001c0001t0001g0078 a0001c0001t0001g0094 |
3 | HG03041.hp1 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.325-2067_325-2048d others(22): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549863 | |||||||
| chr2:164549863 | A | AAAAATAA others(18): Show |
1 | a0001c0001t0001g0005 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.325-2072_325-2048d others(27): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549863 | |||||||
| chr2:164549863 | AAAAAT | A | 66 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0025 others(63): Show |
67 | HG00544.hp2 HG00639.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.325-2052_325-2048d others(7): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549863 | |||||||
| chr2:164549863 | AAAAATAA others(3): Show |
A | 61 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0028 others(58): Show |
62 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.325-2057_325-2048d others(12): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549863 | |||||||
| chr2:164549863 | AAAAATAA others(8): Show |
A | 81 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0022 others(78): Show |
81 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.325-2062_325-2048d others(17): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549863 | |||||||
| chr2:164549863 | AAAAATAA others(13): Show |
A | 28 | a0001c0001t0001g0041 a0001c0001t0001g0100 a0001c0001t0001g0106 others(25): Show |
28 | HG00673.hp1 HG00735.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.325-2067_325-2048d others(22): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549863 | |||||||
| chr2:164549863 | AAAAATAA others(18): Show |
A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0117 others(5): Show |
8 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.325-2072_325-2048d others(27): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549863 | |||||||
| chr2:164549863 | AAAAATAA others(23): Show |
A | 12 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0001g0127 others(9): Show |
12 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.325-2077_325-2048d others(32): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549863 | |||||||
| chr2:164549867 | A | C | 1 | a0001c0001t0004g0076 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.325-2051T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549867 | |||||||
| chr2:164549961 | C | T | 1 | a0001c0001t0006g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.325-2145G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164549961 | |||||||
| chr2:164550009 | T | C | 46 | a0001c0001t0001g0006 a0001c0001t0001g0061 a0001c0001t0001g0064 others(43): Show |
48 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(45): Show |
intron_variant | MODIFIER | c.325-2193A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164550009 | |||||||
| chr2:164550046 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.325-2230C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164550046 | |||||||
| chr2:164550056 | T | A | 1 | a0001c0001t0001g0113 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.325-2240A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164550056 | |||||||
| chr2:164550087 | C | T | 1 | a0002c0002t0003g0210 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.325-2271G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164550087 | |||||||
| chr2:164550121 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0135 a0001c0001t0004g0043 others(3): Show |
6 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.325-2305G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164550121 | |||||||
| chr2:164550299 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.325-2483A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164550299 | |||||||
| chr2:164550428 | C | A | 1 | a0002c0002t0003g0179 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.325-2612G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164550428 | |||||||
| chr2:164550491 | A | G | 1 | a0001c0001t0006g0001 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.325-2675T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164550491 | |||||||
| chr2:164550661 | G | A | 4 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0137 others(1): Show |
4 | HG02109.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.325-2845C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164550661 | |||||||
| chr2:164551012 | T | C | 1 | a0002c0002t0003g0271 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.325-3196A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164551012 | |||||||
| chr2:164551451 | C | T | 3 | a0001c0001t0001g0083 a0002c0002t0005g0222 a0002c0002t0005g0269 |
3 | HG01516.hp1 HG01517.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.325-3635G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164551451 | |||||||
| chr2:164551747 | A | C | 3 | a0001c0001t0004g0098 a0001c0001t0004g0099 a0001c0001t0007g0104 |
3 | HG02622.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.325-3931T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164551747 | |||||||
| chr2:164551761 | G | A | 11 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0137 others(8): Show |
11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.325-3945C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164551761 | |||||||
| chr2:164551824 | T | A | 1 | a0002c0002t0005g0255 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.325-4008A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164551824 | |||||||
| chr2:164551986 | C | A | 1 | a0002c0002t0003g0234 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.325-4170G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164551986 | |||||||
| chr2:164552083 | A | C | 1 | a0001c0001t0001g0113 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.325-4267T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164552083 | |||||||
| chr2:164552154 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.325-4338T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164552154 | |||||||
| chr2:164552190 | G | C | 1 | a0001c0001t0001g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.325-4374C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164552190 | |||||||
| chr2:164553206 | A | T | 177 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(174): Show |
179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.325-5390T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164553206 | |||||||
| chr2:164553207 | A | T | 1 | a0006c0007t0003g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.325-5391T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164553207 | |||||||
| chr2:164553397 | T | A | 1 | a0001c0001t0001g0050 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.325-5581A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164553397 | |||||||
| chr2:164553592 | T | C | 8 | a0001c0001t0001g0007 a0001c0001t0001g0092 a0001c0001t0001g0093 others(5): Show |
8 | HG02109.hp1 HG02572.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.325-5776A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164553592 | |||||||
| chr2:164553765 | G | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0135 a0001c0001t0004g0043 others(3): Show |
6 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.325-5949C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164553765 | |||||||
| chr2:164553795 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.325-5979A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164553795 | |||||||
| chr2:164553877 | C | T | 26 | a0001c0001t0001g0082 a0001c0001t0001g0121 a0001c0001t0004g0107 others(23): Show |
26 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.325-6061G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164553877 | |||||||
| chr2:164553895 | G | A | 2 | a0002c0002t0002g0262 a0002c0002t0002g0264 |
2 | NA18972.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.325-6079C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164553895 | |||||||
| chr2:164554618 | C | T | 18 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(15): Show |
18 | HG01255.hp2 HG01261.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.325-6802G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164554618 | |||||||
| chr2:164554619 | C | T | 45 | a0001c0001t0001g0006 a0001c0001t0001g0061 a0001c0001t0001g0064 others(42): Show |
47 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(44): Show |
intron_variant | MODIFIER | c.325-6803G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164554619 | |||||||
| chr2:164554692 | T | C | 68 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0038 others(65): Show |
68 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.325-6876A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164554692 | |||||||
| chr2:164554912 | T | C | 2 | a0001c0001t0001g0064 a0001c0001t0004g0065 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.325-7096A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164554912 | |||||||
| chr2:164555051 | C | T | 1 | a0001c0001t0001g0025 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.325-7235G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164555051 | |||||||
| chr2:164555149 | G | A | 2 | a0002c0002t0005g0222 a0002c0002t0005g0269 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.325-7333C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164555149 | |||||||
| chr2:164555268 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.325-7452G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164555268 | |||||||
| chr2:164555269 | G | A | 2 | a0001c0003t0001g0049 a0001c0003t0007g0067 |
2 | HG00609.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.325-7453C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164555269 | |||||||
| chr2:164555284 | G | A | 190 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(187): Show |
192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.325-7468C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164555284 | |||||||
| chr2:164555549 | T | C | 1 | a0002c0002t0003g0289 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.325-7733A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164555549 | |||||||
| chr2:164555895 | A | G | 2 | a0001c0001t0004g0059 a0002c0002t0003g0223 |
2 | HG01346.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.325-8079T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164555895 | |||||||
| chr2:164555930 | TTAATAGA others(12): Show |
T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0135 a0001c0001t0004g0043 others(3): Show |
6 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.325-8133_325-8115d others(21): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164555930 | |||||||
| chr2:164555965 | G | A | 1 | a0001c0001t0004g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.325-8149C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164555965 | |||||||
| chr2:164556128 | A | G | 1 | a0002c0002t0003g0292 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.325-8312T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164556128 | |||||||
| chr2:164556189 | T | A | 1 | a0001c0001t0004g0059 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.325-8373A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164556189 | |||||||
| chr2:164556230 | A | T | 1 | a0001c0001t0006g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.325-8414T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164556230 | |||||||
| chr2:164556874 | A | G | 70 | a0001c0001t0001g0006 a0001c0001t0001g0061 a0001c0001t0001g0064 others(67): Show |
72 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.325-9058T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164556874 | |||||||
| chr2:164556938 | AT | A | 29 | a0001c0001t0004g0011 a0001c0001t0004g0029 a0001c0001t0008g0153 others(26): Show |
30 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(27): Show |
intron_variant | MODIFIER | c.325-9123delA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164556938 | |||||||
| chr2:164557084 | T | C | 1 | a0006c0007t0003g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.325-9268A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164557084 | |||||||
| chr2:164557262 | T | G | 3 | a0002c0002t0002g0219 a0002c0002t0002g0224 a0002c0002t0002g0230 |
3 | NA18974.hp1 NA19065.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.325-9446A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164557262 | |||||||
| chr2:164557408 | T | C | 1 | a0001c0001t0007g0073 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.325-9592A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164557408 | |||||||
| chr2:164557642 | G | A | 1 | a0002c0002t0002g0172 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.325-9826C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164557642 | |||||||
| chr2:164557758 | A | G | 1 | a0001c0001t0004g0119 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.325-9942T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164557758 | |||||||
| chr2:164557764 | C | T | 1 | a0002c0002t0002g0273 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.325-9948G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164557764 | |||||||
| chr2:164558063 | G | A | 1 | a0002c0002t0005g0164 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.325-10247C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164558063 | |||||||
| chr2:164558097 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.325-10281C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164558097 | |||||||
| chr2:164558224 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0126 |
2 | HG02886.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.325-10408C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164558224 | |||||||
| chr2:164558231 | C | T | 69 | a0001c0001t0001g0006 a0001c0001t0001g0061 a0001c0001t0001g0064 others(66): Show |
71 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.325-10415G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164558231 | |||||||
| chr2:164558312 | T | C | 1 | a0001c0001t0004g0043 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.325-10496A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164558312 | |||||||
| chr2:164558742 | T | A | 1 | a0001c0001t0001g0061 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.325-10926A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164558742 | |||||||
| chr2:164558944 | C | A | 1 | a0002c0002t0003g0179 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.325-11128G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164558944 | |||||||
| chr2:164559020 | C | A | 1 | a0001c0001t0001g0057 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.325-11204G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164559020 | |||||||
| chr2:164559026 | G | A | 1 | a0001c0001t0004g0046 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.325-11210C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164559026 | |||||||
| chr2:164559237 | T | C | 1 | a0002c0002t0003g0292 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.325-11421A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164559237 | |||||||
| chr2:164559683 | G | A | 1 | a0002c0002t0003g0192 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.325-11867C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164559683 | |||||||
| chr2:164559768 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.325-11952G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164559768 | |||||||
| chr2:164560016 | A | G | 1 | a0001c0001t0001g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.325-12200T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164560016 | |||||||
| chr2:164560080 | A | G | 1 | a0001c0001t0010g0154 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.325-12264T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164560080 | |||||||
| chr2:164560103 | T | C | 195 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(192): Show |
197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.325-12287A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164560103 | |||||||
| chr2:164560162 | G | A | 1 | a0002c0002t0002g0231 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.325-12346C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164560162 | |||||||
| chr2:164560630 | G | C | 11 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0137 others(8): Show |
11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.325-12814C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164560630 | |||||||
| chr2:164560653 | T | C | 11 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0137 others(8): Show |
11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.325-12837A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164560653 | |||||||
| chr2:164560724 | A | C | 195 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(192): Show |
197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.325-12908T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164560724 | |||||||
| chr2:164560733 | G | C | 1 | a0006c0007t0003g0239 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.325-12917C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164560733 | |||||||
| chr2:164560738 | C | G | 194 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(191): Show |
196 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.325-12922G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164560738 | |||||||
| chr2:164560894 | A | T | 194 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(191): Show |
196 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.325-13078T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164560894 | |||||||
| chr2:164560902 | C | T | 1 | a0002c0002t0002g0286 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.325-13086G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164560902 | |||||||
| chr2:164560937 | G | T | 11 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0137 others(8): Show |
11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.325-13121C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164560937 | |||||||
| chr2:164560985 | A | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG01099.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.325-13169T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164560985 | |||||||
| chr2:164560990 | A | G | 11 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0137 others(8): Show |
11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.325-13174T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164560990 | |||||||
| chr2:164561629 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0004g0046 a0001c0001t0004g0074 |
3 | HG02056.hp2 NA18985.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.325-13813C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164561629 | |||||||
| chr2:164561703 | C | A | 11 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0137 others(8): Show |
11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.325-13887G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164561703 | |||||||
| chr2:164561708 | C | T | 1 | a0001c0001t0010g0154 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.325-13892G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164561708 | |||||||
| chr2:164561818 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.325-14002A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164561818 | |||||||
| chr2:164561950 | A | T | 1 | a0002c0002t0005g0178 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.325-14134T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164561950 | |||||||
| chr2:164562181 | G | C | 2 | a0001c0001t0008g0141 a0001c0001t0008g0142 |
2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.325-14365C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164562181 | |||||||
| chr2:164562245 | T | C | 1 | a0001c0001t0004g0015 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.325-14429A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164562245 | |||||||
| chr2:164562262 | C | T | 11 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0137 others(8): Show |
