Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2534 |
| ensemblid | ENSG00000010810.18 |
| hgncid | 4037 |
| symbol | FYN |
| name | FYN proto-oncogene, Src family tyrosine kinase |
| refseq_nuc | NM_002037.5 |
| refseq_prot | NP_002028.1 |
| ensembl_nuc | ENST00000354650.7 |
| ensembl_prot | ENSP00000346671.3 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 111660332 |
| end | 111873452 |
| strand | - |
| ver | v1.2 |
| region | chr6:111660332-111873452 |
| region5000 | chr6:111655332-111878452 |
| regionname0 | FYN_chr6_111660332_111873452 |
| regionname5000 | FYN_chr6_111655332_111878452 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1611 | 227 | 76 | 37 | 90 | 2 | 20 | FYN_chr6_111655332_111878452 | FYN | ATGGG others(1606): Show |
chr6 | 111655332 | 111878452 | ||
| a0001c0002 | 0/0 | 1611 | 5 | 4 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | ATGGG others(1606): Show |
chr6 | 111655332 | 111878452 | ||
| a0001c0003 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | ATGGG others(1606): Show |
chr6 | 111655332 | 111878452 | ||
| a0001c0004 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | ATGGG others(1606): Show |
chr6 | 111655332 | 111878452 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3628 | 57 | 28 | 5 | 16 | 1 | 7 | FYN_chr6_111655332_111878452 | FYN | AGAGC others(3623): Show |
chr6 | 111655332 | 111878452 |
| a0001c0001t0002 | 0/1 | 3628 | 43 | 3 | 11 | 24 | 0 | 4 | FYN_chr6_111655332_111878452 | FYN | AGAGC others(3623): Show |
chr6 | 111655332 | 111878452 |
| a0001c0001t0003 | 1/0 | 3628 | 19 | 3 | 5 | 4 | 0 | 6 | FYN_chr6_111655332_111878452 | FYN | AGAGC others(3623): Show |
chr6 | 111655332 | 111878452 |
| a0001c0001t0004 | 0/0 | 3628 | 18 | 10 | 3 | 5 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | AGAGC others(3623): Show |
chr6 | 111655332 | 111878452 |
| a0001c0001t0005 | 0/0 | 3628 | 15 | 4 | 0 | 11 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | AGAGC others(3623): Show |
chr6 | 111655332 | 111878452 |
| a0001c0001t0006 | 0/0 | 3628 | 13 | 2 | 4 | 7 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | AGAGC others(3623): Show |
chr6 | 111655332 | 111878452 |
| a0001c0001t0007 | 0/0 | 3628 | 13 | 1 | 5 | 6 | 1 | 0 | FYN_chr6_111655332_111878452 | FYN | AGAGC others(3623): Show |
chr6 | 111655332 | 111878452 |
| a0001c0001t0008 | 0/0 | 3628 | 9 | 9 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | AGAGC others(3623): Show |
chr6 | 111655332 | 111878452 |
| a0001c0001t0009 | 0/0 | 3628 | 7 | 0 | 0 | 7 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | AGAGC others(3623): Show |
chr6 | 111655332 | 111878452 |
| a0001c0001t0010 | 0/0 | 3628 | 6 | 6 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | AGAGC others(3623): Show |
chr6 | 111655332 | 111878452 |
| a0001c0001t0011 | 0/0 | 3628 | 5 | 1 | 1 | 2 | 0 | 1 | FYN_chr6_111655332_111878452 | FYN | AGAGC others(3623): Show |
chr6 | 111655332 | 111878452 |
| a0001c0001t0012 | 0/0 | 3628 | 4 | 1 | 1 | 0 | 0 | 2 | FYN_chr6_111655332_111878452 | FYN | AGAGC others(3623): Show |
chr6 | 111655332 | 111878452 |
| a0001c0001t0013 | 0/0 | 3628 | 3 | 0 | 0 | 3 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | AGAGC others(3623): Show |
chr6 | 111655332 | 111878452 |
| a0001c0001t0014 | 0/0 | 3628 | 2 | 2 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | AGAGC others(3623): Show |
chr6 | 111655332 | 111878452 |
| a0001c0001t0015 | 0/0 | 3628 | 2 | 0 | 0 | 2 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | AGAGC others(3623): Show |
chr6 | 111655332 | 111878452 |
| a0001c0001t0016 | 0/0 | 3628 | 2 | 0 | 0 | 2 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | AGAGC others(3623): Show |
chr6 | 111655332 | 111878452 |
| a0001c0001t0017 | 0/0 | 3628 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | AGAGC others(3623): Show |
chr6 | 111655332 | 111878452 |
| a0001c0001t0018 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | AGAGC others(3619): Show |
chr6 | 111655332 | 111878452 |
| a0001c0001t0019 | 0/0 | 3624 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | AGAGC others(3619): Show |
chr6 | 111655332 | 111878452 |
| a0001c0001t0020 | 0/0 | 3628 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | AGAGC others(3623): Show |
chr6 | 111655332 | 111878452 |
| a0001c0001t0021 | 0/0 | 3628 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | AGAGC others(3623): Show |
chr6 | 111655332 | 111878452 |
| a0001c0001t0022 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | AGAGC others(3619): Show |
chr6 | 111655332 | 111878452 |
| a0001c0001t0023 | 0/0 | 3628 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | AGAGC others(3623): Show |
chr6 | 111655332 | 111878452 |
| a0001c0001t0024 | 0/0 | 3628 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | AGAGC others(3623): Show |
chr6 | 111655332 | 111878452 |
| a0001c0001t0025 | 0/0 | 3628 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | AGAGC others(3623): Show |
chr6 | 111655332 | 111878452 |
| a0001c0002t0001 | 0/0 | 3628 | 3 | 2 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | AGAGC others(3623): Show |
chr6 | 111655332 | 111878452 |
| a0001c0002t0004 | 0/0 | 3628 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | AGAGC others(3623): Show |
chr6 | 111655332 | 111878452 |
| a0001c0002t0006 | 0/0 | 3628 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | AGAGC others(3623): Show |
chr6 | 111655332 | 111878452 |
| a0001c0003t0008 | 0/0 | 3628 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | AGAGC others(3623): Show |
chr6 | 111655332 | 111878452 |
| a0001c0004t0001 | 0/0 | 3628 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | AGAGC others(3623): Show |
chr6 | 111655332 | 111878452 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0015 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0003g0023 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0005g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0005g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0005g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0005g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0005g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0005g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0006g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0006g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0006g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0006g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0006g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0006g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0006g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0006g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0006g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0006g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0006g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0006g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0006g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0007g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0007g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0007g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0007g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0007g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0007g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0007g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0007g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0007g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0007g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0007g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0007g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0007g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0008g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0008g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0008g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0008g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0008g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0008g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0008g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0008g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0008g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0009g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0009g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0009g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0009g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0009g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0009g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0009g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0010g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0010g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0010g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0010g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0010g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0010g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0011g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0011g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0011g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0011g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0011g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0012g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0012g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0012g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0012g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0013g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0013g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0013g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0014g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0014g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0015g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0015g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0016g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0016g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0017g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0018g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0019g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0020g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0021g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0022g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0023g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0024g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0001t0025g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0002t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0002t0006g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0003t0008g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| a0001c0004t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00438 | hp1 | a0001 | c0001 | t0006 | g0212 | EAS | CHS | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG00438 | hp2 | a0001 | c0001 | t0005 | g0223 | EAS | CHS | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | CHS | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0193 | EAS | CHS | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG00673 | hp2 | a0001 | c0001 | t0011 | g0076 | EAS | CHS | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG00733 | hp2 | a0001 | c0001 | t0006 | g0228 | AMR | PUR | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG00735 | hp1 | a0001 | c0001 | t0007 | g0011 | AMR | PUR | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG00738 | hp1 | a0001 | c0001 | t0007 | g0088 | AMR | PUR | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0131 | AMR | PUR | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG01069 | hp1 | a0001 | c0001 | t0011 | g0018 | AMR | PUR | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG01069 | hp2 | a0001 | c0001 | t0006 | g0229 | AMR | PUR | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0032 | AMR | PUR | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG01071 | hp2 | a0001 | c0001 | t0006 | g0230 | AMR | PUR | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0094 | AMR | PUR | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | PUR | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG01109 | hp1 | a0001 | c0001 | t0020 | g0095 | AMR | PUR | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG01109 | hp2 | a0001 | c0001 | t0007 | g0028 | AMR | PUR | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0074 | AMR | PUR | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG01175 | hp2 | a0001 | c0001 | t0012 | g0195 | AMR | PUR | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG01243 | hp2 | a0001 | c0001 | t0019 | g0086 | AMR | PUR | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | CLM | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0125 | AMR | CLM | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0138 | AMR | CLM | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | CLM | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG01433 | hp1 | a0001 | c0001 | t0007 | g0073 | AMR | CLM | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG01433 | hp2 | a0001 | c0001 | t0006 | g0232 | AMR | CLM | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG01496 | hp2 | a0001 | c0001 | t0007 | g0072 | AMR | CLM | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0199 | AFR | ACB | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0090 | AFR | ACB | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0098 | AFR | ACB | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PEL | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0137 | AMR | PEL | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0108 | AFR | ACB | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | KHV | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02071 | hp2 | a0001 | c0001 | t0024 | g0219 | EAS | KHV | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02080 | hp1 | a0001 | c0001 | t0005 | g0224 | EAS | KHV | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | KHV | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02083 | hp1 | a0001 | c0001 | t0013 | g0055 | EAS | KHV | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02083 | hp2 | a0001 | c0001 | t0011 | g0021 | EAS | KHV | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | KHV | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02129 | hp2 | a0001 | c0001 | t0005 | g0225 | EAS | KHV | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | ACB | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02165 | hp1 | a0001 | c0001 | t0013 | g0049 | EAS | CDX | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02165 | hp2 | a0001 | c0001 | t0005 | g0203 | EAS | CDX | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0121 | AFR | ACB | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0109 | AFR | ACB | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02280 | hp1 | a0001 | c0001 | t0010 | g0166 | AFR | ACB | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02280 | hp2 | a0001 | c0001 | t0008 | g0116 | AFR | ACB | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0132 | AFR | ACB | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02451 | hp2 | a0001 | c0001 | t0021 | g0119 | AFR | ACB | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0213 | AFR | GWD | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0103 | AFR | GWD | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02622 | hp2 | a0001 | c0001 | t0007 | g0060 | AFR | GWD | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02630 | hp1 | a0001 | c0001 | t0008 | g0104 | AFR | GWD | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0025 | SAS | PJL | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0215 | AFR | GWD | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02717 | hp2 | a0001 | c0004 | t0001 | g0105 | AFR | GWD | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0169 | AFR | GWD | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0135 | AFR | GWD | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02809 | hp1 | a0001 | c0001 | t0018 | g0052 | AFR | GWD | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02895 | hp1 | a0001 | c0001 | t0010 | g0152 | AFR | GWD | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0110 | AFR | GWD | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02922 | hp1 | a0001 | c0001 | t0012 | g0167 | AFR | ESN | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02965 | hp2 | a0001 | c0001 | t0025 | g0233 | AFR | ESN | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0083 | AFR | ESN | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0100 | AFR | ESN | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03017 | hp1 | a0001 | c0001 | t0012 | g0106 | SAS | PJL | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0134 | AFR | GWD | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03041 | hp2 | a0001 | c0001 | t0010 | g0114 | AFR | GWD | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03098 | hp1 | a0001 | c0002 | t0006 | g0198 | AFR | MSL | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0112 | AFR | ESN | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03139 | hp2 | a0001 | c0001 | t0008 | g0120 | AFR | ESN | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03195 | hp1 | a0001 | c0001 | t0010 | g0118 | AFR | ESN | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03225 | hp1 | a0001 | c0002 | t0004 | g0133 | AFR | MSL | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03225 | hp2 | a0001 | c0001 | t0008 | g0097 | AFR | MSL | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0102 | AFR | MSL | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03490 | hp1 | a0001 | c0001 | t0012 | g0156 | SAS | PJL | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03540 | hp2 | a0001 | c0003 | t0008 | g0164 | AFR | GWD | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0163 | AFR | MSL | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03579 | hp2 | a0001 | c0001 | t0017 | g0051 | AFR | MSL | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0085 | SAS | PJL | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0024 | SAS | BEB | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0044 | SAS | BEB | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0030 | SAS | BEB | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG04199 | hp1 | a0001 | c0001 | t0011 | g0029 | SAS | STU | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0043 | SAS | STU | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | STU | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | STU | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0216 | AFR | YRI | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18522 | hp2 | a0001 | c0001 | t0010 | g0174 | AFR | YRI | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0217 | AFR | YRI | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | YRI | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18941 | hp1 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18942 | hp2 | a0001 | c0001 | t0007 | g0020 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18943 | hp1 | a0001 | c0001 | t0005 | g0231 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18945 | hp2 | a0001 | c0001 | t0006 | g0226 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18946 | hp1 | a0001 | c0001 | t0007 | g0019 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18950 | hp1 | a0001 | c0001 | t0007 | g0022 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18950 | hp2 | a0001 | c0001 | t0009 | g0005 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18951 | hp2 | a0001 | c0001 | t0007 | g0067 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18957 | hp2 | a0001 | c0001 | t0013 | g0057 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0192 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18973 | hp1 | a0001 | c0001 | t0007 | g0027 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0194 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18974 | hp1 | a0001 | c0001 | t0016 | g0206 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18974 | hp2 | a0001 | c0001 | t0006 | g0200 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18982 | hp1 | a0001 | c0001 | t0005 | g0220 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18989 | hp2 | a0001 | c0001 | t0009 | g0006 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18993 | hp1 | a0001 | c0001 | t0009 | g0002 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18995 | hp1 | a0001 | c0001 | t0015 | g0211 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19001 | hp2 | a0001 | c0001 | t0006 | g0208 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19006 | hp1 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0227 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19011 | hp1 | a0001 | c0001 | t0006 | g0210 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19011 | hp2 | a0001 | c0001 | t0009 | g0007 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19030 | hp1 | a0001 | c0001 | t0011 | g0016 | AFR | LWK | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19030 | hp2 | a0001 | c0001 | t0014 | g0036 | AFR | LWK | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | LWK | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19043 | hp2 | a0001 | c0001 | t0010 | g0168 | AFR | LWK | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19057 | hp2 | a0001 | c0001 | t0016 | g0207 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19070 | hp1 | a0001 | c0001 | t0005 | g0202 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19074 | hp2 | a0001 | c0001 | t0006 | g0205 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19077 | hp1 | a0001 | c0001 | t0015 | g0204 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0139 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19079 | hp2 | a0001 | c0001 | t0005 | g0201 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19081 | hp1 | a0001 | c0001 | t0007 | g0026 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19081 | hp2 | a0001 | c0001 | t0005 | g0222 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19084 | hp1 | a0001 | c0001 | t0006 | g0209 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19087 | hp2 | a0001 | c0001 | t0009 | g0004 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19088 | hp2 | a0001 | c0001 | t0009 | g0008 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19090 | hp1 | a0001 | c0001 | t0005 | g0221 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19240 | hp1 | a0001 | c0001 | t0023 | g0214 | AFR | YRI | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0172 | AFR | YRI | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | ASW | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ASW | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA20752 | hp1 | a0001 | c0001 | t0007 | g0071 | EUR | TSI | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0160 | EUR | TSI | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0014 | SAS | GIH | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0065 | SAS | GIH | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0171 | AFR | ACB | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03471 | hp1 | a0001 | c0001 | t0008 | g0101 | AFR | MSL | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0218 | AFR | MSL | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA20300 | hp1 | a0001 | c0001 | t0014 | g0047 | AFR | USA | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA20300 | hp2 | a0001 | c0001 | t0022 | g0176 | AFR | USA | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | LWK | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | LWK | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0015 | REF | REF | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0023 | REF | REF | FYN_chr6_111655332_111878452 | FYN | chr6 | 111655332 | 111878452 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:111696350 | G | A | 1 | a0001c0004 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.969C>T | p.His323His | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 10/14 | 1576/3628 | 969/1614 | 323/537 | chr6 | 111696350 | |||
| chr6:111719881 | C | G | 1 | a0001c0003 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.171G>C | p.Gly57Gly | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/14 | 778/3628 | 171/1614 | 57/537 | chr6 | 111719881 | |||
| chr6:111719926 | G | A | 1 | a0001c0002 | 5 | HG00741.hp2 HG02723.hp2 HG03041.hp1 others(2): Show |
synonymous_variant | LOW | c.126C>T | p.Phe42Phe | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/14 | 733/3628 | 126/1614 | 42/537 | chr6 | 111719926 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:111660402 | CAAAT | C | 3 | a0001c0001t0018 a0001c0001t0019 a0001c0001t0022 |
3 | HG01243.hp2 HG02809.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1333_*1336delATTT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 14/14 | 1333 | chr6 | 111660402 | ||||||
| chr6:111660685 | C | T | 1 | a0001c0001t0013 | 3 | HG02083.hp1 HG02165.hp1 NA18957.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1054G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 14/14 | 1054 | chr6 | 111660685 | ||||||
| chr6:111660719 | A | G | 1 | a0001c0001t0024 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1020T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 14/14 | 1020 | chr6 | 111660719 | ||||||
| chr6:111661037 | G | C | 2 | a0001c0001t0017 a0001c0001t0021 |
2 | HG02451.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*702C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 14/14 | 702 | chr6 | 111661037 | ||||||
| chr6:111661054 | A | C | 10 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0007 others(7): Show |
69 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*685T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 14/14 | 685 | chr6 | 111661054 | ||||||
| chr6:111661174 | C | G | 6 | a0001c0001t0008 a0001c0001t0014 a0001c0001t0017 others(3): Show |
15 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*565G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 14/14 | 565 | chr6 | 111661174 | ||||||
| chr6:111780572 | G | T | 22 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(19): Show |
184 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(181): Show |
5_prime_UTR_variant | MODIFIER | c.-18C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/14 | 60521 | chr6 | 111780572 | ||||||
| chr6:111873141 | T | C | 1 | a0001c0001t0020 | 1 | HG01109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-296A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/14 | 153090 | chr6 | 111873141 | ||||||
| chr6:111873230 | C | A | 8 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0009 others(5): Show |
42 | HG00438.hp1 HG00438.hp2 HG00733.hp2 others(39): Show |
5_prime_UTR_variant | MODIFIER | c.-385G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/14 | 153179 | chr6 | 111873230 | ||||||
| chr6:111873293 | G | C | 20 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(17): Show |
145 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(142): Show |
5_prime_UTR_variant | MODIFIER | c.-448C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/14 | 153242 | chr6 | 111873293 | ||||||
| chr6:111873308 | C | T | 1 | a0001c0001t0009 | 7 | NA18941.hp1 NA18950.hp2 NA18989.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-463G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/14 | 153257 | chr6 | 111873308 | ||||||
| chr6:111873399 | C | A | 1 | a0001c0001t0025 | 1 | HG02965.hp2 | 5_prime_UTR_variant | MODIFIER | c.-554G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/14 | 153348 | chr6 | 111873399 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:111662105 | G | A | 15 | a0001c0001t0008g0097 a0001c0001t0008g0100 a0001c0001t0008g0101 others(12): Show |
15 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1406-158C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111662105 | |||||||
| chr6:111662219 | G | A | 15 | a0001c0001t0008g0097 a0001c0001t0008g0100 a0001c0001t0008g0101 others(12): Show |
15 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1406-272C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111662219 | |||||||
| chr6:111662321 | G | C | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1406-374C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111662321 | |||||||
| chr6:111662402 | G | A | 1 | a0001c0002t0006g0198 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1406-455C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111662402 | |||||||
| chr6:111662423 | T | G | 1 | a0001c0001t0012g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1406-476A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111662423 | |||||||
| chr6:111662439 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1406-492G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111662439 | |||||||
| chr6:111662450 | C | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0175 |
2 | HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1406-503G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111662450 | |||||||
| chr6:111662615 | A | G | 106 | a0001c0001t0001g0099 a0001c0001t0001g0107 a0001c0001t0001g0113 others(103): Show |
107 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(104): Show |
intron_variant | MODIFIER | c.1406-668T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111662615 | |||||||
| chr6:111662674 | T | C | 17 | a0001c0001t0001g0173 a0001c0001t0001g0177 a0001c0001t0001g0178 others(14): Show |
17 | HG00673.hp1 HG00733.hp1 HG02698.hp1 others(14): Show |
intron_variant | MODIFIER | c.1406-727A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111662674 | |||||||
| chr6:111662774 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1406-827G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111662774 | |||||||
| chr6:111662818 | G | C | 80 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0122 others(77): Show |
81 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.1406-871C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111662818 | |||||||
| chr6:111662976 | C | T | 194 | a0001c0001t0001g0099 a0001c0001t0001g0107 a0001c0001t0001g0111 others(191): Show |
195 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(192): Show |
intron_variant | MODIFIER | c.1406-1029G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111662976 | |||||||
| chr6:111663112 | A | G | 18 | a0001c0001t0004g0098 a0001c0001t0004g0109 a0001c0001t0004g0112 others(15): Show |
18 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.1406-1165T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111663112 | |||||||
| chr6:111663197 | G | A | 76 | a0001c0001t0001g0107 a0001c0001t0001g0122 a0001c0001t0001g0129 others(73): Show |
77 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.1406-1250C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111663197 | |||||||
| chr6:111663411 | A | G | 3 | a0001c0001t0018g0052 a0001c0001t0019g0086 a0001c0001t0022g0176 |
3 | HG01243.hp2 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1406-1464T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111663411 | |||||||
| chr6:111663598 | C | T | 3 | a0001c0001t0018g0052 a0001c0001t0019g0086 a0001c0001t0022g0176 |
3 | HG01243.hp2 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1406-1651G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111663598 | |||||||
| chr6:111663657 | C | T | 1 | a0001c0001t0006g0217 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1406-1710G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111663657 | |||||||
| chr6:111663729 | C | T | 3 | a0001c0001t0018g0052 a0001c0001t0019g0086 a0001c0001t0022g0176 |
3 | HG01243.hp2 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1406-1782G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111663729 | |||||||
| chr6:111663796 | T | TTTA | 9 | a0001c0001t0002g0041 a0001c0001t0002g0048 a0001c0001t0002g0050 others(6): Show |
9 | HG00558.hp1 HG02080.hp2 NA18945.hp1 others(6): Show |
intron_variant | MODIFIER | c.1406-1850_1406-184 others(7): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111663796 | |||||||
| chr6:111663806 | T | A | 15 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(12): Show |
15 | HG00673.hp1 HG00733.hp1 HG02698.hp1 others(12): Show |
intron_variant | MODIFIER | c.1406-1859A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111663806 | |||||||
| chr6:111663811 | C | T | 1 | a0001c0001t0002g0044 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1406-1864G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111663811 | |||||||
| chr6:111663824 | A | AAATGGGG | 3 | a0001c0001t0018g0052 a0001c0001t0019g0086 a0001c0001t0022g0176 |
3 | HG01243.hp2 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1406-1884_1406-187 others(11): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111663824 | |||||||
| chr6:111663878 | G | A | 69 | a0001c0001t0004g0098 a0001c0001t0004g0103 a0001c0001t0004g0109 others(66): Show |
69 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.1406-1931C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111663878 | |||||||
| chr6:111663914 | C | T | 1 | a0001c0001t0004g0139 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1406-1967G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111663914 | |||||||
| chr6:111663917 | G | A | 15 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(12): Show |
15 | HG00673.hp1 HG00733.hp1 HG02698.hp1 others(12): Show |
intron_variant | MODIFIER | c.1406-1970C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111663917 | |||||||
| chr6:111663995 | T | C | 1 | a0001c0001t0001g0107 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1406-2048A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111663995 | |||||||
| chr6:111664103 | G | T | 1 | a0001c0001t0012g0106 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1406-2156C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111664103 | |||||||
| chr6:111664261 | T | C | 2 | a0001c0001t0017g0051 a0001c0001t0021g0119 |
2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1406-2314A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111664261 | |||||||
| chr6:111664277 | GA | G | 19 | a0001c0001t0004g0103 a0001c0001t0004g0121 a0001c0001t0004g0169 others(16): Show |
19 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.1406-2331delT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111664277 | |||||||
| chr6:111664323 | G | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0175 |
2 | HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1406-2376C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111664323 | |||||||
| chr6:111664615 | C | CTG | 21 | a0001c0001t0001g0111 a0001c0001t0001g0136 a0001c0001t0001g0145 others(18): Show |
21 | HG00673.hp1 HG00733.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.1406-2669_1406-266 others(6): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111664615 | |||||||
| chr6:111664751 | TCTC | T | 15 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(12): Show |
15 | HG00673.hp1 HG00733.hp1 HG02698.hp1 others(12): Show |
intron_variant | MODIFIER | c.1406-2807_1406-280 others(7): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111664751 | |||||||
| chr6:111664770 | C | T | 3 | a0001c0001t0018g0052 a0001c0001t0019g0086 a0001c0001t0022g0176 |
3 | HG01243.hp2 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1406-2823G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111664770 | |||||||
| chr6:111664999 | G | T | 3 | a0001c0001t0018g0052 a0001c0001t0019g0086 a0001c0001t0022g0176 |
3 | HG01243.hp2 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1406-3052C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111664999 | |||||||
| chr6:111665282 | C | T | 1 | a0001c0001t0002g0038 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1406-3335G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111665282 | |||||||
| chr6:111665287 | C | T | 1 | a0001c0001t0012g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1406-3340G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111665287 | |||||||
| chr6:111665306 | AT | A | 15 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(12): Show |
15 | HG00673.hp1 HG00733.hp1 HG02698.hp1 others(12): Show |
intron_variant | MODIFIER | c.1406-3360delA | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111665306 | |||||||
| chr6:111665348 | T | G | 21 | a0001c0001t0001g0111 a0001c0001t0001g0136 a0001c0001t0001g0145 others(18): Show |
21 | HG00673.hp1 HG00733.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.1406-3401A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111665348 | |||||||
| chr6:111665492 | TTTACCTA others(4): Show |
T | 1 | a0001c0001t0006g0226 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1406-3556_1406-354 others(15): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111665492 | |||||||
| chr6:111665591 | T | G | 21 | a0001c0001t0001g0111 a0001c0001t0001g0136 a0001c0001t0001g0145 others(18): Show |
21 | HG00673.hp1 HG00733.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.1406-3644A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111665591 | |||||||
| chr6:111665618 | TTTTA | T | 69 | a0001c0001t0004g0098 a0001c0001t0004g0103 a0001c0001t0004g0109 others(66): Show |
69 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.1406-3675_1406-367 others(8): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111665618 | |||||||
| chr6:111665630 | A | T | 15 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(12): Show |
15 | HG00673.hp1 HG00733.hp1 HG02698.hp1 others(12): Show |
intron_variant | MODIFIER | c.1406-3683T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111665630 | |||||||
| chr6:111665853 | C | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0175 |
2 | HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1406-3906G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111665853 | |||||||
| chr6:111665995 | C | CT | 56 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0117 others(53): Show |
56 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.1406-4049dupA | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111665995 | |||||||
| chr6:111665995 | C | CTT | 7 | a0001c0001t0001g0096 a0001c0001t0001g0142 a0001c0001t0001g0147 others(4): Show |
7 | HG01109.hp2 HG02615.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.1406-4050_1406-404 others(6): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111665995 | |||||||
| chr6:111665995 | CT | C | 11 | a0001c0001t0001g0129 a0001c0001t0009g0002 a0001c0001t0009g0004 others(8): Show |
11 | HG01243.hp2 HG02809.hp1 HG03516.hp2 others(8): Show |
intron_variant | MODIFIER | c.1406-4049delA | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111665995 | |||||||
| chr6:111666018 | T | TTTC | 14 | a0001c0001t0001g0136 a0001c0001t0001g0177 a0001c0001t0001g0179 others(11): Show |
14 | HG00673.hp1 HG00733.hp1 HG02698.hp1 others(11): Show |
intron_variant | MODIFIER | c.1406-4072_1406-407 others(7): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111666018 | |||||||
| chr6:111666065 | A | G | 21 | a0001c0001t0001g0111 a0001c0001t0001g0136 a0001c0001t0001g0145 others(18): Show |
21 | HG00673.hp1 HG00733.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.1406-4118T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111666065 | |||||||
| chr6:111666070 | C | T | 3 | a0001c0001t0018g0052 a0001c0001t0019g0086 a0001c0001t0022g0176 |
3 | HG01243.hp2 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1406-4123G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111666070 | |||||||
| chr6:111666116 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1406-4169G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111666116 | |||||||
| chr6:111666253 | T | C | 4 | a0001c0001t0001g0113 a0001c0001t0001g0146 a0001c0001t0001g0151 others(1): Show |
4 | HG02559.hp1 HG02630.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1406-4306A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111666253 | |||||||
| chr6:111666418 | A | G | 5 | a0001c0001t0001g0117 a0001c0001t0001g0126 a0001c0001t0001g0127 others(2): Show |
5 | HG00639.hp1 NA18942.hp1 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.1406-4471T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111666418 | |||||||
| chr6:111666485 | T | C | 21 | a0001c0001t0001g0111 a0001c0001t0001g0136 a0001c0001t0001g0145 others(18): Show |
21 | HG00673.hp1 HG00733.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.1406-4538A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111666485 | |||||||
| chr6:111666520 | C | T | 9 | a0001c0001t0001g0099 a0001c0001t0001g0143 a0001c0001t0001g0144 others(6): Show |
9 | HG01891.hp2 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1406-4573G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111666520 | |||||||
| chr6:111666630 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1406-4683G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111666630 | |||||||
| chr6:111666762 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1406-4815C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111666762 | |||||||
| chr6:111666835 | C | T | 5 | a0001c0001t0009g0002 a0001c0001t0009g0004 a0001c0001t0009g0005 others(2): Show |
5 | NA18950.hp2 NA18989.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1406-4888G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111666835 | |||||||
| chr6:111667056 | C | T | 7 | a0001c0001t0004g0125 a0001c0001t0004g0138 a0001c0001t0007g0071 others(4): Show |
7 | HG00738.hp1 HG01069.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.1406-5109G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111667056 | |||||||
| chr6:111667200 | A | C | 2 | a0001c0001t0003g0066 a0001c0001t0003g0087 |
2 | NA18939.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1406-5253T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111667200 | |||||||
| chr6:111667343 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1406-5396T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111667343 | |||||||
| chr6:111667428 | T | A | 1 | a0001c0001t0015g0211 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1406-5481A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111667428 | |||||||
| chr6:111667667 | C | T | 6 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0148 others(3): Show |
6 | HG01891.hp2 HG02145.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1406-5720G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111667667 | |||||||
| chr6:111667952 | T | G | 2 | a0001c0001t0001g0184 a0001c0001t0002g0061 |
2 | HG04228.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.1406-6005A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111667952 | |||||||
| chr6:111668022 | A | G | 78 | a0001c0001t0001g0107 a0001c0001t0001g0113 a0001c0001t0001g0115 others(75): Show |
79 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.1406-6075T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111668022 | |||||||
| chr6:111668502 | G | GA | 7 | a0001c0001t0001g0111 a0001c0001t0001g0136 a0001c0001t0001g0141 others(4): Show |
7 | HG01243.hp2 HG02055.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1405+5996dupT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111668502 | |||||||
| chr6:111668502 | G | GAA | 15 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(12): Show |
15 | HG00673.hp1 HG00733.hp1 HG02698.hp1 others(12): Show |
intron_variant | MODIFIER | c.1405+5995_1405+599 others(6): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111668502 | |||||||
| chr6:111668502 | GA | G | 69 | a0001c0001t0004g0098 a0001c0001t0004g0103 a0001c0001t0004g0109 others(66): Show |
69 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.1405+5996delT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111668502 | |||||||
| chr6:111668503 | A | G | 1 | a0001c0001t0002g0040 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1405+5996T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111668503 | |||||||
| chr6:111668559 | G | A | 20 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0117 others(17): Show |
20 | HG00639.hp1 HG01081.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1405+5940C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111668559 | |||||||
| chr6:111668887 | C | T | 1 | a0001c0001t0007g0072 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1405+5612G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111668887 | |||||||
| chr6:111668944 | T | C | 3 | a0001c0001t0018g0052 a0001c0001t0019g0086 a0001c0001t0022g0176 |
3 | HG01243.hp2 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1405+5555A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111668944 | |||||||
| chr6:111669114 | A | G | 1 | a0001c0001t0005g0231 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1405+5385T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111669114 | |||||||
| chr6:111669333 | G | A | 3 | a0001c0001t0018g0052 a0001c0001t0019g0086 a0001c0001t0022g0176 |
3 | HG01243.hp2 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1405+5166C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111669333 | |||||||
| chr6:111669384 | G | A | 58 | a0001c0001t0001g0107 a0001c0001t0001g0122 a0001c0001t0001g0129 others(55): Show |
59 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1405+5115C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111669384 | |||||||
| chr6:111669438 | C | CA | 19 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0148 others(16): Show |
19 | HG00438.hp2 HG01891.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.1405+5060dupT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111669438 | |||||||
| chr6:111669438 | C | CAA | 13 | a0001c0001t0001g0136 a0001c0001t0004g0109 a0001c0001t0008g0097 others(10): Show |
13 | HG02257.hp2 HG02280.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1405+5059_1405+506 others(6): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111669438 | |||||||
| chr6:111669438 | C | CAAA | 18 | a0001c0001t0001g0111 a0001c0001t0001g0145 a0001c0001t0001g0177 others(15): Show |
18 | HG00673.hp1 HG00733.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1405+5058_1405+506 others(7): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111669438 | |||||||
| chr6:111669438 | C | CAAAA | 22 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0117 others(19): Show |
22 | HG00639.hp1 HG01081.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.1405+5057_1405+506 others(8): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111669438 | |||||||
| chr6:111669438 | C | CAAAAA | 47 | a0001c0001t0001g0107 a0001c0001t0001g0124 a0001c0001t0001g0140 others(44): Show |
48 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.1405+5056_1405+506 others(9): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111669438 | |||||||
| chr6:111669438 | C | CAAAAAA | 7 | a0001c0001t0002g0046 a0001c0001t0002g0056 a0001c0001t0002g0059 others(4): Show |
7 | HG00733.hp2 HG02080.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.1405+5055_1405+506 others(10): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111669438 | |||||||
| chr6:111669438 | CA | C | 11 | a0001c0001t0001g0099 a0001c0001t0003g0010 a0001c0001t0003g0066 others(8): Show |
11 | HG01256.hp1 HG01256.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1405+5060delT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111669438 | |||||||
| chr6:111669489 | C | A | 1 | a0001c0001t0017g0051 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1405+5010G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111669489 | |||||||
| chr6:111669505 | G | A | 1 | a0001c0001t0007g0067 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1405+4994C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111669505 | |||||||
| chr6:111669511 | C | T | 3 | a0001c0001t0018g0052 a0001c0001t0019g0086 a0001c0001t0022g0176 |
3 | HG01243.hp2 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1405+4988G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111669511 | |||||||
| chr6:111669625 | C | A | 1 | a0001c0001t0006g0228 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1405+4874G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111669625 | |||||||
| chr6:111669840 | G | A | 1 | a0001c0001t0006g0212 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1405+4659C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111669840 | |||||||
| chr6:111669881 | G | A | 21 | a0001c0001t0001g0111 a0001c0001t0001g0136 a0001c0001t0001g0145 others(18): Show |
21 | HG00673.hp1 HG00733.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.1405+4618C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111669881 | |||||||
| chr6:111669901 | G | A | 50 | a0001c0001t0004g0103 a0001c0001t0004g0110 a0001c0001t0004g0121 others(47): Show |
50 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1405+4598C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111669901 | |||||||
| chr6:111670118 | T | C | 99 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0113 others(96): Show |
100 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.1405+4381A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111670118 | |||||||
| chr6:111670316 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1405+4183G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111670316 | |||||||
| chr6:111670599 | GGAATGAC others(30): Show |
G | 9 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0146 others(6): Show |
9 | HG02559.hp1 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1405+3863_1405+389 others(41): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111670599 | |||||||
| chr6:111670608 | A | G | 21 | a0001c0001t0001g0111 a0001c0001t0001g0136 a0001c0001t0001g0145 others(18): Show |
21 | HG00673.hp1 HG00733.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.1405+3891T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111670608 | |||||||
| chr6:111670631 | T | C | 2 | a0001c0001t0007g0060 a0001c0001t0010g0152 |
2 | HG02622.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1405+3868A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111670631 | |||||||
| chr6:111670640 | T | A | 9 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0146 others(6): Show |
9 | HG02559.hp1 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1405+3859A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111670640 | |||||||
| chr6:111670695 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1405+3804A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111670695 | |||||||
| chr6:111670787 | C | T | 4 | a0001c0001t0018g0052 a0001c0001t0019g0086 a0001c0001t0022g0176 others(1): Show |
4 | HG01243.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1405+3712G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111670787 | |||||||
| chr6:111670909 | C | G | 229 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(226): Show |
230 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(227): Show |
intron_variant | MODIFIER | c.1405+3590G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111670909 | |||||||
| chr6:111670989 | C | T | 3 | a0001c0001t0018g0052 a0001c0001t0019g0086 a0001c0001t0022g0176 |
3 | HG01243.hp2 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1405+3510G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111670989 | |||||||
| chr6:111671025 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1405+3474A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111671025 | |||||||
| chr6:111671060 | G | C | 1 | a0001c0001t0010g0118 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1405+3439C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111671060 | |||||||
| chr6:111671588 | A | G | 2 | a0001c0001t0018g0052 a0001c0001t0022g0176 |
2 | HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1405+2911T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111671588 | |||||||
| chr6:111671624 | C | T | 70 | a0001c0001t0001g0107 a0001c0001t0001g0113 a0001c0001t0001g0115 others(67): Show |
71 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.1405+2875G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111671624 | |||||||
| chr6:111671674 | C | T | 15 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(12): Show |
15 | HG00673.hp1 HG00733.hp1 HG02698.hp1 others(12): Show |
intron_variant | MODIFIER | c.1405+2825G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111671674 | |||||||
| chr6:111671859 | G | C | 1 | a0001c0001t0001g0149 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1405+2640C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111671859 | |||||||
| chr6:111672029 | G | A | 1 | a0001c0001t0002g0040 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1405+2470C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111672029 | |||||||
| chr6:111672170 | T | C | 3 | a0001c0001t0018g0052 a0001c0001t0019g0086 a0001c0001t0022g0176 |
3 | HG01243.hp2 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1405+2329A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111672170 | |||||||
| chr6:111672354 | G | T | 1 | a0001c0001t0001g0140 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1405+2145C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111672354 | |||||||
| chr6:111672434 | A | G | 1 | a0001c0001t0003g0025 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1405+2065T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111672434 | |||||||
| chr6:111672472 | T | C | 1 | a0001c0001t0002g0034 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1405+2027A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111672472 | |||||||
| chr6:111672544 | G | A | 18 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(15): Show |
18 | HG00673.hp1 HG00733.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1405+1955C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111672544 | |||||||
| chr6:111672621 | C | T | 104 | a0001c0001t0001g0099 a0001c0001t0001g0107 a0001c0001t0001g0111 others(101): Show |
105 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.1405+1878G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111672621 | |||||||
| chr6:111672651 | A | G | 3 | a0001c0001t0018g0052 a0001c0001t0019g0086 a0001c0001t0022g0176 |
3 | HG01243.hp2 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1405+1848T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111672651 | |||||||
| chr6:111672760 | C | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0175 |
2 | HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1405+1739G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111672760 | |||||||
| chr6:111672899 | G | A | 2 | a0001c0001t0004g0109 a0001c0001t0004g0112 |
2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1405+1600C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111672899 | |||||||
| chr6:111672902 | C | A | 1 | a0001c0001t0004g0098 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1405+1597G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111672902 | |||||||
| chr6:111673002 | G | A | 4 | a0001c0001t0002g0080 a0001c0001t0013g0049 a0001c0001t0013g0055 others(1): Show |
4 | HG02083.hp1 HG02165.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.1405+1497C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111673002 | |||||||
| chr6:111673046 | T | G | 1 | a0001c0001t0001g0188 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1405+1453A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111673046 | |||||||
| chr6:111673062 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1405+1437C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111673062 | |||||||
