Item | Value |
---|---|
geneid | 56005 |
ensemblid | ENSG00000074842.8 |
hgncid | 16948 |
symbol | MYDGF |
name | myeloid derived growth factor |
refseq_nuc | NM_019107.4 |
refseq_prot | NP_061980.1 |
ensembl_nuc | ENST00000262947.8 |
ensembl_prot | ENSP00000262947.2 |
mane_status | MANE Select |
chr | chr19 |
start | 4657545 |
end | 4670342 |
strand | - |
ver | v1.2 |
region | chr19:4657545-4670342 |
region5000 | chr19:4652545-4675342 |
regionname0 | MYDGF_chr19_4657545_4670342 |
regionname5000 | MYDGF_chr19_4652545_4675342 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 173 | 287 | 30 | 74 | 129 | 15 | 37 | 95 | MYDGF_chr19_4652545_4675342 | MYDGF | MAAPS others(168): Show |
chr19 | 4652545 | 4675342 |
a0002 | 0/0 | 173 | 121 | 63 | 6 | 48 | 3 | 1 | 36 | MYDGF_chr19_4652545_4675342 | MYDGF | MAAPS others(168): Show |
chr19 | 4652545 | 4675342 |
a0003 | 0/0 | 173 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | MAARS others(168): Show |
chr19 | 4652545 | 4675342 |
a0004 | 0/0 | 173 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYDGF_chr19_4652545_4675342 | MYDGF | MAAPS others(168): Show |
chr19 | 4652545 | 4675342 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 519 | 286 | 29 | 74 | 129 | 15 | 37 | MYDGF_chr19_4652545_4675342 | MYDGF | ATGGC others(514): Show |
chr19 | 4652545 | 4675342 | ||
a0001c0006 | 0/0 | 519 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | ATGGC others(514): Show |
chr19 | 4652545 | 4675342 | ||
a0002c0002 | 0/0 | 519 | 85 | 46 | 3 | 34 | 2 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | ATGGC others(514): Show |
chr19 | 4652545 | 4675342 | ||
a0002c0003 | 0/0 | 519 | 35 | 17 | 3 | 13 | 1 | 1 | MYDGF_chr19_4652545_4675342 | MYDGF | ATGGC others(514): Show |
chr19 | 4652545 | 4675342 | ||
a0002c0005 | 0/0 | 519 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | ATGGC others(514): Show |
chr19 | 4652545 | 4675342 | ||
a0003c0007 | 0/0 | 519 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | ATGGC others(514): Show |
chr19 | 4652545 | 4675342 | ||
a0004c0004 | 0/0 | 519 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | ATGGC others(514): Show |
chr19 | 4652545 | 4675342 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 990 | 280 | 29 | 72 | 125 | 15 | 37 | MYDGF_chr19_4652545_4675342 | MYDGF | AGTCC others(985): Show |
chr19 | 4652545 | 4675342 |
a0001c0001t0005 | 0/0 | 990 | 2 | 0 | 2 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | AGTCC others(985): Show |
chr19 | 4652545 | 4675342 |
a0001c0001t0006 | 0/0 | 990 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | AGTCC others(985): Show |
chr19 | 4652545 | 4675342 |
a0001c0001t0007 | 0/0 | 990 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | AGTCC others(985): Show |
chr19 | 4652545 | 4675342 |
a0001c0001t0010 | 0/0 | 990 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | AGTCC others(985): Show |
chr19 | 4652545 | 4675342 |
a0001c0001t0011 | 0/0 | 990 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | AGTCC others(985): Show |
chr19 | 4652545 | 4675342 |
a0001c0006t0001 | 0/0 | 990 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | AGTCC others(985): Show |
chr19 | 4652545 | 4675342 |
a0002c0002t0002 | 0/0 | 990 | 76 | 38 | 3 | 33 | 2 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | AGTCC others(985): Show |
chr19 | 4652545 | 4675342 |
a0002c0002t0003 | 0/0 | 990 | 5 | 5 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | AGTCC others(985): Show |
chr19 | 4652545 | 4675342 |
a0002c0002t0004 | 0/0 | 990 | 2 | 2 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | AGTCC others(985): Show |
chr19 | 4652545 | 4675342 |
a0002c0002t0008 | 0/0 | 980 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | AGTCC others(975): Show |
chr19 | 4652545 | 4675342 |
a0002c0002t0009 | 0/0 | 990 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | AGTCC others(985): Show |
chr19 | 4652545 | 4675342 |
a0002c0003t0001 | 0/0 | 990 | 8 | 0 | 0 | 7 | 0 | 1 | MYDGF_chr19_4652545_4675342 | MYDGF | AGTCC others(985): Show |
chr19 | 4652545 | 4675342 |
a0002c0003t0002 | 0/0 | 990 | 27 | 17 | 3 | 6 | 1 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | AGTCC others(985): Show |
chr19 | 4652545 | 4675342 |
a0002c0005t0001 | 0/0 | 990 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | AGTCC others(985): Show |
chr19 | 4652545 | 4675342 |
a0003c0007t0001 | 0/0 | 990 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | AGTCC others(985): Show |
chr19 | 4652545 | 4675342 |
a0004c0004t0002 | 0/0 | 990 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | AGTCC others(985): Show |
chr19 | 4652545 | 4675342 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 37 | 4 | 6 | 22 | 5 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0002 | 0/0 | 21 | 4 | 7 | 7 | 1 | 2 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0003 | 0/0 | 7 | 0 | 4 | 0 | 2 | 1 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0004 | 0/0 | 6 | 1 | 4 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0005 | 0/0 | 5 | 1 | 0 | 3 | 0 | 1 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 1 | 3 | 1 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0018 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0036 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0040 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0189 