11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.325-14446G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164562262 | |||||||
| chr2:164562283 | C | T | 11 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0137 others(8): Show |
11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.325-14467G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164562283 | |||||||
| chr2:164562293 | G | T | 1 | a0007c0011t0007g0128 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.325-14477C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164562293 | |||||||
| chr2:164562385 | T | A | 3 | a0001c0001t0004g0098 a0001c0001t0004g0099 a0001c0001t0007g0104 |
3 | HG02622.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.325-14569A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164562385 | |||||||
| chr2:164562499 | T | C | 73 | a0001c0001t0001g0006 a0001c0001t0001g0061 a0001c0001t0001g0064 others(70): Show |
75 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.325-14683A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164562499 | |||||||
| chr2:164562501 | T | C | 1 | a0001c0001t0001g0050 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.325-14685A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164562501 | |||||||
| chr2:164562553 | A | G | 1 | a0002c0002t0005g0178 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.325-14737T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164562553 | |||||||
| chr2:164562750 | T | C | 1 | a0001c0001t0001g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.325-14934A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164562750 | |||||||
| chr2:164562837 | T | C | 82 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0038 others(79): Show |
82 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.325-15021A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164562837 | |||||||
| chr2:164562859 | T | A | 204 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(201): Show |
206 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.325-15043A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164562859 | |||||||
| chr2:164562965 | A | G | 82 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0038 others(79): Show |
82 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.325-15149T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164562965 | |||||||
| chr2:164563180 | T | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0135 a0001c0001t0004g0043 others(3): Show |
6 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.325-15364A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164563180 | |||||||
| chr2:164563195 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.325-15379A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164563195 | |||||||
| chr2:164563233 | T | C | 82 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0038 others(79): Show |
82 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.325-15417A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164563233 | |||||||
| chr2:164563891 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.325-16075A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164563891 | |||||||
| chr2:164564027 | T | G | 2 | a0002c0002t0003g0259 a0006c0007t0003g0239 |
2 | HG02080.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.325-16211A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164564027 | |||||||
| chr2:164564165 | G | A | 1 | a0002c0002t0002g0260 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.325-16349C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164564165 | |||||||
| chr2:164564264 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.325-16448A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164564264 | |||||||
| chr2:164564293 | T | C | 1 | a0002c0002t0002g0162 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.325-16477A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164564293 | |||||||
| chr2:164564372 | A | G | 82 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0038 others(79): Show |
82 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.325-16556T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164564372 | |||||||
| chr2:164564539 | G | A | 2 | a0002c0002t0003g0259 a0006c0007t0003g0239 |
2 | HG02080.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.325-16723C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164564539 | |||||||
| chr2:164564604 | A | C | 82 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0038 others(79): Show |
82 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.325-16788T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164564604 | |||||||
| chr2:164565047 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.325-17231T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164565047 | |||||||
| chr2:164565120 | G | C | 1 | a0001c0012t0001g0139 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.325-17304C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164565120 | |||||||
| chr2:164565235 | C | T | 1 | a0001c0001t0004g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.325-17419G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164565235 | |||||||
| chr2:164565278 | T | TCA | 45 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0064 others(42): Show |
45 | HG00544.hp1 HG01070.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.325-17464_325-1746 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164565278 | |||||||
| chr2:164565278 | T | TCACA | 19 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0013 others(16): Show |
20 | HG01069.hp1 HG01071.hp1 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.325-17466_325-1746 others(8): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164565278 | |||||||
| chr2:164565278 | T | TCACACA | 33 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0019 others(30): Show |
33 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.325-17468_325-1746 others(10): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164565278 | |||||||
| chr2:164565292 | A | ACACG | 34 | a0001c0001t0001g0061 a0001c0001t0004g0011 a0001c0001t0004g0029 others(31): Show |
35 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(32): Show |
intron_variant | MODIFIER | c.325-17477_325-1747 others(8): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164565292 | |||||||
| chr2:164565644 | G | A | 2 | a0001c0001t0001g0085 a0001c0001t0006g0001 |
3 | HG01069.hp1 HG01071.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.325-17828C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164565644 | |||||||
| chr2:164565710 | C | A | 2 | a0001c0001t0001g0022 a0001c0001t0004g0074 |
2 | NA18985.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.325-17894G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164565710 | |||||||
| chr2:164565711 | G | C | 83 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0038 others(80): Show |
83 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.325-17895C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164565711 | |||||||
| chr2:164565948 | C | A | 1 | a0002c0002t0003g0183 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.325-18132G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164565948 | |||||||
| chr2:164566083 | C | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(14): Show |
17 | HG01255.hp2 HG01261.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.325-18267G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164566083 | |||||||
| chr2:164566352 | A | G | 197 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(194): Show |
199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.325-18536T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164566352 | |||||||
| chr2:164566367 | G | C | 13 | a0001c0001t0001g0006 a0001c0001t0001g0064 a0001c0001t0001g0084 others(10): Show |
13 | HG01070.hp1 HG01071.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.325-18551C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164566367 | |||||||
| chr2:164566495 | A | G | 9 | a0001c0001t0004g0047 a0001c0001t0004g0062 a0002c0002t0002g0169 others(6): Show |
9 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(6): Show |
intron_variant | MODIFIER | c.325-18679T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164566495 | |||||||
| chr2:164566619 | G | C | 1 | a0002c0002t0003g0184 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.325-18803C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164566619 | |||||||
| chr2:164566679 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0135 a0001c0001t0004g0043 others(3): Show |
6 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.325-18863G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164566679 | |||||||
| chr2:164566774 | A | C | 1 | a0001c0001t0006g0150 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.325-18958T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164566774 | |||||||
| chr2:164567111 | T | C | 1 | a0002c0002t0003g0210 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.325-19295A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164567111 | |||||||
| chr2:164567343 | C | T | 2 | a0002c0002t0003g0259 a0006c0007t0003g0239 |
2 | HG02080.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.325-19527G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164567343 | |||||||
| chr2:164567602 | A | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0135 a0001c0001t0004g0043 others(3): Show |
6 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.325-19786T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164567602 | |||||||
| chr2:164567670 | C | T | 3 | a0002c0002t0003g0209 a0002c0002t0003g0226 a0002c0002t0003g0276 |
3 | NA18998.hp1 NA19081.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.325-19854G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164567670 | |||||||
| chr2:164567699 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.325-19883G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164567699 | |||||||
| chr2:164568065 | G | A | 133 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(130): Show |
134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.325-20249C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164568065 | |||||||
| chr2:164568202 | G | C | 1 | a0001c0001t0001g0131 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.325-20386C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164568202 | |||||||
| chr2:164568288 | GA | G | 7 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0001g0127 others(4): Show |
7 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.325-20473delT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164568288 | |||||||
| chr2:164568327 | A | G | 48 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(45): Show |
49 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(46): Show |
intron_variant | MODIFIER | c.325-20511T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164568327 | |||||||
| chr2:164568407 | G | A | 1 | a0001c0001t0006g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.325-20591C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164568407 | |||||||
| chr2:164568484 | T | C | 83 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0038 others(80): Show |
83 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.325-20668A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164568484 | |||||||
| chr2:164568808 | T | A | 1 | a0001c0001t0004g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.325-20992A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164568808 | |||||||
| chr2:164568809 | A | C | 1 | a0001c0001t0004g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.325-20993T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164568809 | |||||||
| chr2:164568810 | A | T | 1 | a0001c0001t0004g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.325-20994T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164568810 | |||||||
| chr2:164568811 | T | A | 7 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0094 others(4): Show |
7 | HG01891.hp2 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.325-20995A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164568811 | |||||||
| chr2:164569233 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.325-21417T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164569233 | |||||||
| chr2:164569537 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.325-21721A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164569537 | |||||||
| chr2:164569562 | C | T | 1 | a0002c0002t0002g0211 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.325-21746G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164569562 | |||||||
| chr2:164569876 | C | G | 128 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(125): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.325-22060G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164569876 | |||||||
| chr2:164570145 | C | T | 11 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0137 others(8): Show |
11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.325-22329G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164570145 | |||||||
| chr2:164570180 | G | A | 2 | a0002c0002t0003g0200 a0002c0002t0003g0257 |
2 | HG00642.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.325-22364C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164570180 | |||||||
| chr2:164570272 | A | G | 14 | a0001c0001t0001g0090 a0001c0001t0001g0117 a0001c0001t0001g0134 others(11): Show |
14 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.325-22456T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164570272 | |||||||
| chr2:164570275 | T | TA | 61 | a0001c0001t0001g0013 a0001c0001t0001g0079 a0001c0001t0001g0082 others(58): Show |
62 | HG00423.hp1 HG00609.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.325-22460dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164570275 | |||||||
| chr2:164570275 | T | TAA | 6 | a0001c0001t0001g0019 a0001c0001t0004g0047 a0001c0001t0004g0062 others(3): Show |
6 | HG00408.hp2 HG00438.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.325-22461_325-2246 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164570275 | |||||||
| chr2:164570275 | TA | T | 10 | a0001c0001t0001g0030 a0001c0001t0001g0069 a0001c0001t0001g0101 others(7): Show |
10 | HG00738.hp2 HG01255.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.325-22460delT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164570275 | |||||||
| chr2:164570275 | TAA | T | 12 | a0001c0001t0001g0009 a0001c0001t0001g0117 a0001c0001t0001g0134 others(9): Show |
12 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.325-22461_325-2246 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164570275 | |||||||
| chr2:164570368 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.325-22552A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164570368 | |||||||
| chr2:164570546 | C | T | 1 | a0007c0011t0007g0128 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.325-22730G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164570546 | |||||||
| chr2:164570753 | A | G | 14 | a0001c0001t0001g0090 a0001c0001t0001g0117 a0001c0001t0001g0134 others(11): Show |
14 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.325-22937T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164570753 | |||||||
| chr2:164570838 | A | G | 1 | a0002c0002t0003g0248 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.325-23022T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164570838 | |||||||
| chr2:164570878 | C | T | 5 | a0001c0001t0001g0084 a0001c0001t0001g0105 a0001c0001t0006g0151 others(2): Show |
5 | HG02258.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.325-23062G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164570878 | |||||||
| chr2:164571266 | CA | C | 14 | a0001c0001t0001g0090 a0001c0001t0001g0117 a0001c0001t0001g0134 others(11): Show |
14 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.325-23451delT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164571266 | |||||||
| chr2:164571315 | G | C | 47 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(44): Show |
48 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(45): Show |
intron_variant | MODIFIER | c.325-23499C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164571315 | |||||||
| chr2:164571546 | C | G | 1 | a0001c0001t0001g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.325-23730G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164571546 | |||||||
| chr2:164571639 | T | G | 2 | a0001c0001t0006g0147 a0001c0001t0007g0136 |
2 | HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.325-23823A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164571639 | |||||||
| chr2:164571844 | G | A | 1 | a0002c0002t0003g0292 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.325-24028C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164571844 | |||||||
| chr2:164571844 | G | T | 1 | a0001c0001t0001g0070 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.325-24028C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164571844 | |||||||
| chr2:164571951 | C | T | 1 | a0002c0002t0005g0178 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.325-24135G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164571951 | |||||||
| chr2:164571960 | G | A | 14 | a0001c0001t0001g0090 a0001c0001t0001g0117 a0001c0001t0001g0134 others(11): Show |
14 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.325-24144C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164571960 | |||||||
| chr2:164571961 | C | A | 3 | a0002c0002t0002g0194 a0002c0002t0002g0195 a0002c0002t0005g0193 |
3 | HG00639.hp2 HG00738.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.325-24145G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164571961 | |||||||
| chr2:164572462 | G | C | 3 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0002c0002t0003g0165 |
3 | HG00544.hp2 NA18977.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.325-24646C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164572462 | |||||||
| chr2:164572557 | T | C | 3 | a0002c0002t0003g0002 a0002c0002t0003g0192 a0002c0002t0003g0199 |
4 | HG01256.hp1 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.325-24741A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164572557 | |||||||
| chr2:164572629 | G | C | 15 | a0001c0001t0001g0090 a0001c0001t0001g0117 a0001c0001t0001g0134 others(12): Show |
15 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.325-24813C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164572629 | |||||||
| chr2:164572725 | G | A | 47 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(44): Show |
48 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(45): Show |
intron_variant | MODIFIER | c.325-24909C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164572725 | |||||||
| chr2:164572725 | G | T | 4 | a0002c0002t0002g0262 a0002c0002t0002g0263 a0002c0002t0002g0264 others(1): Show |
4 | HG02056.hp1 NA18972.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.325-24909C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164572725 | |||||||
| chr2:164572788 | T | A | 3 | a0001c0001t0001g0090 a0001c0001t0011g0087 a0001c0001t0011g0091 |
3 | HG00735.hp1 HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.325-24972A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164572788 | |||||||
| chr2:164572799 | G | A | 1 | a0002c0002t0003g0245 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.325-24983C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164572799 | |||||||
| chr2:164572917 | C | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(14): Show |
17 | HG01255.hp2 HG01261.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.325-25101G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164572917 | |||||||
| chr2:164573027 | T | C | 31 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(28): Show |
31 | HG01175.hp2 HG01255.hp2 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.325-25211A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164573027 | |||||||
| chr2:164573203 | G | C | 2 | a0002c0002t0003g0259 a0006c0007t0003g0239 |
