Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 285362 |
| ensemblid | ENSG00000144455.14 |
| hgncid | 20376 |
| symbol | SUMF1 |
| name | sulfatase modifying factor 1 |
| refseq_nuc | NM_182760.4 |
| refseq_prot | NP_877437.2 |
| ensembl_nuc | ENST00000272902.10 |
| ensembl_prot | ENSP00000272902.5 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 4361146 |
| end | 4467269 |
| strand | - |
| ver | v1.2 |
| region | chr3:4361146-4467269 |
| region5000 | chr3:4356146-4472269 |
| regionname0 | SUMF1_chr3_4361146_4467269 |
| regionname5000 | SUMF1_chr3_4356146_4472269 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 374 | 359 | 83 | 63 | 168 | 10 | 33 | 130 | SUMF1_chr3_4356146_4472269 | SUMF1 | MAAPA others(369): Show |
chr3 | 4356146 | 4472269 |
| a0002 | 0/0 | 374 | 22 | 7 | 7 | 0 | 4 | 4 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | MAAPA others(369): Show |
chr3 | 4356146 | 4472269 |
| a0003 | 0/0 | 374 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | MAAPA others(369): Show |
chr3 | 4356146 | 4472269 |
| a0004 | 0/0 | 374 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | MAAPA others(369): Show |
chr3 | 4356146 | 4472269 |
| a0005 | 0/0 | 374 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | MAAPA others(369): Show |
chr3 | 4356146 | 4472269 |
| a0006 | 0/0 | 374 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | MAAPA others(369): Show |
chr3 | 4356146 | 4472269 |
| a0007 | 0/0 | 374 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | MAAPA others(369): Show |
chr3 | 4356146 | 4472269 |
| a0008 | 0/0 | 374 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | MAAPA others(369): Show |
chr3 | 4356146 | 4472269 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1122 | 274 | 79 | 44 | 117 | 8 | 26 | SUMF1_chr3_4356146_4472269 | SUMF1 | ATGGC others(1117): Show |
chr3 | 4356146 | 4472269 | ||
| a0001c0002 | 1/1 | 1122 | 84 | 4 | 19 | 50 | 2 | 7 | SUMF1_chr3_4356146_4472269 | SUMF1 | ATGGC others(1117): Show |
chr3 | 4356146 | 4472269 | ||
| a0001c0010 | 0/0 | 1122 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | ATGGC others(1117): Show |
chr3 | 4356146 | 4472269 | ||
| a0002c0003 | 0/0 | 1122 | 15 | 7 | 3 | 0 | 4 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | ATGGC others(1117): Show |
chr3 | 4356146 | 4472269 | ||
| a0002c0004 | 0/0 | 1122 | 7 | 0 | 4 | 0 | 0 | 3 | SUMF1_chr3_4356146_4472269 | SUMF1 | ATGGC others(1117): Show |
chr3 | 4356146 | 4472269 | ||
| a0003c0005 | 0/0 | 1122 | 5 | 5 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | ATGGC others(1117): Show |
chr3 | 4356146 | 4472269 | ||
| a0003c0006 | 0/0 | 1122 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | ATGGC others(1117): Show |
chr3 | 4356146 | 4472269 | ||
| a0004c0011 | 0/0 | 1122 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | ATGGC others(1117): Show |
chr3 | 4356146 | 4472269 | ||
| a0005c0007 | 0/0 | 1122 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | ATGGC others(1117): Show |
chr3 | 4356146 | 4472269 | ||
| a0006c0008 | 0/0 | 1122 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | ATGGC others(1117): Show |
chr3 | 4356146 | 4472269 | ||
| a0007c0009 | 0/0 | 1122 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | ATGGC others(1117): Show |
chr3 | 4356146 | 4472269 | ||
| a0008c0012 | 0/0 | 1122 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | ATGGC others(1117): Show |
chr3 | 4356146 | 4472269 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2147 | 13 | 13 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2142): Show |
chr3 | 4356146 | 4472269 |
| a0001c0001t0002 | 0/0 | 2143 | 87 | 5 | 8 | 61 | 4 | 9 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2138): Show |
chr3 | 4356146 | 4472269 |
| a0001c0001t0003 | 0/0 | 2143 | 54 | 1 | 24 | 22 | 3 | 4 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2138): Show |
chr3 | 4356146 | 4472269 |
| a0001c0001t0004 | 0/0 | 2143 | 51 | 5 | 6 | 30 | 0 | 10 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2138): Show |
chr3 | 4356146 | 4472269 |
| a0001c0001t0005 | 0/0 | 2143 | 28 | 26 | 2 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2138): Show |
chr3 | 4356146 | 4472269 |
| a0001c0001t0006 | 0/0 | 2143 | 9 | 8 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2138): Show |
chr3 | 4356146 | 4472269 |
| a0001c0001t0007 | 0/0 | 2147 | 9 | 8 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2142): Show |
chr3 | 4356146 | 4472269 |
| a0001c0001t0008 | 0/0 | 2143 | 4 | 0 | 2 | 0 | 1 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2138): Show |
chr3 | 4356146 | 4472269 |
| a0001c0001t0009 | 0/0 | 2143 | 3 | 3 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2138): Show |
chr3 | 4356146 | 4472269 |
| a0001c0001t0010 | 0/0 | 2143 | 3 | 3 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2138): Show |
chr3 | 4356146 | 4472269 |
| a0001c0001t0011 | 0/0 | 2143 | 3 | 3 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2138): Show |
chr3 | 4356146 | 4472269 |
| a0001c0001t0012 | 0/0 | 2143 | 2 | 2 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2138): Show |
chr3 | 4356146 | 4472269 |
| a0001c0001t0013 | 0/0 | 2143 | 2 | 0 | 0 | 2 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2138): Show |
chr3 | 4356146 | 4472269 |
| a0001c0001t0017 | 0/0 | 2143 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2138): Show |
chr3 | 4356146 | 4472269 |
| a0001c0001t0018 | 0/0 | 2143 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2138): Show |
chr3 | 4356146 | 4472269 |
| a0001c0001t0019 | 0/0 | 2143 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2138): Show |
chr3 | 4356146 | 4472269 |
| a0001c0001t0020 | 0/0 | 2143 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2138): Show |
chr3 | 4356146 | 4472269 |
| a0001c0001t0021 | 0/0 | 2143 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2138): Show |
chr3 | 4356146 | 4472269 |
| a0001c0001t0022 | 0/0 | 2143 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2138): Show |
chr3 | 4356146 | 4472269 |
| a0001c0002t0001 | 0/1 | 2147 | 82 | 4 | 19 | 50 | 1 | 7 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2142): Show |
chr3 | 4356146 | 4472269 |
| a0001c0002t0014 | 1/0 | 2147 | 1 | 0 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2142): Show |
chr3 | 4356146 | 4472269 |
| a0001c0002t0015 | 0/0 | 2147 | 1 | 0 | 0 | 0 | 1 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2142): Show |
chr3 | 4356146 | 4472269 |
| a0001c0010t0001 | 0/0 | 2147 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2142): Show |
chr3 | 4356146 | 4472269 |
| a0002c0003t0001 | 0/0 | 2147 | 2 | 2 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2142): Show |
chr3 | 4356146 | 4472269 |
| a0002c0003t0002 | 0/0 | 2143 | 5 | 2 | 0 | 0 | 3 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2138): Show |
chr3 | 4356146 | 4472269 |
| a0002c0003t0003 | 0/0 | 2143 | 5 | 1 | 3 | 0 | 1 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2138): Show |
chr3 | 4356146 | 4472269 |
| a0002c0003t0004 | 0/0 | 2143 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2138): Show |
chr3 | 4356146 | 4472269 |
| a0002c0003t0006 | 0/0 | 2143 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2138): Show |
chr3 | 4356146 | 4472269 |
| a0002c0003t0016 | 0/0 | 2143 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2138): Show |
chr3 | 4356146 | 4472269 |
| a0002c0004t0001 | 0/0 | 2147 | 7 | 0 | 4 | 0 | 0 | 3 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2142): Show |
chr3 | 4356146 | 4472269 |
| a0003c0005t0005 | 0/0 | 2143 | 4 | 4 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2138): Show |
chr3 | 4356146 | 4472269 |
| a0003c0005t0009 | 0/0 | 2143 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2138): Show |
chr3 | 4356146 | 4472269 |
| a0003c0006t0001 | 0/0 | 2147 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2142): Show |
chr3 | 4356146 | 4472269 |
| a0004c0011t0004 | 0/0 | 2143 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2138): Show |
chr3 | 4356146 | 4472269 |
| a0005c0007t0001 | 0/0 | 2147 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2142): Show |
chr3 | 4356146 | 4472269 |
| a0006c0008t0002 | 0/0 | 2143 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2138): Show |
chr3 | 4356146 | 4472269 |
| a0007c0009t0004 | 0/0 | 2143 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2138): Show |
chr3 | 4356146 | 4472269 |
| a0008c0012t0004 | 0/0 | 2143 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | GGGTC others(2138): Show |
chr3 | 4356146 | 4472269 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0002g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0003g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0004g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0005g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0005g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0005g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0005g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0005g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0005g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0005g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0005g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0005g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0006g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0006g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0006g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0006g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0006g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0006g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0006g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0007g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0007g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0007g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0007g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0007g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0007g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0007g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0007g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0007g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0008g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0008g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0008g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0008g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0009g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0009g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0009g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0010g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0010g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0010g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0011g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0011g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0011g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0012g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0012g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0013g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0013g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0017g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0018g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0019g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0020g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0021g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0001t0022g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0307 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0014g0048 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0002t0015g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0001c0010t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0002c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0002c0003t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0002c0003t0002g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0002c0003t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0002c0003t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0002c0003t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0002c0003t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0002c0003t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0002c0003t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0002c0003t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0002c0003t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0002c0003t0004g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0002c0003t0006g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0002c0003t0016g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0002c0004t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0002c0004t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0002c0004t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0002c0004t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0002c0004t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0002c0004t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0002c0004t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0003c0005t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0003c0005t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0003c0005t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0003c0005t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0003c0005t0009g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0003c0006t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0004c0011t0004g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0005c0007t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0006c0008t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0007c0009t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| a0008c0012t0004g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0003 | t0002 | g0021 | EUR | GBR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG00140 | hp2 | a0001 | c0002 | t0015 | g0130 | EUR | GBR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG00280 | hp1 | a0001 | c0001 | t0008 | g0314 | EUR | FIN | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0138 | EUR | FIN | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0178 | EUR | FIN | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG00323 | hp2 | a0002 | c0003 | t0003 | g0029 | EUR | FIN | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0374 | EAS | CHS | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0240 | EAS | CHS | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | CHS | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0204 | EAS | CHS | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0246 | EAS | CHS | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0343 | EAS | CHS | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0197 | EAS | CHS | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG00558 | hp2 | a0001 | c0001 | t0021 | g0289 | EAS | CHS | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0309 | EAS | CHS | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | CHS | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | CHS | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0344 | EAS | CHS | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0268 | EAS | CHS | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0294 | EAS | CHS | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0212 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0182 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG00642 | hp2 | a0001 | c0001 | t0008 | g0272 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0359 | EAS | CHS | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | CHS | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0142 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0198 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0229 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0117 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0186 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0187 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0313 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0209 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0085 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0147 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01099 | hp1 | a0002 | c0004 | t0001 | g0038 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01099 | hp2 | a0001 | c0001 | t0008 | g0221 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0206 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0110 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0068 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0166 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0200 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0230 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0231 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0114 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0251 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01192 | hp1 | a0002 | c0004 | t0001 | g0028 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0165 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0184 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0297 | AMR | PUR | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0091 | AMR | CLM | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0208 | AMR | CLM | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0201 | AMR | CLM | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0207 | AMR | CLM | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | CLM | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | CLM | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0139 | AMR | CLM | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | CLM | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01433 | hp1 | a0002 | c0004 | t0001 | g0025 | AMR | CLM | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0276 | AMR | CLM | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0202 | AMR | CLM | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0361 | AMR | CLM | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0173 | EUR | IBS | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01515 | hp2 | a0002 | c0003 | t0002 | g0001 | EUR | IBS | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0004 | EUR | IBS | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0136 | EUR | IBS | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01517 | hp1 | a0002 | c0003 | t0002 | g0001 | EUR | IBS | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | IBS | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0044 | AFR | ACB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01884 | hp2 | a0002 | c0003 | t0002 | g0023 | AFR | ACB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0050 | AFR | ACB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0266 | AFR | ACB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0213 | AMR | PEL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0089 | AMR | PEL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0317 | AMR | PEL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0260 | AMR | PEL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01943 | hp1 | a0002 | c0003 | t0003 | g0022 | AMR | PEL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0219 | AMR | PEL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0086 | AMR | PEL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0175 | AMR | PEL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01981 | hp1 | a0001 | c0001 | t0005 | g0183 | AMR | PEL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0083 | AMR | PEL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01993 | hp1 | a0002 | c0003 | t0003 | g0027 | AMR | PEL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0253 | AMR | PEL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | KHV | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | KHV | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | KHV | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0292 | EAS | KHV | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0064 | AFR | ACB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0372 | AFR | ACB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0367 | EAS | KHV | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0353 | EAS | KHV | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0355 | EAS | KHV | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | KHV | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | KHV | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0346 | EAS | KHV | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | KHV | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | KHV | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0373 | AFR | ACB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | PEL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0164 | AMR | PEL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | CDX | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0350 | EAS | CDX | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0262 | EAS | CDX | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0352 | EAS | CDX | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02257 | hp2 | a0002 | c0003 | t0001 | g0034 | AFR | ACB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0190 | AFR | ACB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0066 | AFR | ACB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02273 | hp1 | a0002 | c0003 | t0003 | g0031 | AMR | PEL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0365 | AMR | PEL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02280 | hp1 | a0001 | c0001 | t0018 | g0310 | AFR | ACB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0094 | AMR | PEL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0194 | AMR | PEL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0095 | AMR | PEL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0199 | AMR | PEL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02451 | hp1 | a0002 | c0003 | t0002 | g0026 | AFR | ACB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0062 | AFR | ACB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0315 | EAS | KHV | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | KHV | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0368 | AFR | GWD | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0051 | AFR | GWD | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0269 | SAS | PJL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0140 | SAS | PJL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0303 | AFR | GWD | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0129 | AFR | GWD | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02630 | hp1 | a0001 | c0001 | t0010 | g0227 | AFR | GWD | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0067 | AFR | GWD | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0180 | AFR | GWD | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0179 | SAS | PJL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0210 | SAS | PJL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02698 | hp1 | a0004 | c0011 | t0004 | g0376 | SAS | PJL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0124 | SAS | PJL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0319 | AFR | GWD | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0133 | AFR | GWD | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02735 | hp1 | a0002 | c0004 | t0001 | g0032 | SAS | PJL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0252 | SAS | PJL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02738 | hp1 | a0002 | c0004 | t0001 | g0037 | SAS | PJL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02738 | hp2 | a0002 | c0004 | t0001 | g0024 | SAS | PJL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0135 | AFR | GWD | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02809 | hp2 | a0002 | c0003 | t0016 | g0035 | AFR | GWD | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0045 | AFR | GWD | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0128 | AFR | GWD | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02886 | hp1 | a0001 | c0001 | t0009 | g0065 | AFR | GWD | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02886 | hp2 | a0002 | c0003 | t0006 | g0036 | AFR | GWD | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0052 | AFR | GWD | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0059 | AFR | GWD | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0060 | AFR | GWD | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02922 | hp1 | a0003 | c0005 | t0005 | g0018 | AFR | ESN | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02922 | hp2 | a0001 | c0001 | t0011 | g0379 | AFR | ESN | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0265 | AFR | ESN | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0236 | AFR | ESN | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0371 | AFR | ESN | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0056 | AFR | ESN | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02976 | hp1 | a0001 | c0001 | t0007 | g0299 | AFR | ESN | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0363 | AFR | ESN | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0233 | SAS | PJL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0244 | SAS | PJL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0106 | AFR | GWD | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0049 | AFR | GWD | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03098 | hp1 | a0001 | c0001 | t0010 | g0041 | AFR | MSL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0234 | AFR | MSL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0075 | AFR | ESN | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0057 | AFR | ESN | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03139 | hp1 | a0003 | c0006 | t0001 | g0014 | AFR | ESN | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03139 | hp2 | a0003 | c0005 | t0005 | g0013 | AFR | ESN | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03195 | hp1 | a0003 | c0005 | t0009 | g0015 | AFR | ESN | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0103 | AFR | ESN | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03209 | hp1 | a0001 | c0001 | t0009 | g0301 | AFR | MSL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03209 | hp2 | a0001 | c0001 | t0011 | g0378 | AFR | MSL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | MSL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03225 | hp2 | a0001 | c0001 | t0009 | g0300 | AFR | MSL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0150 | SAS | PJL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0192 | SAS | PJL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0167 | AFR | MSL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | MSL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0370 | AFR | MSL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0120 | AFR | MSL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0218 | SAS | PJL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0290 | SAS | PJL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0061 | AFR | ESN | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03516 | hp2 | a0005 | c0007 | t0001 | g0019 | AFR | ESN | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03540 | hp2 | a0001 | c0001 | t0011 | g0380 | AFR | GWD | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0131 | AFR | MSL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0102 | AFR | MSL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0270 | SAS | PJL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03669 | hp2 | a0001 | c0001 | t0019 | g0101 | SAS | PJL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0189 | SAS | PJL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03704 | hp2 | a0001 | c0001 | t0022 | g0073 | SAS | PJL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0278 | SAS | PJL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0211 | SAS | BEB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0172 | SAS | BEB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0077 | SAS | BEB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0122 | SAS | BEB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0071 | SAS | BEB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0375 | SAS | BEB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0250 | SAS | BEB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0125 | SAS | BEB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0137 | SAS | STU | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0195 | SAS | STU | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG04184 | hp1 | a0002 | c0003 | t0004 | g0020 | SAS | BEB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0196 | SAS | BEB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0232 | SAS | STU | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0312 | SAS | STU | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | YRI | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18522 | hp2 | a0006 | c0008 | t0002 | g0040 | AFR | YRI | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0337 | EAS | CHB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | CHB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | CHB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0271 | EAS | CHB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18906 | hp1 | a0001 | c0001 | t0017 | g0298 | AFR | YRI | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0043 | AFR | YRI | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0338 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18940 | hp2 | a0001 | c0001 | t0004 | g0160 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0084 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0093 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0325 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0342 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0070 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0356 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0347 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0334 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18962 | hp2 | a0001 | c0001 | t0004 | g0156 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18963 | hp1 | a0001 | c0001 | t0004 | g0090 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0324 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0340 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0288 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0354 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0358 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0316 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0326 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18981 | hp2 | a0001 | c0010 | t0001 | g0264 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0357 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0360 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0335 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0345 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0092 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18997 | hp1 | a0001 | c0001 | t0004 | g0328 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18997 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0293 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0336 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0088 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0349 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0366 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19012 | hp2 | a0001 | c0001 | t0004 | g0155 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | LWK | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0296 | AFR | LWK | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19043 | hp1 | a0003 | c0005 | t0005 | g0017 | AFR | LWK | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0369 | AFR | LWK | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0295 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0153 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19063 | hp2 | a0001 | c0001 | t0004 | g0100 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0280 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0112 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19068 | hp1 | a0001 | c0001 | t0013 | g0284 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0241 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19070 | hp2 | a0001 | c0001 | t0004 | g0339 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19075 | hp1 | a0001 | c0001 | t0004 | g0158 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19075 | hp2 | a0007 | c0009 | t0004 | g0121 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19077 | hp2 | a0008 | c0012 | t0004 | g0377 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19079 | hp1 | a0001 | c0001 | t0020 | g0249 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0286 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0351 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19082 | hp2 | a0001 | c0001 | t0004 | g0087 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19085 | hp2 | a0001 | c0001 | t0013 | g0242 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19090 | hp1 | a0001 | c0001 | t0004 | g0154 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0132 | AFR | YRI | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0107 | AFR | YRI | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0311 | AFR | ASW | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0143 | AFR | ASW | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0247 | EUR | TSI | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0222 | EUR | TSI | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA20905 | hp1 | a0001 | c0001 | t0008 | g0078 | SAS | GIH | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0072 | SAS | GIH | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01123 | hp1 | a0002 | c0004 | t0001 | g0039 | AMR | CLM | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0329 | AMR | CLM | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02109 | hp1 | a0002 | c0003 | t0001 | g0033 | AFR | ACB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0302 | AFR | ACB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0203 | AFR | ACB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0074 | AFR | ACB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02559 | hp1 | a0001 | c0001 | t0012 | g0104 | AFR | ACB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG02559 | hp2 | a0001 | c0001 | t0010 | g0321 | AFR | ACB | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03471 | hp1 | a0001 | c0001 | t0012 | g0362 | AFR | MSL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0055 | AFR | MSL | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0105 | AFR | USA | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| HG06807 | hp2 | a0001 | c0001 | t0007 | g0364 | AFR | USA | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0348 | EAS | JPT | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0304 | AFR | USA | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA20300 | hp2 | a0002 | c0003 | t0003 | g0030 | AFR | USA | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA21309 | hp1 | a0003 | c0005 | t0005 | g0016 | AFR | LWK | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | LWK | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0307 | REF | REF | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0014 | g0048 | REF | REF | SUMF1_chr3_4356146_4472269 | SUMF1 | chr3 | 4356146 | 4472269 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:4410950 | C | G | 1 | a0007 | 1 | NA19075.hp2 | missense_variant | MODERATE | c.869G>C | p.Gly290Ala | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/9 | 893/2147 | 869/1125 | 290/374 | chr3 | 4410950 | |||
| chr3:4467035 | A | G | 1 | a0006 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.211T>C | p.Ser71Pro | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/9 | 235/2147 | 211/1125 | 71/374 | chr3 | 4467035 | |||
| chr3:4467058 | C | T | 1 | a0002 | 22 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(19): Show |
missense_variant | MODERATE | c.188G>A | p.Ser63Asn | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/9 | 212/2147 | 188/1125 | 63/374 | chr3 | 4467058 | |||
| chr3:4467076 | C | T | 1 | a0005 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.170G>A | p.Arg57Gln | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/9 | 194/2147 | 170/1125 | 57/374 | chr3 | 4467076 | |||
| chr3:4467151 | G | A | 1 | a0004 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.95C>T | p.Ala32Val | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/9 | 119/2147 | 95/1125 | 32/374 | chr3 | 4467151 | |||
| chr3:4467187 | A | C | 1 | a0003 | 6 | HG02922.hp1 HG03139.hp1 HG03139.hp2 others(3): Show |
missense_variant | MODERATE | c.59T>G | p.Leu20Arg | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/9 | 83/2147 | 59/1125 | 20/374 | chr3 | 4467187 | |||
| chr3:4467224 | G | C | 1 | a0008 | 1 | NA19077.hp2 | missense_variant | MODERATE | c.22C>G | p.Leu8Val | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/9 | 46/2147 | 22/1125 | 8/374 | chr3 | 4467224 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:4362153 | A | G | 8 | a0001c0001 a0002c0003 a0003c0005 others(5): Show |
299 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(296): Show |
synonymous_variant | LOW | c.1116T>C | p.Thr372Thr | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 9/9 | 1140/2147 | 1116/1125 | 372/374 | chr3 | 4362153 | |||
| chr3:4452897 | G | A | 1 | a0001c0010 | 1 | NA18981.hp2 | synonymous_variant | LOW | c.423C>T | p.Asn141Asn | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/9 | 447/2147 | 423/1125 | 141/374 | chr3 | 4452897 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:4361162 | C | T | 1 | a0001c0001t0017 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*982G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 9/9 | 982 | chr3 | 4361162 | ||||||
| chr3:4361227 | C | A | 2 | a0001c0001t0009 a0003c0005t0009 |
4 | HG02886.hp1 HG03195.hp1 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*917G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 9/9 | 917 | chr3 | 4361227 | ||||||
| chr3:4361308 | G | C | 1 | a0001c0001t0013 | 2 | NA19068.hp1 NA19085.hp2 |
3_prime_UTR_variant | MODIFIER | c.*836C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 9/9 | 836 | chr3 | 4361308 | ||||||
| chr3:4361339 | G | A | 1 | a0001c0001t0012 | 2 | HG02559.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*805C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 9/9 | 805 | chr3 | 4361339 | ||||||
| chr3:4361469 | T | G | 13 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(10): Show |
177 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*675A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 9/9 | 675 | chr3 | 4361469 | ||||||
| chr3:4361576 | C | T | 1 | a0001c0002t0015 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*568G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 9/9 | 568 | chr3 | 4361576 | ||||||
| chr3:4361584 | C | T | 1 | a0001c0001t0020 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*560G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 9/9 | 560 | chr3 | 4361584 | ||||||
| chr3:4361592 | A | C | 2 | a0001c0001t0006 a0002c0003t0006 |
10 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*552T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 9/9 | 552 | chr3 | 4361592 | ||||||
| chr3:4361626 | A | G | 1 | a0001c0001t0007 | 9 | HG01243.hp2 HG02055.hp1 HG02896.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*518T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 9/9 | 518 | chr3 | 4361626 | ||||||
| chr3:4361673 | A | C | 31 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(28): Show |
334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
3_prime_UTR_variant | MODIFIER | c.*471T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 9/9 | 471 | chr3 | 4361673 | ||||||
| chr3:4361680 | TCTCA | T | 28 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(25): Show |
274 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(271): Show |
3_prime_UTR_variant | MODIFIER | c.*460_*463delTGAG | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 9/9 | 460 | chr3 | 4361680 | ||||||
| chr3:4361746 | G | A | 1 | a0001c0001t0021 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*398C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 9/9 | 398 | chr3 | 4361746 | ||||||
| chr3:4361809 | C | T | 1 | a0002c0003t0016 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*335G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 9/9 | 335 | chr3 | 4361809 | ||||||
| chr3:4361852 | A | T | 2 | a0001c0001t0008 a0001c0001t0018 |
5 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*292T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 9/9 | 292 | chr3 | 4361852 | ||||||
| chr3:4361853 | C | T | 12 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0009 others(9): Show |
164 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*291G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 9/9 | 291 | chr3 | 4361853 | ||||||
| chr3:4361926 | A | G | 1 | a0001c0001t0019 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*218T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 9/9 | 218 | chr3 | 4361926 | ||||||
| chr3:4361930 | T | C | 9 | a0001c0001t0001 a0001c0001t0007 a0001c0002t0001 others(6): Show |
116 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*214A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 9/9 | 214 | chr3 | 4361930 | ||||||
| chr3:4361934 | G | A | 1 | a0001c0001t0010 | 3 | HG02559.hp2 HG02630.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*210C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 9/9 | 210 | chr3 | 4361934 | ||||||
| chr3:4361955 | C | T | 1 | a0001c0001t0018 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*189G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 9/9 | 189 | chr3 | 4361955 | ||||||
| chr3:4362052 | T | C | 1 | a0001c0001t0018 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*92A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 9/9 | 92 | chr3 | 4362052 | ||||||
| chr3:4362083 | A | G | 28 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(25): Show |
274 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(271): Show |
3_prime_UTR_variant | MODIFIER | c.*61T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 9/9 | 61 | chr3 | 4362083 | ||||||
| chr3:4362133 | T | A | 29 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(26): Show |
283 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*11A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 9/9 | 11 | chr3 | 4362133 | ||||||
| chr3:4362134 | T | C | 13 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0009 others(10): Show |
165 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*10A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 9/9 | 10 | chr3 | 4362134 | ||||||
| chr3:4467254 | G | A | 1 | a0001c0001t0011 | 3 | HG02922.hp2 HG03209.hp2 HG03540.hp2 |
5_prime_UTR_variant | MODIFIER | c.-9C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/9 | 9 | chr3 | 4467254 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:4362276 | G | A | 3 | a0001c0001t0001g0113 a0001c0002t0001g0311 a0005c0007t0001g0019 |
3 | HG03516.hp2 NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1015-22C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4362276 | |||||||
| chr3:4362319 | A | C | 1 | a0001c0001t0001g0368 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1015-65T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4362319 | |||||||
| chr3:4362320 | G | C | 1 | a0001c0001t0001g0368 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1015-66C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4362320 | |||||||
| chr3:4362403 | A | G | 263 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(260): Show |
274 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1015-149T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4362403 | |||||||
| chr3:4362579 | A | G | 3 | a0001c0001t0001g0305 a0001c0001t0001g0320 a0002c0003t0001g0033 |
3 | HG02109.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1015-325T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4362579 | |||||||
| chr3:4362789 | T | C | 263 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(260): Show |
274 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1015-535A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4362789 | |||||||
| chr3:4362809 | G | C | 6 | a0001c0001t0002g0009 a0001c0001t0002g0171 a0001c0001t0002g0273 others(3): Show |
7 | HG02135.hp1 NA18939.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.1015-555C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4362809 | |||||||
| chr3:4362839 | G | C | 1 | a0001c0001t0002g0239 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1015-585C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4362839 | |||||||
| chr3:4362913 | C | A | 1 | a0001c0001t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1015-659G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4362913 | |||||||
| chr3:4362922 | G | GA | 10 | a0001c0001t0006g0131 a0001c0001t0006g0133 a0001c0001t0006g0184 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1015-669dupT | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4362922 | |||||||
| chr3:4362949 | G | T | 263 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(260): Show |
274 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1015-695C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4362949 | |||||||
| chr3:4363036 | C | T | 263 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(260): Show |
274 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1015-782G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363036 | |||||||
| chr3:4363081 | G | A | 263 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(260): Show |
274 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1015-827C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363081 | |||||||
| chr3:4363082 | T | C | 4 | a0001c0001t0008g0078 a0001c0001t0008g0221 a0001c0001t0008g0272 others(1): Show |
4 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.1015-828A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363082 | |||||||
| chr3:4363091 | T | A | 10 | a0001c0001t0006g0131 a0001c0001t0006g0133 a0001c0001t0006g0184 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1015-837A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363091 | |||||||
| chr3:4363108 | T | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0306 |
2 | HG02615.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1015-854A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363108 | |||||||
| chr3:4363202 | C | T | 263 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(260): Show |
274 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1015-948G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363202 | |||||||
| chr3:4363214 | C | T | 263 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(260): Show |
274 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1015-960G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363214 | |||||||
| chr3:4363235 | T | C | 285 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(282): Show |
296 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.1015-981A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363235 | |||||||
| chr3:4363337 | G | T | 83 | a0001c0001t0004g0002 a0001c0001t0004g0052 a0001c0001t0004g0070 others(80): Show |
84 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.1015-1083C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363337 | |||||||
| chr3:4363343 | A | G | 1 | a0001c0001t0002g0243 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1015-1089T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363343 | |||||||
| chr3:4363352 | T | A | 3 | a0001c0001t0010g0041 a0001c0001t0010g0227 a0001c0001t0010g0321 |
3 | HG02559.hp2 HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1015-1098A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363352 | |||||||
| chr3:4363387 | CT | C | 4 | a0001c0001t0008g0078 a0001c0001t0008g0221 a0001c0001t0008g0272 others(1): Show |
4 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.1015-1134delA | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363387 | |||||||
| chr3:4363392 | A | C | 263 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(260): Show |
274 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1015-1138T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363392 | |||||||
| chr3:4363405 | G | A | 1 | a0001c0001t0004g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1015-1151C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363405 | |||||||
| chr3:4363411 | T | G | 1 | a0001c0001t0007g0297 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1015-1157A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363411 | |||||||
| chr3:4363416 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1015-1162A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363416 | |||||||
| chr3:4363439 | G | A | 4 | a0001c0001t0008g0078 a0001c0001t0008g0221 a0001c0001t0008g0272 others(1): Show |
4 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.1015-1185C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363439 | |||||||
| chr3:4363482 | G | C | 10 | a0001c0001t0006g0131 a0001c0001t0006g0133 a0001c0001t0006g0184 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1015-1228C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363482 | |||||||
| chr3:4363483 | T | C | 264 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(261): Show |
275 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.1015-1229A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363483 | |||||||
| chr3:4363573 | C | T | 272 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(269): Show |
283 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.1015-1319G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363573 | |||||||
| chr3:4363574 | G | A | 1 | a0001c0001t0001g0368 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1015-1320C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363574 | |||||||
| chr3:4363617 | C | T | 55 | a0001c0001t0004g0002 a0001c0001t0004g0052 a0001c0001t0004g0070 others(52): Show |
56 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.1015-1363G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363617 | |||||||
| chr3:4363643 | T | C | 253 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(250): Show |
264 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.1015-1389A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363643 | |||||||
| chr3:4363661 | A | C | 1 | a0001c0001t0019g0101 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1015-1407T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363661 | |||||||
| chr3:4363681 | T | G | 10 | a0001c0001t0006g0131 a0001c0001t0006g0133 a0001c0001t0006g0184 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1015-1427A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363681 | |||||||
| chr3:4363682 | G | C | 253 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(250): Show |
264 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.1015-1428C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363682 | |||||||
| chr3:4363687 | C | T | 253 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(250): Show |
264 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.1015-1433G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363687 | |||||||
| chr3:4363733 | C | T | 253 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(250): Show |
264 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.1015-1479G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363733 | |||||||
| chr3:4363771 | G | A | 253 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(250): Show |
264 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.1015-1517C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363771 | |||||||
| chr3:4363794 | C | CTTGTGCC others(70): Show |
10 | a0001c0001t0006g0131 a0001c0001t0006g0133 a0001c0001t0006g0184 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1015-1541_1015-154 others(81): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363794 | |||||||
| chr3:4363860 | C | T | 272 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(269): Show |
283 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.1015-1606G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363860 | |||||||
