Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 221938 |
| ensemblid | ENSG00000136297.15 |
| hgncid | 30133 |
| symbol | MMD2 |
| name | monocyte to macrophage differentiation associated 2 |
| refseq_nuc | NM_198403.4 |
| refseq_prot | NP_940685.3 |
| ensembl_nuc | ENST00000401401.8 |
| ensembl_prot | ENSP00000384141.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 4905998 |
| end | 4959187 |
| strand | - |
| ver | v1.2 |
| region | chr7:4905998-4959187 |
| region5000 | chr7:4900998-4964187 |
| regionname0 | MMD2_chr7_4905998_4959187 |
| regionname5000 | MMD2_chr7_4900998_4964187 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 738 | 195 | 32 | 31 | 84 | 9 | 38 | MMD2_chr7_4900998_4964187 | MMD2 | ATGTT others(733): Show |
chr7 | 4900998 | 4964187 | ||
| a0001c0002 | 0/1 | 738 | 162 | 58 | 34 | 52 | 7 | 10 | MMD2_chr7_4900998_4964187 | MMD2 | ATGTT others(733): Show |
chr7 | 4900998 | 4964187 | ||
| a0001c0003 | 0/0 | 738 | 21 | 0 | 1 | 20 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | ATGTT others(733): Show |
chr7 | 4900998 | 4964187 | ||
| a0001c0004 | 0/0 | 738 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | ATGTT others(733): Show |
chr7 | 4900998 | 4964187 | ||
| a0001c0005 | 0/0 | 738 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | ATGTT others(733): Show |
chr7 | 4900998 | 4964187 | ||
| a0001c0006 | 0/0 | 738 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | ATGTT others(733): Show |
chr7 | 4900998 | 4964187 | ||
| a0001c0007 | 0/0 | 738 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | ATGTT others(733): Show |
chr7 | 4900998 | 4964187 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2309 | 41 | 11 | 5 | 23 | 0 | 2 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0001t0002 | 0/0 | 2309 | 51 | 4 | 16 | 13 | 5 | 13 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0001t0003 | 1/0 | 2309 | 37 | 5 | 4 | 15 | 2 | 10 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0001t0004 | 0/0 | 2309 | 21 | 3 | 6 | 5 | 1 | 6 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0001t0005 | 0/0 | 2309 | 6 | 0 | 0 | 4 | 0 | 2 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0001t0006 | 0/0 | 2309 | 9 | 0 | 0 | 9 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0001t0008 | 0/0 | 2309 | 2 | 2 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0001t0009 | 0/0 | 2309 | 5 | 0 | 0 | 5 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0001t0010 | 0/0 | 2309 | 3 | 3 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0001t0011 | 0/0 | 2309 | 3 | 0 | 0 | 2 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0001t0012 | 0/0 | 2309 | 2 | 1 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0001t0013 | 0/0 | 2309 | 3 | 0 | 0 | 3 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0001t0014 | 0/0 | 2309 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0001t0015 | 0/0 | 2309 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0001t0017 | 0/0 | 2309 | 2 | 0 | 0 | 1 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0001t0019 | 0/0 | 2297 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2292): Show |
chr7 | 4900998 | 4964187 |
| a0001c0001t0021 | 0/0 | 2309 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0001t0022 | 0/0 | 2309 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0001t0023 | 0/0 | 2309 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0001t0024 | 0/0 | 2309 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0001t0027 | 0/0 | 2309 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0001t0030 | 0/0 | 2309 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0001t0031 | 0/0 | 2309 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0002t0001 | 0/1 | 2309 | 86 | 46 | 15 | 21 | 3 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0002t0002 | 0/0 | 2309 | 10 | 0 | 2 | 1 | 3 | 4 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0002t0003 | 0/0 | 2309 | 17 | 0 | 1 | 12 | 0 | 4 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0002t0004 | 0/0 | 2309 | 5 | 0 | 1 | 4 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0002t0005 | 0/0 | 2309 | 13 | 0 | 5 | 8 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0002t0006 | 0/0 | 2309 | 5 | 0 | 1 | 4 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0002t0007 | 0/0 | 2309 | 10 | 1 | 7 | 0 | 1 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0002t0008 | 0/0 | 2309 | 4 | 4 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0002t0010 | 0/0 | 2309 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0002t0012 | 0/0 | 2309 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0002t0014 | 0/0 | 2309 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0002t0015 | 0/0 | 2309 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0002t0016 | 0/0 | 2309 | 2 | 2 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0002t0018 | 0/0 | 2309 | 2 | 0 | 2 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0002t0020 | 0/0 | 2309 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0002t0028 | 0/0 | 2294 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2289): Show |
chr7 | 4900998 | 4964187 |
| a0001c0002t0029 | 0/0 | 2309 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0002t0032 | 0/0 | 2309 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0003t0001 | 0/0 | 2309 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0003t0003 | 0/0 | 2309 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0003t0004 | 0/0 | 2309 | 17 | 0 | 1 | 16 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0003t0026 | 0/0 | 2309 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0003t0033 | 0/0 | 2309 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0004t0002 | 0/0 | 2309 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0005t0003 | 0/0 | 2309 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0006t0001 | 0/0 | 2309 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| a0001c0007t0025 | 0/0 | 2309 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | GGGCG others(2304): Show |
chr7 | 4900998 | 4964187 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0138 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0003g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0004g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0005g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0005g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0005g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0005g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0005g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0006g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0006g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0006g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0006g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0006g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0006g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0006g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0006g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0006g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0008g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0008g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0009g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0009g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0009g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0009g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0009g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0010g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0010g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0010g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0011g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0011g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0011g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0012g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0012g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0013g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0013g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0013g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0014g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0015g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0017g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0017g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0019g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0021g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0022g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0023g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0024g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0027g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0030g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0001t0031g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0098 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0004g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0004g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0005g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0005g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0005g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0005g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0005g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0005g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0005g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0005g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0005g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0005g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0005g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0006g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0006g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0006g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0006g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0006g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0007g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0007g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0007g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0007g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0007g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0007g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0007g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0007g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0007g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0007g0373 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0008g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0008g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0008g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0008g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0010g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0012g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0014g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0015g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0016g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0016g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0018g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0018g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0020g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0028g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0029g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0002t0032g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0004g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0026g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0003t0033g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0004t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0005t0003g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0006t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| a0001c0007t0025g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0140 | EUR | GBR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00099 | hp2 | a0001 | c0002 | t0002 | g0139 | EUR | GBR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0096 | EUR | GBR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0062 | EUR | GBR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00280 | hp1 | a0001 | c0002 | t0007 | g0373 | EUR | FIN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0130 | EUR | FIN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00408 | hp1 | a0001 | c0003 | t0004 | g0329 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00408 | hp2 | a0001 | c0001 | t0005 | g0083 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00544 | hp2 | a0001 | c0002 | t0005 | g0188 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00558 | hp1 | a0001 | c0002 | t0005 | g0184 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00597 | hp1 | a0001 | c0001 | t0009 | g0377 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00609 | hp1 | a0001 | c0003 | t0004 | g0263 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00621 | hp1 | a0001 | c0002 | t0003 | g0179 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00639 | hp1 | a0001 | c0002 | t0007 | g0372 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0299 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0275 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | CHS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0277 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00735 | hp2 | a0001 | c0002 | t0005 | g0186 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0100 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0238 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0134 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01069 | hp1 | a0001 | c0002 | t0005 | g0185 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0153 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0144 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0276 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0245 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0241 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0113 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0151 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0278 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0285 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0109 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0305 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01167 | hp2 | a0001 | c0002 | t0004 | g0212 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0132 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0304 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01192 | hp2 | a0001 | c0002 | t0007 | g0360 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01243 | hp1 | a0001 | c0002 | t0006 | g0248 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0067 | AMR | CLM | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0099 | AMR | CLM | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0133 | AMR | CLM | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0114 | AMR | CLM | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0294 | AMR | CLM | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0131 | AMR | CLM | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0037 | AMR | CLM | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0150 | AMR | CLM | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01433 | hp2 | a0001 | c0002 | t0007 | g0369 | AMR | CLM | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01496 | hp2 | a0001 | c0005 | t0003 | g0316 | AMR | CLM | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0117 | EUR | IBS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01515 | hp2 | a0001 | c0001 | t0019 | g0004 | EUR | IBS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0128 | EUR | IBS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0306 | EUR | IBS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0116 | EUR | IBS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0307 | EUR | IBS | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0097 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0250 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01891 | hp1 | a0001 | c0001 | t0010 | g0357 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0108 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01928 | hp1 | a0001 | c0002 | t0018 | g0363 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01928 | hp2 | a0001 | c0002 | t0005 | g0191 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01934 | hp1 | a0001 | c0002 | t0003 | g0231 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0149 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01943 | hp1 | a0001 | c0002 | t0007 | g0361 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0300 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0105 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01975 | hp2 | a0001 | c0002 | t0005 | g0193 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01978 | hp1 | a0001 | c0002 | t0018 | g0365 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0296 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01981 | hp1 | a0001 | c0006 | t0001 | g0240 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG01981 | hp2 | a0001 | c0002 | t0007 | g0364 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02004 | hp1 | a0001 | c0003 | t0004 | g0331 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02004 | hp2 | a0001 | c0002 | t0007 | g0371 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0345 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02040 | hp1 | a0001 | c0001 | t0017 | g0053 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02055 | hp1 | a0001 | c0001 | t0010 | g0041 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02055 | hp2 | a0001 | c0004 | t0002 | g0317 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02056 | hp1 | a0001 | c0002 | t0003 | g0201 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02071 | hp1 | a0001 | c0001 | t0009 | g0379 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02071 | hp2 | a0001 | c0002 | t0005 | g0176 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02074 | hp1 | a0001 | c0001 | t0006 | g0049 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0274 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02083 | hp1 | a0001 | c0003 | t0003 | g0320 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02129 | hp2 | a0001 | c0001 | t0006 | g0076 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02132 | hp1 | a0001 | c0002 | t0006 | g0204 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02135 | hp2 | a0001 | c0001 | t0030 | g0091 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0119 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02145 | hp2 | a0001 | c0002 | t0007 | g0366 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02155 | hp1 | a0001 | c0002 | t0003 | g0203 | EAS | CDX | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | CDX | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02165 | hp1 | a0001 | c0001 | t0009 | g0376 | EAS | CDX | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0237 | EAS | CDX | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0257 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02258 | hp2 | a0001 | c0002 | t0008 | g0044 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02293 | hp1 | a0001 | c0002 | t0005 | g0165 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0103 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02300 | hp2 | a0001 | c0002 | t0007 | g0362 | AMR | PEL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0265 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0143 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02523 | hp2 | a0001 | c0001 | t0009 | g0374 | EAS | KHV | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02572 | hp1 | a0001 | c0002 | t0008 | g0040 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02572 | hp2 | a0001 | c0007 | t0025 | g0356 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02602 | hp1 | a0001 | c0001 | t0024 | g0018 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0234 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02615 | hp2 | a0001 | c0001 | t0015 | g0147 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0137 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0270 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02647 | hp2 | a0001 | c0001 | t0008 | g0266 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0281 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0255 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02717 | hp2 | a0001 | c0002 | t0008 | g0043 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0136 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0253 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0016 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0288 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0145 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0110 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0353 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02818 | hp2 | a0001 | c0001 | t0027 | g0346 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0135 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0141 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0355 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0350 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0112 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0152 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0111 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | ESN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | ESN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02965 | hp1 | a0001 | c0002 | t0014 | g0174 | AFR | ESN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0104 | AFR | ESN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | ESN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0348 | AFR | ESN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0272 | AFR | ESN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0095 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03017 | hp2 | a0001 | c0002 | t0007 | g0359 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03041 | hp1 | a0001 | c0001 | t0010 | g0358 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0162 | AFR | MSL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03098 | hp2 | a0001 | c0002 | t0012 | g0198 | AFR | MSL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | ESN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0107 | AFR | ESN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0354 | AFR | ESN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0106 | AFR | ESN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03195 | hp1 | a0001 | c0002 | t0008 | g0042 | AFR | ESN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0225 | AFR | ESN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0161 | AFR | MSL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0258 | AFR | MSL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0269 | AFR | MSL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0352 | AFR | MSL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0309 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0080 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0129 | AFR | MSL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0163 | AFR | MSL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03490 | hp1 | a0001 | c0001 | t0005 | g0312 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03490 | hp2 | a0001 | c0001 | t0021 | g0047 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0284 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0308 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0283 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03492 | hp2 | a0001 | c0001 | t0005 | g0290 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0252 | AFR | ESN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0120 | AFR | ESN | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0268 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0351 | AFR | GWD | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | MSL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0172 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0092 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0298 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03688 | hp1 | a0001 | c0001 | t0031 | g0166 | SAS | STU | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03688 | hp2 | a0001 | c0002 | t0003 | g0171 | SAS | STU | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0314 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0079 | SAS | PJL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03831 | hp1 | a0001 | c0002 | t0029 | g0167 | SAS | BEB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0015 | SAS | BEB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0244 | SAS | BEB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03834 | hp2 | a0001 | c0001 | t0011 | g0066 | SAS | BEB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03927 | hp1 | a0001 | c0001 | t0017 | g0052 | SAS | BEB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0311 | SAS | BEB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0286 | SAS | BEB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0289 | SAS | STU | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG04115 | hp2 | a0001 | c0002 | t0003 | g0200 | SAS | STU | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0034 | SAS | BEB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0303 | SAS | BEB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0035 | SAS | STU | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0071 | SAS | STU | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0075 | SAS | STU | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG04204 | hp2 | a0001 | c0002 | t0003 | g0168 | SAS | STU | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0010 | SAS | STU | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0173 | SAS | STU | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0142 | AFR | YRI | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0211 | AFR | YRI | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | CHB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18612 | hp2 | a0001 | c0002 | t0006 | g0222 | EAS | CHB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | CHB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18906 | hp1 | a0001 | c0002 | t0015 | g0215 | AFR | YRI | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18906 | hp2 | a0001 | c0002 | t0010 | g0155 | AFR | YRI | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18939 | hp2 | a0001 | c0001 | t0012 | g0301 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18942 | hp1 | a0001 | c0002 | t0004 | g0205 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18942 | hp2 | a0001 | c0001 | t0005 | g0077 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18946 | hp1 | a0001 | c0001 | t0013 | g0367 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18950 | hp2 | a0001 | c0003 | t0004 | g0324 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18951 | hp1 | a0001 | c0002 | t0005 | g0196 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18952 | hp1 | a0001 | c0001 | t0011 | g0073 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18952 | hp2 | a0001 | c0002 | t0004 | g0333 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18956 | hp1 | a0001 | c0001 | t0004 | g0347 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18956 | hp2 | a0001 | c0002 | t0003 | g0157 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18959 | hp1 | a0001 | c0003 | t0004 | g0325 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18962 | hp2 | a0001 | c0001 | t0006 | g0088 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18963 | hp1 | a0001 | c0003 | t0004 | g0339 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18966 | hp1 | a0001 | c0002 | t0005 | g0175 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18967 | hp2 | a0001 | c0002 | t0003 | g0208 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18968 | hp2 | a0001 | c0003 | t0004 | g0321 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18969 | hp1 | a0001 | c0003 | t0004 | g0342 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18971 | hp2 | a0001 | c0001 | t0022 | g0293 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18977 | hp2 | a0001 | c0003 | t0004 | g0319 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18980 | hp2 | a0001 | c0002 | t0003 | g0209 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18981 | hp1 | a0001 | c0001 | t0006 | g0064 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18981 | hp2 | a0001 | c0003 | t0004 | g0224 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18982 | hp2 | a0001 | c0001 | t0004 | g0336 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18983 | hp1 | a0001 | c0001 | t0006 | g0086 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18986 | hp2 | a0001 | c0003 | t0001 | g0343 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18991 | hp1 | a0001 | c0003 | t0033 | g0378 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0344 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18992 | hp2 | a0001 | c0002 | t0003 | g0195 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18994 | hp1 | a0001 | c0001 | t0006 | g0207 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18994 | hp2 | a0001 | c0003 | t0004 | g0332 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18998 | hp1 | a0001 | c0002 | t0003 | g0177 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA18998 | hp2 | a0001 | c0003 | t0004 | g0326 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19000 | hp1 | a0001 | c0001 | t0023 | g0313 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19002 | hp1 | a0001 | c0001 | t0006 | g0084 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19002 | hp2 | a0001 | c0001 | t0013 | g0368 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19003 | hp2 | a0001 | c0002 | t0003 | g0156 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19007 | hp1 | a0001 | c0001 | t0009 | g0375 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19009 | hp1 | a0001 | c0002 | t0006 | g0187 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19010 | hp1 | a0001 | c0002 | t0005 | g0194 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19010 | hp2 | a0001 | c0002 | t0003 | g0210 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19011 | hp1 | a0001 | c0003 | t0026 | g0338 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19011 | hp2 | a0001 | c0002 | t0004 | g0190 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19012 | hp2 | a0001 | c0003 | t0004 | g0330 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | LWK | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0213 | AFR | LWK | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19043 | hp1 | a0001 | c0002 | t0016 | g0169 | AFR | LWK | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0121 | AFR | LWK | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19054 | hp1 | a0001 | c0002 | t0005 | g0192 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0334 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19056 | hp1 | a0001 | c0003 | t0004 | g0322 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19057 | hp1 | a0001 | c0001 | t0006 | g0065 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19058 | hp1 | a0001 | c0002 | t0028 | g0178 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19060 | hp2 | a0001 | c0002 | t0020 | g0005 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19064 | hp1 | a0001 | c0001 | t0013 | g0370 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19064 | hp2 | a0001 | c0002 | t0003 | g0189 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19065 | hp1 | a0001 | c0002 | t0003 | g0340 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0335 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19066 | hp1 | a0001 | c0003 | t0004 | g0323 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19066 | hp2 | a0001 | c0001 | t0005 | g0082 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19068 | hp1 | a0001 | c0003 | t0004 | g0327 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19070 | hp2 | a0001 | c0003 | t0004 | g0341 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19074 | hp1 | a0001 | c0001 | t0006 | g0063 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19080 | hp1 | a0001 | c0002 | t0004 | g0328 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19085 | hp2 | a0001 | c0001 | t0005 | g0072 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19087 | hp2 | a0001 | c0001 | t0011 | g0249 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19090 | hp2 | a0001 | c0002 | t0006 | g0180 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19091 | hp1 | a0001 | c0002 | t0005 | g0216 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0254 | AFR | YRI | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | YRI | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0271 | AFR | ASW | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA20129 | hp2 | a0001 | c0002 | t0032 | g0159 | AFR | ASW | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0291 | EUR | TSI | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0059 | EUR | TSI | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0023 | EUR | TSI | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0160 | EUR | TSI | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA20905 | hp1 | a0001 | c0002 | t0003 | g0148 | SAS | GIH | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0318 | SAS | GIH | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0102 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0101 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0349 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0287 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03471 | hp1 | a0001 | c0001 | t0012 | g0251 | AFR | MSL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG06807 | hp1 | a0001 | c0001 | t0014 | g0124 | AFR | USA | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0315 | AFR | USA | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0146 | AFR | USA | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0302 | AFR | USA | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA21309 | hp1 | a0001 | c0002 | t0016 | g0170 | AFR | LWK | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0256 | AFR | LWK | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0098 | REF | REF | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0138 | REF | REF | MMD2_chr7_4900998_4964187 | MMD2 | chr7 | 4900998 | 4964187 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:4907423 | G | A | 1 | a0001c0004 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.714C>T | p.Ser238Ser | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 884/2309 | 714/741 | 238/246 | chr7 | 4907423 | |||