2 | HG02080.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.325-25387C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164573203 | |||||||
| chr2:164573338 | C | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(14): Show |
17 | HG01255.hp2 HG01261.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.325-25522G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164573338 | |||||||
| chr2:164573393 | C | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0063 a0001c0001t0001g0079 |
3 | NA19006.hp2 NA19011.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.325-25577G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164573393 | |||||||
| chr2:164573632 | G | GT | 46 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(43): Show |
46 | HG00735.hp1 HG01175.hp2 HG01255.hp2 others(43): Show |
intron_variant | MODIFIER | c.325-25817dupA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164573632 | |||||||
| chr2:164573711 | C | T | 1 | a0002c0002t0003g0271 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.325-25895G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164573711 | |||||||
| chr2:164573894 | C | T | 7 | a0001c0001t0004g0108 a0001c0001t0004g0109 a0001c0001t0004g0110 others(4): Show |
7 | HG02055.hp2 HG02280.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.325-26078G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164573894 | |||||||
| chr2:164573913 | T | TATGGGTA others(21): Show |
2 | a0001c0001t0001g0044 a0001c0001t0001g0069 |
2 | NA19005.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.325-26125_325-2609 others(32): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164573913 | |||||||
| chr2:164574211 | T | C | 15 | a0001c0001t0001g0090 a0001c0001t0001g0117 a0001c0001t0001g0134 others(12): Show |
15 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.325-26395A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164574211 | |||||||
| chr2:164574241 | CT | C | 20 | a0001c0001t0001g0090 a0001c0001t0001g0093 a0001c0001t0001g0117 others(17): Show |
20 | HG00735.hp1 HG01515.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.325-26426delA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164574241 | |||||||
| chr2:164574335 | G | A | 2 | a0001c0001t0006g0147 a0001c0001t0007g0136 |
2 | HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.325-26519C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164574335 | |||||||
| chr2:164574432 | G | C | 3 | a0001c0001t0004g0098 a0001c0001t0004g0099 a0001c0001t0007g0104 |
3 | HG02622.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.325-26616C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164574432 | |||||||
| chr2:164574469 | G | A | 11 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0137 others(8): Show |
11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.325-26653C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164574469 | |||||||
| chr2:164574473 | T | C | 2 | a0002c0002t0003g0259 a0006c0007t0003g0239 |
2 | HG02080.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.325-26657A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164574473 | |||||||
| chr2:164574546 | T | C | 1 | a0001c0001t0001g0068 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.325-26730A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164574546 | |||||||
| chr2:164574632 | C | A | 15 | a0001c0001t0001g0090 a0001c0001t0001g0117 a0001c0001t0001g0134 others(12): Show |
15 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.325-26816G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164574632 | |||||||
| chr2:164574652 | A | C | 31 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(28): Show |
31 | HG01175.hp2 HG01255.hp2 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.325-26836T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164574652 | |||||||
| chr2:164574659 | G | A | 3 | a0001c0001t0001g0090 a0001c0001t0011g0087 a0001c0001t0011g0091 |
3 | HG00735.hp1 HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.325-26843C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164574659 | |||||||
| chr2:164574661 | T | C | 34 | a0001c0001t0001g0008 a0001c0001t0001g0082 a0001c0001t0001g0085 others(31): Show |
35 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.325-26845A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164574661 | |||||||
| chr2:164574797 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.325-26981C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164574797 | |||||||
| chr2:164574896 | C | T | 2 | a0002c0002t0003g0259 a0006c0007t0003g0239 |
2 | HG02080.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.325-27080G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164574896 | |||||||
| chr2:164575179 | C | A | 1 | a0002c0002t0003g0232 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.325-27363G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164575179 | |||||||
| chr2:164575573 | T | C | 15 | a0001c0001t0001g0090 a0001c0001t0001g0117 a0001c0001t0001g0134 others(12): Show |
15 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.325-27757A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164575573 | |||||||
| chr2:164575681 | G | C | 5 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0009g0102 others(2): Show |
5 | HG02258.hp1 HG02486.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.325-27865C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164575681 | |||||||
| chr2:164575975 | G | A | 33 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(30): Show |
33 | HG00735.hp1 HG01255.hp2 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.325-28159C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164575975 | |||||||
| chr2:164576073 | A | T | 1 | a0002c0002t0002g0230 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.325-28257T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164576073 | |||||||
| chr2:164576356 | ATTTAAC | A | 3 | a0001c0001t0006g0146 a0001c0001t0008g0141 a0001c0001t0008g0142 |
3 | HG02723.hp1 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.325-28546_325-2854 others(10): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164576356 | |||||||
| chr2:164576409 | T | TA | 15 | a0001c0001t0001g0090 a0001c0001t0001g0117 a0001c0001t0001g0134 others(12): Show |
15 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.325-28594dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164576409 | |||||||
| chr2:164576422 | G | C | 1 | a0001c0001t0004g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.325-28606C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164576422 | |||||||
| chr2:164576647 | T | C | 15 | a0001c0001t0001g0090 a0001c0001t0001g0117 a0001c0001t0001g0134 others(12): Show |
15 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.325-28831A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164576647 | |||||||
| chr2:164576708 | G | A | 2 | a0002c0002t0003g0259 a0006c0007t0003g0239 |
2 | HG02080.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.325-28892C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164576708 | |||||||
| chr2:164576733 | T | C | 34 | a0001c0001t0001g0008 a0001c0001t0001g0082 a0001c0001t0001g0085 others(31): Show |
35 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.325-28917A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164576733 | |||||||
| chr2:164576825 | GA | G | 56 | a0001c0001t0001g0006 a0001c0001t0001g0061 a0001c0001t0001g0064 others(53): Show |
57 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(54): Show |
intron_variant | MODIFIER | c.325-29010delT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164576825 | |||||||
| chr2:164576920 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.325-29104T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164576920 | |||||||
| chr2:164576969 | A | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0079 |
2 | NA19006.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.325-29153T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164576969 | |||||||
| chr2:164577055 | T | C | 1 | a0002c0002t0002g0260 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.325-29239A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164577055 | |||||||
| chr2:164577087 | T | C | 46 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(43): Show |
46 | HG00735.hp1 HG01175.hp2 HG01255.hp2 others(43): Show |
intron_variant | MODIFIER | c.325-29271A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164577087 | |||||||
| chr2:164577106 | G | T | 34 | a0001c0001t0001g0008 a0001c0001t0001g0082 a0001c0001t0001g0085 others(31): Show |
35 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.325-29290C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164577106 | |||||||
| chr2:164577178 | T | C | 3 | a0001c0001t0004g0098 a0001c0001t0004g0099 a0001c0001t0007g0104 |
3 | HG02622.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.325-29362A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164577178 | |||||||
| chr2:164577317 | C | T | 15 | a0001c0001t0001g0090 a0001c0001t0001g0117 a0001c0001t0001g0134 others(12): Show |
15 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.325-29501G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164577317 | |||||||
| chr2:164577381 | G | C | 1 | a0001c0001t0001g0082 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.325-29565C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164577381 | |||||||
| chr2:164577386 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.325-29570C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164577386 | |||||||
| chr2:164577508 | A | C | 15 | a0001c0001t0001g0090 a0001c0001t0001g0117 a0001c0001t0001g0134 others(12): Show |
15 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.325-29692T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164577508 | |||||||
| chr2:164577529 | C | T | 2 | a0001c0003t0001g0049 a0001c0003t0007g0067 |
2 | HG00609.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.325-29713G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164577529 | |||||||
| chr2:164577537 | C | A | 3 | a0002c0002t0003g0209 a0002c0002t0003g0226 a0002c0002t0003g0276 |
3 | NA18998.hp1 NA19081.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.325-29721G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164577537 | |||||||
| chr2:164577569 | C | T | 1 | a0002c0002t0003g0183 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.325-29753G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164577569 | |||||||
| chr2:164577676 | C | T | 1 | a0001c0001t0004g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.325-29860G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164577676 | |||||||
| chr2:164577678 | C | G | 2 | a0001c0001t0001g0032 a0001c0001t0001g0055 |
2 | HG02523.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.325-29862G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164577678 | |||||||
| chr2:164577856 | C | G | 1 | a0001c0001t0004g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.325-30040G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164577856 | |||||||
| chr2:164577889 | G | C | 1 | a0001c0001t0001g0131 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.325-30073C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164577889 | |||||||
| chr2:164578295 | G | A | 15 | a0001c0001t0001g0090 a0001c0001t0001g0117 a0001c0001t0001g0134 others(12): Show |
15 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.325-30479C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164578295 | |||||||
| chr2:164578363 | A | G | 15 | a0001c0001t0001g0090 a0001c0001t0001g0117 a0001c0001t0001g0134 others(12): Show |
15 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.325-30547T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164578363 | |||||||
| chr2:164578386 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.325-30570A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164578386 | |||||||
| chr2:164578522 | G | GCA | 16 | a0001c0001t0001g0048 a0001c0001t0001g0100 a0001c0001t0001g0113 others(13): Show |
16 | HG01106.hp1 HG01175.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.325-30708_325-3070 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164578522 | |||||||
| chr2:164578522 | G | GCACA | 27 | a0001c0001t0001g0018 a0001c0001t0001g0038 a0001c0001t0001g0050 others(24): Show |
27 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.325-30710_325-3070 others(8): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164578522 | |||||||
| chr2:164578522 | G | GCACACA | 73 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0064 others(70): Show |
74 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.325-30712_325-3070 others(10): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164578522 | |||||||
| chr2:164578522 | G | GCACACAC others(1): Show |
10 | a0001c0001t0004g0065 a0002c0002t0002g0202 a0002c0002t0002g0219 others(7): Show |
10 | HG01070.hp1 HG01934.hp2 HG04204.hp2 others(7): Show |
intron_variant | MODIFIER | c.325-30714_325-3070 others(12): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164578522 | |||||||
| chr2:164578522 | G | GCACACAC others(3): Show |
1 | a0001c0001t0001g0061 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.325-30716_325-3070 others(14): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164578522 | |||||||
| chr2:164578522 | GCA | G | 15 | a0001c0001t0001g0117 a0001c0001t0001g0120 a0001c0001t0001g0132 others(12): Show |
15 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.325-30708_325-3070 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164578522 | |||||||
| chr2:164578524 | A | G | 3 | a0001c0001t0001g0090 a0001c0001t0011g0087 a0001c0001t0011g0091 |
3 | HG00735.hp1 HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.325-30708T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164578524 | |||||||
| chr2:164578526 | A | G | 11 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0137 others(8): Show |
11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.325-30710T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164578526 | |||||||
| chr2:164578528 | A | G | 4 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0137 others(1): Show |
4 | HG02109.hp2 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.325-30712T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164578528 | |||||||
| chr2:164578542 | A | G | 9 | a0001c0001t0001g0042 a0002c0002t0002g0243 a0002c0002t0003g0186 others(6): Show |
9 | HG00738.hp1 HG01106.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.325-30726T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164578542 | |||||||
| chr2:164578599 | T | G | 3 | a0002c0002t0003g0187 a0002c0002t0003g0242 a0002c0002t0003g0248 |
3 | HG01934.hp1 NA18945.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.325-30783A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164578599 | |||||||
| chr2:164578767 | C | A | 1 | a0002c0002t0002g0219 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.325-30951G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164578767 | |||||||
| chr2:164579032 | T | TAA | 14 | a0001c0001t0001g0090 a0001c0001t0001g0117 a0001c0001t0001g0134 others(11): Show |
14 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.325-31217_325-3121 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579032 | |||||||
| chr2:164579033 | T | A | 34 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(31): Show |
34 | HG00735.hp1 HG01255.hp2 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.325-31217A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579033 | |||||||
| chr2:164579050 | T | C | 15 | a0001c0001t0001g0090 a0001c0001t0001g0117 a0001c0001t0001g0134 others(12): Show |
15 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.325-31234A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579050 | |||||||
| chr2:164579056 | A | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0048 |
2 | NA18979.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.325-31240T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579056 | |||||||
| chr2:164579169 | G | C | 1 | a0001c0001t0007g0136 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.325-31353C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579169 | |||||||
| chr2:164579500 | T | TGCGC | 4 | a0001c0001t0001g0090 a0001c0001t0007g0114 a0001c0001t0011g0087 others(1): Show |
4 | HG00735.hp1 HG02451.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.325-31685_325-3168 others(8): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579500 | |||||||
| chr2:164579500 | T | TGCGCGCA others(1): Show |
10 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0137 others(7): Show |
10 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.325-31685_325-3168 others(12): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579500 | |||||||
| chr2:164579501 | G | GCA | 22 | a0001c0001t0001g0018 a0001c0001t0001g0038 a0001c0001t0001g0041 others(19): Show |
22 | HG00438.hp2 HG00673.hp1 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.325-31687_325-3168 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579501 | |||||||
| chr2:164579501 | G | GCACA | 5 | a0001c0001t0001g0050 a0001c0001t0006g0156 a0002c0002t0003g0220 others(2): Show |
5 | HG01099.hp1 HG02630.hp2 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.325-31689_325-3168 others(8): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579501 | |||||||
| chr2:164579501 | GCA | G | 27 | a0001c0001t0001g0040 a0001c0001t0001g0082 a0001c0001t0001g0113 others(24): Show |
27 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.325-31687_325-3168 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579501 | |||||||
| chr2:164579501 | GCACA | G | 10 | a0001c0003t0001g0049 a0002c0002t0003g0185 a0002c0002t0005g0163 others(7): Show |
10 | HG00642.hp2 HG01257.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.325-31689_325-3168 others(8): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579501 | |||||||
| chr2:164579501 | GCACACAC others(3): Show |
G | 1 | a0002c0002t0002g0170 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.325-31695_325-3168 others(14): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579501 | |||||||
| chr2:164579501 | GCACACAC others(5): Show |
G | 2 | a0001c0001t0001g0005 a0002c0002t0003g0205 |
2 | HG02083.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.325-31697_325-3168 others(16): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579501 | |||||||
| chr2:164579501 | GCACACAC others(7): Show |
G | 72 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(69): Show |
73 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.325-31699_325-3168 others(18): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579501 | |||||||
| chr2:164579501 | GCACACAC others(9): Show |
G | 1 | a0002c0002t0002g0251 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.325-31701_325-3168 others(20): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579501 | |||||||
| chr2:164579503 | A | G | 1 | a0001c0001t0004g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.325-31687T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579503 | |||||||
| chr2:164579505 | A | G | 4 | a0001c0001t0001g0090 a0001c0001t0007g0114 a0001c0001t0011g0087 others(1): Show |
4 | HG00735.hp1 HG02451.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.325-31689T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579505 | |||||||
| chr2:164579545 | A | G | 91 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(88): Show |
92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.325-31729T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579545 | |||||||
| chr2:164579627 | C | T | 11 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0137 others(8): Show |
11 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.325-31811G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579627 | |||||||
| chr2:164579688 | AT | A | 16 | a0001c0001t0001g0090 a0001c0001t0001g0117 a0001c0001t0001g0134 others(13): Show |
16 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.325-31873delA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579688 | |||||||