| chr6:111673139 | C | T | 8 | a0001c0001t0001g0096 a0001c0001t0001g0141 a0001c0001t0001g0142 others(5): Show |
8 | HG01256.hp1 HG02615.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1405+1360G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111673139 | |||||||
| chr6:111673153 | T | C | 19 | a0001c0001t0008g0097 a0001c0001t0008g0100 a0001c0001t0008g0101 others(16): Show |
19 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1405+1346A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111673153 | |||||||
| chr6:111673249 | A | G | 2 | a0001c0001t0018g0052 a0001c0001t0022g0176 |
2 | HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1405+1250T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111673249 | |||||||
| chr6:111673391 | A | G | 26 | a0001c0001t0001g0099 a0001c0001t0001g0143 a0001c0001t0001g0144 others(23): Show |
26 | HG00673.hp1 HG00733.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.1405+1108T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111673391 | |||||||
| chr6:111673529 | G | A | 6 | a0001c0001t0009g0002 a0001c0001t0009g0004 a0001c0001t0009g0005 others(3): Show |
6 | NA18950.hp2 NA18989.hp2 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1405+970C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111673529 | |||||||
| chr6:111673601 | G | T | 2 | a0001c0001t0018g0052 a0001c0001t0022g0176 |
2 | HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1405+898C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111673601 | |||||||
| chr6:111673619 | A | ACTGTTT | 23 | a0001c0001t0001g0099 a0001c0001t0001g0143 a0001c0001t0001g0144 others(20): Show |
23 | HG00673.hp1 HG00733.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.1405+879_1405+880i others(8): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111673619 | |||||||
| chr6:111673622 | G | GTTTTTTT others(2): Show |
11 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0123 others(8): Show |
11 | HG00639.hp1 HG01106.hp2 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.1405+868_1405+876d others(11): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111673622 | |||||||
| chr6:111673622 | G | GTTTTTTT others(3): Show |
54 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0129 others(51): Show |
55 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1405+867_1405+876d others(12): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111673622 | |||||||
| chr6:111673622 | G | GTTTTTTT others(4): Show |
11 | a0001c0001t0001g0107 a0001c0001t0001g0140 a0001c0001t0001g0154 others(8): Show |
11 | HG02071.hp1 HG02080.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.1405+866_1405+876d others(13): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111673622 | |||||||
| chr6:111673622 | G | T | 26 | a0001c0001t0001g0099 a0001c0001t0001g0143 a0001c0001t0001g0144 others(23): Show |
26 | HG00673.hp1 HG00733.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.1405+877C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111673622 | |||||||
| chr6:111673622 | GT | G | 95 | a0001c0001t0001g0096 a0001c0001t0001g0141 a0001c0001t0001g0142 others(92): Show |
95 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(92): Show |
intron_variant | MODIFIER | c.1405+876delA | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111673622 | |||||||
| chr6:111673752 | G | A | 2 | a0001c0001t0017g0051 a0001c0001t0021g0119 |
2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1405+747C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111673752 | |||||||
| chr6:111673813 | G | A | 1 | a0001c0001t0012g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1405+686C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111673813 | |||||||
| chr6:111673858 | T | C | 8 | a0001c0001t0001g0173 a0001c0001t0002g0054 a0001c0001t0003g0014 others(5): Show |
8 | HG01175.hp1 HG03017.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.1405+641A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111673858 | |||||||
| chr6:111673924 | T | C | 1 | a0001c0001t0003g0031 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1405+575A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111673924 | |||||||
| chr6:111673975 | T | TG | 108 | a0001c0001t0001g0099 a0001c0001t0001g0107 a0001c0001t0001g0111 others(105): Show |
109 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.1405+523dupC | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111673975 | |||||||
| chr6:111674104 | A | G | 9 | a0001c0001t0001g0099 a0001c0001t0001g0143 a0001c0001t0001g0144 others(6): Show |
9 | HG01891.hp2 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1405+395T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111674104 | |||||||
| chr6:111674109 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1405+390G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111674109 | |||||||
| chr6:111674194 | G | T | 2 | a0001c0001t0018g0052 a0001c0001t0022g0176 |
2 | HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1405+305C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111674194 | |||||||
| chr6:111674221 | G | C | 1 | a0001c0001t0004g0109 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1405+278C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111674221 | |||||||
| chr6:111674247 | G | C | 3 | a0001c0001t0001g0111 a0001c0001t0001g0136 a0001c0001t0001g0145 |
3 | HG02055.hp1 HG02818.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1405+252C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111674247 | |||||||
| chr6:111674463 | A | G | 69 | a0001c0001t0004g0098 a0001c0001t0004g0103 a0001c0001t0004g0109 others(66): Show |
69 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.1405+36T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 13/13 | chr6 | 111674463 | |||||||
| chr6:111674815 | C | T | 1 | a0001c0001t0002g0042 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1274-185G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111674815 | |||||||
| chr6:111674901 | T | C | 2 | a0001c0001t0001g0113 a0001c0002t0001g0131 |
2 | HG00741.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1274-271A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111674901 | |||||||
| chr6:111674918 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1274-288A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111674918 | |||||||
| chr6:111675048 | G | T | 78 | a0001c0001t0001g0107 a0001c0001t0001g0113 a0001c0001t0001g0115 others(75): Show |
79 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.1274-418C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111675048 | |||||||
| chr6:111675088 | G | A | 54 | a0001c0001t0001g0107 a0001c0001t0001g0140 a0001c0001t0001g0155 others(51): Show |
55 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1274-458C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111675088 | |||||||
| chr6:111675216 | G | A | 78 | a0001c0001t0001g0107 a0001c0001t0001g0113 a0001c0001t0001g0115 others(75): Show |
79 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.1274-586C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111675216 | |||||||
| chr6:111675463 | C | CTTG | 9 | a0001c0001t0001g0099 a0001c0001t0001g0143 a0001c0001t0001g0144 others(6): Show |
9 | HG01891.hp2 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1274-836_1274-834d others(5): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111675463 | |||||||
| chr6:111675720 | G | T | 9 | a0001c0001t0001g0099 a0001c0001t0001g0143 a0001c0001t0001g0144 others(6): Show |
9 | HG01891.hp2 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1274-1090C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111675720 | |||||||
| chr6:111675741 | C | A | 9 | a0001c0001t0001g0099 a0001c0001t0001g0143 a0001c0001t0001g0144 others(6): Show |
9 | HG01891.hp2 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1274-1111G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111675741 | |||||||
| chr6:111675784 | G | A | 69 | a0001c0001t0004g0098 a0001c0001t0004g0103 a0001c0001t0004g0109 others(66): Show |
69 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.1274-1154C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111675784 | |||||||
| chr6:111675814 | A | AAAAT | 10 | a0001c0001t0001g0111 a0001c0001t0001g0136 a0001c0001t0001g0143 others(7): Show |
10 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1274-1188_1274-118 others(8): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111675814 | |||||||
| chr6:111676122 | C | T | 1 | a0001c0001t0019g0086 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1274-1492G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111676122 | |||||||
| chr6:111676131 | T | C | 9 | a0001c0001t0001g0099 a0001c0001t0001g0143 a0001c0001t0001g0144 others(6): Show |
9 | HG01891.hp2 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1274-1501A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111676131 | |||||||
| chr6:111676493 | G | A | 1 | a0001c0001t0025g0233 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1274-1863C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111676493 | |||||||
| chr6:111676525 | T | C | 2 | a0001c0001t0018g0052 a0001c0001t0022g0176 |
2 | HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1274-1895A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111676525 | |||||||
| chr6:111676908 | A | T | 12 | a0001c0001t0008g0097 a0001c0001t0008g0100 a0001c0001t0008g0101 others(9): Show |
12 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1274-2278T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111676908 | |||||||
| chr6:111676973 | T | G | 2 | a0001c0001t0018g0052 a0001c0001t0022g0176 |
2 | HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1274-2343A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111676973 | |||||||
| chr6:111677364 | C | G | 3 | a0001c0001t0001g0111 a0001c0001t0001g0136 a0001c0001t0001g0145 |
3 | HG02055.hp1 HG02818.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1274-2734G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111677364 | |||||||
| chr6:111677402 | T | G | 1 | a0001c0001t0007g0020 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1274-2772A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111677402 | |||||||
| chr6:111677487 | T | C | 9 | a0001c0001t0001g0099 a0001c0001t0001g0143 a0001c0001t0001g0144 others(6): Show |
9 | HG02145.hp1 HG02559.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1274-2857A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111677487 | |||||||
| chr6:111677488 | G | T | 1 | a0001c0001t0004g0132 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1274-2858C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111677488 | |||||||
| chr6:111677543 | T | C | 5 | a0001c0001t0001g0161 a0001c0001t0001g0185 a0001c0001t0003g0010 others(2): Show |
5 | HG00735.hp1 HG01109.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1274-2913A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111677543 | |||||||
| chr6:111677817 | A | T | 86 | a0001c0001t0001g0099 a0001c0001t0001g0107 a0001c0001t0001g0113 others(83): Show |
87 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.1274-3187T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111677817 | |||||||
| chr6:111678096 | G | A | 90 | a0001c0001t0001g0099 a0001c0001t0001g0107 a0001c0001t0001g0113 others(87): Show |
91 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.1274-3466C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678096 | |||||||
| chr6:111678105 | AAT | A | 6 | a0001c0001t0001g0115 a0001c0001t0001g0151 a0001c0001t0001g0165 others(3): Show |
6 | HG02559.hp1 HG02723.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1274-3477_1274-347 others(6): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678105 | |||||||
| chr6:111678106 | ATATG | A | 10 | a0001c0001t0001g0113 a0001c0001t0001g0123 a0001c0001t0001g0146 others(7): Show |
10 | HG00438.hp1 HG00741.hp2 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.1274-3480_1274-347 others(8): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678106 | |||||||
| chr6:111678106 | ATATGTG | A | 63 | a0001c0001t0001g0107 a0001c0001t0001g0117 a0001c0001t0001g0122 others(60): Show |
63 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1274-3482_1274-347 others(10): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678106 | |||||||
| chr6:111678106 | ATATGTGT others(1): Show |
A | 1 | a0001c0001t0002g0001 | 2 | HG01258.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1274-3484_1274-347 others(12): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678106 | |||||||
| chr6:111678108 | A | ATG | 6 | a0001c0001t0001g0162 a0001c0001t0001g0186 a0001c0001t0001g0187 others(3): Show |
6 | HG01071.hp1 HG03225.hp1 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.1274-3480_1274-347 others(6): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678108 | |||||||
| chr6:111678108 | A | ATGTG | 18 | a0001c0001t0001g0170 a0001c0001t0002g0042 a0001c0001t0003g0025 others(15): Show |
18 | HG00438.hp2 HG01243.hp2 HG02129.hp1 others(15): Show |
intron_variant | MODIFIER | c.1274-3482_1274-347 others(8): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678108 | |||||||
| chr6:111678108 | A | ATGTGTG | 10 | a0001c0001t0001g0190 a0001c0001t0004g0112 a0001c0001t0004g0171 others(7): Show |
10 | HG01884.hp1 HG02080.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1274-3484_1274-347 others(10): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678108 | |||||||
| chr6:111678108 | A | ATGTGTGT others(1): Show |
15 | a0001c0001t0001g0180 a0001c0001t0001g0185 a0001c0001t0003g0010 others(12): Show |
15 | HG00673.hp1 HG00738.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.1274-3486_1274-347 others(12): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678108 | |||||||
| chr6:111678108 | A | ATGTGTGT others(3): Show |
23 | a0001c0001t0001g0136 a0001c0001t0001g0161 a0001c0001t0001g0177 others(20): Show |
23 | HG00558.hp2 HG00673.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.1274-3488_1274-347 others(14): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678108 | |||||||
| chr6:111678108 | A | ATGTGTGT others(5): Show |
14 | a0001c0001t0001g0142 a0001c0001t0001g0148 a0001c0001t0001g0157 others(11): Show |
14 | HG00733.hp1 HG02615.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1274-3490_1274-347 others(16): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678108 | |||||||
| chr6:111678108 | A | ATGTGTGT others(7): Show |
11 | a0001c0001t0001g0096 a0001c0001t0002g0053 a0001c0001t0005g0203 others(8): Show |
11 | HG00735.hp1 HG02055.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.1274-3492_1274-347 others(18): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678108 | |||||||
| chr6:111678108 | A | ATGTGTGT others(9): Show |
5 | a0001c0001t0001g0141 a0001c0001t0004g0132 a0001c0001t0008g0100 others(2): Show |
5 | HG02451.hp1 HG02630.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1274-3494_1274-347 others(20): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678108 | |||||||
| chr6:111678108 | A | ATGTGTGT others(12): Show |
1 | a0001c0001t0001g0183 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1274-3479_1274-347 others(23): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678108 | |||||||
| chr6:111678108 | A | ATGTGTGT others(11): Show |
3 | a0001c0001t0001g0178 a0001c0001t0007g0028 a0001c0001t0008g0116 |
3 | HG01109.hp2 HG02280.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1274-3496_1274-347 others(22): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678108 | |||||||
| chr6:111678108 | A | ATGTGTGT others(13): Show |
2 | a0001c0001t0001g0153 a0001c0001t0008g0120 |
2 | HG01891.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1274-3498_1274-347 others(24): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678108 | |||||||
| chr6:111678108 | A | ATGTGTGT others(15): Show |
1 | a0001c0001t0001g0179 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1274-3500_1274-347 others(26): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678108 | |||||||
| chr6:111678108 | A | ATGTGTGT others(17): Show |
1 | a0001c0001t0014g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1274-3502_1274-347 others(28): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678108 | |||||||
| chr6:111678108 | A | G | 1 | a0001c0001t0002g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1274-3478T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678108 | |||||||
| chr6:111678108 | ATG | A | 6 | a0001c0001t0001g0129 a0001c0001t0001g0175 a0001c0001t0002g0054 others(3): Show |
6 | HG02451.hp2 HG02818.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1274-3480_1274-347 others(6): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678108 | |||||||
| chr6:111678108 | ATGTG | A | 2 | a0001c0001t0003g0030 a0001c0001t0012g0167 |
2 | HG02922.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1274-3482_1274-347 others(8): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678108 | |||||||
| chr6:111678108 | ATGTGTGT others(3): Show |
A | 2 | a0001c0001t0018g0052 a0001c0001t0022g0176 |
2 | HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1274-3488_1274-347 others(14): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678108 | |||||||
| chr6:111678108 | ATGTGTGT others(7): Show |
A | 7 | a0001c0001t0001g0099 a0001c0001t0001g0143 a0001c0001t0001g0144 others(4): Show |
7 | HG02145.hp1 HG02559.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1274-3492_1274-347 others(18): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678108 | |||||||
| chr6:111678108 | ATGTGTGT others(11): Show |
A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0145 |
2 | HG02055.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1274-3496_1274-347 others(22): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678108 | |||||||
| chr6:111678175 | T | C | 8 | a0001c0001t0007g0019 a0001c0001t0009g0002 a0001c0001t0009g0004 others(5): Show |
8 | NA18946.hp1 NA18950.hp2 NA18989.hp2 others(5): Show |
intron_variant | MODIFIER | c.1274-3545A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678175 | |||||||
| chr6:111678212 | A | G | 1 | a0001c0001t0005g0225 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1274-3582T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678212 | |||||||
| chr6:111678379 | G | A | 7 | a0001c0001t0001g0096 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
7 | HG01256.hp1 HG02615.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1274-3749C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678379 | |||||||
| chr6:111678502 | T | C | 2 | a0001c0001t0018g0052 a0001c0001t0022g0176 |
2 | HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1274-3872A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678502 | |||||||
| chr6:111678541 | T | A | 3 | a0001c0001t0002g0041 a0001c0001t0002g0048 a0001c0001t0002g0050 |
3 | HG00558.hp1 NA19005.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1274-3911A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678541 | |||||||
| chr6:111678598 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1274-3968G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678598 | |||||||
| chr6:111678697 | C | T | 15 | a0001c0001t0001g0136 a0001c0001t0001g0148 a0001c0001t0001g0153 others(12): Show |
15 | HG01891.hp2 HG02055.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1274-4067G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678697 | |||||||
| chr6:111678892 | C | T | 2 | a0001c0001t0018g0052 a0001c0001t0022g0176 |
2 | HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1274-4262G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678892 | |||||||
| chr6:111678959 | G | A | 86 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0113 others(83): Show |
87 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.1274-4329C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111678959 | |||||||
| chr6:111679277 | C | T | 1 | a0001c0001t0004g0132 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1274-4647G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111679277 | |||||||
| chr6:111679753 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1274-5123C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111679753 | |||||||
| chr6:111680009 | G | C | 1 | a0001c0001t0001g0179 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1274-5379C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111680009 | |||||||
| chr6:111680374 | G | A | 11 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0146 others(8): Show |
11 | HG00741.hp2 HG02559.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1274-5744C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111680374 | |||||||
| chr6:111680555 | T | C | 1 | a0001c0001t0002g0040 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1274-5925A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111680555 | |||||||
| chr6:111680923 | T | C | 85 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0113 others(82): Show |
86 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.1274-6293A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111680923 | |||||||
| chr6:111681032 | A | AT | 86 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0113 others(83): Show |
87 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.1274-6403dupA | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111681032 | |||||||
| chr6:111681076 | G | A | 1 | a0001c0002t0006g0198 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1274-6446C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111681076 | |||||||
| chr6:111681131 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1274-6501T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111681131 | |||||||
| chr6:111681176 | C | T | 2 | a0001c0001t0018g0052 a0001c0001t0022g0176 |
2 | HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1274-6546G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111681176 | |||||||
| chr6:111681534 | T | C | 1 | a0001c0001t0012g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1274-6904A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111681534 | |||||||
| chr6:111681586 | T | C | 9 | a0001c0001t0001g0099 a0001c0001t0001g0143 a0001c0001t0001g0144 others(6): Show |
9 | HG02145.hp1 HG02559.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1274-6956A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111681586 | |||||||
| chr6:111681758 | C | T | 3 | a0001c0001t0001g0111 a0001c0001t0001g0145 a0001c0001t0014g0047 |
3 | HG02055.hp1 HG02818.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1274-7128G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111681758 | |||||||
| chr6:111681840 | G | A | 1 | a0001c0001t0025g0233 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1274-7210C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111681840 | |||||||
| chr6:111681959 | C | T | 8 | a0001c0001t0001g0173 a0001c0001t0002g0054 a0001c0001t0003g0014 others(5): Show |
8 | HG01175.hp1 HG03017.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.1274-7329G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111681959 | |||||||
| chr6:111682282 | A | C | 7 | a0001c0001t0001g0099 a0001c0001t0001g0143 a0001c0001t0001g0144 others(4): Show |
7 | HG02145.hp1 HG02559.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1274-7652T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111682282 | |||||||
| chr6:111682283 | C | T | 1 | a0001c0001t0006g0217 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1274-7653G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111682283 | |||||||
| chr6:111682545 | T | C | 199 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(196): Show |
200 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(197): Show |
intron_variant | MODIFIER | c.1274-7915A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111682545 | |||||||
| chr6:111683038 | A | T | 6 | a0001c0001t0002g0009 a0001c0001t0002g0039 a0001c0001t0002g0058 others(3): Show |
6 | HG00639.hp2 HG00741.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.1274-8408T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111683038 | |||||||
| chr6:111683040 | C | G | 1 | a0001c0001t0002g0080 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1274-8410G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111683040 | |||||||
| chr6:111683152 | G | C | 1 | a0001c0001t0003g0070 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1274-8522C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111683152 | |||||||
| chr6:111683479 | A | G | 1 | a0001c0001t0011g0076 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1274-8849T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111683479 | |||||||
| chr6:111683546 | G | A | 15 | a0001c0001t0001g0136 a0001c0001t0001g0148 a0001c0001t0001g0153 others(12): Show |
15 | HG01891.hp2 HG02055.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1274-8916C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111683546 | |||||||
| chr6:111683568 | G | A | 18 | a0001c0001t0001g0111 a0001c0001t0001g0145 a0001c0001t0001g0177 others(15): Show |
18 | HG00673.hp1 HG00733.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1274-8938C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111683568 | |||||||
| chr6:111683630 | C | G | 19 | a0001c0001t0001g0111 a0001c0001t0001g0145 a0001c0001t0001g0177 others(16): Show |
19 | HG00673.hp1 HG00733.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1274-9000G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111683630 | |||||||
| chr6:111683727 | CA | C | 176 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(173): Show |
177 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(174): Show |
intron_variant | MODIFIER | c.1274-9098delT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111683727 | |||||||
| chr6:111683923 | T | G | 68 | a0001c0001t0001g0147 a0001c0001t0001g0170 a0001c0001t0004g0098 others(65): Show |
68 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.1274-9293A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111683923 | |||||||
| chr6:111684010 | C | T | 2 | a0001c0001t0018g0052 a0001c0001t0022g0176 |
2 | HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1274-9380G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111684010 | |||||||
| chr6:111684123 | T | C | 2 | a0001c0001t0001g0111 a0001c0001t0001g0145 |
2 | HG02055.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1274-9493A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111684123 | |||||||
| chr6:111684180 | G | A | 1 | a0001c0001t0003g0037 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1274-9550C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111684180 | |||||||
| chr6:111684312 | C | T | 8 | a0001c0001t0001g0113 a0001c0001t0001g0146 a0001c0001t0001g0151 others(5): Show |
8 | HG00741.hp2 HG02559.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1274-9682G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111684312 | |||||||
| chr6:111684437 | A | G | 15 | a0001c0001t0001g0136 a0001c0001t0001g0148 a0001c0001t0001g0153 others(12): Show |
15 | HG01891.hp2 HG02055.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1274-9807T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111684437 | |||||||
| chr6:111684771 | G | C | 1 | a0001c0001t0017g0051 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1273+9604C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111684771 | |||||||
| chr6:111684861 | G | A | 1 | a0001c0001t0010g0114 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1273+9514C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111684861 | |||||||
| chr6:111684952 | C | T | 71 | a0001c0001t0001g0099 a0001c0001t0001g0107 a0001c0001t0001g0122 others(68): Show |
72 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.1273+9423G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111684952 | |||||||
| chr6:111685080 | C | T | 15 | a0001c0001t0001g0136 a0001c0001t0001g0148 a0001c0001t0001g0153 others(12): Show |
15 | HG01891.hp2 HG02055.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1273+9295G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111685080 | |||||||
| chr6:111685346 | C | T | 69 | a0001c0001t0001g0099 a0001c0001t0001g0107 a0001c0001t0001g0122 others(66): Show |
70 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.1273+9029G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111685346 | |||||||
| chr6:111685407 | T | C | 117 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(114): Show |
118 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(115): Show |
intron_variant | MODIFIER | c.1273+8968A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111685407 | |||||||
| chr6:111685624 | A | G | 200 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(197): Show |
201 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(198): Show |
intron_variant | MODIFIER | c.1273+8751T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111685624 | |||||||
| chr6:111685792 | C | T | 69 | a0001c0001t0001g0099 a0001c0001t0001g0107 a0001c0001t0001g0122 others(66): Show |
70 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.1273+8583G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111685792 | |||||||
| chr6:111686017 | A | G | 26 | a0001c0001t0001g0096 a0001c0001t0001g0113 a0001c0001t0001g0115 others(23): Show |
26 | HG00639.hp1 HG00741.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.1273+8358T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111686017 | |||||||
| chr6:111686077 | C | A | 114 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(111): Show |
115 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(112): Show |
intron_variant | MODIFIER | c.1273+8298G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111686077 | |||||||
| chr6:111686169 | T | C | 1 | a0001c0001t0003g0033 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1273+8206A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111686169 | |||||||
| chr6:111686198 | C | T | 2 | a0001c0001t0018g0052 a0001c0001t0022g0176 |
2 | HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1273+8177G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111686198 | |||||||
| chr6:111686241 | G | C | 14 | a0001c0001t0001g0170 a0001c0001t0004g0103 a0001c0001t0004g0121 others(11): Show |
14 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1273+8134C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111686241 | |||||||
| chr6:111686513 | G | A | 2 | a0001c0001t0018g0052 a0001c0001t0022g0176 |
2 | HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1273+7862C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111686513 | |||||||
| chr6:111686613 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1273+7762C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111686613 | |||||||
| chr6:111686648 | T | G | 5 | a0001c0001t0008g0116 a0001c0001t0008g0120 a0001c0001t0008g0163 others(2): Show |
5 | HG02280.hp2 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1273+7727A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111686648 | |||||||
| chr6:111686702 | A | G | 2 | a0001c0001t0018g0052 a0001c0001t0022g0176 |
2 | HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1273+7673T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111686702 | |||||||
| chr6:111686770 | G | T | 3 | a0001c0001t0002g0045 a0001c0001t0002g0080 a0001c0001t0006g0212 |
3 | HG00438.hp1 NA18989.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1273+7605C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111686770 | |||||||
| chr6:111686782 | C | T | 200 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(197): Show |
201 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(198): Show |
intron_variant | MODIFIER | c.1273+7593G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111686782 | |||||||
| chr6:111686822 | C | T | 19 | a0001c0001t0001g0111 a0001c0001t0001g0145 a0001c0001t0001g0177 others(16): Show |
19 | HG00673.hp1 HG00733.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1273+7553G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111686822 | |||||||
| chr6:111686858 | T | C | 1 | a0001c0001t0006g0226 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1273+7517A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111686858 | |||||||
| chr6:111686900 | CGTT | C | 24 | a0001c0001t0001g0096 a0001c0001t0001g0113 a0001c0001t0001g0115 others(21): Show |
24 | HG00639.hp1 HG00741.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.1273+7472_1273+747 others(7): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111686900 | |||||||
| chr6:111687044 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1273+7331G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111687044 | |||||||
| chr6:111687115 | T | C | 2 | a0001c0001t0018g0052 a0001c0001t0022g0176 |
2 | HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1273+7260A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111687115 | |||||||
| chr6:111687119 | A | T | 2 | a0001c0001t0018g0052 a0001c0001t0022g0176 |
2 | HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1273+7256T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111687119 | |||||||
| chr6:111687120 | G | T | 2 | a0001c0001t0018g0052 a0001c0001t0022g0176 |
2 | HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1273+7255C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111687120 | |||||||
| chr6:111687574 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0145 |
2 | HG02055.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1273+6801C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111687574 | |||||||
| chr6:111687576 | G | A | 1 | a0001c0001t0015g0204 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1273+6799C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111687576 | |||||||
| chr6:111687595 | G | GGGGT | 102 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0115 others(99): Show |
102 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.1273+6776_1273+677 others(8): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111687595 | |||||||
| chr6:111687605 | G | GGTGGGT | 3 | a0001c0001t0001g0096 a0001c0001t0004g0194 a0001c0001t0005g0225 |
3 | HG02129.hp2 HG03516.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.1273+6769_1273+677 others(10): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111687605 | |||||||
| chr6:111687607 | T | TGG | 3 | a0001c0001t0002g0013 a0001c0001t0018g0052 a0001c0001t0022g0176 |
3 | HG02809.hp1 HG03669.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1273+6767_1273+676 others(6): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111687607 | |||||||
| chr6:111687609 | T | G | 106 | a0001c0001t0001g0099 a0001c0001t0001g0107 a0001c0001t0001g0122 others(103): Show |
107 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.1273+6766A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111687609 | |||||||
| chr6:111687611 | T | G | 2 | a0001c0001t0018g0052 a0001c0001t0022g0176 |
2 | HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1273+6764A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111687611 | |||||||
| chr6:111687613 | T | G | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1273+6762A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111687613 | |||||||
| chr6:111687642 | C | CAGAG | 43 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0113 others(40): Show |
43 | HG00639.hp1 HG00673.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.1273+6729_1273+673 others(8): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111687642 | |||||||
| chr6:111687642 | CAGAG | C | 2 | a0001c0001t0018g0052 a0001c0001t0022g0176 |
2 | HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1273+6729_1273+673 others(8): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111687642 | |||||||
| chr6:111687800 | T | C | 2 | a0001c0001t0004g0193 a0001c0001t0004g0194 |
2 | HG00558.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1273+6575A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111687800 | |||||||
| chr6:111687803 | TATAG | T | 2 | a0001c0001t0018g0052 a0001c0001t0022g0176 |
2 | HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1273+6568_1273+657 others(8): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111687803 | |||||||
| chr6:111687809 | T | G | 1 | a0001c0001t0002g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1273+6566A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111687809 | |||||||
| chr6:111687932 | A | G | 15 | a0001c0001t0001g0136 a0001c0001t0001g0148 a0001c0001t0001g0153 others(12): Show |
15 | HG01891.hp2 HG02055.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1273+6443T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111687932 | |||||||
| chr6:111687980 | A | T | 1 | a0001c0001t0001g0136 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1273+6395T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111687980 | |||||||
| chr6:111688107 | T | G | 5 | a0001c0001t0001g0113 a0001c0001t0001g0146 a0001c0001t0001g0151 others(2): Show |
5 | HG00741.hp2 HG02559.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1273+6268A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111688107 | |||||||
| chr6:111688122 | A | G | 70 | a0001c0001t0001g0096 a0001c0001t0001g0147 a0001c0001t0001g0170 others(67): Show |
70 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.1273+6253T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111688122 | |||||||
| chr6:111688134 | T | A | 1 | a0001c0001t0012g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1273+6241A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111688134 | |||||||
| chr6:111688224 | T | G | 53 | a0001c0001t0001g0099 a0001c0001t0001g0147 a0001c0001t0001g0149 others(50): Show |
53 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.1273+6151A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111688224 | |||||||
| chr6:111688515 | C | T | 8 | a0001c0001t0002g0041 a0001c0001t0002g0048 a0001c0001t0002g0050 others(5): Show |
8 | HG00558.hp1 HG02080.hp2 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.1273+5860G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111688515 | |||||||
| chr6:111688611 | A | G | 9 | a0001c0001t0001g0111 a0001c0001t0001g0143 a0001c0001t0001g0144 others(6): Show |
9 | HG02055.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1273+5764T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111688611 | |||||||
| chr6:111688622 | C | CGCAGCGT others(12): Show |
1 | a0001c0001t0001g0130 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1273+5734_1273+575 others(23): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111688622 | |||||||
| chr6:111688622 | CGCAGCGT others(12): Show |
C | 1 | a0001c0001t0003g0014 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1273+5734_1273+575 others(23): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111688622 | |||||||
| chr6:111688649 | GTGTGTGC others(3): Show |
G | 5 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0149 others(2): Show |
5 | HG02145.hp1 HG02559.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1273+5716_1273+572 others(14): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111688649 | |||||||
| chr6:111688733 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1273+5642A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111688733 | |||||||
| chr6:111688816 | C | T | 61 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(58): Show |
62 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.1273+5559G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111688816 | |||||||
| chr6:111688868 | AG | A | 5 | a0001c0001t0001g0129 a0001c0001t0001g0165 a0001c0001t0008g0097 others(2): Show |
5 | HG02055.hp2 HG03130.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1273+5506delC | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111688868 | |||||||
| chr6:111688920 | C | T | 4 | a0001c0001t0001g0122 a0001c0001t0001g0144 a0001c0001t0004g0112 others(1): Show |
4 | HG02895.hp2 HG03139.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1273+5455G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111688920 | |||||||
| chr6:111689222 | G | A | 13 | a0001c0001t0001g0111 a0001c0001t0001g0146 a0001c0001t0001g0151 others(10): Show |
13 | HG00733.hp2 HG01109.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1273+5153C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111689222 | |||||||
| chr6:111689230 | A | C | 1 | a0001c0001t0010g0166 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1273+5145T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111689230 | |||||||
| chr6:111689461 | C | T | 13 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0141 others(10): Show |
13 | HG00741.hp2 HG02559.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1273+4914G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111689461 | |||||||
| chr6:111689524 | T | C | 20 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0141 others(17): Show |
20 | HG00741.hp2 HG01884.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1273+4851A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111689524 | |||||||
| chr6:111689617 | T | C | 1 | a0001c0001t0011g0029 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1273+4758A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111689617 | |||||||
| chr6:111689903 | C | G | 5 | a0001c0001t0001g0099 a0001c0001t0007g0060 a0001c0001t0010g0152 others(2): Show |
5 | HG02622.hp2 HG02895.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1273+4472G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111689903 | |||||||
| chr6:111689929 | C | T | 5 | a0001c0001t0001g0099 a0001c0001t0007g0060 a0001c0001t0010g0152 others(2): Show |
5 | HG02622.hp2 HG02895.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1273+4446G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111689929 | |||||||
| chr6:111690020 | G | A | 1 | a0001c0001t0002g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1273+4355C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111690020 | |||||||
| chr6:111690171 | AC | A | 5 | a0001c0001t0001g0099 a0001c0001t0007g0060 a0001c0001t0010g0152 others(2): Show |
5 | HG02622.hp2 HG02895.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1273+4203delG | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111690171 | |||||||
| chr6:111690325 | C | T | 1 | a0001c0001t0004g0132 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1273+4050G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111690325 | |||||||
| chr6:111690359 | G | A | 1 | a0001c0001t0002g0035 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1273+4016C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111690359 | |||||||
| chr6:111690388 | G | A | 5 | a0001c0001t0005g0220 a0001c0001t0005g0224 a0001c0001t0005g0231 others(2): Show |
5 | HG02071.hp2 HG02080.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.1273+3987C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111690388 | |||||||
| chr6:111690760 | A | G | 19 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0141 others(16): Show |
19 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.1273+3615T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111690760 | |||||||
| chr6:111690823 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1273+3552G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111690823 | |||||||
| chr6:111690841 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1273+3534C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111690841 | |||||||
| chr6:111691087 | C | A | 1 | a0001c0001t0005g0215 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1273+3288G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111691087 | |||||||
| chr6:111691160 | C | T | 5 | a0001c0001t0001g0099 a0001c0001t0007g0060 a0001c0001t0010g0152 others(2): Show |
5 | HG02622.hp2 HG02895.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1273+3215G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111691160 | |||||||
| chr6:111691316 | G | A | 21 | a0001c0001t0001g0173 a0001c0001t0001g0177 a0001c0001t0001g0178 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.1273+3059C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111691316 | |||||||
| chr6:111691450 | T | C | 28 | a0001c0001t0001g0173 a0001c0001t0001g0177 a0001c0001t0001g0178 others(25): Show |
28 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.1273+2925A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111691450 | |||||||
| chr6:111691474 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1273+2901C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111691474 | |||||||
| chr6:111691487 | G | A | 18 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0141 others(15): Show |
18 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.1273+2888C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111691487 | |||||||
| chr6:111691559 | T | A | 1 | a0001c0001t0019g0086 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1273+2816A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111691559 | |||||||
| chr6:111691584 | C | T | 18 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0141 others(15): Show |
18 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.1273+2791G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111691584 | |||||||
| chr6:111691970 | C | A | 2 | a0001c0001t0004g0125 a0001c0001t0004g0138 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1273+2405G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111691970 | |||||||
| chr6:111692101 | T | C | 5 | a0001c0001t0001g0099 a0001c0001t0007g0060 a0001c0001t0010g0152 others(2): Show |
5 | HG02622.hp2 HG02895.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1273+2274A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111692101 | |||||||
| chr6:111692101 | T | TC | 29 | a0001c0001t0001g0096 a0001c0001t0001g0122 a0001c0001t0001g0123 others(26): Show |
29 | HG00639.hp1 HG01175.hp1 HG01261.hp2 others(26): Show |
intron_variant | MODIFIER | c.1273+2273dupG | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111692101 | |||||||
| chr6:111692103 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1273+2272G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111692103 | |||||||
| chr6:111692104 | C | A | 3 | a0001c0001t0001g0111 a0001c0001t0004g0109 a0001c0001t0004g0112 |
3 | HG02257.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1273+2271G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111692104 | |||||||
| chr6:111692104 | C | G | 1 | a0001c0001t0004g0132 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1273+2271G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111692104 | |||||||
| chr6:111692104 | C | T | 5 | a0001c0001t0001g0099 a0001c0001t0007g0060 a0001c0001t0010g0152 others(2): Show |
5 | HG02622.hp2 HG02895.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1273+2271G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111692104 | |||||||
| chr6:111692107 | C | G | 28 | a0001c0001t0001g0173 a0001c0001t0001g0177 a0001c0001t0001g0178 others(25): Show |
28 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.1273+2268G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111692107 | |||||||
| chr6:111692108 | C | G | 4 | a0001c0001t0006g0228 a0001c0001t0006g0229 a0001c0001t0006g0230 others(1): Show |
4 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1273+2267G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111692108 | |||||||
| chr6:111692110 | C | G | 1 | a0001c0001t0006g0217 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1273+2265G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111692110 | |||||||
| chr6:111692399 | GAGGGCAG others(17): Show |
G | 4 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0149 others(1): Show |
4 | HG02145.hp1 HG02559.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1273+1952_1273+197 others(28): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111692399 | |||||||
| chr6:111693029 | G | A | 21 | a0001c0001t0001g0173 a0001c0001t0001g0177 a0001c0001t0001g0178 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.1273+1346C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111693029 | |||||||
| chr6:111693032 | T | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0153 |
2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1273+1343A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111693032 | |||||||
| chr6:111693071 | T | G | 1 | a0001c0001t0001g0140 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1273+1304A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111693071 | |||||||
| chr6:111693112 | A | C | 18 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0141 others(15): Show |
18 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.1273+1263T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111693112 | |||||||
| chr6:111693375 | T | C | 1 | a0001c0001t0021g0119 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1273+1000A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111693375 | |||||||
| chr6:111693708 | A | T | 138 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(135): Show |
138 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(135): Show |
intron_variant | MODIFIER | c.1273+667T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111693708 | |||||||
| chr6:111693833 | T | C | 6 | a0001c0001t0005g0218 a0001c0001t0008g0097 a0001c0001t0008g0100 others(3): Show |
6 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1273+542A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111693833 | |||||||
| chr6:111693852 | C | T | 20 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(17): Show |
20 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1273+523G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111693852 | |||||||
| chr6:111693986 | G | A | 6 | a0001c0001t0005g0218 a0001c0001t0008g0097 a0001c0001t0008g0100 others(3): Show |
6 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1273+389C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111693986 | |||||||
| chr6:111694012 | C | G | 17 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0141 others(14): Show |
17 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1273+363G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111694012 | |||||||
| chr6:111694030 | G | C | 2 | a0001c0001t0006g0229 a0001c0001t0006g0230 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1273+345C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111694030 | |||||||
| chr6:111694093 | A | T | 1 | a0001c0001t0002g0035 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1273+282T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111694093 | |||||||
| chr6:111694170 | T | C | 65 | a0001c0001t0001g0107 a0001c0001t0001g0122 a0001c0001t0001g0129 others(62): Show |
66 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.1273+205A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111694170 | |||||||
| chr6:111694349 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1273+26G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111694349 | |||||||
| chr6:111694356 | T | C | 6 | a0001c0001t0005g0218 a0001c0001t0008g0097 a0001c0001t0008g0100 others(3): Show |
6 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1273+19A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111694356 | |||||||
| chr6:111694367 | G | A | 3 | a0001c0001t0001g0124 a0001c0001t0004g0125 a0001c0001t0004g0138 |
3 | HG01106.hp2 HG01256.hp2 HG01258.hp2 |
splice_region_variant&intron_variant | LOW | c.1273+8C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 12/13 | chr6 | 111694367 | |||||||
| chr6:111694538 | C | T | 6 | a0001c0001t0001g0099 a0001c0001t0002g0092 a0001c0001t0007g0060 others(3): Show |
6 | HG02622.hp2 HG02895.hp1 NA19030.hp2 others(3): Show |
intron_variant | MODIFIER | c.1120-10G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 11/13 | chr6 | 111694538 | |||||||
| chr6:111694620 | G | T | 6 | a0001c0001t0001g0099 a0001c0001t0002g0092 a0001c0001t0007g0060 others(3): Show |
6 | HG02622.hp2 HG02895.hp1 NA19030.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1119+8C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 11/13 | chr6 | 111694620 | |||||||
| chr6:111694860 | A | G | 1 | a0001c0001t0002g0044 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1043-156T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 10/13 | chr6 | 111694860 | |||||||
| chr6:111694888 | C | T | 1 | a0001c0001t0021g0119 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1043-184G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 10/13 | chr6 | 111694888 | |||||||
| chr6:111695058 | G | A | 64 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0117 others(61): Show |
64 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.1043-354C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 10/13 | chr6 | 111695058 | |||||||
| chr6:111695081 | C | T | 5 | a0001c0001t0002g0009 a0001c0001t0002g0058 a0001c0001t0002g0093 others(2): Show |
5 | HG00741.hp1 HG01074.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.1043-377G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 10/13 | chr6 | 111695081 | |||||||
| chr6:111695183 | C | T | 64 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0117 others(61): Show |
64 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.1043-479G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 10/13 | chr6 | 111695183 | |||||||
| chr6:111695184 | A | C | 1 | a0001c0001t0001g0197 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1043-480T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 10/13 | chr6 | 111695184 | |||||||
| chr6:111695185 | G | C | 1 | a0001c0001t0001g0197 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1043-481C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 10/13 | chr6 | 111695185 | |||||||
| chr6:111695186 | A | C | 1 | a0001c0001t0001g0197 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1043-482T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 10/13 | chr6 | 111695186 | |||||||
| chr6:111695567 | C | A | 17 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0141 others(14): Show |
17 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1042+710G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 10/13 | chr6 | 111695567 | |||||||
| chr6:111695567 | C | T | 1 | a0001c0001t0003g0085 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1042+710G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 10/13 | chr6 | 111695567 | |||||||
| chr6:111695584 | A | T | 17 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0141 others(14): Show |
17 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1042+693T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 10/13 | chr6 | 111695584 | |||||||
| chr6:111696052 | T | C | 2 | a0001c0001t0002g0092 a0001c0004t0001g0105 |
2 | HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1042+225A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 10/13 | chr6 | 111696052 | |||||||
| chr6:111696068 | C | T | 29 | a0001c0001t0001g0173 a0001c0001t0001g0177 a0001c0001t0001g0178 others(26): Show |
29 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.1042+209G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 10/13 | chr6 | 111696068 | |||||||
| chr6:111696232 | C | T | 3 | a0001c0001t0002g0013 a0001c0001t0003g0010 a0001c0001t0003g0031 |
3 | HG01074.hp2 HG01256.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1042+45G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 10/13 | chr6 | 111696232 | |||||||
| chr6:111696245 | G | C | 6 | a0001c0001t0001g0099 a0001c0001t0001g0175 a0001c0001t0007g0060 others(3): Show |