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0005g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0005g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0006g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0007g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0010g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0001t0011g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0001c0006t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0013 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0003g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0008g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0002t0009g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0003t0001g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0003t0002g0007 | 0/0 | 4 | 3 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0003t0002g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0003t0002g0021 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0003t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0003t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0003t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0003t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0003t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0003t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0003t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0003t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0003t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0003t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0003t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0003t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0003t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0003t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0003t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0003t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0003t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0002c0005t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0003c0007t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
a0004c0004t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0206 | EUR | GBR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | FIN | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00597 | hp1 | a0002 | c0002 | t0002 | g0119 | EAS | CHS | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | CHS | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00609 | hp1 | a0002 | c0002 | t0002 | g0121 | EAS | CHS | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00738 | hp2 | a0001 | c0001 | t0005 | g0199 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01109 | hp1 | a0002 | c0002 | t0002 | g0087 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01167 | hp2 | a0002 | c0002 | t0002 | g0013 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01243 | hp1 | a0002 | c0002 | t0002 | g0079 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0225 | AMR | PUR | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01515 | hp1 | a0002 | c0002 | t0002 | g0013 | EUR | IBS | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01517 | hp1 | a0002 | c0002 | t0002 | g0013 | EUR | IBS | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0218 | EUR | IBS | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01884 | hp1 | a0002 | c0003 | t0002 | g0007 | AFR | ACB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01884 | hp2 | a0002 | c0002 | t0002 | g0111 | AFR | ACB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01891 | hp1 | a0002 | c0003 | t0002 | g0011 | AFR | ACB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01891 | hp2 | a0002 | c0002 | t0002 | g0012 | AFR | ACB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02015 | hp2 | a0002 | c0002 | t0002 | g0117 | EAS | KHV | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02027 | hp1 | a0002 | c0002 | t0002 | g0128 | EAS | KHV | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02040 | hp2 | a0002 | c0002 | t0002 | g0110 | EAS | KHV | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02055 | hp2 | a0002 | c0002 | t0002 | g0089 | AFR | ACB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02056 | hp1 | a0002 | c0003 | t0002 | g0050 | EAS | KHV | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02080 | hp1 | a0002 | c0003 | t0002 | g0060 | EAS | KHV | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02132 | hp2 | a0002 | c0002 | t0002 | g0118 | EAS | KHV | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02135 | hp1 | a0002 | c0003 | t0001 | g0065 | EAS | KHV | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02145 | hp1 | a0002 | c0002 | t0004 | g0070 | AFR | ACB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02148 | hp2 | a0002 | c0003 | t0002 | g0053 | AMR | PEL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02155 | hp1 | a0002 | c0002 | t0002 | g0134 | EAS | CDX | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02155 | hp2 | a0002 | c0003 | t0001 | g0068 | EAS | CDX | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CDX | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CDX | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02257 | hp1 | a0002 | c0003 | t0002 | g0057 | AFR | ACB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02257 | hp2 | a0002 | c0002 | t0002 | g0081 | AFR | ACB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02258 | hp1 | a0002 | c0003 | t0002 | g0055 | AFR | ACB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02273 | hp1 | a0002 | c0003 | t0002 | g0054 | AMR | PEL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02280 | hp1 | a0002 | c0002 | t0002 | g0074 | AFR | ACB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02280 | hp2 | a0002 | c0002 | t0002 | g0076 | AFR | ACB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02300 | hp1 | a0002 | c0003 | t0002 | g0058 | AMR | PEL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02451 | hp1 | a0002 | c0002 | t0002 | g0101 | AFR | ACB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02451 | hp2 | a0002 | c0003 | t0002 | g0048 | AFR | ACB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02523 | hp1 | a0002 | c0002 | t0002 | g0104 | EAS | KHV | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02572 | hp1 | a0002 | c0002 | t0002 | g0099 | AFR | GWD | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02572 | hp2 | a0002 | c0002 | t0002 | g0085 | AFR | GWD | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02615 | hp1 | a0002 | c0003 | t0002 | g0047 | AFR | GWD | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02622 | hp1 | a0002 | c0002 | t0002 | g0100 | AFR | GWD | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02622 | hp2 | a0002 | c0002 | t0002 | g0026 | AFR | GWD | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02630 | hp1 | a0002 | c0002 | t0003 | g0024 | AFR | GWD | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02630 | hp2 | a0002 | c0002 | t0002 | g0091 | AFR | GWD | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02647 | hp2 | a0002 | c0002 | t0002 | g0086 | AFR | GWD | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02723 | hp2 | a0002 | c0002 | t0003 | g0024 | AFR | GWD | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02809 | hp2 | a0002 | c0002 | t0002 | g0026 | AFR | GWD | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02818 | hp1 | a0002 | c0002 | t0002 | g0097 | AFR | GWD | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02818 | hp2 | a0002 | c0002 | t0002 | g0113 | AFR | GWD | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02897 | hp1 | a0002 | c0002 | t0002 | g0098 | AFR | GWD | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02897 | hp2 | a0002 | c0002 | t0002 | g0082 | AFR | GWD | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02922 | hp1 | a0002 | c0002 | t0002 | g0012 | AFR | ESN | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02965 | hp1 | a0002 | c0002 | t0002 | g0083 | AFR | ESN | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | ESN | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02970 | hp1 | a0002 | c0003 | t0002 | g0049 | AFR | ESN | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02970 | hp2 | a0002 | c0003 | t0002 | g0011 | AFR | ESN | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02976 | hp1 | a0002 | c0002 | t0002 | g0088 | AFR | ESN | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02976 | hp2 | a0002 | c0002 | t0002 | g0078 | AFR | ESN | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03041 | hp1 | a0002 | c0003 | t0002 | g0051 | AFR | GWD | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03041 | hp2 | a0002 | c0002 | t0002 | g0077 | AFR | GWD | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03098 | hp2 | a0002 | c0002 | t0003 | g0084 | AFR | MSL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03130 | hp1 | a0002 | c0003 | t0002 | g0045 | AFR | ESN | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03139 | hp2 | a0002 | c0002 | t0002 | g0093 | AFR | ESN | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03195 | hp1 | a0002 | c0002 | t0002 | g0120 | AFR | ESN | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03209 | hp1 | a0002 | c0003 | t0002 | g0007 | AFR | MSL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03209 | hp2 | a0002 | c0002 | t0002 | g0096 | AFR | MSL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03225 | hp1 | a0002 | c0003 | t0002 | g0011 | AFR | MSL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03225 | hp2 | a0002 | c0002 | t0003 | g0023 | AFR | MSL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03453 | hp1 | a0002 | c0002 | t0002 | g0025 | AFR | MSL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | MSL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03486 | hp1 | a0002 | c0002 | t0002 | g0109 | AFR | MSL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03486 | hp2 | a0003 | c0007 | t0001 | g0279 | AFR | MSL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03540 | hp1 | a0002 | c0002 | t0002 | g0069 | AFR | GWD | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03540 | hp2 | a0002 | c0003 | t0002 | g0056 | AFR | GWD | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03579 | hp1 | a0002 | c0002 | t0002 | g0025 | AFR | MSL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03579 | hp2 | a0002 | c0002 | t0003 | g0023 | AFR | MSL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | STU | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | BEB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | BEB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | BEB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | BEB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | STU | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG04184 | hp2 | a0002 | c0003 | t0001 | g0022 | SAS | BEB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | STU | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | STU | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | YRI | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18906 | hp1 | a0002 | c0003 | t0002 | g0046 | AFR | YRI | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18906 | hp2 | a0002 | c0002 | t0002 | g0095 | AFR | YRI | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18943 | hp1 | a0002 | c0002 | t0002 | g0123 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18943 | hp2 | a0002 | c0003 | t0001 | g0064 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18944 | hp1 | a0002 | c0002 | t0002 | g0114 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18946 | hp1 | a0002 | c0003 | t0001 | g0063 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18946 | hp2 | a0002 | c0002 | t0002 | g0130 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18947 | hp1 | a0002 | c0002 | t0002 | g0122 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18951 | hp1 | a0001 | c0001 | t0011 | g0236 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18953 | hp1 | a0002 | c0002 | t0002 | g0124 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18953 | hp2 | a0001 | c0001 | t0006 | g0182 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18954 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18963 | hp2 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18964 | hp1 | a0002 | c0002 | t0002 | g0112 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18969 | hp1 | a0002 | c0002 | t0002 | g0129 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18973 | hp2 | a0002 | c0002 | t0002 | g0135 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18974 | hp1 | a0002 | c0002 | t0002 | g0105 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18974 | hp2 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18977 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18982 | hp1 | a0002 | c0002 | t0002 | g0127 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18984 | hp1 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18986 | hp2 | a0002 | c0003 | t0001 | g0066 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18998 | hp2 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18999 | hp1 | a0002 | c0002 | t0002 | g0116 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19001 | hp1 | a0002 | c0003 | t0002 | g0052 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19005 | hp2 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19007 | hp2 | a0001 | c0001 | t0010 | g0241 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19011 | hp1 | a0002 | c0003 | t0001 | g0022 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | LWK | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19030 | hp2 | a0002 | c0003 | t0002 | g0059 | AFR | LWK | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | LWK | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19043 | hp2 | a0002 | c0002 | t0002 | g0080 | AFR | LWK | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19057 | hp2 | a0004 | c0004 | t0002 | g0102 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19059 | hp1 | a0002 | c0002 | t0008 | g0106 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19059 | hp2 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19060 | hp1 | a0002 | c0003 | t0002 | g0021 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19062 | hp1 | a0001 | c0001 | t0007 | g0200 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19064 | hp1 | a0002 | c0005 | t0001 | g0108 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19070 | hp1 | a0002 | c0003 | t0002 | g0062 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19074 | hp2 | a0002 | c0002 | t0002 | g0115 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19079 | hp1 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19079 | hp2 | a0002 | c0002 | t0002 | g0125 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19082 | hp2 | a0002 | c0003 | t0001 | g0067 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19084 | hp2 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19086 | hp1 | a0002 | c0002 | t0002 | g0133 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19087 | hp2 | a0002 | c0003 | t0002 | g0007 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19090 | hp2 | a0002 | c0002 | t0002 | g0131 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19240 | hp1 | a0002 | c0002 | t0004 | g0071 | AFR | YRI | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA19240 | hp2 | a0001 | c0006 | t0001 | g0136 | AFR | YRI | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ASW | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA20129 | hp2 | a0002 | c0002 | t0002 | g0073 | AFR | ASW | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA20752 | hp1 | a0002 | c0003 | t0002 | g0021 | EUR | TSI | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0201 | EUR | TSI | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0216 | EUR | TSI | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0277 | EUR | TSI | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02109 | hp1 | a0002 | c0002 | t0002 | g0075 | AFR | ACB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02109 | hp2 | a0002 | c0002 | t0002 | g0092 | AFR | ACB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02486 | hp1 | a0002 | c0002 | t0002 | g0012 | AFR | ACB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02486 | hp2 | a0002 | c0003 | t0002 | g0061 | AFR | ACB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02559 | hp1 | a0002 | c0003 | t0002 | g0007 | AFR | ACB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG03471 | hp2 | a0002 | c0002 | t0009 | g0072 | AFR | MSL | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG06807 | hp1 | a0002 | c0002 | t0002 | g0090 | AFR | USA | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | USA | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