| chr3:4363870 | T | C | 1 | a0001c0001t0004g0112 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1015-1616A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363870 | |||||||
| chr3:4363937 | T | C | 1 | a0001c0001t0002g0136 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1015-1683A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363937 | |||||||
| chr3:4363944 | A | C | 1 | a0001c0001t0001g0134 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1015-1690T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363944 | |||||||
| chr3:4363947 | G | T | 10 | a0001c0001t0006g0131 a0001c0001t0006g0133 a0001c0001t0006g0184 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1015-1693C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363947 | |||||||
| chr3:4363957 | C | T | 9 | a0001c0001t0007g0057 a0001c0001t0007g0059 a0001c0001t0007g0060 others(6): Show |
9 | HG01243.hp2 HG02055.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1015-1703G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363957 | |||||||
| chr3:4363974 | G | C | 1 | a0001c0001t0002g0318 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1015-1720C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4363974 | |||||||
| chr3:4364018 | G | C | 1 | a0001c0001t0011g0378 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1015-1764C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4364018 | |||||||
| chr3:4364023 | C | T | 154 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(151): Show |
164 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1015-1769G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4364023 | |||||||
| chr3:4364024 | A | G | 155 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(152): Show |
165 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1015-1770T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4364024 | |||||||
| chr3:4364031 | C | G | 263 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(260): Show |
274 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1015-1777G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4364031 | |||||||
| chr3:4364039 | T | C | 1 | a0001c0001t0004g0241 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1015-1785A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4364039 | |||||||
| chr3:4364207 | C | T | 154 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(151): Show |
164 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1015-1953G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4364207 | |||||||
| chr3:4364227 | T | A | 2 | a0001c0001t0012g0104 a0001c0001t0012g0362 |
2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1015-1973A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4364227 | |||||||
| chr3:4364239 | C | A | 159 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(156): Show |
169 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.1015-1985G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4364239 | |||||||
| chr3:4364309 | C | T | 1 | a0001c0002t0001g0167 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1015-2055G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4364309 | |||||||
| chr3:4364321 | G | C | 272 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(269): Show |
283 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.1015-2067C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4364321 | |||||||
| chr3:4364332 | C | T | 1 | a0001c0002t0001g0139 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1015-2078G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4364332 | |||||||
| chr3:4364410 | T | G | 263 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(260): Show |
274 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1015-2156A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4364410 | |||||||
| chr3:4364424 | G | C | 153 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(150): Show |
163 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.1015-2170C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4364424 | |||||||
| chr3:4364457 | G | A | 1 | a0001c0001t0001g0368 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1015-2203C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4364457 | |||||||
| chr3:4364589 | A | C | 1 | a0002c0004t0001g0037 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1015-2335T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4364589 | |||||||
| chr3:4364639 | C | T | 1 | a0001c0001t0004g0251 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1015-2385G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4364639 | |||||||
| chr3:4364682 | G | C | 1 | a0001c0001t0007g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1015-2428C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4364682 | |||||||
| chr3:4364690 | A | G | 1 | a0001c0001t0003g0257 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1015-2436T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4364690 | |||||||
| chr3:4364796 | G | A | 1 | a0001c0001t0003g0257 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1015-2542C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4364796 | |||||||
| chr3:4364822 | A | G | 1 | a0001c0001t0003g0257 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1015-2568T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4364822 | |||||||
| chr3:4364826 | A | G | 1 | a0001c0001t0002g0318 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1015-2572T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4364826 | |||||||
| chr3:4364843 | C | T | 2 | a0001c0001t0002g0126 a0001c0001t0002g0127 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1015-2589G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4364843 | |||||||
| chr3:4364854 | G | A | 1 | a0001c0001t0003g0257 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1015-2600C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4364854 | |||||||
| chr3:4364861 | T | C | 1 | a0001c0001t0018g0310 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1015-2607A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4364861 | |||||||
| chr3:4364935 | T | C | 126 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(123): Show |
127 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1015-2681A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4364935 | |||||||
| chr3:4364943 | T | A | 1 | a0002c0004t0001g0037 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1015-2689A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4364943 | |||||||
| chr3:4365022 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1015-2768C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4365022 | |||||||
| chr3:4365171 | G | A | 1 | a0001c0001t0003g0222 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1015-2917C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4365171 | |||||||
| chr3:4365186 | T | C | 10 | a0001c0001t0006g0131 a0001c0001t0006g0133 a0001c0001t0006g0184 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1015-2932A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4365186 | |||||||
| chr3:4365191 | T | C | 115 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(112): Show |
116 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1015-2937A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4365191 | |||||||
| chr3:4365233 | T | C | 119 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(116): Show |
120 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.1015-2979A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4365233 | |||||||
| chr3:4365234 | G | A | 119 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(116): Show |
120 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.1015-2980C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4365234 | |||||||
| chr3:4365247 | C | G | 1 | a0001c0001t0002g0205 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1015-2993G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4365247 | |||||||
| chr3:4365254 | C | G | 289 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(286): Show |
300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.1015-3000G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4365254 | |||||||
| chr3:4365287 | C | T | 115 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(112): Show |
116 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1015-3033G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4365287 | |||||||
| chr3:4365335 | T | G | 2 | a0001c0001t0012g0104 a0001c0001t0012g0362 |
2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1015-3081A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4365335 | |||||||
| chr3:4365350 | T | C | 2 | a0001c0001t0010g0041 a0001c0001t0010g0227 |
2 | HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1015-3096A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4365350 | |||||||
| chr3:4365376 | T | C | 115 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(112): Show |
116 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1015-3122A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4365376 | |||||||
| chr3:4365379 | G | C | 154 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(151): Show |
164 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1015-3125C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4365379 | |||||||
| chr3:4365399 | T | C | 115 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(112): Show |
116 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1015-3145A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4365399 | |||||||
| chr3:4365439 | G | C | 115 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(112): Show |
116 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1015-3185C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4365439 | |||||||
| chr3:4365491 | G | T | 1 | a0001c0001t0005g0363 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1015-3237C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4365491 | |||||||
| chr3:4365768 | G | C | 1 | a0001c0002t0001g0346 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1015-3514C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4365768 | |||||||
| chr3:4365809 | T | C | 263 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(260): Show |
274 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1015-3555A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4365809 | |||||||
| chr3:4365817 | G | C | 1 | a0002c0004t0001g0039 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1015-3563C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4365817 | |||||||
| chr3:4365841 | G | T | 9 | a0001c0001t0007g0057 a0001c0001t0007g0059 a0001c0001t0007g0060 others(6): Show |
9 | HG01243.hp2 HG02055.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1015-3587C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4365841 | |||||||
| chr3:4365856 | G | A | 3 | a0001c0001t0002g0375 a0001c0001t0012g0104 a0001c0001t0012g0362 |
3 | HG02559.hp1 HG03471.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1015-3602C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4365856 | |||||||
| chr3:4365906 | G | A | 4 | a0001c0001t0007g0057 a0001c0001t0007g0061 a0001c0001t0007g0102 others(1): Show |
4 | HG02976.hp1 HG03130.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1015-3652C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4365906 | |||||||
| chr3:4365951 | T | G | 1 | a0001c0001t0004g0084 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1015-3697A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4365951 | |||||||
| chr3:4365954 | C | T | 1 | a0001c0001t0004g0084 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1015-3700G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4365954 | |||||||
| chr3:4365955 | T | A | 1 | a0001c0001t0002g0277 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1015-3701A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4365955 | |||||||
| chr3:4365972 | A | T | 2 | a0001c0001t0012g0104 a0001c0001t0012g0362 |
2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1015-3718T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4365972 | |||||||
| chr3:4366077 | G | A | 323 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(320): Show |
334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.1015-3823C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366077 | |||||||
| chr3:4366086 | G | A | 115 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(112): Show |
116 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1015-3832C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366086 | |||||||
| chr3:4366110 | T | A | 9 | a0001c0001t0007g0057 a0001c0001t0007g0059 a0001c0001t0007g0060 others(6): Show |
9 | HG01243.hp2 HG02055.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1015-3856A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366110 | |||||||
| chr3:4366111 | C | T | 1 | a0001c0002t0001g0210 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1015-3857G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366111 | |||||||
| chr3:4366147 | G | A | 4 | a0001c0001t0008g0078 a0001c0001t0008g0221 a0001c0001t0008g0272 others(1): Show |
4 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.1015-3893C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366147 | |||||||
| chr3:4366148 | C | T | 4 | a0001c0001t0008g0078 a0001c0001t0008g0221 a0001c0001t0008g0272 others(1): Show |
4 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.1015-3894G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366148 | |||||||
| chr3:4366183 | T | C | 275 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(272): Show |
286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.1015-3929A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366183 | |||||||
| chr3:4366249 | T | C | 4 | a0001c0001t0008g0078 a0001c0001t0008g0221 a0001c0001t0008g0272 others(1): Show |
4 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.1015-3995A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366249 | |||||||
| chr3:4366264 | G | C | 263 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(260): Show |
274 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1015-4010C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366264 | |||||||
| chr3:4366273 | G | C | 1 | a0001c0001t0010g0321 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1015-4019C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366273 | |||||||
| chr3:4366278 | G | T | 1 | a0001c0002t0001g0172 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1015-4024C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366278 | |||||||
| chr3:4366334 | C | CT | 3 | a0001c0002t0001g0080 a0001c0002t0001g0082 a0001c0002t0001g0096 |
3 | NA18984.hp2 NA19005.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1015-4081_1015-408 others(5): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366334 | |||||||
| chr3:4366335 | C | A | 3 | a0001c0002t0001g0080 a0001c0002t0001g0082 a0001c0002t0001g0096 |
3 | NA18984.hp2 NA19005.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1015-4081G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366335 | |||||||
| chr3:4366336 | G | A | 3 | a0001c0002t0001g0080 a0001c0002t0001g0082 a0001c0002t0001g0096 |
3 | NA18984.hp2 NA19005.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1015-4082C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366336 | |||||||
| chr3:4366361 | C | T | 1 | a0001c0001t0003g0187 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1015-4107G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366361 | |||||||
| chr3:4366449 | G | A | 1 | a0001c0001t0002g0332 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1015-4195C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366449 | |||||||
| chr3:4366454 | A | G | 1 | a0001c0001t0005g0062 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1015-4200T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366454 | |||||||
| chr3:4366510 | A | G | 263 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(260): Show |
274 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1015-4256T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366510 | |||||||
| chr3:4366520 | C | T | 1 | a0001c0001t0018g0310 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1015-4266G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366520 | |||||||
| chr3:4366526 | T | C | 263 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(260): Show |
274 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1015-4272A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366526 | |||||||
| chr3:4366535 | C | T | 1 | a0001c0001t0004g0197 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1015-4281G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366535 | |||||||
| chr3:4366536 | G | A | 155 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(152): Show |
165 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1015-4282C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366536 | |||||||
| chr3:4366537 | T | G | 263 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(260): Show |
274 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1015-4283A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366537 | |||||||
| chr3:4366544 | C | T | 1 | a0001c0001t0002g0375 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1015-4290G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366544 | |||||||
| chr3:4366578 | T | A | 263 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(260): Show |
274 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1015-4324A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366578 | |||||||
| chr3:4366694 | C | T | 4 | a0001c0001t0004g0100 a0001c0001t0004g0156 a0001c0001t0004g0158 others(1): Show |
4 | NA18940.hp1 NA18962.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.1015-4440G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366694 | |||||||
| chr3:4366751 | G | C | 98 | a0001c0001t0004g0002 a0001c0001t0004g0052 a0001c0001t0004g0070 others(95): Show |
99 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.1015-4497C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366751 | |||||||
| chr3:4366786 | G | C | 240 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(237): Show |
251 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.1015-4532C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366786 | |||||||
| chr3:4366788 | C | T | 1 | a0001c0001t0004g0002 | 2 | HG00642.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.1015-4534G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366788 | |||||||
| chr3:4366800 | TA | T | 263 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(260): Show |
274 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1015-4547delT | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366800 | |||||||
| chr3:4366903 | C | T | 115 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(112): Show |
116 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1015-4649G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366903 | |||||||
| chr3:4366951 | T | G | 2 | a0001c0001t0012g0104 a0001c0001t0012g0362 |
2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1015-4697A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366951 | |||||||
| chr3:4366961 | T | C | 10 | a0001c0001t0006g0131 a0001c0001t0006g0133 a0001c0001t0006g0184 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1015-4707A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366961 | |||||||
| chr3:4366962 | TGGAGTTT others(121): Show |
T | 1 | a0001c0001t0001g0134 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1015-4836_1015-470 others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4366962 | |||||||
| chr3:4367010 | C | T | 263 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(260): Show |
274 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1015-4756G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367010 | |||||||
| chr3:4367094 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1015-4840C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367094 | |||||||
| chr3:4367099 | C | T | 1 | a0001c0001t0018g0310 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1015-4845G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367099 | |||||||
| chr3:4367103 | C | T | 2 | a0001c0002t0001g0255 a0001c0002t0001g0356 |
2 | NA18959.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1015-4849G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367103 | |||||||
| chr3:4367106 | G | T | 1 | a0001c0002t0001g0356 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1015-4852C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367106 | |||||||
| chr3:4367128 | C | T | 1 | a0002c0004t0001g0025 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1015-4874G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367128 | |||||||
| chr3:4367136 | G | T | 1 | a0001c0001t0003g0163 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1015-4882C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367136 | |||||||
| chr3:4367143 | A | C | 132 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0046 others(129): Show |
136 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.1015-4889T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367143 | |||||||
| chr3:4367174 | G | T | 2 | a0001c0001t0005g0135 a0001c0001t0011g0379 |
2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1015-4920C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367174 | |||||||
| chr3:4367183 | T | G | 3 | a0001c0002t0001g0186 a0001c0002t0001g0203 a0001c0002t0001g0212 |
3 | HG00639.hp1 HG01070.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1015-4929A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367183 | |||||||
| chr3:4367200 | C | A | 1 | a0001c0001t0002g0345 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1015-4946G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367200 | |||||||
| chr3:4367201 | A | G | 2 | a0001c0001t0002g0345 a0006c0008t0002g0040 |
2 | NA18522.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1015-4947T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367201 | |||||||
| chr3:4367220 | C | T | 1 | a0001c0001t0004g0128 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1015-4966G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367220 | |||||||
| chr3:4367221 | G | A | 9 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(6): Show |
9 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1015-4967C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367221 | |||||||
| chr3:4367290 | T | C | 10 | a0001c0002t0001g0118 a0001c0002t0001g0123 a0001c0002t0001g0161 others(7): Show |
10 | HG00408.hp2 HG00597.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.1015-5036A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367290 | |||||||
| chr3:4367381 | G | A | 115 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(112): Show |
116 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1015-5127C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367381 | |||||||
| chr3:4367400 | G | A | 12 | a0001c0001t0002g0003 a0001c0001t0002g0097 a0001c0001t0002g0098 others(9): Show |
13 | HG00741.hp1 HG02165.hp2 HG03239.hp2 others(10): Show |
intron_variant | MODIFIER | c.1015-5146C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367400 | |||||||
| chr3:4367472 | T | C | 5 | a0001c0001t0001g0368 a0001c0001t0009g0065 a0001c0001t0009g0300 others(2): Show |
5 | HG02572.hp1 HG02886.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1015-5218A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367472 | |||||||
| chr3:4367482 | C | A | 50 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0002g0069 others(47): Show |
53 | HG00544.hp2 HG00609.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.1015-5228G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367482 | |||||||
| chr3:4367505 | T | C | 50 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0002g0069 others(47): Show |
53 | HG00544.hp2 HG00609.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.1015-5251A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367505 | |||||||
| chr3:4367514 | G | A | 10 | a0001c0001t0006g0131 a0001c0001t0006g0133 a0001c0001t0006g0184 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1015-5260C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367514 | |||||||
| chr3:4367518 | G | A | 10 | a0001c0001t0006g0131 a0001c0001t0006g0133 a0001c0001t0006g0184 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1015-5264C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367518 | |||||||
| chr3:4367522 | C | T | 1 | a0001c0001t0009g0301 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1015-5268G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367522 | |||||||
| chr3:4367523 | A | G | 328 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(325): Show |
339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.1015-5269T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367523 | |||||||
| chr3:4367692 | A | G | 93 | a0001c0001t0002g0196 a0001c0001t0004g0002 a0001c0001t0004g0052 others(90): Show |
94 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.1015-5438T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367692 | |||||||
| chr3:4367747 | A | G | 9 | a0001c0001t0007g0057 a0001c0001t0007g0059 a0001c0001t0007g0060 others(6): Show |
9 | HG01243.hp2 HG02055.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1015-5493T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367747 | |||||||
| chr3:4367759 | G | T | 1 | a0001c0001t0004g0197 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1015-5505C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367759 | |||||||
| chr3:4367773 | G | A | 28 | a0001c0001t0005g0043 a0001c0001t0005g0044 a0001c0001t0005g0049 others(25): Show |
28 | HG00639.hp2 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1015-5519C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367773 | |||||||
| chr3:4367781 | A | G | 263 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(260): Show |
274 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1015-5527T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367781 | |||||||
| chr3:4367839 | G | C | 1 | a0001c0001t0003g0188 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1015-5585C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367839 | |||||||
| chr3:4367871 | G | A | 283 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(280): Show |
294 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.1015-5617C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367871 | |||||||
| chr3:4367942 | T | C | 1 | a0001c0001t0005g0075 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1015-5688A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367942 | |||||||
| chr3:4367970 | G | T | 4 | a0001c0001t0003g0079 a0001c0001t0003g0108 a0001c0001t0003g0148 others(1): Show |
4 | HG02155.hp1 NA18942.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.1015-5716C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4367970 | |||||||
| chr3:4368002 | A | C | 1 | a0001c0002t0001g0179 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1015-5748T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368002 | |||||||
| chr3:4368002 | A | G | 253 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(250): Show |
264 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.1015-5748T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368002 | |||||||
| chr3:4368022 | A | C | 1 | a0001c0002t0001g0246 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1015-5768T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368022 | |||||||
| chr3:4368044 | C | T | 27 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0046 others(24): Show |
29 | HG00140.hp1 HG00323.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.1015-5790G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368044 | |||||||
| chr3:4368075 | G | A | 7 | a0001c0001t0004g0241 a0001c0001t0004g0344 a0001c0001t0004g0348 others(4): Show |
7 | HG00280.hp1 HG00609.hp2 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.1015-5821C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368075 | |||||||
| chr3:4368108 | A | G | 1 | a0001c0001t0021g0289 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1015-5854T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368108 | |||||||
| chr3:4368123 | G | C | 263 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(260): Show |
274 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1015-5869C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368123 | |||||||
| chr3:4368172 | C | T | 263 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(260): Show |
274 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1015-5918G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368172 | |||||||
| chr3:4368204 | G | C | 4 | a0001c0001t0008g0078 a0001c0001t0008g0221 a0001c0001t0008g0272 others(1): Show |
4 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.1015-5950C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368204 | |||||||
| chr3:4368226 | A | G | 10 | a0001c0001t0006g0131 a0001c0001t0006g0133 a0001c0001t0006g0184 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1015-5972T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368226 | |||||||
| chr3:4368227 | C | G | 2 | a0001c0001t0002g0063 a0006c0008t0002g0040 |
2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1015-5973G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368227 | |||||||
| chr3:4368249 | C | T | 12 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(9): Show |
12 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1015-5995G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368249 | |||||||
| chr3:4368253 | C | A | 4 | a0001c0001t0008g0078 a0001c0001t0008g0221 a0001c0001t0008g0272 others(1): Show |
4 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.1015-5999G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368253 | |||||||
| chr3:4368273 | A | G | 2 | a0001c0001t0002g0063 a0006c0008t0002g0040 |
2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1015-6019T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368273 | |||||||
| chr3:4368429 | C | T | 1 | a0001c0001t0002g0177 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1015-6175G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368429 | |||||||
| chr3:4368459 | C | T | 28 | a0001c0001t0005g0043 a0001c0001t0005g0044 a0001c0001t0005g0049 others(25): Show |
28 | HG00639.hp2 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1015-6205G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368459 | |||||||
| chr3:4368477 | C | T | 253 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(250): Show |
264 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.1015-6223G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368477 | |||||||
| chr3:4368526 | A | T | 13 | a0001c0001t0005g0045 a0001c0001t0005g0050 a0001c0001t0005g0051 others(10): Show |
13 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1015-6272T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368526 | |||||||
| chr3:4368538 | G | A | 11 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(8): Show |
11 | HG02109.hp1 HG02145.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1015-6284C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368538 | |||||||
| chr3:4368548 | T | C | 4 | a0001c0001t0008g0078 a0001c0001t0008g0221 a0001c0001t0008g0272 others(1): Show |
4 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.1015-6294A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368548 | |||||||
| chr3:4368591 | T | A | 33 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0046 others(30): Show |
36 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.1015-6337A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368591 | |||||||
| chr3:4368599 | C | A | 272 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(269): Show |
283 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.1015-6345G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368599 | |||||||
| chr3:4368604 | C | T | 272 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(269): Show |
283 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.1015-6350G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368604 | |||||||
| chr3:4368666 | C | G | 1 | a0001c0001t0005g0266 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1015-6412G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368666 | |||||||
| chr3:4368679 | C | G | 9 | a0001c0001t0007g0057 a0001c0001t0007g0059 a0001c0001t0007g0060 others(6): Show |
9 | HG01243.hp2 HG02055.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1015-6425G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368679 | |||||||
| chr3:4368702 | T | C | 9 | a0001c0001t0007g0057 a0001c0001t0007g0059 a0001c0001t0007g0060 others(6): Show |
9 | HG01243.hp2 HG02055.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1015-6448A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368702 | |||||||
| chr3:4368734 | C | T | 1 | a0001c0001t0002g0178 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1015-6480G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368734 | |||||||
| chr3:4368735 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1015-6481C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368735 | |||||||
| chr3:4368748 | A | G | 289 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(286): Show |
300 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.1015-6494T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368748 | |||||||
| chr3:4368834 | C | A | 4 | a0001c0001t0008g0078 a0001c0001t0008g0221 a0001c0001t0008g0272 others(1): Show |
4 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.1015-6580G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368834 | |||||||
| chr3:4368850 | C | T | 153 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(150): Show |
162 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.1015-6596G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368850 | |||||||
| chr3:4368856 | A | G | 1 | a0001c0001t0003g0124 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1015-6602T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368856 | |||||||
| chr3:4368935 | G | C | 154 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(151): Show |
164 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1015-6681C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4368935 | |||||||
| chr3:4369034 | T | C | 261 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(258): Show |
272 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.1015-6780A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4369034 | |||||||
| chr3:4369043 | AAAGGTTT others(4): Show |
A | 117 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(114): Show |
118 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1015-6800_1015-679 others(15): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4369043 | |||||||
| chr3:4369047 | G | GT | 20 | a0001c0001t0002g0333 a0001c0001t0002g0340 a0001c0001t0004g0197 others(17): Show |
20 | HG00558.hp1 HG01243.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.1015-6794dupA | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4369047 | |||||||
| chr3:4369055 | T | C | 117 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(114): Show |
118 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1015-6801A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4369055 | |||||||
| chr3:4369062 | TA | T | 10 | a0001c0001t0002g0223 a0001c0001t0004g0293 a0001c0001t0005g0067 others(7): Show |
10 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.1015-6809delT | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4369062 | |||||||
| chr3:4369063 | A | T | 251 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(248): Show |
262 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.1015-6809T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4369063 | |||||||
| chr3:4369272 | A | G | 262 | a0001c0001t0001g0047 a0001c0001t0001g0109 a0001c0001t0001g0134 others(259): Show |
273 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(270): Show |
intron_variant | MODIFIER | c.1015-7018T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4369272 | |||||||
| chr3:4369274 | A | G | 262 | a0001c0001t0001g0047 a0001c0001t0001g0109 a0001c0001t0001g0134 others(259): Show |
273 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(270): Show |
intron_variant | MODIFIER | c.1015-7020T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4369274 | |||||||
| chr3:4369345 | A | C | 60 | a0001c0001t0002g0196 a0001c0001t0002g0318 a0001c0001t0002g0327 others(57): Show |
61 | HG00408.hp1 HG00558.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.1014+6985T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4369345 | |||||||
| chr3:4369381 | T | C | 19 | a0001c0001t0001g0134 a0001c0001t0004g0052 a0001c0001t0005g0045 others(16): Show |
19 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1014+6949A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4369381 | |||||||
| chr3:4369382 | G | A | 6 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0055 others(3): Show |
6 | HG01891.hp1 HG02572.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1014+6948C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4369382 | |||||||
| chr3:4369429 | G | A | 6 | a0001c0001t0005g0043 a0001c0001t0007g0059 a0001c0001t0007g0060 others(3): Show |
6 | HG01243.hp2 HG02055.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1014+6901C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4369429 | |||||||
| chr3:4369572 | T | A | 361 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(358): Show |
373 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(370): Show |
intron_variant | MODIFIER | c.1014+6758A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4369572 | |||||||
| chr3:4369586 | T | C | 1 | a0001c0002t0001g0119 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1014+6744A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4369586 | |||||||
| chr3:4369611 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0012g0104 |
2 | HG02559.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1014+6719G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4369611 | |||||||
| chr3:4369641 | T | A | 1 | a0001c0002t0001g0146 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1014+6689A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4369641 | |||||||
| chr3:4369686 | T | A | 1 | a0001c0001t0004g0269 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1014+6644A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4369686 | |||||||
| chr3:4369712 | A | T | 1 | a0003c0006t0001g0014 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1014+6618T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4369712 | |||||||
| chr3:4369750 | T | C | 1 | a0001c0002t0001g0286 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1014+6580A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4369750 | |||||||
| chr3:4369949 | T | C | 2 | a0001c0001t0002g0336 a0001c0001t0002g0347 |
2 | NA18960.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1014+6381A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4369949 | |||||||
| chr3:4369959 | G | A | 17 | a0001c0001t0005g0045 a0001c0001t0005g0050 a0001c0001t0005g0051 others(14): Show |
17 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1014+6371C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4369959 | |||||||
| chr3:4370007 | C | T | 203 | a0001c0001t0001g0042 a0001c0001t0001g0053 a0001c0001t0001g0054 others(200): Show |
209 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.1014+6323G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4370007 | |||||||
| chr3:4370211 | G | A | 6 | a0001c0001t0005g0044 a0001c0001t0011g0378 a0003c0005t0005g0013 others(3): Show |
6 | HG01884.hp1 HG02922.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1014+6119C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4370211 | |||||||
| chr3:4370295 | G | T | 1 | a0001c0001t0021g0289 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1014+6035C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4370295 | |||||||
| chr3:4370344 | G | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0134 |
2 | HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1014+5986C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4370344 | |||||||
| chr3:4370368 | C | T | 219 | a0001c0001t0001g0042 a0001c0001t0001g0053 a0001c0001t0001g0054 others(216): Show |
227 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.1014+5962G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4370368 | |||||||
| chr3:4370429 | T | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0134 |
2 | HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1014+5901A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4370429 | |||||||
| chr3:4370445 | G | A | 5 | a0001c0001t0006g0184 a0001c0001t0006g0190 a0001c0001t0006g0369 others(2): Show |
5 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1014+5885C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4370445 | |||||||
| chr3:4370576 | T | C | 1 | a0001c0001t0001g0368 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1014+5754A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4370576 | |||||||
| chr3:4370753 | C | A | 6 | a0001c0001t0003g0124 a0001c0001t0005g0120 a0001c0001t0005g0266 others(3): Show |
6 | HG01891.hp2 HG02109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1014+5577G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4370753 | |||||||
| chr3:4370772 | C | T | 228 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(225): Show |
236 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.1014+5558G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4370772 | |||||||
| chr3:4370781 | A | G | 10 | a0001c0001t0007g0057 a0001c0001t0007g0061 a0001c0001t0007g0064 others(7): Show |
10 | HG01243.hp2 HG02055.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1014+5549T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4370781 | |||||||
| chr3:4370870 | T | C | 1 | a0001c0001t0017g0298 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1014+5460A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4370870 | |||||||
| chr3:4370921 | C | G | 71 | a0001c0001t0001g0320 a0001c0001t0002g0063 a0001c0001t0002g0220 others(68): Show |
72 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.1014+5409G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4370921 | |||||||
| chr3:4371247 | C | T | 1 | a0001c0002t0001g0186 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1014+5083G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4371247 | |||||||
| chr3:4371397 | G | C | 1 | a0001c0002t0001g0170 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1014+4933C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4371397 | |||||||
| chr3:4371441 | T | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0134 |
2 | HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1014+4889A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4371441 | |||||||
| chr3:4371460 | T | G | 312 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(309): Show |
323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.1014+4870A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4371460 | |||||||
| chr3:4371518 | T | C | 243 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(240): Show |
252 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.1014+4812A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4371518 | |||||||
| chr3:4371662 | C | T | 7 | a0001c0001t0003g0006 a0001c0001t0003g0011 a0001c0001t0003g0111 others(4): Show |
9 | HG01257.hp1 HG01258.hp2 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.1014+4668G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4371662 | |||||||
| chr3:4371682 | G | A | 2 | a0001c0002t0001g0138 a0002c0004t0001g0032 |
2 | HG00280.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1014+4648C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4371682 | |||||||
| chr3:4371702 | C | T | 1 | a0001c0001t0002g0178 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1014+4628G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4371702 | |||||||
| chr3:4371722 | C | T | 4 | a0001c0001t0001g0320 a0001c0001t0002g0063 a0003c0006t0001g0014 others(1): Show |
4 | HG03139.hp1 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1014+4608G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4371722 | |||||||
| chr3:4371747 | G | A | 309 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(306): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.1014+4583C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4371747 | |||||||
| chr3:4371768 | C | T | 1 | a0001c0001t0004g0072 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1014+4562G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4371768 | |||||||
| chr3:4371801 | T | C | 1 | a0001c0002t0001g0342 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1014+4529A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4371801 | |||||||
| chr3:4371805 | G | C | 4 | a0001c0001t0004g0070 a0001c0001t0004g0204 a0001c0001t0004g0288 others(1): Show |
4 | HG00438.hp2 NA18954.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.1014+4525C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4371805 | |||||||
| chr3:4371892 | G | C | 1 | a0001c0002t0001g0007 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1014+4438C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4371892 | |||||||
| chr3:4371918 | T | C | 232 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(229): Show |
241 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.1014+4412A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4371918 | |||||||
| chr3:4371946 | C | A | 11 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0058 others(8): Show |
11 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1014+4384G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4371946 | |||||||
| chr3:4372030 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1014+4300C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4372030 | |||||||
| chr3:4372171 | C | T | 5 | a0001c0001t0002g0223 a0001c0001t0008g0078 a0001c0001t0008g0221 others(2): Show |
5 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.1014+4159G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4372171 | |||||||
| chr3:4372223 | C | T | 2 | a0001c0001t0002g0223 a0001c0001t0008g0314 |
2 | HG00280.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1014+4107G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4372223 | |||||||
| chr3:4372280 | C | G | 157 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0076 others(154): Show |
160 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.1014+4050G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4372280 | |||||||
| chr3:4372327 | C | A | 48 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0046 others(45): Show |
50 | HG00140.hp1 HG00323.hp1 HG01106.hp2 others(47): Show |
intron_variant | MODIFIER | c.1014+4003G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4372327 | |||||||
| chr3:4372422 | AT | A | 8 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0098 others(5): Show |
10 | HG02135.hp1 HG02895.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.1014+3907delA | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4372422 | |||||||
| chr3:4372669 | T | G | 155 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0058 others(152): Show |
158 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.1014+3661A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4372669 | |||||||
| chr3:4372689 | C | T | 3 | a0001c0001t0001g0320 a0001c0001t0002g0063 a0006c0008t0002g0040 |
3 | HG03225.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1014+3641G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4372689 | |||||||
| chr3:4372905 | A | T | 146 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0076 others(143): Show |
149 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.1014+3425T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4372905 | |||||||
| chr3:4372976 | G | A | 10 | a0001c0001t0007g0057 a0001c0001t0007g0061 a0001c0001t0007g0064 others(7): Show |
10 | HG01243.hp2 HG02055.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1014+3354C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4372976 | |||||||
| chr3:4372997 | C | A | 2 | a0001c0001t0002g0211 a0001c0001t0002g0352 |
2 | HG02165.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1014+3333G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4372997 | |||||||
| chr3:4373121 | C | A | 220 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0109 others(217): Show |
229 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.1014+3209G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4373121 | |||||||
| chr3:4373194 | C | T | 3 | a0001c0001t0001g0320 a0001c0001t0002g0063 a0006c0008t0002g0040 |
3 | HG03225.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1014+3136G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4373194 | |||||||
| chr3:4373203 | GACAA | G | 235 | a0001c0001t0001g0042 a0001c0001t0001g0053 a0001c0001t0001g0054 others(232): Show |
244 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(241): Show |
intron_variant | MODIFIER | c.1014+3123_1014+312 others(8): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4373203 | |||||||
| chr3:4373226 | T | C | 2 | a0001c0001t0005g0182 a0001c0001t0005g0183 |
2 | HG00639.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1014+3104A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4373226 | |||||||
| chr3:4373229 | G | C | 2 | a0001c0001t0005g0182 a0001c0001t0005g0183 |
2 | HG00639.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1014+3101C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4373229 | |||||||
| chr3:4373344 | A | G | 1 | a0001c0001t0002g0192 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1014+2986T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4373344 | |||||||
| chr3:4373463 | G | GAA | 245 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(242): Show |
254 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(251): Show |
intron_variant | MODIFIER | c.1014+2865_1014+286 others(6): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4373463 | |||||||
| chr3:4373592 | G | A | 220 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0109 others(217): Show |
229 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.1014+2738C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4373592 | |||||||
| chr3:4373663 | CA | C | 249 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(246): Show |
258 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.1014+2666delT | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4373663 | |||||||
| chr3:4373696 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0134 |
2 | HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1014+2634G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4373696 | |||||||
| chr3:4373719 | C | A | 1 | a0001c0002t0001g0077 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1014+2611G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4373719 | |||||||
| chr3:4373742 | G | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0134 |
2 | HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1014+2588C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4373742 | |||||||
| chr3:4373807 | CA | C | 311 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(308): Show |
322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.1014+2522delT | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4373807 | |||||||
| chr3:4373817 | T | TA | 38 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0046 others(35): Show |
40 | HG00140.hp1 HG00323.hp1 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.1014+2512dupT | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4373817 | |||||||
| chr3:4373866 | A | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0134 |
2 | HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1014+2464T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4373866 | |||||||
| chr3:4373949 | A | G | 250 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(247): Show |
259 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.1014+2381T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4373949 | |||||||
| chr3:4373994 | T | TA | 223 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0109 others(220): Show |
232 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.1014+2335dupT | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4373994 | |||||||
| chr3:4374080 | T | C | 1 | a0001c0001t0007g0364 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1014+2250A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4374080 | |||||||