| chr7:4909920 | G | A | 1 | a0001c0006 | 1 | HG01981.hp1 | synonymous_variant | LOW | c.498C>T | p.Val166Val | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/7 | 668/2309 | 498/741 | 166/246 | chr7 | 4909920 | |||
| chr7:4911222 | G | C | 1 | a0001c0005 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.390C>G | p.Pro130Pro | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/7 | 560/2309 | 390/741 | 130/246 | chr7 | 4911222 | |||
| chr7:4916022 | C | T | 1 | a0001c0003 | 21 | HG00408.hp1 HG00609.hp1 HG02004.hp1 others(18): Show |
synonymous_variant | LOW | c.348G>A | p.Ala116Ala | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/7 | 518/2309 | 348/741 | 116/246 | chr7 | 4916022 | |||
| chr7:4920176 | G | A | 2 | a0001c0002 a0001c0006 |
162 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(159): Show |
synonymous_variant | LOW | c.285C>T | p.His95His | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/7 | 455/2309 | 285/741 | 95/246 | chr7 | 4920176 | |||
| chr7:4920278 | G | A | 1 | a0001c0007 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.183C>T | p.Asp61Asp | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/7 | 353/2309 | 183/741 | 61/246 | chr7 | 4920278 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:4906123 | G | C | 2 | a0001c0001t0014 a0001c0002t0014 |
2 | HG02965.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1273C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 1273 | chr7 | 4906123 | ||||||
| chr7:4906274 | G | A | 1 | a0001c0002t0016 | 2 | NA19043.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1122C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 1122 | chr7 | 4906274 | ||||||
| chr7:4906319 | G | A | 1 | a0001c0001t0011 | 3 | HG03834.hp2 NA18952.hp1 NA19087.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1077C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 1077 | chr7 | 4906319 | ||||||
| chr7:4906486 | G | A | 1 | a0001c0002t0029 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*910C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 910 | chr7 | 4906486 | ||||||
| chr7:4906526 | TCTCTGGA others(8): Show |
T | 1 | a0001c0002t0028 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*855_*869delTCCAAA others(9): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 855 | chr7 | 4906526 | ||||||
| chr7:4906544 | T | C | 8 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0019 others(5): Show |
71 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*852A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 852 | chr7 | 4906544 | ||||||
| chr7:4906584 | T | C | 1 | a0001c0001t0017 | 2 | HG02040.hp1 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*812A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 812 | chr7 | 4906584 | ||||||
| chr7:4906595 | T | C | 6 | a0001c0001t0004 a0001c0001t0022 a0001c0002t0004 others(3): Show |
46 | HG00099.hp1 HG00408.hp1 HG00609.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*801A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 801 | chr7 | 4906595 | ||||||
| chr7:4906656 | C | T | 36 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(33): Show |
310 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(307): Show |
3_prime_UTR_variant | MODIFIER | c.*740G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 740 | chr7 | 4906656 | ||||||
| chr7:4906712 | T | G | 2 | a0001c0001t0015 a0001c0002t0015 |
2 | HG02615.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*684A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 684 | chr7 | 4906712 | ||||||
| chr7:4906873 | A | C | 2 | a0001c0001t0008 a0001c0002t0008 |
6 | HG02258.hp2 HG02572.hp1 HG02647.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*523T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 523 | chr7 | 4906873 | ||||||
| chr7:4906974 | G | A | 5 | a0001c0001t0004 a0001c0001t0022 a0001c0002t0004 others(2): Show |
45 | HG00099.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*422C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 422 | chr7 | 4906974 | ||||||
| chr7:4907036 | G | A | 1 | a0001c0001t0027 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*360C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 360 | chr7 | 4907036 | ||||||
| chr7:4907069 | A | G | 4 | a0001c0001t0005 a0001c0002t0005 a0001c0002t0018 others(1): Show |
22 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*327T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 327 | chr7 | 4907069 | ||||||
| chr7:4907169 | T | C | 1 | a0001c0001t0030 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*227A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 227 | chr7 | 4907169 | ||||||
| chr7:4907200 | T | C | 1 | a0001c0001t0027 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*196A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 196 | chr7 | 4907200 | ||||||
| chr7:4907229 | G | A | 10 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(7): Show |
46 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*167C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 167 | chr7 | 4907229 | ||||||
| chr7:4907233 | G | A | 1 | a0001c0002t0032 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*163C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 163 | chr7 | 4907233 | ||||||
| chr7:4907246 | T | C | 41 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(38): Show |
316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
3_prime_UTR_variant | MODIFIER | c.*150A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 150 | chr7 | 4907246 | ||||||
| chr7:4907320 | G | A | 5 | a0001c0001t0004 a0001c0001t0022 a0001c0002t0004 others(2): Show |
45 | HG00099.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*76C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 76 | chr7 | 4907320 | ||||||
| chr7:4907330 | G | C | 1 | a0001c0001t0022 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*66C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 66 | chr7 | 4907330 | ||||||
| chr7:4907342 | A | G | 37 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(34): Show |
311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
3_prime_UTR_variant | MODIFIER | c.*54T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 54 | chr7 | 4907342 | ||||||
| chr7:4907343 | C | T | 1 | a0001c0001t0024 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*53G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 53 | chr7 | 4907343 | ||||||
| chr7:4907347 | A | T | 1 | a0001c0001t0023 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*49T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 49 | chr7 | 4907347 | ||||||
| chr7:4907350 | G | A | 2 | a0001c0001t0010 a0001c0002t0010 |
4 | HG01891.hp1 HG02055.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*46C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 46 | chr7 | 4907350 | ||||||
| chr7:4907352 | G | C | 5 | a0001c0001t0004 a0001c0001t0022 a0001c0002t0004 others(2): Show |
45 | HG00099.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*44C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 44 | chr7 | 4907352 | ||||||
| chr7:4907382 | A | G | 5 | a0001c0001t0004 a0001c0001t0022 a0001c0002t0004 others(2): Show |
45 | HG00099.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*14T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 14 | chr7 | 4907382 | ||||||
| chr7:4907393 | A | G | 1 | a0001c0001t0021 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 7/7 | 3 | chr7 | 4907393 | ||||||
| chr7:4959079 | G | A | 3 | a0001c0001t0013 a0001c0002t0007 a0001c0002t0018 |
15 | HG00280.hp1 HG00639.hp1 HG01192.hp2 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-62C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/7 | 62 | chr7 | 4959079 | ||||||
| chr7:4959082 | G | A | 2 | a0001c0001t0009 a0001c0003t0033 |
6 | HG00597.hp1 HG02071.hp1 HG02165.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-65C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/7 | 65 | chr7 | 4959082 | ||||||
| chr7:4959153 | C | G | 1 | a0001c0002t0020 | 1 | NA19060.hp2 | 5_prime_UTR_variant | MODIFIER | c.-136G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/7 | 136 | chr7 | 4959153 | ||||||
| chr7:4959154 | G | T | 1 | a0001c0002t0020 | 1 | NA19060.hp2 | 5_prime_UTR_variant | MODIFIER | c.-137C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/7 | 137 | chr7 | 4959154 | ||||||
| chr7:4959154 | GGAGCCGG others(5): Show |
G | 1 | a0001c0001t0019 | 1 | HG01515.hp2 | 5_prime_UTR_variant | MODIFIER | c.-149_-138delGGGCTC others(6): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/7 | 138 | chr7 | 4959154 | ||||||
| chr7:4959160 | G | C | 6 | a0001c0001t0002 a0001c0001t0013 a0001c0002t0001 others(3): Show |
35 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(32): Show |
5_prime_UTR_variant | MODIFIER | c.-143C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/7 | 143 | chr7 | 4959160 | ||||||
| chr7:4959160 | G | GGAGCCC | 2 | a0001c0002t0001 a0001c0002t0002 |
4 | HG02602.hp2 HG03225.hp1 HG03540.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-149_-144dupGGGCTC | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/7 | 144 | chr7 | 4959160 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:4907616 | G | T | 2 | a0001c0001t0002g0026 a0001c0004t0002g0317 |
2 | HG02055.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.538-17C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4907616 | |||||||
| chr7:4907651 | C | G | 2 | a0001c0001t0004g0353 a0001c0001t0004g0354 |
2 | HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.538-52G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4907651 | |||||||
| chr7:4907728 | G | C | 6 | a0001c0002t0001g0108 a0001c0002t0001g0119 a0001c0002t0001g0120 others(3): Show |
6 | HG01891.hp2 HG02145.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.538-129C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4907728 | |||||||
| chr7:4907736 | A | G | 2 | a0001c0001t0002g0282 a0001c0002t0002g0237 |
2 | HG02165.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.538-137T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4907736 | |||||||
| chr7:4907768 | A | C | 95 | a0001c0001t0001g0032 a0001c0001t0001g0094 a0001c0001t0001g0125 others(92): Show |
96 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.538-169T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4907768 | |||||||
| chr7:4907853 | C | T | 46 | a0001c0001t0005g0072 a0001c0001t0005g0077 a0001c0001t0005g0082 others(43): Show |
46 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.538-254G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4907853 | |||||||
| chr7:4907854 | G | A | 2 | a0001c0001t0010g0041 a0001c0002t0010g0155 |
2 | HG02055.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.538-255C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4907854 | |||||||
| chr7:4907874 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.538-275C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4907874 | |||||||
| chr7:4907883 | T | C | 1 | a0001c0002t0032g0159 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.538-284A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4907883 | |||||||
| chr7:4907970 | G | A | 14 | a0001c0001t0001g0123 a0001c0002t0001g0102 a0001c0002t0001g0103 others(11): Show |
14 | HG00280.hp1 HG00639.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.538-371C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4907970 | |||||||
| chr7:4908002 | A | G | 4 | a0001c0001t0002g0001 a0001c0001t0002g0277 a0001c0001t0002g0278 others(1): Show |
5 | HG00735.hp1 HG00741.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.538-403T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908002 | |||||||
| chr7:4908059 | C | T | 1 | a0001c0007t0025g0356 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.538-460G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908059 | |||||||
| chr7:4908105 | C | T | 2 | a0001c0001t0001g0352 a0001c0002t0001g0113 |
2 | HG01081.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.538-506G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908105 | |||||||
| chr7:4908147 | G | GT | 76 | a0001c0001t0001g0007 a0001c0001t0001g0123 a0001c0001t0001g0125 others(73): Show |
76 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.538-549dupA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908147 | |||||||
| chr7:4908147 | G | T | 1 | a0001c0002t0001g0268 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.538-548C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908147 | |||||||
| chr7:4908148 | T | C | 2 | a0001c0001t0001g0267 a0001c0002t0001g0213 |
2 | NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.538-549A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908148 | |||||||
| chr7:4908186 | G | C | 1 | a0001c0001t0012g0251 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.538-587C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908186 | |||||||
| chr7:4908213 | T | C | 45 | a0001c0001t0003g0288 a0001c0001t0004g0003 a0001c0001t0004g0140 others(42): Show |
46 | HG00099.hp1 HG00408.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.538-614A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908213 | |||||||
| chr7:4908219 | G | C | 45 | a0001c0001t0003g0288 a0001c0001t0004g0003 a0001c0001t0004g0140 others(42): Show |
46 | HG00099.hp1 HG00408.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.538-620C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908219 | |||||||
| chr7:4908255 | C | A | 6 | a0001c0002t0003g0156 a0001c0002t0003g0177 a0001c0002t0003g0189 others(3): Show |
6 | NA18992.hp2 NA18998.hp1 NA19003.hp2 others(3): Show |
intron_variant | MODIFIER | c.538-656G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908255 | |||||||
| chr7:4908266 | C | T | 2 | a0001c0002t0001g0116 a0001c0002t0001g0117 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.538-667G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908266 | |||||||
| chr7:4908267 | G | A | 3 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0221 |
3 | NA18747.hp2 NA18939.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.538-668C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908267 | |||||||
| chr7:4908276 | G | T | 1 | a0001c0002t0001g0243 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.538-677C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908276 | |||||||
| chr7:4908288 | T | C | 204 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0048 others(201): Show |
206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.538-689A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908288 | |||||||
| chr7:4908303 | G | A | 1 | a0001c0003t0001g0343 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.538-704C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908303 | |||||||
| chr7:4908340 | C | T | 1 | a0001c0001t0027g0346 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.538-741G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908340 | |||||||
| chr7:4908412 | G | C | 22 | a0001c0001t0001g0007 a0001c0001t0002g0001 a0001c0001t0002g0011 others(19): Show |
23 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.538-813C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908412 | |||||||
| chr7:4908431 | T | C | 165 | a0001c0001t0001g0007 a0001c0001t0001g0061 a0001c0001t0001g0122 others(162): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.538-832A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908431 | |||||||
| chr7:4908471 | C | T | 1 | a0001c0001t0027g0346 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.538-872G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908471 | |||||||
| chr7:4908530 | T | C | 1 | a0001c0001t0001g0273 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.538-931A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908530 | |||||||
| chr7:4908609 | T | C | 6 | a0001c0001t0001g0118 a0001c0001t0001g0126 a0001c0001t0001g0127 others(3): Show |
6 | HG01496.hp1 HG02055.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.538-1010A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908609 | |||||||
| chr7:4908627 | C | T | 150 | a0001c0001t0001g0020 a0001c0001t0001g0048 a0001c0001t0001g0070 others(147): Show |
151 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.538-1028G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908627 | |||||||
| chr7:4908661 | G | A | 3 | a0001c0001t0001g0123 a0001c0001t0027g0346 a0001c0007t0025g0356 |
3 | HG02559.hp1 HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.538-1062C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908661 | |||||||
| chr7:4908673 | C | T | 4 | a0001c0002t0001g0006 a0001c0002t0001g0008 a0001c0002t0001g0143 others(1): Show |
4 | HG02451.hp2 HG02970.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.538-1074G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908673 | |||||||
| chr7:4908680 | C | T | 2 | a0001c0001t0004g0294 a0001c0001t0004g0296 |
2 | HG01257.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.538-1081G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908680 | |||||||
| chr7:4908688 | G | C | 1 | a0001c0001t0002g0012 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.538-1089C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908688 | |||||||
| chr7:4908694 | C | G | 1 | a0001c0001t0003g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.538-1095G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908694 | |||||||
| chr7:4908694 | C | T | 5 | a0001c0001t0003g0067 a0001c0002t0003g0156 a0001c0002t0003g0189 others(2): Show |
5 | HG01255.hp1 NA18992.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.538-1095G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908694 | |||||||
| chr7:4908702 | G | T | 1 | a0001c0002t0001g0105 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.538-1103C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908702 | |||||||
| chr7:4908724 | C | T | 1 | a0001c0002t0032g0159 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.538-1125G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908724 | |||||||
| chr7:4908736 | A | C | 3 | a0001c0002t0001g0149 a0001c0002t0001g0150 a0001c0002t0001g0151 |
3 | HG01099.hp1 HG01433.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.538-1137T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908736 | |||||||
| chr7:4908745 | T | A | 6 | a0001c0002t0001g0104 a0001c0002t0001g0107 a0001c0002t0001g0109 others(3): Show |
6 | HG01109.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.537+1136A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908745 | |||||||
| chr7:4908745 | T | C | 250 | a0001c0001t0001g0007 a0001c0001t0001g0061 a0001c0001t0001g0070 others(247): Show |
252 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.537+1136A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908745 | |||||||
| chr7:4908754 | G | T | 1 | a0001c0001t0012g0301 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.537+1127C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908754 | |||||||
| chr7:4908756 | G | A | 1 | a0001c0002t0001g0253 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.537+1125C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908756 | |||||||
| chr7:4908766 | A | G | 1 | a0001c0002t0003g0171 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.537+1115T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908766 | |||||||
| chr7:4908770 | G | A | 1 | a0001c0002t0003g0171 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.537+1111C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908770 | |||||||
| chr7:4908833 | G | T | 1 | a0001c0001t0027g0346 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.537+1048C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908833 | |||||||
| chr7:4908841 | A | G | 1 | a0001c0001t0002g0281 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.537+1040T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908841 | |||||||
| chr7:4908846 | G | A | 1 | a0001c0004t0002g0317 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.537+1035C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908846 | |||||||
| chr7:4908874 | G | C | 1 | a0001c0001t0003g0311 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.537+1007C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908874 | |||||||
| chr7:4908896 | C | CA | 9 | a0001c0001t0001g0118 a0001c0001t0001g0127 a0001c0001t0001g0310 others(6): Show |
9 | HG01109.hp1 HG02056.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.537+984dupT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908896 | |||||||
| chr7:4908896 | CA | C | 56 | a0001c0001t0001g0219 a0001c0001t0001g0352 a0001c0001t0002g0012 others(53): Show |
57 | HG00099.hp1 HG00408.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.537+984delT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908896 | |||||||
| chr7:4908987 | G | A | 1 | a0001c0002t0001g0120 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.537+894C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4908987 | |||||||
| chr7:4909070 | T | G | 7 | a0001c0001t0001g0273 a0001c0002t0001g0002 a0001c0002t0001g0225 others(4): Show |
8 | HG02451.hp1 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.537+811A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4909070 | |||||||
| chr7:4909203 | T | C | 15 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0122 others(12): Show |
15 | HG01496.hp1 HG02559.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.537+678A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4909203 | |||||||
| chr7:4909208 | G | A | 2 | a0001c0001t0010g0357 a0001c0001t0010g0358 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.537+673C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4909208 | |||||||
| chr7:4909241 | C | A | 1 | a0001c0001t0027g0346 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.537+640G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4909241 | |||||||
| chr7:4909363 | A | G | 1 | a0001c0002t0004g0212 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.537+518T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4909363 | |||||||
| chr7:4909432 | C | CA | 13 | a0001c0001t0001g0007 a0001c0001t0002g0028 a0001c0001t0002g0031 others(10): Show |
13 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(10): Show |
intron_variant | MODIFIER | c.537+448dupT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4909432 | |||||||
| chr7:4909432 | C | CAA | 226 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0081 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.537+447_537+448dup others(2): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4909432 | |||||||
| chr7:4909432 | C | CAAA | 6 | a0001c0001t0003g0288 a0001c0002t0003g0189 a0001c0002t0004g0205 others(3): Show |
6 | HG02738.hp2 NA18942.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.537+446_537+448dup others(3): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4909432 | |||||||
| chr7:4909438 | A | C | 1 | a0001c0001t0015g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.537+443T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4909438 | |||||||
| chr7:4909491 | G | A | 8 | a0001c0001t0001g0297 a0001c0002t0001g0226 a0001c0002t0001g0229 others(5): Show |
8 | HG02083.hp2 NA18951.hp2 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.537+390C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4909491 | |||||||
| chr7:4909502 | G | A | 178 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0081 others(175): Show |
179 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.537+379C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4909502 | |||||||
| chr7:4909512 | G | A | 178 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0081 others(175): Show |
179 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.537+369C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4909512 | |||||||
| chr7:4909582 | A | G | 51 | a0001c0001t0001g0214 a0001c0001t0001g0337 a0001c0001t0001g0352 others(48): Show |
52 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.537+299T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4909582 | |||||||
| chr7:4909600 | T | G | 1 | a0001c0001t0015g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.537+281A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4909600 | |||||||
| chr7:4909659 | T | C | 16 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0122 others(13): Show |
16 | HG01496.hp1 HG02559.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.537+222A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 6/6 | chr7 | 4909659 | |||||||
| chr7:4910034 | G | A | 1 | a0001c0001t0001g0007 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.468-84C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910034 | |||||||
| chr7:4910092 | T | G | 1 | a0001c0002t0003g0208 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.468-142A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910092 | |||||||
| chr7:4910129 | G | A | 1 | a0001c0001t0010g0041 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.468-179C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910129 | |||||||
| chr7:4910180 | C | T | 235 | a0001c0001t0001g0007 a0001c0001t0001g0048 a0001c0001t0001g0054 others(232): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.468-230G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910180 | |||||||
| chr7:4910287 | T | C | 1 | a0001c0001t0001g0007 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.468-337A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910287 | |||||||
| chr7:4910318 | A | G | 1 | a0001c0002t0001g0235 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.468-368T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910318 | |||||||
| chr7:4910382 | T | A | 3 | a0001c0001t0001g0267 a0001c0001t0008g0266 a0001c0001t0008g0272 |
3 | HG02647.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.468-432A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910382 | |||||||
| chr7:4910575 | AC | A | 4 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0126 others(1): Show |
4 | HG01496.hp1 HG02886.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.467+569delG | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910575 | |||||||
| chr7:4910590 | C | G | 1 | a0001c0002t0002g0237 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.467+555G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910590 | |||||||
| chr7:4910599 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.467+546C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910599 | |||||||
| chr7:4910659 | T | C | 286 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0048 others(283): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.467+486A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910659 | |||||||
| chr7:4910681 | C | T | 7 | a0001c0002t0001g0252 a0001c0002t0001g0253 a0001c0002t0001g0254 others(4): Show |
7 | HG02258.hp1 HG02717.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.467+464G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910681 | |||||||
| chr7:4910687 | G | A | 3 | a0001c0001t0001g0267 a0001c0001t0008g0266 a0001c0001t0008g0272 |
3 | HG02647.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.467+458C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910687 | |||||||
| chr7:4910721 | C | T | 1 | a0001c0001t0030g0091 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.467+424G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910721 | |||||||
| chr7:4910780 | C | T | 6 | a0001c0002t0001g0160 a0001c0002t0001g0161 a0001c0002t0001g0162 others(3): Show |
6 | HG03098.hp1 HG03209.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.467+365G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910780 | |||||||
| chr7:4910843 | G | C | 3 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0001c0002t0001g0121 |
3 | HG02145.hp1 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.467+302C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910843 | |||||||