NA20300 | hp2 | a0002 | c0002 | t0002 | g0094 | AFR | USA | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0189 | REF | REF | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0036 | REF | REF | MYDGF_chr19_4652545_4675342 | MYDGF | chr19 | 4652545 | 4675342 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:4664934 | A | G | 1 | a0004 | 1 | NA19057.hp2 | missense_variant | MODERATE | c.229T>C | p.Trp77Arg | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/6 | 237/990 | 229/522 | 77/173 | chr19 | 4664934 | |||
chr19:4670301 | C | G | 2 | a0002 a0004 |
122 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(119): Show |
missense_variant | MODERATE | c.34G>C | p.Gly12Arg | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 1/6 | 42/990 | 34/522 | 12/173 | chr19 | 4670301 | |||
chr19:4670324 | G | C | 1 | a0003 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.11C>G | p.Pro4Arg | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 1/6 | 19/990 | 11/522 | 4/173 | chr19 | 4670324 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:4658035 | A | G | 2 | a0002c0002 a0004c0004 |
86 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(83): Show |
synonymous_variant | LOW | c.492T>C | p.Ile164Ile | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 6/6 | 500/990 | 492/522 | 164/173 | chr19 | 4658035 | |||
chr19:4660681 | G | A | 1 | a0001c0006 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.357C>T | p.Tyr119Tyr | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 4/6 | 365/990 | 357/522 | 119/173 | chr19 | 4660681 | |||
chr19:4670224 | C | G | 1 | a0002c0003 | 35 | HG01884.hp1 HG01891.hp1 HG02056.hp1 others(32): Show |
synonymous_variant | LOW | c.111G>C | p.Thr37Thr | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 1/6 | 119/990 | 111/522 | 37/173 | chr19 | 4670224 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:4657592 | C | G | 1 | a0001c0001t0010 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*413G>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 6/6 | 413 | chr19 | 4657592 | ||||||
chr19:4657612 | A | C | 1 | a0002c0002t0009 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393T>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 6/6 | 393 | chr19 | 4657612 | ||||||
chr19:4657697 | TTTCCCCA others(3): Show |
T | 1 | a0002c0002t0008 | 1 | NA19059.hp1 | 3_prime_UTR_variant | MODIFIER | c.*298_*307delTGCTGG others(4): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 6/6 | 298 | chr19 | 4657697 | ||||||
chr19:4657812 | G | A | 1 | a0001c0001t0011 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*193C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 6/6 | 193 | chr19 | 4657812 | ||||||
chr19:4657852 | C | T | 1 | a0002c0002t0004 | 2 | HG02145.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*153G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 6/6 | 153 | chr19 | 4657852 | ||||||
chr19:4657945 | A | C | 7 | a0002c0002t0002 a0002c0002t0003 a0002c0002t0004 others(4): Show |
113 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*60T>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 6/6 | 60 | chr19 | 4657945 | ||||||
chr19:4657948 | C | T | 1 | a0001c0001t0007 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*57G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 6/6 | 57 | chr19 | 4657948 | ||||||
chr19:4657951 | G | T | 1 | a0001c0001t0006 | 1 | NA18953.hp2 | 3_prime_UTR_variant | MODIFIER | c.*54C>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 6/6 | 54 | chr19 | 4657951 | ||||||
chr19:4657967 | C | T | 3 | a0001c0001t0005 a0002c0002t0003 a0002c0002t0004 |
9 | HG00738.hp2 HG01243.hp2 HG02145.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*38G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 6/6 | 38 | chr19 | 4657967 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:4658139 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.443-55G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 5/5 | chr19 | 4658139 | |||||||
chr19:4658242 | C | T | 37 | a0002c0002t0002g0013 a0002c0002t0002g0027 a0002c0002t0002g0028 others(34): Show |
42 | HG00597.hp1 HG00609.hp1 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.443-158G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 5/5 | chr19 | 4658242 | |||||||
chr19:4658274 | G | C | 5 | a0002c0002t0003g0023 a0002c0002t0003g0024 a0002c0002t0003g0084 others(2): Show |
7 | HG02145.hp1 HG02630.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.443-190C>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 5/5 | chr19 | 4658274 | |||||||
chr19:4658389 | G | A | 75 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0025 others(72): Show |
86 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(83): Show |
intron_variant | MODIFIER | c.443-305C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 5/5 | chr19 | 4658389 | |||||||
chr19:4658409 | G | T | 3 | a0002c0002t0002g0027 a0002c0002t0002g0115 a0002c0002t0002g0127 |
4 | NA18954.hp1 NA18977.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.443-325C>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 5/5 | chr19 | 4658409 | |||||||