| chr3:4374096 | A | T | 1 | a0001c0001t0002g0296 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1014+2234T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4374096 | |||||||
| chr3:4374106 | T | C | 1 | a0001c0001t0004g0112 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1014+2224A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4374106 | |||||||
| chr3:4374189 | C | T | 2 | a0001c0001t0005g0182 a0001c0001t0005g0183 |
2 | HG00639.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1014+2141G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4374189 | |||||||
| chr3:4374242 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1014+2088G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4374242 | |||||||
| chr3:4374393 | T | C | 3 | a0001c0001t0003g0335 a0001c0002t0001g0248 a0001c0002t0001g0280 |
3 | NA18966.hp1 NA18991.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1014+1937A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4374393 | |||||||
| chr3:4374436 | AT | A | 5 | a0001c0001t0005g0120 a0001c0001t0005g0266 a0001c0001t0005g0302 others(2): Show |
5 | HG01891.hp2 HG02109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1014+1893delA | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4374436 | |||||||
| chr3:4374438 | A | C | 5 | a0001c0001t0005g0120 a0001c0001t0005g0266 a0001c0001t0005g0302 others(2): Show |
5 | HG01891.hp2 HG02109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1014+1892T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4374438 | |||||||
| chr3:4374497 | C | T | 1 | a0001c0001t0003g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1014+1833G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4374497 | |||||||
| chr3:4374528 | C | T | 4 | a0001c0001t0005g0043 a0001c0001t0007g0059 a0001c0001t0007g0060 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1014+1802G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4374528 | |||||||
| chr3:4374615 | T | C | 1 | a0001c0001t0005g0049 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1014+1715A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4374615 | |||||||
| chr3:4374723 | C | T | 67 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0076 others(64): Show |
69 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.1014+1607G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4374723 | |||||||
| chr3:4374809 | A | T | 1 | a0001c0001t0001g0368 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1014+1521T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4374809 | |||||||
| chr3:4374810 | C | T | 2 | a0001c0001t0001g0368 a0002c0003t0003g0031 |
2 | HG02273.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1014+1520G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4374810 | |||||||
| chr3:4374844 | C | G | 1 | a0001c0001t0003g0122 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1014+1486G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4374844 | |||||||
| chr3:4374880 | G | C | 1 | a0001c0001t0002g0215 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1014+1450C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4374880 | |||||||
| chr3:4374888 | A | G | 274 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(271): Show |
283 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.1014+1442T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4374888 | |||||||
| chr3:4374904 | G | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0134 |
2 | HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1014+1426C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4374904 | |||||||
| chr3:4375075 | G | A | 5 | a0001c0001t0002g0223 a0001c0001t0008g0078 a0001c0001t0008g0221 others(2): Show |
5 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.1014+1255C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4375075 | |||||||
| chr3:4375134 | C | CA | 16 | a0001c0001t0001g0054 a0001c0001t0001g0134 a0001c0001t0002g0126 others(13): Show |
16 | HG00438.hp1 HG00597.hp1 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.1014+1195dupT | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4375134 | |||||||
| chr3:4375134 | CA | C | 97 | a0001c0001t0001g0109 a0001c0001t0001g0368 a0001c0001t0002g0003 others(94): Show |
102 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.1014+1195delT | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4375134 | |||||||
| chr3:4375134 | CAA | C | 6 | a0001c0001t0003g0224 a0001c0001t0003g0230 a0001c0001t0003g0271 others(3): Show |
6 | HG01168.hp1 HG02273.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.1014+1194_1014+119 others(6): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4375134 | |||||||
| chr3:4375134 | CAAAA | C | 36 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0046 others(33): Show |
38 | HG00140.hp1 HG00323.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.1014+1192_1014+119 others(8): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4375134 | |||||||
| chr3:4375134 | CAAAAA | C | 12 | a0001c0001t0002g0189 a0001c0001t0004g0128 a0001c0001t0004g0293 others(9): Show |
12 | HG02135.hp2 HG02145.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1014+1191_1014+119 others(9): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4375134 | |||||||
| chr3:4375134 | CAAAAAA | C | 49 | a0001c0001t0001g0320 a0001c0001t0002g0063 a0001c0001t0002g0220 others(46): Show |
50 | HG00408.hp1 HG00558.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.1014+1190_1014+119 others(10): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4375134 | |||||||
| chr3:4375199 | T | C | 1 | a0001c0001t0007g0297 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1014+1131A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4375199 | |||||||
| chr3:4375311 | C | T | 290 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0058 others(287): Show |
300 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.1014+1019G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4375311 | |||||||
| chr3:4375496 | A | G | 18 | a0001c0001t0005g0045 a0001c0001t0005g0050 a0001c0001t0005g0051 others(15): Show |
18 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1014+834T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4375496 | |||||||
| chr3:4375653 | A | G | 24 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0076 others(21): Show |
24 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1014+677T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4375653 | |||||||
| chr3:4375740 | T | C | 18 | a0001c0001t0002g0375 a0001c0001t0004g0002 a0001c0001t0004g0084 others(15): Show |
19 | HG00408.hp1 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1014+590A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4375740 | |||||||
| chr3:4375982 | C | T | 1 | a0001c0001t0001g0368 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1014+348G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4375982 | |||||||
| chr3:4376005 | G | A | 1 | a0001c0001t0002g0252 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1014+325C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4376005 | |||||||
| chr3:4376305 | A | C | 8 | a0001c0001t0003g0006 a0001c0001t0003g0011 a0001c0001t0003g0111 others(5): Show |
10 | HG01257.hp1 HG01258.hp2 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.1014+25T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 8/8 | chr3 | 4376305 | |||||||
| chr3:4376433 | C | T | 8 | a0001c0001t0001g0042 a0001c0001t0001g0134 a0001c0001t0005g0043 others(5): Show |
8 | HG00639.hp2 HG01981.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.955-44G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4376433 | |||||||
| chr3:4376710 | C | A | 5 | a0001c0001t0002g0223 a0001c0001t0008g0078 a0001c0001t0008g0221 others(2): Show |
5 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.955-321G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4376710 | |||||||
| chr3:4376792 | T | G | 5 | a0001c0001t0002g0223 a0001c0001t0008g0078 a0001c0001t0008g0221 others(2): Show |
5 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.955-403A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4376792 | |||||||
| chr3:4376865 | A | G | 5 | a0001c0001t0002g0223 a0001c0001t0008g0078 a0001c0001t0008g0221 others(2): Show |
5 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.955-476T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4376865 | |||||||
| chr3:4376885 | A | T | 5 | a0001c0001t0002g0223 a0001c0001t0008g0078 a0001c0001t0008g0221 others(2): Show |
5 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.955-496T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4376885 | |||||||
| chr3:4376899 | A | G | 2 | a0001c0001t0002g0136 a0002c0003t0002g0026 |
2 | HG01516.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.955-510T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4376899 | |||||||
| chr3:4377087 | C | T | 1 | a0001c0002t0001g0309 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.955-698G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4377087 | |||||||
| chr3:4377105 | T | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0134 |
2 | HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.955-716A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4377105 | |||||||
| chr3:4377227 | A | C | 1 | a0001c0001t0003g0191 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.955-838T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4377227 | |||||||
| chr3:4377353 | A | G | 1 | a0001c0002t0001g0286 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.955-964T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4377353 | |||||||
| chr3:4377385 | C | T | 247 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(244): Show |
256 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.955-996G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4377385 | |||||||
| chr3:4377574 | C | T | 2 | a0001c0001t0002g0046 a0001c0001t0002g0233 |
2 | HG03017.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.955-1185G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4377574 | |||||||
| chr3:4377699 | T | A | 1 | a0001c0001t0002g0220 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.955-1310A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4377699 | |||||||
| chr3:4377722 | G | C | 5 | a0001c0001t0002g0223 a0001c0001t0008g0078 a0001c0001t0008g0221 others(2): Show |
5 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.955-1333C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4377722 | |||||||
| chr3:4377778 | T | A | 4 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0113 others(1): Show |
4 | HG02630.hp2 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.955-1389A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4377778 | |||||||
| chr3:4377790 | A | G | 5 | a0001c0001t0002g0223 a0001c0001t0008g0078 a0001c0001t0008g0221 others(2): Show |
5 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.955-1401T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4377790 | |||||||
| chr3:4377822 | C | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0134 |
2 | HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.955-1433G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4377822 | |||||||
| chr3:4377965 | G | A | 1 | a0001c0001t0005g0236 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.955-1576C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4377965 | |||||||
| chr3:4378032 | C | T | 291 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0058 others(288): Show |
302 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.955-1643G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4378032 | |||||||
| chr3:4378281 | G | A | 45 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0046 others(42): Show |
48 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.955-1892C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4378281 | |||||||
| chr3:4378370 | T | C | 1 | a0001c0001t0022g0073 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.955-1981A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4378370 | |||||||
| chr3:4378426 | C | T | 1 | a0001c0001t0011g0378 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.955-2037G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4378426 | |||||||
| chr3:4378484 | A | G | 6 | a0001c0001t0002g0009 a0001c0001t0002g0098 a0001c0001t0002g0171 others(3): Show |
7 | HG02135.hp1 NA18939.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.955-2095T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4378484 | |||||||
| chr3:4378571 | T | G | 42 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0046 others(39): Show |
45 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.955-2182A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4378571 | |||||||
| chr3:4378635 | A | T | 40 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0046 others(37): Show |
43 | HG00140.hp1 HG00323.hp1 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.955-2246T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4378635 | |||||||
| chr3:4379029 | C | T | 241 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(238): Show |
249 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.955-2640G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4379029 | |||||||
| chr3:4379036 | G | A | 5 | a0001c0001t0002g0223 a0001c0001t0008g0078 a0001c0001t0008g0221 others(2): Show |
5 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.955-2647C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4379036 | |||||||
| chr3:4379235 | G | A | 7 | a0001c0001t0002g0223 a0001c0001t0005g0182 a0001c0001t0005g0183 others(4): Show |
7 | HG00280.hp1 HG00639.hp2 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.955-2846C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4379235 | |||||||
| chr3:4379248 | C | G | 85 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0113 others(82): Show |
86 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.955-2859G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4379248 | |||||||
| chr3:4379312 | C | T | 5 | a0001c0001t0002g0223 a0001c0001t0008g0078 a0001c0001t0008g0221 others(2): Show |
5 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.955-2923G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4379312 | |||||||
| chr3:4379352 | G | T | 16 | a0001c0002t0001g0089 a0001c0002t0001g0099 a0001c0002t0001g0150 others(13): Show |
16 | HG00673.hp2 HG01928.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.955-2963C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4379352 | |||||||
| chr3:4379356 | G | C | 1 | a0001c0001t0004g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.955-2967C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4379356 | |||||||
| chr3:4379369 | AACACAGA others(7): Show |
A | 1 | a0001c0002t0001g0276 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.955-2994_955-2981d others(16): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4379369 | |||||||
| chr3:4379417 | G | T | 1 | a0001c0001t0007g0297 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.955-3028C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4379417 | |||||||
| chr3:4379612 | GAGGTCAA others(7): Show |
G | 1 | a0002c0003t0001g0033 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.955-3237_955-3224d others(16): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4379612 | |||||||
| chr3:4379628 | G | C | 1 | a0001c0002t0001g0167 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.955-3239C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4379628 | |||||||
| chr3:4379649 | C | CT | 14 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0076 others(11): Show |
14 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.955-3261dupA | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4379649 | |||||||
| chr3:4379684 | A | C | 1 | a0001c0001t0001g0368 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.955-3295T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4379684 | |||||||
| chr3:4379703 | G | A | 2 | a0001c0001t0003g0175 a0001c0002t0001g0361 |
2 | HG01496.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.955-3314C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4379703 | |||||||
| chr3:4379767 | G | A | 2 | a0001c0001t0018g0310 a0001c0002t0001g0311 |
2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.955-3378C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4379767 | |||||||
| chr3:4379773 | C | T | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.955-3384G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4379773 | |||||||
| chr3:4379819 | C | A | 2 | a0001c0001t0005g0182 a0001c0001t0005g0183 |
2 | HG00639.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.955-3430G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4379819 | |||||||
| chr3:4379840 | C | CA | 11 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0004g0071 others(8): Show |
11 | HG01175.hp2 HG02135.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.955-3452dupT | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4379840 | |||||||
| chr3:4379840 | CA | C | 86 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0046 others(83): Show |
89 | HG00140.hp1 HG00323.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.955-3452delT | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4379840 | |||||||
| chr3:4379840 | CAA | C | 203 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0109 others(200): Show |
211 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.955-3453_955-3452d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4379840 | |||||||
| chr3:4379840 | CAAA | C | 7 | a0001c0001t0002g0192 a0001c0001t0002g0347 a0001c0001t0005g0182 others(4): Show |
7 | HG00639.hp2 HG01258.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.955-3454_955-3452d others(5): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4379840 | |||||||
| chr3:4379897 | C | T | 5 | a0001c0001t0002g0223 a0001c0001t0008g0078 a0001c0001t0008g0221 others(2): Show |
5 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.955-3508G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4379897 | |||||||
| chr3:4379928 | G | A | 2 | a0001c0001t0009g0300 a0001c0001t0009g0301 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.955-3539C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4379928 | |||||||
| chr3:4379971 | C | CA | 7 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0076 others(4): Show |
7 | HG02109.hp1 HG02145.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.955-3583dupT | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4379971 | |||||||
| chr3:4380126 | T | C | 5 | a0001c0001t0002g0223 a0001c0001t0008g0078 a0001c0001t0008g0221 others(2): Show |
5 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.955-3737A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4380126 | |||||||
| chr3:4380143 | G | A | 1 | a0001c0001t0005g0135 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.955-3754C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4380143 | |||||||
| chr3:4380206 | T | C | 5 | a0001c0001t0002g0223 a0001c0001t0008g0078 a0001c0001t0008g0221 others(2): Show |
5 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.955-3817A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4380206 | |||||||
| chr3:4380213 | T | G | 1 | a0001c0002t0001g0167 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.955-3824A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4380213 | |||||||
| chr3:4380235 | A | G | 91 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0109 others(88): Show |
93 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.955-3846T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4380235 | |||||||
| chr3:4380314 | C | T | 1 | a0001c0002t0001g0246 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.955-3925G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4380314 | |||||||
| chr3:4380374 | A | G | 5 | a0001c0001t0002g0223 a0001c0001t0008g0078 a0001c0001t0008g0221 others(2): Show |
5 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.955-3985T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4380374 | |||||||
| chr3:4380401 | A | G | 42 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0046 others(39): Show |
45 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.955-4012T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4380401 | |||||||
| chr3:4380428 | G | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0134 |
2 | HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.955-4039C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4380428 | |||||||
| chr3:4380522 | G | A | 1 | a0001c0001t0022g0073 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.955-4133C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4380522 | |||||||
| chr3:4380526 | C | T | 4 | a0001c0001t0005g0043 a0001c0001t0007g0059 a0001c0001t0007g0060 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.955-4137G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4380526 | |||||||
| chr3:4380635 | G | A | 2 | a0001c0001t0005g0182 a0001c0001t0005g0183 |
2 | HG00639.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.955-4246C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4380635 | |||||||
| chr3:4380708 | T | C | 1 | a0001c0001t0002g0189 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.955-4319A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4380708 | |||||||
| chr3:4380715 | G | C | 61 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0076 others(58): Show |
64 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.955-4326C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4380715 | |||||||
| chr3:4380750 | G | T | 2 | a0001c0001t0002g0178 a0002c0003t0002g0026 |
2 | HG00323.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.955-4361C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4380750 | |||||||
| chr3:4380770 | A | G | 25 | a0001c0001t0001g0042 a0001c0001t0001g0134 a0001c0001t0002g0223 others(22): Show |
25 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.955-4381T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4380770 | |||||||
| chr3:4380777 | T | G | 1 | a0001c0001t0002g0319 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.955-4388A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4380777 | |||||||
| chr3:4380954 | G | A | 1 | a0001c0001t0002g0012 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.955-4565C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4380954 | |||||||
| chr3:4380965 | A | T | 4 | a0001c0001t0011g0378 a0003c0005t0005g0016 a0003c0005t0005g0017 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.955-4576T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4380965 | |||||||
| chr3:4381024 | G | A | 1 | a0001c0001t0002g0063 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.955-4635C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4381024 | |||||||
| chr3:4381168 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.955-4779G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4381168 | |||||||
| chr3:4381255 | T | C | 16 | a0001c0002t0001g0089 a0001c0002t0001g0099 a0001c0002t0001g0150 others(13): Show |
16 | HG00673.hp2 HG01928.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.955-4866A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4381255 | |||||||
| chr3:4381256 | A | G | 5 | a0001c0001t0002g0223 a0001c0001t0008g0078 a0001c0001t0008g0221 others(2): Show |
5 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.955-4867T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4381256 | |||||||
| chr3:4381300 | G | C | 1 | a0001c0001t0001g0320 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.955-4911C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4381300 | |||||||
| chr3:4381348 | A | AG | 7 | a0001c0001t0002g0126 a0001c0001t0003g0224 a0001c0001t0005g0183 others(4): Show |
7 | HG01109.hp1 HG01496.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.955-4960dupC | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4381348 | |||||||
| chr3:4381357 | C | G | 5 | a0001c0001t0002g0223 a0001c0001t0008g0078 a0001c0001t0008g0221 others(2): Show |
5 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.955-4968G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4381357 | |||||||
| chr3:4381357 | C | T | 1 | a0001c0002t0001g0166 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.955-4968G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4381357 | |||||||
| chr3:4381371 | C | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0134 |
2 | HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.955-4982G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4381371 | |||||||
| chr3:4381446 | A | G | 1 | a0001c0001t0004g0312 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.955-5057T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4381446 | |||||||
| chr3:4381602 | C | G | 1 | a0001c0002t0001g0311 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.955-5213G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4381602 | |||||||
| chr3:4381883 | A | G | 6 | a0001c0001t0007g0057 a0001c0001t0007g0061 a0001c0001t0007g0064 others(3): Show |
6 | HG01243.hp2 HG02055.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.955-5494T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4381883 | |||||||
| chr3:4381902 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0134 |
2 | HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.955-5513G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4381902 | |||||||
| chr3:4381924 | T | C | 58 | a0001c0001t0001g0042 a0001c0001t0001g0134 a0001c0001t0002g0009 others(55): Show |
61 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.955-5535A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4381924 | |||||||
| chr3:4381929 | T | C | 307 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(304): Show |
318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.955-5540A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4381929 | |||||||
| chr3:4382002 | C | T | 5 | a0001c0001t0002g0223 a0001c0001t0008g0078 a0001c0001t0008g0221 others(2): Show |
5 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.955-5613G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4382002 | |||||||
| chr3:4382160 | G | A | 1 | a0001c0002t0001g0096 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.955-5771C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4382160 | |||||||
| chr3:4382215 | A | G | 1 | a0001c0002t0001g0176 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.955-5826T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4382215 | |||||||
| chr3:4382319 | TAC | T | 7 | a0001c0001t0001g0305 a0001c0001t0002g0357 a0001c0001t0002g0358 others(4): Show |
7 | HG00673.hp1 HG02109.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.955-5932_955-5931d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4382319 | |||||||
| chr3:4382327 | C | CAT | 5 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0076 others(2): Show |
5 | HG02145.hp2 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.955-5939_955-5938i others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4382327 | |||||||
| chr3:4382331 | T | TGCACACA others(6): Show |
5 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0076 others(2): Show |
5 | HG02145.hp2 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.955-5943_955-5942i others(15): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4382331 | |||||||
| chr3:4382335 | T | C | 5 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0076 others(2): Show |
5 | HG02145.hp2 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.955-5946A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4382335 | |||||||
| chr3:4382336 | G | A | 5 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0076 others(2): Show |
5 | HG02145.hp2 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.955-5947C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4382336 | |||||||
| chr3:4382336 | G | GCA | 4 | a0001c0001t0001g0113 a0001c0001t0004g0084 a0001c0001t0010g0321 others(1): Show |
4 | HG02559.hp2 HG03516.hp2 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.955-5949_955-5948d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4382336 | |||||||
| chr3:4382336 | G | GCAAACAC others(8): Show |
2 | a0001c0001t0005g0043 a0001c0001t0007g0364 |
2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.955-5948_955-5947i others(17): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4382336 | |||||||
| chr3:4382336 | G | GCACACAC others(4): Show |
25 | a0001c0001t0002g0223 a0001c0001t0006g0131 a0001c0001t0006g0133 others(22): Show |
25 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.955-5958_955-5948d others(13): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4382336 | |||||||
| chr3:4382336 | G | GCACACAC others(6): Show |
28 | a0001c0001t0001g0042 a0001c0001t0002g0009 a0001c0001t0002g0012 others(25): Show |
30 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.955-5948_955-5947i others(15): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4382336 | |||||||
| chr3:4382336 | G | GCACACAC others(8): Show |
18 | a0001c0001t0001g0134 a0001c0001t0001g0305 a0001c0001t0005g0044 others(15): Show |
18 | HG01884.hp1 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.955-5948_955-5947i others(17): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4382336 | |||||||
| chr3:4382336 | G | GCACACAC others(10): Show |
2 | a0001c0001t0005g0135 a0001c0001t0005g0363 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.955-5948_955-5947i others(19): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4382336 | |||||||
| chr3:4382403 | G | A | 12 | a0001c0001t0001g0042 a0001c0001t0001g0134 a0001c0001t0007g0057 others(9): Show |
12 | HG01243.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.955-6014C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4382403 | |||||||
| chr3:4382621 | A | C | 10 | a0001c0001t0006g0131 a0001c0001t0006g0133 a0001c0001t0006g0184 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.955-6232T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4382621 | |||||||
| chr3:4382631 | T | C | 1 | a0001c0002t0001g0167 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.955-6242A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4382631 | |||||||
| chr3:4382648 | T | C | 15 | a0001c0001t0002g0223 a0001c0001t0006g0131 a0001c0001t0006g0133 others(12): Show |
15 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.955-6259A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4382648 | |||||||
| chr3:4382675 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.955-6286C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4382675 | |||||||
| chr3:4382778 | GATGAAGC others(8): Show |
G | 10 | a0001c0001t0003g0124 a0001c0001t0003g0143 a0001c0001t0003g0165 others(7): Show |
10 | HG01071.hp2 HG01074.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.955-6404_955-6390d others(17): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4382778 | |||||||
| chr3:4382798 | T | A | 2 | a0001c0001t0002g0336 a0001c0001t0002g0347 |
2 | NA18960.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.955-6409A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4382798 | |||||||
| chr3:4382799 | T | C | 10 | a0001c0001t0003g0124 a0001c0001t0003g0143 a0001c0001t0003g0165 others(7): Show |
10 | HG01071.hp2 HG01074.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.955-6410A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4382799 | |||||||
| chr3:4382862 | T | G | 1 | a0001c0001t0006g0372 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.955-6473A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4382862 | |||||||
| chr3:4382895 | G | T | 1 | a0001c0001t0018g0310 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.955-6506C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4382895 | |||||||
| chr3:4382908 | T | C | 1 | a0001c0002t0001g0337 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.955-6519A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4382908 | |||||||
| chr3:4382924 | G | A | 5 | a0001c0001t0002g0223 a0001c0001t0008g0078 a0001c0001t0008g0221 others(2): Show |
5 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.955-6535C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4382924 | |||||||
| chr3:4383077 | GA | G | 303 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(300): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.955-6689delT | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4383077 | |||||||
| chr3:4383126 | C | T | 128 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(125): Show |
135 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.955-6737G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4383126 | |||||||
| chr3:4383153 | C | T | 1 | a0001c0001t0002g0349 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.955-6764G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4383153 | |||||||
| chr3:4383182 | C | T | 1 | a0001c0001t0001g0368 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.955-6793G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4383182 | |||||||
| chr3:4383238 | T | C | 1 | a0001c0001t0002g0318 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.955-6849A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4383238 | |||||||
| chr3:4383377 | T | G | 1 | a0001c0001t0004g0269 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.955-6988A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4383377 | |||||||
| chr3:4383511 | G | A | 2 | a0001c0001t0002g0178 a0002c0003t0002g0026 |
2 | HG00323.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.955-7122C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4383511 | |||||||
| chr3:4383557 | G | A | 1 | a0001c0002t0001g0263 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.955-7168C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4383557 | |||||||
| chr3:4383597 | A | T | 66 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0076 others(63): Show |
69 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.955-7208T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4383597 | |||||||
| chr3:4383829 | A | C | 101 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0058 others(98): Show |
104 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.955-7440T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4383829 | |||||||
| chr3:4383958 | T | A | 3 | a0001c0002t0001g0123 a0001c0002t0001g0240 a0001c0002t0001g0355 |
3 | HG00408.hp2 HG02071.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.955-7569A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4383958 | |||||||
| chr3:4384000 | G | GTTATTAT others(39): Show |
5 | a0001c0001t0002g0223 a0001c0001t0008g0078 a0001c0001t0008g0221 others(2): Show |
5 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.955-7612_955-7611i others(48): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4384000 | |||||||
| chr3:4384038 | A | G | 67 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0076 others(64): Show |
70 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.955-7649T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4384038 | |||||||
| chr3:4384044 | G | T | 99 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0058 others(96): Show |
101 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.955-7655C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4384044 | |||||||
| chr3:4384172 | A | C | 58 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0076 others(55): Show |
60 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.955-7783T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4384172 | |||||||
| chr3:4384186 | T | C | 35 | a0001c0001t0001g0042 a0001c0001t0001g0134 a0001c0001t0002g0223 others(32): Show |
35 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.955-7797A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4384186 | |||||||
| chr3:4384373 | C | G | 10 | a0001c0001t0006g0131 a0001c0001t0006g0133 a0001c0001t0006g0184 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.955-7984G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4384373 | |||||||
| chr3:4384461 | T | TA | 4 | a0001c0002t0001g0080 a0001c0002t0001g0081 a0001c0002t0001g0082 others(1): Show |
4 | NA18961.hp2 NA18984.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.955-8073dupT | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4384461 | |||||||
| chr3:4384543 | T | G | 2 | a0001c0001t0018g0310 a0001c0002t0001g0311 |
2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.955-8154A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4384543 | |||||||
| chr3:4384619 | A | G | 1 | a0001c0002t0001g0007 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.955-8230T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4384619 | |||||||
| chr3:4384626 | T | A | 2 | a0001c0001t0007g0059 a0001c0001t0007g0060 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.955-8237A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4384626 | |||||||
| chr3:4384745 | C | T | 2 | a0001c0001t0005g0182 a0001c0001t0005g0183 |
2 | HG00639.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.955-8356G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4384745 | |||||||
| chr3:4384809 | A | G | 2 | a0001c0001t0010g0041 a0001c0001t0010g0227 |
2 | HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.955-8420T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4384809 | |||||||
| chr3:4384848 | A | C | 58 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0076 others(55): Show |
61 | HG00140.hp1 HG00323.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.955-8459T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4384848 | |||||||
| chr3:4384882 | T | G | 16 | a0001c0002t0001g0089 a0001c0002t0001g0099 a0001c0002t0001g0150 others(13): Show |
16 | HG00673.hp2 HG01928.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.955-8493A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4384882 | |||||||
| chr3:4384885 | C | CT | 56 | a0001c0001t0001g0047 a0001c0001t0001g0076 a0001c0001t0001g0306 others(53): Show |
59 | HG00140.hp1 HG00323.hp1 HG01106.hp2 others(56): Show |
intron_variant | MODIFIER | c.955-8497dupA | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4384885 | |||||||
| chr3:4384892 | C | CT | 6 | a0001c0001t0004g0100 a0001c0001t0004g0153 a0001c0001t0004g0154 others(3): Show |
6 | NA18962.hp2 NA19058.hp2 NA19063.hp2 others(3): Show |
intron_variant | MODIFIER | c.955-8504dupA | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4384892 | |||||||
| chr3:4384892 | C | T | 2 | a0001c0001t0001g0058 a0001c0001t0001g0305 |
2 | HG02896.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.955-8503G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4384892 | |||||||
| chr3:4384893 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.955-8504A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4384893 | |||||||
| chr3:4384939 | G | A | 1 | a0001c0002t0001g0176 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.955-8550C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4384939 | |||||||
| chr3:4384990 | A | T | 1 | a0001c0001t0004g0244 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.955-8601T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4384990 | |||||||
| chr3:4385007 | A | T | 58 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0076 others(55): Show |
61 | HG00140.hp1 HG00323.hp1 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.955-8618T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4385007 | |||||||
| chr3:4385056 | C | T | 1 | a0001c0001t0007g0297 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.955-8667G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4385056 | |||||||
| chr3:4385068 | C | T | 53 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0076 others(50): Show |
56 | HG00140.hp1 HG00323.hp1 HG01106.hp2 others(53): Show |
intron_variant | MODIFIER | c.955-8679G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4385068 | |||||||
| chr3:4385107 | A | C | 73 | a0001c0001t0002g0003 a0001c0001t0002g0097 a0001c0001t0002g0192 others(70): Show |
78 | HG00323.hp2 HG00558.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.955-8718T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4385107 | |||||||
| chr3:4385204 | G | C | 1 | a0001c0002t0001g0216 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.955-8815C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4385204 | |||||||
| chr3:4385509 | G | A | 289 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(286): Show |
300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.955-9120C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4385509 | |||||||
| chr3:4385663 | G | A | 2 | a0001c0001t0018g0310 a0001c0002t0001g0311 |
2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.955-9274C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4385663 | |||||||
| chr3:4385845 | C | T | 1 | a0001c0001t0012g0104 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.955-9456G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4385845 | |||||||
| chr3:4385941 | A | G | 1 | a0001c0002t0001g0172 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.955-9552T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4385941 | |||||||
| chr3:4385952 | C | T | 12 | a0001c0001t0001g0042 a0001c0001t0001g0134 a0001c0001t0007g0057 others(9): Show |
12 | HG01243.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.955-9563G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4385952 | |||||||
| chr3:4385978 | C | A | 7 | a0001c0001t0005g0043 a0001c0001t0005g0266 a0001c0001t0007g0059 others(4): Show |
7 | HG01891.hp2 HG02280.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.955-9589G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4385978 | |||||||
| chr3:4386036 | A | AAGT | 17 | a0001c0001t0001g0042 a0001c0001t0001g0134 a0001c0001t0002g0223 others(14): Show |
17 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.955-9650_955-9648d others(5): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4386036 | |||||||
| chr3:4386112 | T | C | 42 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0046 others(39): Show |
45 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.955-9723A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4386112 | |||||||
| chr3:4386150 | T | C | 1 | a0002c0003t0002g0026 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.955-9761A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4386150 | |||||||
| chr3:4386300 | G | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0134 |
2 | HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.955-9911C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4386300 | |||||||
| chr3:4386344 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.955-9955T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4386344 | |||||||
| chr3:4386441 | C | T | 13 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0076 others(10): Show |
13 | HG02109.hp1 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.955-10052G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4386441 | |||||||
| chr3:4386589 | T | A | 4 | a0001c0001t0005g0120 a0001c0001t0005g0302 a0001c0001t0012g0104 others(1): Show |
4 | HG02109.hp2 HG02559.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.955-10200A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4386589 | |||||||
| chr3:4386736 | A | G | 10 | a0001c0001t0006g0131 a0001c0001t0006g0133 a0001c0001t0006g0184 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.955-10347T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4386736 | |||||||
| chr3:4386766 | T | A | 12 | a0001c0001t0003g0083 a0001c0001t0003g0094 a0001c0001t0003g0095 others(9): Show |
12 | HG00323.hp2 HG00741.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.955-10377A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4386766 | |||||||
| chr3:4386859 | T | G | 2 | a0001c0001t0018g0310 a0001c0002t0001g0311 |
2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.955-10470A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4386859 | |||||||
| chr3:4386863 | G | GT | 6 | a0001c0001t0002g0223 a0001c0001t0003g0095 a0001c0001t0008g0078 others(3): Show |
6 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.955-10475dupA | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4386863 | |||||||
| chr3:4386905 | A | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0134 |
2 | HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.955-10516T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4386905 | |||||||
| chr3:4386941 | C | T | 1 | a0001c0001t0002g0254 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.955-10552G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4386941 | |||||||
| chr3:4387005 | T | G | 4 | a0001c0001t0009g0065 a0001c0001t0009g0300 a0001c0001t0009g0301 others(1): Show |
4 | HG02886.hp1 HG03195.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.955-10616A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4387005 | |||||||
| chr3:4387006 | T | C | 4 | a0001c0001t0002g0009 a0001c0001t0002g0098 a0001c0001t0002g0171 others(1): Show |
5 | NA18939.hp2 NA18959.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.955-10617A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4387006 | |||||||
| chr3:4387060 | C | T | 351 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(348): Show |
363 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.955-10671G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4387060 | |||||||
| chr3:4387108 | G | A | 2 | a0001c0001t0010g0041 a0001c0001t0010g0227 |
2 | HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.955-10719C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4387108 | |||||||
| chr3:4387115 | G | C | 9 | a0001c0002t0001g0166 a0001c0002t0001g0167 a0001c0002t0001g0172 others(6): Show |
10 | HG00140.hp2 HG00639.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.955-10726C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4387115 | |||||||
| chr3:4387206 | A | G | 25 | a0001c0001t0002g0223 a0001c0001t0006g0131 a0001c0001t0006g0133 others(22): Show |
25 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.955-10817T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4387206 | |||||||
| chr3:4387402 | C | G | 15 | a0001c0001t0002g0223 a0001c0001t0006g0131 a0001c0001t0006g0133 others(12): Show |
15 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.955-11013G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4387402 | |||||||
| chr3:4387468 | C | T | 25 | a0001c0001t0002g0223 a0001c0001t0006g0131 a0001c0001t0006g0133 others(22): Show |
25 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.955-11079G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4387468 | |||||||
| chr3:4387551 | A | G | 25 | a0001c0001t0002g0223 a0001c0001t0006g0131 a0001c0001t0006g0133 others(22): Show |
25 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.955-11162T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4387551 | |||||||
| chr3:4387654 | G | C | 25 | a0001c0001t0002g0223 a0001c0001t0006g0131 a0001c0001t0006g0133 others(22): Show |
25 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.955-11265C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4387654 | |||||||
| chr3:4387667 | A | G | 25 | a0001c0001t0002g0223 a0001c0001t0006g0131 a0001c0001t0006g0133 others(22): Show |
25 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.955-11278T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4387667 | |||||||
| chr3:4387716 | T | C | 1 | a0001c0001t0002g0177 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.955-11327A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4387716 | |||||||
| chr3:4387718 | C | T | 25 | a0001c0001t0002g0223 a0001c0001t0006g0131 a0001c0001t0006g0133 others(22): Show |
25 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.955-11329G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4387718 | |||||||
| chr3:4387845 | C | T | 1 | a0001c0001t0004g0088 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.955-11456G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4387845 | |||||||
| chr3:4387948 | T | C | 50 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0076 others(47): Show |
53 | HG00140.hp1 HG00323.hp1 HG01106.hp2 others(50): Show |
intron_variant | MODIFIER | c.955-11559A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4387948 | |||||||
| chr3:4388020 | A | G | 2 | a0001c0002t0001g0161 a0001c0002t0001g0162 |
2 | NA18968.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.955-11631T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4388020 | |||||||
| chr3:4388023 | A | C | 25 | a0001c0001t0002g0223 a0001c0001t0006g0131 a0001c0001t0006g0133 others(22): Show |
25 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.955-11634T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4388023 | |||||||
| chr3:4388095 | T | C | 1 | a0003c0005t0005g0017 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.955-11706A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4388095 | |||||||
| chr3:4388148 | A | T | 128 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(125): Show |
136 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.955-11759T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4388148 | |||||||
| chr3:4388312 | C | T | 1 | a0001c0001t0005g0266 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.955-11923G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4388312 | |||||||
| chr3:4388327 | C | T | 1 | a0001c0001t0003g0232 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.955-11938G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4388327 | |||||||
| chr3:4388340 | T | G | 67 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0058 others(64): Show |
69 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.955-11951A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4388340 | |||||||
| chr3:4388407 | A | G | 4 | a0001c0001t0002g0211 a0001c0001t0002g0260 a0001c0001t0002g0352 others(1): Show |
4 | HG01934.hp2 HG02165.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.955-12018T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4388407 | |||||||
| chr3:4388643 | C | T | 4 | a0001c0001t0005g0043 a0001c0001t0007g0059 a0001c0001t0007g0060 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.955-12254G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4388643 | |||||||
| chr3:4388652 | G | A | 1 | a0001c0001t0005g0266 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.955-12263C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4388652 | |||||||
| chr3:4388661 | T | C | 1 | a0001c0001t0004g0374 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.955-12272A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4388661 | |||||||
| chr3:4388700 | G | T | 1 | a0001c0001t0005g0266 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.955-12311C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4388700 | |||||||
| chr3:4388703 | A | C | 1 | a0001c0001t0005g0266 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.955-12314T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4388703 | |||||||
| chr3:4388759 | G | C | 16 | a0001c0001t0002g0252 a0001c0002t0001g0089 a0001c0002t0001g0099 others(13): Show |
16 | HG00673.hp2 HG01928.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.955-12370C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4388759 | |||||||
| chr3:4388838 | T | A | 2 | a0001c0001t0005g0182 a0001c0001t0005g0183 |
2 | HG00639.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.955-12449A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4388838 | |||||||
| chr3:4388866 | C | T | 8 | a0001c0001t0002g0003 a0001c0001t0002g0097 a0001c0001t0002g0215 others(5): Show |
9 | HG00741.hp1 NA18964.hp1 NA18971.hp2 others(6): Show |
intron_variant | MODIFIER | c.955-12477G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4388866 | |||||||
| chr3:4389034 | A | T | 3 | a0001c0001t0001g0368 a0001c0001t0018g0310 a0001c0002t0001g0311 |
3 | HG02280.hp1 HG02572.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.955-12645T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4389034 | |||||||
| chr3:4389039 | T | C | 4 | a0001c0001t0005g0043 a0001c0001t0007g0059 a0001c0001t0007g0060 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.955-12650A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4389039 | |||||||
| chr3:4389047 | C | T | 2 | a0001c0001t0005g0182 a0001c0001t0005g0183 |
2 | HG00639.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.955-12658G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4389047 | |||||||
| chr3:4389121 | T | A | 1 | a0002c0003t0002g0026 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.955-12732A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4389121 | |||||||
| chr3:4389140 | A | G | 8 | a0001c0001t0002g0211 a0001c0001t0002g0260 a0001c0001t0002g0352 others(5): Show |
8 | HG01934.hp2 HG02109.hp2 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.955-12751T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4389140 | |||||||