| chr2:164579797 | C | T | 14 | a0001c0001t0004g0024 a0001c0001t0010g0157 a0002c0002t0002g0188 others(11): Show |
14 | HG00544.hp1 HG02056.hp1 NA18944.hp2 others(11): Show |
intron_variant | MODIFIER | c.325-31981G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579797 | |||||||
| chr2:164579919 | C | A | 15 | a0001c0001t0001g0090 a0001c0001t0001g0117 a0001c0001t0001g0134 others(12): Show |
15 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.325-32103G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164579919 | |||||||
| chr2:164580069 | A | G | 61 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(58): Show |
62 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.325-32253T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580069 | |||||||
| chr2:164580085 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.325-32269A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580085 | |||||||
| chr2:164580096 | AT | A | 100 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0017 others(97): Show |
100 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.325-32281delA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580096 | |||||||
| chr2:164580096 | ATTTT | A | 15 | a0001c0001t0001g0090 a0001c0001t0001g0117 a0001c0001t0001g0134 others(12): Show |
15 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.325-32284_325-3228 others(8): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580096 | |||||||
| chr2:164580238 | G | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0135 a0001c0001t0004g0043 others(3): Show |
6 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.325-32422C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580238 | |||||||
| chr2:164580268 | T | C | 1 | a0001c0001t0004g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.325-32452A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580268 | |||||||
| chr2:164580281 | C | T | 2 | a0002c0002t0003g0259 a0006c0007t0003g0239 |
2 | HG02080.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.325-32465G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580281 | |||||||
| chr2:164580324 | C | T | 18 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(15): Show |
18 | HG01255.hp2 HG01261.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.325-32508G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580324 | |||||||
| chr2:164580430 | C | T | 2 | a0002c0002t0002g0252 a0002c0002t0002g0284 |
2 | HG00140.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.325-32614G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580430 | |||||||
| chr2:164580539 | T | A | 43 | a0001c0001t0001g0006 a0001c0001t0001g0061 a0001c0001t0001g0064 others(40): Show |
44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.325-32723A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580539 | |||||||
| chr2:164580580 | T | C | 13 | a0001c0001t0001g0100 a0001c0001t0001g0106 a0001c0001t0001g0120 others(10): Show |
13 | HG01175.hp2 HG02258.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.325-32764A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580580 | |||||||
| chr2:164580586 | C | T | 3 | a0001c0001t0001g0083 a0002c0002t0005g0222 a0002c0002t0005g0269 |
3 | HG01516.hp1 HG01517.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.325-32770G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580586 | |||||||
| chr2:164580628 | C | T | 6 | a0002c0002t0002g0256 a0002c0002t0002g0291 a0002c0002t0003g0002 others(3): Show |
7 | HG01256.hp1 HG01257.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.325-32812G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580628 | |||||||
| chr2:164580629 | G | T | 1 | a0001c0001t0001g0042 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.325-32813C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580629 | |||||||
| chr2:164580709 | GA | G | 115 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(112): Show |
117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.325-32894delT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580709 | |||||||
| chr2:164580709 | GAA | G | 18 | a0001c0001t0001g0090 a0001c0001t0001g0100 a0001c0001t0001g0117 others(15): Show |
18 | HG00735.hp1 HG01993.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.325-32895_325-3289 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580709 | |||||||
| chr2:164580726 | G | A | 15 | a0001c0001t0001g0090 a0001c0001t0001g0117 a0001c0001t0001g0134 others(12): Show |
15 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.325-32910C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580726 | |||||||
| chr2:164580770 | A | G | 9 | a0001c0001t0004g0047 a0001c0001t0004g0062 a0002c0002t0002g0169 others(6): Show |
9 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(6): Show |
intron_variant | MODIFIER | c.325-32954T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580770 | |||||||
| chr2:164580910 | T | C | 1 | a0001c0001t0004g0046 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.325-33094A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164580910 | |||||||
| chr2:164581034 | C | G | 53 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0030 others(50): Show |
54 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(51): Show |
intron_variant | MODIFIER | c.325-33218G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164581034 | |||||||
| chr2:164581067 | T | C | 1 | a0001c0001t0009g0102 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.325-33251A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164581067 | |||||||
| chr2:164581082 | A | G | 78 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(75): Show |
79 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.325-33266T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164581082 | |||||||
| chr2:164581212 | A | G | 200 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(197): Show |
202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.325-33396T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164581212 | |||||||
| chr2:164581226 | C | G | 108 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0022 others(105): Show |
109 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.325-33410G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164581226 | |||||||
| chr2:164581380 | G | C | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.325-33564C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164581380 | |||||||
| chr2:164581702 | T | C | 1 | a0001c0001t0001g0131 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.325-33886A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164581702 | |||||||
| chr2:164581720 | G | A | 118 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0022 others(115): Show |
118 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.325-33904C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164581720 | |||||||
| chr2:164581749 | G | C | 2 | a0001c0001t0001g0038 a0001c0001t0001g0050 |
2 | HG02027.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.325-33933C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164581749 | |||||||
| chr2:164581871 | T | A | 4 | a0001c0001t0001g0093 a0001c0001t0001g0115 a0001c0001t0001g0122 others(1): Show |
4 | HG02976.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.325-34055A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164581871 | |||||||
| chr2:164581886 | G | A | 6 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0004g0123 others(3): Show |
6 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.325-34070C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164581886 | |||||||
| chr2:164581963 | T | C | 64 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(61): Show |
64 | HG00140.hp1 HG00609.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.325-34147A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164581963 | |||||||
| chr2:164582140 | G | A | 1 | a0001c0001t0004g0059 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.325-34324C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582140 | |||||||
| chr2:164582150 | C | A | 27 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(24): Show |
27 | HG00140.hp1 HG01175.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.325-34334G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582150 | |||||||
| chr2:164582193 | A | G | 3 | a0001c0001t0004g0098 a0001c0001t0004g0099 a0001c0001t0007g0104 |
3 | HG02622.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.325-34377T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582193 | |||||||
| chr2:164582420 | TA | T | 8 | a0001c0001t0001g0084 a0001c0001t0001g0113 a0001c0001t0004g0108 others(5): Show |
8 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.325-34605delT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582420 | |||||||
| chr2:164582421 | A | T | 1 | a0001c0001t0004g0109 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.325-34605T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582421 | |||||||
| chr2:164582422 | TTA | T | 42 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0078 others(39): Show |
43 | HG00642.hp2 HG00733.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.325-34608_325-3460 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582422 | |||||||
| chr2:164582423 | T | A | 1 | a0001c0001t0001g0084 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.325-34607A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582423 | |||||||
| chr2:164582423 | TA | T | 35 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0030 others(32): Show |
35 | HG00609.hp1 HG01175.hp2 HG02027.hp2 others(32): Show |
intron_variant | MODIFIER | c.325-34608delT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582423 | |||||||
| chr2:164582424 | A | T | 11 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0113 others(8): Show |
11 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.325-34608T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582424 | |||||||
| chr2:164582424 | AT | A | 117 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(114): Show |
118 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.325-34609delA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582424 | |||||||
| chr2:164582425 | T | A | 2 | a0001c0001t0001g0082 a0001c0001t0004g0043 |
2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.325-34609A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582425 | |||||||
| chr2:164582426 | T | A | 31 | a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0038 others(28): Show |
31 | HG00609.hp1 HG01175.hp2 HG02027.hp2 others(28): Show |
intron_variant | MODIFIER | c.325-34610A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582426 | |||||||
| chr2:164582427 | T | A | 39 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0090 others(36): Show |
40 | HG00642.hp2 HG00733.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.325-34611A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582427 | |||||||
| chr2:164582428 | T | A | 1 | a0002c0002t0002g0273 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.325-34612A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582428 | |||||||
| chr2:164582430 | T | A | 8 | a0001c0001t0001g0093 a0001c0001t0001g0122 a0001c0001t0001g0129 others(5): Show |
8 | HG02109.hp2 HG02886.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.325-34614A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582430 | |||||||
| chr2:164582431 | T | A | 32 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0100 others(29): Show |
33 | HG00642.hp2 HG00733.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.325-34615A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582431 | |||||||
| chr2:164582435 | T | A | 1 | a0001c0001t0006g0148 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.325-34619A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582435 | |||||||
| chr2:164582490 | C | T | 1 | a0002c0002t0003g0183 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.325-34674G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582490 | |||||||
| chr2:164582618 | G | A | 9 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0100 others(6): Show |
9 | HG00735.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.325-34802C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582618 | |||||||
| chr2:164582715 | G | A | 3 | a0001c0001t0001g0033 a0001c0001t0004g0076 a0001c0001t0006g0156 |
3 | HG00099.hp2 HG00621.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.325-34899C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582715 | |||||||
| chr2:164582768 | G | C | 1 | a0002c0002t0002g0162 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.325-34952C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164582768 | |||||||
| chr2:164583168 | C | T | 14 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(11): Show |
14 | HG00140.hp1 HG01261.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.325-35352G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164583168 | |||||||
| chr2:164583469 | T | C | 2 | a0001c0001t0001g0120 a0001c0001t0001g0126 |
2 | HG02886.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.325-35653A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164583469 | |||||||
| chr2:164583864 | T | C | 11 | a0001c0001t0001g0006 a0001c0001t0001g0083 a0001c0001t0001g0090 others(8): Show |
11 | HG00735.hp1 HG01255.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.324+35823A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164583864 | |||||||
| chr2:164584049 | G | A | 1 | a0002c0002t0002g0208 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.324+35638C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164584049 | |||||||
| chr2:164584132 | A | C | 1 | a0001c0001t0004g0108 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.324+35555T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164584132 | |||||||
| chr2:164584147 | A | AT | 16 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0054 others(13): Show |
16 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.324+35539dupA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164584147 | |||||||
| chr2:164584147 | AT | A | 144 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(141): Show |
146 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.324+35539delA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164584147 | |||||||
| chr2:164584147 | ATT | A | 12 | a0001c0001t0001g0134 a0001c0001t0004g0074 a0001c0001t0004g0098 others(9): Show |
12 | HG01517.hp1 HG02080.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.324+35538_324+3553 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164584147 | |||||||
| chr2:164584147 | ATTTTTTT others(5): Show |
A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0079 |
2 | NA19006.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.324+35528_324+3553 others(16): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164584147 | |||||||
| chr2:164584240 | G | A | 6 | a0002c0002t0002g0171 a0002c0002t0002g0172 a0002c0002t0002g0174 others(3): Show |
6 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(3): Show |
intron_variant | MODIFIER | c.324+35447C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164584240 | |||||||
| chr2:164584433 | G | A | 3 | a0001c0001t0004g0098 a0001c0001t0004g0099 a0001c0001t0007g0104 |
3 | HG02622.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.324+35254C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164584433 | |||||||
| chr2:164584585 | T | TA | 7 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0052 others(4): Show |
7 | HG01255.hp2 HG01884.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.324+35101dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164584585 | |||||||
| chr2:164584949 | G | A | 2 | a0001c0001t0004g0060 a0009c0006t0001g0003 |
2 | HG04184.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.324+34738C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164584949 | |||||||
| chr2:164584986 | GGCTAGAG others(1): Show |
G | 45 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(42): Show |
46 | HG00642.hp2 HG00733.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.324+34693_324+3470 others(12): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164584986 | |||||||
| chr2:164585085 | C | CT | 8 | a0001c0001t0001g0033 a0001c0001t0001g0055 a0001c0001t0001g0071 others(5): Show |
8 | HG00621.hp1 HG01255.hp2 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.324+34601dupA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | |||||||
| chr2:164585085 | C | CTTTTT | 7 | a0001c0001t0001g0044 a0001c0001t0001g0069 a0001c0001t0001g0113 others(4): Show |
7 | HG02922.hp1 HG03540.hp2 NA18991.hp2 others(4): Show |
intron_variant | MODIFIER | c.324+34597_324+3460 others(9): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | |||||||
| chr2:164585085 | C | CTTTTTT | 6 | a0001c0001t0001g0051 a0001c0001t0004g0108 a0001c0001t0004g0109 others(3): Show |
6 | HG02055.hp2 HG02071.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.324+34596_324+3460 others(10): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | |||||||
| chr2:164585085 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0054 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.324+34591_324+3460 others(15): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | |||||||
| chr2:164585085 | CT | C | 37 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0025 others(34): Show |
37 | HG00408.hp1 HG00544.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.324+34601delA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | |||||||
| chr2:164585085 | CTT | C | 16 | a0001c0001t0001g0016 a0001c0001t0001g0045 a0001c0001t0001g0077 others(13): Show |
17 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.324+34600_324+3460 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | |||||||
| chr2:164585085 | CTTT | C | 8 | a0001c0001t0001g0132 a0001c0001t0006g0148 a0001c0001t0006g0151 others(5): Show |
8 | HG00733.hp2 HG01099.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.324+34599_324+3460 others(7): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | |||||||
| chr2:164585085 | CTTTT | C | 9 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0078 others(6): Show |
9 | HG00735.hp1 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.324+34598_324+3460 others(8): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | |||||||
| chr2:164585085 | CTTTTTTT others(1): Show |
C | 27 | a0001c0001t0001g0038 a0001c0001t0001g0048 a0001c0001t0001g0085 others(24): Show |
27 | HG01123.hp1 HG01169.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.324+34594_324+3460 others(12): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | |||||||
| chr2:164585085 | CTTTTTTT others(2): Show |
C | 83 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0042 others(80): Show |
84 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.324+34593_324+3460 others(13): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | |||||||
| chr2:164585085 | CTTTTTTT others(3): Show |
C | 10 | a0001c0001t0001g0084 a0001c0001t0001g0120 a0001c0001t0001g0126 others(7): Show |
10 | HG01975.hp1 HG02258.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.324+34592_324+3460 others(14): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | |||||||
| chr2:164585085 | CTTTTTTT others(4): Show |
C | 7 | a0001c0001t0001g0093 a0001c0001t0001g0115 a0001c0001t0001g0122 others(4): Show |
7 | HG02622.hp1 HG02895.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.324+34591_324+3460 others(15): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | |||||||
| chr2:164585085 | CTTTTTTT others(5): Show |
C | 1 | a0002c0002t0002g0166 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.324+34590_324+3460 others(16): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | |||||||
| chr2:164585085 | CTTTTTTT others(6): Show |
C | 1 | a0009c0006t0001g0003 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.324+34589_324+3460 others(17): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | |||||||
| chr2:164585085 | CTTTTTTT others(9): Show |