chr19:4658420 | G | A | 21 | a0002c0003t0002g0007 a0002c0003t0002g0011 a0002c0003t0002g0021 others(18): Show |
27 | HG01884.hp1 HG01891.hp1 HG02056.hp1 others(24): Show |
intron_variant | MODIFIER | c.443-336C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 5/5 | chr19 | 4658420 | |||||||
chr19:4658551 | G | A | 96 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0025 others(93): Show |
113 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(110): Show |
intron_variant | MODIFIER | c.443-467C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 5/5 | chr19 | 4658551 | |||||||
chr19:4658586 | C | A | 1 | a0002c0002t0002g0069 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.443-502G>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 5/5 | chr19 | 4658586 | |||||||
chr19:4658595 | C | T | 25 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0031 others(22): Show |
32 | HG00733.hp1 HG01192.hp1 HG01358.hp2 others(29): Show |
intron_variant | MODIFIER | c.443-511G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 5/5 | chr19 | 4658595 | |||||||
chr19:4658730 | C | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0149 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.443-646G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 5/5 | chr19 | 4658730 | |||||||
chr19:4658745 | C | G | 1 | a0002c0002t0002g0069 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.443-661G>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 5/5 | chr19 | 4658745 | |||||||
chr19:4658801 | A | T | 75 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0025 others(72): Show |
86 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(83): Show |
intron_variant | MODIFIER | c.443-717T>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 5/5 | chr19 | 4658801 | |||||||
chr19:4658802 | A | T | 1 | a0002c0002t0002g0086 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.443-718T>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 5/5 | chr19 | 4658802 | |||||||
chr19:4658872 | G | A | 1 | a0001c0001t0006g0182 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.443-788C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 5/5 | chr19 | 4658872 | |||||||
chr19:4658945 | A | G | 1 | a0002c0002t0002g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.443-861T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 5/5 | chr19 | 4658945 | |||||||
chr19:4659030 | T | C | 1 | a0001c0006t0001g0136 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.442+901A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 5/5 | chr19 | 4659030 | |||||||
chr19:4659047 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.442+884C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 5/5 | chr19 | 4659047 | |||||||
chr19:4659086 | T | C | 1 | a0001c0001t0001g0248 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.442+845A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 5/5 | chr19 | 4659086 | |||||||
chr19:4659139 | G | A | 1 | a0002c0002t0002g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.442+792C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 5/5 | chr19 | 4659139 | |||||||
chr19:4659160 | C | T | 1 | a0002c0002t0002g0120 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.442+771G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 5/5 | chr19 | 4659160 | |||||||
chr19:4659292 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.442+639T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 5/5 | chr19 | 4659292 | |||||||
chr19:4659313 | T | A | 1 | a0002c0002t0002g0113 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.442+618A>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 5/5 | chr19 | 4659313 | |||||||
chr19:4659466 | C | T | 1 | a0002c0002t0002g0069 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.442+465G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 5/5 | chr19 | 4659466 | |||||||
chr19:4659473 | C | T | 6 | a0002c0002t0002g0069 a0002c0002t0003g0023 a0002c0002t0003g0024 others(3): Show |
8 | HG02145.hp1 HG02630.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.442+458G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 5/5 | chr19 | 4659473 | |||||||
chr19:4659476 | G | A | 2 | a0001c0001t0001g0166 a0001c0001t0001g0186 |
2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.442+455C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 5/5 | chr19 | 4659476 | |||||||
chr19:4659516 | A | G | 97 | a0001c0006t0001g0136 a0002c0002t0002g0012 a0002c0002t0002g0013 others(94): Show |
114 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(111): Show |
intron_variant | MODIFIER | c.442+415T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 5/5 | chr19 | 4659516 | |||||||
chr19:4659598 | A | G | 6 | a0002c0002t0002g0069 a0002c0002t0003g0023 a0002c0002t0003g0024 others(3): Show |
8 | HG02145.hp1 HG02630.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.442+333T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 5/5 | chr19 | 4659598 | |||||||
chr19:4659652 | G | A | 92 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0025 others(89): Show |
107 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(104): Show |
intron_variant | MODIFIER | c.442+279C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 5/5 | chr19 | 4659652 | |||||||
chr19:4659653 | C | T | 5 | a0001c0001t0001g0180 a0002c0003t0002g0011 a0002c0003t0002g0047 others(2): Show |