| chr3:4389154 | C | T | 1 | a0001c0002t0001g0118 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.955-12765G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4389154 | |||||||
| chr3:4389164 | C | T | 200 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0058 others(197): Show |
209 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.955-12775G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4389164 | |||||||
| chr3:4389165 | A | G | 2 | a0001c0001t0004g0241 a0001c0002t0001g0169 |
2 | NA18747.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.955-12776T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4389165 | |||||||
| chr3:4389182 | G | C | 1 | a0001c0001t0002g0229 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.955-12793C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4389182 | |||||||
| chr3:4389202 | A | G | 2 | a0001c0001t0018g0310 a0001c0002t0001g0311 |
2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.955-12813T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4389202 | |||||||
| chr3:4389332 | GT | G | 32 | a0001c0001t0001g0305 a0001c0001t0002g0189 a0001c0001t0002g0375 others(29): Show |
33 | HG00408.hp1 HG01071.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.955-12944delA | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4389332 | |||||||
| chr3:4389332 | GTTT | G | 27 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0005g0045 others(24): Show |
27 | HG00140.hp2 HG01070.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.955-12946_955-1294 others(7): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4389332 | |||||||
| chr3:4389346 | T | C | 1 | a0001c0002t0001g0138 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.955-12957A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4389346 | |||||||
| chr3:4389386 | A | G | 4 | a0001c0001t0009g0065 a0001c0001t0009g0300 a0001c0001t0009g0301 others(1): Show |
4 | HG02886.hp1 HG03195.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.955-12997T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4389386 | |||||||
| chr3:4389395 | CT | C | 28 | a0001c0001t0002g0110 a0001c0001t0002g0136 a0001c0001t0002g0173 others(25): Show |
28 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.955-13007delA | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4389395 | |||||||
| chr3:4389401 | T | C | 28 | a0001c0001t0002g0110 a0001c0001t0002g0136 a0001c0001t0002g0173 others(25): Show |
28 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.955-13012A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4389401 | |||||||
| chr3:4389464 | G | A | 31 | a0001c0001t0001g0042 a0001c0001t0001g0053 a0001c0001t0001g0054 others(28): Show |
32 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.955-13075C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4389464 | |||||||
| chr3:4389503 | A | G | 33 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0113 others(30): Show |
33 | HG01243.hp1 HG01243.hp2 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.955-13114T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4389503 | |||||||
| chr3:4389514 | G | T | 10 | a0001c0001t0006g0131 a0001c0001t0006g0133 a0001c0001t0006g0184 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.955-13125C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4389514 | |||||||
| chr3:4389541 | G | T | 97 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(94): Show |
102 | HG00558.hp1 HG00609.hp1 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.955-13152C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4389541 | |||||||
| chr3:4389548 | C | T | 7 | a0001c0001t0001g0042 a0001c0001t0001g0368 a0001c0001t0007g0057 others(4): Show |
7 | HG00280.hp1 HG02572.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.955-13159G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4389548 | |||||||
| chr3:4389599 | G | A | 6 | a0001c0001t0001g0047 a0001c0001t0001g0305 a0001c0001t0001g0368 others(3): Show |
6 | HG00280.hp1 HG02055.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.955-13210C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4389599 | |||||||
| chr3:4389603 | A | T | 163 | a0001c0001t0001g0042 a0001c0001t0001g0076 a0001c0001t0001g0109 others(160): Show |
169 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.955-13214T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4389603 | |||||||
| chr3:4389672 | C | T | 100 | a0001c0001t0001g0047 a0001c0001t0001g0076 a0001c0001t0001g0113 others(97): Show |
104 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.955-13283G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4389672 | |||||||
| chr3:4389720 | T | C | 2 | a0001c0001t0003g0188 a0001c0001t0004g0294 |
2 | HG00438.hp1 HG00621.hp2 |
intron_variant | MODIFIER | c.955-13331A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4389720 | |||||||
| chr3:4389721 | C | T | 1 | a0002c0003t0003g0027 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.955-13332G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4389721 | |||||||
| chr3:4389725 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.955-13336G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4389725 | |||||||
| chr3:4389732 | G | A | 14 | a0001c0001t0001g0042 a0001c0001t0001g0134 a0001c0001t0001g0368 others(11): Show |
14 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.955-13343C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4389732 | |||||||
| chr3:4389831 | T | C | 3 | a0001c0001t0008g0078 a0001c0001t0008g0314 a0002c0004t0001g0028 |
3 | HG00280.hp1 HG01192.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.955-13442A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4389831 | |||||||
| chr3:4389845 | C | A | 1 | a0001c0001t0003g0202 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.955-13456G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4389845 | |||||||
| chr3:4389963 | G | A | 2 | a0002c0004t0001g0025 a0002c0004t0001g0037 |
2 | HG01433.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.955-13574C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4389963 | |||||||
| chr3:4389991 | T | G | 1 | a0001c0001t0009g0300 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.955-13602A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4389991 | |||||||
| chr3:4390004 | G | A | 1 | a0001c0001t0002g0358 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.955-13615C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4390004 | |||||||
| chr3:4390138 | G | C | 1 | a0001c0001t0003g0202 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.955-13749C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4390138 | |||||||
| chr3:4390298 | T | C | 1 | a0001c0001t0018g0310 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.955-13909A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4390298 | |||||||
| chr3:4390349 | G | T | 117 | a0001c0001t0001g0076 a0001c0001t0001g0113 a0001c0001t0002g0005 others(114): Show |
120 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.955-13960C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4390349 | |||||||
| chr3:4390377 | C | A | 117 | a0001c0001t0001g0076 a0001c0001t0001g0113 a0001c0001t0002g0005 others(114): Show |
120 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.955-13988G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4390377 | |||||||
| chr3:4390423 | G | T | 2 | a0001c0001t0005g0182 a0001c0001t0005g0183 |
2 | HG00639.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.955-14034C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4390423 | |||||||
| chr3:4390432 | C | T | 112 | a0001c0001t0001g0076 a0001c0001t0001g0113 a0001c0001t0002g0005 others(109): Show |
115 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.955-14043G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4390432 | |||||||
| chr3:4390747 | T | A | 2 | a0001c0001t0001g0320 a0001c0001t0005g0265 |
2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.955-14358A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4390747 | |||||||
| chr3:4391178 | CTTG | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0134 a0001c0001t0001g0368 |
3 | HG02257.hp1 HG02572.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.955-14792_955-1479 others(7): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4391178 | |||||||
| chr3:4391185 | T | A | 1 | a0006c0008t0002g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.955-14796A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4391185 | |||||||
| chr3:4391236 | TTTTTTG | T | 22 | a0001c0001t0001g0306 a0001c0001t0002g0285 a0001c0001t0002g0287 others(19): Show |
22 | HG00544.hp2 HG00558.hp1 HG02615.hp1 others(19): Show |
intron_variant | MODIFIER | c.955-14853_955-1484 others(10): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4391236 | |||||||
| chr3:4391520 | G | T | 3 | a0001c0001t0001g0076 a0001c0001t0003g0094 a0002c0003t0001g0034 |
3 | HG02257.hp2 HG02280.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.955-15131C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4391520 | |||||||
| chr3:4391589 | C | G | 2 | a0001c0002t0001g0142 a0001c0002t0001g0164 |
2 | HG00738.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.955-15200G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4391589 | |||||||
| chr3:4391797 | G | A | 7 | a0001c0001t0006g0133 a0001c0001t0006g0184 a0001c0001t0006g0190 others(4): Show |
7 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.955-15408C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4391797 | |||||||
| chr3:4391831 | CT | C | 20 | a0001c0001t0001g0109 a0001c0001t0001g0306 a0001c0001t0003g0274 others(17): Show |
20 | HG01099.hp2 HG01891.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.955-15443delA | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4391831 | |||||||
| chr3:4391831 | CTT | C | 34 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0134 others(31): Show |
34 | HG00558.hp1 HG01175.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.955-15444_955-1544 others(6): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4391831 | |||||||
| chr3:4391831 | CTTT | C | 18 | a0001c0001t0002g0223 a0001c0001t0003g0011 a0001c0001t0003g0213 others(15): Show |
19 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.955-15445_955-1544 others(7): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4391831 | |||||||
| chr3:4391903 | C | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0134 a0001c0001t0001g0368 |
3 | HG02257.hp1 HG02572.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.955-15514G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4391903 | |||||||
| chr3:4392081 | G | C | 20 | a0001c0001t0002g0223 a0001c0001t0003g0011 a0001c0001t0003g0114 others(17): Show |
21 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.955-15692C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392081 | |||||||
| chr3:4392086 | C | T | 2 | a0001c0002t0001g0115 a0001c0002t0001g0116 |
2 | HG02015.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.955-15697G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392086 | |||||||
| chr3:4392164 | A | G | 5 | a0001c0001t0001g0305 a0001c0001t0004g0103 a0001c0001t0004g0304 others(2): Show |
5 | HG01243.hp2 HG03195.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.955-15775T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392164 | |||||||
| chr3:4392236 | C | T | 1 | a0001c0001t0003g0187 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.955-15847G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392236 | |||||||
| chr3:4392265 | C | A | 1 | a0001c0002t0001g0250 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.955-15876G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392265 | |||||||
| chr3:4392282 | A | G | 11 | a0001c0001t0002g0285 a0001c0001t0002g0287 a0001c0001t0002g0291 others(8): Show |
11 | HG00558.hp1 HG02630.hp1 HG03098.hp1 others(8): Show |
intron_variant | MODIFIER | c.955-15893T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392282 | |||||||
| chr3:4392294 | A | G | 1 | a0001c0001t0004g0348 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.955-15905T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392294 | |||||||
| chr3:4392315 | G | A | 60 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0134 others(57): Show |
61 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.955-15926C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392315 | |||||||
| chr3:4392593 | A | ATG | 60 | a0001c0001t0002g0009 a0001c0001t0002g0205 a0001c0001t0002g0211 others(57): Show |
62 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.955-16206_955-1620 others(6): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392593 | |||||||
| chr3:4392593 | A | ATGTG | 2 | a0001c0001t0002g0196 a0001c0001t0003g0004 |
3 | HG01516.hp1 HG01517.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.955-16208_955-1620 others(8): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392593 | |||||||
| chr3:4392593 | A | G | 2 | a0001c0001t0005g0049 a0001c0002t0001g0166 |
2 | HG01109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.955-16204T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392593 | |||||||
| chr3:4392594 | T | C | 1 | a0001c0001t0002g0277 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.955-16205A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392594 | |||||||
| chr3:4392611 | GTGTGTAT others(1): Show |
G | 3 | a0001c0001t0001g0042 a0001c0001t0001g0134 a0001c0001t0001g0368 |
3 | HG02257.hp1 HG02572.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.955-16230_955-1622 others(12): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392611 | |||||||
| chr3:4392611 | GTGTGTAT others(3): Show |
G | 2 | a0001c0001t0007g0057 a0001c0001t0007g0102 |
2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.955-16232_955-1622 others(14): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392611 | |||||||
| chr3:4392611 | GTGTGTAT others(5): Show |
G | 19 | a0001c0001t0002g0223 a0001c0001t0003g0011 a0001c0001t0003g0114 others(16): Show |
20 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.955-16234_955-1622 others(16): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392611 | |||||||
| chr3:4392613 | G | GTA | 5 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0005g0135 others(2): Show |
5 | HG02630.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.955-16225_955-1622 others(6): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392613 | |||||||
| chr3:4392613 | GTGTATA | G | 8 | a0001c0001t0001g0306 a0001c0001t0009g0065 a0001c0001t0009g0300 others(5): Show |
8 | HG02615.hp1 HG02886.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.955-16230_955-1622 others(10): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392613 | |||||||
| chr3:4392613 | GTGTATAT others(1): Show |
G | 23 | a0001c0001t0001g0047 a0001c0001t0001g0305 a0001c0001t0002g0285 others(20): Show |
23 | HG00558.hp1 HG01243.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.955-16232_955-1622 others(12): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392613 | |||||||
| chr3:4392613 | GTGTATAT others(3): Show |
G | 1 | a0001c0002t0001g0164 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.955-16234_955-1622 others(14): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392613 | |||||||
| chr3:4392615 | G | A | 12 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(9): Show |
12 | HG02055.hp1 HG02622.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.955-16226C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392615 | |||||||
| chr3:4392615 | G | GTA | 11 | a0001c0001t0001g0113 a0001c0001t0002g0098 a0001c0001t0003g0095 others(8): Show |
11 | HG00438.hp1 HG00639.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.955-16228_955-1622 others(6): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392615 | |||||||
| chr3:4392615 | G | GTGTA | 6 | a0001c0001t0002g0258 a0001c0001t0002g0259 a0001c0001t0005g0363 others(3): Show |
6 | HG02976.hp2 NA19060.hp2 NA19079.hp1 others(3): Show |
intron_variant | MODIFIER | c.955-16227_955-1622 others(8): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392615 | |||||||
| chr3:4392615 | GTA | G | 44 | a0001c0001t0002g0005 a0001c0001t0002g0046 a0001c0001t0002g0110 others(41): Show |
48 | HG00323.hp1 HG00621.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.955-16228_955-1622 others(6): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392615 | |||||||
| chr3:4392615 | GTATA | G | 4 | a0001c0001t0004g0103 a0001c0001t0004g0312 a0001c0002t0001g0167 others(1): Show |
4 | HG01496.hp2 HG03195.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.955-16230_955-1622 others(8): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392615 | |||||||
| chr3:4392615 | GTATATA | G | 10 | a0001c0001t0001g0076 a0001c0001t0003g0094 a0001c0001t0004g0128 others(7): Show |
10 | HG01243.hp2 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.955-16232_955-1622 others(10): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392615 | |||||||
| chr3:4392617 | A | G | 7 | a0001c0001t0002g0233 a0001c0001t0002g0366 a0001c0001t0003g0232 others(4): Show |
7 | HG02602.hp2 HG03017.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.955-16228T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392617 | |||||||
| chr3:4392619 | A | G | 2 | a0001c0001t0017g0298 a0001c0002t0001g0139 |
2 | HG01346.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.955-16230T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392619 | |||||||
| chr3:4392621 | A | G | 2 | a0001c0001t0004g0103 a0001c0002t0001g0167 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.955-16232T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392621 | |||||||
| chr3:4392623 | A | G | 1 | a0001c0001t0007g0297 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.955-16234T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392623 | |||||||
| chr3:4392637 | A | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0134 a0001c0001t0001g0368 |
3 | HG02257.hp1 HG02572.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.955-16248T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392637 | |||||||
| chr3:4392637 | ATATC | A | 59 | a0001c0001t0002g0149 a0001c0001t0002g0277 a0001c0001t0002g0322 others(56): Show |
59 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.955-16252_955-1624 others(8): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392637 | |||||||
| chr3:4392640 | T | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0134 a0001c0001t0001g0368 |
3 | HG02257.hp1 HG02572.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.955-16251A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392640 | |||||||
| chr3:4392641 | C | A | 2 | a0001c0001t0002g0192 a0001c0002t0001g0317 |
2 | HG01934.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.955-16252G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392641 | |||||||
| chr3:4392671 | C | A | 40 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0134 others(37): Show |
40 | HG00558.hp1 HG01243.hp1 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.955-16282G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392671 | |||||||
| chr3:4392725 | T | C | 1 | a0001c0002t0015g0130 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.955-16336A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392725 | |||||||
| chr3:4392731 | T | TTTTTG | 3 | a0003c0005t0005g0016 a0003c0005t0005g0017 a0003c0005t0005g0018 |
3 | HG02922.hp1 NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.955-16347_955-1634 others(9): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392731 | |||||||
| chr3:4392731 | TTTTTGTT others(3): Show |
T | 2 | a0001c0001t0004g0103 a0001c0002t0001g0167 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.955-16352_955-1634 others(14): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392731 | |||||||
| chr3:4392739 | C | T | 202 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0076 others(199): Show |
208 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.955-16350G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392739 | |||||||
| chr3:4392832 | A | T | 1 | a0001c0001t0002g0291 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.955-16443T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392832 | |||||||
| chr3:4392859 | A | AT | 42 | a0001c0001t0002g0005 a0001c0001t0002g0046 a0001c0001t0002g0110 others(39): Show |
46 | HG00323.hp1 HG00738.hp2 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.955-16471dupA | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392859 | |||||||
| chr3:4392889 | C | G | 1 | a0001c0002t0001g0150 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.955-16500G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392889 | |||||||
| chr3:4392908 | T | C | 1 | a0001c0002t0001g0157 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.955-16519A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4392908 | |||||||
| chr3:4393168 | G | A | 1 | a0001c0001t0002g0110 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.955-16779C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4393168 | |||||||
| chr3:4393209 | G | A | 1 | a0001c0001t0002g0189 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.955-16820C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4393209 | |||||||
| chr3:4393300 | G | C | 1 | a0001c0001t0021g0289 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.955-16911C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4393300 | |||||||
| chr3:4393367 | G | C | 62 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0134 others(59): Show |
63 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.955-16978C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4393367 | |||||||
| chr3:4393384 | A | G | 3 | a0001c0002t0001g0089 a0001c0002t0001g0194 a0001c0002t0001g0199 |
3 | HG01928.hp2 HG02293.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.955-16995T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4393384 | |||||||
| chr3:4393471 | T | C | 1 | a0001c0001t0003g0367 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.955-17082A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4393471 | |||||||
| chr3:4393738 | C | A | 10 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0055 others(7): Show |
10 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.954+17127G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4393738 | |||||||
| chr3:4393830 | G | A | 20 | a0001c0001t0002g0223 a0001c0001t0003g0011 a0001c0001t0003g0114 others(17): Show |
21 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.954+17035C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4393830 | |||||||
| chr3:4393892 | C | A | 13 | a0001c0001t0001g0047 a0001c0001t0005g0050 a0001c0001t0005g0051 others(10): Show |
13 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.954+16973G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4393892 | |||||||
| chr3:4394034 | A | C | 1 | a0001c0001t0002g0366 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.954+16831T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4394034 | |||||||
| chr3:4394406 | T | C | 23 | a0001c0001t0001g0042 a0001c0001t0001g0134 a0001c0001t0001g0368 others(20): Show |
24 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.954+16459A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4394406 | |||||||
| chr3:4394439 | TG | T | 3 | a0001c0001t0001g0076 a0001c0001t0003g0094 a0002c0003t0001g0034 |
3 | HG02257.hp2 HG02280.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.954+16425delC | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4394439 | |||||||
| chr3:4394452 | C | T | 1 | a0002c0003t0003g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.954+16413G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4394452 | |||||||
| chr3:4394488 | C | T | 59 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0134 others(56): Show |
60 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.954+16377G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4394488 | |||||||
| chr3:4394570 | T | C | 1 | a0001c0002t0001g0144 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.954+16295A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4394570 | |||||||
| chr3:4394590 | A | G | 8 | a0001c0001t0001g0306 a0001c0001t0009g0065 a0001c0001t0009g0300 others(5): Show |
8 | HG02615.hp1 HG02886.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.954+16275T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4394590 | |||||||
| chr3:4394711 | T | A | 2 | a0001c0001t0005g0056 a0001c0001t0005g0132 |
2 | HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.954+16154A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4394711 | |||||||
| chr3:4394719 | C | A | 4 | a0001c0001t0002g0110 a0001c0001t0002g0173 a0001c0001t0002g0189 others(1): Show |
4 | HG01106.hp2 HG01515.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.954+16146G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4394719 | |||||||
| chr3:4395030 | G | A | 39 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0002g0136 others(36): Show |
39 | HG00558.hp1 HG01175.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.954+15835C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4395030 | |||||||
| chr3:4395068 | C | T | 1 | a0001c0001t0005g0266 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.954+15797G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4395068 | |||||||
| chr3:4395081 | A | C | 2 | a0001c0001t0004g0103 a0001c0002t0001g0167 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.954+15784T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4395081 | |||||||
| chr3:4395233 | G | A | 8 | a0001c0001t0001g0306 a0001c0001t0009g0065 a0001c0001t0009g0300 others(5): Show |
8 | HG02615.hp1 HG02886.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.954+15632C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4395233 | |||||||
| chr3:4395351 | G | A | 1 | a0001c0001t0003g0271 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.954+15514C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4395351 | |||||||
| chr3:4395572 | G | A | 8 | a0001c0001t0001g0306 a0001c0001t0009g0065 a0001c0001t0009g0300 others(5): Show |
8 | HG02615.hp1 HG02886.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.954+15293C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4395572 | |||||||
| chr3:4395613 | C | T | 20 | a0001c0001t0002g0223 a0001c0001t0003g0011 a0001c0001t0003g0114 others(17): Show |
21 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.954+15252G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4395613 | |||||||
| chr3:4395674 | T | C | 137 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0076 others(134): Show |
139 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.954+15191A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4395674 | |||||||
| chr3:4395800 | T | C | 48 | a0001c0001t0001g0113 a0001c0001t0002g0005 a0001c0001t0002g0046 others(45): Show |
52 | HG00323.hp1 HG00558.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.954+15065A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4395800 | |||||||
| chr3:4396030 | G | C | 21 | a0001c0001t0001g0320 a0001c0001t0002g0063 a0001c0001t0002g0196 others(18): Show |
21 | HG02056.hp1 HG02145.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.954+14835C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4396030 | |||||||
| chr3:4396046 | T | C | 1 | a0001c0001t0002g0261 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.954+14819A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4396046 | |||||||
| chr3:4396135 | C | G | 1 | a0006c0008t0002g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.954+14730G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4396135 | |||||||
| chr3:4396515 | C | G | 2 | a0001c0001t0004g0103 a0001c0002t0001g0167 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.954+14350G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4396515 | |||||||
| chr3:4396557 | G | A | 1 | a0001c0002t0001g0082 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.954+14308C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4396557 | |||||||
| chr3:4396824 | T | A | 11 | a0001c0001t0001g0076 a0001c0001t0001g0109 a0001c0001t0003g0094 others(8): Show |
11 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.954+14041A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4396824 | |||||||
| chr3:4396841 | A | T | 4 | a0001c0001t0004g0128 a0001c0001t0005g0236 a0001c0001t0005g0266 others(1): Show |
4 | HG01891.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.954+14024T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4396841 | |||||||
| chr3:4397027 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.954+13838T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4397027 | |||||||
| chr3:4397151 | C | A | 1 | a0001c0001t0003g0175 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.954+13714G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4397151 | |||||||
| chr3:4397197 | G | A | 3 | a0001c0001t0001g0076 a0001c0001t0003g0094 a0002c0003t0001g0034 |
3 | HG02257.hp2 HG02280.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.954+13668C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4397197 | |||||||
| chr3:4397236 | T | G | 2 | a0001c0001t0001g0305 a0001c0001t0004g0304 |
2 | NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.954+13629A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4397236 | |||||||
| chr3:4397391 | G | A | 11 | a0001c0001t0001g0076 a0001c0001t0001g0109 a0001c0001t0003g0094 others(8): Show |
11 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.954+13474C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4397391 | |||||||
| chr3:4397598 | T | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0134 a0001c0001t0001g0368 |
3 | HG02257.hp1 HG02572.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.954+13267A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4397598 | |||||||
| chr3:4397613 | G | A | 1 | a0001c0001t0003g0117 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.954+13252C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4397613 | |||||||
| chr3:4397903 | T | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0134 a0001c0001t0001g0368 |
3 | HG02257.hp1 HG02572.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.954+12962A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4397903 | |||||||
| chr3:4398046 | T | C | 1 | a0001c0001t0002g0136 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.954+12819A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4398046 | |||||||
| chr3:4398189 | C | T | 1 | a0002c0003t0003g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.954+12676G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4398189 | |||||||
| chr3:4398200 | T | C | 1 | a0003c0005t0005g0013 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.954+12665A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4398200 | |||||||
| chr3:4398221 | G | A | 1 | a0001c0001t0003g0094 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.954+12644C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4398221 | |||||||
| chr3:4398358 | TATGCATA others(14): Show |
T | 2 | a0001c0001t0005g0043 a0001c0001t0007g0364 |
2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.954+12486_954+1250 others(25): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4398358 | |||||||
| chr3:4398448 | T | G | 3 | a0001c0001t0006g0131 a0001c0001t0006g0234 a0001c0001t0006g0303 |
3 | HG02615.hp2 HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.954+12417A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4398448 | |||||||
| chr3:4398498 | A | C | 1 | a0001c0001t0001g0042 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.954+12367T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4398498 | |||||||
| chr3:4398990 | C | T | 17 | a0001c0001t0001g0042 a0001c0001t0001g0076 a0001c0001t0001g0109 others(14): Show |
17 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.954+11875G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4398990 | |||||||
| chr3:4399047 | ATCT | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0134 a0001c0001t0001g0368 |
3 | HG02257.hp1 HG02572.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.954+11815_954+1181 others(7): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4399047 | |||||||
| chr3:4399090 | A | C | 1 | a0001c0001t0003g0268 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.954+11775T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4399090 | |||||||
| chr3:4399097 | G | A | 4 | a0001c0001t0001g0109 a0001c0001t0007g0059 a0001c0001t0007g0060 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.954+11768C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4399097 | |||||||
| chr3:4399105 | G | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0134 a0001c0001t0001g0368 |
3 | HG02257.hp1 HG02572.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.954+11760C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4399105 | |||||||
| chr3:4399206 | C | T | 8 | a0001c0001t0001g0306 a0001c0001t0009g0065 a0001c0001t0009g0300 others(5): Show |
8 | HG02615.hp1 HG02886.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.954+11659G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4399206 | |||||||
| chr3:4399285 | A | G | 1 | a0001c0001t0004g0112 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.954+11580T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4399285 | |||||||
| chr3:4399301 | C | T | 1 | a0001c0001t0017g0298 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.954+11564G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4399301 | |||||||
| chr3:4399391 | C | G | 1 | a0006c0008t0002g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.954+11474G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4399391 | |||||||
| chr3:4399399 | T | C | 1 | a0006c0008t0002g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.954+11466A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4399399 | |||||||
| chr3:4399736 | G | A | 5 | a0001c0001t0001g0058 a0001c0001t0004g0052 a0001c0001t0004g0129 others(2): Show |
5 | HG00323.hp2 HG02622.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.954+11129C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4399736 | |||||||
| chr3:4399803 | C | G | 371 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(368): Show |
383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.954+11062G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4399803 | |||||||
| chr3:4400051 | T | G | 14 | a0001c0001t0001g0047 a0001c0001t0005g0050 a0001c0001t0005g0051 others(11): Show |
14 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.954+10814A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4400051 | |||||||
| chr3:4400202 | G | A | 1 | a0001c0002t0001g0263 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.954+10663C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4400202 | |||||||
| chr3:4400378 | G | T | 4 | a0001c0001t0004g0128 a0001c0001t0005g0236 a0001c0001t0005g0266 others(1): Show |
4 | HG01891.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.954+10487C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4400378 | |||||||
| chr3:4400463 | T | A | 1 | a0003c0005t0005g0013 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.954+10402A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4400463 | |||||||
| chr3:4400579 | C | T | 4 | a0001c0001t0004g0128 a0001c0001t0005g0236 a0001c0001t0005g0266 others(1): Show |
4 | HG01891.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.954+10286G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4400579 | |||||||
| chr3:4400650 | G | A | 1 | a0001c0001t0005g0363 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.954+10215C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4400650 | |||||||
| chr3:4400783 | G | A | 36 | a0001c0001t0001g0047 a0001c0001t0001g0320 a0001c0001t0002g0063 others(33): Show |
36 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.954+10082C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4400783 | |||||||
| chr3:4400965 | T | TC | 19 | a0001c0001t0002g0223 a0001c0001t0003g0011 a0001c0001t0003g0114 others(16): Show |
21 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.954+9899dupG | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4400965 | |||||||
| chr3:4401002 | C | T | 4 | a0001c0001t0004g0128 a0001c0001t0005g0236 a0001c0001t0005g0266 others(1): Show |
4 | HG01891.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.954+9863G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4401002 | |||||||
| chr3:4401036 | C | T | 14 | a0001c0001t0001g0076 a0001c0001t0001g0109 a0001c0001t0003g0094 others(11): Show |
14 | HG01891.hp2 HG02257.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.954+9829G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4401036 | |||||||
| chr3:4401065 | T | C | 14 | a0001c0001t0001g0076 a0001c0001t0001g0109 a0001c0001t0003g0094 others(11): Show |
14 | HG01891.hp2 HG02257.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.954+9800A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4401065 | |||||||
| chr3:4401066 | C | T | 14 | a0001c0001t0001g0076 a0001c0001t0001g0109 a0001c0001t0003g0094 others(11): Show |
14 | HG01891.hp2 HG02257.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.954+9799G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4401066 | |||||||
| chr3:4401085 | A | C | 1 | a0001c0002t0001g0212 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.954+9780T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4401085 | |||||||
| chr3:4401180 | T | C | 8 | a0001c0001t0001g0306 a0001c0001t0009g0065 a0001c0001t0009g0300 others(5): Show |
8 | HG02615.hp1 HG02886.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.954+9685A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4401180 | |||||||
| chr3:4401204 | T | C | 17 | a0001c0001t0001g0042 a0001c0001t0001g0076 a0001c0001t0001g0109 others(14): Show |
17 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.954+9661A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4401204 | |||||||
| chr3:4401221 | A | G | 2 | a0001c0001t0005g0043 a0001c0001t0007g0364 |
2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.954+9644T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4401221 | |||||||
| chr3:4401312 | G | T | 1 | a0001c0001t0003g0079 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.954+9553C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4401312 | |||||||
| chr3:4401368 | T | C | 1 | a0001c0002t0001g0263 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.954+9497A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4401368 | |||||||
| chr3:4401444 | A | C | 35 | a0001c0001t0001g0076 a0001c0001t0001g0109 a0001c0001t0002g0223 others(32): Show |
37 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.954+9421T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4401444 | |||||||
| chr3:4401446 | A | T | 36 | a0001c0001t0001g0047 a0001c0001t0001g0320 a0001c0001t0002g0063 others(33): Show |
36 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.954+9419T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4401446 | |||||||
| chr3:4401490 | C | T | 21 | a0001c0001t0002g0223 a0001c0001t0003g0011 a0001c0001t0003g0114 others(18): Show |
23 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.954+9375G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4401490 | |||||||
| chr3:4401530 | G | A | 17 | a0001c0001t0001g0042 a0001c0001t0001g0076 a0001c0001t0001g0109 others(14): Show |
17 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.954+9335C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4401530 | |||||||
| chr3:4401545 | G | A | 1 | a0001c0001t0006g0372 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.954+9320C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4401545 | |||||||
| chr3:4401545 | G | T | 14 | a0001c0001t0001g0076 a0001c0001t0001g0109 a0001c0001t0003g0094 others(11): Show |
14 | HG01891.hp2 HG02257.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.954+9320C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4401545 | |||||||
| chr3:4401547 | G | A | 14 | a0001c0001t0001g0076 a0001c0001t0001g0109 a0001c0001t0003g0094 others(11): Show |
14 | HG01891.hp2 HG02257.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.954+9318C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4401547 | |||||||
| chr3:4401576 | C | T | 4 | a0001c0001t0004g0128 a0001c0001t0005g0236 a0001c0001t0005g0266 others(1): Show |
4 | HG01891.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.954+9289G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4401576 | |||||||
| chr3:4401655 | T | C | 77 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0069 others(74): Show |
80 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.954+9210A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4401655 | |||||||
| chr3:4401864 | G | A | 8 | a0001c0001t0001g0076 a0001c0001t0003g0094 a0001c0001t0004g0128 others(5): Show |
8 | HG01891.hp2 HG02257.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.954+9001C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4401864 | |||||||
| chr3:4401926 | G | C | 1 | a0001c0001t0007g0297 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.954+8939C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4401926 | |||||||
| chr3:4401969 | T | A | 14 | a0001c0001t0001g0076 a0001c0001t0001g0109 a0001c0001t0003g0094 others(11): Show |
14 | HG01891.hp2 HG02257.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.954+8896A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4401969 | |||||||
| chr3:4402082 | T | C | 2 | a0001c0001t0001g0320 a0001c0001t0005g0265 |
2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.954+8783A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4402082 | |||||||
| chr3:4402183 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0047 |
2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.954+8682A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4402183 | |||||||
| chr3:4402516 | T | C | 12 | a0001c0001t0001g0047 a0001c0001t0005g0370 a0001c0001t0006g0133 others(9): Show |
12 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.954+8349A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4402516 | |||||||
| chr3:4402522 | G | A | 1 | a0001c0002t0001g0169 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.954+8343C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4402522 | |||||||
| chr3:4402543 | G | C | 2 | a0001c0001t0004g0103 a0001c0002t0001g0167 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.954+8322C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4402543 | |||||||
| chr3:4402660 | C | T | 1 | a0001c0001t0002g0177 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.954+8205G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4402660 | |||||||
| chr3:4402756 | T | G | 1 | a0001c0002t0001g0219 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.954+8109A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4402756 | |||||||
| chr3:4403027 | T | C | 74 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0076 others(71): Show |
76 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.954+7838A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4403027 | |||||||
| chr3:4403036 | A | C | 6 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0005g0135 others(3): Show |
6 | HG02055.hp1 HG02630.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.954+7829T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4403036 | |||||||
| chr3:4403083 | C | T | 1 | a0001c0002t0001g0199 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.954+7782G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4403083 | |||||||
| chr3:4403105 | G | A | 12 | a0001c0001t0001g0076 a0001c0001t0001g0109 a0001c0001t0003g0094 others(9): Show |
12 | HG01891.hp2 HG02257.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.954+7760C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4403105 | |||||||
| chr3:4403232 | G | A | 2 | a0001c0001t0005g0043 a0001c0001t0007g0364 |
2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.954+7633C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4403232 | |||||||
| chr3:4403463 | T | C | 4 | a0001c0001t0004g0128 a0001c0001t0005g0236 a0001c0001t0005g0266 others(1): Show |
4 | HG01891.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.954+7402A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4403463 | |||||||
| chr3:4403660 | T | C | 2 | a0001c0001t0005g0043 a0001c0001t0007g0364 |
2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.954+7205A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4403660 | |||||||
| chr3:4403752 | C | T | 10 | a0001c0001t0001g0076 a0001c0001t0003g0094 a0001c0001t0004g0128 others(7): Show |
10 | HG01891.hp2 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.954+7113G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4403752 | |||||||
| chr3:4403899 | G | A | 2 | a0001c0001t0005g0043 a0001c0001t0007g0364 |
2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.954+6966C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4403899 | |||||||
| chr3:4403915 | C | T | 1 | a0001c0001t0008g0078 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.954+6950G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4403915 | |||||||
| chr3:4403965 | G | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0134 a0001c0001t0001g0368 |
3 | HG02257.hp1 HG02572.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.954+6900C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4403965 | |||||||
| chr3:4404024 | G | A | 10 | a0001c0001t0001g0076 a0001c0001t0003g0094 a0001c0001t0004g0128 others(7): Show |
10 | HG01891.hp2 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.954+6841C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4404024 | |||||||
| chr3:4404114 | C | T | 1 | a0001c0001t0019g0101 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.954+6751G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4404114 | |||||||
| chr3:4404336 | C | A | 8 | a0001c0001t0001g0076 a0001c0001t0003g0094 a0001c0001t0004g0128 others(5): Show |
8 | HG01891.hp2 HG02257.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.954+6529G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4404336 | |||||||
| chr3:4404385 | G | A | 10 | a0001c0001t0001g0076 a0001c0001t0003g0094 a0001c0001t0004g0128 others(7): Show |
10 | HG01891.hp2 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.954+6480C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4404385 | |||||||
| chr3:4404419 | T | C | 1 | a0001c0001t0003g0147 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.954+6446A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4404419 | |||||||
| chr3:4404482 | GTGCAGTG others(5): Show |
G | 20 | a0001c0001t0002g0223 a0001c0001t0003g0011 a0001c0001t0003g0114 others(17): Show |
22 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.954+6371_954+6382d others(14): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4404482 | |||||||
| chr3:4404569 | C | T | 1 | a0001c0002t0001g0237 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.954+6296G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4404569 | |||||||
| chr3:4404579 | G | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0134 a0001c0001t0001g0368 |
3 | HG02257.hp1 HG02572.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.954+6286C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4404579 | |||||||
| chr3:4404641 | G | A | 2 | a0001c0001t0001g0113 a0005c0007t0001g0019 |
2 | HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.954+6224C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4404641 | |||||||
| chr3:4404690 | G | A | 6 | a0001c0001t0002g0331 a0001c0001t0002g0332 a0001c0001t0002g0333 others(3): Show |
6 | HG01934.hp1 NA18960.hp1 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.954+6175C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4404690 | |||||||
| chr3:4404736 | T | C | 2 | a0001c0001t0001g0305 a0001c0001t0004g0304 |
2 | NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.954+6129A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4404736 | |||||||
| chr3:4404736 | T | G | 4 | a0001c0001t0001g0109 a0001c0001t0007g0059 a0001c0001t0007g0060 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.954+6129A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4404736 | |||||||
| chr3:4404917 | A | G | 1 | a0001c0002t0001g0194 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.954+5948T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4404917 | |||||||
| chr3:4404919 | T | C | 4 | a0001c0001t0004g0128 a0001c0001t0005g0236 a0001c0001t0005g0266 others(1): Show |
4 | HG01891.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.954+5946A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4404919 | |||||||
| chr3:4404966 | G | A | 1 | a0001c0001t0003g0137 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.954+5899C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4404966 | |||||||
| chr3:4405153 | T | A | 49 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0076 others(46): Show |
49 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(46): Show |
intron_variant | MODIFIER | c.954+5712A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4405153 | |||||||
| chr3:4405284 | G | T | 1 | a0001c0002t0001g0263 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.954+5581C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4405284 | |||||||
| chr3:4405438 | G | A | 1 | a0001c0001t0003g0147 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.954+5427C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4405438 | |||||||
| chr3:4405577 | G | A | 4 | a0001c0002t0001g0142 a0001c0002t0001g0164 a0002c0004t0001g0024 others(1): Show |
4 | HG00738.hp1 HG01099.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.954+5288C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4405577 | |||||||
| chr3:4405707 | A | T | 8 | a0001c0001t0001g0076 a0001c0001t0003g0094 a0001c0001t0004g0128 others(5): Show |
8 | HG01891.hp2 HG02257.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.954+5158T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4405707 | |||||||
| chr3:4405752 | C | T | 1 | a0001c0001t0004g0112 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.954+5113G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4405752 | |||||||
| chr3:4405788 | C | T | 1 | a0001c0002t0001g0355 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.954+5077G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4405788 | |||||||
| chr3:4405796 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.954+5069C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4405796 | |||||||
| chr3:4405936 | G | A | 20 | a0001c0001t0002g0223 a0001c0001t0003g0011 a0001c0001t0003g0114 others(17): Show |
22 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.954+4929C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4405936 | |||||||
| chr3:4406060 | G | T | 1 | a0001c0001t0003g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.954+4805C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4406060 | |||||||
| chr3:4406131 | A | T | 1 | a0001c0002t0001g0275 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.954+4734T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4406131 | |||||||
| chr3:4406163 | A | G | 4 | a0001c0001t0001g0113 a0001c0001t0005g0363 a0001c0001t0010g0321 others(1): Show |
4 | HG02559.hp2 HG02976.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.954+4702T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4406163 | |||||||
| chr3:4406235 | C | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0134 |
2 | HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.954+4630G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4406235 | |||||||
| chr3:4406277 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0134 |
2 | HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.954+4588A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4406277 | |||||||
| chr3:4406324 | G | A | 14 | a0001c0001t0001g0076 a0001c0001t0001g0109 a0001c0001t0003g0094 others(11): Show |
14 | HG01891.hp2 HG02257.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.954+4541C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4406324 | |||||||
| chr3:4406345 | T | A | 53 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0076 others(50): Show |
53 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(50): Show |
intron_variant | MODIFIER | c.954+4520A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4406345 | |||||||
| chr3:4406386 | T | C | 4 | a0001c0001t0001g0109 a0001c0001t0007g0059 a0001c0001t0007g0060 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.954+4479A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4406386 | |||||||
| chr3:4406529 | G | A | 1 | a0001c0001t0003g0222 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.954+4336C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4406529 | |||||||