6 | HG02622.hp2 HG02818.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1042+32C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 10/13 | chr6 | 111696245 | |||||||
| chr6:111696542 | T | G | 1 | a0001c0001t0021g0119 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.863-86A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111696542 | |||||||
| chr6:111696689 | A | C | 1 | a0001c0001t0005g0199 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.863-233T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111696689 | |||||||
| chr6:111696807 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.863-351G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111696807 | |||||||
| chr6:111697173 | T | TA | 17 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0141 others(14): Show |
17 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.863-718dupT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111697173 | |||||||
| chr6:111697259 | G | A | 2 | a0001c0001t0002g0034 a0001c0001t0002g0091 |
2 | NA18963.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.863-803C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111697259 | |||||||
| chr6:111697394 | T | C | 17 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0141 others(14): Show |
17 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.863-938A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111697394 | |||||||
| chr6:111697423 | T | G | 1 | a0001c0001t0002g0056 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.863-967A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111697423 | |||||||
| chr6:111697428 | T | A | 1 | a0001c0001t0002g0053 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.863-972A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111697428 | |||||||
| chr6:111697717 | G | A | 18 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0141 others(15): Show |
18 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.863-1261C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111697717 | |||||||
| chr6:111697907 | G | A | 5 | a0001c0001t0002g0034 a0001c0001t0002g0035 a0001c0001t0002g0046 others(2): Show |
5 | NA18963.hp2 NA18985.hp1 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.863-1451C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111697907 | |||||||
| chr6:111698000 | T | G | 1 | a0001c0001t0001g0143 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.863-1544A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111698000 | |||||||
| chr6:111698007 | T | C | 1 | a0001c0001t0002g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.863-1551A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111698007 | |||||||
| chr6:111698019 | T | G | 1 | a0001c0001t0001g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.863-1563A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111698019 | |||||||
| chr6:111698037 | CTATT | C | 9 | a0001c0001t0001g0143 a0001c0001t0001g0149 a0001c0001t0001g0150 others(6): Show |
9 | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.863-1585_863-1582d others(6): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111698037 | |||||||
| chr6:111698063 | T | C | 1 | a0001c0001t0004g0132 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.863-1607A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111698063 | |||||||
| chr6:111698117 | T | C | 19 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0141 others(16): Show |
19 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.863-1661A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111698117 | |||||||
| chr6:111698134 | T | C | 58 | a0001c0001t0001g0117 a0001c0001t0001g0123 a0001c0001t0001g0124 others(55): Show |
58 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.863-1678A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111698134 | |||||||
| chr6:111698147 | C | T | 13 | a0001c0001t0002g0054 a0001c0001t0003g0014 a0001c0001t0003g0030 others(10): Show |
13 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.863-1691G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111698147 | |||||||
| chr6:111698176 | AGTGCAAT others(1): Show |
A | 112 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(109): Show |
112 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.863-1728_863-1721d others(10): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111698176 | |||||||
| chr6:111698413 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.862+1691C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111698413 | |||||||
| chr6:111698589 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.862+1515C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111698589 | |||||||
| chr6:111698807 | G | A | 58 | a0001c0001t0001g0113 a0001c0001t0001g0117 a0001c0001t0001g0123 others(55): Show |
58 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.862+1297C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111698807 | |||||||
| chr6:111699001 | C | G | 21 | a0001c0001t0001g0173 a0001c0001t0001g0177 a0001c0001t0001g0178 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.862+1103G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111699001 | |||||||
| chr6:111699038 | G | A | 1 | a0001c0001t0003g0031 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.862+1066C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111699038 | |||||||
| chr6:111699044 | T | C | 2 | a0001c0001t0002g0046 a0001c0001t0002g0056 |
2 | NA18985.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.862+1060A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111699044 | |||||||
| chr6:111699051 | C | G | 1 | a0001c0001t0003g0090 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.862+1053G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111699051 | |||||||
| chr6:111699156 | T | C | 2 | a0001c0001t0001g0161 a0001c0001t0002g0092 |
2 | HG03942.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.862+948A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111699156 | |||||||
| chr6:111699171 | A | G | 1 | a0001c0001t0004g0139 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.862+933T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111699171 | |||||||
| chr6:111699174 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.862+930A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111699174 | |||||||
| chr6:111699211 | T | C | 138 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(135): Show |
138 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(135): Show |
intron_variant | MODIFIER | c.862+893A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111699211 | |||||||
| chr6:111699223 | C | T | 3 | a0001c0001t0001g0111 a0001c0001t0004g0109 a0001c0001t0004g0112 |
3 | HG02257.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.862+881G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111699223 | |||||||
| chr6:111699350 | CA | C | 5 | a0001c0001t0001g0165 a0001c0001t0008g0116 a0001c0001t0008g0120 others(2): Show |
5 | HG02280.hp2 HG03130.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.862+753delT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111699350 | |||||||
| chr6:111699398 | T | A | 1 | a0001c0001t0001g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.862+706A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111699398 | |||||||
| chr6:111699913 | C | CT | 12 | a0001c0001t0001g0129 a0001c0001t0001g0183 a0001c0001t0002g0064 others(9): Show |
12 | HG00438.hp1 HG02055.hp2 HG02976.hp2 others(9): Show |
intron_variant | MODIFIER | c.862+190dupA | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111699913 | |||||||
| chr6:111699913 | C | CTTT | 15 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(12): Show |
15 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.862+188_862+190dup others(3): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111699913 | |||||||
| chr6:111699913 | CT | C | 57 | a0001c0001t0001g0107 a0001c0001t0001g0113 a0001c0001t0001g0145 others(54): Show |
57 | HG00438.hp2 HG00733.hp2 HG01071.hp2 others(54): Show |
intron_variant | MODIFIER | c.862+190delA | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111699913 | |||||||
| chr6:111699913 | CTT | C | 14 | a0001c0001t0001g0117 a0001c0001t0001g0123 a0001c0001t0001g0124 others(11): Show |
14 | HG00639.hp1 HG01069.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.862+189_862+190del others(2): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111699913 | |||||||
| chr6:111699913 | CTTTTT | C | 13 | a0001c0001t0001g0143 a0001c0001t0001g0146 a0001c0001t0001g0149 others(10): Show |
13 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.862+186_862+190del others(5): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 9/13 | chr6 | 111699913 | |||||||
| chr6:111700355 | G | A | 11 | a0001c0001t0001g0115 a0001c0001t0001g0141 a0001c0001t0001g0142 others(8): Show |
11 | HG00741.hp2 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.698-87C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 8/13 | chr6 | 111700355 | |||||||
| chr6:111700357 | C | T | 1 | a0001c0001t0005g0215 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.698-89G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 8/13 | chr6 | 111700357 | |||||||
| chr6:111700451 | C | T | 1 | a0001c0001t0010g0114 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.698-183G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 8/13 | chr6 | 111700451 | |||||||
| chr6:111700473 | C | T | 5 | a0001c0001t0001g0111 a0001c0001t0004g0109 a0001c0001t0004g0112 others(2): Show |
5 | HG02257.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.698-205G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 8/13 | chr6 | 111700473 | |||||||
| chr6:111700530 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.698-262G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 8/13 | chr6 | 111700530 | |||||||
| chr6:111700671 | T | C | 7 | a0001c0001t0001g0099 a0001c0001t0001g0136 a0001c0001t0007g0060 others(4): Show |
7 | HG02622.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.698-403A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 8/13 | chr6 | 111700671 | |||||||
| chr6:111700861 | T | C | 16 | a0001c0001t0001g0115 a0001c0001t0001g0141 a0001c0001t0001g0142 others(13): Show |
16 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.698-593A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 8/13 | chr6 | 111700861 | |||||||
| chr6:111700916 | C | T | 17 | a0001c0001t0001g0115 a0001c0001t0001g0141 a0001c0001t0001g0142 others(14): Show |
17 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.698-648G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 8/13 | chr6 | 111700916 | |||||||
| chr6:111700982 | TA | T | 14 | a0001c0001t0001g0099 a0001c0001t0001g0115 a0001c0001t0001g0141 others(11): Show |
14 | HG00741.hp2 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.698-715delT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 8/13 | chr6 | 111700982 | |||||||
| chr6:111700993 | A | C | 5 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0149 others(2): Show |
5 | HG02145.hp1 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.698-725T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 8/13 | chr6 | 111700993 | |||||||
| chr6:111701346 | G | C | 1 | a0001c0001t0002g0041 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.698-1078C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 8/13 | chr6 | 111701346 | |||||||
| chr6:111701403 | T | G | 1 | a0001c0001t0002g0034 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.698-1135A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 8/13 | chr6 | 111701403 | |||||||
| chr6:111701442 | G | A | 1 | a0001c0001t0002g0042 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.698-1174C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 8/13 | chr6 | 111701442 | |||||||
| chr6:111701565 | T | A | 2 | a0001c0001t0001g0161 a0001c0001t0002g0092 |
2 | HG03942.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.698-1297A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 8/13 | chr6 | 111701565 | |||||||
| chr6:111701875 | T | A | 4 | a0001c0001t0001g0111 a0001c0001t0004g0109 a0001c0001t0004g0112 others(1): Show |
4 | HG02257.hp2 HG02451.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.697+1010A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 8/13 | chr6 | 111701875 | |||||||
| chr6:111701927 | C | T | 2 | a0001c0001t0006g0205 a0001c0001t0006g0210 |
2 | NA19011.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.697+958G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 8/13 | chr6 | 111701927 | |||||||
| chr6:111701928 | G | A | 1 | a0001c0001t0006g0208 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.697+957C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 8/13 | chr6 | 111701928 | |||||||
| chr6:111702093 | T | A | 2 | a0001c0001t0005g0220 a0001c0001t0024g0219 |
2 | HG02071.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.697+792A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 8/13 | chr6 | 111702093 | |||||||
| chr6:111702125 | C | T | 2 | a0001c0001t0001g0154 a0001c0004t0001g0105 |
2 | HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.697+760G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 8/13 | chr6 | 111702125 | |||||||
| chr6:111702211 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.697+674A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 8/13 | chr6 | 111702211 | |||||||
| chr6:111702265 | T | C | 21 | a0001c0001t0001g0173 a0001c0001t0001g0177 a0001c0001t0001g0178 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.697+620A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 8/13 | chr6 | 111702265 | |||||||
| chr6:111702290 | T | A | 7 | a0001c0001t0001g0099 a0001c0001t0001g0136 a0001c0001t0007g0060 others(4): Show |
7 | HG02622.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.697+595A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 8/13 | chr6 | 111702290 | |||||||
| chr6:111702319 | T | C | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0157 |
3 | HG02615.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.697+566A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 8/13 | chr6 | 111702319 | |||||||
| chr6:111702496 | T | C | 1 | a0001c0001t0002g0042 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.697+389A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 8/13 | chr6 | 111702496 | |||||||
| chr6:111703059 | A | C | 59 | a0001c0001t0001g0113 a0001c0001t0001g0117 a0001c0001t0001g0123 others(56): Show |
59 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.548-25T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 7/13 | chr6 | 111703059 | |||||||
| chr6:111703237 | C | A | 5 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0149 others(2): Show |
5 | HG02145.hp1 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.548-203G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 7/13 | chr6 | 111703237 | |||||||
| chr6:111703287 | C | T | 8 | a0001c0001t0001g0099 a0001c0001t0001g0136 a0001c0001t0001g0161 others(5): Show |
8 | HG02622.hp2 HG02895.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.548-253G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 7/13 | chr6 | 111703287 | |||||||
| chr6:111703447 | G | C | 23 | a0001c0001t0001g0117 a0001c0001t0001g0123 a0001c0001t0001g0124 others(20): Show |
23 | HG00639.hp1 HG01081.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.548-413C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 7/13 | chr6 | 111703447 | |||||||
| chr6:111703739 | C | T | 28 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0115 others(25): Show |
28 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(25): Show |
intron_variant | MODIFIER | c.547+260G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 7/13 | chr6 | 111703739 | |||||||
| chr6:111703763 | T | A | 28 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0115 others(25): Show |
28 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(25): Show |
intron_variant | MODIFIER | c.547+236A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 7/13 | chr6 | 111703763 | |||||||
| chr6:111703888 | G | A | 3 | a0001c0001t0017g0051 a0001c0001t0018g0052 a0001c0001t0022g0176 |
3 | HG02809.hp1 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.547+111C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 7/13 | chr6 | 111703888 | |||||||
| chr6:111704353 | A | G | 8 | a0001c0001t0001g0099 a0001c0001t0001g0136 a0001c0001t0001g0161 others(5): Show |
8 | HG02622.hp2 HG02895.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.444-251T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111704353 | |||||||
| chr6:111704400 | C | G | 1 | a0001c0001t0006g0209 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.444-298G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111704400 | |||||||
| chr6:111704457 | A | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0175 |
2 | HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.444-355T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111704457 | |||||||
| chr6:111704612 | G | T | 8 | a0001c0001t0001g0099 a0001c0001t0001g0136 a0001c0001t0001g0161 others(5): Show |
8 | HG02622.hp2 HG02895.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.444-510C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111704612 | |||||||
| chr6:111705063 | T | A | 28 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0115 others(25): Show |
28 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(25): Show |
intron_variant | MODIFIER | c.444-961A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111705063 | |||||||
| chr6:111705197 | T | C | 59 | a0001c0001t0001g0113 a0001c0001t0001g0117 a0001c0001t0001g0123 others(56): Show |
59 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.444-1095A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111705197 | |||||||
| chr6:111705269 | A | C | 6 | a0001c0001t0005g0218 a0001c0001t0008g0097 a0001c0001t0008g0100 others(3): Show |
6 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.444-1167T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111705269 | |||||||
| chr6:111705286 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.444-1184A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111705286 | |||||||
| chr6:111705355 | T | C | 17 | a0001c0001t0001g0115 a0001c0001t0001g0141 a0001c0001t0001g0142 others(14): Show |
17 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.444-1253A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111705355 | |||||||
| chr6:111705376 | T | A | 21 | a0001c0001t0001g0173 a0001c0001t0001g0177 a0001c0001t0001g0178 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.444-1274A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111705376 | |||||||
| chr6:111705384 | C | CT | 23 | a0001c0001t0001g0115 a0001c0001t0001g0141 a0001c0001t0001g0142 others(20): Show |
23 | HG00741.hp2 HG02055.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.444-1283dupA | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111705384 | |||||||
| chr6:111705477 | T | G | 79 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0117 others(76): Show |
79 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(76): Show |
intron_variant | MODIFIER | c.444-1375A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111705477 | |||||||
| chr6:111705567 | G | A | 60 | a0001c0001t0001g0113 a0001c0001t0001g0117 a0001c0001t0001g0123 others(57): Show |
60 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.444-1465C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111705567 | |||||||
| chr6:111705646 | C | T | 8 | a0001c0001t0001g0099 a0001c0001t0001g0136 a0001c0001t0001g0161 others(5): Show |
8 | HG02622.hp2 HG02895.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.444-1544G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111705646 | |||||||
| chr6:111705679 | A | G | 5 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0149 others(2): Show |
5 | HG02145.hp1 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.444-1577T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111705679 | |||||||
| chr6:111705797 | T | C | 207 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(204): Show |
208 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(205): Show |
intron_variant | MODIFIER | c.444-1695A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111705797 | |||||||
| chr6:111705817 | C | G | 15 | a0001c0001t0001g0162 a0001c0001t0002g0054 a0001c0001t0003g0014 others(12): Show |
15 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.444-1715G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111705817 | |||||||
| chr6:111705875 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.444-1773G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111705875 | |||||||
| chr6:111705994 | A | G | 3 | a0001c0001t0001g0143 a0001c0001t0001g0149 a0001c0001t0001g0150 |
3 | HG02145.hp1 HG02559.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.444-1892T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111705994 | |||||||
| chr6:111706257 | G | A | 8 | a0001c0001t0001g0099 a0001c0001t0001g0136 a0001c0001t0001g0161 others(5): Show |
8 | HG02622.hp2 HG02895.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.443+1665C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111706257 | |||||||
| chr6:111706305 | T | C | 3 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0020g0095 |
3 | HG01109.hp1 HG02486.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.443+1617A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111706305 | |||||||
| chr6:111706482 | A | G | 8 | a0001c0001t0001g0099 a0001c0001t0001g0136 a0001c0001t0001g0161 others(5): Show |
8 | HG02622.hp2 HG02895.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.443+1440T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111706482 | |||||||
| chr6:111707117 | C | T | 1 | a0001c0001t0003g0025 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.443+805G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111707117 | |||||||
| chr6:111707424 | T | C | 6 | a0001c0001t0005g0218 a0001c0001t0008g0097 a0001c0001t0008g0100 others(3): Show |
6 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.443+498A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111707424 | |||||||
| chr6:111707546 | T | A | 1 | a0001c0001t0001g0154 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.443+376A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111707546 | |||||||
| chr6:111707560 | CTCT | C | 60 | a0001c0001t0001g0113 a0001c0001t0001g0117 a0001c0001t0001g0123 others(57): Show |
60 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.443+359_443+361del others(3): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111707560 | |||||||
| chr6:111707575 | G | C | 20 | a0001c0001t0001g0162 a0001c0001t0001g0165 a0001c0001t0002g0054 others(17): Show |
20 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.443+347C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111707575 | |||||||
| chr6:111707633 | T | G | 1 | a0001c0001t0003g0024 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.443+289A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111707633 | |||||||
| chr6:111707664 | A | G | 1 | a0001c0004t0001g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.443+258T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111707664 | |||||||
| chr6:111707758 | G | A | 1 | a0001c0001t0014g0047 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.443+164C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111707758 | |||||||
| chr6:111707760 | G | A | 1 | a0001c0002t0001g0131 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.443+162C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111707760 | |||||||
| chr6:111707817 | C | T | 13 | a0001c0001t0001g0115 a0001c0001t0001g0141 a0001c0001t0001g0142 others(10): Show |
13 | HG00741.hp2 HG02559.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.443+105G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111707817 | |||||||
| chr6:111707866 | T | C | 2 | a0001c0001t0002g0053 a0001c0001t0002g0081 |
2 | NA19070.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.443+56A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 6/13 | chr6 | 111707866 | |||||||
| chr6:111708128 | G | A | 15 | a0001c0001t0001g0162 a0001c0001t0002g0054 a0001c0001t0003g0014 others(12): Show |
15 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.345-108C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111708128 | |||||||
| chr6:111708130 | T | C | 1 | a0001c0001t0006g0217 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.345-110A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111708130 | |||||||
| chr6:111708153 | C | G | 3 | a0001c0001t0001g0111 a0001c0001t0004g0109 a0001c0001t0004g0112 |
3 | HG02257.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.345-133G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111708153 | |||||||
| chr6:111708199 | C | T | 20 | a0001c0001t0001g0162 a0001c0001t0001g0165 a0001c0001t0002g0054 others(17): Show |
20 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.345-179G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111708199 | |||||||
| chr6:111708282 | C | T | 2 | a0001c0001t0002g0046 a0001c0001t0002g0056 |
2 | NA18985.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.345-262G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111708282 | |||||||
| chr6:111708302 | G | C | 66 | a0001c0001t0001g0107 a0001c0001t0001g0122 a0001c0001t0001g0129 others(63): Show |
67 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.345-282C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111708302 | |||||||
| chr6:111708331 | T | C | 33 | a0001c0001t0001g0099 a0001c0001t0001g0115 a0001c0001t0001g0136 others(30): Show |
33 | HG00741.hp2 HG02055.hp2 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.345-311A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111708331 | |||||||
| chr6:111708401 | T | C | 20 | a0001c0001t0001g0162 a0001c0001t0001g0165 a0001c0001t0002g0054 others(17): Show |
20 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.345-381A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111708401 | |||||||
| chr6:111708461 | CCT | C | 8 | a0001c0001t0001g0099 a0001c0001t0001g0136 a0001c0001t0001g0161 others(5): Show |
8 | HG02622.hp2 HG02895.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-443_345-442del others(2): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111708461 | |||||||
| chr6:111708506 | T | C | 59 | a0001c0001t0001g0113 a0001c0001t0001g0117 a0001c0001t0001g0123 others(56): Show |
59 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.345-486A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111708506 | |||||||
| chr6:111708559 | G | A | 12 | a0001c0001t0001g0115 a0001c0001t0001g0141 a0001c0001t0001g0142 others(9): Show |
12 | HG00741.hp2 HG02559.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.345-539C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111708559 | |||||||
| chr6:111708781 | C | T | 24 | a0001c0001t0001g0111 a0001c0001t0001g0173 a0001c0001t0001g0177 others(21): Show |
24 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.345-761G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111708781 | |||||||
| chr6:111708782 | G | A | 24 | a0001c0001t0001g0115 a0001c0001t0001g0141 a0001c0001t0001g0142 others(21): Show |
24 | HG00741.hp2 HG02055.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.345-762C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111708782 | |||||||
| chr6:111708953 | T | C | 57 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0115 others(54): Show |
57 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.345-933A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111708953 | |||||||
| chr6:111708960 | C | T | 1 | a0001c0001t0002g0034 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.345-940G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111708960 | |||||||
| chr6:111708971 | T | C | 6 | a0001c0001t0005g0218 a0001c0001t0008g0097 a0001c0001t0008g0100 others(3): Show |
6 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-951A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111708971 | |||||||
| chr6:111708976 | A | G | 25 | a0001c0001t0001g0115 a0001c0001t0001g0141 a0001c0001t0001g0142 others(22): Show |
25 | HG00741.hp2 HG02055.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.345-956T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111708976 | |||||||
| chr6:111709043 | T | C | 33 | a0001c0001t0001g0099 a0001c0001t0001g0115 a0001c0001t0001g0136 others(30): Show |
33 | HG00741.hp2 HG02055.hp2 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.345-1023A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111709043 | |||||||
| chr6:111709132 | G | C | 33 | a0001c0001t0001g0099 a0001c0001t0001g0115 a0001c0001t0001g0136 others(30): Show |
33 | HG00741.hp2 HG02055.hp2 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.345-1112C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111709132 | |||||||
| chr6:111709190 | TA | T | 33 | a0001c0001t0001g0099 a0001c0001t0001g0115 a0001c0001t0001g0136 others(30): Show |
33 | HG00741.hp2 HG02055.hp2 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.345-1171delT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111709190 | |||||||
| chr6:111709192 | A | T | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.345-1172T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111709192 | |||||||
| chr6:111709202 | G | A | 25 | a0001c0001t0001g0115 a0001c0001t0001g0141 a0001c0001t0001g0142 others(22): Show |
25 | HG00741.hp2 HG02055.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.345-1182C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111709202 | |||||||
| chr6:111709260 | A | G | 57 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0115 others(54): Show |
57 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.345-1240T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111709260 | |||||||
| chr6:111709321 | C | T | 1 | a0001c0001t0005g0213 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.345-1301G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111709321 | |||||||
| chr6:111709441 | C | T | 49 | a0001c0001t0001g0111 a0001c0001t0001g0115 a0001c0001t0001g0141 others(46): Show |
49 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.345-1421G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111709441 | |||||||
| chr6:111709497 | C | T | 57 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0115 others(54): Show |
57 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.345-1477G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111709497 | |||||||
| chr6:111709693 | T | C | 7 | a0001c0001t0001g0099 a0001c0001t0001g0136 a0001c0001t0007g0060 others(4): Show |
7 | HG02622.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-1673A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111709693 | |||||||
| chr6:111709808 | T | G | 1 | a0001c0001t0001g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.345-1788A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111709808 | |||||||
| chr6:111709838 | C | T | 49 | a0001c0001t0001g0111 a0001c0001t0001g0115 a0001c0001t0001g0141 others(46): Show |
49 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.345-1818G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111709838 | |||||||
| chr6:111709891 | G | T | 8 | a0001c0001t0001g0099 a0001c0001t0001g0136 a0001c0001t0001g0161 others(5): Show |
8 | HG02622.hp2 HG02895.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-1871C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111709891 | |||||||
| chr6:111709895 | C | T | 20 | a0001c0001t0001g0162 a0001c0001t0001g0165 a0001c0001t0002g0054 others(17): Show |
20 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.345-1875G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111709895 | |||||||
| chr6:111709997 | GA | G | 57 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0115 others(54): Show |
57 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.345-1978delT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111709997 | |||||||
| chr6:111710108 | C | T | 57 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0115 others(54): Show |
57 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.345-2088G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111710108 | |||||||
| chr6:111710173 | G | A | 24 | a0001c0001t0001g0111 a0001c0001t0001g0173 a0001c0001t0001g0177 others(21): Show |
24 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.345-2153C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111710173 | |||||||
| chr6:111710238 | T | A | 7 | a0001c0001t0001g0099 a0001c0001t0001g0136 a0001c0001t0007g0060 others(4): Show |
7 | HG02622.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-2218A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111710238 | |||||||
| chr6:111710964 | C | A | 6 | a0001c0001t0005g0218 a0001c0001t0008g0097 a0001c0001t0008g0100 others(3): Show |
6 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-2944G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111710964 | |||||||
| chr6:111711030 | C | T | 1 | a0001c0001t0002g0084 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.345-3010G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111711030 | |||||||
| chr6:111711117 | C | T | 1 | a0001c0001t0002g0059 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.345-3097G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111711117 | |||||||
| chr6:111711146 | C | A | 7 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0183 others(4): Show |
7 | HG02083.hp2 HG03834.hp1 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-3126G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111711146 | |||||||
| chr6:111711210 | C | T | 8 | a0001c0001t0001g0099 a0001c0001t0001g0136 a0001c0001t0001g0161 others(5): Show |
8 | HG02622.hp2 HG02895.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.344+3137G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111711210 | |||||||
| chr6:111711477 | C | T | 1 | a0001c0001t0002g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.344+2870G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111711477 | |||||||
| chr6:111711957 | A | G | 2 | a0001c0001t0003g0083 a0001c0001t0003g0090 |
2 | HG01884.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.344+2390T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111711957 | |||||||
| chr6:111712022 | T | C | 1 | a0001c0001t0006g0205 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.344+2325A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111712022 | |||||||
| chr6:111712167 | C | T | 57 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0115 others(54): Show |
57 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.344+2180G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111712167 | |||||||
| chr6:111712303 | C | T | 8 | a0001c0001t0001g0099 a0001c0001t0001g0136 a0001c0001t0001g0161 others(5): Show |
8 | HG02622.hp2 HG02895.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.344+2044G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111712303 | |||||||
| chr6:111712384 | G | A | 1 | a0001c0001t0004g0110 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.344+1963C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111712384 | |||||||
| chr6:111712529 | G | GC | 57 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0115 others(54): Show |
57 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.344+1817dupG | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111712529 | |||||||
| chr6:111712690 | T | C | 1 | a0001c0001t0007g0072 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.344+1657A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111712690 | |||||||
| chr6:111712793 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.344+1554A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111712793 | |||||||
| chr6:111712797 | T | C | 7 | a0001c0001t0001g0099 a0001c0001t0001g0136 a0001c0001t0007g0060 others(4): Show |
7 | HG02622.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.344+1550A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111712797 | |||||||
| chr6:111713068 | G | A | 49 | a0001c0001t0001g0111 a0001c0001t0001g0115 a0001c0001t0001g0141 others(46): Show |
49 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.344+1279C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111713068 | |||||||
| chr6:111713073 | A | C | 1 | a0001c0001t0002g0013 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.344+1274T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111713073 | |||||||
| chr6:111713090 | T | C | 49 | a0001c0001t0001g0111 a0001c0001t0001g0115 a0001c0001t0001g0141 others(46): Show |
49 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.344+1257A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111713090 | |||||||
| chr6:111713165 | C | T | 49 | a0001c0001t0001g0111 a0001c0001t0001g0115 a0001c0001t0001g0141 others(46): Show |
49 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.344+1182G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111713165 | |||||||
| chr6:111713551 | C | G | 1 | a0001c0001t0004g0109 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.344+796G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111713551 | |||||||
| chr6:111713574 | T | C | 54 | a0001c0001t0001g0111 a0001c0001t0001g0115 a0001c0001t0001g0141 others(51): Show |
54 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.344+773A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111713574 | |||||||
| chr6:111713653 | G | A | 1 | a0001c0001t0002g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.344+694C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111713653 | |||||||
| chr6:111713666 | T | C | 7 | a0001c0001t0002g0054 a0001c0001t0003g0014 a0001c0001t0003g0074 others(4): Show |
7 | HG01175.hp1 HG03490.hp1 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.344+681A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111713666 | |||||||
| chr6:111713799 | A | G | 207 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(204): Show |
208 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(205): Show |
intron_variant | MODIFIER | c.344+548T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111713799 | |||||||
| chr6:111713847 | T | C | 138 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(135): Show |
138 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(135): Show |
intron_variant | MODIFIER | c.344+500A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111713847 | |||||||
| chr6:111713852 | T | C | 1 | a0001c0004t0001g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.344+495A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111713852 | |||||||
| chr6:111713860 | C | T | 1 | a0001c0001t0011g0029 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.344+487G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111713860 | |||||||
| chr6:111713905 | T | C | 138 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(135): Show |
138 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(135): Show |
intron_variant | MODIFIER | c.344+442A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 5/13 | chr6 | 111713905 | |||||||
| chr6:111714644 | C | G | 1 | a0001c0001t0001g0188 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.248-201G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111714644 | |||||||
| chr6:111714654 | A | C | 57 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0115 others(54): Show |
57 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.248-211T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111714654 | |||||||
| chr6:111714722 | T | C | 1 | a0001c0001t0006g0217 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.248-279A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111714722 | |||||||
| chr6:111715144 | T | G | 1 | a0001c0001t0020g0095 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.248-701A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111715144 | |||||||
| chr6:111715245 | C | CT | 54 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0115 others(51): Show |
54 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.248-803dupA | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111715245 | |||||||
| chr6:111715273 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.248-830C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111715273 | |||||||
| chr6:111715275 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.248-832G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111715275 | |||||||
| chr6:111715358 | G | C | 1 | a0001c0001t0012g0106 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.248-915C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111715358 | |||||||
| chr6:111715370 | T | C | 62 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0115 others(59): Show |
62 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.248-927A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111715370 | |||||||
| chr6:111715459 | G | A | 8 | a0001c0001t0001g0099 a0001c0001t0001g0136 a0001c0001t0001g0161 others(5): Show |
8 | HG02622.hp2 HG02895.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.248-1016C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111715459 | |||||||
| chr6:111715500 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.248-1057C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111715500 | |||||||
| chr6:111715544 | G | A | 21 | a0001c0001t0001g0173 a0001c0001t0001g0177 a0001c0001t0001g0178 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.248-1101C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111715544 | |||||||
| chr6:111715987 | T | C | 21 | a0001c0001t0001g0162 a0001c0001t0001g0165 a0001c0001t0002g0054 others(18): Show |
21 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.248-1544A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111715987 | |||||||
| chr6:111716003 | T | C | 229 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(226): Show |
230 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(227): Show |
intron_variant | MODIFIER | c.248-1560A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111716003 | |||||||
| chr6:111716184 | C | T | 3 | a0001c0001t0001g0111 a0001c0001t0004g0109 a0001c0001t0004g0112 |
3 | HG02257.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.248-1741G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111716184 | |||||||
| chr6:111716282 | T | C | 2 | a0001c0001t0003g0010 a0001c0001t0003g0031 |
2 | HG01074.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.248-1839A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111716282 | |||||||
| chr6:111716410 | C | T | 57 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0115 others(54): Show |
57 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.248-1967G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111716410 | |||||||
| chr6:111716654 | TA | T | 57 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0115 others(54): Show |
57 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.248-2212delT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111716654 | |||||||
| chr6:111716683 | G | A | 1 | a0001c0001t0004g0132 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.248-2240C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111716683 | |||||||
| chr6:111716702 | T | TA | 21 | a0001c0001t0001g0173 a0001c0001t0001g0177 a0001c0001t0001g0178 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.248-2260dupT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111716702 | |||||||
| chr6:111716733 | C | A | 1 | a0001c0001t0003g0074 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.248-2290G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111716733 | |||||||
| chr6:111716754 | T | C | 21 | a0001c0001t0001g0162 a0001c0001t0001g0165 a0001c0001t0002g0054 others(18): Show |
21 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.248-2311A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111716754 | |||||||
| chr6:111716783 | ATT | A | 46 | a0001c0001t0001g0115 a0001c0001t0001g0141 a0001c0001t0001g0142 others(43): Show |
46 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.248-2342_248-2341d others(4): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111716783 | |||||||
| chr6:111716783 | ATTT | A | 8 | a0001c0001t0001g0099 a0001c0001t0001g0136 a0001c0001t0001g0161 others(5): Show |
8 | HG02622.hp2 HG02895.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.248-2343_248-2341d others(5): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111716783 | |||||||
| chr6:111716800 | T | C | 57 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0115 others(54): Show |
57 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.248-2357A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111716800 | |||||||
| chr6:111716824 | G | A | 24 | a0001c0001t0001g0111 a0001c0001t0001g0173 a0001c0001t0001g0177 others(21): Show |
24 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.248-2381C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111716824 | |||||||
| chr6:111716832 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.248-2389A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111716832 | |||||||
| chr6:111716853 | C | T | 57 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0115 others(54): Show |
57 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.248-2410G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111716853 | |||||||
| chr6:111716857 | T | C | 21 | a0001c0001t0001g0162 a0001c0001t0001g0165 a0001c0001t0002g0054 others(18): Show |
21 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.248-2414A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111716857 | |||||||
| chr6:111717011 | C | T | 5 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0149 others(2): Show |
5 | HG02145.hp1 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.248-2568G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111717011 | |||||||
| chr6:111717285 | T | C | 1 | a0001c0001t0002g0042 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.247+2520A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111717285 | |||||||
| chr6:111717295 | A | G | 59 | a0001c0001t0001g0113 a0001c0001t0001g0117 a0001c0001t0001g0123 others(56): Show |
59 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.247+2510T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111717295 | |||||||
| chr6:111717386 | C | A | 1 | a0001c0001t0002g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.247+2419G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111717386 | |||||||
| chr6:111717437 | C | G | 8 | a0001c0001t0001g0099 a0001c0001t0001g0136 a0001c0001t0001g0161 others(5): Show |
8 | HG02622.hp2 HG02895.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.247+2368G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111717437 | |||||||
| chr6:111717549 | C | T | 8 | a0001c0001t0001g0099 a0001c0001t0001g0136 a0001c0001t0001g0161 others(5): Show |
8 | HG02622.hp2 HG02895.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.247+2256G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111717549 | |||||||
| chr6:111717615 | C | T | 24 | a0001c0001t0001g0111 a0001c0001t0001g0173 a0001c0001t0001g0177 others(21): Show |
24 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.247+2190G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111717615 | |||||||
| chr6:111717752 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.247+2053G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111717752 | |||||||
| chr6:111717900 | T | C | 1 | a0001c0001t0012g0106 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.247+1905A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111717900 | |||||||
| chr6:111718109 | C | A | 1 | a0001c0001t0002g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.247+1696G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111718109 | |||||||
| chr6:111718276 | T | C | 21 | a0001c0001t0001g0173 a0001c0001t0001g0177 a0001c0001t0001g0178 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.247+1529A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111718276 | |||||||
| chr6:111718281 | G | A | 6 | a0001c0001t0005g0218 a0001c0001t0008g0097 a0001c0001t0008g0100 others(3): Show |
6 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.247+1524C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111718281 | |||||||
| chr6:111718368 | T | G | 12 | a0001c0001t0001g0115 a0001c0001t0001g0141 a0001c0001t0001g0142 others(9): Show |
12 | HG00741.hp2 HG02559.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.247+1437A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111718368 | |||||||
| chr6:111718417 | C | T | 1 | a0001c0001t0003g0033 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.247+1388G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111718417 | |||||||
| chr6:111718428 | C | T | 1 | a0001c0001t0008g0100 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.247+1377G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111718428 | |||||||
| chr6:111718519 | G | A | 8 | a0001c0001t0001g0099 a0001c0001t0001g0136 a0001c0001t0001g0161 others(5): Show |
8 | HG02622.hp2 HG02895.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.247+1286C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111718519 | |||||||
| chr6:111718564 | G | T | 35 | a0001c0001t0001g0113 a0001c0001t0001g0147 a0001c0001t0001g0148 others(32): Show |
35 | HG00438.hp2 HG00733.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.247+1241C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111718564 | |||||||
| chr6:111718806 | ACTT | A | 8 | a0001c0001t0001g0099 a0001c0001t0001g0136 a0001c0001t0001g0161 others(5): Show |
8 | HG02622.hp2 HG02895.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.247+996_247+998del others(3): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111718806 | |||||||
| chr6:111718869 | C | T | 8 | a0001c0001t0001g0099 a0001c0001t0001g0136 a0001c0001t0001g0161 others(5): Show |
8 | HG02622.hp2 HG02895.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.247+936G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111718869 | |||||||
| chr6:111719126 | G | C | 3 | a0001c0001t0001g0111 a0001c0001t0004g0109 a0001c0001t0004g0112 |
3 | HG02257.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.247+679C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111719126 | |||||||
| chr6:111719310 | CA | C | 8 | a0001c0001t0001g0155 a0001c0001t0001g0191 a0001c0001t0002g0034 others(5): Show |
8 | HG01081.hp1 HG02451.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.247+494delT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111719310 | |||||||
| chr6:111719463 | G | A | 24 | a0001c0001t0001g0111 a0001c0001t0001g0173 a0001c0001t0001g0177 others(21): Show |
24 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.247+342C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 4/13 | chr6 | 111719463 | |||||||
| chr6:111720156 | T | C | 139 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(136): Show |
139 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(136): Show |
intron_variant | MODIFIER | c.-11-94A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111720156 | |||||||
| chr6:111720165 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-11-103A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111720165 | |||||||
| chr6:111720248 | G | A | 1 | a0001c0001t0002g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-11-186C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111720248 | |||||||
| chr6:111720378 | T | G | 1 | a0001c0001t0007g0073 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-11-316A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111720378 | |||||||
| chr6:111720429 | T | C | 4 | a0001c0001t0007g0071 a0001c0001t0007g0072 a0001c0001t0007g0073 others(1): Show |
4 | HG00738.hp1 HG01433.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-367A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111720429 | |||||||
| chr6:111720448 | A | C | 9 | a0001c0001t0001g0113 a0001c0001t0001g0147 a0001c0001t0001g0148 others(6): Show |
9 | HG01891.hp2 HG01952.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-11-386T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111720448 | |||||||
| chr6:111720662 | A | G | 8 | a0001c0001t0001g0099 a0001c0001t0001g0136 a0001c0001t0001g0161 others(5): Show |
8 | HG02622.hp2 HG02895.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.-11-600T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111720662 | |||||||
| chr6:111720826 | G | A | 2 | a0001c0001t0001g0096 a0001c0001t0023g0214 |
2 | HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-11-764C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111720826 | |||||||
| chr6:111720874 | C | T | 1 | a0001c0001t0002g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-11-812G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111720874 | |||||||
| chr6:111720949 | T | G | 4 | a0001c0001t0007g0060 a0001c0001t0010g0152 a0001c0001t0014g0036 others(1): Show |
4 | HG02622.hp2 HG02895.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-887A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111720949 | |||||||
| chr6:111720951 | A | T | 1 | a0001c0001t0007g0072 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-11-889T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111720951 | |||||||
| chr6:111721136 | C | T | 4 | a0001c0001t0001g0144 a0001c0001t0001g0149 a0001c0001t0001g0175 others(1): Show |
4 | HG02622.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-1074G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111721136 | |||||||
| chr6:111721458 | C | T | 3 | a0001c0001t0001g0117 a0001c0001t0001g0127 a0001c0001t0001g0128 |
3 | NA18946.hp2 NA18951.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.-11-1396G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111721458 | |||||||
| chr6:111721472 | C | T | 33 | a0001c0001t0001g0099 a0001c0001t0001g0115 a0001c0001t0001g0136 others(30): Show |
33 | HG00741.hp2 HG02055.hp2 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.-11-1410G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111721472 | |||||||
| chr6:111721488 | G | A | 61 | a0001c0001t0001g0096 a0001c0001t0001g0113 a0001c0001t0001g0117 others(58): Show |
61 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.-11-1426C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111721488 | |||||||
| chr6:111721550 | C | T | 7 | a0001c0001t0006g0209 a0001c0001t0009g0002 a0001c0001t0009g0004 others(4): Show |
7 | NA18950.hp2 NA18989.hp2 NA18993.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11-1488G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111721550 | |||||||
| chr6:111721598 | T | G | 1 | a0001c0001t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-11-1536A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111721598 | |||||||
| chr6:111721614 | A | T | 57 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0115 others(54): Show |
57 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.-11-1552T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111721614 | |||||||
| chr6:111721675 | C | G | 207 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(204): Show |
208 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(205): Show |
intron_variant | MODIFIER | c.-11-1613G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111721675 | |||||||
| chr6:111721715 | C | G | 1 | a0001c0001t0006g0226 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-11-1653G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111721715 | |||||||