| chr7:4910968 | G | C | 6 | a0001c0002t0001g0104 a0001c0002t0001g0107 a0001c0002t0001g0109 others(3): Show |
6 | HG01109.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.467+177C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910968 | |||||||
| chr7:4910981 | T | A | 4 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(1): Show |
4 | NA18980.hp1 NA19007.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.467+164A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 5/6 | chr7 | 4910981 | |||||||
| chr7:4911380 | C | T | 1 | a0001c0001t0002g0011 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.366-134G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4911380 | |||||||
| chr7:4911414 | G | C | 3 | a0001c0001t0001g0267 a0001c0001t0008g0266 a0001c0001t0008g0272 |
3 | HG02647.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.366-168C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4911414 | |||||||
| chr7:4911502 | T | A | 182 | a0001c0001t0001g0007 a0001c0001t0001g0048 a0001c0001t0001g0054 others(179): Show |
183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.366-256A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4911502 | |||||||
| chr7:4911502 | T | C | 14 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0123 others(11): Show |
14 | HG01496.hp1 HG02559.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.366-256A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4911502 | |||||||
| chr7:4911570 | C | T | 1 | a0001c0002t0002g0128 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.366-324G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4911570 | |||||||
| chr7:4911571 | G | A | 3 | a0001c0003t0003g0320 a0001c0003t0004g0326 a0001c0003t0004g0327 |
3 | HG02083.hp1 NA18998.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.366-325C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4911571 | |||||||
| chr7:4911584 | A | G | 286 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0048 others(283): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.366-338T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4911584 | |||||||
| chr7:4911598 | G | GTTTTA | 286 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0048 others(283): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.366-357_366-353dup others(5): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4911598 | |||||||
| chr7:4911630 | T | G | 1 | a0001c0002t0005g0176 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.366-384A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4911630 | |||||||
| chr7:4911705 | G | A | 1 | a0001c0002t0008g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.366-459C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4911705 | |||||||
| chr7:4911734 | C | T | 10 | a0001c0001t0001g0158 a0001c0001t0001g0197 a0001c0001t0001g0199 others(7): Show |
10 | HG02056.hp2 HG02135.hp1 NA18747.hp2 others(7): Show |
intron_variant | MODIFIER | c.366-488G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4911734 | |||||||
| chr7:4911961 | A | C | 1 | a0001c0002t0001g0114 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.366-715T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4911961 | |||||||
| chr7:4911987 | T | C | 1 | a0001c0001t0002g0281 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.366-741A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4911987 | |||||||
| chr7:4912153 | G | T | 2 | a0001c0001t0001g0214 a0001c0001t0001g0352 |
2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.366-907C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4912153 | |||||||
| chr7:4912199 | G | A | 1 | a0001c0002t0001g0243 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.366-953C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4912199 | |||||||
| chr7:4912297 | G | A | 1 | a0001c0001t0002g0012 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.366-1051C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4912297 | |||||||
| chr7:4912362 | T | C | 2 | a0001c0001t0002g0085 a0001c0001t0002g0100 |
2 | HG00642.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.366-1116A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4912362 | |||||||
| chr7:4912425 | G | A | 87 | a0001c0001t0001g0020 a0001c0001t0001g0214 a0001c0001t0001g0297 others(84): Show |
88 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.366-1179C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4912425 | |||||||
| chr7:4912479 | G | A | 3 | a0001c0002t0002g0172 a0001c0002t0002g0173 a0001c0002t0003g0171 |
3 | HG03654.hp1 HG03688.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.366-1233C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4912479 | |||||||
| chr7:4912488 | G | A | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0267 others(3): Show |
6 | HG02559.hp1 HG02647.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.366-1242C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4912488 | |||||||
| chr7:4912519 | G | A | 2 | a0001c0001t0010g0357 a0001c0001t0010g0358 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.366-1273C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4912519 | |||||||
| chr7:4912561 | C | CA | 7 | a0001c0001t0001g0220 a0001c0001t0002g0280 a0001c0002t0001g0014 others(4): Show |
7 | HG01981.hp1 NA18983.hp2 NA18995.hp1 others(4): Show |
intron_variant | MODIFIER | c.366-1316dupT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4912561 | |||||||
| chr7:4912651 | A | G | 284 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0048 others(281): Show |
286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.366-1405T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4912651 | |||||||
| chr7:4912674 | G | C | 78 | a0001c0001t0001g0020 a0001c0001t0001g0297 a0001c0001t0001g0314 others(75): Show |
79 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.366-1428C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4912674 | |||||||
| chr7:4912677 | T | C | 1 | a0001c0002t0001g0241 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.366-1431A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4912677 | |||||||
| chr7:4912882 | G | A | 1 | a0001c0002t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.366-1636C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4912882 | |||||||
| chr7:4912959 | C | A | 2 | a0001c0002t0001g0006 a0001c0002t0001g0008 |
2 | HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.366-1713G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4912959 | |||||||
| chr7:4912983 | C | T | 2 | a0001c0002t0006g0180 a0001c0002t0006g0187 |
2 | NA19009.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.366-1737G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4912983 | |||||||
| chr7:4913000 | G | T | 2 | a0001c0001t0010g0357 a0001c0001t0010g0358 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.366-1754C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913000 | |||||||
| chr7:4913028 | G | C | 1 | a0001c0001t0003g0010 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.366-1782C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913028 | |||||||
| chr7:4913199 | G | A | 1 | a0001c0001t0012g0251 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.366-1953C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913199 | |||||||
| chr7:4913265 | A | C | 2 | a0001c0001t0010g0357 a0001c0001t0010g0358 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.366-2019T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913265 | |||||||
| chr7:4913334 | C | A | 7 | a0001c0002t0001g0101 a0001c0002t0001g0160 a0001c0002t0001g0161 others(4): Show |
7 | HG02109.hp2 HG03098.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.366-2088G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913334 | |||||||
| chr7:4913341 | T | G | 1 | a0001c0001t0015g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.366-2095A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913341 | |||||||
| chr7:4913385 | G | A | 7 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0264 others(4): Show |
7 | HG02559.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.366-2139C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913385 | |||||||
| chr7:4913443 | G | A | 268 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0048 others(265): Show |
270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.366-2197C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913443 | |||||||
| chr7:4913448 | G | A | 1 | a0001c0001t0027g0346 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.366-2202C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913448 | |||||||
| chr7:4913549 | C | A | 1 | a0001c0001t0003g0039 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.366-2303G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913549 | |||||||
| chr7:4913567 | A | G | 1 | a0001c0003t0003g0320 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.366-2321T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913567 | |||||||
| chr7:4913653 | G | A | 1 | a0001c0002t0001g0102 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.365+2352C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913653 | |||||||
| chr7:4913721 | C | CA | 31 | a0001c0001t0001g0032 a0001c0001t0001g0057 a0001c0001t0001g0061 others(28): Show |
31 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.365+2283dupT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913721 | |||||||
| chr7:4913721 | CA | C | 218 | a0001c0001t0001g0007 a0001c0001t0001g0048 a0001c0001t0001g0081 others(215): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.365+2283delT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913721 | |||||||
| chr7:4913721 | CAA | C | 8 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0126 others(5): Show |
8 | HG01496.hp1 HG02572.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.365+2282_365+2283d others(4): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913721 | |||||||
| chr7:4913721 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0019g0004 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.365+2273_365+2283d others(13): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913721 | |||||||
| chr7:4913766 | A | G | 264 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0048 others(261): Show |
266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.365+2239T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913766 | |||||||
| chr7:4913792 | G | T | 5 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0126 others(2): Show |
5 | HG01496.hp1 HG02886.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.365+2213C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913792 | |||||||
| chr7:4913810 | T | C | 3 | a0001c0001t0001g0214 a0001c0001t0001g0352 a0001c0001t0009g0377 |
3 | HG00597.hp1 HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.365+2195A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913810 | |||||||
| chr7:4913822 | C | T | 12 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0123 others(9): Show |
12 | HG01496.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.365+2183G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913822 | |||||||
| chr7:4913851 | C | T | 1 | a0001c0001t0009g0375 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.365+2154G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4913851 | |||||||
| chr7:4914013 | C | A | 280 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0118 others(277): Show |
282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.365+1992G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4914013 | |||||||
| chr7:4914052 | C | G | 2 | a0001c0002t0001g0233 a0001c0002t0001g0236 |
2 | NA18977.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.365+1953G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4914052 | |||||||
| chr7:4914070 | T | C | 373 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0048 others(370): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.365+1935A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4914070 | |||||||
| chr7:4914090 | G | A | 282 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0048 others(279): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.365+1915C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4914090 | |||||||
| chr7:4914254 | T | C | 2 | a0001c0002t0001g0136 a0001c0002t0001g0145 |
2 | HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.365+1751A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4914254 | |||||||
| chr7:4914264 | G | A | 3 | a0001c0002t0001g0217 a0001c0002t0005g0216 a0001c0002t0020g0005 |
3 | NA19060.hp2 NA19074.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.365+1741C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4914264 | |||||||
| chr7:4914315 | A | G | 179 | a0001c0001t0001g0007 a0001c0001t0001g0048 a0001c0001t0001g0054 others(176): Show |
180 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.365+1690T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4914315 | |||||||
| chr7:4914502 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.365+1503A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4914502 | |||||||
| chr7:4914566 | C | A | 1 | a0001c0001t0027g0346 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.365+1439G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4914566 | |||||||
| chr7:4914657 | A | G | 284 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0048 others(281): Show |
286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.365+1348T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4914657 | |||||||
| chr7:4914667 | G | A | 7 | a0001c0002t0001g0101 a0001c0002t0001g0160 a0001c0002t0001g0161 others(4): Show |
7 | HG02109.hp2 HG03098.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.365+1338C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4914667 | |||||||
| chr7:4914895 | C | T | 1 | a0001c0002t0007g0359 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.365+1110G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4914895 | |||||||
| chr7:4915063 | A | C | 89 | a0001c0001t0001g0020 a0001c0001t0001g0214 a0001c0001t0001g0297 others(86): Show |
90 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.365+942T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915063 | |||||||
| chr7:4915114 | T | C | 1 | a0001c0007t0025g0356 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.365+891A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915114 | |||||||
| chr7:4915119 | A | G | 2 | a0001c0001t0002g0026 a0001c0004t0002g0317 |
2 | HG02055.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.365+886T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915119 | |||||||
| chr7:4915129 | A | C | 10 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0013 others(7): Show |
11 | HG01069.hp2 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.365+876T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915129 | |||||||
| chr7:4915176 | T | C | 282 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0048 others(279): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.365+829A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915176 | |||||||
| chr7:4915339 | G | C | 1 | a0001c0001t0015g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.365+666C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915339 | |||||||
| chr7:4915459 | G | A | 2 | a0001c0002t0001g0106 a0001c0002t0001g0113 |
2 | HG01081.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.365+546C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915459 | |||||||
| chr7:4915530 | A | G | 2 | a0001c0001t0002g0283 a0001c0001t0002g0284 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.365+475T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915530 | |||||||
| chr7:4915633 | G | C | 1 | a0001c0001t0012g0251 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.365+372C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915633 | |||||||
| chr7:4915640 | A | T | 1 | a0001c0007t0025g0356 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.365+365T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915640 | |||||||
| chr7:4915659 | C | G | 282 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0048 others(279): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.365+346G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915659 | |||||||
| chr7:4915750 | G | GA | 25 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0123 others(22): Show |
25 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.365+254dupT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915750 | |||||||
| chr7:4915779 | T | TTTTTCTG others(26): Show |
97 | a0001c0001t0001g0020 a0001c0001t0001g0158 a0001c0001t0001g0214 others(94): Show |
98 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.365+193_365+225dup others(33): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915779 | |||||||
| chr7:4915779 | T | TTTTTCTG others(59): Show |
1 | a0001c0001t0004g0334 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.365+225_365+226ins others(66): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915779 | |||||||
| chr7:4915804 | A | AGTGAGTT others(26): Show |
3 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0001g0223 |
3 | HG02135.hp1 NA18967.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.365+200_365+201ins others(33): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915804 | |||||||
| chr7:4915845 | A | G | 1 | a0001c0001t0004g0345 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.365+160T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915845 | |||||||
| chr7:4915867 | GAA | G | 4 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0126 others(1): Show |
4 | HG01496.hp1 HG02886.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+136_365+137del others(2): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915867 | |||||||
| chr7:4915976 | G | C | 1 | a0001c0001t0001g0070 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.365+29C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915976 | |||||||
| chr7:4915990 | C | T | 5 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0126 others(2): Show |
5 | HG01496.hp1 HG02886.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.365+15G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 4/6 | chr7 | 4915990 | |||||||
| chr7:4916086 | C | T | 2 | a0001c0001t0012g0251 a0001c0002t0004g0212 |
2 | HG01167.hp2 HG03471.hp1 |
splice_region_variant&intron_variant | LOW | c.291-7G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4916086 | |||||||
| chr7:4916174 | A | G | 14 | a0001c0001t0003g0288 a0001c0001t0004g0003 a0001c0001t0004g0140 others(11): Show |
15 | HG00099.hp1 HG00639.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.291-95T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4916174 | |||||||
| chr7:4916258 | T | A | 1 | a0001c0001t0003g0035 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.291-179A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4916258 | |||||||
| chr7:4916371 | C | CT | 17 | a0001c0001t0001g0262 a0001c0001t0002g0034 a0001c0001t0002g0093 others(14): Show |
17 | HG00408.hp2 HG01109.hp1 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.291-293dupA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4916371 | |||||||
| chr7:4916371 | CT | C | 171 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0158 others(168): Show |
171 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.291-293delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4916371 | |||||||
| chr7:4916371 | CTT | C | 66 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0081 others(63): Show |
67 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.291-294_291-293del others(2): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4916371 | |||||||
| chr7:4916371 | CTTT | C | 7 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0267 others(4): Show |
7 | HG01074.hp2 HG02559.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.291-295_291-293del others(3): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4916371 | |||||||
| chr7:4916371 | CTTTTTTT others(7): Show |
C | 5 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0126 others(2): Show |
5 | HG01496.hp1 HG02886.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.291-306_291-293del others(14): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4916371 | |||||||
| chr7:4916434 | G | A | 4 | a0001c0001t0001g0061 a0001c0001t0005g0072 a0001c0001t0005g0077 others(1): Show |
4 | HG00408.hp2 NA18942.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.291-355C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4916434 | |||||||
| chr7:4916572 | G | A | 5 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0126 others(2): Show |
5 | HG01496.hp1 HG02886.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.291-493C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4916572 | |||||||
| chr7:4916672 | C | T | 7 | a0001c0002t0001g0101 a0001c0002t0001g0160 a0001c0002t0001g0161 others(4): Show |
7 | HG02109.hp2 HG03098.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.291-593G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4916672 | |||||||
| chr7:4916777 | A | G | 1 | a0001c0007t0025g0356 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.291-698T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4916777 | |||||||
| chr7:4916939 | G | C | 5 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0126 others(2): Show |
5 | HG01496.hp1 HG02886.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.291-860C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4916939 | |||||||
| chr7:4917045 | C | A | 1 | a0001c0002t0003g0200 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.291-966G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4917045 | |||||||
| chr7:4917191 | T | A | 1 | a0001c0001t0002g0115 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.291-1112A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4917191 | |||||||
| chr7:4917281 | G | A | 1 | a0001c0001t0002g0115 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.291-1202C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4917281 | |||||||
| chr7:4917342 | C | T | 139 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0081 others(136): Show |
140 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.291-1263G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4917342 | |||||||
| chr7:4917386 | G | C | 7 | a0001c0002t0001g0101 a0001c0002t0001g0160 a0001c0002t0001g0161 others(4): Show |
7 | HG02109.hp2 HG03098.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.291-1307C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4917386 | |||||||
| chr7:4917498 | C | T | 2 | a0001c0001t0002g0085 a0001c0001t0002g0100 |
2 | HG00642.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.291-1419G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4917498 | |||||||
| chr7:4917549 | G | A | 7 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0264 others(4): Show |
7 | HG02559.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.291-1470C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4917549 | |||||||
| chr7:4917664 | C | T | 148 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0081 others(145): Show |
149 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.291-1585G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4917664 | |||||||
| chr7:4917702 | AT | A | 4 | a0001c0001t0001g0158 a0001c0001t0001g0246 a0001c0001t0003g0351 others(1): Show |
4 | HG03540.hp2 NA18946.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.291-1624delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4917702 | |||||||
| chr7:4917703 | T | A | 101 | a0001c0001t0001g0020 a0001c0001t0001g0197 a0001c0001t0001g0199 others(98): Show |
102 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.291-1624A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4917703 | |||||||
| chr7:4917704 | A | T | 1 | a0001c0001t0003g0062 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.291-1625T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4917704 | |||||||
| chr7:4917779 | C | T | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0267 others(3): Show |
6 | HG02559.hp1 HG02647.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.291-1700G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4917779 | |||||||
| chr7:4917785 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.291-1706G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4917785 | |||||||
| chr7:4917835 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.291-1756C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4917835 | |||||||
| chr7:4918428 | G | C | 153 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0081 others(150): Show |
154 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(151): Show |
intron_variant | MODIFIER | c.290+1743C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4918428 | |||||||
| chr7:4918446 | G | A | 1 | a0001c0002t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.290+1725C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4918446 | |||||||
| chr7:4918483 | C | CT | 14 | a0001c0001t0001g0061 a0001c0001t0001g0260 a0001c0001t0001g0352 others(11): Show |
14 | HG01516.hp2 HG01517.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.290+1687dupA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4918483 | |||||||
| chr7:4918483 | CT | C | 10 | a0001c0001t0001g0246 a0001c0001t0003g0016 a0001c0001t0003g0274 others(7): Show |
10 | HG01515.hp1 HG01975.hp1 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.290+1687delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4918483 | |||||||
| chr7:4918483 | CTTT | C | 138 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0081 others(135): Show |
139 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(136): Show |
intron_variant | MODIFIER | c.290+1685_290+1687d others(5): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4918483 | |||||||
| chr7:4918483 | CTTTT | C | 15 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0123 others(12): Show |
15 | HG01496.hp1 HG01891.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.290+1684_290+1687d others(6): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4918483 | |||||||
| chr7:4918494 | T | C | 1 | a0001c0001t0004g0287 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.290+1677A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4918494 | |||||||
| chr7:4918628 | T | C | 2 | a0001c0001t0004g0304 a0001c0001t0004g0305 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.290+1543A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4918628 | |||||||
| chr7:4918792 | A | AT | 11 | a0001c0001t0002g0085 a0001c0002t0001g0101 a0001c0002t0001g0160 others(8): Show |
11 | HG00642.hp2 HG02109.hp2 HG03098.hp1 others(8): Show |
intron_variant | MODIFIER | c.290+1378dupA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4918792 | |||||||
| chr7:4919047 | C | T | 107 | a0001c0001t0001g0020 a0001c0001t0001g0158 a0001c0001t0001g0197 others(104): Show |
108 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.290+1124G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4919047 | |||||||
| chr7:4919068 | C | T | 1 | a0001c0001t0001g0007 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.290+1103G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4919068 | |||||||
| chr7:4919115 | C | A | 1 | a0001c0001t0027g0346 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.290+1056G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4919115 | |||||||
| chr7:4919156 | A | T | 3 | a0001c0001t0001g0267 a0001c0001t0008g0266 a0001c0001t0008g0272 |
3 | HG02647.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.290+1015T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4919156 | |||||||
| chr7:4919168 | A | G | 1 | a0001c0001t0002g0291 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.290+1003T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4919168 | |||||||
| chr7:4919405 | C | T | 72 | a0001c0002t0001g0006 a0001c0002t0001g0008 a0001c0002t0001g0036 others(69): Show |
72 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.290+766G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4919405 | |||||||
| chr7:4919406 | A | G | 1 | a0001c0002t0004g0205 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.290+765T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4919406 | |||||||
| chr7:4919519 | G | C | 1 | a0001c0007t0025g0356 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.290+652C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4919519 | |||||||
| chr7:4919561 | C | G | 2 | a0001c0001t0010g0357 a0001c0001t0010g0358 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.290+610G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4919561 | |||||||
| chr7:4919664 | C | T | 2 | a0001c0002t0010g0155 a0001c0002t0014g0174 |
2 | HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.290+507G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4919664 | |||||||
| chr7:4919715 | A | G | 3 | a0001c0001t0001g0032 a0001c0001t0001g0094 a0001c0001t0019g0004 |
3 | HG01106.hp2 HG01515.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.290+456T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4919715 | |||||||
| chr7:4919950 | G | A | 178 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0122 others(175): Show |
179 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.290+221C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4919950 | |||||||
| chr7:4919953 | G | C | 7 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0264 others(4): Show |
7 | HG02559.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.290+218C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4919953 | |||||||
| chr7:4919959 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.290+212G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4919959 | |||||||
| chr7:4919971 | A | G | 161 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0008 others(158): Show |
162 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.290+200T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4919971 | |||||||
| chr7:4920158 | G | A | 161 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0008 others(158): Show |
162 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.290+13C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 3/6 | chr7 | 4920158 | |||||||
| chr7:4920420 | G | A | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0267 others(3): Show |
6 | HG02559.hp1 HG02647.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.130-89C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4920420 | |||||||
| chr7:4920498 | G | A | 2 | a0001c0002t0001g0213 a0001c0002t0015g0215 |
2 | NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.130-167C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4920498 | |||||||
| chr7:4920522 | T | C | 1 | a0001c0001t0015g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.130-191A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4920522 | |||||||
| chr7:4920638 | C | A | 1 | a0001c0002t0001g0101 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.130-307G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4920638 | |||||||
| chr7:4920668 | C | T | 1 | a0001c0001t0015g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.130-337G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4920668 | |||||||
| chr7:4920688 | TCCTCCCT others(1): Show |
T | 268 | a0001c0001t0001g0020 a0001c0001t0001g0118 a0001c0001t0001g0122 others(265): Show |