| chr3:4406577 | C | T | 145 | a0001c0001t0001g0076 a0001c0001t0001g0109 a0001c0001t0001g0113 others(142): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.954+4288G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4406577 | |||||||
| chr3:4406678 | C | A | 1 | a0001c0001t0002g0330 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.954+4187G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4406678 | |||||||
| chr3:4406683 | A | G | 3 | a0001c0001t0001g0305 a0001c0001t0004g0304 a0001c0001t0007g0297 |
3 | HG01243.hp2 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.954+4182T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4406683 | |||||||
| chr3:4406730 | A | G | 1 | a0001c0002t0001g0311 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.954+4135T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4406730 | |||||||
| chr3:4406743 | C | T | 1 | a0001c0001t0006g0372 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.954+4122G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4406743 | |||||||
| chr3:4406782 | C | T | 1 | a0001c0001t0002g0192 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.954+4083G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4406782 | |||||||
| chr3:4406977 | T | C | 1 | a0001c0001t0003g0274 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.954+3888A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4406977 | |||||||
| chr3:4407085 | G | GAC | 46 | a0001c0001t0001g0109 a0001c0001t0001g0305 a0001c0001t0002g0009 others(43): Show |
47 | HG00639.hp2 HG01243.hp1 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.954+3778_954+3779d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4407085 | |||||||
| chr3:4407085 | G | GACAC | 5 | a0001c0001t0001g0047 a0001c0001t0001g0076 a0001c0001t0003g0274 others(2): Show |
5 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.954+3776_954+3779d others(6): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4407085 | |||||||
| chr3:4407085 | G | GACACACA others(3): Show |
3 | a0001c0001t0002g0063 a0001c0001t0005g0075 a0001c0001t0005g0373 |
3 | HG02145.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.954+3770_954+3779d others(12): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4407085 | |||||||
| chr3:4407085 | G | GACACACA others(7): Show |
1 | a0001c0001t0005g0067 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.954+3766_954+3779d others(16): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4407085 | |||||||
| chr3:4407085 | GAC | G | 127 | a0001c0001t0001g0042 a0001c0001t0001g0113 a0001c0001t0001g0134 others(124): Show |
131 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.954+3778_954+3779d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4407085 | |||||||
| chr3:4407085 | GACAC | G | 5 | a0001c0001t0002g0173 a0001c0001t0002g0189 a0001c0001t0003g0010 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.954+3776_954+3779d others(6): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4407085 | |||||||
| chr3:4407085 | GACACACA others(3): Show |
G | 1 | a0001c0001t0003g0329 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.954+3770_954+3779d others(12): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4407085 | |||||||
| chr3:4407140 | C | A | 53 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0076 others(50): Show |
53 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(50): Show |
intron_variant | MODIFIER | c.954+3725G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4407140 | |||||||
| chr3:4407228 | A | G | 3 | a0001c0001t0001g0042 a0001c0001t0001g0134 a0001c0001t0001g0368 |
3 | HG02257.hp1 HG02572.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.954+3637T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4407228 | |||||||
| chr3:4407309 | A | G | 1 | a0001c0002t0001g0262 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.954+3556T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4407309 | |||||||
| chr3:4407464 | C | T | 14 | a0001c0001t0001g0076 a0001c0001t0001g0109 a0001c0001t0003g0094 others(11): Show |
14 | HG01891.hp2 HG02257.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.954+3401G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4407464 | |||||||
| chr3:4407465 | G | A | 23 | a0001c0001t0001g0306 a0001c0001t0002g0012 a0001c0001t0002g0285 others(20): Show |
24 | HG00558.hp1 HG02615.hp1 HG02630.hp1 others(21): Show |
intron_variant | MODIFIER | c.954+3400C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4407465 | |||||||
| chr3:4407539 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0134 a0001c0001t0001g0368 |
3 | HG02257.hp1 HG02572.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.954+3326G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4407539 | |||||||
| chr3:4407851 | G | T | 2 | a0001c0001t0007g0059 a0001c0001t0007g0060 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.954+3014C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4407851 | |||||||
| chr3:4407903 | C | T | 24 | a0001c0001t0001g0320 a0001c0001t0002g0063 a0001c0001t0002g0196 others(21): Show |
24 | HG01891.hp1 HG02056.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.954+2962G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4407903 | |||||||
| chr3:4408004 | T | A | 1 | a0001c0001t0006g0371 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.954+2861A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4408004 | |||||||
| chr3:4408112 | C | T | 1 | a0001c0001t0005g0132 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.954+2753G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4408112 | |||||||
| chr3:4408378 | T | C | 65 | a0001c0001t0001g0113 a0001c0001t0002g0005 a0001c0001t0002g0046 others(62): Show |
68 | HG00323.hp1 HG00558.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.954+2487A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4408378 | |||||||
| chr3:4408501 | T | C | 1 | a0001c0002t0001g0311 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.954+2364A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4408501 | |||||||
| chr3:4408527 | C | T | 1 | a0001c0002t0001g0210 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.954+2338G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4408527 | |||||||
| chr3:4408606 | T | C | 1 | a0001c0002t0001g0350 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.954+2259A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4408606 | |||||||
| chr3:4408616 | C | T | 1 | a0001c0001t0002g0349 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.954+2249G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4408616 | |||||||
| chr3:4408664 | C | T | 4 | a0001c0001t0002g0110 a0001c0001t0002g0173 a0001c0001t0002g0189 others(1): Show |
4 | HG01106.hp2 HG01515.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.954+2201G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4408664 | |||||||
| chr3:4408722 | G | A | 2 | a0001c0001t0004g0251 a0001c0002t0001g0180 |
2 | HG01175.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.954+2143C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4408722 | |||||||
| chr3:4408765 | G | C | 2 | a0001c0001t0002g0009 a0001c0001t0002g0273 |
3 | NA18939.hp2 NA18959.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.954+2100C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4408765 | |||||||
| chr3:4408952 | A | G | 2 | a0001c0001t0004g0103 a0001c0002t0001g0167 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.954+1913T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4408952 | |||||||
| chr3:4409012 | T | A | 1 | a0001c0001t0002g0345 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.954+1853A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4409012 | |||||||
| chr3:4409343 | G | A | 2 | a0001c0002t0001g0255 a0001c0002t0001g0256 |
2 | NA18989.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.954+1522C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4409343 | |||||||
| chr3:4409394 | T | A | 3 | a0001c0001t0006g0131 a0001c0001t0006g0234 a0001c0001t0006g0303 |
3 | HG02615.hp2 HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.954+1471A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4409394 | |||||||
| chr3:4409406 | T | C | 4 | a0001c0001t0001g0109 a0001c0001t0007g0059 a0001c0001t0007g0060 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.954+1459A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4409406 | |||||||
| chr3:4409557 | A | G | 1 | a0006c0008t0002g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.954+1308T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4409557 | |||||||
| chr3:4409598 | G | A | 1 | a0001c0001t0003g0175 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.954+1267C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4409598 | |||||||
| chr3:4409626 | G | A | 10 | a0001c0001t0001g0076 a0001c0001t0003g0094 a0001c0001t0004g0128 others(7): Show |
10 | HG01891.hp2 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.954+1239C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4409626 | |||||||
| chr3:4409736 | G | A | 88 | a0001c0001t0001g0058 a0001c0001t0002g0003 a0001c0001t0002g0008 others(85): Show |
91 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.954+1129C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4409736 | |||||||
| chr3:4409743 | C | T | 1 | a0001c0001t0007g0297 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.954+1122G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4409743 | |||||||
| chr3:4409865 | T | C | 15 | a0001c0001t0001g0320 a0001c0001t0002g0063 a0001c0001t0005g0050 others(12): Show |
15 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.954+1000A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4409865 | |||||||
| chr3:4409892 | CTCAGGCA others(7): Show |
C | 1 | a0001c0001t0004g0328 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.954+959_954+972del others(14): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4409892 | |||||||
| chr3:4409932 | T | C | 8 | a0001c0001t0005g0370 a0001c0001t0006g0133 a0001c0001t0006g0184 others(5): Show |
8 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.954+933A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4409932 | |||||||
| chr3:4410000 | T | C | 1 | a0001c0002t0001g0007 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.954+865A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4410000 | |||||||
| chr3:4410193 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.954+672A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4410193 | |||||||
| chr3:4410310 | T | C | 40 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0076 others(37): Show |
42 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.954+555A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4410310 | |||||||
| chr3:4410323 | T | C | 1 | a0001c0001t0002g0260 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.954+542A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4410323 | |||||||
| chr3:4410573 | A | C | 4 | a0001c0001t0001g0109 a0001c0001t0007g0059 a0001c0001t0007g0060 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.954+292T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4410573 | |||||||
| chr3:4410618 | T | C | 2 | a0001c0001t0004g0103 a0001c0002t0001g0167 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.954+247A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4410618 | |||||||
| chr3:4410754 | A | G | 4 | a0001c0001t0001g0058 a0001c0001t0004g0052 a0001c0001t0004g0129 others(1): Show |
4 | HG02622.hp1 HG02809.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.954+111T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 7/8 | chr3 | 4410754 | |||||||
| chr3:4410992 | C | T | 4 | a0001c0001t0004g0128 a0001c0001t0005g0236 a0001c0001t0005g0266 others(1): Show |
4 | HG01891.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.841-14G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4410992 | |||||||
| chr3:4411053 | G | A | 186 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0076 others(183): Show |
191 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.841-75C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4411053 | |||||||
| chr3:4411071 | G | T | 1 | a0001c0001t0002g0358 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.841-93C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4411071 | |||||||
| chr3:4411255 | C | A | 4 | a0001c0001t0001g0076 a0001c0001t0003g0094 a0001c0001t0018g0310 others(1): Show |
4 | HG02257.hp2 HG02280.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.841-277G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4411255 | |||||||
| chr3:4411393 | A | G | 1 | a0001c0001t0003g0117 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.841-415T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4411393 | |||||||
| chr3:4411438 | C | G | 48 | a0001c0001t0002g0149 a0001c0001t0002g0277 a0001c0001t0002g0322 others(45): Show |
48 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.841-460G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4411438 | |||||||
| chr3:4411518 | A | T | 14 | a0001c0001t0002g0285 a0001c0001t0002g0287 a0001c0001t0002g0291 others(11): Show |
14 | HG02109.hp2 HG02559.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.841-540T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4411518 | |||||||
| chr3:4411705 | G | GA | 61 | a0001c0001t0001g0047 a0001c0001t0001g0320 a0001c0001t0001g0368 others(58): Show |
63 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.841-728dupT | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4411705 | |||||||
| chr3:4411705 | G | GAAA | 8 | a0001c0001t0001g0076 a0001c0001t0001g0109 a0001c0001t0003g0094 others(5): Show |
8 | HG02257.hp2 HG02280.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.841-730_841-728dup others(3): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4411705 | |||||||
| chr3:4411705 | GA | G | 8 | a0001c0001t0002g0270 a0001c0001t0004g0128 a0001c0001t0004g0304 others(5): Show |
9 | HG01070.hp1 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.841-728delT | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4411705 | |||||||
| chr3:4411873 | G | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0134 a0001c0001t0001g0368 |
3 | HG02257.hp1 HG02572.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.841-895C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4411873 | |||||||
| chr3:4412037 | T | C | 1 | a0001c0001t0005g0050 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.841-1059A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4412037 | |||||||
| chr3:4412308 | G | A | 1 | a0001c0001t0006g0131 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.841-1330C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4412308 | |||||||
| chr3:4412436 | C | T | 1 | a0001c0001t0004g0293 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.841-1458G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4412436 | |||||||
| chr3:4412612 | C | G | 30 | a0001c0001t0001g0076 a0001c0001t0001g0109 a0001c0001t0002g0223 others(27): Show |
32 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.841-1634G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4412612 | |||||||
| chr3:4412643 | G | A | 2 | a0001c0001t0004g0103 a0001c0002t0001g0167 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.841-1665C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4412643 | |||||||
| chr3:4412689 | G | A | 3 | a0001c0001t0001g0320 a0001c0001t0005g0074 a0001c0001t0005g0265 |
3 | HG02486.hp2 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.841-1711C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4412689 | |||||||
| chr3:4412701 | T | C | 5 | a0001c0001t0003g0006 a0001c0001t0003g0217 a0001c0001t0003g0226 others(2): Show |
6 | NA18953.hp1 NA18960.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.841-1723A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4412701 | |||||||
| chr3:4412753 | C | T | 22 | a0001c0001t0002g0223 a0001c0001t0003g0011 a0001c0001t0003g0114 others(19): Show |
24 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.841-1775G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4412753 | |||||||
| chr3:4412950 | T | C | 8 | a0001c0001t0001g0076 a0001c0001t0001g0109 a0001c0001t0003g0094 others(5): Show |
8 | HG02257.hp2 HG02280.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.841-1972A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4412950 | |||||||
| chr3:4413018 | T | G | 1 | a0001c0001t0003g0187 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.841-2040A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4413018 | |||||||
| chr3:4413130 | G | A | 20 | a0001c0001t0002g0223 a0001c0001t0003g0011 a0001c0001t0003g0114 others(17): Show |
22 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.841-2152C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4413130 | |||||||
| chr3:4413157 | A | C | 1 | a0001c0001t0004g0195 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.841-2179T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4413157 | |||||||
| chr3:4413165 | C | T | 34 | a0001c0001t0001g0042 a0001c0001t0001g0320 a0001c0001t0002g0063 others(31): Show |
34 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.841-2187G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4413165 | |||||||
| chr3:4413365 | G | C | 12 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0305 others(9): Show |
12 | HG01891.hp2 HG02055.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.841-2387C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4413365 | |||||||
| chr3:4413534 | C | T | 8 | a0001c0001t0005g0370 a0001c0001t0006g0133 a0001c0001t0006g0184 others(5): Show |
8 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.841-2556G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4413534 | |||||||
| chr3:4413614 | C | G | 1 | a0001c0001t0011g0379 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.841-2636G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4413614 | |||||||
| chr3:4413632 | C | G | 2 | a0001c0001t0001g0305 a0001c0001t0004g0304 |
2 | NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.841-2654G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4413632 | |||||||
| chr3:4413703 | C | T | 1 | a0001c0001t0007g0364 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.841-2725G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4413703 | |||||||
| chr3:4413708 | T | C | 4 | a0001c0001t0004g0128 a0001c0001t0005g0236 a0001c0001t0005g0266 others(1): Show |
4 | HG01891.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.841-2730A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4413708 | |||||||
| chr3:4413745 | G | C | 2 | a0001c0001t0002g0258 a0001c0001t0002g0259 |
2 | NA19060.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.841-2767C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4413745 | |||||||
| chr3:4413873 | T | A | 1 | a0001c0001t0001g0047 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.841-2895A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4413873 | |||||||
| chr3:4413886 | T | C | 22 | a0001c0001t0002g0223 a0001c0001t0003g0011 a0001c0001t0003g0114 others(19): Show |
24 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.841-2908A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4413886 | |||||||
| chr3:4413943 | A | T | 15 | a0001c0001t0002g0223 a0001c0001t0003g0011 a0001c0001t0003g0114 others(12): Show |
16 | HG00140.hp1 HG00323.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.841-2965T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4413943 | |||||||
| chr3:4413989 | G | C | 22 | a0001c0001t0002g0223 a0001c0001t0003g0011 a0001c0001t0003g0114 others(19): Show |
24 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.841-3011C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4413989 | |||||||
| chr3:4414025 | G | A | 1 | a0001c0001t0002g0333 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.841-3047C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4414025 | |||||||
| chr3:4414192 | A | G | 7 | a0001c0001t0002g0220 a0001c0001t0002g0243 a0001c0001t0004g0295 others(4): Show |
7 | HG02015.hp1 HG02040.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.840+2936T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4414192 | |||||||
| chr3:4414349 | C | A | 1 | a0001c0002t0001g0248 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.840+2779G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4414349 | |||||||
| chr3:4414365 | A | G | 1 | a0001c0001t0003g0232 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.840+2763T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4414365 | |||||||
| chr3:4414371 | T | A | 4 | a0001c0001t0001g0109 a0001c0001t0007g0059 a0001c0001t0007g0060 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+2757A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4414371 | |||||||
| chr3:4414488 | C | T | 1 | a0001c0001t0003g0095 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.840+2640G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4414488 | |||||||
| chr3:4414501 | G | T | 198 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0113 others(195): Show |
204 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.840+2627C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4414501 | |||||||
| chr3:4414504 | A | G | 2 | a0001c0001t0001g0134 a0001c0001t0001g0368 |
2 | HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.840+2624T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4414504 | |||||||
| chr3:4414526 | A | T | 2 | a0001c0001t0002g0336 a0001c0001t0002g0347 |
2 | NA18960.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.840+2602T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4414526 | |||||||
| chr3:4414567 | G | T | 1 | a0001c0002t0015g0130 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.840+2561C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4414567 | |||||||
| chr3:4414624 | G | C | 4 | a0001c0001t0004g0128 a0001c0001t0005g0236 a0001c0001t0005g0266 others(1): Show |
4 | HG01891.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.840+2504C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4414624 | |||||||
| chr3:4414939 | G | C | 1 | a0001c0001t0003g0122 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.840+2189C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4414939 | |||||||
| chr3:4415017 | G | C | 2 | a0001c0001t0005g0043 a0001c0001t0007g0364 |
2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.840+2111C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4415017 | |||||||
| chr3:4415055 | T | C | 3 | a0001c0001t0002g0178 a0001c0002t0001g0007 a0001c0002t0001g0276 |
4 | HG00323.hp1 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+2073A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4415055 | |||||||
| chr3:4415107 | A | G | 2 | a0001c0001t0005g0043 a0001c0001t0007g0364 |
2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.840+2021T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4415107 | |||||||
| chr3:4415146 | G | C | 4 | a0001c0001t0001g0109 a0001c0001t0007g0059 a0001c0001t0007g0060 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+1982C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4415146 | |||||||
| chr3:4415159 | G | A | 2 | a0001c0001t0003g0335 a0001c0001t0004g0086 |
2 | HG01978.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.840+1969C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4415159 | |||||||
| chr3:4415226 | C | CA | 31 | a0001c0001t0001g0047 a0001c0001t0001g0109 a0001c0001t0002g0063 others(28): Show |
31 | HG01243.hp1 HG01891.hp1 HG01934.hp2 others(28): Show |
intron_variant | MODIFIER | c.840+1901dupT | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4415226 | |||||||
| chr3:4415226 | C | CAA | 14 | a0001c0001t0001g0042 a0001c0001t0001g0320 a0001c0001t0002g0196 others(11): Show |
14 | HG02056.hp1 HG02145.hp1 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.840+1900_840+1901d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4415226 | |||||||
| chr3:4415226 | CA | C | 35 | a0001c0001t0001g0076 a0001c0001t0001g0134 a0001c0001t0001g0305 others(32): Show |
37 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.840+1901delT | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4415226 | |||||||
| chr3:4415293 | G | A | 1 | a0002c0003t0003g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.840+1835C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4415293 | |||||||
| chr3:4415425 | G | A | 2 | a0001c0002t0001g0255 a0001c0002t0001g0256 |
2 | NA18989.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.840+1703C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4415425 | |||||||
| chr3:4415439 | C | T | 4 | a0001c0001t0004g0128 a0001c0001t0005g0236 a0001c0001t0005g0266 others(1): Show |
4 | HG01891.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.840+1689G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4415439 | |||||||
| chr3:4415463 | GA | G | 44 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0076 others(41): Show |
44 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(41): Show |
intron_variant | MODIFIER | c.840+1664delT | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4415463 | |||||||
| chr3:4415695 | C | G | 2 | a0001c0001t0001g0305 a0001c0001t0004g0304 |
2 | NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.840+1433G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4415695 | |||||||
| chr3:4415933 | C | T | 2 | a0001c0001t0001g0113 a0005c0007t0001g0019 |
2 | HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.840+1195G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4415933 | |||||||
| chr3:4416314 | C | A | 4 | a0001c0001t0001g0109 a0001c0001t0007g0059 a0001c0001t0007g0060 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+814G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4416314 | |||||||
| chr3:4416416 | A | C | 2 | a0001c0001t0004g0103 a0001c0002t0001g0167 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.840+712T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4416416 | |||||||
| chr3:4416525 | T | C | 2 | a0001c0001t0002g0281 a0001c0001t0002g0282 |
2 | NA18999.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.840+603A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4416525 | |||||||
| chr3:4416567 | T | C | 32 | a0001c0001t0001g0076 a0001c0001t0001g0109 a0001c0001t0001g0134 others(29): Show |
34 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.840+561A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4416567 | |||||||
| chr3:4416736 | GGC | G | 185 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0076 others(182): Show |
190 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.840+390_840+391del others(2): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4416736 | |||||||
| chr3:4416759 | C | T | 1 | a0001c0002t0001g0342 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.840+369G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4416759 | |||||||
| chr3:4416995 | C | A | 2 | a0001c0001t0001g0305 a0001c0001t0004g0304 |
2 | NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.840+133G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4416995 | |||||||
| chr3:4417071 | A | C | 2 | a0001c0001t0006g0184 a0001c0001t0006g0190 |
2 | HG01243.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.840+57T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 6/8 | chr3 | 4417071 | |||||||
| chr3:4417543 | T | C | 1 | a0001c0002t0001g0169 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.726-301A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 5/8 | chr3 | 4417543 | |||||||
| chr3:4417757 | C | G | 8 | a0001c0001t0002g0220 a0001c0001t0002g0243 a0001c0001t0004g0295 others(5): Show |
8 | HG01943.hp2 HG02015.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.725+253G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 5/8 | chr3 | 4417757 | |||||||
| chr3:4417802 | C | T | 11 | a0001c0001t0001g0320 a0001c0001t0002g0196 a0001c0001t0002g0296 others(8): Show |
11 | HG02056.hp1 HG02523.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.725+208G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 5/8 | chr3 | 4417802 | |||||||
| chr3:4417859 | T | C | 1 | a0001c0001t0004g0125 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.725+151A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 5/8 | chr3 | 4417859 | |||||||
| chr3:4417905 | C | T | 2 | a0001c0001t0005g0043 a0001c0001t0007g0364 |
2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.725+105G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 5/8 | chr3 | 4417905 | |||||||
| chr3:4417969 | T | C | 1 | a0001c0001t0004g0129 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.725+41A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 5/8 | chr3 | 4417969 | |||||||
| chr3:4417996 | G | A | 1 | a0001c0001t0004g0290 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.725+14C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 5/8 | chr3 | 4417996 | |||||||
| chr3:4418189 | G | A | 1 | a0001c0001t0007g0297 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.603-57C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 4/8 | chr3 | 4418189 | |||||||
| chr3:4418206 | G | A | 1 | a0001c0001t0010g0321 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.603-74C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 4/8 | chr3 | 4418206 | |||||||
| chr3:4418235 | A | G | 2 | a0001c0001t0003g0188 a0001c0002t0001g0248 |
2 | HG00438.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.603-103T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 4/8 | chr3 | 4418235 | |||||||
| chr3:4418288 | A | G | 346 | a0001c0001t0001g0042 a0001c0001t0001g0053 a0001c0001t0001g0054 others(343): Show |
358 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.603-156T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 4/8 | chr3 | 4418288 | |||||||
| chr3:4418382 | C | T | 1 | a0001c0001t0003g0004 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.603-250G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 4/8 | chr3 | 4418382 | |||||||
| chr3:4418436 | A | G | 4 | a0001c0001t0001g0305 a0001c0001t0004g0304 a0001c0001t0010g0321 others(1): Show |
4 | HG02257.hp2 HG02559.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.603-304T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 4/8 | chr3 | 4418436 | |||||||
| chr3:4418457 | C | T | 6 | a0001c0001t0001g0134 a0001c0001t0001g0368 a0001c0001t0005g0043 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.603-325G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 4/8 | chr3 | 4418457 | |||||||
| chr3:4418533 | C | A | 1 | a0001c0002t0001g0311 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.603-401G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 4/8 | chr3 | 4418533 | |||||||
| chr3:4418971 | C | G | 1 | a0001c0002t0001g0311 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.603-839G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 4/8 | chr3 | 4418971 | |||||||
| chr3:4418999 | T | A | 5 | a0001c0001t0003g0202 a0001c0001t0003g0222 a0001c0001t0008g0221 others(2): Show |
5 | HG01099.hp2 HG01257.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.603-867A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 4/8 | chr3 | 4418999 | |||||||
| chr3:4419251 | G | A | 3 | a0001c0001t0001g0076 a0001c0001t0006g0303 a0001c0001t0018g0310 |
3 | HG02280.hp1 HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.602+813C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 4/8 | chr3 | 4419251 | |||||||
| chr3:4419333 | T | C | 1 | a0001c0002t0001g0311 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.602+731A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 4/8 | chr3 | 4419333 | |||||||
| chr3:4419640 | C | T | 50 | a0001c0001t0001g0305 a0001c0001t0002g0149 a0001c0001t0002g0252 others(47): Show |
50 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.602+424G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 4/8 | chr3 | 4419640 | |||||||
| chr3:4419694 | A | G | 2 | a0001c0001t0001g0076 a0001c0001t0018g0310 |
2 | HG02280.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.602+370T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 4/8 | chr3 | 4419694 | |||||||
| chr3:4419885 | G | A | 283 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(280): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.602+179C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 4/8 | chr3 | 4419885 | |||||||
| chr3:4419946 | C | T | 4 | a0001c0001t0005g0182 a0001c0001t0005g0183 a0001c0001t0005g0236 others(1): Show |
4 | HG00639.hp2 HG01981.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.602+118G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 4/8 | chr3 | 4419946 | |||||||
| chr3:4420014 | C | T | 338 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(335): Show |
350 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.602+50G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 4/8 | chr3 | 4420014 | |||||||
| chr3:4420051 | G | A | 21 | a0001c0001t0002g0189 a0001c0001t0002g0281 a0001c0001t0002g0282 others(18): Show |
21 | HG00639.hp2 HG01981.hp1 HG02965.hp2 others(18): Show |
intron_variant | MODIFIER | c.602+13C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 4/8 | chr3 | 4420051 | |||||||
| chr3:4420173 | G | A | 3 | a0001c0001t0002g0003 a0001c0001t0002g0098 a0001c0001t0002g0354 |
4 | NA18971.hp1 NA19009.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-27C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4420173 | |||||||
| chr3:4420176 | A | C | 1 | a0001c0001t0002g0340 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.520-30T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4420176 | |||||||
| chr3:4420185 | C | CATCAACT others(10): Show |
3 | a0001c0001t0001g0305 a0001c0001t0001g0368 a0001c0001t0004g0304 |
3 | HG02572.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.520-56_520-40dupAT others(15): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4420185 | |||||||
| chr3:4420233 | A | G | 2 | a0001c0001t0001g0076 a0001c0001t0018g0310 |
2 | HG02280.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.520-87T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4420233 | |||||||
| chr3:4420397 | A | AT | 140 | a0001c0001t0001g0058 a0001c0001t0001g0109 a0001c0001t0001g0113 others(137): Show |
146 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.520-252dupA | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4420397 | |||||||
| chr3:4420397 | A | ATT | 193 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0002g0003 others(190): Show |
199 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.520-253_520-252dup others(2): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4420397 | |||||||
| chr3:4420433 | T | C | 1 | a0001c0002t0001g0216 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.520-287A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4420433 | |||||||
| chr3:4420522 | G | C | 2 | a0001c0001t0001g0076 a0001c0001t0018g0310 |
2 | HG02280.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.520-376C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4420522 | |||||||
| chr3:4420528 | C | T | 3 | a0001c0001t0001g0305 a0001c0001t0001g0368 a0001c0001t0004g0304 |
3 | HG02572.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.520-382G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4420528 | |||||||
| chr3:4420543 | C | T | 1 | a0001c0001t0006g0372 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.520-397G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4420543 | |||||||
| chr3:4420560 | C | A | 3 | a0001c0001t0001g0305 a0001c0001t0001g0368 a0001c0001t0004g0304 |
3 | HG02572.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.520-414G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4420560 | |||||||
| chr3:4420561 | G | A | 1 | a0001c0001t0002g0220 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.520-415C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4420561 | |||||||
| chr3:4420597 | T | C | 3 | a0001c0001t0003g0108 a0001c0001t0003g0148 a0001c0002t0001g0140 |
3 | HG02602.hp2 NA18942.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.520-451A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4420597 | |||||||
| chr3:4420598 | C | G | 3 | a0001c0001t0003g0108 a0001c0001t0003g0148 a0001c0002t0001g0140 |
3 | HG02602.hp2 NA18942.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.520-452G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4420598 | |||||||
| chr3:4420618 | G | A | 2 | a0001c0001t0001g0305 a0001c0001t0004g0304 |
2 | NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.520-472C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4420618 | |||||||
| chr3:4420686 | A | G | 377 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(374): Show |
389 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.520-540T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4420686 | |||||||
| chr3:4420743 | C | G | 3 | a0001c0001t0001g0305 a0001c0001t0001g0368 a0001c0001t0004g0304 |
3 | HG02572.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.520-597G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4420743 | |||||||
| chr3:4420776 | T | C | 1 | a0001c0001t0004g0128 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.520-630A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4420776 | |||||||
| chr3:4420860 | C | T | 25 | a0001c0001t0002g0223 a0001c0001t0003g0011 a0001c0001t0004g0103 others(22): Show |
27 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.520-714G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4420860 | |||||||
| chr3:4420897 | C | T | 11 | a0001c0001t0002g0005 a0001c0001t0002g0110 a0001c0001t0002g0171 others(8): Show |
12 | HG01106.hp2 HG01515.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.520-751G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4420897 | |||||||
| chr3:4420898 | G | A | 3 | a0001c0001t0001g0076 a0001c0001t0006g0303 a0001c0001t0018g0310 |
3 | HG02280.hp1 HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.520-752C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4420898 | |||||||
| chr3:4421090 | G | A | 332 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(329): Show |
344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.520-944C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4421090 | |||||||
| chr3:4421138 | T | C | 3 | a0001c0001t0004g0312 a0001c0002t0001g0068 a0001c0002t0001g0361 |
3 | HG01109.hp1 HG01496.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.520-992A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4421138 | |||||||
| chr3:4421308 | A | C | 2 | a0001c0001t0001g0305 a0001c0001t0004g0304 |
2 | NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.520-1162T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4421308 | |||||||
| chr3:4421318 | A | G | 1 | a0001c0001t0002g0253 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.520-1172T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4421318 | |||||||
| chr3:4421324 | A | C | 25 | a0001c0001t0002g0223 a0001c0001t0003g0011 a0001c0001t0004g0103 others(22): Show |
27 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.520-1178T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4421324 | |||||||
| chr3:4421484 | A | G | 4 | a0001c0001t0007g0059 a0001c0001t0007g0060 a0001c0002t0001g0311 others(1): Show |
4 | HG02109.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-1338T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4421484 | |||||||
| chr3:4421488 | G | C | 7 | a0001c0001t0002g0220 a0001c0001t0002g0243 a0001c0002t0001g0115 others(4): Show |
7 | HG01943.hp2 HG02015.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.520-1342C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4421488 | |||||||
| chr3:4421592 | G | A | 2 | a0001c0001t0007g0057 a0001c0001t0007g0102 |
2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.520-1446C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4421592 | |||||||
| chr3:4421628 | C | T | 3 | a0001c0001t0001g0305 a0001c0001t0001g0368 a0001c0001t0004g0304 |
3 | HG02572.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.520-1482G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4421628 | |||||||
| chr3:4421771 | T | C | 338 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(335): Show |
350 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.520-1625A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4421771 | |||||||
| chr3:4421919 | T | C | 3 | a0001c0001t0001g0076 a0001c0001t0006g0303 a0001c0001t0018g0310 |
3 | HG02280.hp1 HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.520-1773A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4421919 | |||||||
| chr3:4422069 | A | T | 3 | a0001c0001t0001g0076 a0001c0001t0006g0303 a0001c0001t0018g0310 |
3 | HG02280.hp1 HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.520-1923T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4422069 | |||||||
| chr3:4422087 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.520-1941T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4422087 | |||||||
| chr3:4422197 | G | A | 3 | a0001c0001t0002g0069 a0001c0001t0002g0245 a0001c0001t0002g0253 |
3 | HG01261.hp2 HG01993.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.520-2051C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4422197 | |||||||
| chr3:4422374 | A | T | 1 | a0001c0001t0009g0300 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.520-2228T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4422374 | |||||||
| chr3:4422492 | T | A | 5 | a0001c0001t0002g0233 a0001c0001t0005g0182 a0001c0001t0005g0183 others(2): Show |
5 | HG00639.hp2 HG01981.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.520-2346A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4422492 | |||||||
| chr3:4422492 | T | TA | 15 | a0001c0001t0001g0306 a0001c0001t0001g0368 a0001c0001t0002g0012 others(12): Show |
16 | HG02572.hp1 HG02615.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.520-2347dupT | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4422492 | |||||||
| chr3:4422505 | A | C | 1 | a0001c0001t0004g0294 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.520-2359T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4422505 | |||||||
| chr3:4422547 | G | A | 4 | a0001c0001t0001g0047 a0001c0001t0001g0134 a0001c0001t0007g0057 others(1): Show |
4 | HG02145.hp2 HG02257.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.520-2401C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4422547 | |||||||
| chr3:4422564 | G | A | 189 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(186): Show |
196 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.520-2418C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4422564 | |||||||
| chr3:4422632 | T | C | 1 | a0001c0002t0001g0176 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.520-2486A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4422632 | |||||||
| chr3:4422635 | G | A | 20 | a0001c0001t0002g0223 a0001c0001t0003g0011 a0001c0002t0001g0142 others(17): Show |
22 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.520-2489C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4422635 | |||||||
| chr3:4422767 | CT | C | 15 | a0001c0001t0002g0063 a0001c0001t0002g0345 a0001c0001t0003g0335 others(12): Show |
15 | HG01891.hp2 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.520-2622delA | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4422767 | |||||||
| chr3:4422777 | T | A | 4 | a0001c0001t0001g0076 a0001c0001t0004g0295 a0001c0001t0018g0310 others(1): Show |
4 | HG02280.hp1 HG02280.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-2631A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4422777 | |||||||
| chr3:4422778 | T | A | 341 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(338): Show |
353 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.520-2632A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4422778 | |||||||
| chr3:4422791 | G | T | 1 | a0001c0001t0001g0368 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.520-2645C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4422791 | |||||||
| chr3:4422830 | G | C | 307 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(304): Show |
317 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(314): Show |
intron_variant | MODIFIER | c.520-2684C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4422830 | |||||||
| chr3:4422863 | C | G | 2 | a0001c0001t0010g0041 a0001c0001t0010g0227 |
2 | HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.520-2717G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4422863 | |||||||
| chr3:4422886 | T | C | 307 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(304): Show |
317 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(314): Show |
intron_variant | MODIFIER | c.520-2740A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4422886 | |||||||
| chr3:4422892 | C | T | 3 | a0001c0001t0001g0305 a0001c0001t0001g0368 a0001c0001t0004g0304 |
3 | HG02572.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.520-2746G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4422892 | |||||||
| chr3:4422948 | CCT | C | 118 | a0001c0001t0001g0109 a0001c0001t0001g0113 a0001c0001t0002g0005 others(115): Show |
121 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.520-2804_520-2803d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4422948 | |||||||
| chr3:4423032 | T | C | 3 | a0001c0001t0001g0076 a0001c0001t0006g0303 a0001c0001t0018g0310 |
3 | HG02280.hp1 HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.520-2886A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4423032 | |||||||
| chr3:4423279 | T | TAC | 38 | a0001c0001t0001g0042 a0001c0001t0001g0076 a0001c0001t0001g0109 others(35): Show |
38 | HG00609.hp2 HG00639.hp2 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.520-3135_520-3134d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4423279 | |||||||
| chr3:4423279 | T | TACAC | 123 | a0001c0001t0001g0047 a0001c0001t0001g0134 a0001c0001t0002g0003 others(120): Show |
127 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.520-3137_520-3134d others(6): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4423279 | |||||||
| chr3:4423279 | T | TACACAC | 35 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(32): Show |
36 | HG00438.hp1 HG00438.hp2 HG01257.hp2 others(33): Show |
intron_variant | MODIFIER | c.520-3139_520-3134d others(8): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4423279 | |||||||
| chr3:4423279 | T | TACACACA others(1): Show |
5 | a0001c0001t0003g0122 a0001c0001t0005g0135 a0001c0001t0010g0041 others(2): Show |
5 | HG02630.hp1 HG02809.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.520-3141_520-3134d others(10): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4423279 | |||||||
| chr3:4423279 | T | TACATACA others(3): Show |
2 | a0001c0001t0001g0305 a0001c0001t0004g0304 |
2 | NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.520-3134_520-3133i others(12): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4423279 | |||||||
| chr3:4423279 | TAC | T | 69 | a0001c0001t0001g0306 a0001c0001t0001g0320 a0001c0001t0002g0005 others(66): Show |
72 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.520-3135_520-3134d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4423279 | |||||||
| chr3:4423279 | TACAC | T | 11 | a0001c0001t0002g0063 a0001c0001t0005g0062 a0001c0001t0005g0066 others(8): Show |
11 | HG01891.hp2 HG02145.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.520-3137_520-3134d others(6): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4423279 | |||||||
| chr3:4423279 | TACACACA others(1): Show |
T | 25 | a0001c0001t0002g0223 a0001c0001t0003g0011 a0001c0001t0004g0103 others(22): Show |
27 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.520-3141_520-3134d others(10): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4423279 | |||||||
| chr3:4423315 | C | A | 1 | a0001c0001t0005g0056 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.520-3169G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4423315 | |||||||
| chr3:4423373 | T | C | 1 | a0001c0001t0004g0218 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.520-3227A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4423373 | |||||||
| chr3:4423402 | G | A | 1 | a0001c0001t0003g0175 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.520-3256C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4423402 | |||||||
| chr3:4423421 | A | C | 332 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(329): Show |
344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.520-3275T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4423421 | |||||||
| chr3:4423459 | A | G | 3 | a0001c0001t0001g0305 a0001c0001t0001g0368 a0001c0001t0004g0304 |
3 | HG02572.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.520-3313T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4423459 | |||||||
| chr3:4423482 | C | G | 3 | a0001c0001t0001g0076 a0001c0001t0006g0303 a0001c0001t0018g0310 |
3 | HG02280.hp1 HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.520-3336G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4423482 | |||||||
| chr3:4423523 | T | C | 1 | a0001c0001t0002g0110 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.520-3377A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4423523 | |||||||
| chr3:4423602 | C | T | 3 | a0001c0001t0001g0305 a0001c0001t0001g0368 a0001c0001t0004g0304 |
3 | HG02572.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.520-3456G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4423602 | |||||||
| chr3:4423625 | T | C | 1 | a0001c0001t0001g0368 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.520-3479A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4423625 | |||||||
| chr3:4423772 | C | T | 1 | a0001c0002t0001g0201 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.520-3626G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4423772 | |||||||
| chr3:4423791 | G | A | 3 | a0001c0001t0001g0305 a0001c0001t0001g0368 a0001c0001t0004g0304 |
3 | HG02572.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.520-3645C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4423791 | |||||||
| chr3:4423808 | T | C | 3 | a0001c0001t0001g0305 a0001c0001t0001g0368 a0001c0001t0004g0304 |
3 | HG02572.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.520-3662A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4423808 | |||||||
| chr3:4423901 | C | A | 1 | a0001c0001t0004g0324 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.520-3755G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4423901 | |||||||
| chr3:4424053 | G | C | 306 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(303): Show |
316 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(313): Show |
intron_variant | MODIFIER | c.520-3907C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4424053 | |||||||
| chr3:4424062 | G | A | 3 | a0001c0001t0001g0305 a0001c0001t0001g0368 a0001c0001t0004g0304 |
3 | HG02572.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.520-3916C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4424062 | |||||||
| chr3:4424273 | T | C | 2 | a0001c0002t0001g0311 a0002c0003t0001g0033 |
2 | HG02109.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.520-4127A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4424273 | |||||||
| chr3:4424363 | C | T | 1 | a0001c0002t0001g0077 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.520-4217G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4424363 | |||||||
| chr3:4424372 | C | T | 1 | a0001c0001t0005g0107 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.520-4226G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4424372 | |||||||
| chr3:4424410 | G | C | 1 | a0001c0001t0003g0213 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.520-4264C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4424410 | |||||||
| chr3:4424415 | C | A | 3 | a0001c0001t0004g0103 a0001c0001t0007g0297 a0001c0002t0001g0167 |
3 | HG01243.hp2 HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.520-4269G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4424415 | |||||||
| chr3:4424415 | C | T | 3 | a0001c0001t0001g0076 a0001c0001t0006g0303 a0001c0001t0018g0310 |
3 | HG02280.hp1 HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.520-4269G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4424415 | |||||||
| chr3:4424590 | TAACTTAA others(16): Show |
T | 280 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(277): Show |
289 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.520-4467_520-4445d others(25): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4424590 | |||||||
| chr3:4424652 | G | A | 2 | a0001c0001t0005g0043 a0001c0001t0007g0364 |
2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.520-4506C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4424652 | |||||||
| chr3:4424739 | G | A | 1 | a0001c0002t0001g0317 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.520-4593C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4424739 | |||||||