C | 12 | a0001c0001t0001g0106 a0001c0001t0001g0117 a0001c0001t0001g0121 others(9): Show |
12 | HG01175.hp2 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.324+34586_324+3460 others(20): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | |||||||
| chr2:164585085 | CTTTTTTT others(10): Show |
C | 15 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(12): Show |
15 | HG00140.hp1 HG01261.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.324+34585_324+3460 others(21): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | |||||||
| chr2:164585085 | CTTTTTTT others(14): Show |
C | 1 | a0001c0001t0001g0100 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.324+34581_324+3460 others(25): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | |||||||
| chr2:164585085 | CTTTTTTT others(15): Show |
C | 1 | a0002c0002t0003g0259 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.324+34580_324+3460 others(26): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585085 | |||||||
| chr2:164585168 | G | A | 1 | a0001c0001t0006g0149 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.324+34519C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585168 | |||||||
| chr2:164585198 | T | C | 120 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0030 others(117): Show |
121 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.324+34489A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585198 | |||||||
| chr2:164585341 | A | C | 1 | a0002c0002t0002g0174 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324+34346T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585341 | |||||||
| chr2:164585624 | T | C | 1 | a0001c0012t0001g0139 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.324+34063A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585624 | |||||||
| chr2:164585802 | T | G | 1 | a0001c0001t0001g0082 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.324+33885A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585802 | |||||||
| chr2:164585852 | A | T | 1 | a0001c0001t0001g0041 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.324+33835T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164585852 | |||||||
| chr2:164586215 | T | C | 212 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(209): Show |
214 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.324+33472A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164586215 | |||||||
| chr2:164586292 | T | C | 1 | a0001c0001t0010g0140 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.324+33395A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164586292 | |||||||
| chr2:164586296 | T | C | 1 | a0002c0002t0003g0206 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.324+33391A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164586296 | |||||||
| chr2:164586493 | T | C | 1 | a0002c0002t0002g0288 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.324+33194A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164586493 | |||||||
| chr2:164586617 | T | C | 209 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(206): Show |
211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.324+33070A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164586617 | |||||||
| chr2:164587255 | T | C | 1 | a0008c0009t0005g0250 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.324+32432A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164587255 | |||||||
| chr2:164587336 | T | A | 1 | a0002c0002t0003g0234 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.324+32351A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164587336 | |||||||
| chr2:164587351 | C | T | 27 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(24): Show |
27 | HG00140.hp1 HG01175.hp2 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.324+32336G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164587351 | |||||||
| chr2:164587372 | C | T | 1 | a0002c0002t0002g0191 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.324+32315G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164587372 | |||||||
| chr2:164587380 | T | A | 1 | a0002c0002t0003g0201 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.324+32307A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164587380 | |||||||
| chr2:164587404 | G | T | 3 | a0001c0001t0001g0129 a0001c0001t0004g0107 a0007c0011t0007g0128 |
3 | HG02723.hp2 HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.324+32283C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164587404 | |||||||
| chr2:164587474 | G | A | 15 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0030 others(12): Show |
15 | HG00609.hp1 HG02027.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.324+32213C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164587474 | |||||||
| chr2:164587562 | T | C | 7 | a0002c0002t0002g0256 a0002c0002t0002g0291 a0002c0002t0003g0192 others(4): Show |
7 | HG00642.hp1 HG01256.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.324+32125A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164587562 | |||||||
| chr2:164587714 | C | T | 1 | a0002c0002t0005g0178 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.324+31973G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164587714 | |||||||
| chr2:164587742 | C | T | 7 | a0002c0002t0002g0194 a0002c0002t0002g0195 a0002c0002t0002g0235 others(4): Show |
7 | HG00639.hp2 HG00738.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.324+31945G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164587742 | |||||||
| chr2:164587853 | A | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0051 |
2 | HG02071.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.324+31834T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164587853 | |||||||
| chr2:164588142 | C | A | 1 | a0002c0002t0002g0162 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.324+31545G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164588142 | |||||||
| chr2:164588164 | T | C | 124 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(121): Show |
125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.324+31523A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164588164 | |||||||
| chr2:164588546 | AT | A | 35 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0030 others(32): Show |
35 | HG00609.hp1 HG02027.hp2 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.324+31140delA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164588546 | |||||||
| chr2:164588555 | A | T | 1 | a0001c0001t0004g0031 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.324+31132T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164588555 | |||||||
| chr2:164588556 | C | A | 1 | a0001c0001t0004g0031 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.324+31131G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164588556 | |||||||
| chr2:164588841 | C | T | 4 | a0001c0001t0001g0134 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
4 | HG02109.hp2 HG02257.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.324+30846G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164588841 | |||||||
| chr2:164588888 | G | A | 4 | a0001c0001t0001g0134 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
4 | HG02109.hp2 HG02257.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.324+30799C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164588888 | |||||||
| chr2:164588958 | G | A | 98 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(95): Show |
99 | HG00609.hp1 HG00642.hp2 HG00733.hp2 others(96): Show |
intron_variant | MODIFIER | c.324+30729C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164588958 | |||||||
| chr2:164589110 | T | C | 14 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0030 others(11): Show |
14 | HG00609.hp1 HG02027.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.324+30577A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164589110 | |||||||
| chr2:164589117 | A | G | 1 | a0002c0002t0002g0181 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.324+30570T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164589117 | |||||||
| chr2:164589125 | C | G | 1 | a0002c0002t0003g0245 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.324+30562G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164589125 | |||||||
| chr2:164589285 | C | T | 1 | a0002c0002t0003g0259 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.324+30402G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164589285 | |||||||
| chr2:164589364 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.324+30323T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164589364 | |||||||
| chr2:164589549 | G | C | 6 | a0001c0001t0001g0120 a0001c0001t0001g0126 a0001c0001t0001g0134 others(3): Show |
6 | HG02109.hp2 HG02257.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.324+30138C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164589549 | |||||||
| chr2:164589637 | G | C | 1 | a0001c0001t0001g0106 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.324+30050C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164589637 | |||||||
| chr2:164589877 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.324+29810G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164589877 | |||||||
| chr2:164589901 | G | A | 1 | a0002c0002t0003g0259 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.324+29786C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164589901 | |||||||
| chr2:164590000 | T | C | 6 | a0001c0001t0001g0078 a0001c0001t0001g0135 a0001c0001t0004g0133 others(3): Show |
6 | HG02559.hp2 HG02976.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.324+29687A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164590000 | |||||||
| chr2:164590036 | C | T | 3 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0061 |
3 | HG01070.hp2 HG01099.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.324+29651G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164590036 | |||||||
| chr2:164590052 | C | T | 12 | a0001c0001t0001g0106 a0001c0001t0001g0117 a0001c0001t0001g0121 others(9): Show |
12 | HG01175.hp2 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.324+29635G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164590052 | |||||||
| chr2:164590223 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.324+29464A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164590223 | |||||||
| chr2:164590236 | T | C | 1 | a0001c0001t0001g0131 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.324+29451A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164590236 | |||||||
| chr2:164590314 | A | C | 1 | a0007c0011t0007g0128 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.324+29373T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164590314 | |||||||
| chr2:164590801 | A | G | 3 | a0001c0001t0001g0093 a0001c0001t0001g0115 a0001c0001t0001g0122 |
3 | HG02976.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.324+28886T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164590801 | |||||||
| chr2:164590835 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.324+28852G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164590835 | |||||||
| chr2:164591283 | A | G | 1 | a0001c0001t0006g0149 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.324+28404T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164591283 | |||||||
| chr2:164591344 | T | C | 1 | a0001c0001t0001g0131 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.324+28343A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164591344 | |||||||
| chr2:164591447 | G | A | 1 | a0002c0002t0005g0267 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.324+28240C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164591447 | |||||||
| chr2:164591553 | C | A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0083 a0001c0001t0004g0029 others(1): Show |
4 | HG01255.hp2 HG03239.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+28134G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164591553 | |||||||
| chr2:164591794 | C | A | 28 | a0001c0001t0004g0004 a0002c0002t0002g0169 a0002c0002t0002g0170 others(25): Show |
28 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.324+27893G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164591794 | |||||||
| chr2:164591892 | T | C | 11 | a0001c0001t0001g0006 a0001c0001t0001g0083 a0001c0001t0001g0090 others(8): Show |
11 | HG00735.hp1 HG01255.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.324+27795A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164591892 | |||||||
| chr2:164592079 | G | A | 15 | a0001c0001t0001g0113 a0001c0001t0001g0120 a0001c0001t0001g0126 others(12): Show |
15 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.324+27608C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164592079 | |||||||
| chr2:164592123 | G | GT | 17 | a0001c0001t0001g0037 a0001c0001t0001g0051 a0001c0001t0001g0071 others(14): Show |
17 | HG01123.hp1 HG01934.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.324+27563dupA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164592123 | |||||||
| chr2:164592129 | T | G | 13 | a0001c0001t0001g0027 a0001c0001t0001g0113 a0001c0001t0001g0120 others(10): Show |
13 | HG00423.hp2 HG02055.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.324+27558A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164592129 | |||||||
| chr2:164592236 | G | A | 3 | a0001c0001t0001g0085 a0001c0001t0004g0043 a0002c0002t0003g0292 |
3 | HG02630.hp2 HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.324+27451C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164592236 | |||||||
| chr2:164592355 | C | T | 51 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(48): Show |
52 | HG00642.hp2 HG00733.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.324+27332G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164592355 | |||||||
| chr2:164592544 | G | C | 1 | a0001c0001t0001g0129 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.324+27143C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164592544 | |||||||
| chr2:164592566 | A | G | 1 | a0002c0002t0002g0273 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.324+27121T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164592566 | |||||||
| chr2:164592619 | T | C | 3 | a0001c0001t0001g0085 a0001c0001t0004g0043 a0002c0002t0003g0292 |
3 | HG02630.hp2 HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.324+27068A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164592619 | |||||||
| chr2:164592663 | A | C | 3 | a0001c0001t0001g0093 a0001c0001t0001g0115 a0001c0001t0001g0122 |
3 | HG02976.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.324+27024T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164592663 | |||||||
| chr2:164593110 | T | C | 112 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(109): Show |
113 | HG00140.hp1 HG00609.hp1 HG00642.hp2 others(110): Show |
intron_variant | MODIFIER | c.324+26577A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164593110 | |||||||
| chr2:164593130 | C | T | 4 | a0001c0001t0001g0134 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
4 | HG02109.hp2 HG02257.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.324+26557G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164593130 | |||||||
| chr2:164593139 | A | G | 68 | a0001c0001t0001g0042 a0001c0001t0004g0004 a0001c0001t0004g0047 others(65): Show |
68 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.324+26548T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164593139 | |||||||
| chr2:164593241 | A | G | 52 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(49): Show |
53 | HG00642.hp2 HG00733.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.324+26446T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164593241 | |||||||
| chr2:164593403 | T | C | 6 | a0001c0001t0001g0117 a0001c0001t0001g0124 a0001c0001t0001g0127 others(3): Show |
6 | HG02258.hp1 HG02486.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.324+26284A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164593403 | |||||||
| chr2:164593446 | C | T | 1 | a0001c0001t0006g0148 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.324+26241G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164593446 | |||||||
| chr2:164593453 | C | CA | 4 | a0002c0002t0002g0277 a0002c0002t0003g0209 a0002c0002t0003g0226 others(1): Show |
4 | NA18991.hp1 NA18998.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+26233dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164593453 | |||||||
| chr2:164593614 | T | C | 11 | a0001c0001t0001g0113 a0001c0001t0001g0120 a0001c0001t0001g0126 others(8): Show |
11 | HG02055.hp2 HG02280.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.324+26073A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164593614 | |||||||
| chr2:164593735 | G | T | 1 | a0002c0002t0003g0259 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.324+25952C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164593735 | |||||||
| chr2:164594146 | A | C | 1 | a0001c0001t0004g0047 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.324+25541T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164594146 | |||||||
| chr2:164594236 | C | T | 2 | a0001c0001t0001g0085 a0001c0001t0004g0043 |
2 | HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.324+25451G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164594236 | |||||||
| chr2:164594295 | A | G | 2 | a0003c0004t0008g0152 a0003c0004t0008g0155 |
2 | HG01099.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.324+25392T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164594295 | |||||||
| chr2:164594322 | C | A | 6 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0004g0089 others(3): Show |
6 | HG00735.hp1 HG02109.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.324+25365G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164594322 | |||||||
| chr2:164594490 | G | A | 1 | a0002c0002t0002g0284 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.324+25197C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164594490 | |||||||
| chr2:164594522 | C | G | 1 | a0001c0001t0001g0045 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.324+25165G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164594522 | |||||||
| chr2:164594582 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.324+25105T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164594582 | |||||||
| chr2:164594843 | A | G | 52 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(49): Show |
53 | HG00642.hp2 HG00733.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.324+24844T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164594843 | |||||||
| chr2:164594962 | T | C | 12 | a0001c0001t0001g0106 a0001c0001t0001g0117 a0001c0001t0001g0121 others(9): Show |
12 | HG01175.hp2 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.324+24725A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164594962 | |||||||
| chr2:164595043 | T | C | 1 | a0001c0001t0001g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.324+24644A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164595043 | |||||||
| chr2:164595094 | T | G | 1 | a0001c0001t0001g0007 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.324+24593A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164595094 | |||||||
| chr2:164595226 | C | T | 15 | a0001c0001t0001g0113 a0001c0001t0001g0120 a0001c0001t0001g0126 others(12): Show |
15 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.324+24461G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164595226 | |||||||
| chr2:164595252 | G | C | 19 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0030 others(16): Show |
19 | HG00609.hp1 HG02027.hp2 HG02523.hp1 others(16): Show |
intron_variant | MODIFIER | c.324+24435C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164595252 | |||||||
| chr2:164595280 | A | T | 1 | a0001c0001t0001g0045 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.324+24407T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164595280 | |||||||
| chr2:164595379 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.324+24308G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164595379 | |||||||