| chr6:111721915 | C | A | 138 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(135): Show |
138 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(135): Show |
intron_variant | MODIFIER | c.-11-1853G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111721915 | |||||||
| chr6:111721928 | T | A | 1 | a0001c0001t0002g0094 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-11-1866A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111721928 | |||||||
| chr6:111721930 | C | A | 138 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(135): Show |
138 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(135): Show |
intron_variant | MODIFIER | c.-11-1868G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111721930 | |||||||
| chr6:111721952 | T | G | 1 | a0001c0002t0001g0135 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-11-1890A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111721952 | |||||||
| chr6:111722224 | C | T | 1 | a0001c0001t0004g0109 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-11-2162G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111722224 | |||||||
| chr6:111722313 | T | C | 3 | a0001c0001t0001g0111 a0001c0001t0004g0109 a0001c0001t0004g0112 |
3 | HG02257.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-11-2251A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111722313 | |||||||
| chr6:111722396 | A | C | 57 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0115 others(54): Show |
57 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.-11-2334T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111722396 | |||||||
| chr6:111722634 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-11-2572C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111722634 | |||||||
| chr6:111722655 | G | A | 138 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(135): Show |
138 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(135): Show |
intron_variant | MODIFIER | c.-11-2593C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111722655 | |||||||
| chr6:111722853 | G | A | 138 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(135): Show |
138 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(135): Show |
intron_variant | MODIFIER | c.-11-2791C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111722853 | |||||||
| chr6:111722859 | A | C | 138 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(135): Show |
138 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(135): Show |
intron_variant | MODIFIER | c.-11-2797T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111722859 | |||||||
| chr6:111722902 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-11-2840G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111722902 | |||||||
| chr6:111723114 | A | G | 1 | a0001c0001t0002g0091 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-11-3052T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111723114 | |||||||
| chr6:111723262 | A | G | 59 | a0001c0001t0001g0113 a0001c0001t0001g0117 a0001c0001t0001g0123 others(56): Show |
59 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.-11-3200T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111723262 | |||||||
| chr6:111723315 | G | A | 26 | a0001c0001t0001g0099 a0001c0001t0001g0115 a0001c0001t0001g0136 others(23): Show |
26 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(23): Show |
intron_variant | MODIFIER | c.-11-3253C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111723315 | |||||||
| chr6:111723344 | G | C | 20 | a0001c0001t0001g0162 a0001c0001t0001g0165 a0001c0001t0002g0054 others(17): Show |
20 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.-11-3282C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111723344 | |||||||
| chr6:111723687 | T | C | 1 | a0001c0001t0002g0063 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-11-3625A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111723687 | |||||||
| chr6:111723770 | C | T | 1 | a0001c0001t0009g0003 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-11-3708G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111723770 | |||||||
| chr6:111723787 | A | G | 6 | a0001c0001t0005g0218 a0001c0001t0008g0097 a0001c0001t0008g0100 others(3): Show |
6 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11-3725T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111723787 | |||||||
| chr6:111723919 | T | C | 138 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(135): Show |
138 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(135): Show |
intron_variant | MODIFIER | c.-11-3857A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111723919 | |||||||
| chr6:111724031 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-11-3969C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111724031 | |||||||
| chr6:111724199 | C | T | 6 | a0001c0001t0005g0218 a0001c0001t0008g0097 a0001c0001t0008g0100 others(3): Show |
6 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11-4137G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111724199 | |||||||
| chr6:111724275 | A | C | 138 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(135): Show |
138 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(135): Show |
intron_variant | MODIFIER | c.-11-4213T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111724275 | |||||||
| chr6:111724450 | C | T | 59 | a0001c0001t0001g0113 a0001c0001t0001g0117 a0001c0001t0001g0123 others(56): Show |
59 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.-11-4388G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111724450 | |||||||
| chr6:111724480 | A | C | 17 | a0001c0001t0001g0115 a0001c0001t0001g0141 a0001c0001t0001g0142 others(14): Show |
17 | HG00741.hp2 HG02145.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.-11-4418T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111724480 | |||||||
| chr6:111724794 | C | G | 6 | a0001c0001t0005g0218 a0001c0001t0008g0097 a0001c0001t0008g0100 others(3): Show |
6 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11-4732G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111724794 | |||||||
| chr6:111724807 | C | T | 1 | a0001c0001t0007g0027 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-11-4745G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111724807 | |||||||
| chr6:111725048 | CAGGAATA others(5): Show |
C | 81 | a0001c0001t0001g0096 a0001c0001t0001g0113 a0001c0001t0001g0117 others(78): Show |
81 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.-11-4998_-11-4987d others(14): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111725048 | |||||||
| chr6:111725070 | A | C | 1 | a0001c0004t0001g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-11-5008T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111725070 | |||||||
| chr6:111725121 | T | C | 58 | a0001c0001t0001g0113 a0001c0001t0001g0117 a0001c0001t0001g0123 others(55): Show |
58 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.-11-5059A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111725121 | |||||||
| chr6:111725125 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-11-5063A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111725125 | |||||||
| chr6:111725144 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-11-5082G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111725144 | |||||||
| chr6:111725181 | G | A | 1 | a0001c0001t0003g0074 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-11-5119C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111725181 | |||||||
| chr6:111725206 | G | C | 57 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0115 others(54): Show |
57 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.-11-5144C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111725206 | |||||||
| chr6:111725356 | C | T | 1 | a0001c0001t0002g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-11-5294G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111725356 | |||||||
| chr6:111725402 | T | C | 1 | a0001c0001t0003g0066 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-11-5340A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111725402 | |||||||
| chr6:111725519 | T | TG | 61 | a0001c0001t0001g0096 a0001c0001t0001g0113 a0001c0001t0001g0117 others(58): Show |
61 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.-11-5458dupC | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111725519 | |||||||
| chr6:111725810 | G | A | 1 | a0001c0001t0002g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-11-5748C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111725810 | |||||||
| chr6:111725944 | C | T | 1 | a0001c0001t0006g0217 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-11-5882G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111725944 | |||||||
| chr6:111726253 | A | G | 62 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0115 others(59): Show |
62 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.-11-6191T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111726253 | |||||||
| chr6:111726395 | T | A | 138 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(135): Show |
138 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(135): Show |
intron_variant | MODIFIER | c.-11-6333A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111726395 | |||||||
| chr6:111726915 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-11-6853C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111726915 | |||||||
| chr6:111727000 | G | A | 11 | a0001c0001t0001g0170 a0001c0001t0004g0121 a0001c0001t0004g0169 others(8): Show |
11 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11-6938C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111727000 | |||||||
| chr6:111727086 | T | C | 207 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(204): Show |
208 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(205): Show |
intron_variant | MODIFIER | c.-11-7024A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111727086 | |||||||
| chr6:111727208 | C | T | 57 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0115 others(54): Show |
57 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.-11-7146G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111727208 | |||||||
| chr6:111727225 | C | T | 2 | a0001c0001t0007g0022 a0001c0001t0007g0026 |
2 | NA18950.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-11-7163G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111727225 | |||||||
| chr6:111727318 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-11-7256A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111727318 | |||||||
| chr6:111727665 | T | C | 21 | a0001c0001t0001g0173 a0001c0001t0001g0177 a0001c0001t0001g0178 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-11-7603A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111727665 | |||||||
| chr6:111727747 | C | T | 61 | a0001c0001t0001g0113 a0001c0001t0001g0117 a0001c0001t0001g0123 others(58): Show |
61 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.-11-7685G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111727747 | |||||||
| chr6:111727842 | T | C | 60 | a0001c0001t0001g0113 a0001c0001t0001g0117 a0001c0001t0001g0123 others(57): Show |
60 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.-11-7780A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111727842 | |||||||
| chr6:111727942 | C | T | 5 | a0001c0001t0002g0059 a0001c0001t0002g0063 a0001c0001t0002g0064 others(2): Show |
5 | HG02080.hp2 NA18945.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11-7880G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111727942 | |||||||
| chr6:111728101 | G | C | 6 | a0001c0001t0005g0218 a0001c0001t0008g0097 a0001c0001t0008g0100 others(3): Show |
6 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11-8039C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111728101 | |||||||
| chr6:111728429 | ATTTCCAT others(18): Show |
A | 24 | a0001c0001t0001g0111 a0001c0001t0001g0173 a0001c0001t0001g0177 others(21): Show |
24 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.-11-8392_-11-8368d others(27): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111728429 | |||||||
| chr6:111728570 | T | C | 2 | a0001c0001t0001g0115 a0001c0001t0005g0215 |
2 | HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-11-8508A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111728570 | |||||||
| chr6:111728743 | A | G | 1 | a0001c0001t0002g0056 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-11-8681T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111728743 | |||||||
| chr6:111728849 | A | G | 118 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0113 others(115): Show |
118 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(115): Show |
intron_variant | MODIFIER | c.-11-8787T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111728849 | |||||||
| chr6:111728924 | G | C | 1 | a0001c0001t0021g0119 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-11-8862C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111728924 | |||||||
| chr6:111728938 | G | C | 2 | a0001c0001t0001g0115 a0001c0001t0005g0215 |
2 | HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-11-8876C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111728938 | |||||||
| chr6:111729137 | A | G | 24 | a0001c0001t0001g0111 a0001c0001t0001g0173 a0001c0001t0001g0177 others(21): Show |
24 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.-11-9075T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111729137 | |||||||
| chr6:111729290 | A | G | 20 | a0001c0001t0001g0162 a0001c0001t0001g0165 a0001c0001t0002g0054 others(17): Show |
20 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.-11-9228T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111729290 | |||||||
| chr6:111729487 | AG | A | 57 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0115 others(54): Show |
57 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.-11-9426delC | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111729487 | |||||||
| chr6:111729488 | G | A | 80 | a0001c0001t0001g0113 a0001c0001t0001g0117 a0001c0001t0001g0123 others(77): Show |
80 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(77): Show |
intron_variant | MODIFIER | c.-11-9426C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111729488 | |||||||
| chr6:111729491 | G | T | 137 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0113 others(134): Show |
137 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(134): Show |
intron_variant | MODIFIER | c.-11-9429C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111729491 | |||||||
| chr6:111729581 | T | C | 1 | a0001c0001t0007g0067 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-11-9519A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111729581 | |||||||
| chr6:111730004 | C | G | 1 | a0001c0001t0002g0045 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-11-9942G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111730004 | |||||||
| chr6:111730185 | A | C | 2 | a0001c0001t0006g0200 a0001c0001t0016g0206 |
2 | NA18974.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.-11-10123T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111730185 | |||||||
| chr6:111730201 | G | A | 5 | a0001c0001t0001g0165 a0001c0001t0008g0116 a0001c0001t0008g0120 others(2): Show |
5 | HG02280.hp2 HG03130.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-10139C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111730201 | |||||||
| chr6:111730572 | G | A | 1 | a0001c0001t0021g0119 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-11-10510C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111730572 | |||||||
| chr6:111730630 | T | C | 1 | a0001c0001t0002g0093 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-11-10568A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111730630 | |||||||
| chr6:111730657 | T | G | 1 | a0001c0001t0001g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-11-10595A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111730657 | |||||||
| chr6:111730858 | GA | G | 58 | a0001c0001t0001g0113 a0001c0001t0001g0117 a0001c0001t0001g0123 others(55): Show |
58 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.-11-10797delT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111730858 | |||||||
| chr6:111731091 | A | T | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-11-11029T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111731091 | |||||||
| chr6:111731191 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-11-11129C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111731191 | |||||||
| chr6:111731327 | G | C | 4 | a0001c0001t0007g0060 a0001c0001t0010g0152 a0001c0001t0014g0036 others(1): Show |
4 | HG02622.hp2 HG02895.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-11265C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111731327 | |||||||
| chr6:111731461 | C | G | 5 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0149 others(2): Show |
5 | HG02145.hp1 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11-11399G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111731461 | |||||||
| chr6:111731526 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-11-11464G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111731526 | |||||||
| chr6:111731544 | T | C | 1 | a0001c0001t0005g0215 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-11-11482A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111731544 | |||||||
| chr6:111731726 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-11-11664G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111731726 | |||||||
| chr6:111731879 | G | A | 21 | a0001c0001t0001g0173 a0001c0001t0001g0177 a0001c0001t0001g0178 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-11-11817C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111731879 | |||||||
| chr6:111731902 | G | A | 117 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0113 others(114): Show |
117 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(114): Show |
intron_variant | MODIFIER | c.-11-11840C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111731902 | |||||||
| chr6:111731960 | G | A | 1 | a0001c0001t0004g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-11-11898C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111731960 | |||||||
| chr6:111732125 | C | T | 2 | a0001c0001t0007g0022 a0001c0001t0007g0026 |
2 | NA18950.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-11-12063G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111732125 | |||||||
| chr6:111732214 | T | C | 24 | a0001c0001t0001g0111 a0001c0001t0001g0173 a0001c0001t0001g0177 others(21): Show |
24 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.-11-12152A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111732214 | |||||||
| chr6:111732281 | AATACAAT others(8): Show |
A | 6 | a0001c0001t0005g0218 a0001c0001t0008g0097 a0001c0001t0008g0100 others(3): Show |
6 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11-12234_-11-1222 others(19): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111732281 | |||||||
| chr6:111732371 | T | G | 3 | a0001c0001t0001g0111 a0001c0001t0004g0109 a0001c0001t0004g0112 |
3 | HG02257.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-11-12309A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111732371 | |||||||
| chr6:111732395 | G | A | 1 | a0001c0001t0002g0001 | 2 | HG01258.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-11-12333C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111732395 | |||||||
| chr6:111732486 | A | AGGGTGAA others(3): Show |
1 | a0001c0001t0002g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-11-12434_-11-1242 others(14): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111732486 | |||||||
| chr6:111732524 | G | A | 6 | a0001c0001t0005g0218 a0001c0001t0008g0097 a0001c0001t0008g0100 others(3): Show |
6 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11-12462C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111732524 | |||||||
| chr6:111732770 | T | C | 94 | a0001c0001t0001g0099 a0001c0001t0001g0113 a0001c0001t0001g0115 others(91): Show |
94 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(91): Show |
intron_variant | MODIFIER | c.-11-12708A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111732770 | |||||||
| chr6:111732862 | C | T | 1 | a0001c0001t0002g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-11-12800G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111732862 | |||||||
| chr6:111732916 | C | A | 1 | a0001c0001t0002g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-11-12854G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111732916 | |||||||
| chr6:111733071 | T | C | 67 | a0001c0001t0001g0113 a0001c0001t0001g0117 a0001c0001t0001g0123 others(64): Show |
67 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.-11-13009A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111733071 | |||||||
| chr6:111733099 | G | A | 1 | a0001c0001t0007g0072 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-11-13037C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111733099 | |||||||
| chr6:111733105 | A | G | 1 | a0001c0001t0005g0215 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-11-13043T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111733105 | |||||||
| chr6:111733245 | C | T | 1 | a0001c0001t0002g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-11-13183G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111733245 | |||||||
| chr6:111733418 | G | A | 1 | a0001c0001t0004g0132 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-11-13356C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111733418 | |||||||
| chr6:111733607 | T | G | 21 | a0001c0001t0001g0173 a0001c0001t0001g0177 a0001c0001t0001g0178 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-11-13545A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111733607 | |||||||
| chr6:111733730 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-11-13668C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111733730 | |||||||
| chr6:111733812 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-11-13750C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111733812 | |||||||
| chr6:111733983 | G | A | 4 | a0001c0001t0007g0071 a0001c0001t0007g0072 a0001c0001t0007g0073 others(1): Show |
4 | HG00738.hp1 HG01433.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-13921C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111733983 | |||||||
| chr6:111734073 | T | C | 138 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(135): Show |
138 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(135): Show |
intron_variant | MODIFIER | c.-11-14011A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111734073 | |||||||
| chr6:111734269 | A | T | 2 | a0001c0001t0006g0216 a0001c0001t0023g0214 |
2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-11-14207T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111734269 | |||||||
| chr6:111734346 | G | C | 1 | a0001c0001t0004g0172 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-11-14284C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111734346 | |||||||
| chr6:111734448 | C | T | 7 | a0001c0001t0001g0099 a0001c0001t0001g0136 a0001c0001t0007g0060 others(4): Show |
7 | HG02622.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11-14386G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111734448 | |||||||
| chr6:111734487 | C | T | 1 | a0001c0001t0002g0061 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-11-14425G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111734487 | |||||||
| chr6:111734502 | G | A | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0157 |
3 | HG02615.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-11-14440C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111734502 | |||||||
| chr6:111734576 | T | A | 21 | a0001c0001t0001g0173 a0001c0001t0001g0177 a0001c0001t0001g0178 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-11-14514A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111734576 | |||||||
| chr6:111734657 | TGAAGTTA | T | 71 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0117 others(68): Show |
71 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(68): Show |
intron_variant | MODIFIER | c.-11-14602_-11-1459 others(11): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111734657 | |||||||
| chr6:111734710 | A | G | 1 | a0001c0001t0002g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-11-14648T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111734710 | |||||||
| chr6:111734724 | C | T | 1 | a0001c0001t0002g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-11-14662G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111734724 | |||||||
| chr6:111734794 | C | T | 1 | a0001c0001t0007g0072 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-11-14732G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111734794 | |||||||
| chr6:111735066 | T | C | 1 | a0001c0001t0002g0001 | 2 | HG01258.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-11-15004A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111735066 | |||||||
| chr6:111735141 | T | G | 2 | a0001c0001t0001g0154 a0001c0004t0001g0105 |
2 | HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-11-15079A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111735141 | |||||||
| chr6:111735154 | G | A | 8 | a0001c0001t0001g0117 a0001c0001t0001g0124 a0001c0001t0001g0126 others(5): Show |
8 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11-15092C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111735154 | |||||||
| chr6:111735432 | C | T | 1 | a0001c0004t0001g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-11-15370G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111735432 | |||||||
| chr6:111735556 | A | G | 201 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0111 others(198): Show |
202 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(199): Show |
intron_variant | MODIFIER | c.-11-15494T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111735556 | |||||||
| chr6:111735680 | G | C | 2 | a0001c0001t0003g0087 a0001c0001t0007g0067 |
2 | NA18951.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.-11-15618C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111735680 | |||||||
| chr6:111735702 | A | G | 201 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0111 others(198): Show |
202 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(199): Show |
intron_variant | MODIFIER | c.-11-15640T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111735702 | |||||||
| chr6:111735872 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-11-15810A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111735872 | |||||||
| chr6:111736210 | G | A | 6 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0149 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11-16148C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111736210 | |||||||
| chr6:111736211 | C | A | 6 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0149 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11-16149G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111736211 | |||||||
| chr6:111736299 | A | G | 1 | a0001c0001t0002g0001 | 2 | HG01258.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-11-16237T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111736299 | |||||||
| chr6:111736743 | C | T | 1 | a0001c0001t0003g0032 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-11-16681G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111736743 | |||||||
| chr6:111736908 | C | T | 1 | a0001c0001t0002g0053 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-11-16846G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111736908 | |||||||
| chr6:111737302 | C | T | 1 | a0001c0001t0003g0062 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-11-17240G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111737302 | |||||||
| chr6:111737538 | G | A | 6 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0149 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11-17476C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111737538 | |||||||
| chr6:111737542 | G | A | 14 | a0001c0001t0001g0162 a0001c0001t0002g0054 a0001c0001t0003g0014 others(11): Show |
14 | HG01175.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-11-17480C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111737542 | |||||||
| chr6:111737811 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-11-17749A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111737811 | |||||||
| chr6:111738000 | C | T | 2 | a0001c0001t0004g0181 a0001c0001t0004g0192 |
2 | NA18964.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.-11-17938G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111738000 | |||||||
| chr6:111738018 | A | G | 1 | a0001c0001t0009g0007 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-11-17956T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111738018 | |||||||
| chr6:111738159 | G | A | 1 | a0001c0001t0007g0072 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-11-18097C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111738159 | |||||||
| chr6:111738519 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-11-18457A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111738519 | |||||||
| chr6:111738528 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-11-18466T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111738528 | |||||||
| chr6:111738891 | G | A | 1 | a0001c0001t0002g0013 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-11-18829C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111738891 | |||||||
| chr6:111739095 | A | T | 1 | a0001c0001t0001g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-11-19033T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111739095 | |||||||
| chr6:111739387 | C | T | 1 | a0001c0001t0008g0102 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-11-19325G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111739387 | |||||||
| chr6:111739526 | C | T | 1 | a0001c0001t0013g0055 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-11-19464G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111739526 | |||||||
| chr6:111739554 | T | C | 6 | a0001c0001t0001g0162 a0001c0001t0001g0165 a0001c0001t0008g0116 others(3): Show |
6 | HG02280.hp2 HG03130.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11-19492A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111739554 | |||||||
| chr6:111739596 | G | A | 120 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0111 others(117): Show |
121 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.-11-19534C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111739596 | |||||||
| chr6:111739848 | G | C | 5 | a0001c0001t0008g0097 a0001c0001t0008g0100 a0001c0001t0008g0101 others(2): Show |
5 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-19786C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111739848 | |||||||
| chr6:111739970 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-11-19908G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111739970 | |||||||
| chr6:111740069 | A | AC | 120 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0111 others(117): Show |
121 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.-11-20008dupG | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111740069 | |||||||
| chr6:111740572 | G | A | 24 | a0001c0001t0001g0111 a0001c0001t0001g0173 a0001c0001t0001g0177 others(21): Show |
24 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.-11-20510C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111740572 | |||||||
| chr6:111740882 | G | A | 1 | a0001c0001t0008g0101 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-11-20820C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111740882 | |||||||
| chr6:111740990 | C | T | 1 | a0001c0001t0006g0208 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-11-20928G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111740990 | |||||||
| chr6:111741100 | C | CA | 22 | a0001c0001t0001g0117 a0001c0001t0001g0123 a0001c0001t0001g0124 others(19): Show |
22 | HG00639.hp1 HG01081.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-11-21039dupT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111741100 | |||||||
| chr6:111741158 | G | T | 24 | a0001c0001t0001g0096 a0001c0001t0001g0117 a0001c0001t0001g0123 others(21): Show |
24 | HG00639.hp1 HG01081.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.-11-21096C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111741158 | |||||||
| chr6:111741199 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-11-21137C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111741199 | |||||||
| chr6:111741524 | T | TAAC | 229 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(226): Show |
230 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(227): Show |
intron_variant | MODIFIER | c.-11-21465_-11-2146 others(7): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111741524 | |||||||
| chr6:111741615 | CA | C | 116 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0111 others(113): Show |
117 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.-11-21554delT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111741615 | |||||||
| chr6:111741666 | T | A | 1 | a0001c0001t0003g0070 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-11-21604A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111741666 | |||||||
| chr6:111741945 | A | T | 1 | a0001c0001t0004g0098 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-11-21883T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111741945 | |||||||
| chr6:111742279 | T | C | 121 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0111 others(118): Show |
122 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.-11-22217A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111742279 | |||||||
| chr6:111742340 | A | G | 53 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0117 others(50): Show |
53 | HG00558.hp2 HG00639.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.-11-22278T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111742340 | |||||||
| chr6:111742343 | T | C | 24 | a0001c0001t0001g0111 a0001c0001t0001g0173 a0001c0001t0001g0177 others(21): Show |
24 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.-11-22281A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111742343 | |||||||
| chr6:111742387 | C | T | 115 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0111 others(112): Show |
116 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.-11-22325G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111742387 | |||||||
| chr6:111742468 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-11-22406A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111742468 | |||||||
| chr6:111742573 | G | A | 5 | a0001c0001t0008g0097 a0001c0001t0008g0100 a0001c0001t0008g0101 others(2): Show |
5 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-22511C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111742573 | |||||||
| chr6:111742667 | A | G | 62 | a0001c0001t0001g0107 a0001c0001t0001g0129 a0001c0001t0001g0154 others(59): Show |
63 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.-11-22605T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111742667 | |||||||
| chr6:111742849 | G | A | 53 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0117 others(50): Show |
53 | HG00558.hp2 HG00639.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.-11-22787C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111742849 | |||||||
| chr6:111742957 | T | A | 1 | a0001c0001t0002g0054 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-11-22895A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111742957 | |||||||
| chr6:111742967 | C | CT | 5 | a0001c0001t0008g0097 a0001c0001t0008g0100 a0001c0001t0008g0101 others(2): Show |
5 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-22906dupA | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111742967 | |||||||
| chr6:111742967 | CT | C | 62 | a0001c0001t0001g0107 a0001c0001t0001g0129 a0001c0001t0001g0154 others(59): Show |
63 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.-11-22906delA | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111742967 | |||||||
| chr6:111743032 | T | A | 5 | a0001c0001t0008g0097 a0001c0001t0008g0100 a0001c0001t0008g0101 others(2): Show |
5 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-22970A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111743032 | |||||||
| chr6:111743114 | G | A | 5 | a0001c0001t0008g0097 a0001c0001t0008g0100 a0001c0001t0008g0101 others(2): Show |
5 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-23052C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111743114 | |||||||
| chr6:111744026 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-11-23964C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111744026 | |||||||
| chr6:111744095 | G | C | 50 | a0001c0001t0001g0096 a0001c0001t0001g0117 a0001c0001t0001g0123 others(47): Show |
50 | HG00558.hp2 HG00639.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.-11-24033C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111744095 | |||||||
| chr6:111744361 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-11-24299C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111744361 | |||||||
| chr6:111744370 | G | C | 1 | a0001c0001t0002g0054 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-11-24308C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111744370 | |||||||
| chr6:111744417 | T | C | 53 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0117 others(50): Show |
53 | HG00558.hp2 HG00639.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.-11-24355A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111744417 | |||||||
| chr6:111744427 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-11-24365T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111744427 | |||||||
| chr6:111744496 | G | A | 21 | a0001c0001t0001g0173 a0001c0001t0001g0177 a0001c0001t0001g0178 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-11-24434C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111744496 | |||||||
| chr6:111744498 | T | A | 121 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0111 others(118): Show |
122 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.-11-24436A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111744498 | |||||||
| chr6:111744762 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-11-24700A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111744762 | |||||||
| chr6:111744890 | A | T | 4 | a0001c0001t0001g0143 a0001c0001t0001g0149 a0001c0001t0001g0150 others(1): Show |
4 | HG02145.hp1 HG02559.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-24828T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111744890 | |||||||
| chr6:111744975 | C | A | 5 | a0001c0001t0008g0097 a0001c0001t0008g0100 a0001c0001t0008g0101 others(2): Show |
5 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-24913G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111744975 | |||||||
| chr6:111745050 | G | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0151 |
2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-11-24988C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111745050 | |||||||
| chr6:111745229 | A | G | 122 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0111 others(119): Show |
123 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.-11-25167T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111745229 | |||||||
| chr6:111745405 | T | G | 1 | a0001c0001t0001g0122 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-11-25343A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111745405 | |||||||
| chr6:111745437 | A | C | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0157 |
3 | HG02615.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-11-25375T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111745437 | |||||||
| chr6:111745658 | T | G | 1 | a0001c0001t0001g0129 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-11-25596A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111745658 | |||||||
| chr6:111745667 | G | C | 24 | a0001c0001t0001g0096 a0001c0001t0001g0117 a0001c0001t0001g0123 others(21): Show |
24 | HG00639.hp1 HG01081.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.-11-25605C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111745667 | |||||||
| chr6:111745688 | C | G | 122 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0111 others(119): Show |
123 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.-11-25626G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111745688 | |||||||
| chr6:111746030 | C | T | 53 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0117 others(50): Show |
53 | HG00558.hp2 HG00639.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.-11-25968G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111746030 | |||||||
| chr6:111746031 | G | A | 2 | a0001c0001t0004g0181 a0001c0001t0004g0192 |
2 | NA18964.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.-11-25969C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111746031 | |||||||
| chr6:111746036 | T | C | 1 | a0001c0001t0011g0029 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-11-25974A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111746036 | |||||||
| chr6:111746197 | G | T | 2 | a0001c0001t0005g0220 a0001c0001t0024g0219 |
2 | HG02071.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.-11-26135C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111746197 | |||||||
| chr6:111746452 | T | C | 181 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0111 others(178): Show |
182 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(179): Show |
intron_variant | MODIFIER | c.-11-26390A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111746452 | |||||||
| chr6:111746459 | A | T | 181 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0111 others(178): Show |
182 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(179): Show |
intron_variant | MODIFIER | c.-11-26397T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111746459 | |||||||
| chr6:111746521 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-11-26459A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111746521 | |||||||
| chr6:111746606 | T | C | 3 | a0001c0001t0001g0111 a0001c0001t0004g0109 a0001c0001t0004g0112 |
3 | HG02257.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-11-26544A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111746606 | |||||||
| chr6:111746668 | G | A | 2 | a0001c0001t0002g0075 a0001c0001t0011g0018 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.-11-26606C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111746668 | |||||||
| chr6:111746815 | G | A | 63 | a0001c0001t0001g0107 a0001c0001t0001g0129 a0001c0001t0001g0154 others(60): Show |
64 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.-11-26753C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111746815 | |||||||
| chr6:111746977 | C | T | 53 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0117 others(50): Show |
53 | HG00558.hp2 HG00639.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.-11-26915G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111746977 | |||||||
| chr6:111746979 | G | C | 24 | a0001c0001t0001g0111 a0001c0001t0001g0173 a0001c0001t0001g0177 others(21): Show |
24 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.-11-26917C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111746979 | |||||||
| chr6:111747179 | G | A | 29 | a0001c0001t0001g0096 a0001c0001t0001g0117 a0001c0001t0001g0123 others(26): Show |
29 | HG00639.hp1 HG01081.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.-11-27117C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111747179 | |||||||
| chr6:111747467 | A | G | 5 | a0001c0001t0008g0097 a0001c0001t0008g0100 a0001c0001t0008g0101 others(2): Show |
5 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-27405T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111747467 | |||||||
| chr6:111747521 | C | T | 1 | a0001c0001t0003g0085 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-11-27459G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111747521 | |||||||
| chr6:111747545 | T | C | 5 | a0001c0001t0008g0097 a0001c0001t0008g0100 a0001c0001t0008g0101 others(2): Show |
5 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-27483A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111747545 | |||||||
| chr6:111747596 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-11-27534C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111747596 | |||||||
| chr6:111747629 | A | G | 5 | a0001c0001t0008g0097 a0001c0001t0008g0100 a0001c0001t0008g0101 others(2): Show |
5 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-27567T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111747629 | |||||||
| chr6:111747761 | C | A | 6 | a0001c0001t0001g0162 a0001c0001t0001g0165 a0001c0001t0008g0116 others(3): Show |
6 | HG02280.hp2 HG03130.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11-27699G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111747761 | |||||||
| chr6:111747874 | C | T | 24 | a0001c0001t0001g0096 a0001c0001t0001g0117 a0001c0001t0001g0123 others(21): Show |
24 | HG00639.hp1 HG01081.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.-11-27812G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111747874 | |||||||
| chr6:111747980 | C | A | 62 | a0001c0001t0001g0107 a0001c0001t0001g0129 a0001c0001t0001g0154 others(59): Show |
63 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.-11-27918G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111747980 | |||||||
| chr6:111748006 | G | A | 1 | a0001c0001t0021g0119 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-11-27944C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111748006 | |||||||
| chr6:111748136 | G | A | 3 | a0001c0001t0002g0046 a0001c0001t0002g0056 a0001c0001t0002g0058 |
3 | HG00741.hp1 NA18985.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-11-28074C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111748136 | |||||||
| chr6:111748404 | C | T | 2 | a0001c0001t0001g0184 a0001c0001t0002g0061 |
2 | HG04228.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.-11-28342G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111748404 | |||||||
| chr6:111748459 | C | T | 6 | a0001c0001t0001g0162 a0001c0001t0001g0165 a0001c0001t0008g0116 others(3): Show |
6 | HG02280.hp2 HG03130.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11-28397G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111748459 | |||||||
| chr6:111748982 | C | G | 63 | a0001c0001t0001g0107 a0001c0001t0001g0129 a0001c0001t0001g0154 others(60): Show |
64 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.-11-28920G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111748982 | |||||||
| chr6:111749182 | T | G | 1 | a0001c0001t0012g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-11-29120A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111749182 | |||||||
| chr6:111749342 | C | T | 22 | a0001c0001t0001g0096 a0001c0001t0001g0117 a0001c0001t0001g0123 others(19): Show |
22 | HG00639.hp1 HG01081.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-11-29280G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111749342 | |||||||
| chr6:111749529 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-11-29467A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111749529 | |||||||
| chr6:111749875 | C | A | 63 | a0001c0001t0001g0107 a0001c0001t0001g0129 a0001c0001t0001g0154 others(60): Show |
64 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.-11-29813G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111749875 | |||||||
| chr6:111749882 | A | G | 1 | a0001c0001t0019g0086 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-11-29820T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111749882 | |||||||
| chr6:111749893 | G | A | 3 | a0001c0001t0001g0111 a0001c0001t0004g0109 a0001c0001t0004g0112 |
3 | HG02257.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-11-29831C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111749893 | |||||||
| chr6:111749933 | C | T | 6 | a0001c0001t0001g0162 a0001c0001t0001g0165 a0001c0001t0008g0116 others(3): Show |
6 | HG02280.hp2 HG03130.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11-29871G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111749933 | |||||||
| chr6:111749948 | A | T | 1 | a0001c0001t0002g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-11-29886T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111749948 | |||||||
| chr6:111750224 | A | G | 181 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0111 others(178): Show |
182 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(179): Show |
intron_variant | MODIFIER | c.-11-30162T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111750224 | |||||||
| chr6:111750397 | C | T | 1 | a0001c0001t0006g0232 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-12+30169G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111750397 | |||||||
| chr6:111750448 | C | T | 5 | a0001c0001t0008g0097 a0001c0001t0008g0100 a0001c0001t0008g0101 others(2): Show |
5 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+30118G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111750448 | |||||||
| chr6:111750566 | C | T | 5 | a0001c0001t0008g0097 a0001c0001t0008g0100 a0001c0001t0008g0101 others(2): Show |
5 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+30000G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111750566 | |||||||
| chr6:111750644 | T | G | 55 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0140 others(52): Show |
55 | HG00438.hp2 HG00733.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.-12+29922A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111750644 | |||||||
| chr6:111750717 | A | AT | 115 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0111 others(112): Show |
116 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.-12+29848dupA | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111750717 | |||||||
| chr6:111750717 | AT | A | 9 | a0001c0001t0001g0115 a0001c0001t0001g0145 a0001c0001t0003g0037 others(6): Show |
9 | HG02055.hp1 HG02622.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-12+29848delA | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111750717 | |||||||
| chr6:111750737 | A | G | 1 | a0001c0001t0003g0043 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-12+29829T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111750737 | |||||||
| chr6:111750779 | G | T | 5 | a0001c0001t0008g0097 a0001c0001t0008g0100 a0001c0001t0008g0101 others(2): Show |
5 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+29787C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111750779 | |||||||
| chr6:111750922 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-12+29644A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111750922 | |||||||
| chr6:111751042 | A | G | 1 | a0001c0001t0016g0207 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-12+29524T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111751042 | |||||||
| chr6:111751082 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-12+29484G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111751082 | |||||||
| chr6:111751127 | C | G | 45 | a0001c0001t0001g0096 a0001c0001t0001g0117 a0001c0001t0001g0123 others(42): Show |
45 | HG00558.hp2 HG00639.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.-12+29439G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111751127 | |||||||
| chr6:111751402 | C | T | 22 | a0001c0001t0001g0117 a0001c0001t0001g0123 a0001c0001t0001g0124 others(19): Show |
22 | HG00639.hp1 HG01081.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-12+29164G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111751402 | |||||||
| chr6:111751454 | T | TAACAACA others(5): Show |
116 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0111 others(113): Show |
117 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.-12+29100_-12+2911 others(16): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111751454 | |||||||
| chr6:111751465 | A | AC | 60 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0140 others(57): Show |
60 | HG00438.hp2 HG00733.hp2 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.-12+29100dupG | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111751465 | |||||||
| chr6:111751465 | A | C | 1 | a0001c0001t0005g0203 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-12+29101T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111751465 | |||||||
| chr6:111751489 | A | G | 62 | a0001c0001t0001g0107 a0001c0001t0001g0129 a0001c0001t0001g0154 others(59): Show |
63 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.-12+29077T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111751489 | |||||||
| chr6:111751628 | CT | C | 177 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0111 others(174): Show |
178 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(175): Show |
intron_variant | MODIFIER | c.-12+28937delA | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111751628 | |||||||
| chr6:111751656 | C | T | 6 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0149 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+28910G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111751656 | |||||||
| chr6:111751664 | T | C | 10 | a0001c0001t0001g0170 a0001c0001t0004g0121 a0001c0001t0004g0169 others(7): Show |
10 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-12+28902A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111751664 | |||||||
| chr6:111751965 | T | C | 1 | a0001c0001t0002g0040 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-12+28601A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111751965 | |||||||
| chr6:111752188 | C | T | 3 | a0001c0001t0005g0201 a0001c0001t0005g0202 a0001c0001t0005g0203 |
3 | HG02165.hp2 NA19070.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-12+28378G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111752188 | |||||||
| chr6:111752225 | C | T | 5 | a0001c0001t0008g0097 a0001c0001t0008g0100 a0001c0001t0008g0101 others(2): Show |
5 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+28341G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111752225 | |||||||
| chr6:111752314 | A | G | 1 | a0001c0001t0001g0190 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-12+28252T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111752314 | |||||||
| chr6:111752317 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-12+28249A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111752317 | |||||||
| chr6:111752461 | A | C | 1 | a0001c0001t0001g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-12+28105T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111752461 | |||||||
| chr6:111752867 | G | T | 6 | a0001c0001t0001g0162 a0001c0001t0001g0165 a0001c0001t0008g0116 others(3): Show |
6 | HG02280.hp2 HG03130.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+27699C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111752867 | |||||||
| chr6:111753024 | T | G | 1 | a0001c0001t0002g0080 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-12+27542A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111753024 | |||||||
| chr6:111753072 | A | G | 5 | a0001c0001t0008g0097 a0001c0001t0008g0100 a0001c0001t0008g0101 others(2): Show |
5 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+27494T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111753072 | |||||||