270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.130-365_130-358del others(8): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4920688 | |||||||
| chr7:4920688 | TCCTCCCT others(5): Show |
T | 1 | a0001c0001t0001g0264 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.130-369_130-358del others(12): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4920688 | |||||||
| chr7:4920785 | G | A | 269 | a0001c0001t0001g0020 a0001c0001t0001g0118 a0001c0001t0001g0122 others(266): Show |
271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.130-454C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4920785 | |||||||
| chr7:4920837 | G | C | 283 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0118 others(280): Show |
285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.130-506C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4920837 | |||||||
| chr7:4920865 | C | A | 256 | a0001c0001t0001g0020 a0001c0001t0001g0158 a0001c0001t0001g0197 others(253): Show |
258 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.130-534G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4920865 | |||||||
| chr7:4920996 | C | A | 11 | a0001c0001t0002g0028 a0001c0001t0002g0031 a0001c0001t0002g0034 others(8): Show |
11 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(8): Show |
intron_variant | MODIFIER | c.130-665G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4920996 | |||||||
| chr7:4921016 | C | A | 2 | a0001c0001t0003g0089 a0001c0001t0003g0090 |
2 | HG00558.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.130-685G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4921016 | |||||||
| chr7:4921072 | C | A | 1 | a0001c0001t0015g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.130-741G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4921072 | |||||||
| chr7:4921103 | G | C | 51 | a0001c0002t0001g0002 a0001c0002t0001g0014 a0001c0002t0001g0029 others(48): Show |
52 | HG00738.hp2 HG01074.hp2 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.130-772C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4921103 | |||||||
| chr7:4921417 | G | A | 1 | a0001c0002t0003g0200 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.130-1086C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4921417 | |||||||
| chr7:4921447 | C | T | 1 | a0001c0002t0001g0006 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.130-1116G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4921447 | |||||||
| chr7:4921485 | G | A | 1 | a0001c0001t0002g0021 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.130-1154C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4921485 | |||||||
| chr7:4921494 | A | G | 256 | a0001c0001t0001g0020 a0001c0001t0001g0158 a0001c0001t0001g0197 others(253): Show |
258 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.130-1163T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4921494 | |||||||
| chr7:4921576 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.130-1245C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4921576 | |||||||
| chr7:4921577 | C | T | 234 | a0001c0001t0001g0020 a0001c0001t0001g0158 a0001c0001t0001g0197 others(231): Show |
236 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.130-1246G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4921577 | |||||||
| chr7:4921620 | C | CA | 17 | a0001c0001t0001g0202 a0001c0001t0001g0273 a0001c0001t0002g0344 others(14): Show |
17 | HG00544.hp1 HG02109.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.130-1290dupT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4921620 | |||||||
| chr7:4921620 | CA | C | 27 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0122 others(24): Show |
27 | HG01069.hp1 HG01256.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.130-1290delT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4921620 | |||||||
| chr7:4921742 | G | A | 2 | a0001c0002t0001g0160 a0001c0002t0001g0162 |
2 | HG03098.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.130-1411C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4921742 | |||||||
| chr7:4921749 | G | A | 1 | a0001c0001t0003g0045 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.130-1418C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4921749 | |||||||
| chr7:4921777 | G | A | 95 | a0001c0001t0001g0020 a0001c0001t0001g0158 a0001c0001t0001g0197 others(92): Show |
96 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.130-1446C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4921777 | |||||||
| chr7:4922099 | G | A | 1 | a0001c0001t0002g0038 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.130-1768C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922099 | |||||||
| chr7:4922192 | C | T | 48 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(45): Show |
48 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.130-1861G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922192 | |||||||
| chr7:4922269 | A | T | 252 | a0001c0001t0001g0020 a0001c0001t0001g0158 a0001c0001t0001g0197 others(249): Show |
254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.130-1938T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922269 | |||||||
| chr7:4922341 | A | G | 252 | a0001c0001t0001g0020 a0001c0001t0001g0158 a0001c0001t0001g0197 others(249): Show |
254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.130-2010T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922341 | |||||||
| chr7:4922350 | C | A | 230 | a0001c0001t0001g0020 a0001c0001t0001g0158 a0001c0001t0001g0197 others(227): Show |
232 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.130-2019G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922350 | |||||||
| chr7:4922350 | C | T | 1 | a0001c0001t0002g0038 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.130-2019G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922350 | |||||||
| chr7:4922425 | C | T | 1 | a0001c0001t0008g0272 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.130-2094G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922425 | |||||||
| chr7:4922439 | G | A | 2 | a0001c0002t0001g0141 a0001c0002t0001g0152 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.130-2108C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922439 | |||||||
| chr7:4922475 | A | T | 1 | a0001c0001t0004g0354 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.130-2144T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922475 | |||||||
| chr7:4922587 | T | G | 252 | a0001c0001t0001g0020 a0001c0001t0001g0158 a0001c0001t0001g0197 others(249): Show |
254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.130-2256A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922587 | |||||||
| chr7:4922617 | C | A | 1 | a0001c0001t0010g0041 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.130-2286G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922617 | |||||||
| chr7:4922695 | C | A | 1 | a0001c0002t0001g0136 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.130-2364G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922695 | |||||||
| chr7:4922732 | G | A | 252 | a0001c0001t0001g0020 a0001c0001t0001g0158 a0001c0001t0001g0197 others(249): Show |
254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.130-2401C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922732 | |||||||
| chr7:4922759 | C | T | 97 | a0001c0002t0001g0006 a0001c0002t0001g0008 a0001c0002t0001g0033 others(94): Show |
97 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.130-2428G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922759 | |||||||
| chr7:4922761 | A | G | 7 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0264 others(4): Show |
7 | HG02559.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.130-2430T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922761 | |||||||
| chr7:4922839 | T | C | 14 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0123 others(11): Show |
14 | HG01496.hp1 HG02559.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.130-2508A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922839 | |||||||
| chr7:4922877 | C | T | 1 | a0001c0002t0001g0129 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.130-2546G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4922877 | |||||||
| chr7:4923001 | C | A | 6 | a0001c0002t0002g0172 a0001c0002t0002g0173 a0001c0002t0003g0171 others(3): Show |
6 | HG01243.hp1 HG03654.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+2450G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4923001 | |||||||
| chr7:4923052 | C | A | 5 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0126 others(2): Show |
5 | HG01496.hp1 HG02886.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.129+2399G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4923052 | |||||||
| chr7:4923057 | G | A | 230 | a0001c0001t0001g0020 a0001c0001t0001g0158 a0001c0001t0001g0197 others(227): Show |
232 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.129+2394C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4923057 | |||||||
| chr7:4923101 | C | CT | 18 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0264 others(15): Show |
18 | HG01891.hp1 HG01978.hp1 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.129+2349dupA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4923101 | |||||||
| chr7:4923316 | C | G | 2 | a0001c0001t0010g0357 a0001c0001t0010g0358 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.129+2135G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4923316 | |||||||
| chr7:4923330 | C | T | 1 | a0001c0001t0015g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.129+2121G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4923330 | |||||||
| chr7:4923564 | C | G | 1 | a0001c0007t0025g0356 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.129+1887G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4923564 | |||||||
| chr7:4923617 | A | AC | 247 | a0001c0001t0001g0020 a0001c0001t0001g0118 a0001c0001t0001g0122 others(244): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.129+1833_129+1834i others(3): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4923617 | |||||||
| chr7:4923639 | T | G | 2 | a0001c0001t0010g0357 a0001c0001t0010g0358 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.129+1812A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4923639 | |||||||
| chr7:4923674 | T | A | 231 | a0001c0001t0001g0020 a0001c0001t0001g0158 a0001c0001t0001g0197 others(228): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.129+1777A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4923674 | |||||||
| chr7:4923707 | A | T | 1 | a0001c0002t0008g0040 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.129+1744T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4923707 | |||||||
| chr7:4923717 | A | G | 278 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0118 others(275): Show |
280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.129+1734T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4923717 | |||||||
| chr7:4923931 | A | G | 18 | a0001c0002t0001g0099 a0001c0002t0001g0103 a0001c0002t0001g0105 others(15): Show |
18 | HG00280.hp1 HG00639.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.129+1520T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4923931 | |||||||
| chr7:4923997 | T | C | 3 | a0001c0002t0001g0162 a0001c0002t0008g0044 a0001c0003t0004g0331 |
3 | HG02004.hp1 HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.129+1454A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4923997 | |||||||
| chr7:4924008 | C | T | 1 | a0001c0002t0001g0135 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.129+1443G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924008 | |||||||
| chr7:4924053 | T | G | 7 | a0001c0002t0001g0101 a0001c0002t0001g0160 a0001c0002t0001g0161 others(4): Show |
7 | HG02109.hp2 HG03098.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.129+1398A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924053 | |||||||
| chr7:4924064 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.129+1387G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924064 | |||||||
| chr7:4924109 | A | G | 6 | a0001c0001t0002g0026 a0001c0001t0010g0357 a0001c0001t0010g0358 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+1342T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924109 | |||||||
| chr7:4924149 | A | G | 242 | a0001c0001t0001g0020 a0001c0001t0001g0158 a0001c0001t0001g0197 others(239): Show |
244 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.129+1302T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924149 | |||||||
| chr7:4924185 | T | C | 240 | a0001c0001t0001g0020 a0001c0001t0001g0122 a0001c0001t0001g0123 others(237): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.129+1266A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924185 | |||||||
| chr7:4924309 | T | C | 1 | a0001c0002t0003g0201 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.129+1142A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924309 | |||||||
| chr7:4924371 | G | A | 231 | a0001c0001t0001g0020 a0001c0001t0001g0158 a0001c0001t0001g0197 others(228): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.129+1080C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924371 | |||||||
| chr7:4924421 | C | A | 4 | a0001c0002t0001g0002 a0001c0002t0001g0265 a0001c0002t0001g0270 others(1): Show |
5 | HG02451.hp1 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.129+1030G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924421 | |||||||
| chr7:4924582 | G | T | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0267 others(3): Show |
6 | HG02559.hp1 HG02647.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+869C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924582 | |||||||
| chr7:4924583 | A | C | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0267 others(3): Show |
6 | HG02559.hp1 HG02647.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+868T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924583 | |||||||
| chr7:4924603 | T | C | 6 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0126 others(3): Show |
6 | HG01496.hp1 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+848A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924603 | |||||||
| chr7:4924639 | G | C | 1 | a0001c0001t0001g0264 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.129+812C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924639 | |||||||
| chr7:4924726 | T | C | 1 | a0001c0001t0001g0264 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.129+725A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924726 | |||||||
| chr7:4924749 | G | A | 244 | a0001c0001t0001g0020 a0001c0001t0001g0118 a0001c0001t0001g0122 others(241): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.129+702C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924749 | |||||||
| chr7:4924865 | C | T | 1 | a0001c0001t0030g0091 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.129+586G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924865 | |||||||
| chr7:4924866 | G | A | 11 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0013 others(8): Show |
12 | HG01069.hp2 HG01070.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.129+585C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4924866 | |||||||
| chr7:4925106 | G | C | 1 | a0001c0001t0002g0308 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.129+345C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4925106 | |||||||
| chr7:4925227 | G | A | 2 | a0001c0001t0005g0290 a0001c0001t0005g0312 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.129+224C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4925227 | |||||||
| chr7:4925236 | G | T | 81 | a0001c0001t0001g0020 a0001c0001t0001g0273 a0001c0001t0001g0297 others(78): Show |
82 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.129+215C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4925236 | |||||||
| chr7:4925260 | A | G | 1 | a0001c0001t0027g0346 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.129+191T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4925260 | |||||||
| chr7:4925310 | GCCA | G | 92 | a0001c0001t0001g0020 a0001c0001t0001g0273 a0001c0001t0001g0297 others(89): Show |
93 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.129+138_129+140del others(3): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4925310 | |||||||
| chr7:4925316 | G | C | 92 | a0001c0001t0001g0020 a0001c0001t0001g0273 a0001c0001t0001g0297 others(89): Show |
93 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.129+135C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4925316 | |||||||
| chr7:4925318 | G | C | 92 | a0001c0001t0001g0020 a0001c0001t0001g0273 a0001c0001t0001g0297 others(89): Show |
93 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.129+133C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4925318 | |||||||
| chr7:4925320 | C | CT | 92 | a0001c0001t0001g0020 a0001c0001t0001g0273 a0001c0001t0001g0297 others(89): Show |
93 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.129+130_129+131ins others(1): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4925320 | |||||||
| chr7:4925323 | TCC | T | 92 | a0001c0001t0001g0020 a0001c0001t0001g0273 a0001c0001t0001g0297 others(89): Show |
93 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.129+126_129+127del others(2): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 2/6 | chr7 | 4925323 | |||||||
| chr7:4925564 | C | T | 81 | a0001c0001t0001g0020 a0001c0001t0001g0273 a0001c0001t0001g0297 others(78): Show |
82 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.48-32G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4925564 | |||||||
| chr7:4925632 | G | T | 1 | a0001c0001t0002g0115 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.48-100C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4925632 | |||||||
| chr7:4925702 | T | C | 98 | a0001c0001t0001g0020 a0001c0001t0001g0259 a0001c0001t0001g0260 others(95): Show |
99 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.48-170A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4925702 | |||||||
| chr7:4925707 | G | A | 6 | a0001c0001t0010g0357 a0001c0001t0010g0358 a0001c0002t0007g0360 others(3): Show |
6 | HG00280.hp1 HG01192.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.48-175C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4925707 | |||||||
| chr7:4925834 | A | C | 7 | a0001c0002t0001g0101 a0001c0002t0001g0160 a0001c0002t0001g0161 others(4): Show |
7 | HG02109.hp2 HG03098.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.48-302T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4925834 | |||||||
| chr7:4925948 | G | A | 90 | a0001c0001t0001g0020 a0001c0001t0001g0264 a0001c0001t0001g0273 others(87): Show |
91 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.48-416C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4925948 | |||||||
| chr7:4925951 | G | A | 1 | a0001c0001t0015g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.48-419C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4925951 | |||||||
| chr7:4926104 | C | CT | 11 | a0001c0001t0001g0264 a0001c0001t0002g0280 a0001c0001t0004g0286 others(8): Show |
11 | HG01109.hp2 HG01934.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.48-573dupA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926104 | |||||||
| chr7:4926114 | C | T | 243 | a0001c0001t0001g0020 a0001c0001t0001g0118 a0001c0001t0001g0122 others(240): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.48-582G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926114 | |||||||
| chr7:4926209 | C | T | 1 | a0001c0001t0015g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.48-677G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926209 | |||||||
| chr7:4926287 | G | C | 3 | a0001c0001t0001g0267 a0001c0001t0008g0266 a0001c0001t0008g0272 |
3 | HG02647.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.48-755C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926287 | |||||||
| chr7:4926498 | C | A | 80 | a0001c0001t0001g0273 a0001c0001t0001g0297 a0001c0001t0001g0314 others(77): Show |
81 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.48-966G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926498 | |||||||
| chr7:4926508 | G | A | 2 | a0001c0001t0010g0357 a0001c0001t0010g0358 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.48-976C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926508 | |||||||
| chr7:4926572 | C | G | 4 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0126 others(1): Show |
4 | HG01496.hp1 HG02886.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.48-1040G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926572 | |||||||
| chr7:4926696 | C | T | 2 | a0001c0001t0002g0283 a0001c0001t0002g0284 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.48-1164G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926696 | |||||||
| chr7:4926716 | G | C | 1 | a0001c0002t0003g0208 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.48-1184C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926716 | |||||||
| chr7:4926821 | A | T | 84 | a0001c0001t0001g0273 a0001c0001t0001g0292 a0001c0001t0001g0297 others(81): Show |
85 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.48-1289T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926821 | |||||||
| chr7:4926824 | A | G | 2 | a0001c0002t0001g0002 a0001c0002t0001g0265 |
3 | HG02451.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.48-1292T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926824 | |||||||
| chr7:4926846 | G | A | 11 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0013 others(8): Show |
12 | HG01069.hp2 HG01070.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.48-1314C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926846 | |||||||
| chr7:4926858 | C | G | 83 | a0001c0001t0001g0273 a0001c0001t0001g0292 a0001c0001t0001g0297 others(80): Show |
84 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.48-1326G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926858 | |||||||
| chr7:4926859 | C | G | 1 | a0001c0002t0005g0192 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.48-1327G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926859 | |||||||
| chr7:4926898 | T | C | 1 | a0001c0001t0004g0334 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.48-1366A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926898 | |||||||
| chr7:4926942 | C | T | 1 | a0001c0001t0012g0251 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.48-1410G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926942 | |||||||
| chr7:4926969 | T | C | 270 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0123 others(267): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.48-1437A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926969 | |||||||
| chr7:4926993 | C | G | 1 | a0001c0001t0003g0274 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.48-1461G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4926993 | |||||||
| chr7:4927034 | G | A | 86 | a0001c0001t0001g0273 a0001c0001t0001g0292 a0001c0001t0001g0297 others(83): Show |
87 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.48-1502C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4927034 | |||||||
| chr7:4927303 | A | G | 1 | a0001c0001t0001g0220 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.48-1771T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4927303 | |||||||
| chr7:4927304 | A | G | 1 | a0001c0001t0001g0220 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.48-1772T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4927304 | |||||||
| chr7:4927307 | G | C | 128 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0032 others(125): Show |
129 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.48-1775C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4927307 | |||||||
| chr7:4927337 | G | C | 32 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0001t0002g0011 others(29): Show |
33 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.48-1805C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4927337 | |||||||
| chr7:4927351 | C | T | 1 | a0001c0001t0027g0346 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.48-1819G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4927351 | |||||||
| chr7:4927496 | G | A | 8 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0267 others(5): Show |
8 | HG01891.hp1 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.48-1964C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4927496 | |||||||
| chr7:4927638 | C | T | 1 | a0001c0001t0003g0058 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.48-2106G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4927638 | |||||||
| chr7:4927656 | G | A | 1 | a0001c0001t0012g0251 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.48-2124C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4927656 | |||||||
| chr7:4927724 | A | C | 1 | a0001c0002t0003g0200 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.48-2192T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4927724 | |||||||
| chr7:4927943 | C | T | 6 | a0001c0002t0001g0104 a0001c0002t0001g0107 a0001c0002t0001g0109 others(3): Show |
6 | HG01109.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.48-2411G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4927943 | |||||||
| chr7:4928032 | G | A | 65 | a0001c0001t0001g0032 a0001c0001t0001g0048 a0001c0001t0001g0054 others(62): Show |
65 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.48-2500C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4928032 | |||||||
| chr7:4928234 | G | C | 2 | a0001c0001t0003g0075 a0001c0001t0003g0080 |
2 | HG03239.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.48-2702C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4928234 | |||||||
| chr7:4928288 | T | C | 1 | a0001c0002t0006g0248 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.48-2756A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4928288 | |||||||
| chr7:4928351 | G | A | 1 | a0001c0001t0003g0046 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.48-2819C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4928351 | |||||||
| chr7:4928412 | G | T | 1 | a0001c0002t0001g0269 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.48-2880C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4928412 | |||||||
| chr7:4928494 | C | A | 86 | a0001c0001t0001g0273 a0001c0001t0001g0292 a0001c0001t0001g0297 others(83): Show |
87 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.48-2962G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4928494 | |||||||
| chr7:4928540 | C | T | 1 | a0001c0007t0025g0356 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.48-3008G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4928540 | |||||||
| chr7:4928549 | C | T | 4 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0126 others(1): Show |
4 | HG01496.hp1 HG02886.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.48-3017G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4928549 | |||||||
| chr7:4928689 | G | C | 86 | a0001c0001t0001g0273 a0001c0001t0001g0292 a0001c0001t0001g0297 others(83): Show |
87 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.48-3157C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4928689 | |||||||
| chr7:4928739 | C | A | 1 | a0001c0001t0003g0080 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.48-3207G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4928739 | |||||||
| chr7:4928760 | A | C | 1 | a0001c0002t0005g0184 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.48-3228T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4928760 | |||||||
| chr7:4928787 | A | G | 1 | a0001c0001t0002g0115 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.48-3255T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4928787 | |||||||
| chr7:4928813 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.48-3281G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4928813 | |||||||
| chr7:4928846 | G | A | 24 | a0001c0002t0001g0006 a0001c0002t0001g0008 a0001c0002t0001g0119 others(21): Show |
24 | HG00099.hp2 HG00741.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.48-3314C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4928846 | |||||||
| chr7:4928928 | G | T | 2 | a0001c0001t0001g0297 a0001c0001t0003g0274 |
2 | HG02074.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.48-3396C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4928928 | |||||||
| chr7:4929007 | A | G | 87 | a0001c0001t0001g0273 a0001c0001t0001g0292 a0001c0001t0001g0297 others(84): Show |
88 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.48-3475T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929007 | |||||||
| chr7:4929061 | C | T | 1 | a0001c0002t0001g0106 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.48-3529G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929061 | |||||||
| chr7:4929114 | G | C | 24 | a0001c0002t0001g0006 a0001c0002t0001g0008 a0001c0002t0001g0119 others(21): Show |
24 | HG00099.hp2 HG00741.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.48-3582C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929114 | |||||||
| chr7:4929161 | T | A | 1 | a0001c0001t0001g0264 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.48-3629A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929161 | |||||||
| chr7:4929226 | G | C | 1 | a0001c0001t0004g0309 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.48-3694C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929226 | |||||||
| chr7:4929235 | G | A | 1 | a0001c0003t0004g0332 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.48-3703C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929235 | |||||||
| chr7:4929245 | G | A | 1 | a0001c0001t0027g0346 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.48-3713C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929245 | |||||||
| chr7:4929252 | G | A | 5 | a0001c0001t0002g0050 a0001c0001t0002g0227 a0001c0001t0003g0089 others(2): Show |
5 | HG00558.hp2 HG00673.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.48-3720C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929252 | |||||||
| chr7:4929300 | A | T | 1 | a0001c0002t0001g0110 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.48-3768T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929300 | |||||||
| chr7:4929312 | A | G | 235 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0032 others(232): Show |
237 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(234): Show |
intron_variant | MODIFIER | c.48-3780T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929312 | |||||||
| chr7:4929414 | C | G | 1 | a0001c0001t0015g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.48-3882G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929414 | |||||||
| chr7:4929415 | C | A | 1 | a0001c0001t0004g0347 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.48-3883G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929415 | |||||||
| chr7:4929476 | C | T | 117 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0126 others(114): Show |
118 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.48-3944G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929476 | |||||||
| chr7:4929481 | G | A | 117 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0126 others(114): Show |
118 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.48-3949C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929481 | |||||||