| chr2:164595515 | A | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG01891.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.324+24172T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164595515 | |||||||
| chr2:164595520 | G | A | 1 | a0002c0002t0003g0177 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.324+24167C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164595520 | |||||||
| chr2:164595750 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.324+23937G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164595750 | |||||||
| chr2:164595856 | A | T | 31 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0078 others(28): Show |
32 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.324+23831T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164595856 | |||||||
| chr2:164595905 | G | C | 44 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(41): Show |
45 | HG00140.hp1 HG00408.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.324+23782C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164595905 | |||||||
| chr2:164595952 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.324+23735A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164595952 | |||||||
| chr2:164595991 | G | A | 46 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0078 others(43): Show |
47 | HG00642.hp2 HG00733.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.324+23696C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164595991 | |||||||
| chr2:164595994 | T | G | 8 | a0001c0001t0004g0107 a0001c0001t0004g0108 a0001c0001t0004g0109 others(5): Show |
8 | HG02055.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.324+23693A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164595994 | |||||||
| chr2:164596004 | G | A | 2 | a0001c0001t0001g0129 a0007c0011t0007g0128 |
2 | HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.324+23683C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164596004 | |||||||
| chr2:164596099 | G | C | 2 | a0001c0001t0001g0083 a0002c0002t0002g0162 |
2 | HG01255.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.324+23588C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164596099 | |||||||
| chr2:164596104 | C | G | 2 | a0001c0001t0001g0064 a0001c0001t0004g0065 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.324+23583G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164596104 | |||||||
| chr2:164596232 | C | T | 210 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(207): Show |
212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.324+23455G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164596232 | |||||||
| chr2:164596348 | G | A | 3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0103 |
3 | HG02896.hp1 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.324+23339C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164596348 | |||||||
| chr2:164596398 | T | C | 5 | a0001c0001t0001g0084 a0001c0001t0001g0093 a0001c0001t0001g0120 others(2): Show |
5 | HG02055.hp1 HG02258.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.324+23289A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164596398 | |||||||
| chr2:164596476 | G | C | 34 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0030 others(31): Show |
34 | HG01106.hp1 HG01175.hp2 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.324+23211C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164596476 | |||||||
| chr2:164596738 | T | C | 1 | a0002c0002t0002g0277 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.324+22949A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164596738 | |||||||
| chr2:164596870 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.324+22817A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164596870 | |||||||
| chr2:164596895 | C | A | 102 | a0001c0001t0001g0042 a0001c0001t0004g0047 a0001c0001t0010g0140 others(99): Show |
103 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.324+22792G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164596895 | |||||||
| chr2:164596909 | TA | T | 6 | a0001c0001t0001g0084 a0001c0001t0001g0120 a0001c0001t0001g0121 others(3): Show |
6 | HG02055.hp1 HG02258.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.324+22777delT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164596909 | |||||||
| chr2:164596970 | T | C | 2 | a0002c0002t0002g0190 a0002c0002t0002g0272 |
2 | HG02080.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.324+22717A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164596970 | |||||||
| chr2:164597337 | A | C | 1 | a0001c0001t0001g0093 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.324+22350T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164597337 | |||||||
| chr2:164597352 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.324+22335A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164597352 | |||||||
| chr2:164597450 | A | G | 1 | a0001c0001t0004g0021 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.324+22237T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164597450 | |||||||
| chr2:164597487 | C | A | 13 | a0002c0002t0002g0181 a0002c0002t0003g0160 a0002c0002t0003g0177 others(10): Show |
13 | HG01261.hp1 HG01516.hp1 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.324+22200G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164597487 | |||||||
| chr2:164597555 | T | C | 1 | a0001c0001t0007g0136 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.324+22132A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164597555 | |||||||
| chr2:164597580 | G | A | 1 | a0005c0010t0012g0014 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.324+22107C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164597580 | |||||||
| chr2:164597590 | A | G | 6 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(3): Show |
6 | HG00140.hp1 HG01261.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.324+22097T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164597590 | |||||||
| chr2:164597602 | G | T | 34 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0078 others(31): Show |
35 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.324+22085C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164597602 | |||||||
| chr2:164597777 | A | T | 1 | a0001c0001t0001g0134 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.324+21910T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164597777 | |||||||
| chr2:164598192 | G | A | 10 | a0001c0001t0001g0113 a0001c0001t0004g0107 a0001c0001t0004g0108 others(7): Show |
10 | HG01255.hp2 HG02055.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.324+21495C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164598192 | |||||||
| chr2:164598283 | T | G | 35 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0078 others(32): Show |
36 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.324+21404A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164598283 | |||||||
| chr2:164598467 | T | C | 10 | a0001c0001t0001g0005 a0001c0001t0001g0094 a0001c0001t0001g0095 others(7): Show |
10 | HG02622.hp1 HG02630.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.324+21220A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164598467 | |||||||
| chr2:164598525 | T | C | 102 | a0001c0001t0001g0042 a0001c0001t0004g0047 a0001c0001t0010g0140 others(99): Show |
103 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.324+21162A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164598525 | |||||||
| chr2:164598939 | TAA | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0094 a0001c0001t0001g0095 others(7): Show |
10 | HG02622.hp1 HG02630.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.324+20746_324+2074 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164598939 | |||||||
| chr2:164598943 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.324+20744C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164598943 | |||||||
| chr2:164599308 | CG | C | 198 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(195): Show |
200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.324+20378delC | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164599308 | |||||||
| chr2:164599472 | C | T | 2 | a0001c0001t0008g0141 a0001c0001t0008g0142 |
2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.324+20215G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164599472 | |||||||
| chr2:164599683 | T | C | 19 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(16): Show |
19 | HG00140.hp1 HG01261.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.324+20004A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164599683 | |||||||
| chr2:164599718 | T | C | 2 | a0002c0002t0002g0284 a0002c0002t0002g0286 |
2 | HG01123.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.324+19969A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164599718 | |||||||
| chr2:164600462 | A | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.324+19225T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164600462 | |||||||
| chr2:164600552 | C | A | 4 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0071 others(1): Show |
4 | HG00544.hp2 HG00621.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+19135G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164600552 | |||||||
| chr2:164600585 | G | A | 3 | a0001c0001t0001g0028 a0001c0001t0001g0063 a0001c0001t0004g0062 |
3 | NA19006.hp1 NA19011.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.324+19102C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164600585 | |||||||
| chr2:164600756 | T | A | 200 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(197): Show |
202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.324+18931A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164600756 | |||||||
| chr2:164601041 | C | G | 1 | a0001c0001t0006g0145 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.324+18646G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164601041 | |||||||
| chr2:164601077 | T | C | 1 | a0002c0002t0003g0186 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.324+18610A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164601077 | |||||||
| chr2:164601127 | C | A | 9 | a0001c0001t0001g0113 a0001c0001t0004g0107 a0001c0001t0004g0108 others(6): Show |
9 | HG02055.hp2 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.324+18560G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164601127 | |||||||
| chr2:164601142 | A | G | 2 | a0002c0002t0005g0222 a0002c0002t0005g0269 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.324+18545T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164601142 | |||||||
| chr2:164601612 | T | C | 1 | a0001c0001t0001g0013 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.324+18075A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164601612 | |||||||
| chr2:164601823 | C | T | 198 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(195): Show |
200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.324+17864G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164601823 | |||||||
| chr2:164601843 | T | C | 1 | a0002c0002t0005g0268 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.324+17844A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164601843 | |||||||
| chr2:164601937 | A | G | 198 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(195): Show |
200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.324+17750T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164601937 | |||||||
| chr2:164602012 | G | A | 1 | a0002c0002t0002g0231 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.324+17675C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164602012 | |||||||
| chr2:164602133 | T | A | 1 | a0002c0002t0005g0178 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.324+17554A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164602133 | |||||||
| chr2:164602133 | T | TA | 12 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(9): Show |
12 | HG00140.hp1 HG01261.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.324+17553dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164602133 | |||||||
| chr2:164602134 | A | T | 1 | a0001c0001t0004g0098 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.324+17553T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164602134 | |||||||
| chr2:164602176 | A | G | 1 | a0001c0001t0007g0073 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.324+17511T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164602176 | |||||||
| chr2:164602194 | A | G | 1 | a0001c0001t0004g0043 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.324+17493T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164602194 | |||||||
| chr2:164602198 | A | T | 13 | a0002c0002t0002g0181 a0002c0002t0003g0160 a0002c0002t0003g0177 others(10): Show |
13 | HG01261.hp1 HG01516.hp1 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.324+17489T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164602198 | |||||||
| chr2:164602380 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.324+17307T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164602380 | |||||||
| chr2:164602431 | G | A | 8 | a0001c0001t0004g0107 a0001c0001t0004g0108 a0001c0001t0004g0109 others(5): Show |
8 | HG02055.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.324+17256C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164602431 | |||||||
| chr2:164602638 | G | A | 4 | a0001c0001t0001g0084 a0001c0001t0001g0120 a0001c0001t0001g0121 others(1): Show |
4 | HG02055.hp1 HG02258.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+17049C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164602638 | |||||||
| chr2:164602986 | T | C | 34 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0078 others(31): Show |
35 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.324+16701A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164602986 | |||||||
| chr2:164603239 | GGAAAA | G | 34 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0078 others(31): Show |
35 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.324+16443_324+1644 others(9): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164603239 | |||||||
| chr2:164603568 | G | T | 1 | a0001c0001t0007g0136 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.324+16119C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164603568 | |||||||
| chr2:164603629 | A | C | 198 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(195): Show |
200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.324+16058T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164603629 | |||||||
| chr2:164603662 | C | CAA | 9 | a0001c0001t0001g0005 a0001c0001t0001g0094 a0001c0001t0001g0095 others(6): Show |
9 | HG02622.hp1 HG02630.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.324+16023_324+1602 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164603662 | |||||||
| chr2:164603671 | A | AT | 10 | a0001c0001t0001g0113 a0001c0001t0004g0107 a0001c0001t0004g0108 others(7): Show |
10 | HG01255.hp2 HG02055.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.324+16015_324+1601 others(5): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164603671 | |||||||
| chr2:164603671 | A | T | 3 | a0001c0001t0001g0085 a0001c0001t0004g0020 a0002c0002t0003g0292 |
3 | HG02630.hp2 HG03453.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.324+16016T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164603671 | |||||||
| chr2:164603671 | AAT | A | 16 | a0001c0001t0001g0092 a0001c0001t0001g0106 a0001c0001t0001g0115 others(13): Show |
16 | HG00735.hp1 HG01106.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.324+16014_324+1601 others(6): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164603671 | |||||||
| chr2:164603672 | AT | A | 83 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(80): Show |
85 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.324+16014delA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164603672 | |||||||
| chr2:164603673 | T | A | 98 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0012 others(95): Show |
98 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.324+16014A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164603673 | |||||||
| chr2:164603675 | T | A | 197 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(194): Show |
199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.324+16012A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164603675 | |||||||
| chr2:164603677 | T | A | 191 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(188): Show |
193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.324+16010A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164603677 | |||||||
| chr2:164603692 | C | T | 198 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(195): Show |
200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.324+15995G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164603692 | |||||||
| chr2:164603889 | T | C | 10 | a0001c0001t0001g0113 a0001c0001t0004g0107 a0001c0001t0004g0108 others(7): Show |
10 | HG01255.hp2 HG02055.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.324+15798A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164603889 | |||||||
| chr2:164604203 | C | T | 13 | a0001c0001t0001g0106 a0001c0001t0001g0115 a0001c0001t0001g0117 others(10): Show |
13 | HG01106.hp1 HG01175.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.324+15484G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164604203 | |||||||
| chr2:164604270 | T | C | 2 | a0001c0001t0001g0129 a0007c0011t0007g0128 |
2 | HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.324+15417A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164604270 | |||||||
| chr2:164604294 | G | T | 33 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0078 others(30): Show |
34 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.324+15393C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164604294 | |||||||
| chr2:164604355 | C | T | 2 | a0001c0001t0001g0064 a0001c0001t0004g0065 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.324+15332G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164604355 | |||||||
| chr2:164604419 | C | T | 7 | a0001c0001t0001g0078 a0001c0001t0001g0135 a0001c0001t0004g0133 others(4): Show |
7 | HG02559.hp2 HG02572.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.324+15268G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164604419 | |||||||
| chr2:164604453 | T | C | 1 | a0001c0001t0006g0149 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.324+15234A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164604453 | |||||||
| chr2:164604570 | G | C | 3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0103 |
3 | HG02896.hp1 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.324+15117C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164604570 | |||||||
| chr2:164604606 | A | G | 221 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(218): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.324+15081T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164604606 | |||||||
| chr2:164604858 | C | T | 2 | a0001c0001t0001g0085 a0002c0002t0003g0292 |
2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.324+14829G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164604858 | |||||||
| chr2:164604869 | A | C | 1 | a0002c0002t0002g0278 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.324+14818T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164604869 | |||||||
| chr2:164605011 | G | A | 1 | a0002c0002t0003g0292 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.324+14676C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164605011 | |||||||
| chr2:164605129 | G | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.324+14558C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164605129 | |||||||
| chr2:164605145 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.324+14542A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164605145 | |||||||
| chr2:164605228 | AC | A | 3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0103 |
3 | HG02896.hp1 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.324+14458delG | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164605228 | |||||||