| chr3:4424757 | C | A | 1 | a0001c0001t0002g0345 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.520-4611G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4424757 | |||||||
| chr3:4424960 | T | C | 1 | a0001c0001t0001g0368 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.520-4814A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4424960 | |||||||
| chr3:4425021 | C | A | 1 | a0001c0001t0002g0340 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.520-4875G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4425021 | |||||||
| chr3:4425061 | T | C | 2 | a0001c0001t0004g0125 a0001c0001t0004g0195 |
2 | HG03942.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.520-4915A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4425061 | |||||||
| chr3:4425115 | G | T | 68 | a0001c0001t0001g0109 a0001c0001t0001g0113 a0001c0001t0002g0005 others(65): Show |
71 | HG00280.hp2 HG00558.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.520-4969C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4425115 | |||||||
| chr3:4425135 | A | C | 1 | a0001c0001t0002g0279 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.520-4989T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4425135 | |||||||
| chr3:4425182 | G | A | 1 | a0001c0002t0001g0077 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.520-5036C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4425182 | |||||||
| chr3:4425267 | G | C | 14 | a0001c0001t0002g0239 a0001c0001t0002g0308 a0001c0001t0003g0079 others(11): Show |
14 | HG00408.hp2 HG00597.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.520-5121C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4425267 | |||||||
| chr3:4425268 | C | T | 305 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(302): Show |
315 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(312): Show |
intron_variant | MODIFIER | c.520-5122G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4425268 | |||||||
| chr3:4425429 | A | G | 1 | a0001c0002t0001g0248 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.520-5283T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4425429 | |||||||
| chr3:4425486 | T | C | 4 | a0001c0001t0001g0042 a0001c0001t0005g0050 a0001c0001t0005g0051 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.520-5340A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4425486 | |||||||
| chr3:4425564 | A | G | 337 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(334): Show |
349 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.520-5418T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4425564 | |||||||
| chr3:4425569 | A | G | 337 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(334): Show |
349 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.520-5423T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4425569 | |||||||
| chr3:4425595 | T | G | 1 | a0001c0002t0001g0176 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.520-5449A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4425595 | |||||||
| chr3:4425602 | T | A | 1 | a0001c0001t0005g0135 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.520-5456A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4425602 | |||||||
| chr3:4425603 | C | A | 1 | a0001c0001t0003g0108 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.520-5457G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4425603 | |||||||
| chr3:4425687 | A | C | 27 | a0001c0001t0001g0076 a0001c0001t0002g0223 a0001c0001t0003g0011 others(24): Show |
29 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.520-5541T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4425687 | |||||||
| chr3:4425817 | T | C | 1 | a0001c0001t0001g0368 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.520-5671A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4425817 | |||||||
| chr3:4425840 | G | A | 48 | a0001c0001t0002g0009 a0001c0001t0002g0178 a0001c0001t0002g0205 others(45): Show |
51 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.520-5694C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4425840 | |||||||
| chr3:4425859 | C | G | 337 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(334): Show |
349 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.520-5713G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4425859 | |||||||
| chr3:4425916 | G | A | 1 | a0001c0001t0001g0368 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.520-5770C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4425916 | |||||||
| chr3:4425953 | GAGATCAC others(3): Show |
G | 1 | a0001c0002t0001g0099 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.520-5817_520-5808d others(12): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4425953 | |||||||
| chr3:4426118 | A | G | 3 | a0001c0001t0001g0076 a0001c0001t0006g0303 a0001c0001t0018g0310 |
3 | HG02280.hp1 HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.520-5972T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4426118 | |||||||
| chr3:4426204 | T | G | 15 | a0001c0001t0002g0239 a0001c0001t0002g0308 a0001c0001t0003g0079 others(12): Show |
15 | HG00408.hp2 HG00597.hp1 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.520-6058A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4426204 | |||||||
| chr3:4426396 | C | T | 117 | a0001c0001t0001g0109 a0001c0001t0001g0113 a0001c0001t0002g0005 others(114): Show |
120 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.520-6250G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4426396 | |||||||
| chr3:4426552 | G | A | 2 | a0001c0001t0004g0344 a0001c0001t0004g0348 |
2 | HG00609.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.520-6406C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4426552 | |||||||
| chr3:4426600 | G | A | 1 | a0001c0001t0004g0295 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.520-6454C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4426600 | |||||||
| chr3:4426789 | GAGACAAT others(4): Show |
G | 1 | a0001c0001t0004g0290 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.520-6654_520-6644d others(13): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4426789 | |||||||
| chr3:4426811 | C | A | 1 | a0001c0010t0001g0264 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.520-6665G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4426811 | |||||||
| chr3:4426899 | A | G | 1 | a0001c0001t0001g0368 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.520-6753T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4426899 | |||||||
| chr3:4426914 | C | G | 2 | a0001c0001t0004g0103 a0001c0002t0001g0167 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.520-6768G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4426914 | |||||||
| chr3:4426914 | C | T | 304 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(301): Show |
314 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.520-6768G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4426914 | |||||||
| chr3:4427315 | C | G | 1 | a0001c0001t0006g0303 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.520-7169G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4427315 | |||||||
| chr3:4427508 | T | G | 21 | a0001c0001t0002g0223 a0001c0001t0003g0011 a0001c0001t0003g0165 others(18): Show |
23 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.520-7362A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4427508 | |||||||
| chr3:4427745 | A | G | 72 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0069 others(69): Show |
75 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.520-7599T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4427745 | |||||||
| chr3:4427885 | C | G | 1 | a0001c0001t0001g0368 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.520-7739G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4427885 | |||||||
| chr3:4427932 | G | A | 3 | a0001c0001t0001g0076 a0001c0001t0006g0303 a0001c0001t0018g0310 |
3 | HG02280.hp1 HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.520-7786C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4427932 | |||||||
| chr3:4428200 | T | C | 77 | a0001c0001t0001g0109 a0001c0001t0001g0113 a0001c0001t0002g0005 others(74): Show |
80 | HG00280.hp2 HG00558.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.520-8054A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4428200 | |||||||
| chr3:4428242 | C | A | 9 | a0001c0001t0001g0306 a0001c0001t0002g0012 a0001c0001t0009g0065 others(6): Show |
10 | HG02615.hp1 HG02886.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.520-8096G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4428242 | |||||||
| chr3:4428265 | C | G | 190 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(187): Show |
197 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.520-8119G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4428265 | |||||||
| chr3:4428359 | CTTT | C | 49 | a0001c0001t0002g0149 a0001c0001t0002g0252 a0001c0001t0002g0322 others(46): Show |
49 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.520-8216_520-8214d others(5): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4428359 | |||||||
| chr3:4428388 | C | CT | 26 | a0001c0001t0002g0223 a0001c0001t0003g0011 a0001c0001t0003g0165 others(23): Show |
28 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.520-8243dupA | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4428388 | |||||||
| chr3:4428468 | C | T | 120 | a0001c0001t0001g0109 a0001c0001t0001g0113 a0001c0001t0002g0005 others(117): Show |
123 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.520-8322G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4428468 | |||||||
| chr3:4428485 | T | C | 337 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(334): Show |
349 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.520-8339A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4428485 | |||||||
| chr3:4428538 | C | G | 337 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(334): Show |
349 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.520-8392G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4428538 | |||||||
| chr3:4428679 | G | A | 1 | a0001c0001t0007g0297 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.520-8533C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4428679 | |||||||
| chr3:4428719 | G | GTTTC | 337 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(334): Show |
349 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.520-8574_520-8573i others(6): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4428719 | |||||||
| chr3:4428773 | A | AAAGT | 337 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(334): Show |
349 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.520-8628_520-8627i others(6): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4428773 | |||||||
| chr3:4428792 | G | A | 68 | a0001c0001t0001g0109 a0001c0001t0001g0113 a0001c0001t0002g0005 others(65): Show |
71 | HG00280.hp2 HG00558.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.520-8646C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4428792 | |||||||
| chr3:4428917 | T | C | 7 | a0001c0001t0002g0178 a0001c0001t0003g0206 a0001c0001t0003g0230 others(4): Show |
7 | HG00323.hp1 HG00639.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.520-8771A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4428917 | |||||||
| chr3:4428936 | T | C | 2 | a0001c0001t0004g0288 a0001c0002t0001g0283 |
2 | NA18941.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.520-8790A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4428936 | |||||||
| chr3:4428953 | A | G | 1 | a0001c0002t0001g0167 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.520-8807T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4428953 | |||||||
| chr3:4429006 | C | CTA | 3 | a0001c0001t0001g0076 a0001c0001t0006g0303 a0001c0001t0018g0310 |
3 | HG02280.hp1 HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.520-8862_520-8861d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4429006 | |||||||
| chr3:4429060 | T | C | 1 | a0001c0001t0002g0351 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.520-8914A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4429060 | |||||||
| chr3:4429152 | G | A | 2 | a0001c0002t0001g0207 a0001c0002t0001g0208 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.520-9006C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4429152 | |||||||
| chr3:4429209 | A | T | 26 | a0001c0001t0002g0223 a0001c0001t0003g0011 a0001c0001t0003g0165 others(23): Show |
28 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.520-9063T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4429209 | |||||||
| chr3:4429336 | A | G | 1 | a0001c0001t0007g0102 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.520-9190T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4429336 | |||||||
| chr3:4429441 | C | T | 27 | a0001c0001t0001g0368 a0001c0001t0002g0223 a0001c0001t0003g0011 others(24): Show |
29 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.520-9295G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4429441 | |||||||
| chr3:4429621 | T | C | 1 | a0003c0006t0001g0014 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.520-9475A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4429621 | |||||||
| chr3:4429816 | G | A | 337 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(334): Show |
349 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.520-9670C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4429816 | |||||||
| chr3:4429882 | C | A | 1 | a0001c0001t0004g0072 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.520-9736G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4429882 | |||||||
| chr3:4430005 | T | C | 1 | a0001c0001t0002g0352 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.520-9859A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4430005 | |||||||
| chr3:4430325 | G | T | 6 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0005g0135 others(3): Show |
6 | HG02055.hp1 HG02630.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.520-10179C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4430325 | |||||||
| chr3:4430348 | C | G | 2 | a0001c0001t0005g0043 a0001c0001t0007g0364 |
2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.520-10202G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4430348 | |||||||
| chr3:4430468 | T | C | 26 | a0001c0001t0002g0223 a0001c0001t0003g0011 a0001c0001t0003g0165 others(23): Show |
28 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.520-10322A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4430468 | |||||||
| chr3:4430619 | AG | A | 21 | a0001c0001t0002g0223 a0001c0001t0003g0011 a0001c0001t0003g0165 others(18): Show |
23 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.520-10474delC | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4430619 | |||||||
| chr3:4430642 | G | C | 2 | a0001c0001t0010g0041 a0001c0001t0010g0227 |
2 | HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.520-10496C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4430642 | |||||||
| chr3:4430653 | C | T | 1 | a0002c0004t0001g0039 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.520-10507G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4430653 | |||||||
| chr3:4431194 | G | T | 2 | a0001c0001t0005g0043 a0001c0001t0007g0364 |
2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.520-11048C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4431194 | |||||||
| chr3:4431244 | G | A | 6 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0185 others(3): Show |
6 | NA18612.hp2 NA18990.hp2 NA19001.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-11098C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4431244 | |||||||
| chr3:4431280 | C | T | 1 | a0001c0002t0001g0311 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.520-11134G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4431280 | |||||||
| chr3:4431309 | T | G | 1 | a0001c0001t0003g0232 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.520-11163A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4431309 | |||||||
| chr3:4431450 | A | G | 1 | a0001c0002t0001g0342 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.520-11304T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4431450 | |||||||
| chr3:4431502 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.520-11356G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4431502 | |||||||
| chr3:4431528 | G | A | 26 | a0001c0001t0002g0223 a0001c0001t0003g0011 a0001c0001t0003g0165 others(23): Show |
28 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.520-11382C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4431528 | |||||||
| chr3:4431555 | C | T | 63 | a0001c0001t0001g0109 a0001c0001t0002g0005 a0001c0001t0002g0046 others(60): Show |
66 | HG00280.hp2 HG00558.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.520-11409G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4431555 | |||||||
| chr3:4431556 | G | A | 1 | a0001c0001t0006g0303 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.520-11410C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4431556 | |||||||
| chr3:4431712 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.520-11566A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4431712 | |||||||
| chr3:4431781 | C | T | 15 | a0001c0001t0001g0368 a0001c0001t0002g0239 a0001c0001t0002g0308 others(12): Show |
15 | HG00408.hp2 HG00597.hp1 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.520-11635G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4431781 | |||||||
| chr3:4431853 | C | T | 3 | a0001c0001t0005g0056 a0001c0001t0005g0132 a0001c0001t0005g0266 |
3 | HG01891.hp2 HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.520-11707G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4431853 | |||||||
| chr3:4431862 | G | C | 19 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0285 others(16): Show |
19 | HG00639.hp2 HG01981.hp1 HG02886.hp1 others(16): Show |
intron_variant | MODIFIER | c.520-11716C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4431862 | |||||||
| chr3:4432147 | C | T | 2 | a0001c0001t0006g0184 a0001c0001t0006g0190 |
2 | HG01243.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.520-12001G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4432147 | |||||||
| chr3:4432249 | C | G | 1 | a0001c0002t0001g0176 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.520-12103G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4432249 | |||||||
| chr3:4432395 | C | A | 1 | a0001c0001t0001g0368 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.520-12249G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4432395 | |||||||
| chr3:4432534 | C | G | 1 | a0001c0001t0002g0110 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.520-12388G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4432534 | |||||||
| chr3:4432535 | C | G | 1 | a0001c0001t0002g0110 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.520-12389G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4432535 | |||||||
| chr3:4432536 | C | A | 1 | a0001c0001t0002g0110 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.520-12390G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4432536 | |||||||
| chr3:4432623 | T | A | 1 | a0002c0003t0001g0034 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.520-12477A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4432623 | |||||||
| chr3:4432720 | A | G | 377 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(374): Show |
389 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.520-12574T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4432720 | |||||||
| chr3:4432724 | C | T | 1 | a0001c0001t0008g0272 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.520-12578G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4432724 | |||||||
| chr3:4432791 | G | A | 20 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0002g0239 others(17): Show |
20 | HG00408.hp2 HG00597.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.520-12645C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4432791 | |||||||
| chr3:4432814 | G | T | 26 | a0001c0001t0002g0223 a0001c0001t0003g0011 a0001c0001t0003g0165 others(23): Show |
28 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.520-12668C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4432814 | |||||||
| chr3:4432921 | C | T | 1 | a0001c0001t0002g0341 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.520-12775G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4432921 | |||||||
| chr3:4433043 | A | G | 3 | a0001c0001t0002g0110 a0001c0001t0002g0173 a0001c0002t0001g0172 |
3 | HG01106.hp2 HG01515.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.520-12897T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4433043 | |||||||
| chr3:4433052 | A | C | 77 | a0001c0001t0001g0058 a0001c0001t0002g0003 a0001c0001t0002g0008 others(74): Show |
80 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.520-12906T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4433052 | |||||||
| chr3:4433055 | G | C | 27 | a0001c0001t0001g0368 a0001c0001t0002g0223 a0001c0001t0003g0011 others(24): Show |
29 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.520-12909C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4433055 | |||||||
| chr3:4433202 | A | C | 1 | a0001c0001t0005g0062 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.520-13056T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4433202 | |||||||
| chr3:4433299 | C | A | 1 | a0001c0001t0004g0312 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.520-13153G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4433299 | |||||||
| chr3:4433460 | T | C | 1 | a0001c0001t0002g0192 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.520-13314A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4433460 | |||||||
| chr3:4433528 | T | C | 29 | a0001c0001t0001g0305 a0001c0001t0001g0368 a0001c0001t0002g0223 others(26): Show |
31 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.520-13382A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4433528 | |||||||
| chr3:4433697 | T | C | 1 | a0001c0001t0001g0368 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.520-13551A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4433697 | |||||||
| chr3:4433704 | T | C | 1 | a0002c0003t0001g0033 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.520-13558A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4433704 | |||||||
| chr3:4433806 | C | T | 1 | a0001c0001t0002g0110 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.520-13660G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4433806 | |||||||
| chr3:4433940 | G | C | 3 | a0001c0001t0003g0165 a0002c0004t0001g0024 a0002c0004t0001g0038 |
3 | HG01099.hp1 HG01192.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.520-13794C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4433940 | |||||||
| chr3:4433961 | C | T | 1 | a0007c0009t0004g0121 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.520-13815G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4433961 | |||||||
| chr3:4433995 | G | A | 26 | a0001c0001t0002g0223 a0001c0001t0003g0011 a0001c0001t0003g0165 others(23): Show |
28 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.520-13849C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4433995 | |||||||
| chr3:4434011 | C | T | 1 | a0001c0001t0003g0232 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.520-13865G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4434011 | |||||||
| chr3:4434146 | G | C | 1 | a0001c0001t0005g0049 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.520-14000C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4434146 | |||||||
| chr3:4434200 | TG | T | 3 | a0001c0001t0001g0076 a0001c0001t0006g0303 a0001c0001t0018g0310 |
3 | HG02280.hp1 HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.520-14055delC | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4434200 | |||||||
| chr3:4434258 | T | A | 1 | a0001c0001t0004g0328 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.520-14112A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4434258 | |||||||
| chr3:4434412 | T | G | 2 | a0001c0001t0010g0041 a0001c0001t0010g0227 |
2 | HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.520-14266A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4434412 | |||||||
| chr3:4434475 | G | A | 9 | a0001c0001t0001g0306 a0001c0001t0002g0012 a0001c0001t0009g0065 others(6): Show |
10 | HG02615.hp1 HG02886.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.520-14329C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4434475 | |||||||
| chr3:4434765 | G | C | 208 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(205): Show |
214 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.519+14501C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4434765 | |||||||
| chr3:4434908 | G | C | 3 | a0001c0001t0001g0076 a0001c0001t0006g0303 a0001c0001t0018g0310 |
3 | HG02280.hp1 HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.519+14358C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4434908 | |||||||
| chr3:4434924 | A | G | 1 | a0001c0001t0004g0294 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.519+14342T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4434924 | |||||||
| chr3:4434956 | T | G | 1 | a0001c0001t0002g0243 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.519+14310A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4434956 | |||||||
| chr3:4434988 | C | T | 8 | a0001c0001t0005g0370 a0001c0001t0006g0133 a0001c0001t0006g0184 others(5): Show |
8 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.519+14278G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4434988 | |||||||
| chr3:4435010 | C | T | 2 | a0001c0001t0001g0305 a0001c0001t0004g0304 |
2 | NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.519+14256G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4435010 | |||||||
| chr3:4435021 | A | G | 6 | a0001c0001t0001g0076 a0001c0001t0001g0305 a0001c0001t0001g0368 others(3): Show |
6 | HG02280.hp1 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.519+14245T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4435021 | |||||||
| chr3:4435196 | G | A | 31 | a0001c0001t0001g0306 a0001c0001t0002g0012 a0001c0001t0002g0281 others(28): Show |
32 | HG00639.hp2 HG01981.hp1 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.519+14070C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4435196 | |||||||
| chr3:4435207 | T | G | 337 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(334): Show |
349 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.519+14059A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4435207 | |||||||
| chr3:4435236 | A | G | 1 | a0001c0002t0001g0169 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.519+14030T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4435236 | |||||||
| chr3:4435334 | C | T | 1 | a0001c0001t0022g0073 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.519+13932G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4435334 | |||||||
| chr3:4435664 | A | G | 1 | a0002c0003t0001g0033 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.519+13602T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4435664 | |||||||
| chr3:4436003 | G | A | 151 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(148): Show |
157 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.519+13263C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4436003 | |||||||
| chr3:4436102 | C | T | 3 | a0001c0001t0007g0059 a0001c0001t0007g0060 a0001c0002t0001g0311 |
3 | HG02896.hp2 HG02897.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.519+13164G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4436102 | |||||||
| chr3:4436227 | A | G | 68 | a0001c0001t0001g0109 a0001c0001t0001g0113 a0001c0001t0002g0005 others(65): Show |
71 | HG00280.hp2 HG00558.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.519+13039T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4436227 | |||||||
| chr3:4436383 | C | G | 8 | a0001c0001t0005g0370 a0001c0001t0006g0133 a0001c0001t0006g0184 others(5): Show |
8 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.519+12883G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4436383 | |||||||
| chr3:4436419 | A | G | 3 | a0001c0001t0001g0076 a0001c0001t0006g0303 a0001c0001t0018g0310 |
3 | HG02280.hp1 HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.519+12847T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4436419 | |||||||
| chr3:4436558 | A | G | 1 | a0001c0001t0005g0049 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.519+12708T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4436558 | |||||||
| chr3:4436578 | A | G | 2 | a0001c0001t0013g0284 a0001c0002t0001g0280 |
2 | NA19064.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.519+12688T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4436578 | |||||||
| chr3:4436600 | T | TA | 7 | a0001c0001t0001g0076 a0001c0001t0003g0010 a0001c0001t0003g0329 others(4): Show |
8 | HG01070.hp2 HG01071.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.519+12665dupT | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4436600 | |||||||
| chr3:4436600 | TA | T | 47 | a0001c0001t0001g0042 a0001c0001t0001g0320 a0001c0001t0001g0368 others(44): Show |
49 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.519+12665delT | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4436600 | |||||||
| chr3:4436655 | T | C | 5 | a0001c0001t0002g0258 a0001c0001t0002g0259 a0001c0001t0003g0271 others(2): Show |
5 | NA18747.hp2 NA18964.hp1 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+12611A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4436655 | |||||||
| chr3:4436690 | T | C | 3 | a0001c0001t0007g0059 a0001c0001t0007g0060 a0001c0002t0001g0311 |
3 | HG02896.hp2 HG02897.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.519+12576A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4436690 | |||||||
| chr3:4436702 | C | A | 2 | a0001c0001t0013g0284 a0001c0002t0001g0280 |
2 | NA19064.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.519+12564G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4436702 | |||||||
| chr3:4436733 | T | C | 33 | a0001c0001t0001g0076 a0001c0001t0001g0305 a0001c0001t0001g0368 others(30): Show |
35 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.519+12533A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4436733 | |||||||
| chr3:4436852 | A | T | 2 | a0001c0001t0005g0043 a0001c0001t0007g0364 |
2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.519+12414T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4436852 | |||||||
| chr3:4436863 | AAT | A | 29 | a0001c0001t0001g0076 a0001c0001t0001g0305 a0001c0001t0001g0368 others(26): Show |
31 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.519+12401_519+1240 others(6): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4436863 | |||||||
| chr3:4436864 | AT | A | 122 | a0001c0001t0001g0109 a0001c0001t0001g0113 a0001c0001t0002g0005 others(119): Show |
125 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.519+12401delA | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4436864 | |||||||
| chr3:4436865 | T | A | 200 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0054 others(197): Show |
207 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(204): Show |
intron_variant | MODIFIER | c.519+12401A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4436865 | |||||||
| chr3:4436881 | C | CA | 29 | a0001c0001t0001g0305 a0001c0001t0001g0368 a0001c0001t0002g0223 others(26): Show |
31 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.519+12384dupT | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4436881 | |||||||
| chr3:4436971 | A | G | 1 | a0002c0003t0001g0033 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.519+12295T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4436971 | |||||||
| chr3:4437027 | T | A | 1 | a0001c0002t0001g0077 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.519+12239A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4437027 | |||||||
| chr3:4437094 | T | C | 1 | a0002c0003t0001g0033 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.519+12172A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4437094 | |||||||
| chr3:4437181 | T | C | 3 | a0001c0001t0002g0375 a0001c0001t0004g0292 a0001c0001t0004g0374 |
3 | HG00408.hp1 HG02040.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.519+12085A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4437181 | |||||||
| chr3:4437184 | A | G | 1 | a0001c0001t0001g0368 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.519+12082T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4437184 | |||||||
| chr3:4437280 | G | A | 1 | a0001c0001t0004g0071 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.519+11986C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4437280 | |||||||
| chr3:4437481 | G | A | 3 | a0001c0001t0003g0124 a0001c0001t0003g0200 a0001c0001t0003g0209 |
3 | HG01074.hp2 HG01167.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.519+11785C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4437481 | |||||||
| chr3:4437577 | C | A | 337 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(334): Show |
349 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.519+11689G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4437577 | |||||||
| chr3:4437641 | T | C | 2 | a0001c0002t0001g0255 a0001c0002t0001g0256 |
2 | NA18989.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.519+11625A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4437641 | |||||||
| chr3:4437681 | G | A | 119 | a0001c0001t0001g0109 a0001c0001t0001g0113 a0001c0001t0002g0005 others(116): Show |
122 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.519+11585C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4437681 | |||||||
| chr3:4437777 | A | G | 2 | a0001c0001t0001g0305 a0001c0001t0004g0304 |
2 | NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.519+11489T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4437777 | |||||||
| chr3:4437800 | G | A | 51 | a0001c0001t0002g0149 a0001c0001t0002g0252 a0001c0001t0002g0322 others(48): Show |
51 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.519+11466C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4437800 | |||||||
| chr3:4437827 | T | C | 2 | a0001c0001t0005g0043 a0001c0001t0007g0364 |
2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.519+11439A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4437827 | |||||||
| chr3:4437903 | C | A | 2 | a0001c0001t0007g0059 a0001c0001t0007g0060 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.519+11363G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4437903 | |||||||
| chr3:4438004 | T | C | 3 | a0001c0001t0003g0004 a0001c0001t0003g0114 a0001c0001t0003g0117 |
4 | HG00741.hp2 HG01175.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+11262A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4438004 | |||||||
| chr3:4438229 | CA | C | 303 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(300): Show |
313 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(310): Show |
intron_variant | MODIFIER | c.519+11036delT | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4438229 | |||||||
| chr3:4438230 | A | C | 2 | a0001c0001t0001g0305 a0001c0001t0004g0304 |
2 | NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.519+11036T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4438230 | |||||||
| chr3:4438231 | A | C | 185 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(182): Show |
192 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.519+11035T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4438231 | |||||||
| chr3:4438241 | A | AG | 27 | a0001c0001t0002g0223 a0001c0001t0003g0011 a0001c0001t0003g0165 others(24): Show |
29 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.519+11024_519+1102 others(5): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4438241 | |||||||
| chr3:4438241 | A | G | 307 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(304): Show |
317 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(314): Show |
intron_variant | MODIFIER | c.519+11025T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4438241 | |||||||
| chr3:4438243 | G | GAC | 39 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0134 others(36): Show |
39 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.519+11022_519+1102 others(6): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4438243 | |||||||
| chr3:4438281 | C | T | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.519+10985G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4438281 | |||||||
| chr3:4438871 | T | C | 376 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(373): Show |
388 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.519+10395A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4438871 | |||||||
| chr3:4438991 | T | C | 1 | a0002c0003t0001g0034 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.519+10275A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4438991 | |||||||
| chr3:4439105 | T | C | 30 | a0001c0001t0001g0305 a0001c0001t0001g0368 a0001c0001t0002g0223 others(27): Show |
32 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.519+10161A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4439105 | |||||||
| chr3:4439263 | C | A | 9 | a0001c0001t0001g0306 a0001c0001t0002g0012 a0001c0001t0009g0065 others(6): Show |
10 | HG02615.hp1 HG02886.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.519+10003G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4439263 | |||||||
| chr3:4439298 | C | T | 26 | a0001c0001t0002g0223 a0001c0001t0003g0011 a0001c0001t0003g0165 others(23): Show |
28 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.519+9968G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4439298 | |||||||
| chr3:4439419 | G | A | 4 | a0001c0001t0005g0182 a0001c0001t0005g0183 a0001c0001t0005g0236 others(1): Show |
4 | HG00639.hp2 HG01981.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.519+9847C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4439419 | |||||||
| chr3:4439543 | T | C | 1 | a0001c0001t0001g0368 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.519+9723A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4439543 | |||||||
| chr3:4439547 | T | A | 1 | a0001c0001t0001g0368 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.519+9719A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4439547 | |||||||
| chr3:4439706 | A | G | 4 | a0001c0001t0005g0120 a0001c0001t0005g0302 a0001c0001t0012g0104 others(1): Show |
4 | HG02109.hp2 HG02559.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+9560T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4439706 | |||||||
| chr3:4439758 | T | C | 351 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0054 others(348): Show |
363 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.519+9508A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4439758 | |||||||
| chr3:4439999 | C | T | 1 | a0001c0002t0001g0210 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.519+9267G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4439999 | |||||||
| chr3:4440004 | C | T | 1 | a0001c0001t0003g0315 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.519+9262G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4440004 | |||||||
| chr3:4440133 | G | A | 2 | a0001c0001t0001g0305 a0001c0001t0004g0304 |
2 | NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.519+9133C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4440133 | |||||||
| chr3:4440134 | G | C | 119 | a0001c0001t0001g0109 a0001c0001t0001g0113 a0001c0001t0002g0005 others(116): Show |
122 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.519+9132C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4440134 | |||||||
| chr3:4440177 | T | C | 1 | a0001c0001t0002g0252 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.519+9089A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4440177 | |||||||
| chr3:4440243 | C | CA | 11 | a0001c0001t0001g0047 a0001c0001t0001g0076 a0001c0001t0002g0063 others(8): Show |
11 | HG01243.hp2 HG02145.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+9022dupT | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4440243 | |||||||
| chr3:4440263 | A | AAAC | 20 | a0001c0001t0002g0211 a0001c0001t0002g0243 a0001c0001t0002g0260 others(17): Show |
20 | HG00438.hp1 HG01934.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.519+9002_519+9003i others(5): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4440263 | |||||||
| chr3:4440263 | A | AAC | 158 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0002g0003 others(155): Show |
165 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.519+9002_519+9003i others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4440263 | |||||||
| chr3:4440263 | A | AC | 75 | a0001c0001t0001g0109 a0001c0001t0001g0113 a0001c0001t0001g0306 others(72): Show |
78 | HG00280.hp2 HG00558.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.519+9002_519+9003i others(3): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4440263 | |||||||
| chr3:4440263 | A | C | 50 | a0001c0001t0001g0305 a0001c0001t0002g0171 a0001c0001t0002g0252 others(47): Show |
50 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.519+9003T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4440263 | |||||||
| chr3:4440415 | T | A | 2 | a0001c0001t0005g0236 a0001c0001t0007g0299 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.519+8851A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4440415 | |||||||
| chr3:4440432 | G | A | 2 | a0001c0001t0005g0182 a0001c0001t0005g0183 |
2 | HG00639.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.519+8834C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4440432 | |||||||
| chr3:4440445 | G | A | 1 | a0002c0003t0016g0035 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.519+8821C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4440445 | |||||||
| chr3:4440535 | G | A | 1 | a0001c0002t0001g0212 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.519+8731C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4440535 | |||||||
| chr3:4440613 | C | T | 1 | a0001c0001t0004g0197 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.519+8653G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4440613 | |||||||
| chr3:4440661 | T | A | 3 | a0001c0001t0002g0327 a0001c0001t0002g0366 a0001c0001t0004g0328 |
3 | NA18997.hp1 NA19012.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.519+8605A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4440661 | |||||||
| chr3:4440701 | A | C | 370 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0053 others(367): Show |
382 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.519+8565T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4440701 | |||||||
| chr3:4440789 | C | T | 1 | a0002c0003t0001g0033 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.519+8477G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4440789 | |||||||
| chr3:4440816 | A | G | 1 | a0001c0001t0008g0272 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.519+8450T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4440816 | |||||||
| chr3:4440827 | G | T | 337 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(334): Show |
349 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.519+8439C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4440827 | |||||||
| chr3:4440836 | T | C | 1 | a0001c0001t0013g0242 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.519+8430A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4440836 | |||||||
| chr3:4440844 | G | C | 8 | a0001c0001t0005g0370 a0001c0001t0006g0133 a0001c0001t0006g0184 others(5): Show |
8 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.519+8422C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4440844 | |||||||
| chr3:4440964 | A | C | 1 | a0001c0001t0007g0059 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.519+8302T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4440964 | |||||||
| chr3:4440984 | C | CT | 26 | a0001c0001t0002g0223 a0001c0001t0003g0011 a0001c0001t0003g0165 others(23): Show |
28 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.519+8281dupA | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4440984 | |||||||
| chr3:4441218 | C | T | 1 | a0001c0001t0005g0302 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.519+8048G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4441218 | |||||||
| chr3:4441283 | T | C | 128 | a0001c0001t0001g0109 a0001c0001t0001g0113 a0001c0001t0002g0005 others(125): Show |
131 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.519+7983A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4441283 | |||||||
| chr3:4441621 | C | T | 1 | a0001c0001t0003g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.519+7645G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4441621 | |||||||
| chr3:4441866 | G | C | 26 | a0001c0001t0002g0223 a0001c0001t0003g0011 a0001c0001t0003g0165 others(23): Show |
28 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.519+7400C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4441866 | |||||||
| chr3:4441922 | G | T | 4 | a0001c0001t0007g0059 a0001c0001t0007g0060 a0001c0002t0001g0311 others(1): Show |
4 | HG02109.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+7344C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4441922 | |||||||
| chr3:4442033 | G | A | 1 | a0001c0001t0004g0292 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.519+7233C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4442033 | |||||||
| chr3:4442069 | C | T | 3 | a0001c0001t0003g0108 a0001c0001t0003g0148 a0001c0002t0001g0099 |
3 | NA18942.hp2 NA18974.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.519+7197G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4442069 | |||||||
| chr3:4442194 | T | C | 3 | a0001c0001t0004g0103 a0001c0001t0007g0297 a0001c0002t0001g0167 |
3 | HG01243.hp2 HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.519+7072A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4442194 | |||||||
| chr3:4442204 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.519+7062C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4442204 | |||||||
| chr3:4442257 | C | A | 31 | a0001c0001t0001g0306 a0001c0001t0002g0012 a0001c0001t0002g0281 others(28): Show |
32 | HG00639.hp2 HG01981.hp1 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.519+7009G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4442257 | |||||||
| chr3:4442257 | C | CT | 77 | a0001c0001t0001g0109 a0001c0001t0001g0113 a0001c0001t0002g0005 others(74): Show |
80 | HG00280.hp2 HG00558.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.519+7008dupA | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4442257 | |||||||
| chr3:4442257 | CT | C | 26 | a0001c0001t0001g0320 a0001c0001t0002g0223 a0001c0001t0003g0011 others(23): Show |
28 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.519+7008delA | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4442257 | |||||||
| chr3:4442356 | C | T | 54 | a0001c0001t0001g0076 a0001c0001t0002g0149 a0001c0001t0002g0252 others(51): Show |
54 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.519+6910G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4442356 | |||||||
| chr3:4442357 | G | A | 1 | a0006c0008t0002g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.519+6909C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4442357 | |||||||
| chr3:4442361 | T | TTCTCCTG others(8): Show |
68 | a0001c0001t0001g0109 a0001c0001t0001g0113 a0001c0001t0002g0005 others(65): Show |
71 | HG00280.hp2 HG00558.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.519+6890_519+6904d others(17): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4442361 | |||||||
| chr3:4442400 | C | T | 1 | a0001c0001t0007g0102 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.519+6866G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4442400 | |||||||
| chr3:4442422 | A | AT | 189 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(186): Show |
196 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.519+6843dupA | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4442422 | |||||||
| chr3:4442422 | AT | A | 148 | a0001c0001t0001g0076 a0001c0001t0001g0109 a0001c0001t0001g0113 others(145): Show |
153 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.519+6843delA | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4442422 | |||||||
| chr3:4442625 | AAGAGAGA others(21): Show |
A | 148 | a0001c0001t0001g0076 a0001c0001t0001g0109 a0001c0001t0001g0113 others(145): Show |
153 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.519+6613_519+6640d others(30): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4442625 | |||||||
| chr3:4442638 | G | GAAAA | 10 | a0001c0001t0001g0306 a0001c0001t0002g0012 a0001c0001t0009g0065 others(7): Show |
11 | HG02615.hp1 HG02886.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.519+6624_519+6627d others(6): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4442638 | |||||||
| chr3:4442638 | G | GAAAAAAA others(3): Show |
1 | a0001c0001t0002g0261 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.519+6618_519+6627d others(12): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4442638 | |||||||
| chr3:4442638 | G | GAAAAAAA others(4): Show |
40 | a0001c0001t0002g0009 a0001c0001t0002g0069 a0001c0001t0002g0178 others(37): Show |
43 | HG00323.hp1 HG00639.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.519+6617_519+6627d others(13): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4442638 | |||||||
| chr3:4442638 | G | GAAAAAAA others(5): Show |
78 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0305 others(75): Show |
80 | HG00140.hp2 HG00438.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.519+6616_519+6627d others(14): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4442638 | |||||||
| chr3:4442638 | G | GAAAAAAA others(6): Show |
21 | a0001c0001t0001g0058 a0001c0001t0002g0098 a0001c0001t0002g0220 others(18): Show |
21 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.519+6615_519+6627d others(15): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4442638 | |||||||
| chr3:4442638 | G | GAAAAAAA others(7): Show |
29 | a0001c0001t0002g0239 a0001c0001t0002g0260 a0001c0001t0002g0281 others(26): Show |
30 | HG00408.hp2 HG00597.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.519+6614_519+6627d others(16): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4442638 | |||||||
| chr3:4442638 | G | GAAAAAAA others(8): Show |
6 | a0001c0001t0004g0293 a0001c0001t0005g0120 a0001c0001t0012g0104 others(3): Show |
6 | HG02559.hp1 HG03486.hp2 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.519+6627_519+6628i others(17): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4442638 | |||||||
| chr3:4442651 | A | AAAAAAAA others(5): Show |
1 | a0001c0001t0004g0112 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.519+6614_519+6615i others(14): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4442651 | |||||||
| chr3:4442659 | G | A | 1 | a0001c0002t0001g0140 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.519+6607C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4442659 | |||||||
| chr3:4442762 | T | C | 27 | a0001c0001t0001g0368 a0001c0001t0002g0223 a0001c0001t0003g0011 others(24): Show |
29 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.519+6504A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4442762 | |||||||
| chr3:4442889 | A | T | 1 | a0001c0001t0002g0193 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.519+6377T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4442889 | |||||||
| chr3:4442900 | C | A | 323 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(320): Show |
335 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.519+6366G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4442900 | |||||||
| chr3:4442917 | T | C | 1 | a0001c0002t0001g0267 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.519+6349A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4442917 | |||||||
| chr3:4442950 | CA | C | 20 | a0001c0001t0001g0306 a0001c0001t0002g0357 a0001c0001t0003g0200 others(17): Show |
20 | HG01167.hp2 HG01243.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.519+6315delT | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4442950 | |||||||
| chr3:4443091 | CA | C | 50 | a0001c0001t0002g0149 a0001c0001t0002g0252 a0001c0001t0002g0322 others(47): Show |
50 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.519+6174delT | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4443091 | |||||||
| chr3:4443135 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.519+6131C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4443135 | |||||||
| chr3:4443146 | C | T | 1 | a0001c0001t0002g0358 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.519+6120G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4443146 | |||||||