| chr7:4929564 | G | A | 1 | a0001c0001t0012g0251 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.48-4032C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929564 | |||||||
| chr7:4929574 | G | A | 322 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0032 others(319): Show |
325 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.48-4042C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929574 | |||||||
| chr7:4929596 | C | T | 2 | a0001c0001t0010g0357 a0001c0001t0010g0358 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.48-4064G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929596 | |||||||
| chr7:4929607 | C | G | 1 | a0001c0002t0006g0248 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.48-4075G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929607 | |||||||
| chr7:4929610 | T | C | 1 | a0001c0001t0003g0060 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.48-4078A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929610 | |||||||
| chr7:4929617 | C | T | 1 | a0001c0001t0015g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.48-4085G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929617 | |||||||
| chr7:4929643 | G | A | 1 | a0001c0001t0027g0346 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.48-4111C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929643 | |||||||
| chr7:4929673 | C | T | 2 | a0001c0003t0004g0321 a0001c0003t0004g0322 |
2 | NA18968.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.48-4141G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929673 | |||||||
| chr7:4929825 | G | C | 1 | a0001c0001t0015g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.48-4293C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929825 | |||||||
| chr7:4929881 | G | C | 84 | a0001c0001t0001g0273 a0001c0001t0001g0292 a0001c0001t0001g0297 others(81): Show |
85 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.48-4349C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929881 | |||||||
| chr7:4929985 | C | G | 8 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0267 others(5): Show |
8 | HG02559.hp1 HG02647.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.48-4453G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4929985 | |||||||
| chr7:4930026 | T | G | 37 | a0001c0001t0001g0292 a0001c0001t0001g0297 a0001c0001t0001g0314 others(34): Show |
37 | HG00597.hp1 HG00642.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.48-4494A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930026 | |||||||
| chr7:4930057 | C | G | 1 | a0001c0001t0006g0064 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.48-4525G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930057 | |||||||
| chr7:4930080 | T | C | 1 | a0001c0001t0003g0015 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.48-4548A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930080 | |||||||
| chr7:4930271 | C | CA | 81 | a0001c0001t0006g0065 a0001c0001t0010g0041 a0001c0001t0010g0357 others(78): Show |
82 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.48-4740dupT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930271 | |||||||
| chr7:4930271 | C | CAAA | 27 | a0001c0001t0001g0197 a0001c0001t0001g0199 a0001c0001t0001g0202 others(24): Show |
27 | HG01167.hp2 HG01884.hp2 HG02056.hp1 others(24): Show |
intron_variant | MODIFIER | c.48-4742_48-4740dup others(3): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930271 | |||||||
| chr7:4930271 | CA | C | 6 | a0001c0001t0002g0009 a0001c0001t0003g0016 a0001c0001t0003g0133 others(3): Show |
6 | HG01256.hp1 HG02735.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.48-4740delT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930271 | |||||||
| chr7:4930357 | A | G | 1 | a0001c0002t0005g0184 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.48-4825T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930357 | |||||||
| chr7:4930362 | G | A | 1 | a0001c0001t0003g0079 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.48-4830C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930362 | |||||||
| chr7:4930452 | T | C | 317 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0032 others(314): Show |
320 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.48-4920A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930452 | |||||||
| chr7:4930474 | T | C | 2 | a0001c0002t0001g0006 a0001c0002t0001g0008 |
2 | HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.48-4942A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930474 | |||||||
| chr7:4930505 | G | A | 2 | a0001c0001t0002g0085 a0001c0001t0002g0100 |
2 | HG00642.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.48-4973C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930505 | |||||||
| chr7:4930516 | C | T | 89 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0273 others(86): Show |
90 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.48-4984G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930516 | |||||||
| chr7:4930531 | C | T | 10 | a0001c0001t0001g0007 a0001c0001t0001g0214 a0001c0001t0001g0352 others(7): Show |
10 | HG02486.hp1 HG02559.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.48-4999G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930531 | |||||||
| chr7:4930536 | C | T | 10 | a0001c0001t0001g0007 a0001c0001t0001g0214 a0001c0001t0001g0352 others(7): Show |
10 | HG02486.hp1 HG02559.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.48-5004G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930536 | |||||||
| chr7:4930569 | G | A | 1 | a0001c0001t0003g0062 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.48-5037C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930569 | |||||||
| chr7:4930577 | G | A | 4 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0126 others(1): Show |
4 | HG01496.hp1 HG02886.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.48-5045C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930577 | |||||||
| chr7:4930632 | G | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0214 a0001c0001t0001g0352 others(7): Show |
10 | HG02486.hp1 HG02559.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.48-5100C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930632 | |||||||
| chr7:4930645 | C | CAAAAAAA others(2): Show |
111 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0032 others(108): Show |
112 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.48-5122_48-5114dup others(9): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930645 | |||||||
| chr7:4930645 | C | CAAAAAAA others(3): Show |
116 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0123 others(113): Show |
117 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.48-5123_48-5114dup others(10): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930645 | |||||||
| chr7:4930645 | C | CAAAAAAA others(4): Show |
7 | a0001c0001t0001g0158 a0001c0002t0001g0230 a0001c0002t0001g0271 others(4): Show |
7 | HG01981.hp1 HG02572.hp1 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.48-5114_48-5113ins others(11): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930645 | |||||||
| chr7:4930658 | G | C | 236 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0032 others(233): Show |
238 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(235): Show |
intron_variant | MODIFIER | c.48-5126C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930658 | |||||||
| chr7:4930659 | G | A | 1 | a0001c0001t0003g0068 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.48-5127C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930659 | |||||||
| chr7:4930703 | G | A | 1 | a0001c0002t0001g0163 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.48-5171C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930703 | |||||||
| chr7:4930708 | C | T | 2 | a0001c0001t0010g0357 a0001c0001t0010g0358 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.48-5176G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930708 | |||||||
| chr7:4930722 | C | T | 2 | a0001c0003t0001g0343 a0001c0003t0033g0378 |
2 | NA18986.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.48-5190G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930722 | |||||||
| chr7:4930748 | C | A | 54 | a0001c0001t0001g0158 a0001c0001t0001g0197 a0001c0001t0001g0199 others(51): Show |
55 | HG00738.hp2 HG01074.hp2 HG01081.hp1 others(52): Show |
intron_variant | MODIFIER | c.48-5216G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930748 | |||||||
| chr7:4930764 | T | G | 236 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0032 others(233): Show |
238 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(235): Show |
intron_variant | MODIFIER | c.48-5232A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930764 | |||||||
| chr7:4930920 | G | A | 3 | a0001c0001t0001g0273 a0001c0002t0001g0268 a0001c0002t0001g0269 |
3 | HG02647.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.48-5388C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930920 | |||||||
| chr7:4930956 | C | T | 235 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0048 others(232): Show |
237 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(234): Show |
intron_variant | MODIFIER | c.48-5424G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4930956 | |||||||
| chr7:4931119 | G | A | 1 | a0001c0002t0001g0269 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.48-5587C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4931119 | |||||||
| chr7:4931165 | T | C | 3 | a0001c0001t0001g0273 a0001c0002t0001g0268 a0001c0002t0001g0269 |
3 | HG02647.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.48-5633A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4931165 | |||||||
| chr7:4931444 | C | T | 3 | a0001c0001t0001g0267 a0001c0001t0008g0266 a0001c0001t0008g0272 |
3 | HG02647.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.48-5912G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4931444 | |||||||
| chr7:4931445 | G | A | 5 | a0001c0001t0001g0273 a0001c0001t0012g0251 a0001c0001t0027g0346 others(2): Show |
5 | HG02647.hp1 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.48-5913C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4931445 | |||||||
| chr7:4931898 | A | G | 1 | a0001c0001t0015g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.48-6366T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4931898 | |||||||
| chr7:4931942 | G | C | 1 | a0001c0001t0002g0115 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.48-6410C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4931942 | |||||||
| chr7:4931952 | C | T | 2 | a0001c0001t0011g0066 a0001c0001t0011g0249 |
2 | HG03834.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.48-6420G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4931952 | |||||||
| chr7:4932054 | G | A | 3 | a0001c0001t0001g0267 a0001c0001t0008g0266 a0001c0001t0008g0272 |
3 | HG02647.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.48-6522C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4932054 | |||||||
| chr7:4932117 | G | C | 1 | a0001c0002t0001g0137 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.48-6585C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4932117 | |||||||
| chr7:4932149 | C | A | 1 | a0001c0002t0001g0102 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.48-6617G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4932149 | |||||||
| chr7:4932311 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.48-6779G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4932311 | |||||||
| chr7:4932312 | G | A | 112 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0126 others(109): Show |
113 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.48-6780C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4932312 | |||||||
| chr7:4932417 | T | C | 1 | a0001c0001t0006g0084 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.48-6885A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4932417 | |||||||
| chr7:4932474 | C | T | 4 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0126 others(1): Show |
4 | HG01496.hp1 HG02886.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.48-6942G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4932474 | |||||||
| chr7:4932485 | G | A | 1 | a0001c0001t0003g0089 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.48-6953C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4932485 | |||||||
| chr7:4932501 | C | T | 3 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0001c0002t0001g0121 |
3 | HG02145.hp1 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.48-6969G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4932501 | |||||||
| chr7:4932620 | GTGCATTT others(1013): Show |
G | 1 | a0001c0001t0015g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.48-8108_48-7089del | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4932620 | |||||||
| chr7:4932624 | AT | A | 198 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0032 others(195): Show |
200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.48-7093delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4932624 | |||||||
| chr7:4932957 | T | G | 1 | a0001c0002t0005g0184 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.48-7425A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4932957 | |||||||
| chr7:4932981 | CT | C | 87 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0001g0292 others(84): Show |
88 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.48-7450delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4932981 | |||||||
| chr7:4933104 | G | T | 1 | a0001c0002t0003g0208 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.48-7572C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933104 | |||||||
| chr7:4933124 | C | T | 1 | a0001c0003t0004g0319 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.48-7592G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933124 | |||||||
| chr7:4933190 | G | A | 3 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0001c0002t0001g0121 |
3 | HG02145.hp1 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.48-7658C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933190 | |||||||
| chr7:4933342 | G | A | 247 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0032 others(244): Show |
249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.48-7810C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933342 | |||||||
| chr7:4933427 | T | C | 1 | a0001c0001t0003g0058 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.48-7895A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933427 | |||||||
| chr7:4933471 | G | A | 87 | a0001c0001t0001g0264 a0001c0001t0001g0273 a0001c0001t0001g0292 others(84): Show |
88 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.48-7939C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933471 | |||||||
| chr7:4933569 | T | C | 350 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0048 others(347): Show |
353 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(350): Show |
intron_variant | MODIFIER | c.48-8037A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933569 | |||||||
| chr7:4933640 | A | T | 83 | a0001c0001t0001g0264 a0001c0001t0001g0292 a0001c0001t0001g0297 others(80): Show |
84 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.48-8108T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933640 | |||||||
| chr7:4933644 | AT | A | 9 | a0001c0001t0001g0054 a0001c0001t0002g0295 a0001c0001t0003g0039 others(6): Show |
9 | HG00423.hp1 HG00621.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.48-8113delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933644 | |||||||
| chr7:4933725 | G | A | 129 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0126 others(126): Show |
130 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.48-8193C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933725 | |||||||
| chr7:4933791 | C | A | 1 | a0001c0002t0003g0200 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.48-8259G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933791 | |||||||
| chr7:4933940 | C | CT | 53 | a0001c0001t0001g0122 a0001c0001t0001g0197 a0001c0001t0001g0199 others(50): Show |
54 | HG00738.hp2 HG01074.hp2 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.48-8409dupA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933940 | |||||||
| chr7:4933940 | CT | C | 75 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0048 others(72): Show |
76 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.48-8409delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933940 | |||||||
| chr7:4933940 | CTT | C | 23 | a0001c0001t0001g0055 a0001c0001t0001g0070 a0001c0001t0001g0260 others(20): Show |
23 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(20): Show |
intron_variant | MODIFIER | c.48-8410_48-8409del others(2): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933940 | |||||||
| chr7:4933940 | CTTTT | C | 47 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0126 others(44): Show |
47 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.48-8412_48-8409del others(4): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933940 | |||||||
| chr7:4933940 | CTTTTT | C | 83 | a0001c0001t0001g0264 a0001c0001t0001g0273 a0001c0001t0001g0292 others(80): Show |
84 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.48-8413_48-8409del others(5): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933940 | |||||||
| chr7:4933972 | T | C | 2 | a0001c0002t0001g0116 a0001c0002t0001g0117 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.48-8440A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4933972 | |||||||
| chr7:4934023 | A | G | 351 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0048 others(348): Show |
354 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(351): Show |
intron_variant | MODIFIER | c.48-8491T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934023 | |||||||
| chr7:4934042 | G | A | 1 | a0001c0005t0003g0316 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.48-8510C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934042 | |||||||
| chr7:4934078 | C | T | 1 | a0001c0002t0012g0198 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.48-8546G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934078 | |||||||
| chr7:4934182 | G | A | 7 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0126 others(4): Show |
7 | HG01496.hp1 HG02647.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.48-8650C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934182 | |||||||
| chr7:4934210 | G | A | 1 | a0001c0001t0012g0251 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.48-8678C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934210 | |||||||
| chr7:4934269 | T | C | 1 | a0001c0001t0023g0313 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.48-8737A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934269 | |||||||
| chr7:4934294 | GGGTTTTG others(1): Show |
G | 31 | a0001c0001t0013g0367 a0001c0001t0013g0368 a0001c0001t0013g0370 others(28): Show |
31 | HG00280.hp1 HG00639.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.48-8770_48-8763del others(8): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934294 | |||||||
| chr7:4934304 | A | C | 31 | a0001c0001t0013g0367 a0001c0001t0013g0368 a0001c0001t0013g0370 others(28): Show |
31 | HG00280.hp1 HG00639.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.48-8772T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934304 | |||||||
| chr7:4934325 | A | C | 3 | a0001c0001t0001g0273 a0001c0002t0001g0268 a0001c0002t0001g0269 |
3 | HG02647.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.48-8793T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934325 | |||||||
| chr7:4934334 | T | C | 349 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0048 others(346): Show |
352 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(349): Show |
intron_variant | MODIFIER | c.48-8802A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934334 | |||||||
| chr7:4934350 | C | T | 40 | a0001c0001t0001g0214 a0001c0001t0001g0352 a0001c0001t0002g0115 others(37): Show |
40 | HG00280.hp1 HG00639.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.48-8818G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934350 | |||||||
| chr7:4934429 | C | A | 8 | a0001c0001t0001g0214 a0001c0001t0001g0352 a0001c0001t0003g0348 others(5): Show |
8 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.48-8897G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934429 | |||||||
| chr7:4934468 | G | T | 1 | a0001c0001t0002g0059 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.48-8936C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934468 | |||||||
| chr7:4934497 | C | G | 104 | a0001c0001t0001g0158 a0001c0001t0001g0197 a0001c0001t0001g0199 others(101): Show |
105 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.48-8965G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934497 | |||||||
| chr7:4934570 | C | T | 1 | a0001c0001t0012g0251 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.48-9038G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934570 | |||||||
| chr7:4934854 | A | G | 237 | a0001c0001t0001g0158 a0001c0001t0001g0197 a0001c0001t0001g0199 others(234): Show |
239 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(236): Show |
intron_variant | MODIFIER | c.48-9322T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934854 | |||||||
| chr7:4934872 | A | T | 96 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0048 others(93): Show |
97 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.48-9340T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4934872 | |||||||
| chr7:4935064 | T | C | 130 | a0001c0001t0001g0214 a0001c0001t0001g0264 a0001c0001t0001g0273 others(127): Show |
131 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.48-9532A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935064 | |||||||
| chr7:4935161 | G | A | 1 | a0001c0001t0006g0076 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.48-9629C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935161 | |||||||
| chr7:4935193 | GA | G | 27 | a0001c0001t0001g0158 a0001c0001t0001g0197 a0001c0001t0001g0199 others(24): Show |
27 | HG00642.hp2 HG00738.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.48-9662delT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935193 | |||||||
| chr7:4935285 | G | A | 87 | a0001c0001t0001g0264 a0001c0001t0001g0273 a0001c0001t0001g0292 others(84): Show |
88 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.48-9753C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935285 | |||||||
| chr7:4935288 | G | A | 40 | a0001c0001t0001g0214 a0001c0001t0001g0352 a0001c0001t0002g0115 others(37): Show |
40 | HG00280.hp1 HG00639.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.48-9756C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935288 | |||||||
| chr7:4935379 | G | A | 110 | a0001c0001t0001g0158 a0001c0001t0001g0197 a0001c0001t0001g0199 others(107): Show |
111 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.48-9847C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935379 | |||||||
| chr7:4935398 | C | T | 1 | a0001c0002t0006g0248 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.48-9866G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935398 | |||||||
| chr7:4935473 | A | G | 1 | a0001c0001t0015g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.48-9941T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935473 | |||||||
| chr7:4935677 | C | CA | 29 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0123 others(26): Show |
29 | HG00423.hp2 HG01496.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.48-10146dupT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935677 | |||||||
| chr7:4935677 | CA | C | 119 | a0001c0001t0001g0214 a0001c0001t0001g0273 a0001c0001t0001g0292 others(116): Show |
120 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.48-10146delT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935677 | |||||||
| chr7:4935677 | CAA | C | 51 | a0001c0001t0001g0197 a0001c0001t0001g0199 a0001c0001t0001g0202 others(48): Show |
52 | HG00738.hp2 HG01074.hp2 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.48-10147_48-10146d others(4): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935677 | |||||||
| chr7:4935696 | AAC | A | 28 | a0001c0002t0001g0181 a0001c0002t0001g0182 a0001c0002t0001g0183 others(25): Show |
28 | HG00558.hp1 HG02258.hp1 HG02258.hp2 others(25): Show |
intron_variant | MODIFIER | c.48-10166_48-10165d others(4): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935696 | |||||||
| chr7:4935697 | A | C | 1 | a0001c0002t0001g0105 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.48-10165T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935697 | |||||||
| chr7:4935697 | AC | A | 19 | a0001c0001t0010g0041 a0001c0002t0001g0217 a0001c0002t0001g0252 others(16): Show |
19 | HG00544.hp2 HG00621.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.48-10166delG | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935697 | |||||||
| chr7:4935698 | C | A | 2 | a0001c0002t0003g0156 a0001c0007t0025g0356 |
2 | HG02572.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.48-10166G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935698 | |||||||
| chr7:4935699 | C | A | 1 | a0001c0002t0005g0176 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.48-10167G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935699 | |||||||
| chr7:4935904 | G | C | 1 | a0001c0001t0003g0348 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.48-10372C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935904 | |||||||
| chr7:4935950 | C | T | 110 | a0001c0001t0001g0158 a0001c0001t0001g0197 a0001c0001t0001g0199 others(107): Show |
111 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.48-10418G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4935950 | |||||||
| chr7:4936110 | G | A | 1 | a0001c0002t0001g0247 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.48-10578C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936110 | |||||||
| chr7:4936112 | G | A | 1 | a0001c0001t0002g0021 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.48-10580C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936112 | |||||||
| chr7:4936177 | C | A | 1 | a0001c0001t0027g0346 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.48-10645G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936177 | |||||||
| chr7:4936185 | CA | C | 116 | a0001c0001t0001g0158 a0001c0001t0001g0197 a0001c0001t0001g0199 others(113): Show |
117 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.48-10654delT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936185 | |||||||
| chr7:4936246 | C | A | 80 | a0001c0001t0001g0292 a0001c0001t0001g0297 a0001c0001t0001g0310 others(77): Show |
81 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.48-10714G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936246 | |||||||
| chr7:4936325 | C | A | 83 | a0001c0001t0001g0264 a0001c0001t0001g0292 a0001c0001t0001g0297 others(80): Show |
84 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.48-10793G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936325 | |||||||
| chr7:4936359 | G | C | 1 | a0001c0001t0004g0345 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.48-10827C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936359 | |||||||
| chr7:4936400 | T | C | 4 | a0001c0003t0004g0323 a0001c0003t0004g0339 a0001c0003t0004g0341 others(1): Show |
4 | NA18963.hp1 NA18969.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.48-10868A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936400 | |||||||
| chr7:4936605 | C | G | 1 | a0001c0001t0027g0346 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.48-11073G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936605 | |||||||
| chr7:4936702 | C | A | 1 | a0001c0001t0009g0376 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.48-11170G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936702 | |||||||
| chr7:4936795 | C | T | 40 | a0001c0001t0001g0214 a0001c0001t0001g0352 a0001c0001t0002g0115 others(37): Show |
40 | HG00280.hp1 HG00639.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.48-11263G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936795 | |||||||
| chr7:4936809 | A | G | 113 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0158 others(110): Show |
114 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.48-11277T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936809 | |||||||
| chr7:4936820 | CG | C | 3 | a0001c0001t0001g0267 a0001c0001t0008g0266 a0001c0001t0008g0272 |
3 | HG02647.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.48-11289delC | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936820 | |||||||
| chr7:4936863 | T | A | 52 | a0001c0001t0001g0158 a0001c0001t0001g0197 a0001c0001t0001g0199 others(49): Show |
53 | HG00738.hp2 HG01074.hp2 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.48-11331A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936863 | |||||||
| chr7:4936880 | G | T | 22 | a0001c0001t0013g0367 a0001c0001t0013g0368 a0001c0001t0013g0370 others(19): Show |
22 | HG00280.hp1 HG00639.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.48-11348C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936880 | |||||||
| chr7:4936924 | C | T | 1 | a0001c0001t0002g0280 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.48-11392G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936924 | |||||||
| chr7:4936988 | G | A | 1 | a0001c0002t0001g0114 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.48-11456C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4936988 | |||||||
| chr7:4937168 | G | C | 115 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0048 others(112): Show |
116 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.48-11636C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937168 | |||||||
| chr7:4937233 | C | A | 1 | a0001c0001t0027g0346 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.48-11701G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937233 | |||||||
| chr7:4937346 | G | A | 1 | a0001c0001t0012g0251 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.48-11814C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937346 | |||||||
| chr7:4937432 | A | G | 1 | a0001c0002t0001g0225 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.48-11900T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937432 | |||||||
| chr7:4937463 | A | G | 2 | a0001c0002t0001g0268 a0001c0002t0001g0269 |
2 | HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.48-11931T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937463 | |||||||
| chr7:4937478 | A | T | 107 | a0001c0001t0001g0158 a0001c0001t0001g0197 a0001c0001t0001g0199 others(104): Show |
108 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(105): Show |
intron_variant | MODIFIER | c.48-11946T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937478 | |||||||
| chr7:4937506 | T | C | 1 | a0001c0001t0001g0264 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.48-11974A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937506 | |||||||
| chr7:4937561 | C | T | 1 | a0001c0001t0002g0282 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.48-12029G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937561 | |||||||
| chr7:4937617 | T | C | 2 | a0001c0001t0010g0357 a0001c0001t0010g0358 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.48-12085A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937617 | |||||||