| chr2:164605335 | G | A | 13 | a0001c0001t0001g0106 a0001c0001t0001g0115 a0001c0001t0001g0117 others(10): Show |
13 | HG01106.hp1 HG01175.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.324+14352C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164605335 | |||||||
| chr2:164605465 | C | T | 4 | a0001c0001t0001g0084 a0001c0001t0001g0120 a0001c0001t0001g0121 others(1): Show |
4 | HG02055.hp1 HG02258.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+14222G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164605465 | |||||||
| chr2:164605563 | A | C | 23 | a0001c0001t0001g0005 a0001c0001t0001g0094 a0001c0001t0001g0095 others(20): Show |
23 | HG01261.hp1 HG01516.hp1 HG01517.hp2 others(20): Show |
intron_variant | MODIFIER | c.324+14124T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164605563 | |||||||
| chr2:164605721 | G | A | 42 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(39): Show |
42 | HG00140.hp1 HG01261.hp1 HG01261.hp2 others(39): Show |
intron_variant | MODIFIER | c.324+13966C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164605721 | |||||||
| chr2:164605785 | A | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0037 |
3 | NA18972.hp1 NA19056.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.324+13902T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164605785 | |||||||
| chr2:164605901 | C | A | 108 | a0001c0001t0001g0042 a0001c0001t0001g0090 a0001c0001t0001g0092 others(105): Show |
109 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.324+13786G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164605901 | |||||||
| chr2:164606033 | T | C | 108 | a0001c0001t0001g0042 a0001c0001t0001g0090 a0001c0001t0001g0092 others(105): Show |
109 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.324+13654A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164606033 | |||||||
| chr2:164606417 | A | G | 1 | a0001c0001t0004g0043 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.324+13270T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164606417 | |||||||
| chr2:164606510 | A | G | 2 | a0002c0002t0003g0192 a0002c0002t0003g0283 |
2 | HG03490.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.324+13177T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164606510 | |||||||
| chr2:164606736 | T | C | 2 | a0001c0001t0001g0064 a0001c0001t0004g0065 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.324+12951A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164606736 | |||||||
| chr2:164607219 | G | A | 10 | a0001c0001t0001g0113 a0001c0001t0004g0107 a0001c0001t0004g0108 others(7): Show |
10 | HG01255.hp2 HG02055.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.324+12468C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164607219 | |||||||
| chr2:164607443 | C | G | 211 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(208): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.324+12244G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164607443 | |||||||
| chr2:164608238 | G | A | 1 | a0002c0002t0002g0230 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.324+11449C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164608238 | |||||||
| chr2:164608246 | C | A | 33 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0078 others(30): Show |
34 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.324+11441G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164608246 | |||||||
| chr2:164608330 | C | A | 1 | a0002c0002t0003g0236 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.324+11357G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164608330 | |||||||
| chr2:164608338 | C | T | 197 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(194): Show |
199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.324+11349G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164608338 | |||||||
| chr2:164608447 | A | G | 4 | a0001c0001t0001g0084 a0001c0001t0001g0120 a0001c0001t0001g0121 others(1): Show |
4 | HG02055.hp1 HG02258.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+11240T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164608447 | |||||||
| chr2:164608590 | AG | A | 39 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0103 others(36): Show |
40 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.324+11096delC | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164608590 | |||||||
| chr2:164608591 | G | A | 168 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(165): Show |
169 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.324+11096C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164608591 | |||||||
| chr2:164608592 | A | G | 4 | a0002c0002t0002g0191 a0002c0002t0002g0243 a0002c0002t0002g0246 others(1): Show |
4 | HG01069.hp2 HG01928.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.324+11095T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164608592 | |||||||
| chr2:164608644 | A | T | 1 | a0002c0002t0003g0201 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.324+11043T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164608644 | |||||||
| chr2:164608918 | G | T | 1 | a0001c0003t0007g0067 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.324+10769C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164608918 | |||||||
| chr2:164609084 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.324+10603A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164609084 | |||||||
| chr2:164609316 | C | G | 1 | a0001c0001t0001g0075 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.324+10371G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164609316 | |||||||
| chr2:164609429 | G | A | 1 | a0002c0002t0003g0187 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.324+10258C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164609429 | |||||||
| chr2:164609547 | A | G | 1 | a0002c0002t0003g0259 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.324+10140T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164609547 | |||||||
| chr2:164609588 | T | C | 1 | a0002c0002t0003g0258 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.324+10099A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164609588 | |||||||
| chr2:164609633 | G | A | 1 | a0001c0003t0007g0067 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.324+10054C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164609633 | |||||||
| chr2:164609667 | G | A | 198 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(195): Show |
200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.324+10020C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164609667 | |||||||
| chr2:164609931 | T | G | 1 | a0001c0001t0004g0029 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.324+9756A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164609931 | |||||||
| chr2:164609939 | T | G | 151 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(148): Show |
152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.324+9748A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164609939 | |||||||
| chr2:164609999 | T | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0132 |
3 | HG01891.hp1 HG02818.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.324+9688A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164609999 | |||||||
| chr2:164610059 | G | A | 13 | a0001c0001t0001g0106 a0001c0001t0001g0115 a0001c0001t0001g0117 others(10): Show |
13 | HG01106.hp1 HG01175.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.324+9628C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164610059 | |||||||
| chr2:164610278 | C | T | 1 | a0001c0001t0001g0009 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.324+9409G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164610278 | |||||||
| chr2:164610327 | C | T | 198 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(195): Show |
200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.324+9360G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164610327 | |||||||
| chr2:164610344 | G | A | 199 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(196): Show |
201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.324+9343C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164610344 | |||||||
| chr2:164610384 | A | T | 1 | a0001c0001t0001g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.324+9303T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164610384 | |||||||
| chr2:164610392 | T | A | 1 | a0001c0001t0001g0082 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.324+9295A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164610392 | |||||||
| chr2:164610558 | A | C | 32 | a0002c0002t0002g0168 a0002c0002t0002g0191 a0002c0002t0002g0194 others(29): Show |
33 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.324+9129T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164610558 | |||||||
| chr2:164610562 | T | C | 27 | a0001c0001t0001g0042 a0001c0001t0004g0047 a0002c0002t0002g0188 others(24): Show |
27 | HG00408.hp2 HG00544.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.324+9125A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164610562 | |||||||
| chr2:164610663 | A | G | 2 | a0002c0002t0002g0190 a0002c0002t0002g0272 |
2 | HG02080.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.324+9024T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164610663 | |||||||
| chr2:164610765 | A | G | 10 | a0001c0001t0001g0005 a0001c0001t0001g0094 a0001c0001t0001g0095 others(7): Show |
10 | HG02622.hp1 HG02630.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.324+8922T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164610765 | |||||||
| chr2:164610822 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.324+8865A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164610822 | |||||||
| chr2:164610875 | A | T | 2 | a0001c0001t0001g0085 a0002c0002t0003g0292 |
2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.324+8812T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164610875 | |||||||
| chr2:164610886 | A | C | 31 | a0001c0001t0001g0078 a0001c0001t0001g0105 a0001c0001t0001g0135 others(28): Show |
32 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.324+8801T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164610886 | |||||||
| chr2:164610911 | C | CA | 168 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(165): Show |
170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.324+8775dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164610911 | |||||||
| chr2:164610911 | C | CAA | 9 | a0001c0001t0001g0113 a0002c0002t0002g0171 a0002c0002t0002g0172 others(6): Show |
9 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(6): Show |
intron_variant | MODIFIER | c.324+8774_324+8775d others(4): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164610911 | |||||||
| chr2:164611025 | T | A | 31 | a0001c0001t0001g0078 a0001c0001t0001g0105 a0001c0001t0001g0135 others(28): Show |
32 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.324+8662A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164611025 | |||||||
| chr2:164611270 | G | A | 1 | a0001c0001t0001g0030 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.324+8417C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164611270 | |||||||
| chr2:164611305 | G | A | 3 | a0001c0001t0001g0040 a0001c0001t0004g0031 a0001c0001t0004g0074 |
3 | NA18963.hp2 NA18985.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.324+8382C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164611305 | |||||||
| chr2:164611317 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.324+8370A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164611317 | |||||||
| chr2:164611449 | T | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0069 |
2 | NA19005.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.324+8238A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164611449 | |||||||
| chr2:164611605 | G | A | 2 | a0001c0001t0001g0032 a0002c0002t0002g0167 |
2 | HG00438.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.324+8082C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164611605 | |||||||
| chr2:164611676 | A | G | 10 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(7): Show |
10 | HG00140.hp1 HG01261.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.324+8011T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164611676 | |||||||
| chr2:164611850 | G | T | 12 | a0001c0001t0001g0106 a0001c0001t0001g0115 a0001c0001t0001g0117 others(9): Show |
12 | HG01106.hp1 HG01175.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.324+7837C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164611850 | |||||||
| chr2:164611852 | A | C | 213 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(210): Show |
215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.324+7835T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164611852 | |||||||
| chr2:164611869 | A | G | 213 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(210): Show |
215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.324+7818T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164611869 | |||||||
| chr2:164611879 | T | G | 2 | a0001c0001t0001g0129 a0007c0011t0007g0128 |
2 | HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.324+7808A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164611879 | |||||||
| chr2:164611925 | G | A | 212 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(209): Show |
214 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.324+7762C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164611925 | |||||||
| chr2:164611940 | G | A | 7 | a0002c0002t0002g0219 a0002c0002t0002g0221 a0002c0002t0002g0224 others(4): Show |
7 | NA18941.hp2 NA18974.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.324+7747C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164611940 | |||||||
| chr2:164612001 | G | C | 1 | a0002c0002t0002g0286 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.324+7686C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164612001 | |||||||
| chr2:164612030 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.324+7657A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164612030 | |||||||
| chr2:164612106 | T | G | 211 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(208): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.324+7581A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164612106 | |||||||
| chr2:164612149 | T | A | 1 | a0002c0002t0002g0174 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324+7538A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164612149 | |||||||
| chr2:164612155 | C | T | 3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0103 |
3 | HG02896.hp1 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.324+7532G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164612155 | |||||||
| chr2:164612212 | T | G | 1 | a0001c0001t0006g0150 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.324+7475A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164612212 | |||||||
| chr2:164612240 | T | C | 211 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(208): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.324+7447A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164612240 | |||||||
| chr2:164612433 | T | G | 4 | a0002c0002t0002g0181 a0002c0002t0003g0160 a0002c0002t0003g0182 others(1): Show |
4 | HG01261.hp1 HG02738.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.324+7254A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164612433 | |||||||
| chr2:164612515 | T | C | 211 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(208): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.324+7172A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164612515 | |||||||
| chr2:164612547 | T | C | 12 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0118 others(9): Show |
12 | HG01106.hp1 HG01175.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.324+7140A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164612547 | |||||||
| chr2:164612714 | T | C | 3 | a0001c0001t0001g0105 a0001c0001t0006g0151 a0001c0001t0006g0159 |
3 | HG02895.hp2 HG02897.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.324+6973A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164612714 | |||||||
| chr2:164612791 | C | G | 211 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(208): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.324+6896G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164612791 | |||||||
| chr2:164612807 | G | A | 10 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(7): Show |
10 | HG00140.hp1 HG01261.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.324+6880C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164612807 | |||||||
| chr2:164612936 | T | G | 1 | a0002c0002t0002g0243 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.324+6751A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164612936 | |||||||
| chr2:164613007 | C | G | 28 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(25): Show |
29 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.324+6680G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164613007 | |||||||
| chr2:164613033 | G | A | 4 | a0001c0001t0001g0134 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
4 | HG02109.hp2 HG02257.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.324+6654C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164613033 | |||||||
| chr2:164613042 | G | C | 1 | a0001c0001t0001g0070 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.324+6645C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164613042 | |||||||
| chr2:164613056 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.324+6631C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164613056 | |||||||
| chr2:164613433 | T | G | 211 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(208): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.324+6254A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164613433 | |||||||
| chr2:164613469 | A | G | 1 | a0002c0002t0002g0168 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.324+6218T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164613469 | |||||||
| chr2:164613527 | C | T | 7 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(4): Show |
7 | HG02622.hp1 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.324+6160G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164613527 | |||||||
| chr2:164613703 | A | G | 4 | a0002c0002t0003g0223 a0002c0002t0003g0244 a0002c0002t0005g0222 others(1): Show |
4 | HG01516.hp1 HG01517.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+5984T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164613703 | |||||||
| chr2:164613776 | T | A | 7 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0103 others(4): Show |
7 | HG02109.hp2 HG02257.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.324+5911A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164613776 | |||||||
| chr2:164613991 | C | T | 1 | a0001c0001t0004g0046 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.324+5696G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164613991 | |||||||
| chr2:164614002 | C | T | 3 | a0002c0002t0002g0188 a0002c0002t0002g0189 a0002c0002t0002g0290 |
3 | NA18944.hp2 NA19007.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.324+5685G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164614002 | |||||||
| chr2:164614146 | G | A | 211 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(208): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.324+5541C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164614146 | |||||||
| chr2:164614157 | C | T | 2 | a0001c0005t0001g0035 a0001c0005t0007g0072 |
2 | HG00639.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.324+5530G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164614157 | |||||||
| chr2:164614161 | C | CA | 3 | a0002c0002t0003g0223 a0002c0002t0005g0222 a0002c0002t0005g0269 |
3 | HG01516.hp1 HG01517.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.324+5525dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164614161 | |||||||
| chr2:164614162 | A | C | 4 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0071 others(1): Show |