| chr3:4443161 | C | T | 71 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0069 others(68): Show |
74 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.519+6105G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4443161 | |||||||
| chr3:4443199 | G | T | 26 | a0001c0001t0001g0368 a0001c0001t0002g0223 a0001c0001t0003g0011 others(23): Show |
28 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.519+6067C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4443199 | |||||||
| chr3:4443239 | C | T | 31 | a0001c0001t0001g0368 a0001c0001t0002g0223 a0001c0001t0003g0011 others(28): Show |
33 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.519+6027G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4443239 | |||||||
| chr3:4443264 | C | G | 1 | a0001c0001t0010g0321 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.519+6002G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4443264 | |||||||
| chr3:4443451 | A | C | 75 | a0001c0001t0001g0109 a0001c0001t0001g0113 a0001c0001t0002g0005 others(72): Show |
78 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.519+5815T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4443451 | |||||||
| chr3:4443505 | C | T | 2 | a0001c0001t0001g0076 a0001c0001t0018g0310 |
2 | HG02280.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.519+5761G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4443505 | |||||||
| chr3:4443506 | G | A | 9 | a0001c0001t0003g0004 a0001c0001t0005g0370 a0001c0001t0006g0133 others(6): Show |
10 | HG01243.hp1 HG01516.hp1 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.519+5760C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4443506 | |||||||
| chr3:4443648 | C | G | 143 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0058 others(140): Show |
149 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.519+5618G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4443648 | |||||||
| chr3:4443869 | C | G | 1 | a0001c0001t0002g0319 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.519+5397G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4443869 | |||||||
| chr3:4443884 | A | C | 80 | a0001c0001t0001g0109 a0001c0001t0001g0113 a0001c0001t0002g0005 others(77): Show |
83 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.519+5382T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4443884 | |||||||
| chr3:4443901 | A | C | 1 | a0002c0003t0001g0034 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.519+5365T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4443901 | |||||||
| chr3:4444160 | A | T | 2 | a0001c0001t0001g0076 a0001c0001t0018g0310 |
2 | HG02280.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.519+5106T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4444160 | |||||||
| chr3:4444278 | G | A | 2 | a0001c0001t0001g0134 a0003c0006t0001g0014 |
2 | HG02257.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.519+4988C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4444278 | |||||||
| chr3:4444443 | G | A | 1 | a0001c0002t0001g0350 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.519+4823C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4444443 | |||||||
| chr3:4444450 | T | A | 1 | a0001c0001t0001g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.519+4816A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4444450 | |||||||
| chr3:4444518 | T | C | 15 | a0001c0001t0002g0063 a0001c0001t0004g0052 a0001c0001t0004g0103 others(12): Show |
15 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.519+4748A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4444518 | |||||||
| chr3:4444524 | G | C | 83 | a0001c0001t0002g0069 a0001c0001t0002g0098 a0001c0001t0002g0126 others(80): Show |
85 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.519+4742C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4444524 | |||||||
| chr3:4444578 | T | C | 7 | a0001c0001t0001g0109 a0001c0001t0002g0319 a0001c0001t0005g0055 others(4): Show |
7 | HG01243.hp1 HG01243.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.519+4688A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4444578 | |||||||
| chr3:4444619 | C | A | 70 | a0001c0001t0002g0003 a0001c0001t0002g0098 a0001c0001t0002g0185 others(67): Show |
73 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.519+4647G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4444619 | |||||||
| chr3:4444647 | T | C | 5 | a0001c0001t0001g0368 a0001c0001t0004g0103 a0001c0001t0007g0064 others(2): Show |
5 | HG01243.hp2 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+4619A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4444647 | |||||||
| chr3:4444882 | T | A | 1 | a0001c0001t0007g0297 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.519+4384A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4444882 | |||||||
| chr3:4445031 | G | A | 3 | a0001c0001t0001g0305 a0001c0001t0004g0304 a0001c0001t0006g0303 |
3 | HG02615.hp2 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.519+4235C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4445031 | |||||||
| chr3:4445036 | T | C | 14 | a0001c0001t0001g0306 a0001c0001t0001g0368 a0001c0001t0005g0302 others(11): Show |
14 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.519+4230A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4445036 | |||||||
| chr3:4445159 | G | C | 7 | a0001c0001t0001g0076 a0001c0001t0004g0103 a0001c0001t0004g0128 others(4): Show |
7 | HG02280.hp2 HG02622.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.519+4107C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4445159 | |||||||
| chr3:4445246 | T | C | 1 | a0001c0001t0010g0041 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.519+4020A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4445246 | |||||||
| chr3:4445349 | C | T | 2 | a0001c0001t0001g0368 a0005c0007t0001g0019 |
2 | HG02572.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.519+3917G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4445349 | |||||||
| chr3:4445426 | C | A | 1 | a0001c0001t0001g0368 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.519+3840G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4445426 | |||||||
| chr3:4445434 | C | T | 1 | a0006c0008t0002g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.519+3832G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4445434 | |||||||
| chr3:4445529 | G | A | 1 | a0001c0002t0001g0246 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.519+3737C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4445529 | |||||||
| chr3:4445578 | C | G | 1 | a0001c0001t0002g0319 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.519+3688G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4445578 | |||||||
| chr3:4445582 | T | C | 121 | a0001c0001t0001g0076 a0001c0001t0001g0305 a0001c0001t0001g0306 others(118): Show |
126 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.519+3684A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4445582 | |||||||
| chr3:4445597 | G | A | 3 | a0001c0001t0005g0043 a0001c0001t0005g0363 a0001c0001t0012g0362 |
3 | HG02976.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.519+3669C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4445597 | |||||||
| chr3:4445665 | T | C | 9 | a0001c0001t0002g0005 a0001c0001t0002g0110 a0001c0001t0002g0171 others(6): Show |
10 | HG01106.hp2 HG01515.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.519+3601A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4445665 | |||||||
| chr3:4445958 | A | G | 1 | a0002c0004t0001g0039 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.519+3308T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4445958 | |||||||
| chr3:4445968 | C | G | 1 | a0001c0001t0001g0368 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.519+3298G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4445968 | |||||||
| chr3:4446001 | C | T | 4 | a0002c0003t0001g0033 a0002c0003t0001g0034 a0002c0003t0006g0036 others(1): Show |
4 | HG02109.hp1 HG02257.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.519+3265G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4446001 | |||||||
| chr3:4446224 | TG | T | 3 | a0001c0001t0001g0368 a0001c0001t0005g0373 a0005c0007t0001g0019 |
3 | HG02145.hp1 HG02572.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.519+3041delC | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4446224 | |||||||
| chr3:4446253 | T | G | 3 | a0001c0001t0005g0236 a0001c0001t0006g0234 a0006c0008t0002g0040 |
3 | HG02965.hp2 HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.519+3013A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4446253 | |||||||
| chr3:4446288 | T | C | 1 | a0001c0001t0010g0227 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.519+2978A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4446288 | |||||||
| chr3:4446615 | T | A | 1 | a0001c0001t0002g0136 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.519+2651A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4446615 | |||||||
| chr3:4446636 | A | G | 1 | a0001c0001t0002g0322 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.519+2630T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4446636 | |||||||
| chr3:4446724 | G | A | 4 | a0001c0001t0005g0370 a0001c0001t0006g0369 a0001c0001t0006g0371 others(1): Show |
4 | HG02055.hp2 HG02970.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+2542C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4446724 | |||||||
| chr3:4446858 | C | A | 7 | a0001c0001t0001g0368 a0001c0001t0005g0370 a0001c0001t0005g0373 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.519+2408G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4446858 | |||||||
| chr3:4447021 | G | T | 3 | a0001c0001t0005g0363 a0001c0001t0007g0364 a0001c0001t0012g0362 |
3 | HG02976.hp2 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.519+2245C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4447021 | |||||||
| chr3:4447172 | T | C | 3 | a0001c0001t0003g0011 a0001c0002t0001g0317 a0001c0002t0001g0350 |
4 | HG01257.hp1 HG01258.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+2094A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4447172 | |||||||
| chr3:4447196 | T | A | 75 | a0001c0001t0001g0320 a0001c0001t0001g0368 a0001c0001t0002g0009 others(72): Show |
78 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.519+2070A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4447196 | |||||||
| chr3:4447197 | A | T | 18 | a0001c0001t0001g0076 a0001c0001t0002g0008 a0001c0001t0002g0196 others(15): Show |
19 | HG00738.hp1 HG02056.hp2 HG02165.hp2 others(16): Show |
intron_variant | MODIFIER | c.519+2069T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4447197 | |||||||
| chr3:4447554 | A | G | 2 | a0001c0001t0005g0373 a0005c0007t0001g0019 |
2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.519+1712T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4447554 | |||||||
| chr3:4447860 | T | C | 7 | a0001c0001t0001g0368 a0001c0001t0005g0370 a0001c0001t0005g0373 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.519+1406A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4447860 | |||||||
| chr3:4447878 | T | C | 33 | a0001c0001t0001g0320 a0001c0001t0002g0009 a0001c0001t0002g0318 others(30): Show |
34 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.519+1388A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4447878 | |||||||
| chr3:4447901 | G | A | 6 | a0003c0005t0005g0013 a0003c0005t0005g0016 a0003c0005t0005g0017 others(3): Show |
6 | HG02922.hp1 HG03139.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.519+1365C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4447901 | |||||||
| chr3:4447913 | G | C | 1 | a0001c0001t0001g0306 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.519+1353C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4447913 | |||||||
| chr3:4448015 | C | A | 1 | a0001c0001t0002g0046 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.519+1251G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4448015 | |||||||
| chr3:4448047 | A | AAG | 96 | a0001c0001t0001g0320 a0001c0001t0002g0009 a0001c0001t0002g0069 others(93): Show |
100 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.519+1217_519+1218d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4448047 | |||||||
| chr3:4448056 | G | A | 4 | a0002c0003t0001g0033 a0002c0003t0001g0034 a0002c0003t0006g0036 others(1): Show |
4 | HG02109.hp1 HG02257.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.519+1210C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4448056 | |||||||
| chr3:4448093 | T | C | 95 | a0001c0001t0001g0320 a0001c0001t0002g0009 a0001c0001t0002g0069 others(92): Show |
99 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.519+1173A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4448093 | |||||||
| chr3:4448115 | T | G | 3 | a0001c0001t0002g0223 a0001c0001t0003g0222 a0001c0001t0008g0221 |
3 | HG01099.hp2 HG01261.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.519+1151A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4448115 | |||||||
| chr3:4448169 | T | C | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0004g0304 others(1): Show |
4 | HG02615.hp1 HG02615.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+1097A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4448169 | |||||||
| chr3:4448402 | A | C | 1 | a0001c0001t0002g0193 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.519+864T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4448402 | |||||||
| chr3:4448405 | CCTTCGT | C | 5 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0004g0304 others(2): Show |
5 | HG01243.hp2 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.519+855_519+860del others(6): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4448405 | |||||||
| chr3:4448410 | G | A | 1 | a0001c0001t0005g0302 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.519+856C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4448410 | |||||||
| chr3:4448630 | G | T | 1 | a0001c0002t0001g0283 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.519+636C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4448630 | |||||||
| chr3:4448664 | T | A | 1 | a0002c0003t0003g0022 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.519+602A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4448664 | |||||||
| chr3:4448759 | CT | C | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0004g0304 others(1): Show |
4 | HG02615.hp1 HG02615.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+506delA | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4448759 | |||||||
| chr3:4448829 | G | A | 105 | a0001c0001t0001g0076 a0001c0001t0001g0320 a0001c0001t0001g0368 others(102): Show |
110 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.519+437C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4448829 | |||||||
| chr3:4449016 | C | A | 4 | a0003c0005t0005g0016 a0003c0005t0005g0017 a0003c0005t0005g0018 others(1): Show |
4 | HG02922.hp1 HG03195.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+250G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 3/8 | chr3 | 4449016 | |||||||
| chr3:4449442 | A | G | 58 | a0001c0001t0001g0076 a0001c0001t0001g0320 a0001c0001t0002g0009 others(55): Show |
61 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.445-102T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4449442 | |||||||
| chr3:4449577 | T | G | 95 | a0001c0001t0001g0320 a0001c0001t0002g0009 a0001c0001t0002g0069 others(92): Show |
99 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.445-237A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4449577 | |||||||
| chr3:4449707 | G | A | 3 | a0001c0001t0011g0378 a0001c0001t0011g0379 a0001c0001t0011g0380 |
3 | HG02922.hp2 HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.445-367C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4449707 | |||||||
| chr3:4449772 | G | T | 1 | a0001c0002t0001g0237 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.445-432C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4449772 | |||||||
| chr3:4449827 | C | G | 2 | a0001c0001t0005g0074 a0001c0001t0005g0075 |
2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.445-487G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4449827 | |||||||
| chr3:4449856 | G | C | 68 | a0001c0001t0001g0320 a0001c0001t0002g0009 a0001c0001t0002g0069 others(65): Show |
71 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.445-516C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4449856 | |||||||
| chr3:4449877 | C | T | 2 | a0001c0001t0003g0010 a0001c0001t0003g0329 |
3 | HG01070.hp2 HG01071.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.445-537G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4449877 | |||||||
| chr3:4450011 | G | A | 5 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0004g0304 others(2): Show |
5 | HG01243.hp2 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-671C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4450011 | |||||||
| chr3:4450209 | A | G | 55 | a0001c0001t0001g0320 a0001c0001t0002g0009 a0001c0001t0002g0069 others(52): Show |
58 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.445-869T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4450209 | |||||||
| chr3:4450480 | T | C | 2 | a0001c0001t0003g0010 a0001c0001t0003g0329 |
3 | HG01070.hp2 HG01071.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.445-1140A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4450480 | |||||||
| chr3:4450523 | C | T | 1 | a0001c0001t0002g0012 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.445-1183G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4450523 | |||||||
| chr3:4450647 | A | T | 6 | a0003c0005t0005g0013 a0003c0005t0005g0016 a0003c0005t0005g0017 others(3): Show |
6 | HG02922.hp1 HG03139.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-1307T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4450647 | |||||||
| chr3:4450882 | A | G | 2 | a0001c0001t0003g0315 a0001c0002t0001g0316 |
2 | HG02523.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.445-1542T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4450882 | |||||||
| chr3:4450974 | CAG | C | 6 | a0003c0005t0005g0013 a0003c0005t0005g0016 a0003c0005t0005g0017 others(3): Show |
6 | HG02922.hp1 HG03139.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-1636_445-1635d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4450974 | |||||||
| chr3:4451072 | C | T | 4 | a0001c0002t0001g0138 a0001c0002t0001g0139 a0001c0002t0001g0140 others(1): Show |
4 | HG00280.hp2 HG01109.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.445-1732G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4451072 | |||||||
| chr3:4451091 | AAAAAT | A | 79 | a0001c0001t0001g0076 a0001c0001t0001g0320 a0001c0001t0001g0368 others(76): Show |
82 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.445-1756_445-1752d others(7): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4451091 | |||||||
| chr3:4451354 | T | C | 1 | a0001c0001t0001g0368 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.444+1522A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4451354 | |||||||
| chr3:4451423 | T | G | 17 | a0001c0001t0003g0165 a0002c0003t0002g0001 a0002c0003t0002g0021 others(14): Show |
18 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.444+1453A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4451423 | |||||||
| chr3:4451461 | A | G | 3 | a0001c0001t0011g0378 a0001c0001t0011g0379 a0001c0001t0011g0380 |
3 | HG02922.hp2 HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.444+1415T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4451461 | |||||||
| chr3:4451478 | G | A | 1 | a0001c0001t0004g0244 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.444+1398C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4451478 | |||||||
| chr3:4451606 | A | G | 6 | a0003c0005t0005g0013 a0003c0005t0005g0016 a0003c0005t0005g0017 others(3): Show |
6 | HG02922.hp1 HG03139.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.444+1270T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4451606 | |||||||
| chr3:4451687 | G | T | 68 | a0001c0001t0001g0320 a0001c0001t0002g0009 a0001c0001t0002g0069 others(65): Show |
71 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.444+1189C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4451687 | |||||||
| chr3:4451719 | T | C | 7 | a0001c0001t0001g0368 a0001c0001t0005g0370 a0001c0001t0005g0373 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.444+1157A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4451719 | |||||||
| chr3:4451777 | G | A | 7 | a0001c0001t0001g0368 a0001c0001t0005g0370 a0001c0001t0005g0373 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.444+1099C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4451777 | |||||||
| chr3:4451792 | T | A | 1 | a0001c0001t0002g0351 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.444+1084A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4451792 | |||||||
| chr3:4451842 | C | A | 1 | a0003c0005t0005g0013 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.444+1034G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4451842 | |||||||
| chr3:4451845 | G | A | 1 | a0001c0001t0002g0012 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.444+1031C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4451845 | |||||||
| chr3:4451919 | G | A | 2 | a0001c0001t0005g0373 a0005c0007t0001g0019 |
2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.444+957C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4451919 | |||||||
| chr3:4451975 | G | A | 6 | a0003c0005t0005g0013 a0003c0005t0005g0016 a0003c0005t0005g0017 others(3): Show |
6 | HG02922.hp1 HG03139.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.444+901C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4451975 | |||||||
| chr3:4451983 | CA | C | 3 | a0001c0001t0011g0378 a0001c0001t0011g0379 a0001c0001t0011g0380 |
3 | HG02922.hp2 HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.444+892delT | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4451983 | |||||||
| chr3:4452045 | A | T | 7 | a0001c0001t0001g0368 a0001c0001t0005g0370 a0001c0001t0005g0373 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.444+831T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4452045 | |||||||
| chr3:4452092 | T | G | 1 | a0001c0002t0001g0166 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.444+784A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4452092 | |||||||
| chr3:4452187 | G | A | 25 | a0001c0001t0005g0302 a0001c0001t0007g0299 a0001c0001t0009g0300 others(22): Show |
26 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.444+689C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4452187 | |||||||
| chr3:4452250 | G | C | 9 | a0001c0001t0005g0302 a0001c0001t0007g0299 a0001c0001t0009g0300 others(6): Show |
9 | HG02109.hp1 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.444+626C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4452250 | |||||||
| chr3:4452511 | T | C | 3 | a0001c0001t0011g0378 a0001c0001t0011g0379 a0001c0001t0011g0380 |
3 | HG02922.hp2 HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.444+365A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4452511 | |||||||
| chr3:4452710 | A | G | 1 | a0001c0001t0003g0315 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.444+166T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4452710 | |||||||
| chr3:4452725 | G | A | 3 | a0001c0001t0001g0076 a0001c0001t0008g0078 a0001c0002t0001g0077 |
3 | HG02280.hp2 HG03834.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.444+151C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4452725 | |||||||
| chr3:4452849 | T | C | 3 | a0001c0001t0001g0368 a0001c0001t0005g0373 a0005c0007t0001g0019 |
3 | HG02145.hp1 HG02572.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.444+27A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 2/8 | chr3 | 4452849 | |||||||
| chr3:4453094 | G | A | 1 | a0001c0001t0004g0290 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.271-45C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4453094 | |||||||
| chr3:4453147 | T | C | 7 | a0001c0001t0001g0368 a0001c0001t0005g0370 a0001c0001t0005g0373 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.271-98A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4453147 | |||||||
| chr3:4453179 | C | T | 3 | a0001c0001t0011g0378 a0001c0001t0011g0379 a0001c0001t0011g0380 |
3 | HG02922.hp2 HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.271-130G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4453179 | |||||||
| chr3:4453197 | C | A | 1 | a0001c0002t0001g0167 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.271-148G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4453197 | |||||||
| chr3:4453206 | A | C | 3 | a0001c0001t0002g0239 a0001c0001t0004g0241 a0001c0002t0001g0240 |
3 | HG00408.hp2 NA19001.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.271-157T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4453206 | |||||||
| chr3:4453241 | C | A | 8 | a0001c0001t0001g0042 a0001c0001t0001g0053 a0001c0001t0001g0054 others(5): Show |
8 | HG01891.hp1 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.271-192G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4453241 | |||||||
| chr3:4453285 | A | G | 4 | a0001c0001t0005g0043 a0001c0001t0005g0363 a0001c0001t0007g0364 others(1): Show |
4 | HG02976.hp2 HG03471.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-236T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4453285 | |||||||
| chr3:4453494 | A | G | 25 | a0001c0001t0005g0302 a0001c0001t0007g0299 a0001c0001t0009g0300 others(22): Show |
26 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.271-445T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4453494 | |||||||
| chr3:4453533 | A | AT | 95 | a0001c0001t0001g0076 a0001c0001t0001g0320 a0001c0001t0001g0368 others(92): Show |
100 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.271-485dupA | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4453533 | |||||||
| chr3:4453533 | AT | A | 5 | a0001c0001t0003g0006 a0001c0001t0003g0224 a0001c0001t0003g0226 others(2): Show |
6 | NA18960.hp2 NA18970.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.271-485delA | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4453533 | |||||||
| chr3:4453555 | C | T | 4 | a0001c0001t0005g0043 a0001c0001t0005g0363 a0001c0001t0007g0364 others(1): Show |
4 | HG02976.hp2 HG03471.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-506G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4453555 | |||||||
| chr3:4453601 | A | G | 1 | a0001c0001t0002g0254 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.271-552T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4453601 | |||||||
| chr3:4453615 | C | A | 1 | a0001c0001t0004g0112 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.271-566G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4453615 | |||||||
| chr3:4453706 | G | C | 1 | a0001c0001t0001g0368 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.271-657C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4453706 | |||||||
| chr3:4453795 | A | G | 1 | a0001c0002t0001g0317 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.271-746T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4453795 | |||||||
| chr3:4453963 | C | A | 1 | a0002c0004t0001g0039 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.271-914G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4453963 | |||||||
| chr3:4454001 | T | C | 1 | a0001c0001t0002g0012 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.271-952A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4454001 | |||||||
| chr3:4454055 | T | C | 2 | a0001c0001t0006g0184 a0001c0001t0006g0190 |
2 | HG01243.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.271-1006A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4454055 | |||||||
| chr3:4454236 | A | G | 1 | a0001c0001t0003g0137 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.271-1187T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4454236 | |||||||
| chr3:4454241 | T | C | 107 | a0001c0001t0001g0076 a0001c0001t0001g0320 a0001c0001t0001g0368 others(104): Show |
112 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.271-1192A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4454241 | |||||||
| chr3:4454448 | T | C | 4 | a0001c0001t0005g0370 a0001c0001t0006g0369 a0001c0001t0006g0371 others(1): Show |
4 | HG02055.hp2 HG02970.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-1399A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4454448 | |||||||
| chr3:4454458 | T | C | 2 | a0001c0001t0004g0292 a0001c0001t0021g0289 |
2 | HG00558.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.271-1409A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4454458 | |||||||
| chr3:4454547 | G | C | 3 | a0001c0001t0001g0076 a0001c0001t0008g0078 a0001c0002t0001g0077 |
3 | HG02280.hp2 HG03834.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.271-1498C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4454547 | |||||||
| chr3:4454578 | T | C | 1 | a0001c0001t0004g0086 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.271-1529A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4454578 | |||||||
| chr3:4454736 | T | A | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0004g0304 others(1): Show |
4 | HG02615.hp1 HG02615.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-1687A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4454736 | |||||||
| chr3:4455024 | T | A | 1 | a0001c0001t0005g0043 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.271-1975A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4455024 | |||||||
| chr3:4455181 | C | T | 105 | a0001c0001t0001g0076 a0001c0001t0001g0320 a0001c0001t0001g0368 others(102): Show |
110 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.271-2132G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4455181 | |||||||
| chr3:4455189 | T | C | 1 | a0001c0001t0007g0364 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.271-2140A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4455189 | |||||||
| chr3:4455209 | G | A | 4 | a0001c0001t0001g0042 a0001c0001t0001g0053 a0001c0001t0001g0054 others(1): Show |
4 | HG02622.hp2 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-2160C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4455209 | |||||||
| chr3:4455303 | A | T | 1 | a0005c0007t0001g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.271-2254T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4455303 | |||||||
| chr3:4455383 | C | A | 3 | a0001c0001t0001g0076 a0001c0001t0008g0078 a0001c0002t0001g0077 |
3 | HG02280.hp2 HG03834.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.271-2334G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4455383 | |||||||
| chr3:4455545 | G | A | 1 | a0001c0001t0010g0041 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.271-2496C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4455545 | |||||||
| chr3:4455705 | A | G | 1 | a0001c0001t0002g0323 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.271-2656T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4455705 | |||||||
| chr3:4455712 | G | A | 7 | a0001c0001t0001g0368 a0001c0001t0005g0370 a0001c0001t0005g0373 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.271-2663C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4455712 | |||||||
| chr3:4455736 | A | G | 1 | a0001c0001t0002g0319 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.271-2687T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4455736 | |||||||
| chr3:4455819 | C | T | 6 | a0003c0005t0005g0013 a0003c0005t0005g0016 a0003c0005t0005g0017 others(3): Show |
6 | HG02922.hp1 HG03139.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.271-2770G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4455819 | |||||||
| chr3:4455959 | G | C | 3 | a0001c0001t0001g0134 a0001c0001t0005g0135 a0001c0002t0001g0311 |
3 | HG02257.hp1 HG02809.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.271-2910C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4455959 | |||||||
| chr3:4455970 | T | C | 3 | a0001c0001t0001g0076 a0001c0001t0008g0078 a0001c0002t0001g0077 |
3 | HG02280.hp2 HG03834.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.271-2921A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4455970 | |||||||
| chr3:4456012 | G | T | 1 | a0001c0001t0003g0011 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.271-2963C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456012 | |||||||
| chr3:4456175 | T | C | 3 | a0001c0001t0001g0320 a0001c0001t0002g0319 a0001c0001t0010g0321 |
3 | HG02559.hp2 HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.271-3126A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456175 | |||||||
| chr3:4456397 | C | G | 3 | a0001c0001t0001g0076 a0001c0001t0008g0078 a0001c0002t0001g0077 |
3 | HG02280.hp2 HG03834.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.271-3348G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456397 | |||||||
| chr3:4456454 | G | GTT | 104 | a0001c0001t0001g0076 a0001c0001t0001g0320 a0001c0001t0001g0368 others(101): Show |
109 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.271-3407_271-3406d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456454 | |||||||
| chr3:4456502 | A | C | 1 | a0001c0001t0002g0291 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.271-3453T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456502 | |||||||
| chr3:4456515 | G | A | 1 | a0001c0001t0004g0002 | 2 | HG00642.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.271-3466C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456515 | |||||||
| chr3:4456610 | C | G | 1 | a0001c0001t0008g0078 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.271-3561G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456610 | |||||||
| chr3:4456617 | A | AAT | 10 | a0001c0001t0001g0058 a0001c0001t0001g0368 a0001c0001t0002g0136 others(7): Show |
10 | HG01516.hp2 HG01884.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.271-3570_271-3569d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456617 | |||||||
| chr3:4456618 | A | ATATATAT others(31): Show |
3 | a0001c0001t0011g0378 a0001c0001t0011g0379 a0001c0001t0011g0380 |
3 | HG02922.hp2 HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.271-3570_271-3569i others(40): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456618 | |||||||
| chr3:4456635 | C | CGTGTATA others(13): Show |
1 | a0001c0002t0001g0262 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.271-3606_271-3587d others(22): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456635 | |||||||
| chr3:4456635 | C | T | 1 | a0002c0004t0001g0032 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.271-3586G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456635 | |||||||
| chr3:4456636 | G | A | 1 | a0002c0004t0001g0032 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.271-3587C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456636 | |||||||
| chr3:4456637 | T | C | 1 | a0002c0004t0001g0032 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.271-3588A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456637 | |||||||
| chr3:4456638 | G | GTA | 3 | a0001c0002t0001g0080 a0001c0002t0001g0081 a0001c0002t0001g0082 |
3 | NA18961.hp2 NA18984.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.271-3591_271-3590d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456638 | |||||||
| chr3:4456638 | GTA | G | 27 | a0001c0001t0001g0076 a0001c0001t0005g0302 a0001c0001t0007g0299 others(24): Show |
28 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.271-3591_271-3590d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456638 | |||||||
| chr3:4456640 | A | ATATATAT others(27): Show |
2 | a0001c0001t0003g0011 a0001c0002t0001g0317 |
3 | HG01257.hp1 HG01258.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.271-3592_271-3591i others(36): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456640 | |||||||
| chr3:4456640 | A | ATATATAT others(29): Show |
54 | a0001c0001t0001g0320 a0001c0001t0002g0009 a0001c0001t0002g0069 others(51): Show |
56 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.271-3592_271-3591i others(38): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456640 | |||||||
| chr3:4456640 | A | G | 1 | a0002c0004t0001g0032 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.271-3591T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456640 | |||||||
| chr3:4456642 | A | G | 1 | a0001c0001t0005g0302 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.271-3593T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456642 | |||||||
| chr3:4456648 | A | ATG | 10 | a0001c0001t0005g0043 a0001c0001t0005g0363 a0001c0001t0007g0364 others(7): Show |
10 | HG02922.hp1 HG02976.hp2 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.271-3600_271-3599i others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456648 | |||||||
| chr3:4456650 | A | G | 18 | a0001c0001t0002g0008 a0001c0001t0002g0353 a0001c0001t0002g0354 others(15): Show |
19 | HG02056.hp2 HG02922.hp1 HG02922.hp2 others(16): Show |
intron_variant | MODIFIER | c.271-3601T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456650 | |||||||
| chr3:4456650 | ATG | A | 7 | a0001c0001t0001g0368 a0001c0001t0005g0370 a0001c0001t0005g0373 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.271-3603_271-3602d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456650 | |||||||
| chr3:4456655 | T | TGTGTATA others(11): Show |
1 | a0001c0001t0010g0227 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.271-3624_271-3607d others(20): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456655 | |||||||
| chr3:4456656 | G | GTATATAT others(33): Show |
3 | a0001c0001t0002g0008 a0001c0001t0002g0353 a0001c0001t0002g0354 |
4 | HG02056.hp2 NA18969.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-3608_271-3607i others(42): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456656 | |||||||
| chr3:4456658 | G | A | 5 | a0001c0001t0002g0008 a0001c0001t0002g0012 a0001c0001t0002g0353 others(2): Show |
7 | HG02056.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.271-3609C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456658 | |||||||
| chr3:4456658 | G | GTA | 57 | a0001c0001t0001g0320 a0001c0001t0002g0009 a0001c0001t0002g0069 others(54): Show |
59 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.271-3611_271-3610d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456658 | |||||||
| chr3:4456671 | T | C | 1 | a0001c0002t0001g0228 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.271-3622A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456671 | |||||||
| chr3:4456673 | C | CGTGTATA others(49): Show |
1 | a0001c0001t0005g0302 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.271-3625_271-3624i others(58): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456673 | |||||||
| chr3:4456686 | A | G | 5 | a0001c0001t0005g0370 a0001c0001t0006g0369 a0001c0001t0006g0371 others(2): Show |
5 | HG02055.hp2 HG02293.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.271-3637T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456686 | |||||||
| chr3:4456692 | GTA | G | 6 | a0001c0001t0001g0058 a0001c0001t0003g0329 a0001c0001t0005g0066 others(3): Show |
6 | HG01123.hp2 HG02258.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.271-3645_271-3644d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456692 | |||||||
| chr3:4456694 | A | G | 50 | a0001c0001t0001g0368 a0001c0001t0004g0103 a0001c0001t0005g0043 others(47): Show |
51 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.271-3645T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456694 | |||||||
| chr3:4456701 | T | C | 8 | a0001c0001t0001g0113 a0001c0001t0002g0349 a0001c0001t0005g0105 others(5): Show |
8 | HG01891.hp2 HG02965.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.271-3652A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456701 | |||||||
| chr3:4456703 | T | C | 6 | a0001c0001t0005g0266 a0001c0001t0005g0370 a0001c0001t0006g0369 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.271-3654A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456703 | |||||||
| chr3:4456704 | A | G | 4 | a0001c0001t0005g0370 a0001c0001t0006g0369 a0001c0001t0006g0371 others(1): Show |
4 | HG02055.hp2 HG02970.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-3655T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456704 | |||||||
| chr3:4456705 | C | T | 4 | a0001c0001t0005g0370 a0001c0001t0006g0369 a0001c0001t0006g0371 others(1): Show |
4 | HG02055.hp2 HG02970.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-3656G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456705 | |||||||
| chr3:4456706 | G | A | 4 | a0001c0001t0005g0370 a0001c0001t0006g0369 a0001c0001t0006g0371 others(1): Show |
4 | HG02055.hp2 HG02970.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-3657C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456706 | |||||||
| chr3:4456706 | G | GTA | 76 | a0001c0001t0001g0076 a0001c0001t0001g0320 a0001c0001t0001g0368 others(73): Show |
80 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.271-3659_271-3658d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456706 | |||||||
| chr3:4456706 | G | GTATATAT others(35): Show |
1 | a0001c0001t0002g0360 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.271-3658_271-3657i others(44): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456706 | |||||||
| chr3:4456714 | ATACATAT others(11): Show |
A | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0004g0304 others(1): Show |
4 | HG02615.hp1 HG02615.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-3683_271-3666d others(20): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456714 | |||||||
| chr3:4456739 | T | C | 5 | a0001c0001t0007g0299 a0001c0001t0009g0300 a0001c0001t0009g0301 others(2): Show |
5 | HG02976.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.271-3690A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456739 | |||||||
| chr3:4456739 | T | TAC | 25 | a0001c0001t0011g0378 a0001c0001t0011g0379 a0001c0001t0011g0380 others(22): Show |
26 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.271-3692_271-3691d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456739 | |||||||
| chr3:4456741 | C | CACACATA others(21): Show |
4 | a0001c0001t0001g0134 a0001c0001t0005g0135 a0001c0002t0001g0246 others(1): Show |
4 | HG00544.hp1 HG02257.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-3720_271-3693d others(30): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456741 | |||||||
| chr3:4456753 | CGT | C | 5 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0004g0304 others(2): Show |
5 | HG02615.hp1 HG02615.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.271-3706_271-3705d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456753 | |||||||
| chr3:4456769 | T | C | 35 | a0001c0001t0001g0076 a0001c0001t0002g0281 a0001c0001t0002g0282 others(32): Show |
35 | HG00558.hp2 HG02040.hp2 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.271-3720A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456769 | |||||||
| chr3:4456771 | C | CGTGT | 63 | a0001c0001t0001g0320 a0001c0001t0002g0008 a0001c0001t0002g0009 others(60): Show |
67 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.271-3723_271-3722i others(6): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456771 | |||||||
| chr3:4456772 | A | ACATATAT others(21): Show |
1 | a0001c0001t0004g0091 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.271-3751_271-3724d others(30): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456772 | |||||||
| chr3:4456773 | C | CATATATA others(23): Show |
1 | a0001c0001t0002g0254 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.271-3725_271-3724i others(32): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456773 | |||||||
| chr3:4456773 | C | CATATATA others(23): Show |
2 | a0001c0001t0004g0128 a0001c0001t0004g0129 |
2 | HG02622.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.271-3725_271-3724i others(32): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456773 | |||||||
| chr3:4456773 | C | CATATATA others(129): Show |
1 | a0001c0001t0006g0372 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.271-3725_271-3724i others(138): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456773 | |||||||
| chr3:4456773 | C | CATATATA others(161): Show |
3 | a0001c0001t0005g0370 a0001c0001t0006g0369 a0001c0001t0006g0371 |
3 | HG02970.hp1 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.271-3725_271-3724i others(170): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456773 | |||||||
| chr3:4456773 | C | T | 63 | a0001c0001t0001g0320 a0001c0001t0002g0008 a0001c0001t0002g0009 others(60): Show |
67 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.271-3724G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456773 | |||||||
| chr3:4456783 | T | TGTGTGTA others(307): Show |
2 | a0001c0001t0002g0126 a0001c0001t0002g0127 |
2 | NA19001.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.271-3735_271-3734i others(316): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456783 | |||||||
| chr3:4456786 | G | C | 1 | a0001c0001t0002g0296 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.271-3737C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456786 | |||||||
| chr3:4456790 | G | GTATATAT others(195): Show |
1 | a0002c0003t0003g0022 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.271-3742_271-3741i others(204): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456790 | |||||||
| chr3:4456797 | T | TACGTGTA others(343): Show |
1 | a0001c0001t0005g0067 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.271-3749_271-3748i others(352): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456797 | |||||||
| chr3:4456815 | T | TGTGTGTA others(97): Show |
1 | a0001c0001t0002g0351 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.271-3767_271-3766i others(106): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456815 | |||||||
| chr3:4456815 | T | TGTGTGTG others(97): Show |
4 | a0001c0001t0002g0069 a0001c0001t0004g0312 a0001c0002t0001g0068 others(1): Show |
4 | HG01109.hp1 HG01261.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-3767_271-3766i others(106): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456815 | |||||||
| chr3:4456815 | T | TGTGTGTG others(97): Show |
1 | a0001c0001t0002g0353 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.271-3767_271-3766i others(106): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456815 | |||||||
| chr3:4456815 | T | TGTGTGTG others(99): Show |
49 | a0001c0001t0001g0320 a0001c0001t0002g0008 a0001c0001t0002g0009 others(46): Show |
52 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.271-3767_271-3766i others(108): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456815 | |||||||
| chr3:4456815 | T | TGTGTGTG others(131): Show |
2 | a0001c0001t0003g0011 a0001c0002t0001g0317 |
3 | HG01257.hp1 HG01258.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.271-3767_271-3766i others(140): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456815 | |||||||
| chr3:4456815 | T | TGTGTGTG others(273): Show |
1 | a0001c0001t0003g0083 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.271-3767_271-3766i others(282): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456815 | |||||||
| chr3:4456815 | T | TGTGTGTG others(165): Show |
2 | a0001c0001t0005g0043 a0001c0001t0007g0364 |
2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.271-3767_271-3766i others(174): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456815 | |||||||
| chr3:4456815 | T | TGTGTGTG others(197): Show |
2 | a0001c0001t0011g0379 a0001c0001t0011g0380 |
2 | HG02922.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.271-3767_271-3766i others(206): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456815 | |||||||
| chr3:4456815 | T | TGTGTGTG others(197): Show |
1 | a0003c0005t0005g0013 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.271-3767_271-3766i others(206): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456815 | |||||||
| chr3:4456815 | T | TGTGTGTG others(233): Show |
1 | a0001c0001t0011g0378 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.271-3767_271-3766i others(242): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456815 | |||||||
| chr3:4456815 | T | TGTGTGTG others(201): Show |
2 | a0001c0001t0005g0363 a0001c0001t0012g0362 |
2 | HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.271-3767_271-3766i others(210): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456815 | |||||||
| chr3:4456822 | G | A | 4 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0005g0067 others(1): Show |
4 | HG01943.hp1 HG02647.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-3773C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAC others(279): Show |
1 | a0001c0001t0002g0254 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.271-3774_271-3773i others(288): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(371): Show |
1 | a0001c0001t0001g0306 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.271-3774_271-3773i others(380): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(371): Show |
2 | a0001c0001t0001g0305 a0001c0001t0004g0304 |
2 | NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.271-3774_271-3773i others(380): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(341): Show |
1 | a0001c0001t0006g0190 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.271-3774_271-3773i others(350): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(437): Show |
2 | a0001c0001t0004g0128 a0001c0001t0004g0129 |
2 | HG02622.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.271-3774_271-3773i others(446): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(371): Show |
1 | a0001c0001t0006g0303 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.271-3774_271-3773i others(380): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(309): Show |
1 | a0001c0001t0003g0108 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.271-3774_271-3773i others(318): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(373): Show |
1 | a0001c0001t0005g0045 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.271-3774_271-3773i others(382): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(313): Show |
1 | a0001c0001t0006g0133 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.271-3774_271-3773i others(322): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(281): Show |
2 | a0001c0001t0005g0132 a0001c0001t0006g0131 |
2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.271-3774_271-3773i others(290): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(311): Show |
1 | a0001c0002t0001g0180 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.271-3774_271-3773i others(320): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(309): Show |
3 | a0001c0001t0002g0235 a0001c0001t0005g0236 a0001c0001t0006g0234 |
3 | HG02965.hp2 HG03098.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.271-3774_271-3773i others(318): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(341): Show |
1 | a0001c0002t0001g0169 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.271-3774_271-3773i others(350): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(309): Show |
9 | a0001c0001t0001g0109 a0001c0001t0002g0005 a0001c0001t0002g0110 others(6): Show |
10 | HG01106.hp2 HG01515.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.271-3774_271-3773i others(318): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(311): Show |
2 | a0001c0001t0004g0251 a0001c0002t0001g0250 |
2 | HG01175.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.271-3774_271-3773i others(320): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(311): Show |
5 | a0001c0001t0002g0178 a0001c0001t0008g0272 a0001c0002t0001g0007 others(2): Show |
6 | HG00323.hp1 HG00642.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.271-3774_271-3773i others(320): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(413): Show |
1 | a0001c0001t0002g0046 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.271-3774_271-3773i others(422): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(313): Show |
1 | a0001c0001t0004g0085 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.271-3774_271-3773i others(322): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(281): Show |
1 | a0001c0002t0001g0181 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.271-3774_271-3773i others(290): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(315): Show |
1 | a0001c0001t0002g0177 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.271-3774_271-3773i others(324): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(371): Show |
1 | a0001c0001t0001g0047 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.271-3774_271-3773i others(380): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(341): Show |
2 | a0001c0001t0003g0230 a0001c0001t0003g0231 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.271-3774_271-3773i others(350): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(339): Show |