| chr7:4937653 | C | T | 3 | a0001c0001t0002g0276 a0001c0001t0002g0277 a0001c0001t0002g0278 |
3 | HG00735.hp1 HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.48-12121G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937653 | |||||||
| chr7:4937715 | C | G | 85 | a0001c0001t0001g0292 a0001c0001t0001g0297 a0001c0001t0001g0310 others(82): Show |
86 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.48-12183G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937715 | |||||||
| chr7:4937731 | C | G | 85 | a0001c0001t0001g0292 a0001c0001t0001g0297 a0001c0001t0001g0310 others(82): Show |
86 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.48-12199G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937731 | |||||||
| chr7:4937874 | C | T | 1 | a0001c0001t0027g0346 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.48-12342G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937874 | |||||||
| chr7:4937880 | C | T | 4 | a0001c0001t0001g0273 a0001c0002t0001g0119 a0001c0002t0001g0120 others(1): Show |
4 | HG02145.hp1 HG02647.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.48-12348G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937880 | |||||||
| chr7:4937957 | A | G | 1 | a0001c0001t0006g0076 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.48-12425T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937957 | |||||||
| chr7:4937969 | C | CTTTTTCT others(3): Show |
1 | a0001c0001t0001g0158 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.48-12447_48-12438d others(12): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937969 | |||||||
| chr7:4937969 | C | CTTTTTCT others(4): Show |
47 | a0001c0001t0001g0197 a0001c0001t0001g0199 a0001c0001t0001g0202 others(44): Show |
48 | HG00738.hp2 HG01074.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.48-12448_48-12438d others(13): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937969 | |||||||
| chr7:4937978 | T | C | 2 | a0001c0002t0001g0268 a0001c0002t0001g0269 |
2 | HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.48-12446A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937978 | |||||||
| chr7:4937990 | T | TTTTTTTT others(9): Show |
1 | a0001c0002t0001g0228 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.48-12459_48-12458i others(18): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937990 | |||||||
| chr7:4937994 | C | T | 2 | a0001c0001t0001g0219 a0001c0002t0004g0205 |
2 | NA18939.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.48-12462G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4937994 | |||||||
| chr7:4938002 | C | CT | 85 | a0001c0001t0001g0020 a0001c0001t0001g0054 a0001c0001t0001g0055 others(82): Show |
86 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.48-12471dupA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938002 | |||||||
| chr7:4938002 | C | CTT | 21 | a0001c0001t0001g0048 a0001c0001t0001g0057 a0001c0001t0002g0023 others(18): Show |
21 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.48-12472_48-12471d others(4): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938002 | |||||||
| chr7:4938002 | C | T | 1 | a0001c0002t0001g0228 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.48-12470G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938002 | |||||||
| chr7:4938002 | CT | C | 81 | a0001c0001t0001g0158 a0001c0001t0001g0197 a0001c0001t0001g0199 others(78): Show |
82 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.48-12471delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938002 | |||||||
| chr7:4938002 | CTT | C | 32 | a0001c0001t0001g0352 a0001c0001t0002g0115 a0001c0001t0003g0348 others(29): Show |
32 | HG00280.hp1 HG00639.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.48-12472_48-12471d others(4): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938002 | |||||||
| chr7:4938002 | CTTTT | C | 66 | a0001c0001t0001g0297 a0001c0001t0001g0310 a0001c0001t0001g0314 others(63): Show |
67 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.48-12474_48-12471d others(6): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938002 | |||||||
| chr7:4938002 | CTTTTT | C | 13 | a0001c0001t0001g0292 a0001c0001t0002g0300 a0001c0001t0004g0304 others(10): Show |
13 | HG00741.hp1 HG01169.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.48-12475_48-12471d others(7): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938002 | |||||||
| chr7:4938105 | G | A | 126 | a0001c0001t0001g0214 a0001c0001t0001g0264 a0001c0001t0001g0292 others(123): Show |
127 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.48-12573C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938105 | |||||||
| chr7:4938114 | G | C | 2 | a0001c0001t0010g0357 a0001c0001t0010g0358 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.48-12582C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938114 | |||||||
| chr7:4938200 | G | T | 83 | a0001c0001t0001g0264 a0001c0001t0001g0292 a0001c0001t0001g0297 others(80): Show |
84 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.48-12668C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938200 | |||||||
| chr7:4938292 | A | G | 112 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0048 others(109): Show |
113 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.48-12760T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938292 | |||||||
| chr7:4938304 | C | T | 1 | a0001c0002t0001g0270 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.48-12772G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938304 | |||||||
| chr7:4938353 | A | G | 110 | a0001c0001t0001g0158 a0001c0001t0001g0197 a0001c0001t0001g0199 others(107): Show |
111 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.48-12821T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938353 | |||||||
| chr7:4938400 | G | C | 3 | a0001c0001t0001g0267 a0001c0001t0008g0266 a0001c0001t0008g0272 |
3 | HG02647.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.48-12868C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938400 | |||||||
| chr7:4938446 | A | G | 2 | a0001c0001t0004g0304 a0001c0001t0004g0305 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.48-12914T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938446 | |||||||
| chr7:4938508 | G | A | 2 | a0001c0003t0004g0326 a0001c0003t0026g0338 |
2 | NA18998.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.48-12976C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938508 | |||||||
| chr7:4938509 | C | A | 125 | a0001c0001t0001g0214 a0001c0001t0001g0264 a0001c0001t0001g0292 others(122): Show |
126 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.48-12977G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938509 | |||||||
| chr7:4938660 | T | C | 1 | a0001c0002t0012g0198 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.48-13128A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938660 | |||||||
| chr7:4938808 | C | G | 1 | a0001c0001t0006g0076 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.48-13276G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4938808 | |||||||
| chr7:4939004 | T | G | 1 | a0001c0002t0002g0244 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.48-13472A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939004 | |||||||
| chr7:4939029 | G | A | 1 | a0001c0002t0005g0165 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.48-13497C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939029 | |||||||
| chr7:4939035 | C | G | 88 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(85): Show |
89 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.48-13503G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939035 | |||||||
| chr7:4939188 | C | A | 10 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0123 others(7): Show |
10 | HG01496.hp1 HG02559.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.48-13656G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939188 | |||||||
| chr7:4939196 | C | T | 1 | a0001c0003t0004g0327 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.48-13664G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939196 | |||||||
| chr7:4939274 | G | A | 2 | a0001c0001t0012g0251 a0001c0002t0001g0250 |
2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.48-13742C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939274 | |||||||
| chr7:4939359 | C | A | 1 | a0001c0002t0008g0044 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.48-13827G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939359 | |||||||
| chr7:4939446 | G | C | 1 | a0001c0002t0008g0044 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.48-13914C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939446 | |||||||
| chr7:4939474 | T | C | 1 | a0001c0001t0019g0004 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.48-13942A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939474 | |||||||
| chr7:4939521 | C | T | 45 | a0001c0001t0010g0041 a0001c0002t0001g0181 a0001c0002t0001g0182 others(42): Show |
45 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.48-13989G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939521 | |||||||
| chr7:4939628 | T | C | 107 | a0001c0001t0001g0158 a0001c0001t0001g0197 a0001c0001t0001g0199 others(104): Show |
108 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(105): Show |
intron_variant | MODIFIER | c.48-14096A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939628 | |||||||
| chr7:4939705 | C | T | 142 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0123 others(139): Show |
143 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(140): Show |
intron_variant | MODIFIER | c.48-14173G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939705 | |||||||
| chr7:4939742 | CT | C | 197 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0158 others(194): Show |
199 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(196): Show |
intron_variant | MODIFIER | c.48-14211delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939742 | |||||||
| chr7:4939746 | T | C | 93 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0048 others(90): Show |
94 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.48-14214A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939746 | |||||||
| chr7:4939747 | T | C | 50 | a0001c0001t0001g0158 a0001c0001t0001g0197 a0001c0001t0001g0199 others(47): Show |
51 | HG00738.hp2 HG01074.hp2 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.48-14215A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939747 | |||||||
| chr7:4939748 | T | C | 1 | a0001c0002t0001g0236 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.48-14216A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939748 | |||||||
| chr7:4939752 | T | A | 1 | a0001c0002t0001g0225 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.48-14220A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939752 | |||||||
| chr7:4939767 | G | C | 1 | a0001c0001t0001g0264 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.48-14235C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939767 | |||||||
| chr7:4939793 | T | A | 107 | a0001c0001t0001g0158 a0001c0001t0001g0197 a0001c0001t0001g0199 others(104): Show |
108 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(105): Show |
intron_variant | MODIFIER | c.48-14261A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939793 | |||||||
| chr7:4939823 | C | T | 5 | a0001c0001t0001g0273 a0001c0001t0027g0346 a0001c0002t0001g0119 others(2): Show |
5 | HG02145.hp1 HG02647.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.48-14291G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939823 | |||||||
| chr7:4939883 | G | A | 107 | a0001c0001t0001g0158 a0001c0001t0001g0197 a0001c0001t0001g0199 others(104): Show |
108 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(105): Show |
intron_variant | MODIFIER | c.48-14351C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4939883 | |||||||
| chr7:4940007 | G | A | 45 | a0001c0001t0010g0041 a0001c0002t0001g0181 a0001c0002t0001g0182 others(42): Show |
45 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.48-14475C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4940007 | |||||||
| chr7:4940158 | G | A | 2 | a0001c0001t0010g0357 a0001c0001t0010g0358 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.48-14626C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4940158 | |||||||
| chr7:4940201 | G | A | 1 | a0001c0001t0027g0346 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.48-14669C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4940201 | |||||||
| chr7:4940220 | C | T | 8 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0126 others(5): Show |
8 | HG01496.hp1 HG02145.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.48-14688G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4940220 | |||||||
| chr7:4940230 | G | C | 349 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0048 others(346): Show |
352 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.48-14698C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4940230 | |||||||
| chr7:4940546 | G | C | 2 | a0001c0001t0010g0357 a0001c0001t0010g0358 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.48-15014C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4940546 | |||||||
| chr7:4940565 | C | G | 1 | a0001c0002t0001g0269 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.48-15033G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4940565 | |||||||
| chr7:4940583 | C | T | 1 | a0001c0002t0003g0200 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.48-15051G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4940583 | |||||||
| chr7:4940734 | G | A | 1 | a0001c0002t0015g0215 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.48-15202C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4940734 | |||||||
| chr7:4940775 | C | T | 1 | a0001c0001t0002g0021 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.48-15243G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4940775 | |||||||
| chr7:4940811 | A | G | 1 | a0001c0001t0003g0058 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.48-15279T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4940811 | |||||||
| chr7:4940843 | A | T | 1 | a0001c0001t0002g0021 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.48-15311T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4940843 | |||||||
| chr7:4940908 | C | G | 14 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0123 others(11): Show |
14 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.48-15376G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4940908 | |||||||
| chr7:4940998 | C | A | 1 | a0001c0002t0001g0146 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.48-15466G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4940998 | |||||||
| chr7:4941100 | G | A | 1 | a0001c0001t0002g0009 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.48-15568C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4941100 | |||||||
| chr7:4941430 | G | C | 1 | a0001c0001t0003g0311 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.48-15898C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4941430 | |||||||
| chr7:4941459 | G | A | 1 | a0001c0002t0001g0239 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.48-15927C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4941459 | |||||||
| chr7:4941467 | T | G | 1 | a0001c0002t0003g0231 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.48-15935A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4941467 | |||||||
| chr7:4941495 | T | G | 1 | a0001c0001t0003g0039 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.48-15963A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4941495 | |||||||
| chr7:4941629 | CA | C | 129 | a0001c0001t0001g0158 a0001c0001t0001g0197 a0001c0001t0001g0199 others(126): Show |
129 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.48-16098delT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4941629 | |||||||
| chr7:4941629 | CAA | C | 195 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0048 others(192): Show |
197 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.48-16099_48-16098d others(4): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4941629 | |||||||
| chr7:4941721 | G | A | 107 | a0001c0001t0001g0158 a0001c0001t0001g0197 a0001c0001t0001g0199 others(104): Show |
108 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(105): Show |
intron_variant | MODIFIER | c.48-16189C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4941721 | |||||||
| chr7:4941749 | T | C | 1 | a0001c0001t0027g0346 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.48-16217A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4941749 | |||||||
| chr7:4941859 | A | G | 1 | a0001c0001t0027g0346 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.48-16327T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4941859 | |||||||
| chr7:4941865 | C | T | 4 | a0001c0001t0001g0214 a0001c0002t0001g0213 a0001c0002t0008g0040 others(1): Show |
4 | HG02572.hp1 NA18906.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.48-16333G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4941865 | |||||||
| chr7:4941927 | T | A | 241 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0048 others(238): Show |
243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.48-16395A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4941927 | |||||||
| chr7:4941927 | T | C | 1 | a0001c0002t0001g0243 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.48-16395A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4941927 | |||||||
| chr7:4941951 | T | A | 2 | a0001c0001t0003g0089 a0001c0001t0003g0090 |
2 | HG00558.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.48-16419A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4941951 | |||||||
| chr7:4941984 | C | T | 1 | a0001c0001t0002g0059 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.48-16452G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4941984 | |||||||
| chr7:4941985 | G | A | 1 | a0001c0001t0004g0140 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.48-16453C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4941985 | |||||||
| chr7:4942286 | G | T | 1 | a0001c0002t0001g0226 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.47+16685C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942286 | |||||||
| chr7:4942346 | C | T | 1 | a0001c0001t0002g0308 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.47+16625G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942346 | |||||||
| chr7:4942386 | C | T | 1 | a0001c0001t0002g0028 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.47+16585G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942386 | |||||||
| chr7:4942415 | AT | A | 131 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0122 others(128): Show |
132 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(129): Show |
intron_variant | MODIFIER | c.47+16555delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942415 | |||||||
| chr7:4942415 | ATT | A | 234 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0048 others(231): Show |
236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.47+16554_47+16555d others(4): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942415 | |||||||
| chr7:4942435 | A | T | 1 | a0001c0001t0002g0282 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.47+16536T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942435 | |||||||
| chr7:4942441 | T | C | 1 | a0001c0001t0002g0308 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.47+16530A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942441 | |||||||
| chr7:4942442 | T | A | 2 | a0001c0001t0002g0283 a0001c0001t0002g0284 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.47+16529A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942442 | |||||||
| chr7:4942524 | T | C | 17 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0123 others(14): Show |
17 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.47+16447A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942524 | |||||||
| chr7:4942562 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.47+16409G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942562 | |||||||
| chr7:4942617 | CT | C | 94 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0048 others(91): Show |
95 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.47+16353delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942617 | |||||||
| chr7:4942704 | G | C | 373 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0032 others(370): Show |
376 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(373): Show |
intron_variant | MODIFIER | c.47+16267C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942704 | |||||||
| chr7:4942730 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.47+16241G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942730 | |||||||
| chr7:4942777 | G | A | 30 | a0001c0002t0001g0181 a0001c0002t0001g0182 a0001c0002t0001g0183 others(27): Show |
30 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.47+16194C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942777 | |||||||
| chr7:4942779 | C | G | 1 | a0001c0001t0027g0346 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.47+16192G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942779 | |||||||
| chr7:4942822 | A | C | 2 | a0001c0001t0006g0063 a0001c0001t0006g0064 |
2 | NA18981.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.47+16149T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942822 | |||||||
| chr7:4942906 | G | A | 40 | a0001c0001t0001g0352 a0001c0001t0002g0100 a0001c0001t0002g0115 others(37): Show |
40 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.47+16065C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4942906 | |||||||
| chr7:4943004 | C | CT | 8 | a0001c0001t0003g0348 a0001c0001t0003g0349 a0001c0001t0003g0351 others(5): Show |
8 | HG00741.hp2 HG01109.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.47+15966dupA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943004 | |||||||
| chr7:4943004 | CT | C | 102 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0123 others(99): Show |
103 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.47+15966delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943004 | |||||||
| chr7:4943004 | CTT | C | 94 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0048 others(91): Show |
95 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.47+15965_47+15966d others(4): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943004 | |||||||
| chr7:4943009 | T | C | 1 | a0001c0001t0001g0264 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.47+15962A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943009 | |||||||
| chr7:4943027 | T | G | 1 | a0001c0001t0015g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.47+15944A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943027 | |||||||
| chr7:4943168 | C | T | 14 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0123 others(11): Show |
14 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.47+15803G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943168 | |||||||
| chr7:4943228 | C | A | 2 | a0001c0001t0003g0131 a0001c0001t0003g0133 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.47+15743G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943228 | |||||||
| chr7:4943299 | G | A | 1 | a0001c0002t0003g0203 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.47+15672C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943299 | |||||||
| chr7:4943364 | C | T | 2 | a0001c0002t0001g0002 a0001c0002t0001g0265 |
3 | HG02451.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.47+15607G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943364 | |||||||
| chr7:4943428 | C | G | 1 | a0001c0001t0003g0351 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.47+15543G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943428 | |||||||
| chr7:4943515 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.47+15456C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943515 | |||||||
| chr7:4943622 | A | G | 9 | a0001c0001t0012g0251 a0001c0002t0001g0250 a0001c0002t0001g0252 others(6): Show |
9 | HG01884.hp2 HG02258.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.47+15349T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943622 | |||||||
| chr7:4943638 | G | A | 1 | a0001c0001t0027g0346 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.47+15333C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943638 | |||||||
| chr7:4943834 | C | T | 17 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0123 others(14): Show |
17 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.47+15137G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943834 | |||||||
| chr7:4943853 | G | A | 1 | a0001c0001t0003g0045 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.47+15118C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943853 | |||||||
| chr7:4943950 | C | T | 40 | a0001c0001t0001g0352 a0001c0001t0002g0100 a0001c0001t0002g0115 others(37): Show |
40 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.47+15021G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943950 | |||||||
| chr7:4943978 | T | C | 17 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0123 others(14): Show |
17 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.47+14993A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4943978 | |||||||
| chr7:4944059 | A | C | 1 | a0001c0001t0002g0085 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.47+14912T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944059 | |||||||
| chr7:4944244 | C | A | 4 | a0001c0001t0003g0037 a0001c0001t0003g0071 a0001c0001t0003g0075 others(1): Show |
4 | HG01346.hp2 HG03239.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.47+14727G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944244 | |||||||
| chr7:4944443 | G | A | 1 | a0001c0001t0027g0346 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.47+14528C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944443 | |||||||
| chr7:4944515 | CTCAGCAC others(30): Show |
C | 1 | a0001c0001t0011g0249 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.47+14419_47+14455d others(39): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944515 | |||||||
| chr7:4944530 | A | G | 1 | a0001c0002t0003g0208 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.47+14441T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944530 | |||||||
| chr7:4944617 | G | T | 2 | a0001c0001t0012g0251 a0001c0002t0001g0250 |
2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.47+14354C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944617 | |||||||
| chr7:4944700 | T | C | 2 | a0001c0001t0010g0357 a0001c0001t0010g0358 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.47+14271A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944700 | |||||||
| chr7:4944745 | C | T | 3 | a0001c0001t0010g0357 a0001c0001t0010g0358 a0001c0002t0003g0156 |
3 | HG01891.hp1 HG03041.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.47+14226G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944745 | |||||||
| chr7:4944760 | C | CT | 38 | a0001c0001t0001g0055 a0001c0001t0001g0094 a0001c0001t0001g0264 others(35): Show |
38 | HG01256.hp2 HG01433.hp2 HG01517.hp1 others(35): Show |
intron_variant | MODIFIER | c.47+14210dupA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944760 | |||||||
| chr7:4944760 | CT | C | 96 | a0001c0001t0001g0032 a0001c0001t0001g0061 a0001c0001t0001g0126 others(93): Show |
97 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.47+14210delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944760 | |||||||
| chr7:4944760 | CTT | C | 70 | a0001c0001t0001g0020 a0001c0001t0001g0197 a0001c0001t0002g0012 others(67): Show |
71 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.47+14209_47+14210d others(4): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944760 | |||||||
| chr7:4944760 | CTTT | C | 6 | a0001c0002t0001g0252 a0001c0002t0001g0253 a0001c0002t0001g0254 others(3): Show |
6 | HG00735.hp2 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.47+14208_47+14210d others(5): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944760 | |||||||
| chr7:4944762 | T | TC | 4 | a0001c0002t0001g0228 a0001c0002t0001g0268 a0001c0002t0003g0156 others(1): Show |
4 | HG03098.hp2 HG03540.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+14208_47+14209i others(3): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944762 | |||||||
| chr7:4944763 | T | C | 2 | a0001c0002t0001g0233 a0001c0002t0001g0269 |
2 | HG03225.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.47+14208A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944763 | |||||||
| chr7:4944764 | T | A | 4 | a0001c0001t0001g0214 a0001c0002t0001g0213 a0001c0002t0008g0040 others(1): Show |
4 | HG02572.hp1 NA18906.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+14207A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944764 | |||||||
| chr7:4944764 | T | C | 25 | a0001c0001t0001g0158 a0001c0001t0001g0199 a0001c0001t0001g0202 others(22): Show |
25 | HG01167.hp2 HG01981.hp1 HG02056.hp1 others(22): Show |
intron_variant | MODIFIER | c.47+14207A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944764 | |||||||
| chr7:4944765 | T | C | 24 | a0001c0001t0001g0197 a0001c0002t0001g0002 a0001c0002t0001g0225 others(21): Show |
25 | HG00738.hp2 HG01074.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.47+14206A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944765 | |||||||
| chr7:4944801 | T | C | 2 | a0001c0002t0001g0268 a0001c0002t0001g0269 |
2 | HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.47+14170A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944801 | |||||||
| chr7:4944804 | G | A | 3 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0001c0002t0001g0121 |
3 | HG02145.hp1 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.47+14167C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944804 | |||||||
| chr7:4944888 | C | T | 87 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(84): Show |
88 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.47+14083G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944888 | |||||||
| chr7:4944902 | G | A | 1 | a0001c0001t0002g0298 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.47+14069C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944902 | |||||||
| chr7:4944923 | A | G | 1 | a0001c0001t0002g0009 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.47+14048T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4944923 | |||||||
| chr7:4945078 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.47+13893G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945078 | |||||||
| chr7:4945184 | C | CCTTCTT | 4 | a0001c0001t0001g0055 a0001c0002t0005g0165 a0001c0002t0010g0155 others(1): Show |
4 | HG02293.hp1 HG02300.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+13786_47+13787i others(8): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945184 | |||||||
| chr7:4945184 | C | CCTTCTTC others(2): Show |
4 | a0001c0002t0003g0171 a0001c0002t0005g0184 a0001c0002t0005g0194 others(1): Show |
4 | HG00558.hp1 HG03688.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+13786_47+13787i others(11): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945184 | |||||||
| chr7:4945184 | C | CCTTCTTC others(5): Show |
7 | a0001c0002t0003g0156 a0001c0002t0003g0179 a0001c0002t0003g0195 others(4): Show |