7 | HG01891.hp1 HG02451.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.442+278G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 5/5 | chr19 | 4659653 | |||||||
chr19:4659654 | G | A | 1 | a0002c0002t0002g0110 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.442+277C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 5/5 | chr19 | 4659654 | |||||||
chr19:4659800 | G | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0257 |
3 | HG02165.hp1 NA19065.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.442+131C>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 5/5 | chr19 | 4659800 | |||||||
chr19:4659912 | C | T | 17 | a0002c0003t0002g0007 a0002c0003t0002g0021 a0002c0003t0002g0045 others(14): Show |
21 | HG01884.hp1 HG02056.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.442+19G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 5/5 | chr19 | 4659912 | |||||||
chr19:4660063 | C | T | 18 | a0001c0001t0001g0010 a0001c0001t0001g0039 a0001c0001t0001g0044 others(15): Show |
23 | HG00438.hp1 HG01081.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.370-60G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 4/5 | chr19 | 4660063 | |||||||
chr19:4660160 | C | A | 1 | a0001c0001t0001g0252 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.370-157G>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 4/5 | chr19 | 4660160 | |||||||
chr19:4660407 | C | T | 21 | a0001c0001t0001g0010 a0001c0001t0001g0039 a0001c0001t0001g0044 others(18): Show |
26 | HG00408.hp1 HG00438.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.369+262G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 4/5 | chr19 | 4660407 | |||||||
chr19:4660483 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.369+186G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 4/5 | chr19 | 4660483 | |||||||
chr19:4660507 | G | A | 1 | a0001c0006t0001g0136 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.369+162C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 4/5 | chr19 | 4660507 | |||||||
chr19:4660606 | T | C | 1 | a0001c0001t0001g0204 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.369+63A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 4/5 | chr19 | 4660606 | |||||||
chr19:4660647 | T | G | 2 | a0001c0001t0001g0227 a0001c0001t0001g0243 |
2 | NA18995.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.369+22A>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 4/5 | chr19 | 4660647 | |||||||
chr19:4660783 | C | T | 3 | a0002c0002t0002g0081 a0002c0002t0002g0100 a0002c0002t0002g0101 |
3 | HG02257.hp2 HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.288-33G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4660783 | |||||||
chr19:4660787 | C | T | 95 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0025 others(92): Show |
112 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(109): Show |
intron_variant | MODIFIER | c.288-37G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4660787 | |||||||
chr19:4660845 | G | T | 1 | a0001c0001t0001g0217 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.288-95C>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4660845 | |||||||
chr19:4660855 | C | G | 1 | a0001c0006t0001g0136 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.288-105G>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4660855 | |||||||
chr19:4660888 | C | T | 5 | a0002c0002t0002g0012 a0002c0002t0002g0074 a0002c0002t0002g0075 others(2): Show |
7 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.288-138G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4660888 | |||||||
chr19:4660894 | C | T | 71 | a0001c0001t0001g0251 a0002c0002t0002g0012 a0002c0002t0002g0013 others(68): Show |
80 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(77): Show |
intron_variant | MODIFIER | c.288-144G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4660894 | |||||||
chr19:4660918 | T | C | 102 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0025 others(99): Show |
120 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(117): Show |
intron_variant | MODIFIER | c.288-168A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4660918 | |||||||
chr19:4660919 | G | A | 102 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0025 others(99): Show |
120 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(117): Show |
intron_variant | MODIFIER | c.288-169C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4660919 | |||||||
chr19:4660933 | C | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0240 |
3 | HG03654.hp1 HG03834.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.288-183G>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4660933 | |||||||
chr19:4660964 | A | AT | 7 | a0002c0002t0002g0013 a0002c0002t0002g0081 a0002c0002t0002g0113 others(4): Show |
9 | HG01167.hp2 HG01515.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.288-215dupA | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4660964 | |||||||
chr19:4660964 | AT | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(157): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.288-215delA | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4660964 | |||||||
chr19:4660964 | ATT | A | 8 | a0001c0001t0001g0037 a0001c0001t0001g0160 a0001c0001t0001g0175 others(5): Show |
9 | HG00438.hp2 HG01070.hp1 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.288-216_288-215del others(2): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4660964 | |||||||