4 | HG00544.hp2 HG00621.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+5525T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164614162 | |||||||
| chr2:164614225 | T | C | 3 | a0001c0001t0008g0153 a0003c0004t0008g0152 a0003c0004t0008g0155 |
3 | HG00733.hp2 HG01099.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.324+5462A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164614225 | |||||||
| chr2:164614399 | T | C | 1 | a0001c0001t0004g0043 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.324+5288A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164614399 | |||||||
| chr2:164614460 | A | G | 12 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0118 others(9): Show |
12 | HG01106.hp1 HG01175.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.324+5227T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164614460 | |||||||
| chr2:164614494 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.324+5193G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164614494 | |||||||
| chr2:164614588 | GGGT | G | 4 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0071 others(1): Show |
4 | HG00544.hp2 HG00621.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+5096_324+5098d others(5): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164614588 | |||||||
| chr2:164614638 | T | A | 1 | a0002c0002t0002g0224 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.324+5049A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164614638 | |||||||
| chr2:164614886 | G | C | 1 | a0001c0001t0001g0106 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.324+4801C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164614886 | |||||||
| chr2:164615014 | A | T | 1 | a0001c0001t0001g0045 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.324+4673T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164615014 | |||||||
| chr2:164615069 | C | T | 1 | a0002c0002t0003g0177 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.324+4618G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164615069 | |||||||
| chr2:164615088 | C | G | 1 | a0001c0001t0001g0044 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.324+4599G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164615088 | |||||||
| chr2:164615097 | C | T | 2 | a0001c0001t0008g0141 a0001c0001t0008g0142 |
2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.324+4590G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164615097 | |||||||
| chr2:164615328 | T | C | 3 | a0001c0001t0001g0042 a0001c0005t0001g0035 a0001c0005t0007g0072 |
3 | HG00639.hp1 HG01106.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.324+4359A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164615328 | |||||||
| chr2:164615371 | A | G | 9 | a0002c0002t0002g0243 a0002c0002t0003g0186 a0002c0002t0003g0187 others(6): Show |
9 | HG00738.hp1 HG01255.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.324+4316T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164615371 | |||||||
| chr2:164615509 | A | T | 23 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0113 others(20): Show |
23 | HG01261.hp1 HG01891.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.324+4178T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164615509 | |||||||
| chr2:164615832 | A | T | 8 | a0001c0001t0001g0113 a0001c0001t0004g0107 a0001c0001t0004g0108 others(5): Show |
8 | HG02055.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.324+3855T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164615832 | |||||||
| chr2:164615838 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.324+3849T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164615838 | |||||||
| chr2:164615858 | T | A | 1 | a0001c0001t0001g0036 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.324+3829A>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164615858 | |||||||
| chr2:164615895 | C | T | 209 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(206): Show |
211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.324+3792G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164615895 | |||||||
| chr2:164615967 | A | C | 1 | a0001c0001t0001g0137 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.324+3720T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164615967 | |||||||
| chr2:164616287 | G | A | 1 | a0001c0001t0001g0008 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.324+3400C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616287 | |||||||
| chr2:164616425 | C | CA | 28 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0038 others(25): Show |
28 | HG00438.hp1 HG00438.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.324+3261dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616425 | |||||||
| chr2:164616425 | CA | C | 115 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(112): Show |
116 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.324+3261delT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616425 | |||||||
| chr2:164616425 | CAAAAAAA others(5): Show |
C | 3 | a0002c0002t0003g0232 a0002c0002t0003g0240 a0006c0007t0003g0239 |
3 | NA18940.hp2 NA18954.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.324+3250_324+3261d others(14): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616425 | |||||||
| chr2:164616470 | C | T | 211 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(208): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.324+3217G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616470 | |||||||
| chr2:164616720 | T | C | 1 | a0001c0001t0001g0005 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.324+2967A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616720 | |||||||
| chr2:164616837 | G | T | 1 | a0002c0002t0003g0161 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.324+2850C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616837 | |||||||
| chr2:164616840 | A | C | 1 | a0002c0002t0003g0161 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.324+2847T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616840 | |||||||
| chr2:164616844 | T | C | 1 | a0002c0002t0003g0161 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.324+2843A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616844 | |||||||
| chr2:164616845 | C | T | 1 | a0002c0002t0003g0161 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.324+2842G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616845 | |||||||
| chr2:164616847 | C | A | 1 | a0002c0002t0003g0161 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.324+2840G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616847 | |||||||
| chr2:164616850 | A | C | 1 | a0001c0001t0001g0042 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.324+2837T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616850 | |||||||
| chr2:164616861 | A | T | 1 | a0002c0002t0003g0161 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.324+2826T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616861 | |||||||
| chr2:164616871 | A | T | 1 | a0002c0002t0003g0161 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.324+2816T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616871 | |||||||
| chr2:164616872 | T | G | 1 | a0002c0002t0003g0161 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.324+2815A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616872 | |||||||
| chr2:164616881 | G | T | 1 | a0002c0002t0003g0161 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.324+2806C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616881 | |||||||
| chr2:164616906 | C | G | 1 | a0002c0002t0003g0161 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.324+2781G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616906 | |||||||
| chr2:164616916 | G | T | 1 | a0002c0002t0003g0161 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.324+2771C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616916 | |||||||
| chr2:164616930 | A | C | 1 | a0002c0002t0003g0161 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.324+2757T>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164616930 | |||||||
| chr2:164617002 | A | G | 203 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0077 others(200): Show |
205 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.324+2685T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617002 | |||||||
| chr2:164617272 | C | T | 12 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0118 others(9): Show |
12 | HG01106.hp1 HG01175.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.324+2415G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617272 | |||||||
| chr2:164617273 | G | A | 1 | a0001c0001t0001g0005 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.324+2414C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617273 | |||||||
| chr2:164617372 | C | A | 1 | a0001c0001t0004g0074 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.324+2315G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617372 | |||||||
| chr2:164617523 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.324+2164G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617523 | |||||||
| chr2:164617903 | T | C | 206 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0077 others(203): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.324+1784A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617903 | |||||||
| chr2:164617925 | A | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0080 |
2 | NA18940.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.324+1762T>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617925 | |||||||
| chr2:164617951 | C | CT | 66 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0117 others(63): Show |
67 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.324+1735dupA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617951 | |||||||
| chr2:164617959 | T | G | 1 | a0001c0001t0001g0075 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.324+1728A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617959 | |||||||
| chr2:164617959 | T | TTG | 50 | a0001c0001t0001g0127 a0001c0001t0007g0104 a0001c0001t0010g0140 others(47): Show |
50 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.324+1727_324+1728i others(4): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617959 | |||||||
| chr2:164617959 | T | TTGG | 7 | a0002c0002t0002g0284 a0002c0002t0002g0286 a0002c0002t0002g0287 others(4): Show |
7 | HG01123.hp2 HG02071.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.324+1727_324+1728i others(5): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617959 | |||||||
| chr2:164617959 | TG | T | 53 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(50): Show |
53 | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.324+1727delC | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617959 | |||||||
| chr2:164617959 | TGG | T | 55 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(52): Show |
56 | HG00140.hp1 HG00733.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.324+1726_324+1727d others(4): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617959 | |||||||
| chr2:164617960 | G | T | 17 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0124 others(14): Show |
17 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.324+1727C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617960 | |||||||
| chr2:164617961 | G | T | 17 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0080 others(14): Show |
17 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.324+1726C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617961 | |||||||
| chr2:164617962 | G | T | 42 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(39): Show |
43 | HG00733.hp2 HG00735.hp1 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.324+1725C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617962 | |||||||
| chr2:164617963 | G | T | 1 | a0001c0001t0001g0082 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.324+1724C>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617963 | |||||||
| chr2:164617967 | G | C | 1 | a0002c0002t0002g0288 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.324+1720C>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617967 | |||||||
| chr2:164617973 | T | G | 1 | a0001c0001t0004g0046 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.324+1714A>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617973 | |||||||
| chr2:164617999 | C | G | 7 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(4): Show |
7 | HG00140.hp1 HG01261.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.324+1688G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164617999 | |||||||
| chr2:164618011 | G | A | 194 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(191): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.324+1676C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164618011 | |||||||
| chr2:164618053 | G | A | 185 | a0001c0001t0001g0006 a0001c0001t0001g0077 a0001c0001t0001g0078 others(182): Show |
187 | HG00140.hp2 HG00544.hp1 HG00639.hp2 others(184): Show |
intron_variant | MODIFIER | c.324+1634C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164618053 | |||||||
| chr2:164618084 | C | T | 1 | a0002c0002t0002g0162 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.324+1603G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164618084 | |||||||
| chr2:164618266 | A | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0132 |
3 | HG01891.hp1 HG02818.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.324+1421T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164618266 | |||||||
| chr2:164618275 | CT | C | 23 | a0001c0001t0001g0105 a0001c0001t0006g0001 a0001c0001t0006g0143 others(20): Show |
24 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.324+1411delA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164618275 | |||||||
| chr2:164618353 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.324+1334G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164618353 | |||||||
| chr2:164618388 | G | GT | 3 | a0001c0001t0001g0006 a0001c0001t0001g0083 a0002c0002t0003g0161 |
3 | HG04204.hp1 NA19001.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.324+1298dupA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164618388 | |||||||
| chr2:164618453 | T | C | 2 | a0001c0001t0001g0129 a0007c0011t0007g0128 |
2 | HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.324+1234A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164618453 | |||||||
| chr2:164618751 | C | T | 1 | a0002c0002t0003g0160 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.324+936G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164618751 | |||||||
| chr2:164619507 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.324+180C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164619507 | |||||||
| chr2:164619616 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.324+71C>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 2/13 | chr2 | 164619616 | |||||||
| chr2:164620038 | G | GTC | 5 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 others(2): Show |
5 | HG02258.hp2 HG02630.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.192-221_192-220dup others(2): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620038 | |||||||
| chr2:164620038 | GTCTC | G | 177 | a0001c0001t0001g0106 a0001c0001t0001g0113 a0001c0001t0001g0115 others(174): Show |
179 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.192-223_192-220del others(4): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620038 | |||||||
| chr2:164620038 | GTCTCTCT others(1): Show |
G | 21 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0093 others(18): Show |
21 | HG00735.hp1 HG02109.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.192-227_192-220del others(8): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620038 | |||||||
| chr2:164620054 | CTCT | C | 4 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
4 | HG02257.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.192-238_192-236del others(3): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620054 | |||||||
| chr2:164620059 | T | C | 4 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
4 | HG02257.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.192-240A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620059 | |||||||
| chr2:164620067 | C | A | 4 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
4 | HG02257.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.192-248G>T | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620067 | |||||||
| chr2:164620073 | A | AC | 29 | a0001c0001t0006g0145 a0001c0001t0006g0151 a0001c0001t0006g0156 others(26): Show |
29 | HG00544.hp1 HG00673.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.192-255dupG | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620073 | |||||||
| chr2:164620073 | A | ACC | 11 | a0001c0001t0006g0144 a0001c0001t0010g0140 a0001c0001t0010g0154 others(8): Show |
11 | HG00438.hp1 HG01099.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.192-256_192-255dup others(2): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620073 | |||||||
| chr2:164620076 | C | G | 4 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
4 | HG02257.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.192-257G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620076 | |||||||
| chr2:164620076 | C | T | 8 | a0001c0001t0001g0113 a0001c0001t0004g0107 a0001c0001t0004g0108 others(5): Show |
8 | HG02055.hp2 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.192-257G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620076 | |||||||
| chr2:164620076 | CCT | C | 30 | a0001c0001t0001g0092 a0001c0001t0001g0095 a0001c0001t0001g0096 others(27): Show |
30 | HG00099.hp1 HG00639.hp2 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.192-259_192-258del others(2): Show |
GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620076 | |||||||
| chr2:164620077 | CT | C | 73 | a0001c0001t0001g0094 a0001c0001t0001g0097 a0001c0001t0001g0105 others(70): Show |
74 | HG00140.hp2 HG00438.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.192-259delA | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620077 | |||||||
| chr2:164620078 | T | C | 96 | a0001c0001t0001g0093 a0001c0001t0001g0100 a0001c0001t0001g0101 others(93): Show |
97 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.192-259A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620078 | |||||||
| chr2:164620078 | T | TC | 30 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(27): Show |
30 | HG00544.hp2 HG00621.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.192-260dupG | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620078 | |||||||
| chr2:164620083 | C | G | 1 | a0001c0001t0001g0005 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.192-264G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620083 | |||||||
| chr2:164620092 | C | T | 6 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0004g0089 others(3): Show |
6 | HG00735.hp1 HG02109.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.192-273G>A | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620092 | |||||||
| chr2:164620518 | G | GA | 207 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0093 others(204): Show |
209 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.191+600dupT | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620518 | |||||||
| chr2:164620652 | C | G | 1 | a0001c0001t0004g0004 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.191+467G>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620652 | |||||||
| chr2:164620741 | T | C | 6 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(3): Show |
6 | HG02109.hp2 HG02257.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.191+378A>G | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620741 | |||||||
| chr2:164620826 | A | G | 21 | a0001c0001t0006g0001 a0001c0001t0006g0143 a0001c0001t0006g0144 others(18): Show |
22 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.191+293T>C | GRB14 | ENSG00000115290.11 | transcript | ENST00000263915.8 | protein_coding | 1/13 | chr2 | 164620826 |