7 | HG00621.hp1 HG01975.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.47+13786_47+13787i others(14): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945184 | |||||||
| chr7:4945184 | C | CCTTCTTC others(8): Show |
9 | a0001c0002t0001g0183 a0001c0002t0001g0252 a0001c0002t0001g0258 others(6): Show |
9 | HG01928.hp2 HG03209.hp2 HG03516.hp1 others(6): Show |
intron_variant | MODIFIER | c.47+13786_47+13787i others(17): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945184 | |||||||
| chr7:4945184 | C | CCTTCTTC others(11): Show |
7 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0002t0001g0182 others(4): Show |
7 | HG01069.hp2 HG01071.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.47+13786_47+13787i others(20): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945184 | |||||||
| chr7:4945184 | C | CCTTCTTC others(14): Show |
4 | a0001c0002t0001g0181 a0001c0002t0001g0254 a0001c0002t0003g0177 others(1): Show |
4 | HG00544.hp2 NA18990.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+13786_47+13787i others(23): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945184 | |||||||
| chr7:4945184 | C | CCTTCTTC others(17): Show |
4 | a0001c0002t0001g0253 a0001c0002t0003g0340 a0001c0002t0006g0187 others(1): Show |
4 | HG02723.hp2 NA19009.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+13786_47+13787i others(26): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945184 | |||||||
| chr7:4945184 | C | CCTTCTTC others(23): Show |
1 | a0001c0002t0006g0180 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.47+13786_47+13787i others(32): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945184 | |||||||
| chr7:4945184 | C | CCTTCTTC others(35): Show |
1 | a0001c0002t0005g0176 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.47+13786_47+13787i others(44): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945184 | |||||||
| chr7:4945185 | T | C | 46 | a0001c0001t0001g0055 a0001c0001t0002g0024 a0001c0001t0002g0025 others(43): Show |
46 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.47+13786A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | |||||||
| chr7:4945185 | T | TCTTCTTC others(6): Show |
1 | a0001c0002t0006g0248 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.47+13785_47+13786i others(15): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | |||||||
| chr7:4945185 | T | TCTTCTTC others(36): Show |
1 | a0001c0001t0004g0336 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.47+13785_47+13786i others(45): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | |||||||
| chr7:4945185 | T | TTCTTCCT others(15): Show |
1 | a0001c0002t0001g0228 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.47+13785_47+13786i others(24): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | |||||||
| chr7:4945185 | T | TTCTTCTT others(4): Show |
2 | a0001c0001t0002g0344 a0001c0003t0033g0378 |
2 | NA18991.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.47+13785_47+13786i others(13): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | |||||||
| chr7:4945185 | T | TTCTTCTT others(37): Show |
1 | a0001c0003t0004g0224 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.47+13785_47+13786i others(46): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | |||||||
| chr7:4945185 | T | TTTC | 13 | a0001c0001t0002g0031 a0001c0001t0003g0039 a0001c0001t0003g0045 others(10): Show |
13 | HG00140.hp2 HG00423.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.47+13783_47+13785d others(5): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | |||||||
| chr7:4945185 | T | TTTCTTC | 18 | a0001c0001t0001g0032 a0001c0001t0001g0260 a0001c0001t0001g0261 others(15): Show |
18 | HG00609.hp1 HG01070.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.47+13780_47+13785d others(8): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | |||||||
| chr7:4945185 | T | TTTCTTCT others(2): Show |
28 | a0001c0001t0001g0057 a0001c0001t0001g0061 a0001c0001t0001g0259 others(25): Show |
29 | HG00099.hp2 HG00438.hp2 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.47+13777_47+13785d others(11): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | |||||||
| chr7:4945185 | T | TTTCTTCT others(5): Show |
31 | a0001c0001t0001g0020 a0001c0001t0001g0070 a0001c0001t0001g0122 others(28): Show |
31 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.47+13774_47+13785d others(14): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | |||||||
| chr7:4945185 | T | TTTCTTCT others(23): Show |
1 | a0001c0001t0027g0346 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.47+13785_47+13786i others(32): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | |||||||
| chr7:4945185 | T | TTTCTTCT others(8): Show |
51 | a0001c0001t0001g0007 a0001c0001t0001g0158 a0001c0001t0001g0246 others(48): Show |
52 | HG00408.hp1 HG00639.hp1 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.47+13771_47+13785d others(17): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | |||||||
| chr7:4945185 | T | TTTCTTCT others(11): Show |
37 | a0001c0001t0001g0054 a0001c0001t0001g0199 a0001c0001t0001g0218 others(34): Show |
37 | HG00280.hp1 HG00423.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.47+13768_47+13785d others(20): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | |||||||
| chr7:4945185 | T | TTTCTTCT others(14): Show |
42 | a0001c0001t0001g0197 a0001c0001t0001g0202 a0001c0001t0001g0214 others(39): Show |
42 | HG00408.hp2 HG00639.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.47+13765_47+13785d others(23): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | |||||||
| chr7:4945185 | T | TTTCTTCT others(17): Show |
24 | a0001c0001t0001g0081 a0001c0001t0002g0009 a0001c0001t0002g0023 others(21): Show |
24 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.47+13762_47+13785d others(26): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | |||||||
| chr7:4945185 | T | TTTCTTCT others(20): Show |
15 | a0001c0001t0001g0048 a0001c0001t0001g0094 a0001c0001t0001g0219 others(12): Show |
15 | HG00558.hp2 HG00597.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.47+13759_47+13785d others(29): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | |||||||
| chr7:4945185 | T | TTTCTTCT others(23): Show |
10 | a0001c0001t0002g0095 a0001c0001t0002g0302 a0001c0001t0003g0016 others(7): Show |
10 | HG01978.hp2 HG02486.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.47+13756_47+13785d others(32): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | |||||||
| chr7:4945185 | T | TTTCTTCT others(26): Show |
6 | a0001c0001t0001g0220 a0001c0001t0003g0288 a0001c0001t0004g0303 others(3): Show |
6 | HG01169.hp2 HG02055.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.47+13753_47+13785d others(35): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | |||||||
| chr7:4945185 | T | TTTCTTCT others(29): Show |
6 | a0001c0001t0001g0337 a0001c0001t0002g0306 a0001c0001t0002g0307 others(3): Show |
6 | HG01167.hp1 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.47+13750_47+13785d others(38): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | |||||||
| chr7:4945185 | T | TTTCTTCT others(32): Show |
5 | a0001c0001t0002g0275 a0001c0001t0003g0090 a0001c0001t0004g0294 others(2): Show |
5 | HG00642.hp1 HG00673.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.47+13747_47+13785d others(41): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | |||||||
| chr7:4945185 | T | TTTCTTCT others(35): Show |
1 | a0001c0001t0002g0280 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.47+13744_47+13785d others(44): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | |||||||
| chr7:4945185 | T | TTTCTTCT others(38): Show |
1 | a0001c0001t0002g0308 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.47+13741_47+13785d others(47): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | |||||||
| chr7:4945185 | T | TTTCTTCT others(41): Show |
3 | a0001c0001t0004g0309 a0001c0001t0004g0335 a0001c0002t0007g0359 |
3 | HG03017.hp2 HG03239.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.47+13738_47+13785d others(50): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | |||||||
| chr7:4945185 | T | TTTCTTCT others(44): Show |
2 | a0001c0001t0005g0290 a0001c0001t0005g0312 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.47+13735_47+13785d others(53): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | |||||||
| chr7:4945185 | T | TTTCTTCT others(47): Show |
1 | a0001c0002t0002g0237 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.47+13732_47+13785d others(56): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | |||||||
| chr7:4945185 | T | TTTCTTCT others(50): Show |
2 | a0001c0001t0001g0267 a0001c0002t0001g0036 |
2 | NA18990.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.47+13785_47+13786i others(59): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | |||||||
| chr7:4945185 | T | TTTCTTCT others(56): Show |
1 | a0001c0001t0001g0310 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.47+13785_47+13786i others(65): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | |||||||
| chr7:4945185 | T | TTTCTTCT others(59): Show |
1 | a0001c0001t0004g0003 | 2 | HG02735.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.47+13785_47+13786i others(68): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | |||||||
| chr7:4945185 | T | TTTCTTCT others(65): Show |
2 | a0001c0001t0002g0279 a0001c0002t0004g0328 |
2 | NA19080.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.47+13785_47+13786i others(74): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | |||||||
| chr7:4945185 | T | TTTCTTCT others(32): Show |
1 | a0001c0002t0001g0268 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.47+13785_47+13786i others(41): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | |||||||
| chr7:4945185 | T | TTTCTTCT others(44): Show |
1 | a0001c0002t0001g0269 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.47+13785_47+13786i others(53): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | |||||||
| chr7:4945185 | TTTC | T | 5 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0002t0002g0130 others(2): Show |
5 | HG00280.hp2 HG01168.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.47+13783_47+13785d others(5): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945185 | |||||||
| chr7:4945198 | T | G | 1 | a0001c0001t0027g0346 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.47+13773A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945198 | |||||||
| chr7:4945203 | C | CTTCTTCT others(7): Show |
2 | a0001c0002t0001g0116 a0001c0002t0001g0117 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.47+13754_47+13767d others(16): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945203 | |||||||
| chr7:4945206 | C | CTTCTTCT others(31): Show |
1 | a0001c0001t0012g0251 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.47+13764_47+13765i others(40): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945206 | |||||||
| chr7:4945206 | C | CTTCTTCT others(34): Show |
1 | a0001c0002t0001g0250 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.47+13764_47+13765i others(43): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945206 | |||||||
| chr7:4945237 | T | TTCTTCTT others(22): Show |
1 | a0001c0001t0001g0314 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.47+13733_47+13734i others(31): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945237 | |||||||
| chr7:4945240 | C | T | 3 | a0001c0001t0002g0013 a0001c0001t0002g0027 a0001c0002t0001g0228 |
3 | HG01168.hp1 HG01169.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.47+13731G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945240 | |||||||
| chr7:4945250 | T | C | 1 | a0001c0002t0015g0215 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.47+13721A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945250 | |||||||
| chr7:4945263 | C | T | 40 | a0001c0001t0001g0352 a0001c0001t0002g0100 a0001c0001t0002g0115 others(37): Show |
40 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.47+13708G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945263 | |||||||
| chr7:4945378 | C | G | 2 | a0001c0001t0012g0251 a0001c0002t0001g0250 |
2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.47+13593G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945378 | |||||||
| chr7:4945409 | C | CAGGTGCC others(8): Show |
1 | a0001c0002t0001g0116 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.47+13547_47+13561d others(17): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945409 | |||||||
| chr7:4945493 | C | T | 32 | a0001c0001t0002g0100 a0001c0001t0013g0367 a0001c0001t0013g0368 others(29): Show |
32 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.47+13478G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945493 | |||||||
| chr7:4945543 | G | A | 1 | a0001c0001t0001g0337 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.47+13428C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945543 | |||||||
| chr7:4945553 | G | C | 18 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0123 others(15): Show |
18 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.47+13418C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945553 | |||||||
| chr7:4945630 | A | AGTGGCGC others(32): Show |
1 | a0001c0001t0011g0249 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.47+13302_47+13340d others(41): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945630 | |||||||
| chr7:4945635 | C | T | 38 | a0001c0001t0001g0055 a0001c0001t0010g0041 a0001c0002t0001g0181 others(35): Show |
38 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.47+13336G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945635 | |||||||
| chr7:4945775 | ATGT | A | 40 | a0001c0001t0001g0352 a0001c0001t0002g0100 a0001c0001t0002g0115 others(37): Show |
40 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.47+13193_47+13195d others(5): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945775 | |||||||
| chr7:4945917 | A | C | 2 | a0001c0002t0016g0169 a0001c0002t0016g0170 |
2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.47+13054T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4945917 | |||||||
| chr7:4946030 | T | C | 2 | a0001c0001t0004g0353 a0001c0001t0004g0354 |
2 | HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.47+12941A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4946030 | |||||||
| chr7:4946093 | A | G | 1 | a0001c0001t0003g0096 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.47+12878T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4946093 | |||||||
| chr7:4946095 | A | G | 41 | a0001c0001t0001g0352 a0001c0001t0002g0100 a0001c0001t0002g0115 others(38): Show |
41 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.47+12876T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4946095 | |||||||
| chr7:4946102 | T | C | 94 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0048 others(91): Show |
95 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.47+12869A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4946102 | |||||||
| chr7:4946115 | A | G | 83 | a0001c0001t0001g0292 a0001c0001t0001g0297 a0001c0001t0001g0310 others(80): Show |
84 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.47+12856T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4946115 | |||||||
| chr7:4946181 | A | G | 13 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0123 others(10): Show |
13 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.47+12790T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4946181 | |||||||
| chr7:4946183 | A | G | 148 | a0001c0001t0001g0020 a0001c0001t0001g0054 a0001c0001t0001g0122 others(145): Show |
150 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(147): Show |
intron_variant | MODIFIER | c.47+12788T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4946183 | |||||||
| chr7:4946226 | TACACGCA others(3): Show |
T | 2 | a0001c0001t0002g0279 a0001c0002t0004g0328 |
2 | NA19080.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.47+12735_47+12744d others(12): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4946226 | |||||||
| chr7:4946397 | A | G | 1 | a0001c0001t0003g0062 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.47+12574T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4946397 | |||||||
| chr7:4946546 | T | A | 3 | a0001c0001t0001g0273 a0001c0002t0001g0268 a0001c0002t0001g0269 |
3 | HG02647.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.47+12425A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4946546 | |||||||
| chr7:4946834 | G | A | 2 | a0001c0001t0012g0251 a0001c0002t0001g0250 |
2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.47+12137C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4946834 | |||||||
| chr7:4946884 | G | T | 19 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0002g0001 others(16): Show |
20 | HG01069.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.47+12087C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4946884 | |||||||
| chr7:4947000 | G | A | 2 | a0001c0002t0001g0238 a0001c0002t0002g0244 |
2 | HG00738.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.47+11971C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947000 | |||||||
| chr7:4947014 | C | T | 5 | a0001c0002t0001g0181 a0001c0002t0001g0182 a0001c0002t0001g0183 others(2): Show |
5 | HG00558.hp1 HG00621.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.47+11957G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947014 | |||||||
| chr7:4947133 | G | A | 4 | a0001c0003t0003g0320 a0001c0003t0004g0326 a0001c0003t0004g0327 others(1): Show |
4 | HG02083.hp1 NA18998.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+11838C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947133 | |||||||
| chr7:4947164 | C | T | 16 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0126 others(13): Show |
17 | HG01496.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.47+11807G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947164 | |||||||
| chr7:4947171 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.47+11800C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947171 | |||||||
| chr7:4947177 | C | T | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+11794G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947177 | |||||||
| chr7:4947203 | G | A | 3 | a0001c0001t0002g0012 a0001c0001t0002g0092 a0001c0001t0002g0095 |
3 | HG01070.hp1 HG03017.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.47+11768C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947203 | |||||||
| chr7:4947253 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.47+11718T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947253 | |||||||
| chr7:4947280 | C | T | 20 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0126 others(17): Show |
21 | HG01496.hp1 HG02145.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.47+11691G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947280 | |||||||
| chr7:4947311 | T | G | 82 | a0001c0001t0001g0292 a0001c0001t0001g0297 a0001c0001t0001g0310 others(79): Show |
83 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.47+11660A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947311 | |||||||
| chr7:4947398 | C | CT | 328 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0048 others(325): Show |
331 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.47+11572dupA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947398 | |||||||
| chr7:4947398 | C | CTT | 11 | a0001c0001t0001g0061 a0001c0001t0001g0352 a0001c0001t0003g0348 others(8): Show |
11 | HG02486.hp1 HG02818.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.47+11571_47+11572d others(4): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947398 | |||||||
| chr7:4947518 | C | T | 1 | a0001c0001t0005g0083 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.47+11453G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947518 | |||||||
| chr7:4947539 | G | A | 1 | a0001c0001t0005g0082 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.47+11432C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947539 | |||||||
| chr7:4947567 | G | A | 106 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0158 others(103): Show |
106 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.47+11404C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947567 | |||||||
| chr7:4947628 | G | A | 1 | a0001c0001t0015g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.47+11343C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947628 | |||||||
| chr7:4947692 | C | CT | 6 | a0001c0001t0004g0353 a0001c0002t0001g0101 a0001c0002t0001g0116 others(3): Show |
6 | HG01517.hp1 HG01978.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.47+11278dupA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947692 | |||||||
| chr7:4947692 | CT | C | 112 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0048 others(109): Show |
113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.47+11278delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947692 | |||||||
| chr7:4947692 | CTT | C | 165 | a0001c0001t0001g0220 a0001c0001t0001g0264 a0001c0001t0001g0267 others(162): Show |
167 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(164): Show |
intron_variant | MODIFIER | c.47+11277_47+11278d others(4): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947692 | |||||||
| chr7:4947692 | CTTT | C | 31 | a0001c0001t0001g0158 a0001c0001t0001g0197 a0001c0001t0001g0199 others(28): Show |
31 | HG00609.hp1 HG01070.hp2 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.47+11276_47+11278d others(5): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947692 | |||||||
| chr7:4947692 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0002g0115 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.47+11267_47+11278d others(14): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947692 | |||||||
| chr7:4947692 | CTTTTTTT others(8): Show |
C | 1 | a0001c0003t0004g0322 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.47+11264_47+11278d others(17): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947692 | |||||||
| chr7:4947753 | A | G | 128 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0123 others(125): Show |
129 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(126): Show |
intron_variant | MODIFIER | c.47+11218T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947753 | |||||||
| chr7:4947758 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.47+11213C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947758 | |||||||
| chr7:4947764 | A | G | 2 | a0001c0001t0003g0089 a0001c0001t0003g0090 |
2 | HG00558.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.47+11207T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4947764 | |||||||
| chr7:4948121 | C | A | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10850G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948121 | |||||||
| chr7:4948122 | A | T | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10849T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948122 | |||||||
| chr7:4948124 | C | G | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10847G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948124 | |||||||
| chr7:4948125 | C | G | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10846G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948125 | |||||||
| chr7:4948127 | A | T | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10844T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948127 | |||||||
| chr7:4948136 | A | G | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10835T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948136 | |||||||
| chr7:4948139 | A | T | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10832T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948139 | |||||||
| chr7:4948141 | A | T | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10830T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948141 | |||||||
| chr7:4948142 | A | C | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10829T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948142 | |||||||
| chr7:4948143 | C | A | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10828G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948143 | |||||||
| chr7:4948154 | A | G | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10817T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948154 | |||||||
| chr7:4948157 | G | T | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10814C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948157 | |||||||
| chr7:4948158 | G | A | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10813C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948158 | |||||||
| chr7:4948160 | G | C | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10811C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948160 | |||||||
| chr7:4948171 | G | T | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10800C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948171 | |||||||
| chr7:4948173 | T | C | 2 | a0001c0001t0012g0251 a0001c0002t0001g0250 |
2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.47+10798A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948173 | |||||||
| chr7:4948176 | A | C | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10795T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948176 | |||||||
| chr7:4948178 | A | C | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10793T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948178 | |||||||
| chr7:4948180 | C | T | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10791G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948180 | |||||||
| chr7:4948181 | A | T | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10790T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948181 | |||||||
| chr7:4948182 | T | G | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10789A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948182 | |||||||
| chr7:4948183 | A | G | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10788T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948183 | |||||||
| chr7:4948185 | C | T | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10786G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948185 | |||||||
| chr7:4948186 | A | G | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10785T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948186 | |||||||
| chr7:4948188 | A | G | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10783T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948188 | |||||||
| chr7:4948203 | T | A | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10768A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948203 | |||||||
| chr7:4948208 | A | G | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10763T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948208 | |||||||
| chr7:4948209 | C | T | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10762G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948209 | |||||||
| chr7:4948215 | G | C | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10756C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948215 | |||||||
| chr7:4948217 | T | A | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10754A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948217 | |||||||
| chr7:4948233 | T | G | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10738A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948233 | |||||||
| chr7:4948236 | A | T | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10735T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948236 | |||||||
| chr7:4948254 | T | C | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10717A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948254 | |||||||
| chr7:4948290 | A | G | 1 | a0001c0001t0002g0295 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.47+10681T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948290 | |||||||
| chr7:4948305 | T | A | 1 | a0001c0001t0002g0028 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.47+10666A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948305 | |||||||
| chr7:4948440 | T | A | 1 | a0001c0002t0003g0148 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.47+10531A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948440 | |||||||
| chr7:4948478 | G | A | 1 | a0001c0001t0015g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.47+10493C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948478 | |||||||
| chr7:4948527 | GA | G | 6 | a0001c0001t0001g0352 a0001c0001t0002g0315 a0001c0001t0003g0348 others(3): Show |
6 | HG02486.hp1 HG02896.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.47+10443delT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948527 | |||||||
| chr7:4948716 | G | A | 1 | a0001c0001t0006g0084 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.47+10255C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948716 | |||||||
| chr7:4948746 | A | C | 2 | a0001c0001t0010g0357 a0001c0001t0010g0358 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.47+10225T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4948746 | |||||||
| chr7:4949057 | A | G | 1 | a0001c0001t0027g0346 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.47+9914T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949057 | |||||||
| chr7:4949071 | G | A | 2 | a0001c0001t0003g0096 a0001c0001t0003g0097 |
2 | HG00140.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.47+9900C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949071 | |||||||
| chr7:4949085 | C | G | 2 | a0001c0001t0004g0294 a0001c0001t0004g0296 |
2 | HG01257.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.47+9886G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949085 | |||||||
| chr7:4949146 | G | T | 1 | a0001c0002t0003g0200 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.47+9825C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949146 | |||||||
| chr7:4949159 | G | A | 82 | a0001c0001t0001g0292 a0001c0001t0001g0297 a0001c0001t0001g0310 others(79): Show |
83 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.47+9812C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949159 | |||||||
| chr7:4949207 | C | A | 20 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0229 others(17): Show |
20 | HG00738.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.47+9764G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949207 | |||||||
| chr7:4949322 | C | A | 3 | a0001c0002t0001g0014 a0001c0002t0001g0029 a0001c0002t0001g0030 |
3 | NA18983.hp2 NA18995.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.47+9649G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949322 | |||||||
| chr7:4949374 | G | A | 375 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0032 others(372): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.47+9597C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949374 | |||||||
| chr7:4949390 | C | T | 349 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0048 others(346): Show |
352 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.47+9581G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949390 | |||||||
| chr7:4949531 | T | A | 1 | a0001c0002t0003g0148 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.47+9440A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949531 | |||||||
| chr7:4949696 | G | A | 11 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0126 others(8): Show |