| chr6:111753145 | G | C | 64 | a0001c0001t0001g0107 a0001c0001t0001g0129 a0001c0001t0001g0145 others(61): Show |
65 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.-12+27421C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111753145 | |||||||
| chr6:111753200 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-12+27366C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111753200 | |||||||
| chr6:111753210 | T | C | 63 | a0001c0001t0001g0107 a0001c0001t0001g0129 a0001c0001t0001g0154 others(60): Show |
64 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.-12+27356A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111753210 | |||||||
| chr6:111753283 | T | C | 53 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0117 others(50): Show |
53 | HG00558.hp2 HG00639.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.-12+27283A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111753283 | |||||||
| chr6:111753349 | T | C | 10 | a0001c0001t0001g0170 a0001c0001t0004g0121 a0001c0001t0004g0169 others(7): Show |
10 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-12+27217A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111753349 | |||||||
| chr6:111753381 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-12+27185C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111753381 | |||||||
| chr6:111753638 | A | G | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0157 |
3 | HG02615.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-12+26928T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111753638 | |||||||
| chr6:111753836 | A | G | 3 | a0001c0001t0010g0166 a0001c0001t0010g0168 a0001c0001t0025g0233 |
3 | HG02280.hp1 HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-12+26730T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111753836 | |||||||
| chr6:111753858 | C | T | 116 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0111 others(113): Show |
117 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.-12+26708G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111753858 | |||||||
| chr6:111754054 | C | T | 115 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0111 others(112): Show |
116 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.-12+26512G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111754054 | |||||||
| chr6:111754191 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-12+26375C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111754191 | |||||||
| chr6:111754249 | T | A | 3 | a0001c0001t0004g0139 a0001c0001t0004g0181 a0001c0001t0004g0192 |
3 | NA18964.hp1 NA19006.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-12+26317A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111754249 | |||||||
| chr6:111754269 | G | A | 229 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(226): Show |
230 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(227): Show |
intron_variant | MODIFIER | c.-12+26297C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111754269 | |||||||
| chr6:111754649 | G | A | 61 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0140 others(58): Show |
61 | HG00438.hp2 HG00733.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.-12+25917C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111754649 | |||||||
| chr6:111754662 | A | T | 1 | a0001c0001t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-12+25904T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111754662 | |||||||
| chr6:111754710 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-12+25856A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111754710 | |||||||
| chr6:111754725 | A | G | 180 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0111 others(177): Show |
181 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(178): Show |
intron_variant | MODIFIER | c.-12+25841T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111754725 | |||||||
| chr6:111754762 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-12+25804C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111754762 | |||||||
| chr6:111754853 | C | A | 21 | a0001c0001t0001g0173 a0001c0001t0001g0177 a0001c0001t0001g0178 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-12+25713G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111754853 | |||||||
| chr6:111754859 | A | G | 4 | a0001c0001t0002g0077 a0001c0001t0002g0078 a0001c0001t0002g0079 others(1): Show |
4 | HG02071.hp1 NA18964.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+25707T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111754859 | |||||||
| chr6:111754910 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-12+25656A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111754910 | |||||||
| chr6:111754968 | G | GT | 23 | a0001c0001t0001g0117 a0001c0001t0001g0123 a0001c0001t0001g0124 others(20): Show |
23 | HG00639.hp1 HG01081.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.-12+25597dupA | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111754968 | |||||||
| chr6:111754968 | G | GTT | 31 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0173 others(28): Show |
31 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.-12+25596_-12+2559 others(6): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111754968 | |||||||
| chr6:111754968 | GT | G | 67 | a0001c0001t0001g0107 a0001c0001t0001g0129 a0001c0001t0001g0147 others(64): Show |
68 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.-12+25597delA | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111754968 | |||||||
| chr6:111755124 | TAGATG | T | 8 | a0001c0001t0001g0180 a0001c0001t0001g0182 a0001c0001t0001g0189 others(5): Show |
8 | HG00558.hp2 HG00673.hp1 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12+25437_-12+2544 others(9): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111755124 | |||||||
| chr6:111755252 | G | A | 5 | a0001c0001t0008g0097 a0001c0001t0008g0100 a0001c0001t0008g0101 others(2): Show |
5 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+25314C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111755252 | |||||||
| chr6:111755253 | A | T | 5 | a0001c0001t0008g0097 a0001c0001t0008g0100 a0001c0001t0008g0101 others(2): Show |
5 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+25313T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111755253 | |||||||
| chr6:111755309 | C | A | 53 | a0001c0001t0001g0096 a0001c0001t0001g0117 a0001c0001t0001g0123 others(50): Show |
53 | HG00558.hp2 HG00639.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.-12+25257G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111755309 | |||||||
| chr6:111755373 | G | C | 1 | a0001c0001t0009g0005 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-12+25193C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111755373 | |||||||
| chr6:111755492 | T | C | 24 | a0001c0001t0001g0096 a0001c0001t0001g0117 a0001c0001t0001g0123 others(21): Show |
24 | HG00639.hp1 HG01081.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.-12+25074A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111755492 | |||||||
| chr6:111755573 | C | G | 1 | a0001c0001t0016g0207 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-12+24993G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111755573 | |||||||
| chr6:111755779 | A | C | 53 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0117 others(50): Show |
53 | HG00558.hp2 HG00639.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.-12+24787T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111755779 | |||||||
| chr6:111755813 | T | A | 2 | a0001c0001t0001g0115 a0001c0004t0001g0105 |
2 | HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-12+24753A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111755813 | |||||||
| chr6:111756049 | G | A | 3 | a0001c0001t0004g0139 a0001c0001t0004g0181 a0001c0001t0004g0192 |
3 | NA18964.hp1 NA19006.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-12+24517C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111756049 | |||||||
| chr6:111756062 | G | C | 1 | a0001c0001t0001g0162 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-12+24504C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111756062 | |||||||
| chr6:111756147 | A | G | 1 | a0001c0001t0011g0076 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-12+24419T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111756147 | |||||||
| chr6:111756204 | T | C | 55 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0140 others(52): Show |
55 | HG00438.hp2 HG00733.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.-12+24362A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111756204 | |||||||
| chr6:111756278 | T | A | 5 | a0001c0001t0001g0158 a0001c0001t0001g0160 a0001c0001t0002g0013 others(2): Show |
5 | HG01074.hp2 HG01256.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+24288A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111756278 | |||||||
| chr6:111756296 | T | C | 1 | a0001c0001t0002g0041 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-12+24270A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111756296 | |||||||
| chr6:111756416 | T | TA | 29 | a0001c0001t0001g0096 a0001c0001t0001g0117 a0001c0001t0001g0123 others(26): Show |
29 | HG00639.hp1 HG01081.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.-12+24149dupT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111756416 | |||||||
| chr6:111756422 | A | C | 1 | a0001c0001t0001g0162 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-12+24144T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111756422 | |||||||
| chr6:111756447 | C | A | 116 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0111 others(113): Show |
117 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.-12+24119G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111756447 | |||||||
| chr6:111756518 | G | C | 1 | a0001c0001t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-12+24048C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111756518 | |||||||
| chr6:111756902 | A | G | 6 | a0001c0001t0001g0162 a0001c0001t0001g0165 a0001c0001t0008g0116 others(3): Show |
6 | HG02280.hp2 HG03130.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+23664T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111756902 | |||||||
| chr6:111757078 | T | C | 1 | a0001c0001t0002g0050 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-12+23488A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111757078 | |||||||
| chr6:111757466 | T | C | 1 | a0001c0001t0004g0098 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-12+23100A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111757466 | |||||||
| chr6:111757789 | T | G | 1 | a0001c0001t0001g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-12+22777A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111757789 | |||||||
| chr6:111758062 | A | T | 61 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0140 others(58): Show |
61 | HG00438.hp2 HG00733.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.-12+22504T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111758062 | |||||||
| chr6:111758590 | G | T | 5 | a0001c0001t0008g0097 a0001c0001t0008g0100 a0001c0001t0008g0101 others(2): Show |
5 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+21976C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111758590 | |||||||
| chr6:111758591 | C | T | 5 | a0001c0001t0008g0097 a0001c0001t0008g0100 a0001c0001t0008g0101 others(2): Show |
5 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+21975G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111758591 | |||||||
| chr6:111758611 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-12+21955G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111758611 | |||||||
| chr6:111758710 | C | G | 56 | a0001c0001t0001g0096 a0001c0001t0001g0117 a0001c0001t0001g0123 others(53): Show |
56 | HG00558.hp2 HG00639.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.-12+21856G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111758710 | |||||||
| chr6:111758797 | G | C | 1 | a0001c0001t0003g0010 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-12+21769C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111758797 | |||||||
| chr6:111758822 | AG | A | 62 | a0001c0001t0001g0107 a0001c0001t0001g0129 a0001c0001t0001g0154 others(59): Show |
63 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.-12+21743delC | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111758822 | |||||||
| chr6:111759017 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-12+21549C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111759017 | |||||||
| chr6:111759030 | C | A | 1 | a0001c0001t0004g0193 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-12+21536G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111759030 | |||||||
| chr6:111759557 | G | A | 45 | a0001c0001t0001g0096 a0001c0001t0001g0117 a0001c0001t0001g0123 others(42): Show |
45 | HG00558.hp2 HG00639.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.-12+21009C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111759557 | |||||||
| chr6:111759560 | G | A | 3 | a0001c0001t0001g0111 a0001c0001t0004g0109 a0001c0001t0004g0112 |
3 | HG02257.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-12+21006C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111759560 | |||||||
| chr6:111759600 | C | A | 5 | a0001c0001t0005g0220 a0001c0001t0005g0224 a0001c0001t0005g0231 others(2): Show |
5 | HG02071.hp2 HG02080.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+20966G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111759600 | |||||||
| chr6:111759899 | C | T | 1 | a0001c0001t0010g0114 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-12+20667G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111759899 | |||||||
| chr6:111759986 | AT | A | 10 | a0001c0001t0001g0111 a0001c0001t0001g0127 a0001c0001t0001g0162 others(7): Show |
10 | HG02257.hp2 HG02280.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12+20579delA | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111759986 | |||||||
| chr6:111760097 | G | A | 21 | a0001c0001t0001g0173 a0001c0001t0001g0177 a0001c0001t0001g0178 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-12+20469C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111760097 | |||||||
| chr6:111760104 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-12+20462C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111760104 | |||||||
| chr6:111760182 | C | T | 1 | a0001c0001t0003g0074 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-12+20384G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111760182 | |||||||
| chr6:111760413 | G | A | 63 | a0001c0001t0001g0107 a0001c0001t0001g0129 a0001c0001t0001g0154 others(60): Show |
64 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.-12+20153C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111760413 | |||||||
| chr6:111760418 | T | C | 1 | a0001c0001t0013g0057 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-12+20148A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111760418 | |||||||
| chr6:111760532 | C | T | 121 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0111 others(118): Show |
122 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.-12+20034G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111760532 | |||||||
| chr6:111760596 | G | A | 63 | a0001c0001t0001g0107 a0001c0001t0001g0129 a0001c0001t0001g0154 others(60): Show |
64 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.-12+19970C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111760596 | |||||||
| chr6:111760655 | T | C | 122 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0111 others(119): Show |
123 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.-12+19911A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111760655 | |||||||
| chr6:111760730 | A | C | 1 | a0001c0001t0001g0154 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-12+19836T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111760730 | |||||||
| chr6:111760735 | C | T | 45 | a0001c0001t0001g0096 a0001c0001t0001g0117 a0001c0001t0001g0123 others(42): Show |
45 | HG00558.hp2 HG00639.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.-12+19831G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111760735 | |||||||
| chr6:111760786 | T | A | 1 | a0001c0001t0016g0207 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-12+19780A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111760786 | |||||||
| chr6:111761057 | T | C | 3 | a0001c0001t0001g0111 a0001c0001t0004g0109 a0001c0001t0004g0112 |
3 | HG02257.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-12+19509A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111761057 | |||||||
| chr6:111761139 | T | A | 63 | a0001c0001t0001g0107 a0001c0001t0001g0129 a0001c0001t0001g0154 others(60): Show |
64 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.-12+19427A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111761139 | |||||||
| chr6:111761238 | T | A | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-12+19328A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111761238 | |||||||
| chr6:111761515 | T | C | 6 | a0001c0001t0001g0162 a0001c0001t0001g0165 a0001c0001t0008g0116 others(3): Show |
6 | HG02280.hp2 HG03130.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+19051A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111761515 | |||||||
| chr6:111761541 | T | A | 53 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0117 others(50): Show |
53 | HG00558.hp2 HG00639.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.-12+19025A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111761541 | |||||||
| chr6:111761679 | C | T | 1 | a0001c0001t0014g0047 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-12+18887G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111761679 | |||||||
| chr6:111761831 | C | T | 5 | a0001c0001t0001g0158 a0001c0001t0001g0160 a0001c0001t0002g0013 others(2): Show |
5 | HG01074.hp2 HG01256.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+18735G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111761831 | |||||||
| chr6:111761858 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-12+18708A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111761858 | |||||||
| chr6:111762024 | G | A | 5 | a0001c0001t0008g0097 a0001c0001t0008g0100 a0001c0001t0008g0101 others(2): Show |
5 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+18542C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111762024 | |||||||
| chr6:111762050 | G | C | 1 | a0001c0001t0002g0040 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-12+18516C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111762050 | |||||||
| chr6:111762102 | A | G | 1 | a0001c0001t0006g0226 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-12+18464T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111762102 | |||||||
| chr6:111762452 | T | C | 6 | a0001c0001t0001g0162 a0001c0001t0001g0165 a0001c0001t0008g0116 others(3): Show |
6 | HG02280.hp2 HG03130.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+18114A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111762452 | |||||||
| chr6:111762465 | T | A | 6 | a0001c0001t0001g0162 a0001c0001t0001g0165 a0001c0001t0008g0116 others(3): Show |
6 | HG02280.hp2 HG03130.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+18101A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111762465 | |||||||
| chr6:111762645 | C | T | 178 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0111 others(175): Show |
179 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(176): Show |
intron_variant | MODIFIER | c.-12+17921G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111762645 | |||||||
| chr6:111762696 | C | T | 121 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0111 others(118): Show |
122 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.-12+17870G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111762696 | |||||||
| chr6:111762788 | T | C | 62 | a0001c0001t0001g0107 a0001c0001t0001g0129 a0001c0001t0001g0154 others(59): Show |
63 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.-12+17778A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111762788 | |||||||
| chr6:111762854 | A | G | 65 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0129 others(62): Show |
66 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.-12+17712T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111762854 | |||||||
| chr6:111762923 | T | C | 6 | a0001c0001t0001g0162 a0001c0001t0001g0165 a0001c0001t0008g0116 others(3): Show |
6 | HG02280.hp2 HG03130.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+17643A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111762923 | |||||||
| chr6:111763062 | C | T | 10 | a0001c0001t0001g0170 a0001c0001t0004g0121 a0001c0001t0004g0169 others(7): Show |
10 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-12+17504G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111763062 | |||||||
| chr6:111763210 | A | C | 65 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0129 others(62): Show |
66 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.-12+17356T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111763210 | |||||||
| chr6:111763542 | G | A | 4 | a0001c0001t0002g0009 a0001c0001t0002g0093 a0001c0001t0002g0094 others(1): Show |
4 | HG01074.hp1 HG01243.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+17024C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111763542 | |||||||
| chr6:111763774 | A | C | 1 | a0001c0001t0003g0032 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-12+16792T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111763774 | |||||||
| chr6:111764035 | A | G | 63 | a0001c0001t0001g0107 a0001c0001t0001g0129 a0001c0001t0001g0154 others(60): Show |
64 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.-12+16531T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111764035 | |||||||
| chr6:111764160 | T | TA | 25 | a0001c0001t0001g0096 a0001c0001t0001g0117 a0001c0001t0001g0123 others(22): Show |
25 | HG00639.hp1 HG01081.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.-12+16405dupT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111764160 | |||||||
| chr6:111764216 | C | CA | 48 | a0001c0001t0001g0122 a0001c0001t0001g0136 a0001c0001t0001g0147 others(45): Show |
48 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.-12+16349dupT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111764216 | |||||||
| chr6:111764216 | C | CAAAAAA | 51 | a0001c0001t0001g0107 a0001c0001t0001g0129 a0001c0001t0001g0154 others(48): Show |
52 | HG00438.hp1 HG00639.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.-12+16344_-12+1634 others(10): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111764216 | |||||||
| chr6:111764216 | C | CAAAAAAA | 9 | a0001c0001t0001g0143 a0001c0001t0001g0161 a0001c0001t0002g0046 others(6): Show |
9 | HG01109.hp1 HG01433.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-12+16343_-12+1634 others(11): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111764216 | |||||||
| chr6:111764216 | C | CAAAAAAA others(1): Show |
13 | a0001c0001t0001g0142 a0001c0001t0001g0144 a0001c0001t0001g0149 others(10): Show |
13 | HG02145.hp1 HG02280.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.-12+16342_-12+1634 others(12): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111764216 | |||||||
| chr6:111764216 | C | CAAAAAAA others(2): Show |
32 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0140 others(29): Show |
32 | HG00438.hp2 HG00733.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.-12+16341_-12+1634 others(13): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111764216 | |||||||
| chr6:111764216 | C | CAAAAAAA others(3): Show |
17 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0001g0151 others(14): Show |
17 | HG01884.hp1 HG01952.hp2 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.-12+16340_-12+1634 others(14): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111764216 | |||||||
| chr6:111764216 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0004g0181 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-12+16339_-12+1634 others(15): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111764216 | |||||||
| chr6:111764216 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-12+16337_-12+1634 others(17): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111764216 | |||||||
| chr6:111764228 | A | AAAAAAAG | 8 | a0001c0001t0001g0182 a0001c0001t0001g0185 a0001c0001t0001g0190 others(5): Show |
8 | HG02055.hp2 HG02976.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12+16337_-12+1633 others(11): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111764228 | |||||||
| chr6:111764228 | A | AAAAAAG | 21 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0173 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-12+16337_-12+1633 others(10): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111764228 | |||||||
| chr6:111764228 | A | AAAAAG | 21 | a0001c0001t0001g0117 a0001c0001t0001g0123 a0001c0001t0001g0124 others(18): Show |
21 | HG00639.hp1 HG01081.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12+16333_-12+1633 others(9): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111764228 | |||||||
| chr6:111764233 | G | A | 3 | a0001c0001t0004g0098 a0001c0001t0004g0194 a0001c0001t0011g0018 |
3 | HG01069.hp1 HG01891.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.-12+16333C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111764233 | |||||||
| chr6:111764398 | A | T | 1 | a0001c0001t0004g0181 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-12+16168T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111764398 | |||||||
| chr6:111764486 | A | T | 1 | a0001c0001t0004g0181 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-12+16080T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111764486 | |||||||
| chr6:111764508 | A | T | 1 | a0001c0001t0004g0181 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-12+16058T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111764508 | |||||||
| chr6:111764534 | T | C | 24 | a0001c0001t0001g0173 a0001c0001t0001g0177 a0001c0001t0001g0178 others(21): Show |
24 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.-12+16032A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111764534 | |||||||
| chr6:111764568 | G | T | 1 | a0001c0001t0004g0181 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-12+15998C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111764568 | |||||||
| chr6:111764634 | T | A | 1 | a0001c0001t0004g0181 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-12+15932A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111764634 | |||||||
| chr6:111764929 | G | T | 27 | a0001c0001t0001g0117 a0001c0001t0001g0123 a0001c0001t0001g0124 others(24): Show |
27 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(24): Show |
intron_variant | MODIFIER | c.-12+15637C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111764929 | |||||||
| chr6:111765475 | A | G | 5 | a0001c0001t0001g0165 a0001c0001t0008g0116 a0001c0001t0008g0120 others(2): Show |
5 | HG02280.hp2 HG03130.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+15091T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111765475 | |||||||
| chr6:111765507 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-12+15059A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111765507 | |||||||
| chr6:111765681 | C | T | 47 | a0001c0001t0001g0117 a0001c0001t0001g0123 a0001c0001t0001g0124 others(44): Show |
47 | HG00558.hp2 HG00639.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.-12+14885G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111765681 | |||||||
| chr6:111765761 | A | G | 21 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0123 others(18): Show |
21 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12+14805T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111765761 | |||||||
| chr6:111765768 | A | T | 1 | a0001c0001t0004g0181 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-12+14798T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111765768 | |||||||
| chr6:111765774 | TA | T | 164 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0111 others(161): Show |
165 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(162): Show |
intron_variant | MODIFIER | c.-12+14791delT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111765774 | |||||||
| chr6:111765774 | TAA | T | 9 | a0001c0001t0001g0113 a0001c0001t0001g0127 a0001c0001t0002g0069 others(6): Show |
9 | HG01069.hp1 HG02451.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12+14790_-12+1479 others(6): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111765774 | |||||||
| chr6:111765853 | G | C | 1 | a0001c0001t0002g0065 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-12+14713C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111765853 | |||||||
| chr6:111766252 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-12+14314C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111766252 | |||||||
| chr6:111766475 | TA | T | 3 | a0001c0001t0001g0111 a0001c0001t0004g0109 a0001c0001t0004g0112 |
3 | HG02257.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-12+14090delT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111766475 | |||||||
| chr6:111766565 | G | A | 173 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0111 others(170): Show |
174 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(171): Show |
intron_variant | MODIFIER | c.-12+14001C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111766565 | |||||||
| chr6:111766803 | A | G | 6 | a0001c0001t0004g0098 a0001c0001t0008g0097 a0001c0001t0008g0100 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+13763T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111766803 | |||||||
| chr6:111767028 | C | T | 165 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0111 others(162): Show |
166 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(163): Show |
intron_variant | MODIFIER | c.-12+13538G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111767028 | |||||||
| chr6:111767089 | C | G | 1 | a0001c0001t0010g0114 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-12+13477G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111767089 | |||||||
| chr6:111767182 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-12+13384A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111767182 | |||||||
| chr6:111767297 | T | C | 78 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0117 others(75): Show |
78 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.-12+13269A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111767297 | |||||||
| chr6:111767302 | T | C | 6 | a0001c0001t0004g0098 a0001c0001t0008g0097 a0001c0001t0008g0100 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+13264A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111767302 | |||||||
| chr6:111767434 | C | T | 2 | a0001c0001t0001g0111 a0001c0001t0004g0109 |
2 | HG02257.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-12+13132G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111767434 | |||||||
| chr6:111767641 | C | T | 3 | a0001c0001t0001g0111 a0001c0001t0004g0109 a0001c0001t0004g0112 |
3 | HG02257.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-12+12925G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111767641 | |||||||
| chr6:111767658 | C | A | 1 | a0001c0001t0001g0161 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-12+12908G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111767658 | |||||||
| chr6:111767715 | G | C | 6 | a0001c0001t0001g0162 a0001c0001t0001g0165 a0001c0001t0008g0116 others(3): Show |
6 | HG02280.hp2 HG03130.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+12851C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111767715 | |||||||
| chr6:111767903 | T | C | 7 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0149 others(4): Show |
7 | HG02145.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-12+12663A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111767903 | |||||||
| chr6:111768317 | G | A | 66 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0111 others(63): Show |
67 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.-12+12249C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111768317 | |||||||
| chr6:111768465 | G | A | 167 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0111 others(164): Show |
168 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(165): Show |
intron_variant | MODIFIER | c.-12+12101C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111768465 | |||||||
| chr6:111768735 | T | C | 1 | a0001c0004t0001g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-12+11831A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111768735 | |||||||
| chr6:111768874 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-12+11692A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111768874 | |||||||
| chr6:111769400 | T | C | 1 | a0001c0001t0006g0212 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-12+11166A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111769400 | |||||||
| chr6:111769410 | C | G | 20 | a0001c0001t0001g0173 a0001c0001t0001g0177 a0001c0001t0001g0178 others(17): Show |
20 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.-12+11156G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111769410 | |||||||
| chr6:111769558 | T | C | 4 | a0001c0001t0001g0165 a0001c0001t0008g0120 a0001c0001t0008g0163 others(1): Show |
4 | HG03130.hp1 HG03139.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+11008A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111769558 | |||||||
| chr6:111769737 | A | AC | 5 | a0001c0001t0001g0162 a0001c0001t0001g0165 a0001c0001t0008g0120 others(2): Show |
5 | HG03130.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+10828_-12+1082 others(5): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111769737 | |||||||
| chr6:111769743 | C | G | 6 | a0001c0001t0004g0098 a0001c0001t0008g0097 a0001c0001t0008g0100 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+10823G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111769743 | |||||||
| chr6:111769958 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-12+10608C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111769958 | |||||||
| chr6:111770122 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-12+10444G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111770122 | |||||||
| chr6:111770170 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-12+10396A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111770170 | |||||||
| chr6:111770318 | T | C | 1 | a0001c0001t0008g0108 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-12+10248A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111770318 | |||||||
| chr6:111770356 | C | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0151 |
2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-12+10210G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111770356 | |||||||
| chr6:111770380 | A | T | 1 | a0001c0001t0002g0075 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-12+10186T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111770380 | |||||||
| chr6:111770708 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-12+9858A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111770708 | |||||||
| chr6:111770744 | G | T | 1 | a0001c0001t0002g0035 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-12+9822C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111770744 | |||||||
| chr6:111771000 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-12+9566C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111771000 | |||||||
| chr6:111771421 | A | G | 1 | a0001c0001t0003g0030 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-12+9145T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111771421 | |||||||
| chr6:111771587 | TAAA | T | 3 | a0001c0001t0001g0099 a0001c0001t0001g0130 a0001c0001t0001g0145 |
3 | HG01081.hp2 HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-12+8976_-12+8978d others(5): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111771587 | |||||||
| chr6:111771732 | C | A | 6 | a0001c0001t0004g0098 a0001c0001t0008g0097 a0001c0001t0008g0100 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+8834G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111771732 | |||||||
| chr6:111771821 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0153 |
2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-12+8745C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111771821 | |||||||
| chr6:111771882 | C | T | 1 | a0001c0001t0012g0106 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-12+8684G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111771882 | |||||||
| chr6:111772116 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-12+8450G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111772116 | |||||||
| chr6:111772224 | C | CCAGGTGA others(15): Show |
1 | a0001c0001t0002g0034 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-12+8320_-12+8341d others(24): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111772224 | |||||||
| chr6:111772256 | C | T | 3 | a0001c0001t0001g0099 a0001c0001t0001g0130 a0001c0001t0001g0145 |
3 | HG01081.hp2 HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-12+8310G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111772256 | |||||||
| chr6:111772295 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-12+8271C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111772295 | |||||||
| chr6:111772571 | G | A | 20 | a0001c0001t0001g0096 a0001c0001t0001g0117 a0001c0001t0001g0122 others(17): Show |
20 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.-12+7995C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111772571 | |||||||
| chr6:111772855 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-12+7711C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111772855 | |||||||
| chr6:111773014 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-12+7552G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773014 | |||||||
| chr6:111773119 | G | T | 3 | a0001c0001t0017g0051 a0001c0001t0018g0052 a0001c0001t0022g0176 |
3 | HG02809.hp1 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-12+7447C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773119 | |||||||
| chr6:111773135 | C | T | 165 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(162): Show |
166 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(163): Show |
intron_variant | MODIFIER | c.-12+7431G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773135 | |||||||
| chr6:111773150 | A | G | 1 | a0001c0001t0003g0024 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-12+7416T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773150 | |||||||
| chr6:111773212 | T | C | 1 | a0001c0001t0010g0118 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-12+7354A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773212 | |||||||
| chr6:111773318 | GAGGGGGA others(11): Show |
G | 20 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(17): Show |
20 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.-12+7230_-12+7247d others(20): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773318 | |||||||
| chr6:111773323 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-12+7243C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773323 | |||||||
| chr6:111773323 | GGAGGGAG others(17): Show |
G | 1 | a0001c0001t0002g0065 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-12+7219_-12+7242d others(26): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773323 | |||||||
| chr6:111773335 | AAAGGGAG others(10): Show |
A | 1 | a0001c0001t0001g0196 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-12+7214_-12+7230d others(19): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773335 | |||||||
| chr6:111773379 | A | AG | 14 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0150 others(11): Show |
14 | HG01069.hp2 HG01243.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12+7186dupC | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773379 | |||||||
| chr6:111773394 | G | A | 8 | a0001c0001t0001g0115 a0001c0001t0001g0165 a0001c0001t0001g0170 others(5): Show |
8 | HG02486.hp2 HG02723.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12+7172C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773394 | |||||||
| chr6:111773405 | A | AG | 8 | a0001c0001t0001g0182 a0001c0001t0002g0075 a0001c0001t0002g0084 others(5): Show |
8 | HG00735.hp1 HG00738.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12+7160dupC | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773405 | |||||||
| chr6:111773476 | C | CCAGAGGG others(41): Show |
21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-12+7089_-12+7090i others(50): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773476 | |||||||
| chr6:111773476 | CGAGAGG | C | 2 | a0001c0001t0002g0075 a0001c0001t0011g0018 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.-12+7084_-12+7089d others(8): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773476 | |||||||
| chr6:111773477 | G | A | 20 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0123 others(17): Show |
20 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.-12+7089C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773477 | |||||||
| chr6:111773477 | G | C | 118 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0113 others(115): Show |
119 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.-12+7089C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773477 | |||||||
| chr6:111773480 | A | G | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-12+7086T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773480 | |||||||
| chr6:111773483 | G | C | 2 | a0001c0001t0002g0075 a0001c0001t0011g0018 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.-12+7083C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773483 | |||||||
| chr6:111773487 | G | A | 6 | a0001c0001t0004g0098 a0001c0001t0008g0097 a0001c0001t0008g0100 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+7079C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773487 | |||||||
| chr6:111773528 | G | GGGGAGA | 112 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0113 others(109): Show |
113 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.-12+7032_-12+7037d others(8): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773528 | |||||||
| chr6:111773528 | G | GGGGAGAG others(5): Show |
2 | a0001c0001t0002g0077 a0001c0001t0006g0208 |
2 | NA19001.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-12+7026_-12+7037d others(14): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773528 | |||||||
| chr6:111773558 | A | C | 2 | a0001c0001t0004g0125 a0001c0001t0004g0138 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-12+7008T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773558 | |||||||
| chr6:111773559 | G | GGAGGGA | 123 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0113 others(120): Show |
124 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.-12+7001_-12+7006d others(8): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773559 | |||||||
| chr6:111773577 | G | A | 21 | a0001c0001t0001g0099 a0001c0001t0001g0117 a0001c0001t0001g0122 others(18): Show |
21 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12+6989C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773577 | |||||||
| chr6:111773589 | A | G | 21 | a0001c0001t0001g0099 a0001c0001t0001g0117 a0001c0001t0001g0122 others(18): Show |
21 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12+6977T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773589 | |||||||
| chr6:111773590 | A | G | 21 | a0001c0001t0001g0099 a0001c0001t0001g0117 a0001c0001t0001g0122 others(18): Show |
21 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12+6976T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773590 | |||||||
| chr6:111773596 | A | AAGGGAGA others(7): Show |
14 | a0001c0001t0001g0111 a0001c0001t0001g0136 a0001c0001t0001g0143 others(11): Show |
14 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-12+6956_-12+6969d others(16): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773596 | |||||||
| chr6:111773596 | A | AAGGGAGA others(20): Show |
1 | a0001c0001t0001g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-12+6969_-12+6970i others(29): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773596 | |||||||
| chr6:111773596 | A | G | 2 | a0001c0001t0001g0130 a0001c0001t0001g0145 |
2 | HG01081.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-12+6970T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773596 | |||||||
| chr6:111773616 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-12+6950C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773616 | |||||||
| chr6:111773616 | G | GAGAGGGG others(7): Show |
3 | a0001c0001t0001g0130 a0001c0001t0001g0145 a0001c0001t0008g0101 |
3 | HG01081.hp2 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-12+6949_-12+6950i others(16): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773616 | |||||||
| chr6:111773616 | G | GAGAGGGG others(21): Show |
46 | a0001c0001t0001g0096 a0001c0001t0001g0117 a0001c0001t0001g0122 others(43): Show |
46 | HG00558.hp2 HG00639.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.-12+6949_-12+6950i others(30): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773616 | |||||||
| chr6:111773616 | G | GAGAGGGG others(35): Show |
75 | a0001c0001t0001g0107 a0001c0001t0001g0115 a0001c0001t0001g0129 others(72): Show |
76 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.-12+6949_-12+6950i others(44): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773616 | |||||||
| chr6:111773616 | G | GAGAGGGG others(248): Show |
1 | a0001c0001t0006g0228 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-12+6949_-12+6950i others(257): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773616 | |||||||
| chr6:111773616 | G | GAGAGGGG others(64): Show |
1 | a0001c0001t0005g0221 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-12+6949_-12+6950i others(73): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773616 | |||||||
| chr6:111773616 | G | GAGAGGGG others(49): Show |
10 | a0001c0001t0001g0113 a0001c0001t0001g0140 a0001c0001t0005g0199 others(7): Show |
10 | HG01884.hp1 HG02630.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12+6949_-12+6950i others(58): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773616 | |||||||
| chr6:111773616 | G | GAGAGGGG others(62): Show |
1 | a0001c0001t0004g0181 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-12+6949_-12+6950i others(71): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773616 | |||||||
| chr6:111773616 | G | GAGAGGGG others(63): Show |
19 | a0001c0001t0004g0139 a0001c0001t0004g0192 a0001c0001t0005g0201 others(16): Show |
19 | HG00438.hp2 HG01069.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.-12+6949_-12+6950i others(72): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773616 | |||||||
| chr6:111773616 | G | GAGAGGGG others(77): Show |
1 | a0001c0001t0006g0209 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-12+6949_-12+6950i others(86): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773616 | |||||||
| chr6:111773616 | G | GAGAGGGG others(36): Show |
1 | a0001c0001t0001g0142 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-12+6949_-12+6950i others(45): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773616 | |||||||
| chr6:111773616 | G | GAGAGGGG others(50): Show |
1 | a0001c0001t0005g0215 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-12+6949_-12+6950i others(59): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773616 | |||||||
| chr6:111773616 | G | GAGAGGGG others(64): Show |
2 | a0001c0001t0005g0220 a0001c0001t0009g0006 |
2 | NA18982.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.-12+6949_-12+6950i others(73): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773616 | |||||||
| chr6:111773616 | G | GAGAGGGG others(22): Show |
1 | a0001c0001t0001g0196 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-12+6949_-12+6950i others(31): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773616 | |||||||
| chr6:111773616 | G | GAGGAGGG others(36): Show |
1 | a0001c0001t0001g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-12+6949_-12+6950i others(45): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773616 | |||||||
| chr6:111773619 | A | AGGGGGAG others(65): Show |
1 | a0001c0001t0009g0002 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-12+6946_-12+6947i others(74): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773619 | |||||||
| chr6:111773844 | C | T | 1 | a0001c0001t0002g0059 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-12+6722G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773844 | |||||||
| chr6:111773938 | C | T | 1 | a0001c0001t0010g0174 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-12+6628G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111773938 | |||||||
| chr6:111774043 | C | A | 117 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(114): Show |
117 | HG00558.hp2 HG00639.hp1 HG00673.hp1 others(114): Show |
intron_variant | MODIFIER | c.-12+6523G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111774043 | |||||||
| chr6:111774064 | A | C | 1 | a0001c0001t0003g0090 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-12+6502T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111774064 | |||||||
| chr6:111774318 | A | T | 2 | a0001c0001t0001g0136 a0001c0001t0001g0175 |
2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-12+6248T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111774318 | |||||||
| chr6:111774364 | A | T | 6 | a0001c0001t0004g0098 a0001c0001t0008g0097 a0001c0001t0008g0100 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+6202T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111774364 | |||||||
| chr6:111774586 | C | A | 1 | a0001c0001t0015g0204 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-12+5980G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111774586 | |||||||
| chr6:111775142 | T | C | 116 | a0001c0001t0001g0107 a0001c0001t0001g0113 a0001c0001t0001g0115 others(113): Show |
117 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.-12+5424A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111775142 | |||||||
| chr6:111775189 | T | C | 1 | a0001c0001t0006g0200 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-12+5377A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111775189 | |||||||
| chr6:111775191 | G | C | 1 | a0001c0001t0004g0132 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-12+5375C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111775191 | |||||||
| chr6:111775370 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-12+5196A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111775370 | |||||||
| chr6:111775558 | G | T | 22 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0123 others(19): Show |
22 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.-12+5008C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111775558 | |||||||
| chr6:111775963 | A | T | 1 | a0001c0001t0008g0102 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-12+4603T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111775963 | |||||||
| chr6:111775978 | T | C | 117 | a0001c0001t0001g0107 a0001c0001t0001g0113 a0001c0001t0001g0115 others(114): Show |
118 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.-12+4588A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111775978 | |||||||
| chr6:111776073 | T | C | 1 | a0001c0001t0012g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-12+4493A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111776073 | |||||||
| chr6:111776074 | T | C | 2 | a0001c0001t0003g0025 a0001c0001t0003g0043 |
2 | HG02698.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-12+4492A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111776074 | |||||||
| chr6:111776397 | G | A | 59 | a0001c0001t0001g0107 a0001c0001t0001g0129 a0001c0001t0001g0155 others(56): Show |
60 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.-12+4169C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111776397 | |||||||
| chr6:111776698 | C | T | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0185 |
3 | HG03490.hp2 HG03942.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-12+3868G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111776698 | |||||||
| chr6:111776840 | T | C | 14 | a0001c0001t0001g0111 a0001c0001t0001g0136 a0001c0001t0001g0143 others(11): Show |
14 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-12+3726A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111776840 | |||||||
| chr6:111776862 | G | A | 114 | a0001c0001t0001g0107 a0001c0001t0001g0113 a0001c0001t0001g0115 others(111): Show |
115 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.-12+3704C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111776862 | |||||||
| chr6:111776959 | A | T | 1 | a0001c0001t0002g0001 | 2 | HG01258.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-12+3607T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111776959 | |||||||
| chr6:111776982 | T | C | 3 | a0001c0001t0001g0099 a0001c0001t0001g0130 a0001c0001t0001g0145 |
3 | HG01081.hp2 HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-12+3584A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111776982 | |||||||
| chr6:111777061 | A | G | 184 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(181): Show |
185 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(182): Show |
intron_variant | MODIFIER | c.-12+3505T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111777061 | |||||||
| chr6:111777073 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0153 |
2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-12+3493G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111777073 | |||||||
| chr6:111777155 | T | A | 1 | a0001c0001t0001g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-12+3411A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111777155 | |||||||
| chr6:111777209 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-12+3357A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111777209 | |||||||
| chr6:111777492 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-12+3074C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111777492 | |||||||
| chr6:111777693 | T | C | 184 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(181): Show |
185 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(182): Show |
intron_variant | MODIFIER | c.-12+2873A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111777693 | |||||||
| chr6:111777772 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-12+2794A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111777772 | |||||||
| chr6:111777884 | C | G | 22 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0123 others(19): Show |
22 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.-12+2682G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111777884 | |||||||
| chr6:111777947 | T | C | 13 | a0001c0001t0001g0111 a0001c0001t0001g0143 a0001c0001t0001g0144 others(10): Show |
13 | HG02145.hp1 HG02257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.-12+2619A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111777947 | |||||||
| chr6:111778319 | T | C | 2 | a0001c0001t0002g0053 a0001c0001t0002g0081 |