1 | a0001c0002t0015g0130 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.271-3774_271-3773i others(348): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(433): Show |
1 | a0001c0001t0007g0297 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.271-3774_271-3773i others(442): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(341): Show |
1 | a0001c0002t0001g0116 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.271-3774_271-3773i others(350): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(341): Show |
1 | a0001c0001t0004g0091 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.271-3774_271-3773i others(350): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(309): Show |
1 | a0001c0001t0004g0002 | 2 | HG00642.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.271-3774_271-3773i others(318): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(277): Show |
1 | a0001c0001t0002g0247 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.271-3774_271-3773i others(286): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(347): Show |
1 | a0007c0009t0004g0121 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.271-3774_271-3773i others(356): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(343): Show |
1 | a0001c0001t0004g0092 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.271-3774_271-3773i others(352): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(341): Show |
1 | a0001c0001t0003g0094 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.271-3774_271-3773i others(350): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(373): Show |
1 | a0001c0001t0004g0090 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.271-3774_271-3773i others(382): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(309): Show |
2 | a0001c0001t0002g0258 a0001c0001t0002g0259 |
2 | NA19060.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.271-3774_271-3773i others(318): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(309): Show |
1 | a0001c0001t0003g0257 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.271-3774_271-3773i others(318): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(341): Show |
2 | a0001c0001t0020g0249 a0001c0002t0001g0248 |
2 | NA18966.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.271-3774_271-3773i others(350): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(309): Show |
1 | a0001c0002t0001g0246 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.271-3774_271-3773i others(318): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(339): Show |
1 | a0001c0001t0003g0365 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.271-3774_271-3773i others(348): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(341): Show |
1 | a0001c0001t0004g0093 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.271-3774_271-3773i others(350): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(373): Show |
2 | a0001c0001t0004g0087 a0001c0001t0004g0088 |
2 | NA19007.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.271-3774_271-3773i others(382): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(341): Show |
2 | a0001c0001t0004g0086 a0001c0002t0001g0256 |
2 | HG01978.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.271-3774_271-3773i others(350): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(327): Show |
1 | a0001c0001t0003g0095 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.271-3774_271-3773i others(336): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(309): Show |
1 | a0001c0001t0002g0252 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.271-3774_271-3773i others(318): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(341): Show |
13 | a0001c0001t0002g0239 a0001c0001t0002g0243 a0001c0001t0002g0277 others(10): Show |
13 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(10): Show |
intron_variant | MODIFIER | c.271-3774_271-3773i others(350): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(501): Show |
1 | a0001c0002t0001g0255 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.271-3774_271-3773i others(510): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(373): Show |
1 | a0001c0001t0003g0079 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.271-3774_271-3773i others(382): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(341): Show |
3 | a0001c0001t0004g0294 a0001c0002t0001g0081 a0001c0002t0001g0082 |
3 | HG00621.hp2 NA18961.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.271-3774_271-3773i others(350): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(373): Show |
1 | a0001c0001t0002g0308 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.271-3774_271-3773i others(382): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(379): Show |
1 | a0001c0001t0002g0296 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.271-3774_271-3773i others(388): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(373): Show |
2 | a0001c0001t0005g0075 a0001c0002t0001g0080 |
2 | HG03130.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.271-3774_271-3773i others(382): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(307): Show |
1 | a0001c0001t0003g0117 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.271-3774_271-3773i others(316): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(409): Show |
1 | a0001c0001t0012g0104 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.271-3774_271-3773i others(418): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(309): Show |
8 | a0001c0001t0002g0233 a0001c0001t0003g0004 a0001c0001t0003g0114 others(5): Show |
9 | HG01175.hp1 HG01516.hp1 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.271-3774_271-3773i others(318): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(341): Show |
57 | a0001c0001t0001g0113 a0001c0001t0002g0003 a0001c0001t0002g0097 others(54): Show |
59 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.271-3774_271-3773i others(350): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(373): Show |
17 | a0001c0001t0001g0058 a0001c0001t0002g0063 a0001c0001t0002g0189 others(14): Show |
17 | HG00438.hp1 HG00558.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.271-3774_271-3773i others(382): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(405): Show |
6 | a0001c0001t0002g0261 a0001c0001t0005g0056 a0001c0001t0005g0105 others(3): Show |
6 | HG00639.hp2 HG01243.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.271-3774_271-3773i others(414): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(437): Show |
8 | a0001c0001t0001g0042 a0001c0001t0001g0053 a0001c0001t0001g0054 others(5): Show |
8 | HG01891.hp1 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.271-3774_271-3773i others(446): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(469): Show |
1 | a0001c0001t0003g0122 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.271-3774_271-3773i others(478): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(373): Show |
2 | a0001c0001t0001g0134 a0001c0001t0005g0044 |
2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.271-3774_271-3773i others(382): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(341): Show |
54 | a0001c0001t0002g0136 a0001c0001t0002g0149 a0001c0001t0002g0270 others(51): Show |
54 | HG00280.hp2 HG00673.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.271-3774_271-3773i others(350): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(309): Show |
1 | a0001c0002t0001g0170 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.271-3774_271-3773i others(318): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(372): Show |
1 | a0001c0001t0005g0066 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.271-3774_271-3773i others(381): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(343): Show |
1 | a0006c0008t0002g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.271-3774_271-3773i others(352): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(373): Show |
1 | a0001c0001t0003g0271 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.271-3774_271-3773i others(382): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(135): Show |
1 | a0002c0003t0001g0033 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.271-3774_271-3773i others(144): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(345): Show |
1 | a0001c0002t0001g0237 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.271-3774_271-3773i others(354): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(341): Show |
1 | a0001c0002t0001g0118 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.271-3774_271-3773i others(350): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(373): Show |
1 | a0001c0002t0001g0089 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.271-3774_271-3773i others(382): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(309): Show |
1 | a0001c0001t0002g0253 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.271-3774_271-3773i others(318): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(341): Show |
1 | a0001c0001t0002g0245 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.271-3774_271-3773i others(350): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(373): Show |
1 | a0001c0001t0002g0238 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.271-3774_271-3773i others(382): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(371): Show |
1 | a0001c0001t0004g0293 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.271-3774_271-3773i others(380): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(373): Show |
3 | a0001c0001t0002g0192 a0001c0001t0002g0193 a0001c0001t0003g0191 |
3 | HG02155.hp1 HG03239.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.271-3774_271-3773i others(382): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(405): Show |
2 | a0001c0001t0002g0185 a0001c0001t0007g0057 |
2 | HG03130.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.271-3774_271-3773i others(414): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(373): Show |
2 | a0001c0001t0002g0281 a0001c0001t0002g0282 |
2 | NA18999.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.271-3774_271-3773i others(382): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(135): Show |
9 | a0001c0001t0001g0076 a0001c0001t0005g0302 a0001c0001t0007g0299 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.271-3774_271-3773i others(144): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(167): Show |
19 | a0001c0001t0008g0078 a0002c0003t0002g0001 a0002c0003t0002g0023 others(16): Show |
20 | HG00323.hp2 HG01099.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.271-3774_271-3773i others(176): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(169): Show |
1 | a0001c0001t0010g0041 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.271-3774_271-3773i others(178): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(107): Show |
1 | a0002c0003t0002g0021 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.271-3774_271-3773i others(116): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(345): Show |
1 | a0001c0001t0002g0229 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.271-3774_271-3773i others(354): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456822 | G | GTATATAT others(341): Show |
1 | a0001c0001t0004g0290 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.271-3774_271-3773i others(350): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456822 | |||||||
| chr3:4456828 | A | ATACGTGT others(311): Show |
1 | a0001c0001t0002g0012 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.271-3780_271-3779i others(320): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456828 | |||||||
| chr3:4456829 | T | TACGTGTA others(277): Show |
1 | a0001c0001t0002g0260 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.271-3781_271-3780i others(286): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456829 | |||||||
| chr3:4456829 | T | TACGTGTA others(341): Show |
1 | a0001c0002t0001g0096 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.271-3781_271-3780i others(350): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456829 | |||||||
| chr3:4456836 | A | ATATATAT others(147): Show |
1 | a0001c0001t0005g0373 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.271-3788_271-3787i others(156): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456836 | |||||||
| chr3:4456836 | A | ATATATAT others(119): Show |
1 | a0005c0007t0001g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.271-3788_271-3787i others(128): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456836 | |||||||
| chr3:4456836 | A | ATATATAT others(211): Show |
1 | a0001c0001t0001g0368 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.271-3788_271-3787i others(220): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456836 | |||||||
| chr3:4456846 | G | GTGTGTGT others(161): Show |
1 | a0001c0001t0002g0366 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-3798_271-3797i others(170): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456846 | |||||||
| chr3:4456846 | G | GTGTGTGT others(131): Show |
2 | a0001c0001t0002g0327 a0001c0001t0004g0328 |
2 | NA18997.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.271-3798_271-3797i others(140): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456846 | |||||||
| chr3:4456847 | T | TGTGTGTG others(163): Show |
1 | a0003c0006t0001g0014 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.271-3799_271-3798i others(172): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456847 | |||||||
| chr3:4456854 | A | G | 1 | a0003c0006t0001g0014 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.271-3805T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456854 | |||||||
| chr3:4456861 | T | C | 1 | a0001c0001t0017g0298 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.271-3812A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456861 | |||||||
| chr3:4456865 | T | TATATATA others(99): Show |
1 | a0001c0001t0017g0298 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.271-3817_271-3816i others(108): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456865 | |||||||
| chr3:4456874 | C | A | 1 | a0001c0001t0017g0298 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.271-3825G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456874 | |||||||
| chr3:4456879 | T | C | 1 | a0001c0001t0017g0298 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.271-3830A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456879 | |||||||
| chr3:4456880 | G | A | 108 | a0001c0001t0001g0076 a0001c0001t0001g0320 a0001c0001t0001g0368 others(105): Show |
113 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.271-3831C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456880 | |||||||
| chr3:4456881 | T | C | 108 | a0001c0001t0001g0076 a0001c0001t0001g0320 a0001c0001t0001g0368 others(105): Show |
113 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.271-3832A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456881 | |||||||
| chr3:4456886 | GTA | G | 7 | a0001c0001t0003g0011 a0001c0001t0004g0125 a0001c0001t0005g0370 others(4): Show |
8 | HG01257.hp1 HG01258.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.271-3839_271-3838d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456886 | |||||||
| chr3:4456915 | C | T | 2 | a0002c0004t0001g0037 a0002c0004t0001g0038 |
2 | HG01099.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.271-3866G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456915 | |||||||
| chr3:4456916 | G | GTGTGTAT others(5): Show |
1 | a0001c0001t0017g0298 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.271-3868_271-3867i others(14): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456916 | |||||||
| chr3:4456926 | A | G | 60 | a0001c0001t0001g0320 a0001c0001t0002g0008 a0001c0001t0002g0009 others(57): Show |
64 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.271-3877T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456926 | |||||||
| chr3:4456936 | G | A | 6 | a0001c0001t0001g0368 a0001c0001t0005g0370 a0001c0001t0005g0373 others(3): Show |
6 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.271-3887C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456936 | |||||||
| chr3:4456942 | G | GTATATAT others(13): Show |
1 | a0001c0001t0003g0329 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.271-3894_271-3893i others(22): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456942 | |||||||
| chr3:4456942 | G | GTATATAT others(55): Show |
1 | a0001c0001t0002g0360 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.271-3894_271-3893i others(64): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456942 | |||||||
| chr3:4456945 | C | T | 109 | a0001c0001t0001g0076 a0001c0001t0001g0320 a0001c0001t0001g0368 others(106): Show |
114 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.271-3896G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456945 | |||||||
| chr3:4456960 | G | GTA | 99 | a0001c0001t0001g0076 a0001c0001t0001g0320 a0001c0001t0001g0368 others(96): Show |
104 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.271-3913_271-3912d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456960 | |||||||
| chr3:4456960 | G | GTATA | 4 | a0001c0001t0002g0008 a0001c0001t0002g0352 a0001c0001t0002g0353 others(1): Show |
5 | HG02056.hp2 HG02165.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.271-3915_271-3912d others(6): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456960 | |||||||
| chr3:4456960 | G | GTATATAT others(15): Show |
1 | a0001c0001t0002g0330 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.271-3912_271-3911i others(24): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456960 | |||||||
| chr3:4456962 | A | G | 3 | a0001c0001t0005g0105 a0001c0001t0005g0106 a0001c0001t0005g0107 |
3 | HG03041.hp1 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.271-3913T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456962 | |||||||
| chr3:4456971 | C | T | 3 | a0001c0001t0007g0299 a0001c0001t0009g0300 a0001c0001t0009g0301 |
3 | HG02976.hp1 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.271-3922G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456971 | |||||||
| chr3:4456972 | G | A | 3 | a0001c0001t0007g0299 a0001c0001t0009g0300 a0001c0001t0009g0301 |
3 | HG02976.hp1 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.271-3923C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456972 | |||||||
| chr3:4456973 | T | C | 3 | a0001c0001t0007g0299 a0001c0001t0009g0300 a0001c0001t0009g0301 |
3 | HG02976.hp1 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.271-3924A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456973 | |||||||
| chr3:4456978 | GTA | G | 4 | a0001c0001t0002g0360 a0001c0001t0003g0124 a0001c0001t0003g0367 others(1): Show |
4 | HG02056.hp1 HG02698.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-3931_271-3930d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456978 | |||||||
| chr3:4456980 | A | ATATATAT others(11): Show |
1 | a0001c0001t0003g0329 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.271-3949_271-3932d others(20): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456980 | |||||||
| chr3:4456980 | A | ATATATAT others(31): Show |
9 | a0001c0001t0001g0320 a0001c0001t0002g0008 a0001c0001t0002g0319 others(6): Show |
10 | HG02056.hp2 HG02559.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.271-3932_271-3931i others(40): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456980 | |||||||
| chr3:4456980 | A | G | 3 | a0001c0001t0007g0299 a0001c0001t0009g0300 a0001c0001t0009g0301 |
3 | HG02976.hp1 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.271-3931T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456980 | |||||||
| chr3:4456991 | C | T | 1 | a0001c0001t0007g0297 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.271-3942G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4456991 | |||||||
| chr3:4457000 | A | G | 1 | a0001c0002t0001g0123 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.271-3951T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457000 | |||||||
| chr3:4457007 | TAC | T | 7 | a0001c0001t0001g0368 a0001c0001t0005g0370 a0001c0001t0005g0373 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.271-3960_271-3959d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457007 | |||||||
| chr3:4457008 | A | ATACGTGT others(53): Show |
46 | a0001c0001t0002g0009 a0001c0001t0002g0069 a0001c0001t0002g0318 others(43): Show |
49 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.271-3960_271-3959i others(62): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457008 | |||||||
| chr3:4457009 | C | CGTGTGTG others(33): Show |
2 | a0001c0001t0003g0315 a0001c0001t0008g0314 |
2 | HG00280.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.271-3961_271-3960i others(42): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457009 | |||||||
| chr3:4457009 | C | T | 46 | a0001c0001t0002g0009 a0001c0001t0002g0069 a0001c0001t0002g0318 others(43): Show |
49 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.271-3960G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457009 | |||||||
| chr3:4457019 | C | T | 48 | a0001c0001t0002g0009 a0001c0001t0002g0069 a0001c0001t0002g0318 others(45): Show |
51 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.271-3970G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457019 | |||||||
| chr3:4457030 | G | A | 1 | a0001c0001t0002g0261 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.271-3981C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457030 | |||||||
| chr3:4457038 | G | GTATA | 9 | a0001c0001t0002g0009 a0001c0001t0002g0323 a0001c0001t0003g0011 others(6): Show |
11 | HG01257.hp1 HG01258.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.271-3993_271-3990d others(6): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457038 | |||||||
| chr3:4457038 | G | GTATATA | 38 | a0001c0001t0002g0069 a0001c0001t0002g0318 a0001c0001t0002g0331 others(35): Show |
39 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.271-3995_271-3990d others(8): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457038 | |||||||
| chr3:4457038 | G | GTATATAT others(21): Show |
3 | a0001c0001t0002g0008 a0001c0001t0002g0353 a0001c0001t0002g0354 |
4 | HG02056.hp2 NA18969.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-3990_271-3989i others(30): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457038 | |||||||
| chr3:4457038 | G | GTATATAT others(35): Show |
1 | a0001c0001t0008g0078 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.271-3990_271-3989i others(44): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457038 | |||||||
| chr3:4457038 | G | GTATATAT others(43): Show |
1 | a0003c0005t0005g0018 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.271-4039_271-3990d others(52): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457038 | |||||||
| chr3:4457038 | G | GTATATAT others(21): Show |
1 | a0001c0001t0002g0330 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.271-3990_271-3989i others(30): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457038 | |||||||
| chr3:4457044 | A | G | 1 | a0001c0001t0002g0012 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.271-3995T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457044 | |||||||
| chr3:4457051 | C | CGTGT | 4 | a0001c0001t0005g0370 a0001c0001t0006g0369 a0001c0001t0006g0371 others(1): Show |
4 | HG02055.hp2 HG02970.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-4006_271-4003d others(6): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457051 | |||||||
| chr3:4457051 | C | CGTGTGTA others(39): Show |
2 | a0001c0001t0001g0076 a0001c0002t0001g0077 |
2 | HG02280.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.271-4003_271-4002i others(48): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457051 | |||||||
| chr3:4457058 | G | GTA | 21 | a0001c0001t0002g0012 a0001c0001t0005g0043 a0001c0001t0005g0067 others(18): Show |
22 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.271-4011_271-4010d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457058 | |||||||
| chr3:4457058 | G | GTATA | 3 | a0001c0001t0003g0315 a0003c0005t0005g0018 a0005c0007t0001g0019 |
3 | HG02523.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.271-4013_271-4010d others(6): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457058 | |||||||
| chr3:4457058 | G | GTATATA | 48 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0069 others(45): Show |
52 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.271-4015_271-4010d others(8): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457058 | |||||||
| chr3:4457058 | G | GTATATAT others(47): Show |
1 | a0003c0005t0005g0013 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.271-4010_271-4009i others(56): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457058 | |||||||
| chr3:4457058 | G | GTATATAT others(47): Show |
1 | a0003c0005t0005g0017 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.271-4010_271-4009i others(56): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457058 | |||||||
| chr3:4457058 | G | GTATATAT others(29): Show |
1 | a0001c0002t0001g0355 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.271-4010_271-4009i others(38): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457058 | |||||||
| chr3:4457058 | G | GTGTATAT others(27): Show |
4 | a0001c0001t0002g0327 a0001c0001t0002g0366 a0001c0001t0003g0329 others(1): Show |
4 | HG01123.hp2 NA18997.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-4010_271-4009i others(36): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457058 | |||||||
| chr3:4457058 | G | GTGTATAT others(27): Show |
3 | a0001c0001t0001g0320 a0001c0001t0002g0319 a0001c0001t0010g0321 |
3 | HG02559.hp2 HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.271-4010_271-4009i others(36): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457058 | |||||||
| chr3:4457065 | T | TACGTGTG others(5): Show |
1 | a0002c0003t0004g0020 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.271-4017_271-4016i others(14): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457065 | |||||||
| chr3:4457065 | T | TATACGTG others(7): Show |
15 | a0002c0003t0002g0001 a0002c0003t0002g0021 a0002c0003t0002g0023 others(12): Show |
16 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.271-4017_271-4016i others(16): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457065 | |||||||
| chr3:4457084 | A | G | 16 | a0002c0003t0002g0001 a0002c0003t0002g0021 a0002c0003t0002g0023 others(13): Show |
17 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.271-4035T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457084 | |||||||
| chr3:4457093 | TA | T | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0004g0304 others(1): Show |
4 | HG02615.hp1 HG02615.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-4045delT | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457093 | |||||||
| chr3:4457094 | A | ATATATAC others(48): Show |
3 | a0003c0005t0005g0016 a0003c0005t0009g0015 a0003c0006t0001g0014 |
3 | HG03139.hp1 HG03195.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.271-4046_271-4045i others(57): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457094 | |||||||
| chr3:4457094 | A | T | 7 | a0001c0001t0001g0076 a0001c0001t0005g0302 a0001c0001t0007g0297 others(4): Show |
8 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.271-4045T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457094 | |||||||
| chr3:4457096 | T | A | 12 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0357 others(9): Show |
14 | HG00621.hp1 HG00673.hp1 HG02895.hp2 others(11): Show |
intron_variant | MODIFIER | c.271-4047A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457096 | |||||||
| chr3:4457098 | T | G | 17 | a0001c0001t0005g0373 a0002c0003t0002g0001 a0002c0003t0002g0021 others(14): Show |
18 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.271-4049A>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457098 | |||||||
| chr3:4457243 | G | C | 1 | a0001c0002t0001g0077 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.271-4194C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457243 | |||||||
| chr3:4457662 | C | T | 108 | a0001c0001t0001g0076 a0001c0001t0001g0320 a0001c0001t0001g0368 others(105): Show |
113 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.271-4613G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457662 | |||||||
| chr3:4457814 | C | T | 3 | a0001c0002t0001g0080 a0001c0002t0001g0081 a0001c0002t0001g0082 |
3 | NA18961.hp2 NA18984.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.271-4765G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457814 | |||||||
| chr3:4457864 | C | T | 109 | a0001c0001t0001g0076 a0001c0001t0001g0320 a0001c0001t0001g0368 others(106): Show |
115 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.271-4815G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4457864 | |||||||
| chr3:4458086 | A | G | 1 | a0001c0001t0003g0271 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.271-5037T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4458086 | |||||||
| chr3:4458119 | A | G | 1 | a0001c0001t0003g0122 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.271-5070T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4458119 | |||||||
| chr3:4458400 | A | G | 2 | a0001c0001t0005g0074 a0001c0001t0005g0075 |
2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.271-5351T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4458400 | |||||||
| chr3:4458780 | T | C | 354 | a0001c0001t0001g0076 a0001c0001t0001g0109 a0001c0001t0001g0113 others(351): Show |
366 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(363): Show |
intron_variant | MODIFIER | c.271-5731A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4458780 | |||||||
| chr3:4458811 | G | A | 2 | a0001c0001t0005g0265 a0001c0001t0005g0266 |
2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.271-5762C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4458811 | |||||||
| chr3:4458831 | G | C | 2 | a0001c0001t0003g0268 a0001c0002t0001g0267 |
2 | HG00621.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.271-5782C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4458831 | |||||||
| chr3:4458998 | A | G | 1 | a0007c0009t0004g0121 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.271-5949T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4458998 | |||||||
| chr3:4459081 | A | G | 1 | a0001c0001t0005g0120 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.271-6032T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4459081 | |||||||
| chr3:4459164 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.271-6115G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4459164 | |||||||
| chr3:4459165 | G | A | 1 | a0001c0001t0010g0041 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.271-6116C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4459165 | |||||||
| chr3:4459313 | A | C | 4 | a0001c0001t0005g0370 a0001c0001t0006g0369 a0001c0001t0006g0371 others(1): Show |
4 | HG02055.hp2 HG02970.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-6264T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4459313 | |||||||
| chr3:4459455 | A | C | 1 | a0003c0005t0005g0013 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.271-6406T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4459455 | |||||||
| chr3:4459550 | G | A | 22 | a0001c0001t0002g0012 a0001c0002t0001g0118 a0002c0003t0001g0033 others(19): Show |
24 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.271-6501C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4459550 | |||||||
| chr3:4459642 | A | G | 1 | a0001c0001t0010g0041 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.271-6593T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4459642 | |||||||
| chr3:4459699 | T | A | 1 | a0001c0002t0001g0119 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.271-6650A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4459699 | |||||||
| chr3:4459707 | G | C | 1 | a0001c0001t0001g0368 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.271-6658C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4459707 | |||||||
| chr3:4459774 | G | C | 4 | a0001c0001t0005g0370 a0001c0001t0006g0369 a0001c0001t0006g0371 others(1): Show |
4 | HG02055.hp2 HG02970.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-6725C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4459774 | |||||||
| chr3:4459781 | G | T | 1 | a0001c0001t0003g0365 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.271-6732C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4459781 | |||||||
| chr3:4459912 | T | C | 21 | a0001c0001t0002g0012 a0002c0003t0001g0033 a0002c0003t0001g0034 others(18): Show |
23 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.271-6863A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4459912 | |||||||
| chr3:4460100 | C | T | 1 | a0001c0001t0007g0297 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.270+6876G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4460100 | |||||||
| chr3:4460197 | T | C | 2 | a0001c0001t0002g0270 a0001c0001t0004g0269 |
2 | HG02602.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.270+6779A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4460197 | |||||||
| chr3:4460232 | A | T | 1 | a0001c0001t0003g0367 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.270+6744T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4460232 | |||||||
| chr3:4460315 | A | T | 21 | a0001c0001t0002g0012 a0002c0003t0001g0033 a0002c0003t0001g0034 others(18): Show |
23 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.270+6661T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4460315 | |||||||
| chr3:4460329 | C | G | 21 | a0001c0001t0002g0012 a0002c0003t0001g0033 a0002c0003t0001g0034 others(18): Show |
23 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.270+6647G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4460329 | |||||||
| chr3:4460441 | AGAGCTCA others(11): Show |
A | 1 | a0001c0002t0001g0099 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.270+6517_270+6534d others(20): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4460441 | |||||||
| chr3:4460481 | C | T | 73 | a0001c0001t0001g0320 a0001c0001t0002g0008 a0001c0001t0002g0009 others(70): Show |
77 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.270+6495G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4460481 | |||||||
| chr3:4460599 | A | AGT | 85 | a0001c0001t0001g0047 a0001c0001t0001g0076 a0001c0001t0001g0109 others(82): Show |
88 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.270+6375_270+6376d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4460599 | |||||||
| chr3:4460599 | A | AGTGT | 5 | a0001c0001t0003g0004 a0001c0001t0003g0315 a0001c0001t0004g0103 others(2): Show |
6 | HG01516.hp1 HG01517.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.270+6373_270+6376d others(6): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4460599 | |||||||
| chr3:4460599 | AGT | A | 8 | a0001c0001t0002g0273 a0001c0001t0003g0011 a0001c0001t0003g0271 others(5): Show |
9 | HG00642.hp2 HG01257.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.270+6375_270+6376d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4460599 | |||||||
| chr3:4460599 | AGTGT | A | 10 | a0001c0001t0001g0368 a0001c0001t0002g0277 a0001c0001t0004g0295 others(7): Show |
10 | HG00609.hp1 HG01433.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.270+6373_270+6376d others(6): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4460599 | |||||||
| chr3:4460623 | T | A | 3 | a0001c0001t0011g0378 a0001c0001t0011g0379 a0001c0001t0011g0380 |
3 | HG02922.hp2 HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.270+6353A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4460623 | |||||||
| chr3:4460623 | TGAGA | T | 3 | a0001c0001t0001g0305 a0001c0001t0004g0304 a0001c0001t0006g0303 |
3 | HG02615.hp2 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.270+6349_270+6352d others(6): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4460623 | |||||||
| chr3:4460625 | A | T | 1 | a0001c0001t0004g0278 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.270+6351T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4460625 | |||||||
| chr3:4460627 | A | T | 2 | a0001c0001t0001g0306 a0001c0001t0010g0041 |
2 | HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.270+6349T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4460627 | |||||||
| chr3:4460631 | T | A | 1 | a0001c0001t0004g0278 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.270+6345A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4460631 | |||||||
| chr3:4460649 | CAT | C | 6 | a0003c0005t0005g0013 a0003c0005t0005g0016 a0003c0005t0005g0017 others(3): Show |
6 | HG02922.hp1 HG03139.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.270+6325_270+6326d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4460649 | |||||||
| chr3:4460666 | A | T | 6 | a0001c0001t0001g0368 a0001c0001t0002g0012 a0001c0001t0004g0071 others(3): Show |
7 | HG02572.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.270+6310T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4460666 | |||||||
| chr3:4460668 | T | A | 3 | a0001c0001t0002g0375 a0001c0001t0004g0374 a0001c0001t0005g0302 |
3 | HG00408.hp1 HG02109.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.270+6308A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4460668 | |||||||
| chr3:4460764 | T | C | 1 | a0001c0001t0002g0279 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.270+6212A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4460764 | |||||||
| chr3:4461003 | T | C | 22 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0285 others(19): Show |
22 | HG00558.hp2 HG00621.hp2 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.270+5973A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4461003 | |||||||
| chr3:4461018 | G | A | 1 | a0001c0001t0003g0365 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.270+5958C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4461018 | |||||||
| chr3:4461031 | C | T | 1 | a0001c0001t0019g0101 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.270+5945G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4461031 | |||||||
| chr3:4461224 | T | C | 106 | a0001c0001t0001g0076 a0001c0001t0001g0320 a0001c0001t0001g0368 others(103): Show |
112 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.270+5752A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4461224 | |||||||
| chr3:4461237 | G | A | 21 | a0001c0001t0002g0012 a0002c0003t0001g0033 a0002c0003t0001g0034 others(18): Show |
23 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.270+5739C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4461237 | |||||||
| chr3:4461268 | C | CT | 21 | a0001c0001t0002g0012 a0002c0003t0001g0033 a0002c0003t0001g0034 others(18): Show |
23 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.270+5707dupA | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4461268 | |||||||
| chr3:4461277 | G | T | 1 | a0001c0001t0004g0100 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.270+5699C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4461277 | |||||||
| chr3:4461498 | C | A | 1 | a0001c0001t0008g0078 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.270+5478G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4461498 | |||||||
| chr3:4461866 | TTTAGTCA others(15): Show |
T | 1 | a0001c0001t0002g0366 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.270+5088_270+5109d others(24): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4461866 | |||||||
| chr3:4461937 | C | T | 1 | a0001c0002t0001g0099 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.270+5039G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4461937 | |||||||
| chr3:4461950 | C | A | 20 | a0002c0003t0001g0033 a0002c0003t0001g0034 a0002c0003t0002g0001 others(17): Show |
21 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.270+5026G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4461950 | |||||||
| chr3:4462091 | C | T | 3 | a0001c0001t0001g0076 a0001c0001t0008g0078 a0001c0002t0001g0077 |
3 | HG02280.hp2 HG03834.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.270+4885G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4462091 | |||||||
| chr3:4462184 | C | T | 3 | a0001c0001t0002g0003 a0001c0001t0002g0097 a0001c0001t0002g0098 |
4 | NA18971.hp2 NA19009.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.270+4792G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4462184 | |||||||
| chr3:4462433 | C | T | 1 | a0001c0001t0010g0041 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.270+4543G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4462433 | |||||||
| chr3:4462436 | A | G | 77 | a0001c0001t0001g0320 a0001c0001t0002g0008 a0001c0001t0002g0009 others(74): Show |
81 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.270+4540T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4462436 | |||||||
| chr3:4462643 | C | T | 16 | a0002c0003t0002g0001 a0002c0003t0002g0021 a0002c0003t0002g0023 others(13): Show |
17 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.270+4333G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4462643 | |||||||
| chr3:4462902 | T | A | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0004g0304 others(1): Show |
4 | HG02615.hp1 HG02615.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.270+4074A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4462902 | |||||||
| chr3:4462925 | G | C | 1 | a0001c0001t0002g0296 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.270+4051C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4462925 | |||||||
| chr3:4462940 | T | C | 63 | a0001c0001t0001g0320 a0001c0001t0002g0008 a0001c0001t0002g0009 others(60): Show |
67 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.270+4036A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4462940 | |||||||
| chr3:4462992 | A | G | 1 | a0001c0001t0005g0044 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.270+3984T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4462992 | |||||||
| chr3:4463214 | G | A | 10 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0004g0304 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.270+3762C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4463214 | |||||||
| chr3:4463230 | G | A | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0004g0304 others(1): Show |
4 | HG02615.hp1 HG02615.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.270+3746C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4463230 | |||||||
| chr3:4463278 | T | A | 3 | a0001c0001t0001g0368 a0001c0001t0005g0373 a0005c0007t0001g0019 |
3 | HG02145.hp1 HG02572.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.270+3698A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4463278 | |||||||
| chr3:4463288 | G | A | 4 | a0002c0003t0001g0033 a0002c0003t0001g0034 a0002c0003t0006g0036 others(1): Show |
4 | HG02109.hp1 HG02257.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+3688C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4463288 | |||||||
| chr3:4463313 | A | C | 11 | a0001c0001t0005g0043 a0001c0001t0005g0363 a0001c0001t0007g0364 others(8): Show |
11 | HG02922.hp1 HG02976.hp2 HG03139.hp1 others(8): Show |
intron_variant | MODIFIER | c.270+3663T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4463313 | |||||||
| chr3:4463443 | T | C | 7 | a0001c0001t0001g0368 a0001c0001t0005g0370 a0001c0001t0005g0373 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.270+3533A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4463443 | |||||||
| chr3:4463464 | T | C | 2 | a0001c0001t0002g0308 a0001c0002t0001g0309 |
2 | HG00597.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.270+3512A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4463464 | |||||||
| chr3:4463727 | A | C | 4 | a0001c0001t0005g0043 a0001c0001t0005g0363 a0001c0001t0007g0364 others(1): Show |
4 | HG02976.hp2 HG03471.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+3249T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4463727 | |||||||
| chr3:4463958 | C | T | 106 | a0001c0001t0001g0076 a0001c0001t0001g0320 a0001c0001t0001g0368 others(103): Show |
112 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.270+3018G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4463958 | |||||||
| chr3:4463959 | G | T | 19 | a0001c0001t0003g0083 a0001c0001t0003g0094 a0001c0001t0003g0095 others(16): Show |
20 | HG00642.hp1 HG01081.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.270+3017C>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4463959 | |||||||
| chr3:4464276 | CTT | C | 103 | a0001c0001t0001g0320 a0001c0001t0001g0368 a0001c0001t0002g0008 others(100): Show |
109 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.270+2698_270+2699d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4464276 | |||||||
| chr3:4464299 | C | T | 6 | a0003c0005t0005g0013 a0003c0005t0005g0016 a0003c0005t0005g0017 others(3): Show |
6 | HG02922.hp1 HG03139.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.270+2677G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4464299 | |||||||
| chr3:4464338 | G | A | 1 | a0001c0001t0011g0380 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.270+2638C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4464338 | |||||||
| chr3:4464356 | C | T | 1 | a0001c0001t0003g0079 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.270+2620G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4464356 | |||||||
| chr3:4464412 | T | TTG | 6 | a0001c0001t0003g0313 a0001c0001t0008g0314 a0001c0001t0011g0378 others(3): Show |
6 | HG00280.hp1 HG01074.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.270+2562_270+2563d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4464412 | |||||||
| chr3:4464412 | T | TTGTG | 66 | a0001c0001t0001g0320 a0001c0001t0002g0008 a0001c0001t0002g0009 others(63): Show |
70 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.270+2560_270+2563d others(6): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4464412 | |||||||
| chr3:4464412 | TTG | T | 3 | a0001c0001t0001g0076 a0001c0001t0008g0078 a0001c0002t0001g0077 |
3 | HG02280.hp2 HG03834.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.270+2562_270+2563d others(4): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4464412 | |||||||
| chr3:4464430 | G | C | 1 | a0001c0002t0001g0007 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.270+2546C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4464430 | |||||||
| chr3:4464431 | T | A | 21 | a0001c0001t0002g0012 a0002c0003t0001g0033 a0002c0003t0001g0034 others(18): Show |
23 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.270+2545A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4464431 | |||||||
| chr3:4464431 | T | TGTGTGA | 3 | a0001c0001t0005g0373 a0003c0005t0005g0013 a0005c0007t0001g0019 |
3 | HG02145.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.270+2544_270+2545i others(8): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4464431 | |||||||
| chr3:4464431 | T | TGTGTGTG others(1): Show |
5 | a0003c0005t0005g0016 a0003c0005t0005g0017 a0003c0005t0005g0018 others(2): Show |
5 | HG02922.hp1 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.270+2544_270+2545i others(10): Show |
SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4464431 | |||||||
| chr3:4464433 | A | T | 2 | a0001c0001t0005g0074 a0001c0001t0005g0075 |
2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.270+2543T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4464433 | |||||||
| chr3:4464507 | C | T | 5 | a0001c0001t0003g0367 a0001c0001t0004g0071 a0001c0001t0004g0072 others(2): Show |
5 | HG02056.hp1 HG02698.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.270+2469G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4464507 | |||||||
| chr3:4464532 | T | C | 82 | a0001c0001t0001g0320 a0001c0001t0001g0368 a0001c0001t0002g0008 others(79): Show |
86 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.270+2444A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4464532 | |||||||
| chr3:4464546 | G | A | 60 | a0001c0001t0001g0320 a0001c0001t0002g0008 a0001c0001t0002g0009 others(57): Show |
64 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.270+2430C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4464546 | |||||||
| chr3:4464622 | T | A | 1 | a0001c0002t0001g0361 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.270+2354A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4464622 | |||||||
| chr3:4464797 | T | A | 10 | a0001c0001t0005g0043 a0001c0001t0005g0363 a0001c0001t0007g0364 others(7): Show |
10 | HG02922.hp1 HG02976.hp2 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.270+2179A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4464797 | |||||||
| chr3:4464912 | C | G | 1 | a0001c0001t0004g0070 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.270+2064G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4464912 | |||||||
| chr3:4464935 | C | T | 21 | a0001c0001t0002g0012 a0002c0003t0001g0033 a0002c0003t0001g0034 others(18): Show |
23 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.270+2041G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4464935 | |||||||
| chr3:4465213 | A | G | 2 | a0001c0001t0002g0069 a0001c0002t0001g0068 |
2 | HG01109.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.270+1763T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4465213 | |||||||
| chr3:4465359 | C | A | 1 | a0001c0001t0003g0365 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.270+1617G>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4465359 | |||||||
| chr3:4465488 | A | T | 16 | a0002c0003t0002g0001 a0002c0003t0002g0021 a0002c0003t0002g0023 others(13): Show |
17 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.270+1488T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4465488 | |||||||
| chr3:4465520 | T | C | 2 | a0002c0004t0001g0037 a0002c0004t0001g0038 |
2 | HG01099.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.270+1456A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4465520 | |||||||
| chr3:4465629 | T | C | 357 | a0001c0001t0001g0076 a0001c0001t0001g0109 a0001c0001t0001g0113 others(354): Show |
369 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.270+1347A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4465629 | |||||||
| chr3:4465630 | G | A | 1 | a0001c0001t0002g0366 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.270+1346C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4465630 | |||||||
| chr3:4465632 | T | A | 1 | a0001c0001t0003g0367 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.270+1344A>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4465632 | |||||||
| chr3:4465825 | A | C | 1 | a0001c0001t0002g0046 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.270+1151T>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4465825 | |||||||
| chr3:4466193 | C | G | 22 | a0001c0001t0002g0012 a0001c0001t0005g0045 a0002c0003t0001g0033 others(19): Show |
24 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.270+783G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4466193 | |||||||
| chr3:4466296 | G | C | 7 | a0001c0001t0001g0368 a0001c0001t0005g0370 a0001c0001t0005g0373 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.270+680C>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4466296 | |||||||
| chr3:4466301 | G | A | 1 | a0001c0001t0002g0012 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.270+675C>T | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4466301 | |||||||
| chr3:4466324 | C | G | 1 | a0001c0001t0005g0044 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.270+652G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4466324 | |||||||
| chr3:4466341 | A | G | 1 | a0001c0001t0010g0041 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.270+635T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4466341 | |||||||
| chr3:4466376 | C | T | 20 | a0002c0003t0001g0033 a0002c0003t0001g0034 a0002c0003t0002g0001 others(17): Show |
21 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.270+600G>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4466376 | |||||||
| chr3:4466412 | A | T | 1 | a0001c0001t0005g0043 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.270+564T>A | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4466412 | |||||||
| chr3:4466490 | T | C | 2 | a0001c0001t0002g0375 a0001c0001t0004g0374 |
2 | HG00408.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.270+486A>G | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4466490 | |||||||
| chr3:4466655 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.270+321T>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4466655 | |||||||
| chr3:4466783 | C | G | 1 | a0001c0001t0010g0041 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.270+193G>C | SUMF1 | ENSG00000144455.14 | transcript | ENST00000272902.10 | protein_coding | 1/8 | chr3 | 4466783 |