11 | HG01496.hp1 HG02145.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.47+9275C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949696 | |||||||
| chr7:4949712 | A | C | 2 | a0001c0001t0017g0052 a0001c0001t0017g0053 |
2 | HG02040.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.47+9259T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949712 | |||||||
| chr7:4949727 | G | T | 99 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0158 others(96): Show |
99 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.47+9244C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949727 | |||||||
| chr7:4949749 | G | A | 99 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0158 others(96): Show |
99 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.47+9222C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949749 | |||||||
| chr7:4949811 | G | C | 1 | a0001c0001t0027g0346 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.47+9160C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949811 | |||||||
| chr7:4949966 | G | A | 80 | a0001c0001t0001g0292 a0001c0001t0001g0297 a0001c0001t0001g0310 others(77): Show |
81 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.47+9005C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949966 | |||||||
| chr7:4949998 | G | A | 9 | a0001c0001t0012g0251 a0001c0002t0001g0250 a0001c0002t0001g0252 others(6): Show |
9 | HG01884.hp2 HG02258.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.47+8973C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4949998 | |||||||
| chr7:4950007 | C | T | 2 | a0001c0002t0010g0155 a0001c0002t0014g0174 |
2 | HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.47+8964G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950007 | |||||||
| chr7:4950079 | T | TTG | 5 | a0001c0002t0001g0006 a0001c0002t0001g0008 a0001c0002t0001g0149 others(2): Show |
5 | HG01099.hp1 HG01433.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.47+8890_47+8891dup others(2): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950079 | |||||||
| chr7:4950079 | TTG | T | 9 | a0001c0001t0001g0199 a0001c0001t0001g0264 a0001c0001t0002g0031 others(6): Show |
9 | HG01884.hp1 HG02615.hp1 HG03831.hp2 others(6): Show |
intron_variant | MODIFIER | c.47+8890_47+8891del others(2): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950079 | |||||||
| chr7:4950079 | TTGTG | T | 337 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0048 others(334): Show |
340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.47+8888_47+8891del others(4): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950079 | |||||||
| chr7:4950112 | G | T | 4 | a0001c0001t0003g0348 a0001c0001t0003g0349 a0001c0001t0003g0350 others(1): Show |
4 | HG02486.hp1 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+8859C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950112 | |||||||
| chr7:4950117 | A | T | 1 | a0001c0002t0003g0157 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.47+8854T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950117 | |||||||
| chr7:4950247 | C | T | 2 | a0001c0001t0002g0050 a0001c0001t0003g0051 |
2 | NA18993.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.47+8724G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950247 | |||||||
| chr7:4950297 | C | T | 7 | a0001c0001t0001g0352 a0001c0001t0003g0348 a0001c0001t0003g0349 others(4): Show |
7 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.47+8674G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950297 | |||||||
| chr7:4950300 | G | T | 1 | a0001c0003t0004g0323 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.47+8671C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950300 | |||||||
| chr7:4950378 | G | C | 5 | a0001c0002t0001g0002 a0001c0002t0001g0265 a0001c0002t0001g0270 others(2): Show |
6 | HG02451.hp1 HG02622.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.47+8593C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950378 | |||||||
| chr7:4950380 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.47+8591C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950380 | |||||||
| chr7:4950420 | C | A | 101 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0158 others(98): Show |
101 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.47+8551G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950420 | |||||||
| chr7:4950499 | T | A | 2 | a0001c0002t0001g0241 a0001c0006t0001g0240 |
2 | HG01081.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.47+8472A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950499 | |||||||
| chr7:4950607 | C | T | 2 | a0001c0003t0004g0324 a0001c0003t0004g0325 |
2 | NA18950.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.47+8364G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950607 | |||||||
| chr7:4950665 | G | A | 1 | a0001c0002t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.47+8306C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950665 | |||||||
| chr7:4950709 | C | T | 13 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0214 others(10): Show |
13 | HG02559.hp1 HG02572.hp1 HG03098.hp1 others(10): Show |
intron_variant | MODIFIER | c.47+8262G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950709 | |||||||
| chr7:4950712 | CT | C | 202 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0048 others(199): Show |
205 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.47+8258delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950712 | |||||||
| chr7:4950771 | T | G | 1 | a0001c0002t0001g0225 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.47+8200A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4950771 | |||||||
| chr7:4951009 | G | A | 25 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0002g0001 others(22): Show |
26 | HG00423.hp2 HG01069.hp2 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.47+7962C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4951009 | |||||||
| chr7:4951087 | A | C | 1 | a0001c0001t0001g0197 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.47+7884T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4951087 | |||||||
| chr7:4951088 | C | A | 1 | a0001c0001t0001g0197 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.47+7883G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4951088 | |||||||
| chr7:4951089 | A | C | 1 | a0001c0001t0001g0197 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.47+7882T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4951089 | |||||||
| chr7:4951249 | TC | T | 3 | a0001c0001t0001g0197 a0001c0001t0003g0350 a0001c0001t0005g0312 |
3 | HG02896.hp1 HG03490.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.47+7721delG | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4951249 | |||||||
| chr7:4951342 | C | T | 237 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0048 others(234): Show |
240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.47+7629G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4951342 | |||||||
| chr7:4951388 | C | T | 6 | a0001c0001t0001g0264 a0001c0002t0001g0002 a0001c0002t0001g0265 others(3): Show |
7 | HG02451.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.47+7583G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4951388 | |||||||
| chr7:4951418 | C | A | 1 | a0001c0001t0001g0197 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.47+7553G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4951418 | |||||||
| chr7:4951446 | C | G | 1 | a0001c0001t0001g0048 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.47+7525G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4951446 | |||||||
| chr7:4951494 | A | G | 4 | a0001c0001t0001g0214 a0001c0002t0001g0211 a0001c0002t0001g0213 others(1): Show |
4 | HG02572.hp1 NA18522.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+7477T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4951494 | |||||||
| chr7:4951628 | C | A | 61 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0126 others(58): Show |
62 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.47+7343G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4951628 | |||||||
| chr7:4951771 | T | A | 1 | a0001c0001t0001g0197 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.47+7200A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4951771 | |||||||
| chr7:4951774 | A | T | 1 | a0001c0001t0001g0197 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.47+7197T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4951774 | |||||||
| chr7:4951811 | A | T | 1 | a0001c0001t0001g0118 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.47+7160T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4951811 | |||||||
| chr7:4951945 | C | T | 1 | a0001c0001t0003g0016 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.47+7026G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4951945 | |||||||
| chr7:4951986 | T | G | 1 | a0001c0001t0002g0012 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.47+6985A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4951986 | |||||||
| chr7:4952028 | G | C | 8 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0126 others(5): Show |
8 | HG01496.hp1 HG02145.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.47+6943C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4952028 | |||||||
| chr7:4952182 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.47+6789C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4952182 | |||||||
| chr7:4952262 | C | G | 11 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0126 others(8): Show |
11 | HG01496.hp1 HG02145.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.47+6709G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4952262 | |||||||
| chr7:4952640 | C | G | 1 | a0001c0001t0022g0293 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.47+6331G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4952640 | |||||||
| chr7:4952655 | C | T | 89 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0048 others(86): Show |
90 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.47+6316G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4952655 | |||||||
| chr7:4952675 | G | A | 74 | a0001c0001t0001g0297 a0001c0001t0001g0310 a0001c0001t0001g0337 others(71): Show |
75 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.47+6296C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4952675 | |||||||
| chr7:4952689 | A | AT | 19 | a0001c0001t0001g0199 a0001c0001t0001g0218 a0001c0001t0001g0219 others(16): Show |
19 | HG00741.hp2 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.47+6281dupA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4952689 | |||||||
| chr7:4952689 | AT | A | 214 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0048 others(211): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.47+6281delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4952689 | |||||||
| chr7:4952714 | CAG | C | 29 | a0001c0002t0001g0036 a0001c0002t0001g0181 a0001c0002t0001g0182 others(26): Show |
29 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.47+6255_47+6256del others(2): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4952714 | |||||||
| chr7:4952797 | T | G | 2 | a0001c0003t0004g0321 a0001c0003t0004g0322 |
2 | NA18968.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.47+6174A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4952797 | |||||||
| chr7:4952898 | C | T | 87 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(84): Show |
88 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.47+6073G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4952898 | |||||||
| chr7:4952995 | G | GT | 64 | a0001c0001t0001g0158 a0001c0001t0001g0197 a0001c0001t0001g0199 others(61): Show |
64 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.47+5975dupA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4952995 | |||||||
| chr7:4953001 | T | C | 1 | a0001c0001t0027g0346 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.47+5970A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4953001 | |||||||
| chr7:4953006 | T | G | 1 | a0001c0002t0001g0211 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.47+5965A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4953006 | |||||||
| chr7:4953023 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.47+5948T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4953023 | |||||||
| chr7:4953247 | C | T | 1 | a0001c0002t0005g0175 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.47+5724G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4953247 | |||||||
| chr7:4953321 | C | T | 93 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0048 others(90): Show |
94 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.47+5650G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4953321 | |||||||
| chr7:4953455 | A | G | 1 | a0001c0001t0003g0349 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.47+5516T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4953455 | |||||||
| chr7:4953475 | CT | C | 97 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0048 others(94): Show |
98 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.47+5495delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4953475 | |||||||
| chr7:4953584 | C | T | 98 | a0001c0001t0001g0158 a0001c0001t0001g0197 a0001c0001t0001g0199 others(95): Show |
98 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.47+5387G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4953584 | |||||||
| chr7:4953748 | G | A | 1 | a0001c0007t0025g0356 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.47+5223C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4953748 | |||||||
| chr7:4953761 | G | A | 13 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0123 others(10): Show |
13 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.47+5210C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4953761 | |||||||
| chr7:4953796 | T | A | 1 | a0001c0001t0001g0197 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.47+5175A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4953796 | |||||||
| chr7:4953808 | A | T | 1 | a0001c0001t0001g0197 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.47+5163T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4953808 | |||||||
| chr7:4953822 | T | A | 4 | a0001c0002t0001g0160 a0001c0002t0001g0161 a0001c0002t0001g0162 others(1): Show |
4 | HG03098.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.47+5149A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4953822 | |||||||
| chr7:4953869 | G | A | 2 | a0001c0001t0002g0034 a0001c0002t0001g0243 |
2 | HG04184.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.47+5102C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4953869 | |||||||
| chr7:4953998 | G | A | 25 | a0001c0002t0001g0036 a0001c0002t0001g0181 a0001c0002t0001g0182 others(22): Show |
25 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.47+4973C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4953998 | |||||||
| chr7:4954106 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.47+4865T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954106 | |||||||
| chr7:4954125 | C | T | 85 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(82): Show |
86 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.47+4846G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954125 | |||||||
| chr7:4954418 | A | AT | 93 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0048 others(90): Show |
94 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.47+4552dupA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954418 | |||||||
| chr7:4954444 | G | T | 2 | a0001c0001t0002g0344 a0001c0003t0001g0343 |
2 | NA18986.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.47+4527C>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954444 | |||||||
| chr7:4954451 | T | G | 1 | a0001c0002t0001g0163 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.47+4520A>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954451 | |||||||
| chr7:4954520 | C | A | 20 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0123 others(17): Show |
21 | HG01496.hp1 HG02145.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.47+4451G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954520 | |||||||
| chr7:4954542 | T | C | 1 | a0001c0001t0001g0264 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.47+4429A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954542 | |||||||
| chr7:4954619 | A | G | 39 | a0001c0001t0010g0041 a0001c0002t0001g0036 a0001c0002t0001g0181 others(36): Show |
39 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.47+4352T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954619 | |||||||
| chr7:4954621 | G | A | 3 | a0001c0001t0001g0214 a0001c0002t0001g0213 a0001c0002t0015g0215 |
3 | NA18906.hp1 NA19030.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.47+4350C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954621 | |||||||
| chr7:4954647 | G | A | 9 | a0001c0001t0012g0251 a0001c0002t0001g0250 a0001c0002t0001g0252 others(6): Show |
9 | HG01884.hp2 HG02258.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.47+4324C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954647 | |||||||
| chr7:4954671 | G | A | 81 | a0001c0001t0001g0292 a0001c0001t0001g0297 a0001c0001t0001g0310 others(78): Show |
82 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.47+4300C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954671 | |||||||
| chr7:4954685 | T | C | 2 | a0001c0001t0002g0344 a0001c0003t0001g0343 |
2 | NA18986.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.47+4286A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954685 | |||||||
| chr7:4954859 | A | T | 1 | a0001c0001t0003g0039 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.47+4112T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954859 | |||||||
| chr7:4954906 | G | C | 12 | a0001c0001t0001g0094 a0001c0001t0002g0009 a0001c0001t0002g0092 others(9): Show |
12 | HG00140.hp1 HG00558.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.47+4065C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954906 | |||||||
| chr7:4954920 | A | G | 1 | a0001c0001t0002g0038 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.47+4051T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954920 | |||||||
| chr7:4954937 | T | A | 1 | a0001c0001t0027g0346 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.47+4034A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954937 | |||||||
| chr7:4954941 | T | C | 2 | a0001c0001t0012g0251 a0001c0002t0001g0250 |
2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.47+4030A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4954941 | |||||||
| chr7:4955132 | C | T | 295 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0048 others(292): Show |
297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.47+3839G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4955132 | |||||||
| chr7:4955189 | G | A | 1 | a0001c0001t0031g0166 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.47+3782C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4955189 | |||||||
| chr7:4955351 | G | A | 1 | a0001c0001t0027g0346 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.47+3620C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4955351 | |||||||
| chr7:4955461 | A | T | 1 | a0001c0001t0031g0166 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.47+3510T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4955461 | |||||||
| chr7:4955548 | T | C | 1 | a0001c0002t0002g0244 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.47+3423A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4955548 | |||||||
| chr7:4955607 | T | C | 8 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(5): Show |
8 | HG02135.hp1 NA18612.hp2 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.47+3364A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4955607 | |||||||
| chr7:4955957 | G | A | 1 | a0001c0002t0001g0225 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.47+3014C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4955957 | |||||||
| chr7:4955968 | G | A | 22 | a0001c0001t0002g0227 a0001c0001t0003g0164 a0001c0002t0001g0226 others(19): Show |
22 | HG00738.hp2 HG01074.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.47+3003C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4955968 | |||||||
| chr7:4956013 | A | G | 14 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0123 others(11): Show |
14 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.47+2958T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4956013 | |||||||
| chr7:4956014 | T | C | 5 | a0001c0002t0001g0002 a0001c0002t0001g0265 a0001c0002t0001g0270 others(2): Show |
6 | HG02451.hp1 HG02622.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.47+2957A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4956014 | |||||||
| chr7:4956119 | A | G | 2 | a0001c0001t0009g0374 a0001c0001t0027g0346 |
2 | HG02523.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.47+2852T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4956119 | |||||||
| chr7:4956162 | C | T | 1 | a0001c0001t0009g0375 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.47+2809G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4956162 | |||||||
| chr7:4956216 | T | C | 349 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0048 others(346): Show |
352 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.47+2755A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4956216 | |||||||
| chr7:4956247 | A | G | 1 | a0001c0002t0005g0165 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.47+2724T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4956247 | |||||||
| chr7:4956252 | A | G | 7 | a0001c0002t0001g0252 a0001c0002t0001g0253 a0001c0002t0001g0254 others(4): Show |
7 | HG02258.hp1 HG02717.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.47+2719T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4956252 | |||||||
| chr7:4956362 | G | C | 1 | a0001c0002t0001g0245 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.47+2609C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4956362 | |||||||
| chr7:4956425 | TA | T | 28 | a0001c0001t0001g0158 a0001c0001t0002g0011 a0001c0001t0002g0115 others(25): Show |
28 | HG01517.hp1 HG01884.hp2 HG01943.hp1 others(25): Show |
intron_variant | MODIFIER | c.47+2545delT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4956425 | |||||||
| chr7:4956678 | T | C | 1 | a0001c0001t0001g0246 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.47+2293A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4956678 | |||||||
| chr7:4956781 | G | C | 1 | a0001c0001t0003g0037 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.47+2190C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4956781 | |||||||
| chr7:4956816 | G | A | 1 | a0001c0007t0025g0356 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.47+2155C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4956816 | |||||||
| chr7:4956918 | C | G | 1 | a0001c0001t0001g0264 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.47+2053G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4956918 | |||||||
| chr7:4957091 | G | A | 1 | a0001c0001t0027g0346 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.47+1880C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957091 | |||||||
| chr7:4957163 | C | CAA | 8 | a0001c0001t0002g0115 a0001c0002t0001g0252 a0001c0002t0001g0253 others(5): Show |
8 | HG02258.hp1 HG02717.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.47+1806_47+1807dup others(2): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957163 | |||||||
| chr7:4957163 | CAA | C | 100 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0259 others(97): Show |
102 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.47+1806_47+1807del others(2): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957163 | |||||||
| chr7:4957173 | A | AT | 4 | a0001c0001t0003g0131 a0001c0001t0003g0133 a0001c0002t0002g0130 others(1): Show |
4 | HG00280.hp2 HG01168.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+1797_47+1798ins others(1): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957173 | |||||||
| chr7:4957173 | A | T | 16 | a0001c0001t0002g0275 a0001c0001t0002g0276 a0001c0001t0002g0277 others(13): Show |
16 | HG00642.hp1 HG00735.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.47+1798T>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957173 | |||||||
| chr7:4957173 | AAT | A | 72 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(69): Show |
72 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.47+1796_47+1797del others(2): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957173 | |||||||
| chr7:4957174 | AT | A | 50 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0123 others(47): Show |
50 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.47+1796delA | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957174 | |||||||
| chr7:4957175 | T | A | 93 | a0001c0001t0001g0158 a0001c0001t0001g0197 a0001c0001t0001g0199 others(90): Show |
93 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.47+1796A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957175 | |||||||
| chr7:4957177 | T | A | 38 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0202 others(35): Show |
38 | HG00738.hp2 HG01074.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.47+1794A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957177 | |||||||
| chr7:4957179 | T | A | 1 | a0001c0002t0001g0247 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.47+1792A>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957179 | |||||||
| chr7:4957310 | A | C | 7 | a0001c0001t0001g0352 a0001c0001t0003g0348 a0001c0001t0003g0349 others(4): Show |
7 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.47+1661T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957310 | |||||||
| chr7:4957375 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.47+1596C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957375 | |||||||
| chr7:4957469 | A | G | 1 | a0001c0003t0004g0319 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.47+1502T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957469 | |||||||
| chr7:4957471 | AC | A | 316 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0048 others(313): Show |
318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.47+1499delG | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957471 | |||||||
| chr7:4957472 | C | A | 1 | a0001c0003t0004g0319 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.47+1499G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957472 | |||||||
| chr7:4957499 | A | G | 41 | a0001c0001t0001g0352 a0001c0001t0002g0100 a0001c0001t0002g0115 others(38): Show |
41 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.47+1472T>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957499 | |||||||
| chr7:4957526 | G | A | 41 | a0001c0001t0001g0352 a0001c0001t0002g0100 a0001c0001t0002g0115 others(38): Show |
41 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.47+1445C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957526 | |||||||
| chr7:4957542 | G | C | 7 | a0001c0002t0001g0252 a0001c0002t0001g0253 a0001c0002t0001g0254 others(4): Show |
7 | HG02258.hp1 HG02717.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.47+1429C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957542 | |||||||
| chr7:4957563 | C | A | 1 | a0001c0004t0002g0317 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.47+1408G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957563 | |||||||
| chr7:4957633 | G | C | 2 | a0001c0002t0001g0116 a0001c0002t0001g0117 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.47+1338C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957633 | |||||||
| chr7:4957636 | C | A | 1 | a0001c0001t0002g0318 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.47+1335G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957636 | |||||||
| chr7:4957651 | G | GA | 96 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0048 others(93): Show |
97 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.47+1319dupT | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957651 | |||||||
| chr7:4957682 | A | C | 1 | a0001c0002t0007g0359 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.47+1289T>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957682 | |||||||
| chr7:4957918 | C | G | 22 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0123 others(19): Show |
23 | HG01496.hp1 HG02145.hp1 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.47+1053G>C | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4957918 | |||||||
| chr7:4958173 | T | C | 9 | a0001c0001t0012g0251 a0001c0002t0001g0250 a0001c0002t0001g0252 others(6): Show |
9 | HG01884.hp2 HG02258.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.47+798A>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4958173 | |||||||
| chr7:4958217 | G | A | 32 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(29): Show |
32 | HG00408.hp1 HG00609.hp1 HG02004.hp1 others(29): Show |
intron_variant | MODIFIER | c.47+754C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4958217 | |||||||
| chr7:4958261 | C | T | 41 | a0001c0001t0001g0352 a0001c0001t0002g0100 a0001c0001t0002g0115 others(38): Show |
41 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.47+710G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4958261 | |||||||
| chr7:4958395 | G | C | 90 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0001g0273 others(87): Show |
92 | HG00408.hp1 HG00597.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.47+576C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4958395 | |||||||
| chr7:4958512 | C | T | 92 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0048 others(89): Show |
93 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.47+459G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4958512 | |||||||
| chr7:4958515 | C | T | 3 | a0001c0001t0001g0007 a0001c0002t0001g0006 a0001c0002t0001g0008 |
3 | HG02559.hp2 HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.47+456G>A | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4958515 | |||||||
| chr7:4958601 | G | A | 1 | a0001c0001t0027g0346 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.47+370C>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4958601 | |||||||
| chr7:4958693 | CGCATAAC others(9): Show |
C | 1 | a0001c0001t0004g0347 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.47+262_47+277delAA others(14): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4958693 | |||||||
| chr7:4958809 | C | A | 8 | a0001c0001t0001g0352 a0001c0001t0003g0348 a0001c0001t0003g0349 others(5): Show |
8 | HG02486.hp1 HG02818.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.47+162G>T | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4958809 | |||||||
| chr7:4958892 | G | C | 3 | a0001c0001t0010g0357 a0001c0001t0010g0358 a0001c0007t0025g0356 |
3 | HG01891.hp1 HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.47+79C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4958892 | |||||||
| chr7:4958912 | G | C | 1 | a0001c0002t0020g0005 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.47+59C>G | MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4958912 | |||||||
| chr7:4958915 | C | CCCGCCGC others(40): Show |
1 | a0001c0002t0007g0359 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.47+9_47+55dupCGGCC others(42): Show |
MMD2 | ENSG00000136297.15 | transcript | ENST00000401401.8 | protein_coding | 1/6 | chr7 | 4958915 |