2 | NA19070.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-12+2247A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111778319 | |||||||
| chr6:111778331 | G | A | 20 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(17): Show |
20 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.-12+2235C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111778331 | |||||||
| chr6:111778594 | C | A | 184 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(181): Show |
185 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(182): Show |
intron_variant | MODIFIER | c.-12+1972G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111778594 | |||||||
| chr6:111778800 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0153 |
2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-12+1766G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111778800 | |||||||
| chr6:111779039 | T | C | 21 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0123 others(18): Show |
21 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12+1527A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111779039 | |||||||
| chr6:111779120 | C | CA | 4 | a0001c0001t0001g0179 a0001c0001t0002g0061 a0001c0001t0008g0100 others(1): Show |
4 | HG02083.hp2 HG02976.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+1445dupT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111779120 | |||||||
| chr6:111779120 | C | CT | 15 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0126 others(12): Show |
15 | HG00639.hp1 HG01952.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.-12+1445_-12+1446i others(3): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111779120 | |||||||
| chr6:111779120 | C | CTT | 4 | a0001c0001t0001g0161 a0001c0001t0004g0121 a0001c0001t0004g0125 others(1): Show |
4 | HG01256.hp2 HG01258.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12+1445_-12+1446i others(4): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111779120 | |||||||
| chr6:111779121 | A | AT | 121 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0111 others(118): Show |
122 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.-12+1444dupA | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111779121 | |||||||
| chr6:111779121 | A | ATT | 17 | a0001c0001t0001g0150 a0001c0001t0001g0153 a0001c0001t0002g0012 others(14): Show |
17 | HG00735.hp2 HG01106.hp1 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.-12+1443_-12+1444d others(4): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111779121 | |||||||
| chr6:111779121 | A | T | 21 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0123 others(18): Show |
21 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12+1445T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111779121 | |||||||
| chr6:111779121 | AT | A | 5 | a0001c0001t0001g0185 a0001c0001t0002g0091 a0001c0001t0008g0097 others(2): Show |
5 | HG02055.hp2 HG03225.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+1444delA | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111779121 | |||||||
| chr6:111779122 | T | A | 19 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(16): Show |
19 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.-12+1444A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111779122 | |||||||
| chr6:111779123 | T | A | 4 | a0001c0001t0001g0185 a0001c0001t0008g0097 a0001c0001t0008g0102 others(1): Show |
4 | HG02055.hp2 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+1443A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111779123 | |||||||
| chr6:111779267 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-12+1299G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111779267 | |||||||
| chr6:111779297 | C | T | 1 | a0001c0001t0010g0118 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-12+1269G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111779297 | |||||||
| chr6:111779568 | A | T | 6 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 others(3): Show |
6 | NA18941.hp1 NA18950.hp2 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+998T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111779568 | |||||||
| chr6:111779665 | A | G | 22 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0123 others(19): Show |
22 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.-12+901T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111779665 | |||||||
| chr6:111779684 | G | A | 1 | a0001c0001t0002g0069 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-12+882C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111779684 | |||||||
| chr6:111779787 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-12+779G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111779787 | |||||||
| chr6:111780130 | G | A | 1 | a0001c0001t0004g0110 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-12+436C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111780130 | |||||||
| chr6:111780522 | C | A | 183 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(180): Show |
184 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(181): Show |
intron_variant | MODIFIER | c.-12+44G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 3/13 | chr6 | 111780522 | |||||||
| chr6:111780804 | C | T | 117 | a0001c0001t0001g0107 a0001c0001t0001g0113 a0001c0001t0001g0115 others(114): Show |
118 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.-81-169G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111780804 | |||||||
| chr6:111781102 | T | C | 12 | a0001c0001t0001g0111 a0001c0001t0001g0143 a0001c0001t0001g0144 others(9): Show |
12 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-81-467A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111781102 | |||||||
| chr6:111781537 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-81-902G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111781537 | |||||||
| chr6:111782237 | T | C | 6 | a0001c0001t0004g0098 a0001c0001t0008g0097 a0001c0001t0008g0100 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-81-1602A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111782237 | |||||||
| chr6:111782620 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-81-1985A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111782620 | |||||||
| chr6:111782720 | C | A | 3 | a0001c0001t0001g0099 a0001c0001t0001g0130 a0001c0001t0001g0145 |
3 | HG01081.hp2 HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-81-2085G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111782720 | |||||||
| chr6:111782857 | A | G | 1 | a0001c0001t0007g0067 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-81-2222T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111782857 | |||||||
| chr6:111782943 | T | C | 1 | a0001c0001t0004g0132 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-81-2308A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111782943 | |||||||
| chr6:111782988 | A | G | 10 | a0001c0001t0001g0111 a0001c0001t0001g0143 a0001c0001t0001g0144 others(7): Show |
10 | HG02145.hp1 HG02257.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-81-2353T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111782988 | |||||||
| chr6:111783138 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-81-2503A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111783138 | |||||||
| chr6:111783510 | T | C | 1 | a0001c0001t0007g0073 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-81-2875A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111783510 | |||||||
| chr6:111783543 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-81-2908G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111783543 | |||||||
| chr6:111784273 | A | G | 1 | a0001c0001t0015g0204 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-81-3638T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111784273 | |||||||
| chr6:111784462 | T | C | 2 | a0001c0001t0004g0121 a0001c0001t0021g0119 |
2 | HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-81-3827A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111784462 | |||||||
| chr6:111784621 | T | C | 3 | a0001c0001t0001g0148 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG01891.hp2 HG03130.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-81-3986A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111784621 | |||||||
| chr6:111784864 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-81-4229G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111784864 | |||||||
| chr6:111784865 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-81-4230C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111784865 | |||||||
| chr6:111785089 | C | T | 117 | a0001c0001t0001g0107 a0001c0001t0001g0113 a0001c0001t0001g0115 others(114): Show |
118 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.-81-4454G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111785089 | |||||||
| chr6:111785120 | G | C | 1 | a0001c0001t0001g0161 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-81-4485C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111785120 | |||||||
| chr6:111785669 | C | CT | 7 | a0001c0001t0003g0037 a0001c0001t0003g0066 a0001c0001t0003g0087 others(4): Show |
7 | NA18939.hp1 NA18941.hp2 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.-81-5035dupA | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111785669 | |||||||
| chr6:111785717 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-81-5082G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111785717 | |||||||
| chr6:111785742 | CAT | C | 10 | a0001c0001t0001g0111 a0001c0001t0001g0143 a0001c0001t0001g0144 others(7): Show |
10 | HG02145.hp1 HG02257.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-81-5109_-81-5108d others(4): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111785742 | |||||||
| chr6:111785832 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-81-5197G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111785832 | |||||||
| chr6:111785882 | T | C | 118 | a0001c0001t0001g0107 a0001c0001t0001g0113 a0001c0001t0001g0115 others(115): Show |
119 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.-81-5247A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111785882 | |||||||
| chr6:111785912 | T | C | 4 | a0001c0001t0007g0071 a0001c0001t0007g0072 a0001c0001t0007g0073 others(1): Show |
4 | HG00738.hp1 HG01433.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.-81-5277A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111785912 | |||||||
| chr6:111786010 | T | C | 4 | a0001c0001t0007g0060 a0001c0001t0010g0166 a0001c0001t0010g0168 others(1): Show |
4 | HG02280.hp1 HG02622.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-81-5375A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111786010 | |||||||
| chr6:111786107 | C | T | 1 | a0001c0001t0003g0031 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-81-5472G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111786107 | |||||||
| chr6:111786508 | C | G | 1 | a0001c0001t0007g0072 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-81-5873G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111786508 | |||||||
| chr6:111786508 | C | T | 2 | a0001c0001t0001g0136 a0001c0001t0001g0175 |
2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-81-5873G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111786508 | |||||||
| chr6:111786972 | G | T | 1 | a0001c0001t0001g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-81-6337C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111786972 | |||||||
| chr6:111787142 | T | C | 1 | a0001c0001t0013g0055 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-81-6507A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111787142 | |||||||
| chr6:111787279 | C | T | 1 | a0001c0001t0023g0214 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-81-6644G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111787279 | |||||||
| chr6:111787280 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-81-6645C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111787280 | |||||||
| chr6:111787341 | G | T | 4 | a0001c0001t0007g0060 a0001c0001t0010g0166 a0001c0001t0010g0168 others(1): Show |
4 | HG02280.hp1 HG02622.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-81-6706C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111787341 | |||||||
| chr6:111787384 | C | G | 22 | a0001c0001t0001g0136 a0001c0001t0001g0177 a0001c0001t0001g0178 others(19): Show |
22 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.-81-6749G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111787384 | |||||||
| chr6:111787385 | G | A | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-81-6750C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111787385 | |||||||
| chr6:111787605 | C | T | 8 | a0001c0001t0004g0121 a0001c0001t0004g0137 a0001c0001t0005g0213 others(5): Show |
8 | HG01952.hp2 HG02257.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-81-6970G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111787605 | |||||||
| chr6:111787618 | G | A | 1 | a0001c0001t0004g0181 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-81-6983C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111787618 | |||||||
| chr6:111787648 | T | G | 12 | a0001c0001t0001g0111 a0001c0001t0001g0143 a0001c0001t0001g0144 others(9): Show |
12 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-81-7013A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111787648 | |||||||
| chr6:111788023 | G | A | 7 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0008g0097 others(4): Show |
7 | HG02055.hp2 HG02615.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.-81-7388C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111788023 | |||||||
| chr6:111788200 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-81-7565G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111788200 | |||||||
| chr6:111788292 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-81-7657A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111788292 | |||||||
| chr6:111788319 | T | C | 3 | a0001c0001t0003g0025 a0001c0001t0003g0043 a0001c0001t0003g0070 |
3 | HG02698.hp2 HG04199.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-81-7684A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111788319 | |||||||
| chr6:111788329 | G | A | 2 | a0001c0001t0001g0096 a0001c0001t0001g0154 |
2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-81-7694C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111788329 | |||||||
| chr6:111788904 | A | G | 1 | a0001c0001t0002g0034 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-81-8269T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111788904 | |||||||
| chr6:111789114 | G | T | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-81-8479C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111789114 | |||||||
| chr6:111789173 | T | C | 19 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(16): Show |
19 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.-81-8538A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111789173 | |||||||
| chr6:111789325 | T | C | 128 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(125): Show |
128 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(125): Show |
intron_variant | MODIFIER | c.-81-8690A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111789325 | |||||||
| chr6:111789475 | A | G | 1 | a0001c0001t0019g0086 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-81-8840T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111789475 | |||||||
| chr6:111789481 | C | A | 1 | a0001c0001t0014g0047 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-81-8846G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111789481 | |||||||
| chr6:111789625 | T | A | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0185 |
3 | HG03490.hp2 HG03942.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-81-8990A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111789625 | |||||||
| chr6:111789627 | A | G | 1 | a0001c0001t0010g0174 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-81-8992T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111789627 | |||||||
| chr6:111789729 | T | G | 3 | a0001c0001t0001g0124 a0001c0001t0004g0125 a0001c0001t0004g0138 |
3 | HG01106.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-81-9094A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111789729 | |||||||
| chr6:111789866 | C | T | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0185 |
3 | HG03490.hp2 HG03942.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-81-9231G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111789866 | |||||||
| chr6:111790091 | C | CTG | 65 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0113 others(62): Show |
65 | HG00438.hp2 HG00733.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.-81-9458_-81-9457d others(4): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111790091 | |||||||
| chr6:111790091 | C | CTGTG | 13 | a0001c0001t0001g0115 a0001c0001t0001g0161 a0001c0001t0001g0162 others(10): Show |
13 | HG02280.hp1 HG02486.hp2 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.-81-9460_-81-9457d others(6): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111790091 | |||||||
| chr6:111790091 | CTGTG | C | 21 | a0001c0001t0001g0175 a0001c0001t0001g0177 a0001c0001t0001g0178 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-81-9460_-81-9457d others(6): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111790091 | |||||||
| chr6:111790191 | C | A | 130 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(127): Show |
130 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(127): Show |
intron_variant | MODIFIER | c.-81-9556G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111790191 | |||||||
| chr6:111790201 | T | G | 1 | a0001c0001t0001g0107 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-81-9566A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111790201 | |||||||
| chr6:111790247 | T | TAC | 5 | a0001c0001t0001g0096 a0001c0001t0001g0179 a0001c0001t0002g0069 others(2): Show |
5 | HG03516.hp1 NA18950.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.-81-9614_-81-9613d others(4): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111790247 | |||||||
| chr6:111790247 | TAC | T | 52 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0123 others(49): Show |
52 | HG00558.hp1 HG00639.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.-81-9614_-81-9613d others(4): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111790247 | |||||||
| chr6:111790247 | TACAC | T | 61 | a0001c0001t0001g0099 a0001c0001t0001g0107 a0001c0001t0001g0130 others(58): Show |
62 | HG00438.hp1 HG00673.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.-81-9616_-81-9613d others(6): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111790247 | |||||||
| chr6:111790247 | TACACAC | T | 33 | a0001c0001t0001g0113 a0001c0001t0001g0129 a0001c0001t0001g0136 others(30): Show |
33 | HG00558.hp2 HG00639.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.-81-9618_-81-9613d others(8): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111790247 | |||||||
| chr6:111790247 | TACACACA others(1): Show |
T | 25 | a0001c0001t0001g0143 a0001c0001t0001g0145 a0001c0001t0001g0149 others(22): Show |
25 | HG01243.hp1 HG01256.hp1 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.-81-9620_-81-9613d others(10): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111790247 | |||||||
| chr6:111790247 | TACACACA others(3): Show |
T | 23 | a0001c0001t0001g0140 a0001c0001t0005g0201 a0001c0001t0005g0202 others(20): Show |
23 | HG00438.hp2 HG02129.hp2 HG02717.hp1 others(20): Show |
intron_variant | MODIFIER | c.-81-9622_-81-9613d others(12): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111790247 | |||||||
| chr6:111790247 | TACACACA others(5): Show |
T | 8 | a0001c0001t0001g0111 a0001c0001t0001g0141 a0001c0001t0001g0142 others(5): Show |
8 | HG02257.hp2 HG02486.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-81-9624_-81-9613d others(14): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111790247 | |||||||
| chr6:111790247 | TACACACA others(7): Show |
T | 8 | a0001c0001t0003g0037 a0001c0001t0003g0087 a0001c0001t0004g0112 others(5): Show |
8 | HG03139.hp1 NA18941.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.-81-9626_-81-9613d others(16): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111790247 | |||||||
| chr6:111790247 | TACACACA others(9): Show |
T | 4 | a0001c0001t0003g0066 a0001c0001t0006g0228 a0001c0001t0006g0229 others(1): Show |
4 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.-81-9628_-81-9613d others(18): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111790247 | |||||||
| chr6:111790247 | TACACACA others(11): Show |
T | 2 | a0001c0001t0004g0181 a0001c0001t0004g0192 |
2 | NA18964.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.-81-9630_-81-9613d others(20): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111790247 | |||||||
| chr6:111790279 | CACACACA others(13): Show |
C | 1 | a0001c0001t0010g0174 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-81-9664_-81-9645d others(22): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111790279 | |||||||
| chr6:111790416 | T | G | 1 | a0001c0001t0002g0058 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-81-9781A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111790416 | |||||||
| chr6:111790460 | G | A | 1 | a0001c0001t0016g0206 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-81-9825C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111790460 | |||||||
| chr6:111790460 | G | C | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-81-9825C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111790460 | |||||||
| chr6:111790746 | T | C | 30 | a0001c0001t0001g0099 a0001c0001t0001g0117 a0001c0001t0001g0122 others(27): Show |
30 | HG00639.hp1 HG01081.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.-81-10111A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111790746 | |||||||
| chr6:111791009 | A | AT | 4 | a0001c0001t0001g0111 a0001c0001t0002g0084 a0001c0001t0004g0109 others(1): Show |
4 | HG01106.hp1 HG02257.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-81-10375dupA | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111791009 | |||||||
| chr6:111791009 | A | T | 29 | a0001c0001t0001g0099 a0001c0001t0001g0117 a0001c0001t0001g0122 others(26): Show |
29 | HG00639.hp1 HG01081.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.-81-10374T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111791009 | |||||||
| chr6:111791127 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-81-10492C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111791127 | |||||||
| chr6:111791147 | C | A | 3 | a0001c0001t0006g0228 a0001c0001t0006g0229 a0001c0001t0006g0230 |
3 | HG00733.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-81-10512G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111791147 | |||||||
| chr6:111791244 | G | C | 3 | a0001c0001t0001g0124 a0001c0001t0004g0125 a0001c0001t0004g0138 |
3 | HG01106.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-81-10609C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111791244 | |||||||
| chr6:111791386 | C | T | 51 | a0001c0001t0001g0099 a0001c0001t0001g0117 a0001c0001t0001g0122 others(48): Show |
51 | HG00558.hp2 HG00639.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.-81-10751G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111791386 | |||||||
| chr6:111791834 | C | G | 1 | a0001c0001t0005g0224 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-81-11199G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111791834 | |||||||
| chr6:111791886 | T | A | 1 | a0001c0001t0004g0110 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-81-11251A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111791886 | |||||||
| chr6:111791956 | A | G | 1 | a0001c0001t0014g0047 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-81-11321T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111791956 | |||||||
| chr6:111791961 | C | A | 1 | a0001c0001t0010g0174 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-81-11326G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111791961 | |||||||
| chr6:111792032 | AT | A | 63 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0129 others(60): Show |
63 | HG00438.hp2 HG00733.hp2 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.-81-11398delA | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111792032 | |||||||
| chr6:111792390 | G | A | 7 | a0001c0001t0003g0037 a0001c0001t0003g0066 a0001c0001t0003g0087 others(4): Show |
7 | NA18939.hp1 NA18941.hp2 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.-81-11755C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111792390 | |||||||
| chr6:111792534 | C | T | 1 | a0001c0001t0003g0014 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-81-11899G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111792534 | |||||||
| chr6:111792553 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-81-11918C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111792553 | |||||||
| chr6:111792556 | A | G | 1 | a0001c0001t0010g0174 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-81-11921T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111792556 | |||||||
| chr6:111792619 | C | T | 1 | a0001c0001t0003g0070 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-81-11984G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111792619 | |||||||
| chr6:111792691 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-81-12056A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111792691 | |||||||
| chr6:111792707 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0153 |
2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-81-12072G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111792707 | |||||||
| chr6:111792735 | T | C | 130 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(127): Show |
130 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(127): Show |
intron_variant | MODIFIER | c.-81-12100A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111792735 | |||||||
| chr6:111792755 | C | T | 63 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0129 others(60): Show |
63 | HG00438.hp2 HG00733.hp2 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.-81-12120G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111792755 | |||||||
| chr6:111792774 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-81-12139G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111792774 | |||||||
| chr6:111792948 | G | A | 63 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0129 others(60): Show |
63 | HG00438.hp2 HG00733.hp2 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.-81-12313C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111792948 | |||||||
| chr6:111793046 | A | G | 129 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(126): Show |
129 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(126): Show |
intron_variant | MODIFIER | c.-81-12411T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111793046 | |||||||
| chr6:111793105 | C | T | 129 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(126): Show |
129 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(126): Show |
intron_variant | MODIFIER | c.-81-12470G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111793105 | |||||||
| chr6:111793210 | C | T | 3 | a0001c0001t0004g0181 a0001c0001t0004g0192 a0001c0001t0006g0212 |
3 | HG00438.hp1 NA18964.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.-81-12575G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111793210 | |||||||
| chr6:111793384 | G | A | 6 | a0001c0001t0002g0012 a0001c0001t0002g0038 a0001c0001t0002g0040 others(3): Show |
6 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.-81-12749C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111793384 | |||||||
| chr6:111793423 | A | G | 20 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0123 others(17): Show |
20 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.-81-12788T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111793423 | |||||||
| chr6:111793504 | A | G | 20 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0123 others(17): Show |
20 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.-81-12869T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111793504 | |||||||
| chr6:111793509 | A | C | 1 | a0001c0001t0005g0231 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-81-12874T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111793509 | |||||||
| chr6:111793588 | T | C | 129 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(126): Show |
129 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(126): Show |
intron_variant | MODIFIER | c.-81-12953A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111793588 | |||||||
| chr6:111793620 | C | G | 8 | a0001c0001t0005g0199 a0001c0001t0005g0215 a0001c0001t0005g0218 others(5): Show |
8 | HG01884.hp1 HG02630.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-81-12985G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111793620 | |||||||
| chr6:111793664 | A | G | 20 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0123 others(17): Show |
20 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.-81-13029T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111793664 | |||||||
| chr6:111793706 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-81-13071G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111793706 | |||||||
| chr6:111793914 | C | T | 1 | a0001c0001t0012g0106 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-81-13279G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111793914 | |||||||
| chr6:111794093 | C | T | 2 | a0001c0001t0006g0229 a0001c0001t0006g0230 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-81-13458G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111794093 | |||||||
| chr6:111794119 | C | A | 10 | a0001c0001t0001g0115 a0001c0001t0001g0165 a0001c0001t0001g0170 others(7): Show |
10 | HG02280.hp1 HG02486.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.-81-13484G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111794119 | |||||||
| chr6:111794152 | T | C | 130 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(127): Show |
130 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(127): Show |
intron_variant | MODIFIER | c.-81-13517A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111794152 | |||||||
| chr6:111794458 | G | C | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-81-13823C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111794458 | |||||||
| chr6:111794545 | G | A | 30 | a0001c0001t0001g0099 a0001c0001t0001g0130 a0001c0001t0001g0145 others(27): Show |
30 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.-81-13910C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111794545 | |||||||
| chr6:111794720 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-81-14085G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111794720 | |||||||
| chr6:111794790 | G | A | 63 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0129 others(60): Show |
63 | HG00438.hp2 HG00733.hp2 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.-81-14155C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111794790 | |||||||
| chr6:111795007 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-81-14372A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111795007 | |||||||
| chr6:111795169 | C | T | 1 | a0001c0001t0012g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-81-14534G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111795169 | |||||||
| chr6:111795186 | A | G | 2 | a0001c0001t0002g0053 a0001c0001t0002g0081 |
2 | NA19070.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-81-14551T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111795186 | |||||||
| chr6:111795193 | CAG | C | 63 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0129 others(60): Show |
63 | HG00438.hp2 HG00733.hp2 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.-81-14560_-81-1455 others(6): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111795193 | |||||||
| chr6:111795248 | C | T | 130 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(127): Show |
130 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(127): Show |
intron_variant | MODIFIER | c.-81-14613G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111795248 | |||||||
| chr6:111795348 | A | G | 3 | a0001c0001t0001g0099 a0001c0001t0001g0130 a0001c0001t0001g0145 |
3 | HG01081.hp2 HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-81-14713T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111795348 | |||||||
| chr6:111795366 | C | A | 1 | a0001c0001t0003g0014 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-81-14731G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111795366 | |||||||
| chr6:111795624 | G | A | 1 | a0001c0001t0019g0086 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-81-14989C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111795624 | |||||||
| chr6:111795725 | T | C | 1 | a0001c0001t0002g0012 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-81-15090A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111795725 | |||||||
| chr6:111795750 | T | A | 1 | a0001c0001t0011g0029 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-81-15115A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111795750 | |||||||
| chr6:111795902 | G | A | 1 | a0001c0001t0010g0174 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-81-15267C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111795902 | |||||||
| chr6:111796054 | A | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0153 |
2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-81-15419T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111796054 | |||||||
| chr6:111796080 | C | T | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-81-15445G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111796080 | |||||||
| chr6:111796193 | C | G | 20 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(17): Show |
20 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.-81-15558G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111796193 | |||||||
| chr6:111796244 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-81-15609G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111796244 | |||||||
| chr6:111796421 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0153 |
2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-81-15786C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111796421 | |||||||
| chr6:111796551 | G | A | 6 | a0001c0001t0004g0098 a0001c0001t0008g0097 a0001c0001t0008g0100 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-81-15916C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111796551 | |||||||
| chr6:111796713 | C | T | 10 | a0001c0001t0001g0115 a0001c0001t0001g0165 a0001c0001t0001g0170 others(7): Show |
10 | HG02280.hp1 HG02486.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.-81-16078G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111796713 | |||||||
| chr6:111797288 | T | G | 2 | a0001c0001t0002g0048 a0001c0001t0002g0050 |
2 | NA19005.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.-81-16653A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111797288 | |||||||
| chr6:111797302 | A | C | 129 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(126): Show |
129 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(126): Show |
intron_variant | MODIFIER | c.-81-16667T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111797302 | |||||||
| chr6:111797330 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-81-16695A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111797330 | |||||||
| chr6:111797575 | TG | T | 20 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0123 others(17): Show |
20 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.-81-16941delC | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111797575 | |||||||
| chr6:111797577 | G | C | 20 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0123 others(17): Show |
20 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.-81-16942C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111797577 | |||||||
| chr6:111797665 | C | CAT | 4 | a0001c0001t0003g0014 a0001c0001t0003g0024 a0001c0001t0003g0033 others(1): Show |
4 | HG01261.hp1 HG01496.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.-81-17032_-81-1703 others(6): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111797665 | |||||||
| chr6:111797665 | C | CATAT | 5 | a0001c0001t0002g0040 a0001c0001t0003g0010 a0001c0001t0003g0087 others(2): Show |
5 | HG01256.hp1 HG02145.hp2 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.-81-17034_-81-1703 others(8): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111797665 | |||||||
| chr6:111797665 | CAT | C | 16 | a0001c0001t0002g0013 a0001c0001t0002g0039 a0001c0001t0002g0048 others(13): Show |
16 | HG00639.hp2 HG00738.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.-81-17032_-81-1703 others(6): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111797665 | |||||||
| chr6:111797665 | CATAT | C | 17 | a0001c0001t0002g0012 a0001c0001t0002g0034 a0001c0001t0002g0035 others(14): Show |
17 | HG00673.hp2 HG00735.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.-81-17034_-81-1703 others(8): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111797665 | |||||||
| chr6:111797665 | CATATAT | C | 13 | a0001c0001t0001g0173 a0001c0001t0002g0045 a0001c0001t0002g0046 others(10): Show |
13 | HG00735.hp1 HG01074.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-81-17036_-81-1703 others(10): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111797665 | |||||||
| chr6:111797665 | CATATATA others(1): Show |
C | 21 | a0001c0001t0001g0107 a0001c0001t0001g0155 a0001c0001t0002g0044 others(18): Show |
21 | HG00741.hp1 HG01081.hp1 HG02071.hp1 others(18): Show |
intron_variant | MODIFIER | c.-81-17038_-81-1703 others(12): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111797665 | |||||||
| chr6:111797665 | CATATATA others(3): Show |
C | 7 | a0001c0001t0002g0001 a0001c0001t0002g0041 a0001c0001t0002g0042 others(4): Show |
8 | HG00438.hp1 HG00558.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.-81-17040_-81-1703 others(14): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111797665 | |||||||
| chr6:111797665 | CATATATA others(9): Show |
C | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-81-17046_-81-1703 others(20): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111797665 | |||||||
| chr6:111797665 | CATATATA others(11): Show |
C | 3 | a0001c0001t0015g0204 a0001c0001t0016g0206 a0001c0001t0016g0207 |
3 | NA18974.hp1 NA19057.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-81-17048_-81-1703 others(22): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111797665 | |||||||
| chr6:111797665 | CATATATA others(13): Show |
C | 2 | a0001c0001t0001g0122 a0001c0001t0004g0103 |
2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-81-17050_-81-1703 others(24): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111797665 | |||||||
| chr6:111797665 | CATATATA others(15): Show |
C | 9 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0126 others(6): Show |
9 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.-81-17052_-81-1703 others(26): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111797665 | |||||||
| chr6:111797665 | CATATATA others(17): Show |
C | 21 | a0001c0001t0001g0111 a0001c0001t0001g0117 a0001c0001t0001g0127 others(18): Show |
21 | HG01952.hp2 HG02145.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.-81-17054_-81-1703 others(28): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111797665 | |||||||
| chr6:111797665 | CATATATA others(19): Show |
C | 17 | a0001c0001t0001g0113 a0001c0001t0001g0129 a0001c0001t0001g0136 others(14): Show |
17 | HG00741.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.-81-17056_-81-1703 others(30): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111797665 | |||||||
| chr6:111797665 | CATATATA others(21): Show |
C | 58 | a0001c0001t0001g0099 a0001c0001t0001g0115 a0001c0001t0001g0130 others(55): Show |
58 | HG00438.hp2 HG00733.hp2 HG01069.hp2 others(55): Show |
intron_variant | MODIFIER | c.-81-17058_-81-1703 others(32): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111797665 | |||||||
| chr6:111797665 | CATATATA others(25): Show |
C | 2 | a0001c0001t0003g0085 a0001c0001t0012g0156 |
2 | HG03490.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.-81-17062_-81-1703 others(36): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111797665 | |||||||
| chr6:111797683 | TATATATA others(23): Show |
T | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-81-17078_-81-1704 others(34): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111797683 | |||||||
| chr6:111797685 | TATATATA others(21): Show |
T | 1 | a0001c0001t0001g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-81-17078_-81-1705 others(32): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111797685 | |||||||
| chr6:111797709 | T | C | 4 | a0001c0001t0001g0122 a0001c0001t0002g0082 a0001c0001t0003g0074 others(1): Show |
4 | HG01175.hp1 HG01243.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.-81-17074A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111797709 | |||||||
| chr6:111797711 | T | C | 87 | a0001c0001t0001g0113 a0001c0001t0001g0117 a0001c0001t0001g0122 others(84): Show |
87 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(84): Show |
intron_variant | MODIFIER | c.-81-17076A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111797711 | |||||||
| chr6:111797727 | C | T | 1 | a0001c0001t0002g0082 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-81-17092G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111797727 | |||||||
| chr6:111797728 | A | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0153 |
2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-81-17093T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111797728 | |||||||
| chr6:111797729 | T | C | 84 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0129 others(81): Show |
84 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(81): Show |
intron_variant | MODIFIER | c.-81-17094A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111797729 | |||||||
| chr6:111797804 | C | T | 1 | a0001c0001t0015g0204 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-81-17169G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111797804 | |||||||
| chr6:111797841 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0153 |
2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-81-17206G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111797841 | |||||||
| chr6:111797856 | A | G | 130 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(127): Show |
130 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(127): Show |
intron_variant | MODIFIER | c.-81-17221T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111797856 | |||||||
| chr6:111798011 | C | A | 1 | a0001c0001t0002g0065 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-81-17376G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111798011 | |||||||
| chr6:111798416 | C | T | 130 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(127): Show |
130 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(127): Show |
intron_variant | MODIFIER | c.-81-17781G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111798416 | |||||||
| chr6:111798499 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-81-17864C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111798499 | |||||||
| chr6:111798525 | TC | T | 14 | a0001c0001t0001g0096 a0001c0001t0001g0115 a0001c0001t0001g0154 others(11): Show |
14 | HG02280.hp1 HG02486.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.-81-17891delG | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111798525 | |||||||
| chr6:111798544 | C | A | 6 | a0001c0001t0004g0098 a0001c0001t0008g0097 a0001c0001t0008g0100 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-81-17909G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111798544 | |||||||
| chr6:111798662 | CTTCCT | C | 14 | a0001c0001t0001g0096 a0001c0001t0001g0115 a0001c0001t0001g0154 others(11): Show |
14 | HG02280.hp1 HG02486.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.-81-18032_-81-1802 others(9): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111798662 | |||||||
| chr6:111798668 | G | A | 14 | a0001c0001t0001g0096 a0001c0001t0001g0115 a0001c0001t0001g0154 others(11): Show |
14 | HG02280.hp1 HG02486.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.-81-18033C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111798668 | |||||||
| chr6:111798778 | A | G | 130 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(127): Show |
130 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(127): Show |
intron_variant | MODIFIER | c.-81-18143T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111798778 | |||||||
| chr6:111798933 | T | C | 1 | a0001c0001t0011g0029 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-81-18298A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111798933 | |||||||
| chr6:111798962 | A | G | 1 | a0001c0001t0002g0075 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-81-18327T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111798962 | |||||||
| chr6:111799192 | A | C | 1 | a0001c0001t0001g0173 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-81-18557T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111799192 | |||||||
| chr6:111799544 | T | A | 1 | a0001c0001t0007g0071 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-81-18909A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111799544 | |||||||
| chr6:111799836 | T | C | 1 | a0001c0001t0004g0132 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-81-19201A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111799836 | |||||||
| chr6:111799893 | G | A | 127 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(124): Show |
127 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(124): Show |
intron_variant | MODIFIER | c.-81-19258C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111799893 | |||||||
| chr6:111799983 | G | T | 1 | a0001c0001t0004g0137 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-81-19348C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111799983 | |||||||
| chr6:111800025 | G | A | 130 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(127): Show |
130 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(127): Show |
intron_variant | MODIFIER | c.-81-19390C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111800025 | |||||||
| chr6:111800240 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-81-19605A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111800240 | |||||||
| chr6:111800427 | G | A | 3 | a0001c0001t0001g0099 a0001c0001t0001g0130 a0001c0001t0001g0145 |
3 | HG01081.hp2 HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-81-19792C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111800427 | |||||||
| chr6:111800563 | C | T | 129 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(126): Show |
129 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(126): Show |
intron_variant | MODIFIER | c.-81-19928G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111800563 | |||||||
| chr6:111800953 | T | G | 3 | a0001c0001t0001g0111 a0001c0001t0004g0109 a0001c0001t0004g0112 |
3 | HG02257.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-81-20318A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111800953 | |||||||
| chr6:111801023 | C | T | 129 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(126): Show |
129 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(126): Show |
intron_variant | MODIFIER | c.-81-20388G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111801023 | |||||||
| chr6:111801170 | C | T | 58 | a0001c0001t0001g0107 a0001c0001t0001g0155 a0001c0001t0001g0173 others(55): Show |
59 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.-81-20535G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111801170 | |||||||
| chr6:111801183 | G | C | 1 | a0001c0001t0001g0126 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-81-20548C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111801183 | |||||||
| chr6:111801184 | G | T | 1 | a0001c0001t0001g0126 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-81-20549C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111801184 | |||||||
| chr6:111801193 | C | T | 1 | a0001c0001t0005g0213 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-81-20558G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111801193 | |||||||
| chr6:111801458 | C | T | 1 | a0001c0001t0003g0032 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-81-20823G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111801458 | |||||||
| chr6:111801960 | C | G | 1 | a0001c0001t0003g0062 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-81-21325G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111801960 | |||||||
| chr6:111802224 | CTCCCCCT others(13): Show |
C | 1 | a0001c0001t0016g0207 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-81-21609_-81-2159 others(24): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111802224 | |||||||
| chr6:111802233 | TCCTCTCC others(8): Show |
T | 1 | a0001c0001t0001g0122 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-81-21613_-81-2159 others(19): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111802233 | |||||||
| chr6:111802433 | TC | T | 128 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(125): Show |
128 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(125): Show |
intron_variant | MODIFIER | c.-81-21799delG | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111802433 | |||||||
| chr6:111802436 | C | T | 1 | a0001c0001t0005g0221 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-81-21801G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111802436 | |||||||
| chr6:111802457 | G | A | 1 | a0001c0001t0002g0084 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-81-21822C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111802457 | |||||||
| chr6:111802718 | C | T | 1 | a0001c0001t0005g0201 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-81-22083G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111802718 | |||||||
| chr6:111802790 | AAT | A | 62 | a0001c0001t0001g0113 a0001c0001t0001g0117 a0001c0001t0001g0122 others(59): Show |
62 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.-81-22157_-81-2215 others(6): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111802790 | |||||||
| chr6:111802791 | AT | A | 23 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0129 others(20): Show |
23 | HG02083.hp2 HG02145.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.-81-22157delA | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111802791 | |||||||
| chr6:111802792 | T | A | 44 | a0001c0001t0001g0099 a0001c0001t0001g0115 a0001c0001t0001g0130 others(41): Show |
44 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.-81-22157A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111802792 | |||||||
| chr6:111802845 | A | T | 1 | a0001c0001t0002g0080 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-81-22210T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111802845 | |||||||
| chr6:111802884 | T | C | 1 | a0001c0001t0004g0132 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-81-22249A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111802884 | |||||||
| chr6:111802913 | A | G | 20 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0123 others(17): Show |
20 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.-81-22278T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111802913 | |||||||
| chr6:111802997 | G | A | 1 | a0001c0001t0003g0024 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-81-22362C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111802997 | |||||||
| chr6:111803144 | A | T | 1 | a0001c0001t0003g0090 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-81-22509T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111803144 | |||||||
| chr6:111803235 | C | G | 129 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(126): Show |
129 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(126): Show |
intron_variant | MODIFIER | c.-81-22600G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111803235 | |||||||
| chr6:111803237 | C | T | 130 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(127): Show |
130 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(127): Show |
intron_variant | MODIFIER | c.-81-22602G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111803237 | |||||||
| chr6:111803567 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-81-22932A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111803567 | |||||||
| chr6:111803766 | T | C | 1 | a0001c0001t0002g0064 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-81-23131A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111803766 | |||||||
| chr6:111804057 | T | C | 4 | a0001c0001t0005g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(1): Show |
4 | HG02717.hp1 NA18522.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-81-23422A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111804057 | |||||||
| chr6:111804132 | T | C | 130 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(127): Show |
130 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(127): Show |
intron_variant | MODIFIER | c.-81-23497A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111804132 | |||||||
| chr6:111804193 | C | T | 9 | a0001c0001t0001g0099 a0001c0001t0001g0130 a0001c0001t0001g0145 others(6): Show |
9 | HG01081.hp2 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-81-23558G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111804193 | |||||||
| chr6:111804250 | C | G | 83 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0117 others(80): Show |
83 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(80): Show |
intron_variant | MODIFIER | c.-81-23615G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111804250 | |||||||
| chr6:111804484 | A | T | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0151 others(1): Show |
4 | HG02559.hp1 HG02630.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-81-23849T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111804484 | |||||||
| chr6:111804864 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-81-24229A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111804864 | |||||||
| chr6:111805100 | G | A | 67 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0129 others(64): Show |
67 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.-81-24465C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111805100 | |||||||
| chr6:111805136 | G | A | 66 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0115 others(63): Show |
66 | HG00558.hp2 HG00639.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.-81-24501C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111805136 | |||||||
| chr6:111805232 | T | C | 14 | a0001c0001t0001g0096 a0001c0001t0001g0115 a0001c0001t0001g0154 others(11): Show |
14 | HG02280.hp1 HG02486.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.-81-24597A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111805232 | |||||||
| chr6:111805422 | G | C | 14 | a0001c0001t0001g0096 a0001c0001t0001g0115 a0001c0001t0001g0154 others(11): Show |
14 | HG02280.hp1 HG02486.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.-81-24787C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111805422 | |||||||
| chr6:111805552 | G | T | 46 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0115 others(43): Show |
46 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.-81-24917C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111805552 | |||||||
| chr6:111805559 | T | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0153 |
2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-81-24924A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111805559 | |||||||
| chr6:111805840 | C | T | 30 | a0001c0001t0001g0099 a0001c0001t0001g0130 a0001c0001t0001g0145 others(27): Show |
30 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.-81-25205G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111805840 | |||||||
| chr6:111806032 | A | G | 1 | a0001c0001t0010g0118 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-81-25397T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111806032 | |||||||
| chr6:111806051 | G | A | 1 | a0001c0001t0003g0062 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-81-25416C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111806051 | |||||||
| chr6:111806136 | T | C | 20 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0123 others(17): Show |
20 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.-81-25501A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111806136 | |||||||
| chr6:111806210 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-81-25575G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111806210 | |||||||
| chr6:111806437 | G | A | 46 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0115 others(43): Show |
46 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.-81-25802C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111806437 | |||||||
| chr6:111806680 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-81-26045T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111806680 | |||||||
| chr6:111807196 | T | C | 4 | a0001c0001t0002g0009 a0001c0001t0002g0093 a0001c0001t0002g0094 others(1): Show |
4 | HG01074.hp1 HG01243.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.-81-26561A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111807196 | |||||||
| chr6:111807337 | T | G | 14 | a0001c0001t0001g0096 a0001c0001t0001g0115 a0001c0001t0001g0154 others(11): Show |
14 | HG02280.hp1 HG02486.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.-81-26702A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111807337 | |||||||
| chr6:111807571 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-81-26936C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111807571 | |||||||
| chr6:111807708 | T | C | 1 | a0001c0001t0005g0203 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-81-27073A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111807708 | |||||||
| chr6:111807744 | T | C | 130 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(127): Show |
130 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(127): Show |
intron_variant | MODIFIER | c.-81-27109A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111807744 | |||||||
| chr6:111807910 | C | T | 1 | a0001c0001t0020g0095 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-81-27275G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111807910 | |||||||
| chr6:111807979 | G | A | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-81-27344C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111807979 | |||||||
| chr6:111808162 | C | T | 9 | a0001c0001t0001g0099 a0001c0001t0001g0130 a0001c0001t0001g0145 others(6): Show |
9 | HG01081.hp2 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-81-27527G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111808162 | |||||||
| chr6:111808216 | A | G | 1 | a0001c0001t0008g0101 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-81-27581T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111808216 | |||||||
| chr6:111808433 | G | A | 64 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0129 others(61): Show |
64 | HG00438.hp2 HG00733.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.-81-27798C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111808433 | |||||||
| chr6:111808745 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-81-28110C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111808745 | |||||||
| chr6:111809057 | G | A | 14 | a0001c0001t0001g0096 a0001c0001t0001g0115 a0001c0001t0001g0154 others(11): Show |
14 | HG02280.hp1 HG02486.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.-81-28422C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111809057 | |||||||
| chr6:111809275 | C | T | 130 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(127): Show |
130 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(127): Show |
intron_variant | MODIFIER | c.-81-28640G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111809275 | |||||||
| chr6:111809497 | G | A | 4 | a0001c0001t0003g0037 a0001c0001t0007g0019 a0001c0001t0007g0020 others(1): Show |
4 | NA18941.hp2 NA18942.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.-81-28862C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111809497 | |||||||
| chr6:111809517 | C | T | 1 | a0001c0001t0014g0047 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-81-28882G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111809517 | |||||||
| chr6:111809863 | T | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0153 |
2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-81-29228A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111809863 | |||||||
| chr6:111810000 | A | G | 1 | a0001c0001t0002g0093 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-81-29365T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111810000 | |||||||
| chr6:111810245 | T | C | 1 | a0001c0001t0006g0209 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-81-29610A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111810245 | |||||||
| chr6:111810284 | T | C | 1 | a0001c0001t0019g0086 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-81-29649A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111810284 | |||||||
| chr6:111810375 | G | A | 130 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(127): Show |
130 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(127): Show |
intron_variant | MODIFIER | c.-81-29740C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111810375 | |||||||
| chr6:111810400 | C | T | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02486.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-81-29765G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111810400 | |||||||
| chr6:111810445 | T | C | 50 | a0001c0001t0001g0113 a0001c0001t0001g0140 a0001c0001t0001g0141 others(47): Show |
50 | HG00438.hp2 HG00733.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.-81-29810A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111810445 | |||||||
| chr6:111810455 | A | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0153 |
2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-81-29820T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111810455 | |||||||
| chr6:111810681 | G | T | 1 | a0001c0001t0001g0157 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-81-30046C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111810681 | |||||||
| chr6:111810765 | T | C | 1 | a0001c0001t0010g0114 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-81-30130A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111810765 | |||||||
| chr6:111810772 | T | G | 32 | a0001c0001t0001g0099 a0001c0001t0001g0130 a0001c0001t0001g0145 others(29): Show |
32 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.-81-30137A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111810772 | |||||||
| chr6:111810783 | C | T | 1 | a0001c0001t0002g0012 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-81-30148G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111810783 | |||||||
| chr6:111810829 | T | C | 130 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(127): Show |
130 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(127): Show |
intron_variant | MODIFIER | c.-81-30194A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111810829 | |||||||
| chr6:111811342 | T | C | 14 | a0001c0001t0001g0096 a0001c0001t0001g0115 a0001c0001t0001g0154 others(11): Show |
14 | HG02280.hp1 HG02486.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.-81-30707A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111811342 | |||||||
| chr6:111811602 | T | C | 3 | a0001c0001t0005g0201 a0001c0001t0005g0202 a0001c0001t0006g0200 |
3 | NA18974.hp2 NA19070.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-81-30967A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111811602 | |||||||
| chr6:111811716 | C | T | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-81-31081G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111811716 | |||||||
| chr6:111811749 | C | T | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-81-31114G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111811749 | |||||||
| chr6:111811793 | T | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0153 |
2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-81-31158A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111811793 | |||||||
| chr6:111811835 | G | A | 2 | a0001c0001t0003g0025 a0001c0001t0003g0043 |
2 | HG02698.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-81-31200C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111811835 | |||||||
| chr6:111811854 | CT | C | 9 | a0001c0001t0001g0099 a0001c0001t0001g0130 a0001c0001t0001g0145 others(6): Show |
9 | HG01081.hp2 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-81-31220delA | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111811854 | |||||||
| chr6:111812327 | T | C | 41 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0123 others(38): Show |
41 | HG00558.hp2 HG00639.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.-81-31692A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111812327 | |||||||
| chr6:111812393 | G | A | 2 | a0001c0001t0003g0025 a0001c0001t0003g0043 |
2 | HG02698.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-81-31758C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111812393 | |||||||
| chr6:111812517 | C | T | 1 | a0001c0001t0002g0089 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-81-31882G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111812517 | |||||||
| chr6:111812604 | C | CT | 10 | a0001c0001t0001g0155 a0001c0001t0001g0159 a0001c0001t0002g0046 others(7): Show |
10 | HG01081.hp1 HG01109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-81-31970dupA | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111812604 | |||||||
| chr6:111812604 | CT | C | 24 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(21): Show |
24 | HG00673.hp1 HG00733.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.-81-31970delA | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111812604 | |||||||
| chr6:111812604 | CTTTTTTT others(11): Show |
C | 20 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0123 others(17): Show |
20 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.-81-31987_-81-3197 others(22): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111812604 | |||||||
| chr6:111813093 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-81-32458T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111813093 | |||||||
| chr6:111813520 | C | G | 6 | a0001c0001t0004g0098 a0001c0001t0008g0097 a0001c0001t0008g0100 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-81-32885G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111813520 | |||||||
| chr6:111813888 | C | T | 33 | a0001c0001t0005g0199 a0001c0001t0005g0201 a0001c0001t0005g0202 others(30): Show |
33 | HG00438.hp2 HG00733.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.-82+32701G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111813888 | |||||||
| chr6:111813904 | G | A | 23 | a0001c0001t0001g0148 a0001c0001t0001g0153 a0001c0001t0001g0177 others(20): Show |
23 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.-82+32685C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111813904 | |||||||
| chr6:111814022 | G | A | 6 | a0001c0001t0004g0098 a0001c0001t0008g0097 a0001c0001t0008g0100 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-82+32567C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111814022 | |||||||
| chr6:111814038 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-82+32551A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111814038 | |||||||
| chr6:111814056 | C | T | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-82+32533G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111814056 | |||||||
| chr6:111814070 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-82+32519C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111814070 | |||||||
| chr6:111814133 | T | A | 1 | a0001c0001t0020g0095 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-82+32456A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111814133 | |||||||
| chr6:111814260 | CTTTCAGA others(25): Show |
C | 6 | a0001c0001t0004g0098 a0001c0001t0008g0097 a0001c0001t0008g0100 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-82+32297_-82+3232 others(36): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111814260 | |||||||
| chr6:111814714 | C | T | 4 | a0001c0001t0002g0061 a0001c0001t0004g0181 a0001c0001t0004g0192 others(1): Show |
4 | HG00438.hp1 HG04228.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.-82+31875G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111814714 | |||||||
| chr6:111814939 | A | G | 20 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(17): Show |
20 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.-82+31650T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111814939 | |||||||
| chr6:111815123 | A | G | 9 | a0001c0001t0001g0099 a0001c0001t0001g0130 a0001c0001t0001g0145 others(6): Show |
9 | HG01081.hp2 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-82+31466T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111815123 | |||||||
| chr6:111815173 | T | TA | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-82+31415dupT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111815173 | |||||||
| chr6:111815246 | G | C | 1 | a0001c0001t0015g0204 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-82+31343C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111815246 | |||||||
| chr6:111815472 | C | T | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-82+31117G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111815472 | |||||||
| chr6:111815712 | CT | C | 128 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(125): Show |
128 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(125): Show |
intron_variant | MODIFIER | c.-82+30876delA | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111815712 | |||||||
| chr6:111815935 | A | G | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-82+30654T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111815935 | |||||||
| chr6:111816145 | A | G | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-82+30444T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111816145 | |||||||
| chr6:111816557 | T | C | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-82+30032A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111816557 | |||||||
| chr6:111816644 | T | C | 1 | a0001c0001t0003g0033 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-82+29945A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111816644 | |||||||
| chr6:111816801 | C | A | 1 | a0001c0001t0010g0174 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-82+29788G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111816801 | |||||||
| chr6:111817091 | T | C | 119 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0113 others(116): Show |
119 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(116): Show |
intron_variant | MODIFIER | c.-82+29498A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111817091 | |||||||
| chr6:111817094 | AATAGATT | A | 130 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(127): Show |
130 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(127): Show |
intron_variant | MODIFIER | c.-82+29488_-82+2949 others(11): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111817094 | |||||||
| chr6:111817513 | A | G | 1 | a0001c0001t0007g0067 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-82+29076T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111817513 | |||||||
| chr6:111817534 | C | T | 3 | a0001c0001t0001g0099 a0001c0001t0001g0130 a0001c0001t0001g0145 |
3 | HG01081.hp2 HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-82+29055G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111817534 | |||||||
| chr6:111817679 | G | A | 98 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0113 others(95): Show |
98 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(95): Show |
intron_variant | MODIFIER | c.-82+28910C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111817679 | |||||||
| chr6:111817721 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-82+28868A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111817721 | |||||||
| chr6:111817790 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-82+28799T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111817790 | |||||||
| chr6:111818501 | G | A | 5 | a0001c0001t0005g0220 a0001c0001t0005g0224 a0001c0001t0005g0231 others(2): Show |
5 | HG02071.hp2 HG02080.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.-82+28088C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111818501 | |||||||
| chr6:111818803 | A | G | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-82+27786T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111818803 | |||||||
| chr6:111818869 | C | T | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-82+27720G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111818869 | |||||||
| chr6:111818892 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-82+27697G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111818892 | |||||||
| chr6:111819071 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-82+27518T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111819071 | |||||||
| chr6:111819349 | C | T | 1 | a0001c0001t0003g0014 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-82+27240G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111819349 | |||||||
| chr6:111820062 | T | C | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-82+26527A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111820062 | |||||||
| chr6:111820332 | C | T | 3 | a0001c0001t0001g0182 a0001c0001t0001g0189 a0001c0001t0001g0196 |
3 | NA18957.hp1 NA18963.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.-82+26257G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111820332 | |||||||
| chr6:111820406 | T | A | 6 | a0001c0001t0001g0117 a0001c0001t0001g0126 a0001c0001t0001g0127 others(3): Show |
6 | HG00639.hp1 NA18942.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.-82+26183A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111820406 | |||||||
| chr6:111820468 | A | C | 1 | a0001c0001t0021g0119 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-82+26121T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111820468 | |||||||
| chr6:111820490 | AAT | A | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-82+26097_-82+2609 others(6): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111820490 | |||||||
| chr6:111820529 | T | C | 130 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(127): Show |
130 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(127): Show |
intron_variant | MODIFIER | c.-82+26060A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111820529 | |||||||
| chr6:111820705 | A | G | 130 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(127): Show |
130 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(127): Show |
intron_variant | MODIFIER | c.-82+25884T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111820705 | |||||||
| chr6:111820782 | A | ATT | 12 | a0001c0001t0001g0115 a0001c0001t0001g0161 a0001c0001t0001g0162 others(9): Show |
12 | HG02280.hp1 HG02486.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.-82+25806_-82+2580 others(6): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111820782 | |||||||
| chr6:111820870 | T | C | 10 | a0001c0001t0001g0115 a0001c0001t0001g0165 a0001c0001t0001g0170 others(7): Show |
10 | HG02280.hp1 HG02486.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.-82+25719A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111820870 | |||||||
| chr6:111820887 | C | T | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-82+25702G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111820887 | |||||||
| chr6:111820922 | G | A | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-82+25667C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111820922 | |||||||
| chr6:111821019 | T | A | 9 | a0001c0001t0001g0099 a0001c0001t0001g0130 a0001c0001t0001g0145 others(6): Show |
9 | HG01081.hp2 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-82+25570A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111821019 | |||||||
| chr6:111821214 | C | T | 208 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(205): Show |
209 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(206): Show |
intron_variant | MODIFIER | c.-82+25375G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111821214 | |||||||
| chr6:111821215 | A | G | 209 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(206): Show |
210 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(207): Show |
intron_variant | MODIFIER | c.-82+25374T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111821215 | |||||||
| chr6:111821271 | G | C | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-82+25318C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111821271 | |||||||
| chr6:111821438 | G | A | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-82+25151C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111821438 | |||||||
| chr6:111821504 | C | A | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-82+25085G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111821504 | |||||||
| chr6:111821513 | C | T | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-82+25076G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111821513 | |||||||
| chr6:111821605 | C | A | 22 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(19): Show |
22 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.-82+24984G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111821605 | |||||||
| chr6:111821664 | C | A | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-82+24925G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111821664 | |||||||
| chr6:111821788 | G | C | 1 | a0001c0001t0012g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-82+24801C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111821788 | |||||||
| chr6:111821798 | C | A | 1 | a0001c0001t0002g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-82+24791G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111821798 | |||||||
| chr6:111821816 | G | A | 1 | a0001c0001t0007g0027 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-82+24773C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111821816 | |||||||
| chr6:111821882 | A | C | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-82+24707T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111821882 | |||||||
| chr6:111821963 | T | TA | 98 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0113 others(95): Show |
98 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(95): Show |
intron_variant | MODIFIER | c.-82+24625dupT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111821963 | |||||||
| chr6:111822116 | C | A | 107 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(104): Show |
107 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(104): Show |
intron_variant | MODIFIER | c.-82+24473G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111822116 | |||||||
| chr6:111822251 | T | C | 19 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0123 others(16): Show |
19 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.-82+24338A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111822251 | |||||||
| chr6:111822269 | G | A | 64 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0129 others(61): Show |
64 | HG00438.hp2 HG00733.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.-82+24320C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111822269 | |||||||
| chr6:111822483 | G | A | 1 | a0001c0001t0010g0174 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-82+24106C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111822483 | |||||||
| chr6:111822494 | C | G | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-82+24095G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111822494 | |||||||
| chr6:111822494 | C | T | 1 | a0001c0001t0002g0091 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-82+24095G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111822494 | |||||||
| chr6:111822716 | T | A | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-82+23873A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111822716 | |||||||
| chr6:111822716 | T | G | 19 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0123 others(16): Show |
19 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.-82+23873A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111822716 | |||||||
| chr6:111822718 | A | G | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-82+23871T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111822718 | |||||||
| chr6:111822719 | A | G | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-82+23870T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111822719 | |||||||
| chr6:111822723 | T | C | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-82+23866A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111822723 | |||||||
| chr6:111822827 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-82+23762C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111822827 | |||||||
| chr6:111822900 | T | C | 1 | a0001c0001t0007g0028 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-82+23689A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111822900 | |||||||
| chr6:111822946 | C | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0153 |
2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-82+23643G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111822946 | |||||||
| chr6:111824306 | G | T | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-82+22283C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111824306 | |||||||
| chr6:111824356 | A | G | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-82+22233T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111824356 | |||||||
| chr6:111824573 | G | A | 2 | a0001c0001t0004g0193 a0001c0001t0004g0194 |
2 | HG00558.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.-82+22016C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111824573 | |||||||
| chr6:111824586 | A | G | 1 | a0001c0001t0002g0040 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-82+22003T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111824586 | |||||||
| chr6:111824835 | T | G | 1 | a0001c0001t0016g0207 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-82+21754A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111824835 | |||||||
| chr6:111824904 | A | T | 20 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0123 others(17): Show |
20 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.-82+21685T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111824904 | |||||||
| chr6:111824922 | G | A | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-82+21667C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111824922 | |||||||
| chr6:111824998 | T | C | 1 | a0001c0001t0007g0067 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-82+21591A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111824998 | |||||||
| chr6:111825091 | G | A | 3 | a0001c0001t0001g0117 a0001c0001t0001g0127 a0001c0001t0001g0128 |
3 | NA18946.hp2 NA18951.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.-82+21498C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111825091 | |||||||
| chr6:111825177 | G | C | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-82+21412C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111825177 | |||||||
| chr6:111825364 | A | C | 1 | a0001c0001t0002g0045 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-82+21225T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111825364 | |||||||
| chr6:111825550 | A | T | 1 | a0001c0001t0015g0204 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-82+21039T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111825550 | |||||||
| chr6:111825588 | G | A | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | HG02486.hp1 HG03209.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-82+21001C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111825588 | |||||||
| chr6:111825904 | C | T | 130 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(127): Show |
130 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(127): Show |
intron_variant | MODIFIER | c.-82+20685G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111825904 | |||||||
| chr6:111825951 | T | C | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG02615.hp2 HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-82+20638A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111825951 | |||||||
| chr6:111826120 | C | G | 209 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(206): Show |
210 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(207): Show |
intron_variant | MODIFIER | c.-82+20469G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111826120 | |||||||
| chr6:111826335 | C | T | 1 | a0001c0001t0010g0166 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-82+20254G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111826335 | |||||||
| chr6:111826357 | T | C | 1 | a0001c0001t0002g0061 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-82+20232A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111826357 | |||||||
| chr6:111826529 | T | TA | 9 | a0001c0001t0001g0099 a0001c0001t0001g0130 a0001c0001t0001g0145 others(6): Show |
9 | HG01081.hp2 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-82+20059dupT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111826529 | |||||||
| chr6:111826701 | C | T | 1 | a0001c0001t0010g0174 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-82+19888G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111826701 | |||||||
| chr6:111826706 | T | C | 66 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0129 others(63): Show |
66 | HG00438.hp2 HG00733.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.-82+19883A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111826706 | |||||||
| chr6:111827090 | C | T | 130 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(127): Show |
130 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(127): Show |
intron_variant | MODIFIER | c.-82+19499G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111827090 | |||||||
| chr6:111827355 | C | T | 1 | a0001c0001t0003g0033 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-82+19234G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111827355 | |||||||
| chr6:111827447 | C | T | 1 | a0001c0001t0005g0213 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-82+19142G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111827447 | |||||||
| chr6:111827539 | C | A | 2 | a0001c0001t0004g0103 a0001c0001t0011g0016 |
2 | HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-82+19050G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111827539 | |||||||
| chr6:111827540 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-82+19049C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111827540 | |||||||
| chr6:111827648 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-82+18941G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111827648 | |||||||
| chr6:111827720 | C | A | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-82+18869G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111827720 | |||||||
| chr6:111827929 | T | C | 3 | a0001c0001t0001g0111 a0001c0001t0004g0109 a0001c0001t0004g0112 |
3 | HG02257.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-82+18660A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111827929 | |||||||
| chr6:111828125 | G | C | 1 | a0001c0001t0004g0109 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-82+18464C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111828125 | |||||||
| chr6:111828170 | A | G | 130 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(127): Show |
130 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(127): Show |
intron_variant | MODIFIER | c.-82+18419T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111828170 | |||||||
| chr6:111828283 | T | A | 66 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0129 others(63): Show |
66 | HG00438.hp2 HG00733.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.-82+18306A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111828283 | |||||||
| chr6:111828431 | G | A | 1 | a0001c0001t0020g0095 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-82+18158C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111828431 | |||||||
| chr6:111828460 | T | G | 20 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(17): Show |
20 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.-82+18129A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111828460 | |||||||
| chr6:111828575 | T | TAAAAAGG others(330): Show |
1 | a0001c0001t0003g0010 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-82+18013_-82+1801 others(341): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111828575 | |||||||
| chr6:111828714 | G | A | 22 | a0001c0001t0001g0175 a0001c0001t0001g0177 a0001c0001t0001g0178 others(19): Show |
22 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.-82+17875C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111828714 | |||||||
| chr6:111828729 | G | A | 1 | a0001c0001t0005g0225 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-82+17860C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111828729 | |||||||
| chr6:111828764 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-82+17825C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111828764 | |||||||
| chr6:111829227 | A | G | 99 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0113 others(96): Show |
99 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(96): Show |
intron_variant | MODIFIER | c.-82+17362T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111829227 | |||||||
| chr6:111829426 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-82+17163G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111829426 | |||||||
| chr6:111829436 | T | C | 1 | a0001c0001t0012g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-82+17153A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111829436 | |||||||
| chr6:111829596 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-82+16993G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111829596 | |||||||
| chr6:111829674 | C | T | 14 | a0001c0001t0001g0096 a0001c0001t0001g0115 a0001c0001t0001g0154 others(11): Show |
14 | HG02280.hp1 HG02486.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.-82+16915G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111829674 | |||||||
| chr6:111829695 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-82+16894G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111829695 | |||||||
| chr6:111829699 | C | T | 1 | a0001c0001t0002g0044 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-82+16890G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111829699 | |||||||
| chr6:111829853 | T | C | 36 | a0001c0001t0001g0096 a0001c0001t0001g0115 a0001c0001t0001g0154 others(33): Show |
36 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.-82+16736A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111829853 | |||||||
| chr6:111829892 | T | A | 14 | a0001c0001t0001g0096 a0001c0001t0001g0115 a0001c0001t0001g0154 others(11): Show |
14 | HG02280.hp1 HG02486.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.-82+16697A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111829892 | |||||||
| chr6:111830081 | C | T | 9 | a0001c0001t0001g0099 a0001c0001t0001g0130 a0001c0001t0001g0145 others(6): Show |
9 | HG01081.hp2 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-82+16508G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111830081 | |||||||
| chr6:111830158 | C | A | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG02615.hp2 HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-82+16431G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111830158 | |||||||
| chr6:111830213 | A | G | 1 | a0001c0001t0001g0183 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-82+16376T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111830213 | |||||||
| chr6:111830241 | C | G | 106 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(103): Show |
106 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(103): Show |
intron_variant | MODIFIER | c.-82+16348G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111830241 | |||||||
| chr6:111830249 | G | A | 80 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(77): Show |
80 | HG00438.hp2 HG00733.hp2 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.-82+16340C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111830249 | |||||||
| chr6:111830324 | T | G | 24 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(21): Show |
24 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.-82+16265A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111830324 | |||||||
| chr6:111830327 | C | G | 1 | a0001c0001t0002g0012 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-82+16262G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111830327 | |||||||
| chr6:111830513 | G | GGA | 129 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0111 others(126): Show |
129 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.-82+16074_-82+1607 others(6): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111830513 | |||||||
| chr6:111830731 | G | A | 4 | a0001c0001t0001g0113 a0001c0002t0001g0134 a0001c0002t0001g0135 others(1): Show |
4 | HG02723.hp2 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-82+15858C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111830731 | |||||||
| chr6:111830772 | T | A | 134 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(131): Show |
134 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.-82+15817A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111830772 | |||||||
| chr6:111830903 | TTTGTAGA others(2): Show |
T | 32 | a0001c0001t0005g0199 a0001c0001t0005g0201 a0001c0001t0005g0202 others(29): Show |
32 | HG00438.hp1 HG00438.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.-82+15677_-82+1568 others(13): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111830903 | |||||||
| chr6:111830947 | T | C | 1 | a0001c0001t0005g0227 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-82+15642A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111830947 | |||||||
| chr6:111831010 | G | C | 1 | a0001c0001t0001g0155 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-82+15579C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111831010 | |||||||
| chr6:111831085 | T | C | 1 | a0001c0001t0010g0174 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-82+15504A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111831085 | |||||||
| chr6:111831185 | G | C | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-82+15404C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111831185 | |||||||
| chr6:111831212 | G | A | 71 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0113 others(68): Show |
71 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.-82+15377C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111831212 | |||||||
| chr6:111831291 | G | A | 71 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0113 others(68): Show |
71 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.-82+15298C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111831291 | |||||||
| chr6:111831357 | C | T | 71 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0113 others(68): Show |
71 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.-82+15232G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111831357 | |||||||
| chr6:111831565 | C | T | 71 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0113 others(68): Show |
71 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.-82+15024G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111831565 | |||||||
| chr6:111831622 | ATATGTGA others(6): Show |
A | 7 | a0001c0001t0001g0170 a0001c0001t0004g0169 a0001c0001t0004g0171 others(4): Show |
7 | HG02280.hp1 HG02486.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-82+14954_-82+1496 others(17): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111831622 | |||||||
| chr6:111831711 | A | G | 33 | a0001c0001t0005g0199 a0001c0001t0005g0201 a0001c0001t0005g0202 others(30): Show |
33 | HG00438.hp1 HG00438.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.-82+14878T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111831711 | |||||||
| chr6:111831770 | A | T | 1 | a0001c0001t0001g0173 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-82+14819T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111831770 | |||||||
| chr6:111831873 | T | C | 7 | a0001c0001t0001g0170 a0001c0001t0004g0169 a0001c0001t0004g0171 others(4): Show |
7 | HG02280.hp1 HG02486.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-82+14716A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111831873 | |||||||
| chr6:111832219 | A | C | 41 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0129 others(38): Show |
41 | HG00741.hp2 HG01081.hp2 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.-82+14370T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111832219 | |||||||
| chr6:111832380 | A | C | 31 | a0001c0001t0001g0099 a0001c0001t0001g0177 a0001c0001t0001g0178 others(28): Show |
31 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.-82+14209T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111832380 | |||||||
| chr6:111832511 | C | G | 1 | a0001c0001t0001g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-82+14078G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111832511 | |||||||
| chr6:111832601 | G | GATC | 132 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(129): Show |
132 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.-82+13985_-82+1398 others(7): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111832601 | |||||||
| chr6:111832696 | A | T | 17 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0123 others(14): Show |
17 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.-82+13893T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111832696 | |||||||
| chr6:111832818 | C | T | 81 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(78): Show |
81 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.-82+13771G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111832818 | |||||||
| chr6:111832997 | A | G | 81 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(78): Show |
81 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.-82+13592T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111832997 | |||||||
| chr6:111833041 | A | T | 81 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(78): Show |
81 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.-82+13548T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111833041 | |||||||
| chr6:111833047 | G | A | 2 | a0001c0001t0004g0125 a0001c0001t0004g0138 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-82+13542C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111833047 | |||||||
| chr6:111833175 | T | TATC | 81 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(78): Show |
81 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.-82+13413_-82+1341 others(7): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111833175 | |||||||
| chr6:111833645 | T | C | 132 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(129): Show |
132 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.-82+12944A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111833645 | |||||||
| chr6:111833731 | G | A | 1 | a0001c0001t0019g0086 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-82+12858C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111833731 | |||||||
| chr6:111833954 | T | C | 33 | a0001c0001t0005g0199 a0001c0001t0005g0201 a0001c0001t0005g0202 others(30): Show |
33 | HG00438.hp1 HG00438.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.-82+12635A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111833954 | |||||||
| chr6:111834268 | GGATT | G | 5 | a0001c0001t0001g0115 a0001c0001t0001g0165 a0001c0001t0004g0137 others(2): Show |
5 | HG01952.hp2 HG02965.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-82+12317_-82+1232 others(8): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111834268 | |||||||
| chr6:111834270 | A | G | 76 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(73): Show |
76 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.-82+12319T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111834270 | |||||||
| chr6:111834274 | T | C | 17 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0123 others(14): Show |
17 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.-82+12315A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111834274 | |||||||
| chr6:111834274 | T | G | 5 | a0001c0001t0001g0115 a0001c0001t0001g0165 a0001c0001t0004g0137 others(2): Show |
5 | HG01952.hp2 HG02965.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-82+12315A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111834274 | |||||||
| chr6:111834358 | A | G | 10 | a0001c0001t0001g0099 a0001c0001t0004g0098 a0001c0001t0004g0103 others(7): Show |
10 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-82+12231T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111834358 | |||||||
| chr6:111834467 | T | G | 133 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(130): Show |
133 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.-82+12122A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111834467 | |||||||
| chr6:111834519 | C | T | 50 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0113 others(47): Show |
50 | HG00741.hp2 HG01081.hp2 HG01891.hp2 others(47): Show |
intron_variant | MODIFIER | c.-82+12070G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111834519 | |||||||
| chr6:111834586 | G | A | 50 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0113 others(47): Show |
50 | HG00741.hp2 HG01081.hp2 HG01891.hp2 others(47): Show |
intron_variant | MODIFIER | c.-82+12003C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111834586 | |||||||
| chr6:111834649 | G | A | 33 | a0001c0001t0005g0199 a0001c0001t0005g0201 a0001c0001t0005g0202 others(30): Show |
33 | HG00438.hp1 HG00438.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.-82+11940C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111834649 | |||||||
| chr6:111834874 | C | A | 1 | a0001c0001t0001g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-82+11715G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111834874 | |||||||
| chr6:111835260 | G | A | 50 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0113 others(47): Show |
50 | HG00741.hp2 HG01081.hp2 HG01891.hp2 others(47): Show |
intron_variant | MODIFIER | c.-82+11329C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111835260 | |||||||
| chr6:111835367 | C | T | 50 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0113 others(47): Show |
50 | HG00741.hp2 HG01081.hp2 HG01891.hp2 others(47): Show |
intron_variant | MODIFIER | c.-82+11222G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111835367 | |||||||
| chr6:111835497 | G | A | 17 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0123 others(14): Show |
17 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.-82+11092C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111835497 | |||||||
| chr6:111835570 | T | C | 1 | a0001c0001t0002g0064 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-82+11019A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111835570 | |||||||
| chr6:111835628 | T | C | 1 | a0001c0001t0012g0195 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-82+10961A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111835628 | |||||||
| chr6:111835630 | A | AT | 9 | a0001c0001t0001g0111 a0001c0001t0001g0148 a0001c0001t0001g0149 others(6): Show |
9 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-82+10958dupA | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111835630 | |||||||
| chr6:111835773 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-82+10816C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111835773 | |||||||
| chr6:111835806 | AG | A | 48 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0113 others(45): Show |
48 | HG00741.hp2 HG01081.hp2 HG01891.hp2 others(45): Show |
intron_variant | MODIFIER | c.-82+10782delC | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111835806 | |||||||
| chr6:111835817 | G | C | 133 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(130): Show |
133 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.-82+10772C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111835817 | |||||||
| chr6:111835894 | T | C | 48 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0113 others(45): Show |
48 | HG00741.hp2 HG01081.hp2 HG01891.hp2 others(45): Show |
intron_variant | MODIFIER | c.-82+10695A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111835894 | |||||||
| chr6:111835910 | G | A | 1 | a0001c0001t0020g0095 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-82+10679C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111835910 | |||||||
| chr6:111836379 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-82+10210G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111836379 | |||||||
| chr6:111836412 | T | C | 131 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0111 others(128): Show |
131 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.-82+10177A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111836412 | |||||||
| chr6:111836412 | T | G | 1 | a0001c0001t0001g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-82+10177A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111836412 | |||||||
| chr6:111836447 | C | CCAA | 33 | a0001c0001t0005g0199 a0001c0001t0005g0201 a0001c0001t0005g0202 others(30): Show |
33 | HG00438.hp1 HG00438.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.-82+10139_-82+1014 others(7): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111836447 | |||||||
| chr6:111836489 | G | A | 3 | a0001c0001t0001g0170 a0001c0001t0004g0171 a0001c0001t0004g0172 |
3 | HG02486.hp2 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-82+10100C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111836489 | |||||||
| chr6:111836493 | G | A | 1 | a0001c0001t0002g0063 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-82+10096C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111836493 | |||||||
| chr6:111836531 | A | G | 66 | a0001c0001t0001g0099 a0001c0001t0001g0107 a0001c0001t0001g0173 others(63): Show |
66 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.-82+10058T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111836531 | |||||||
| chr6:111836791 | C | T | 3 | a0001c0001t0002g0012 a0001c0001t0002g0075 a0001c0001t0011g0018 |
3 | HG00735.hp2 HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.-82+9798G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111836791 | |||||||
| chr6:111836931 | G | A | 33 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0129 others(30): Show |
33 | HG00741.hp2 HG01081.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.-82+9658C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111836931 | |||||||
| chr6:111837012 | A | G | 133 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(130): Show |
133 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.-82+9577T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111837012 | |||||||
| chr6:111837240 | T | C | 19 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0122 others(16): Show |
19 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.-82+9349A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111837240 | |||||||
| chr6:111837256 | C | G | 1 | a0001c0001t0001g0173 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-82+9333G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111837256 | |||||||
| chr6:111837336 | T | G | 1 | a0001c0001t0003g0032 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-82+9253A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111837336 | |||||||
| chr6:111837343 | T | G | 2 | a0001c0001t0004g0103 a0001c0001t0008g0104 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-82+9246A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111837343 | |||||||
| chr6:111837413 | A | G | 1 | a0001c0001t0002g0064 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-82+9176T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111837413 | |||||||
| chr6:111837414 | G | A | 1 | a0001c0001t0002g0064 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-82+9175C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111837414 | |||||||
| chr6:111837463 | A | G | 1 | a0001c0001t0002g0040 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-82+9126T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111837463 | |||||||
| chr6:111837527 | T | C | 1 | a0001c0001t0002g0065 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-82+9062A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111837527 | |||||||
| chr6:111837624 | C | T | 10 | a0001c0001t0001g0099 a0001c0001t0004g0098 a0001c0001t0004g0103 others(7): Show |
10 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-82+8965G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111837624 | |||||||
| chr6:111837785 | A | G | 85 | a0001c0001t0001g0099 a0001c0001t0001g0107 a0001c0001t0001g0115 others(82): Show |
85 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.-82+8804T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111837785 | |||||||
| chr6:111837809 | C | T | 1 | a0001c0001t0002g0013 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-82+8780G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111837809 | |||||||
| chr6:111837812 | CGCT | C | 19 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0122 others(16): Show |
19 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.-82+8774_-82+8776d others(5): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111837812 | |||||||
| chr6:111837865 | C | T | 133 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(130): Show |
133 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.-82+8724G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111837865 | |||||||
| chr6:111837884 | G | A | 1 | a0001c0001t0002g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-82+8705C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111837884 | |||||||
| chr6:111838646 | T | C | 33 | a0001c0001t0005g0199 a0001c0001t0005g0201 a0001c0001t0005g0202 others(30): Show |
33 | HG00438.hp1 HG00438.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.-82+7943A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111838646 | |||||||
| chr6:111839110 | G | A | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-82+7479C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111839110 | |||||||
| chr6:111839459 | G | C | 7 | a0001c0001t0001g0170 a0001c0001t0004g0169 a0001c0001t0004g0171 others(4): Show |
7 | HG02280.hp1 HG02486.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-82+7130C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111839459 | |||||||
| chr6:111839628 | T | C | 1 | a0001c0001t0002g0091 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-82+6961A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111839628 | |||||||
| chr6:111839693 | A | C | 10 | a0001c0001t0001g0099 a0001c0001t0004g0098 a0001c0001t0004g0103 others(7): Show |
10 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-82+6896T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111839693 | |||||||
| chr6:111839889 | G | A | 48 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0113 others(45): Show |
48 | HG00741.hp2 HG01081.hp2 HG01891.hp2 others(45): Show |
intron_variant | MODIFIER | c.-82+6700C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111839889 | |||||||
| chr6:111840079 | G | T | 1 | a0001c0001t0007g0088 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-82+6510C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111840079 | |||||||
| chr6:111840328 | T | C | 7 | a0001c0001t0001g0170 a0001c0001t0004g0169 a0001c0001t0004g0171 others(4): Show |
7 | HG02280.hp1 HG02486.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-82+6261A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111840328 | |||||||
| chr6:111840439 | T | A | 1 | a0001c0001t0010g0174 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-82+6150A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111840439 | |||||||
| chr6:111840503 | A | G | 9 | a0001c0001t0004g0098 a0001c0001t0004g0103 a0001c0001t0008g0097 others(6): Show |
9 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-82+6086T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111840503 | |||||||
| chr6:111840583 | G | A | 131 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(128): Show |
131 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.-82+6006C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111840583 | |||||||
| chr6:111840754 | G | C | 1 | a0001c0001t0002g0001 | 2 | HG01258.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-82+5835C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111840754 | |||||||
| chr6:111840800 | T | G | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-82+5789A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111840800 | |||||||
| chr6:111841008 | G | A | 1 | a0001c0001t0022g0176 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-82+5581C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111841008 | |||||||
| chr6:111841106 | C | G | 1 | a0001c0004t0001g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-82+5483G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111841106 | |||||||
| chr6:111841113 | G | A | 3 | a0001c0001t0006g0228 a0001c0001t0006g0229 a0001c0001t0006g0230 |
3 | HG00733.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-82+5476C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111841113 | |||||||
| chr6:111841520 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG03942.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-82+5069G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111841520 | |||||||
| chr6:111841555 | C | T | 1 | a0001c0001t0002g0039 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-82+5034G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111841555 | |||||||
| chr6:111841576 | A | G | 19 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0122 others(16): Show |
19 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.-82+5013T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111841576 | |||||||
| chr6:111841778 | AT | A | 22 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(19): Show |
22 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.-82+4810delA | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111841778 | |||||||
| chr6:111841817 | A | G | 1 | a0001c0001t0012g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-82+4772T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111841817 | |||||||
| chr6:111841844 | C | T | 11 | a0001c0001t0001g0099 a0001c0001t0001g0173 a0001c0001t0004g0098 others(8): Show |
11 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-82+4745G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111841844 | |||||||
| chr6:111841897 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-82+4692G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111841897 | |||||||
| chr6:111841917 | T | C | 33 | a0001c0001t0005g0199 a0001c0001t0005g0201 a0001c0001t0005g0202 others(30): Show |
33 | HG00438.hp1 HG00438.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.-82+4672A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111841917 | |||||||
| chr6:111841988 | A | AAC | 8 | a0001c0001t0002g0038 a0001c0001t0002g0068 a0001c0001t0003g0037 others(5): Show |
8 | HG01261.hp2 HG02071.hp2 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.-82+4599_-82+4600d others(4): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111841988 | |||||||
| chr6:111841988 | AAC | A | 94 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0113 others(91): Show |
94 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.-82+4599_-82+4600d others(4): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111841988 | |||||||
| chr6:111842133 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-82+4456A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111842133 | |||||||
| chr6:111842157 | G | C | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-82+4432C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111842157 | |||||||
| chr6:111842295 | C | T | 2 | a0001c0001t0005g0199 a0001c0002t0006g0198 |
2 | HG01884.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-82+4294G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111842295 | |||||||
| chr6:111842305 | T | C | 6 | a0001c0001t0001g0130 a0001c0001t0001g0143 a0001c0001t0001g0144 others(3): Show |
6 | HG01081.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-82+4284A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111842305 | |||||||
| chr6:111842501 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-82+4088G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111842501 | |||||||
| chr6:111842871 | G | A | 33 | a0001c0001t0005g0199 a0001c0001t0005g0201 a0001c0001t0005g0202 others(30): Show |
33 | HG00438.hp1 HG00438.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.-82+3718C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111842871 | |||||||
| chr6:111843110 | G | A | 131 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(128): Show |
131 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.-82+3479C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111843110 | |||||||
| chr6:111843238 | A | G | 131 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(128): Show |
131 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.-82+3351T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111843238 | |||||||
| chr6:111843306 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-82+3283G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111843306 | |||||||
| chr6:111843713 | G | C | 10 | a0001c0001t0001g0099 a0001c0001t0004g0098 a0001c0001t0004g0103 others(7): Show |
10 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-82+2876C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111843713 | |||||||
| chr6:111843714 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-82+2875C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111843714 | |||||||
| chr6:111843871 | C | T | 1 | a0001c0001t0003g0033 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-82+2718G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111843871 | |||||||
| chr6:111843897 | G | A | 3 | a0001c0001t0006g0228 a0001c0001t0006g0229 a0001c0001t0006g0230 |
3 | HG00733.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-82+2692C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111843897 | |||||||
| chr6:111843898 | T | C | 19 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0122 others(16): Show |
19 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.-82+2691A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111843898 | |||||||
| chr6:111843974 | C | A | 1 | a0001c0001t0003g0085 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-82+2615G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111843974 | |||||||
| chr6:111843999 | T | C | 33 | a0001c0001t0005g0199 a0001c0001t0005g0201 a0001c0001t0005g0202 others(30): Show |
33 | HG00438.hp1 HG00438.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.-82+2590A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111843999 | |||||||
| chr6:111844075 | A | G | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-82+2514T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111844075 | |||||||
| chr6:111844178 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-82+2411A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111844178 | |||||||
| chr6:111844373 | T | C | 41 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0129 others(38): Show |
41 | HG00741.hp2 HG01081.hp2 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.-82+2216A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111844373 | |||||||
| chr6:111844383 | C | T | 10 | a0001c0001t0001g0099 a0001c0001t0004g0098 a0001c0001t0004g0103 others(7): Show |
10 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-82+2206G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111844383 | |||||||
| chr6:111844738 | C | T | 10 | a0001c0001t0001g0099 a0001c0001t0004g0098 a0001c0001t0004g0103 others(7): Show |
10 | HG01891.hp1 HG02055.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-82+1851G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111844738 | |||||||
| chr6:111844892 | C | T | 1 | a0001c0001t0007g0088 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-82+1697G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111844892 | |||||||
| chr6:111844923 | C | A | 19 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0122 others(16): Show |
19 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.-82+1666G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111844923 | |||||||
| chr6:111844952 | G | T | 19 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0122 others(16): Show |
19 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.-82+1637C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111844952 | |||||||
| chr6:111845018 | C | A | 7 | a0001c0001t0001g0096 a0001c0001t0001g0154 a0001c0001t0001g0161 others(4): Show |
7 | HG03130.hp1 HG03453.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.-82+1571G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111845018 | |||||||
| chr6:111845276 | CCAGAAGG others(10): Show |
C | 4 | a0001c0001t0004g0181 a0001c0001t0004g0192 a0001c0001t0004g0193 others(1): Show |
4 | HG00558.hp2 NA18964.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.-82+1296_-82+1312d others(19): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111845276 | |||||||
| chr6:111845486 | T | C | 1 | a0001c0001t0010g0152 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-82+1103A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111845486 | |||||||
| chr6:111845650 | C | A | 2 | a0001c0001t0001g0188 a0001c0001t0012g0195 |
2 | HG00733.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.-82+939G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111845650 | |||||||
| chr6:111846016 | G | A | 8 | a0001c0001t0001g0170 a0001c0001t0001g0175 a0001c0001t0004g0169 others(5): Show |
8 | HG02280.hp1 HG02486.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-82+573C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111846016 | |||||||
| chr6:111846404 | A | C | 1 | a0001c0001t0006g0228 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-82+185T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111846404 | |||||||
| chr6:111846406 | A | G | 50 | a0001c0001t0001g0099 a0001c0001t0001g0115 a0001c0001t0001g0117 others(47): Show |
50 | HG00558.hp2 HG00639.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.-82+183T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 2/13 | chr6 | 111846406 | |||||||
| chr6:111846917 | T | TAC | 3 | a0001c0001t0006g0228 a0001c0001t0006g0229 a0001c0001t0006g0230 |
3 | HG00733.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-122-290_-122-289d others(4): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111846917 | |||||||
| chr6:111846933 | A | C | 1 | a0001c0001t0014g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-122-304T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111846933 | |||||||
| chr6:111846936 | A | G | 1 | a0001c0001t0010g0174 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-122-307T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111846936 | |||||||
| chr6:111846984 | T | C | 1 | a0001c0001t0020g0095 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-122-355A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111846984 | |||||||
| chr6:111847086 | T | C | 1 | a0001c0001t0001g0160 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-122-457A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111847086 | |||||||
| chr6:111847106 | G | A | 131 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(128): Show |
131 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.-122-477C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111847106 | |||||||
| chr6:111847415 | G | A | 19 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0122 others(16): Show |
19 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.-122-786C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111847415 | |||||||
| chr6:111847714 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-122-1085G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111847714 | |||||||
| chr6:111847935 | A | G | 132 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(129): Show |
132 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.-122-1306T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111847935 | |||||||
| chr6:111847945 | G | A | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-122-1316C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111847945 | |||||||
| chr6:111848147 | T | C | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-122-1518A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111848147 | |||||||
| chr6:111848314 | G | A | 1 | a0001c0001t0003g0033 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-122-1685C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111848314 | |||||||
| chr6:111848801 | T | G | 2 | a0001c0001t0001g0129 a0001c0001t0002g0092 |
2 | HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-122-2172A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111848801 | |||||||
| chr6:111848916 | T | C | 9 | a0001c0001t0001g0117 a0001c0001t0001g0123 a0001c0001t0001g0124 others(6): Show |
9 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.-122-2287A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111848916 | |||||||
| chr6:111848988 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-122-2359C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111848988 | |||||||
| chr6:111849019 | C | T | 133 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(130): Show |
133 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.-122-2390G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111849019 | |||||||
| chr6:111849088 | G | A | 33 | a0001c0001t0005g0199 a0001c0001t0005g0201 a0001c0001t0005g0202 others(30): Show |
33 | HG00438.hp1 HG00438.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.-122-2459C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111849088 | |||||||
| chr6:111849483 | A | G | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-122-2854T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111849483 | |||||||
| chr6:111849893 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-122-3264C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111849893 | |||||||
| chr6:111849927 | C | T | 130 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(127): Show |
130 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.-122-3298G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111849927 | |||||||
| chr6:111849955 | G | C | 1 | a0001c0001t0019g0086 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-122-3326C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111849955 | |||||||
| chr6:111850471 | C | A | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-122-3842G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111850471 | |||||||
| chr6:111850478 | G | A | 40 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0122 others(37): Show |
40 | HG00558.hp2 HG00639.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.-122-3849C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111850478 | |||||||
| chr6:111850506 | A | G | 1 | a0001c0001t0014g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-122-3877T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111850506 | |||||||
| chr6:111850539 | G | A | 21 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(18): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-122-3910C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111850539 | |||||||
| chr6:111850799 | C | T | 7 | a0001c0001t0001g0096 a0001c0001t0001g0154 a0001c0001t0001g0161 others(4): Show |
7 | HG03130.hp1 HG03453.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.-122-4170G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111850799 | |||||||
| chr6:111850913 | C | T | 1 | a0001c0001t0011g0021 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-122-4284G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111850913 | |||||||
| chr6:111851006 | G | A | 33 | a0001c0001t0005g0199 a0001c0001t0005g0201 a0001c0001t0005g0202 others(30): Show |
33 | HG00438.hp1 HG00438.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.-122-4377C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111851006 | |||||||
| chr6:111851027 | AACT | A | 9 | a0001c0001t0001g0170 a0001c0001t0001g0175 a0001c0001t0004g0169 others(6): Show |
9 | HG02280.hp1 HG02486.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-122-4401_-122-439 others(7): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111851027 | |||||||
| chr6:111851147 | G | A | 1 | a0001c0001t0005g0199 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-122-4518C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111851147 | |||||||
| chr6:111851281 | C | A | 33 | a0001c0001t0005g0199 a0001c0001t0005g0201 a0001c0001t0005g0202 others(30): Show |
33 | HG00438.hp1 HG00438.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.-122-4652G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111851281 | |||||||
| chr6:111851281 | C | T | 11 | a0001c0001t0001g0111 a0001c0001t0001g0148 a0001c0001t0001g0149 others(8): Show |
11 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-122-4652G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111851281 | |||||||
| chr6:111851380 | G | A | 7 | a0001c0001t0001g0096 a0001c0001t0001g0154 a0001c0001t0001g0161 others(4): Show |
7 | HG03130.hp1 HG03453.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.-122-4751C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111851380 | |||||||
| chr6:111851519 | G | C | 100 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0113 others(97): Show |
100 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.-122-4890C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111851519 | |||||||
| chr6:111851543 | G | A | 131 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(128): Show |
131 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.-122-4914C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111851543 | |||||||
| chr6:111851547 | G | C | 10 | a0001c0001t0001g0180 a0001c0001t0001g0182 a0001c0001t0001g0189 others(7): Show |
10 | HG00558.hp2 HG00673.hp1 NA18939.hp2 others(7): Show |
intron_variant | MODIFIER | c.-122-4918C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111851547 | |||||||
| chr6:111851753 | G | A | 25 | a0001c0001t0005g0201 a0001c0001t0005g0202 a0001c0001t0005g0203 others(22): Show |
25 | HG00438.hp1 HG00438.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.-122-5124C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111851753 | |||||||
| chr6:111851772 | C | A | 31 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0129 others(28): Show |
31 | HG00741.hp2 HG01081.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.-122-5143G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111851772 | |||||||
| chr6:111851803 | C | G | 1 | a0001c0001t0005g0213 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-122-5174G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111851803 | |||||||
| chr6:111851892 | CT | C | 42 | a0001c0001t0001g0096 a0001c0001t0001g0154 a0001c0001t0001g0161 others(39): Show |
42 | HG00438.hp1 HG00438.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.-122-5264delA | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111851892 | |||||||
| chr6:111852070 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-122-5441A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111852070 | |||||||
| chr6:111852218 | A | G | 4 | a0001c0001t0002g0034 a0001c0001t0002g0035 a0001c0001t0002g0091 others(1): Show |
4 | HG00673.hp2 NA18963.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.-122-5589T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111852218 | |||||||
| chr6:111852368 | A | G | 29 | a0001c0001t0001g0099 a0001c0001t0001g0115 a0001c0001t0001g0117 others(26): Show |
29 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(26): Show |
intron_variant | MODIFIER | c.-122-5739T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111852368 | |||||||
| chr6:111852616 | A | T | 1 | a0001c0001t0010g0118 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-122-5987T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111852616 | |||||||
| chr6:111852876 | T | C | 1 | a0001c0001t0022g0176 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-122-6247A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111852876 | |||||||
| chr6:111853116 | T | TC | 92 | a0001c0001t0001g0099 a0001c0001t0001g0107 a0001c0001t0001g0111 others(89): Show |
92 | HG00558.hp2 HG00639.hp1 HG00673.hp1 others(89): Show |
intron_variant | MODIFIER | c.-122-6488_-122-648 others(5): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111853116 | |||||||
| chr6:111853118 | C | G | 92 | a0001c0001t0001g0099 a0001c0001t0001g0107 a0001c0001t0001g0111 others(89): Show |
92 | HG00558.hp2 HG00639.hp1 HG00673.hp1 others(89): Show |
intron_variant | MODIFIER | c.-122-6489G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111853118 | |||||||
| chr6:111853357 | C | CT | 96 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(93): Show |
96 | HG00558.hp2 HG00639.hp1 HG00673.hp1 others(93): Show |
intron_variant | MODIFIER | c.-122-6729dupA | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111853357 | |||||||
| chr6:111853458 | C | T | 2 | a0001c0001t0002g0034 a0001c0001t0011g0076 |
2 | HG00673.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.-122-6829G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111853458 | |||||||
| chr6:111853767 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-122-7138G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111853767 | |||||||
| chr6:111853977 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-122-7348C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111853977 | |||||||
| chr6:111854017 | C | T | 7 | a0001c0001t0001g0096 a0001c0001t0001g0154 a0001c0001t0001g0161 others(4): Show |
7 | HG03130.hp1 HG03453.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.-122-7388G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111854017 | |||||||
| chr6:111854314 | C | T | 40 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0129 others(37): Show |
40 | HG00741.hp2 HG01081.hp2 HG01891.hp2 others(37): Show |
intron_variant | MODIFIER | c.-122-7685G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111854314 | |||||||
| chr6:111854449 | A | G | 19 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0122 others(16): Show |
19 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.-122-7820T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111854449 | |||||||
| chr6:111854532 | A | G | 92 | a0001c0001t0001g0099 a0001c0001t0001g0107 a0001c0001t0001g0111 others(89): Show |
92 | HG00558.hp2 HG00639.hp1 HG00673.hp1 others(89): Show |
intron_variant | MODIFIER | c.-122-7903T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111854532 | |||||||
| chr6:111854551 | T | A | 1 | a0001c0001t0005g0231 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-122-7922A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111854551 | |||||||
| chr6:111854618 | C | T | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG02615.hp2 HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-122-7989G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111854618 | |||||||
| chr6:111854860 | C | T | 1 | a0001c0001t0006g0212 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-122-8231G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111854860 | |||||||
| chr6:111854862 | A | C | 1 | a0001c0001t0012g0195 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-122-8233T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111854862 | |||||||
| chr6:111855036 | A | G | 132 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(129): Show |
132 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.-122-8407T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111855036 | |||||||
| chr6:111855684 | C | T | 5 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(2): Show |
5 | HG03130.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-122-9055G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111855684 | |||||||
| chr6:111855685 | G | A | 18 | a0001c0001t0001g0113 a0001c0001t0001g0140 a0001c0001t0001g0141 others(15): Show |
18 | HG00741.hp2 HG02055.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.-122-9056C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111855685 | |||||||
| chr6:111855984 | A | G | 19 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0122 others(16): Show |
19 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.-122-9355T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111855984 | |||||||
| chr6:111855994 | G | A | 4 | a0001c0001t0002g0068 a0001c0001t0003g0066 a0001c0001t0003g0087 others(1): Show |
4 | NA18939.hp1 NA18943.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.-122-9365C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111855994 | |||||||
| chr6:111856342 | A | T | 1 | a0001c0001t0004g0181 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-122-9713T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111856342 | |||||||
| chr6:111856435 | T | C | 7 | a0001c0001t0001g0096 a0001c0001t0001g0154 a0001c0001t0001g0161 others(4): Show |
7 | HG03130.hp1 HG03453.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.-122-9806A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111856435 | |||||||
| chr6:111856444 | T | TA | 19 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0122 others(16): Show |
19 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.-122-9816dupT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111856444 | |||||||
| chr6:111856763 | T | C | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | HG02486.hp1 HG03209.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-122-10134A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111856763 | |||||||
| chr6:111856865 | C | T | 7 | a0001c0001t0001g0096 a0001c0001t0001g0154 a0001c0001t0001g0161 others(4): Show |
7 | HG03130.hp1 HG03453.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.-122-10236G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111856865 | |||||||
| chr6:111857200 | G | C | 19 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0122 others(16): Show |
19 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.-122-10571C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111857200 | |||||||
| chr6:111857579 | T | C | 1 | a0001c0001t0002g0069 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-122-10950A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111857579 | |||||||
| chr6:111857695 | A | AG | 23 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0122 others(20): Show |
23 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.-122-11067dupC | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111857695 | |||||||
| chr6:111857821 | CCTT | C | 28 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0129 others(25): Show |
28 | HG00741.hp2 HG01081.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.-122-11195_-122-11 others(9): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111857821 | |||||||
| chr6:111857859 | A | AC | 3 | a0001c0001t0001g0175 a0001c0001t0010g0174 a0001c0001t0022g0176 |
3 | HG02818.hp2 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-122-11231_-122-11 others(7): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111857859 | |||||||
| chr6:111857860 | T | G | 3 | a0001c0001t0001g0175 a0001c0001t0010g0174 a0001c0001t0022g0176 |
3 | HG02818.hp2 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-122-11231A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111857860 | |||||||
| chr6:111857861 | G | A | 5 | a0001c0001t0001g0117 a0001c0001t0001g0126 a0001c0001t0001g0127 others(2): Show |
5 | HG00639.hp1 NA18946.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.-122-11232C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111857861 | |||||||
| chr6:111858018 | G | A | 63 | a0001c0001t0001g0170 a0001c0001t0001g0173 a0001c0001t0001g0177 others(60): Show |
63 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.-122-11389C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111858018 | |||||||
| chr6:111858023 | T | C | 133 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(130): Show |
133 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.-122-11394A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111858023 | |||||||
| chr6:111858060 | C | A | 1 | a0001c0001t0001g0173 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-122-11431G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111858060 | |||||||
| chr6:111858256 | G | A | 1 | a0001c0001t0009g0002 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-122-11627C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111858256 | |||||||
| chr6:111858278 | C | T | 1 | a0001c0001t0008g0100 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-122-11649G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111858278 | |||||||
| chr6:111858284 | C | T | 5 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(2): Show |
5 | HG03130.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-122-11655G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111858284 | |||||||
| chr6:111858363 | T | C | 2 | a0001c0001t0004g0171 a0001c0001t0004g0172 |
2 | HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-122-11734A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111858363 | |||||||
| chr6:111858435 | T | G | 72 | a0001c0001t0001g0096 a0001c0001t0001g0154 a0001c0001t0001g0155 others(69): Show |
72 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.-122-11806A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111858435 | |||||||
| chr6:111858729 | G | A | 211 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(208): Show |
212 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(209): Show |
intron_variant | MODIFIER | c.-122-12100C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111858729 | |||||||
| chr6:111858841 | T | TA | 21 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(18): Show |
21 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.-122-12213dupT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111858841 | |||||||
| chr6:111858841 | TA | T | 9 | a0001c0001t0001g0136 a0001c0001t0001g0140 a0001c0001t0001g0177 others(6): Show |
9 | HG01256.hp1 HG02698.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-122-12213delT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111858841 | |||||||
| chr6:111858883 | C | G | 20 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0122 others(17): Show |
20 | HG00639.hp1 HG01106.hp2 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.-122-12254G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111858883 | |||||||
| chr6:111859010 | G | T | 1 | a0001c0001t0001g0173 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-122-12381C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111859010 | |||||||
| chr6:111859287 | C | T | 6 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 others(3): Show |
6 | NA18941.hp1 NA18950.hp2 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.-122-12658G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111859287 | |||||||
| chr6:111859651 | G | A | 1 | a0001c0001t0006g0209 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-122-13022C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111859651 | |||||||
| chr6:111859716 | G | A | 1 | a0001c0001t0012g0195 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-122-13087C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111859716 | |||||||
| chr6:111859779 | A | C | 1 | a0001c0001t0004g0181 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-122-13150T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111859779 | |||||||
| chr6:111860045 | G | A | 9 | a0001c0001t0001g0096 a0001c0001t0001g0154 a0001c0001t0001g0155 others(6): Show |
9 | HG01081.hp1 HG03130.hp1 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.-123+12923C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111860045 | |||||||
| chr6:111860263 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-123+12705A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111860263 | |||||||
| chr6:111860316 | G | A | 1 | a0001c0002t0001g0135 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-123+12652C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111860316 | |||||||
| chr6:111860827 | C | T | 2 | a0001c0001t0002g0075 a0001c0001t0011g0018 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.-123+12141G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111860827 | |||||||
| chr6:111860908 | T | G | 133 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(130): Show |
133 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.-123+12060A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111860908 | |||||||
| chr6:111861000 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-123+11968T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111861000 | |||||||
| chr6:111861081 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-123+11887A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111861081 | |||||||
| chr6:111861151 | AC | A | 37 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0113 others(34): Show |
37 | HG00741.hp2 HG01081.hp2 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.-123+11816delG | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111861151 | |||||||
| chr6:111861249 | C | G | 1 | a0001c0001t0002g0017 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-123+11719G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111861249 | |||||||
| chr6:111861326 | G | A | 3 | a0001c0001t0001g0175 a0001c0001t0010g0174 a0001c0001t0022g0176 |
3 | HG02818.hp2 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-123+11642C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111861326 | |||||||
| chr6:111861468 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-123+11500G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111861468 | |||||||
| chr6:111861505 | G | T | 1 | a0001c0001t0001g0136 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-123+11463C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111861505 | |||||||
| chr6:111861523 | T | C | 1 | a0001c0001t0005g0203 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-123+11445A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111861523 | |||||||
| chr6:111861560 | C | CCT | 9 | a0001c0001t0001g0096 a0001c0001t0001g0154 a0001c0001t0001g0155 others(6): Show |
9 | HG01081.hp1 HG03130.hp1 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.-123+11406_-123+11 others(8): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111861560 | |||||||
| chr6:111861854 | C | G | 1 | a0001c0001t0011g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-123+11114G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111861854 | |||||||
| chr6:111862015 | T | C | 1 | a0001c0001t0003g0070 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-123+10953A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111862015 | |||||||
| chr6:111862031 | T | G | 60 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0113 others(57): Show |
60 | HG00639.hp1 HG00741.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.-123+10937A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111862031 | |||||||
| chr6:111862084 | C | T | 28 | a0001c0001t0001g0170 a0001c0001t0001g0177 a0001c0001t0001g0178 others(25): Show |
28 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.-123+10884G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111862084 | |||||||
| chr6:111862255 | G | C | 62 | a0001c0001t0001g0170 a0001c0001t0001g0177 a0001c0001t0001g0178 others(59): Show |
62 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-123+10713C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111862255 | |||||||
| chr6:111862610 | G | A | 5 | a0001c0001t0003g0074 a0001c0001t0007g0071 a0001c0001t0007g0072 others(2): Show |
5 | HG00738.hp1 HG01175.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.-123+10358C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111862610 | |||||||
| chr6:111862826 | T | G | 5 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(2): Show |
5 | HG03130.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-123+10142A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111862826 | |||||||
| chr6:111862831 | A | G | 9 | a0001c0001t0001g0096 a0001c0001t0001g0154 a0001c0001t0001g0155 others(6): Show |
9 | HG01081.hp1 HG03130.hp1 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.-123+10137T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111862831 | |||||||
| chr6:111863317 | T | C | 133 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(130): Show |
133 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.-123+9651A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111863317 | |||||||
| chr6:111863418 | T | C | 133 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(130): Show |
133 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.-123+9550A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111863418 | |||||||
| chr6:111863502 | G | T | 28 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0129 others(25): Show |
28 | HG00741.hp2 HG01081.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.-123+9466C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111863502 | |||||||
| chr6:111864258 | C | T | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | NA19005.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.-123+8710G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111864258 | |||||||
| chr6:111864486 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-123+8482C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111864486 | |||||||
| chr6:111864502 | G | A | 1 | a0001c0001t0002g0089 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-123+8466C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111864502 | |||||||
| chr6:111864529 | T | C | 133 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(130): Show |
133 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.-123+8439A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111864529 | |||||||
| chr6:111864544 | G | A | 3 | a0001c0001t0001g0111 a0001c0001t0004g0109 a0001c0001t0004g0112 |
3 | HG02257.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-123+8424C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111864544 | |||||||
| chr6:111864561 | G | GGAT | 133 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(130): Show |
133 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.-123+8404_-123+840 others(7): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111864561 | |||||||
| chr6:111864635 | A | G | 133 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(130): Show |
133 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.-123+8333T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111864635 | |||||||
| chr6:111864672 | T | C | 3 | a0001c0001t0001g0175 a0001c0001t0010g0174 a0001c0001t0022g0176 |
3 | HG02818.hp2 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-123+8296A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111864672 | |||||||
| chr6:111864810 | C | A | 60 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0113 others(57): Show |
60 | HG00639.hp1 HG00741.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.-123+8158G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111864810 | |||||||
| chr6:111865787 | C | T | 12 | a0001c0001t0002g0009 a0001c0001t0002g0013 a0001c0001t0003g0014 others(9): Show |
12 | HG01109.hp1 HG01243.hp1 HG03669.hp1 others(9): Show |
intron_variant | MODIFIER | c.-123+7181G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111865787 | |||||||
| chr6:111866105 | C | T | 29 | a0001c0001t0001g0107 a0001c0001t0001g0170 a0001c0001t0001g0177 others(26): Show |
29 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.-123+6863G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111866105 | |||||||
| chr6:111866350 | C | G | 132 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(129): Show |
132 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.-123+6618G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111866350 | |||||||
| chr6:111866450 | G | A | 63 | a0001c0001t0001g0170 a0001c0001t0001g0173 a0001c0001t0001g0177 others(60): Show |
63 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.-123+6518C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111866450 | |||||||
| chr6:111866848 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-123+6120A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111866848 | |||||||
| chr6:111867061 | C | T | 9 | a0001c0001t0001g0096 a0001c0001t0001g0154 a0001c0001t0001g0155 others(6): Show |
9 | HG01081.hp1 HG03130.hp1 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.-123+5907G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111867061 | |||||||
| chr6:111867150 | A | C | 1 | a0001c0001t0001g0177 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-123+5818T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111867150 | |||||||
| chr6:111867322 | T | C | 37 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0113 others(34): Show |
37 | HG00741.hp2 HG01081.hp2 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.-123+5646A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111867322 | |||||||
| chr6:111867353 | G | A | 1 | a0001c0001t0022g0176 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-123+5615C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111867353 | |||||||
| chr6:111867455 | C | CG | 3 | a0001c0001t0002g0012 a0001c0001t0003g0010 a0001c0001t0007g0011 |
3 | HG00735.hp1 HG00735.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.-123+5512dupC | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111867455 | |||||||
| chr6:111867458 | G | GA | 18 | a0001c0001t0002g0001 a0001c0001t0002g0075 a0001c0001t0002g0077 others(15): Show |
19 | HG00673.hp2 HG00738.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.-123+5509dupT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111867458 | |||||||
| chr6:111867458 | G | GAA | 40 | a0001c0001t0001g0111 a0001c0001t0001g0115 a0001c0001t0001g0117 others(37): Show |
40 | HG00639.hp1 HG00741.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.-123+5508_-123+550 others(6): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111867458 | |||||||
| chr6:111867458 | G | GAAA | 9 | a0001c0001t0001g0142 a0001c0001t0001g0145 a0001c0001t0001g0146 others(6): Show |
9 | HG01258.hp2 HG01891.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-123+5507_-123+550 others(7): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111867458 | |||||||
| chr6:111867458 | G | GGAA | 8 | a0001c0001t0001g0099 a0001c0001t0001g0113 a0001c0001t0004g0103 others(5): Show |
8 | HG02622.hp1 HG02630.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.-123+5509_-123+551 others(7): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111867458 | |||||||
| chr6:111867458 | GAAAAAAA others(2): Show |
G | 9 | a0001c0001t0001g0096 a0001c0001t0001g0154 a0001c0001t0001g0155 others(6): Show |
9 | HG01081.hp1 HG03130.hp1 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.-123+5501_-123+550 others(13): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111867458 | |||||||
| chr6:111867459 | A | AAAG | 61 | a0001c0001t0001g0170 a0001c0001t0001g0177 a0001c0001t0001g0178 others(58): Show |
61 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.-123+5508_-123+550 others(7): Show |
FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111867459 | |||||||
| chr6:111867459 | A | G | 1 | a0001c0001t0002g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-123+5509T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111867459 | |||||||
| chr6:111868074 | C | A | 4 | a0001c0001t0001g0175 a0001c0001t0003g0090 a0001c0001t0010g0174 others(1): Show |
4 | HG01884.hp2 HG02818.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-123+4894G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111868074 | |||||||
| chr6:111868091 | T | C | 133 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(130): Show |
133 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.-123+4877A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111868091 | |||||||
| chr6:111868188 | A | G | 1 | a0001c0001t0009g0002 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-123+4780T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111868188 | |||||||
| chr6:111868243 | C | G | 3 | a0001c0001t0001g0175 a0001c0001t0010g0174 a0001c0001t0022g0176 |
3 | HG02818.hp2 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-123+4725G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111868243 | |||||||
| chr6:111868279 | T | G | 1 | a0001c0001t0002g0091 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-123+4689A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111868279 | |||||||
| chr6:111868319 | C | T | 19 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0148 others(16): Show |
19 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-123+4649G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111868319 | |||||||
| chr6:111868320 | G | A | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG02615.hp2 HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-123+4648C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111868320 | |||||||
| chr6:111868509 | T | G | 140 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0111 others(137): Show |
140 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.-123+4459A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111868509 | |||||||
| chr6:111868532 | GA | G | 9 | a0001c0001t0001g0096 a0001c0001t0001g0154 a0001c0001t0001g0155 others(6): Show |
9 | HG01081.hp1 HG03130.hp1 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.-123+4435delT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111868532 | |||||||
| chr6:111868700 | G | A | 1 | a0001c0001t0002g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-123+4268C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111868700 | |||||||
| chr6:111868781 | T | G | 1 | a0001c0001t0020g0095 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-123+4187A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111868781 | |||||||
| chr6:111868813 | G | A | 71 | a0001c0001t0001g0170 a0001c0001t0001g0173 a0001c0001t0001g0177 others(68): Show |
71 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.-123+4155C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111868813 | |||||||
| chr6:111868836 | C | CA | 60 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0113 others(57): Show |
60 | HG00639.hp1 HG00741.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.-123+4131dupT | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111868836 | |||||||
| chr6:111868910 | A | T | 80 | a0001c0001t0001g0096 a0001c0001t0001g0154 a0001c0001t0001g0155 others(77): Show |
80 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.-123+4058T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111868910 | |||||||
| chr6:111868939 | C | A | 28 | a0001c0001t0001g0170 a0001c0001t0001g0177 a0001c0001t0001g0178 others(25): Show |
28 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.-123+4029G>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111868939 | |||||||
| chr6:111869261 | T | C | 5 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-123+3707A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111869261 | |||||||
| chr6:111870046 | G | A | 6 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG01891.hp2 HG02145.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-123+2922C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111870046 | |||||||
| chr6:111870047 | T | A | 6 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG01891.hp2 HG02145.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-123+2921A>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111870047 | |||||||
| chr6:111870288 | A | T | 3 | a0001c0001t0001g0175 a0001c0001t0010g0174 a0001c0001t0022g0176 |
3 | HG02818.hp2 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-123+2680T>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111870288 | |||||||
| chr6:111870523 | A | G | 1 | a0001c0001t0010g0166 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-123+2445T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111870523 | |||||||
| chr6:111870566 | A | C | 42 | a0001c0001t0005g0199 a0001c0001t0005g0201 a0001c0001t0005g0202 others(39): Show |
42 | HG00438.hp1 HG00438.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.-123+2402T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111870566 | |||||||
| chr6:111870608 | T | C | 2 | a0001c0001t0002g0093 a0001c0001t0002g0094 |
2 | HG01074.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.-123+2360A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111870608 | |||||||
| chr6:111870963 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-123+2005G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111870963 | |||||||
| chr6:111870978 | G | A | 5 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(2): Show |
5 | HG03130.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-123+1990C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111870978 | |||||||
| chr6:111871137 | A | G | 3 | a0001c0001t0001g0175 a0001c0001t0010g0174 a0001c0001t0022g0176 |
3 | HG02818.hp2 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-123+1831T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111871137 | |||||||
| chr6:111871174 | G | A | 1 | a0001c0001t0022g0176 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-123+1794C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111871174 | |||||||
| chr6:111871457 | A | C | 4 | a0001c0001t0005g0201 a0001c0001t0005g0202 a0001c0001t0005g0203 others(1): Show |
4 | HG02165.hp2 NA18974.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.-123+1511T>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111871457 | |||||||
| chr6:111871479 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-123+1489C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111871479 | |||||||
| chr6:111871592 | T | C | 144 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0107 others(141): Show |
144 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(141): Show |
intron_variant | MODIFIER | c.-123+1376A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111871592 | |||||||
| chr6:111871609 | C | T | 1 | a0001c0001t0008g0097 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-123+1359G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111871609 | |||||||
| chr6:111871644 | T | C | 13 | a0001c0001t0001g0096 a0001c0001t0001g0154 a0001c0001t0001g0155 others(10): Show |
13 | HG01081.hp1 HG02486.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.-123+1324A>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111871644 | |||||||
| chr6:111871834 | A | G | 1 | a0001c0001t0002g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-123+1134T>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111871834 | |||||||
| chr6:111872095 | G | C | 28 | a0001c0001t0001g0170 a0001c0001t0001g0177 a0001c0001t0001g0178 others(25): Show |
28 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.-123+873C>G | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111872095 | |||||||
| chr6:111872112 | G | T | 1 | a0001c0001t0012g0106 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-123+856C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111872112 | |||||||
| chr6:111872133 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-123+835C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111872133 | |||||||
| chr6:111872210 | C | G | 1 | a0001c0004t0001g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-123+758G>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111872210 | |||||||
| chr6:111872321 | G | A | 41 | a0001c0001t0005g0201 a0001c0001t0005g0202 a0001c0001t0005g0203 others(38): Show |
41 | HG00438.hp1 HG00438.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.-123+647C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111872321 | |||||||
| chr6:111872656 | C | T | 8 | a0001c0001t0001g0099 a0001c0001t0004g0098 a0001c0001t0004g0103 others(5): Show |
8 | HG01891.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-123+312G>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111872656 | |||||||
| chr6:111872733 | T | G | 3 | a0001c0001t0001g0175 a0001c0001t0010g0174 a0001c0001t0022g0176 |
3 | HG02818.hp2 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-123+235A>C | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111872733 | |||||||
| chr6:111872848 | G | A | 62 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(59): Show |
62 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-123+120C>T | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111872848 | |||||||
| chr6:111872958 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-123+10C>A | FYN | ENSG00000010810.18 | transcript | ENST00000354650.7 | protein_coding | 1/13 | chr6 | 111872958 |