chr19:4661047 | G | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0228 a0001c0001t0001g0256 |
4 | NA18980.hp2 NA18998.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.288-297C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4661047 | |||||||
chr19:4661118 | G | A | 3 | a0002c0002t0002g0117 a0002c0002t0002g0128 a0004c0004t0002g0102 |
3 | HG02015.hp2 HG02027.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.288-368C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4661118 | |||||||
chr19:4661146 | T | C | 1 | a0001c0006t0001g0136 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.288-396A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4661146 | |||||||
chr19:4661220 | C | T | 6 | a0002c0002t0002g0025 a0002c0002t0002g0076 a0002c0002t0002g0077 others(3): Show |
7 | HG01243.hp1 HG02280.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.288-470G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4661220 | |||||||
chr19:4661404 | C | T | 1 | a0002c0002t0002g0099 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.288-654G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4661404 | |||||||
chr19:4661454 | G | A | 1 | a0001c0006t0001g0136 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.288-704C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4661454 | |||||||
chr19:4661548 | C | A | 1 | a0001c0001t0001g0204 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.288-798G>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4661548 | |||||||
chr19:4661756 | A | G | 6 | a0002c0002t0002g0069 a0002c0002t0003g0023 a0002c0002t0003g0024 others(3): Show |
8 | HG02145.hp1 HG02630.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.288-1006T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4661756 | |||||||
chr19:4661972 | G | C | 5 | a0002c0002t0003g0023 a0002c0002t0003g0024 a0002c0002t0003g0084 others(2): Show |
7 | HG02145.hp1 HG02630.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.288-1222C>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4661972 | |||||||
chr19:4661981 | C | G | 1 | a0001c0001t0001g0211 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.288-1231G>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4661981 | |||||||
chr19:4662061 | C | G | 103 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0025 others(100): Show |
121 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(118): Show |
intron_variant | MODIFIER | c.288-1311G>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4662061 | |||||||
chr19:4662138 | C | A | 1 | a0002c0003t0002g0052 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.288-1388G>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4662138 | |||||||
chr19:4662165 | G | A | 2 | a0001c0001t0001g0207 a0001c0001t0001g0229 |
2 | HG01074.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.288-1415C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4662165 | |||||||
chr19:4662187 | C | T | 21 | a0002c0003t0002g0007 a0002c0003t0002g0011 a0002c0003t0002g0021 others(18): Show |
27 | HG01884.hp1 HG01891.hp1 HG02056.hp1 others(24): Show |
intron_variant | MODIFIER | c.288-1437G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4662187 | |||||||
chr19:4662254 | G | C | 1 | a0001c0001t0001g0171 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.288-1504C>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4662254 | |||||||
chr19:4662280 | T | G | 1 | a0002c0002t0002g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.288-1530A>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4662280 | |||||||
chr19:4662311 | A | C | 2 | a0001c0001t0001g0151 a0001c0001t0001g0197 |
2 | HG00438.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.288-1561T>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4662311 | |||||||
chr19:4662383 | G | C | 3 | a0001c0001t0001g0038 a0001c0001t0001g0228 a0001c0001t0001g0256 |
4 | NA18980.hp2 NA18998.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.288-1633C>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4662383 | |||||||
chr19:4662416 | C | A | 4 | a0002c0002t0002g0028 a0002c0002t0002g0116 a0002c0002t0002g0122 others(1): Show |
5 | NA18947.hp1 NA18953.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.288-1666G>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4662416 | |||||||
chr19:4662428 | C | T | 6 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0159 others(3): Show |
10 | HG00642.hp1 HG01070.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.288-1678G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4662428 | |||||||
chr19:4662450 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.288-1700G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4662450 | |||||||
chr19:4662564 | G | C | 1 | a0001c0001t0001g0167 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.288-1814C>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4662564 | |||||||
chr19:4662583 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.288-1833C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4662583 | |||||||
chr19:4662790 | C | G | 1 | a0002c0002t0002g0081 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.288-2040G>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4662790 | |||||||
chr19:4662847 | G | C | 1 | a0002c0002t0002g0073 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.287+2029C>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4662847 | |||||||
chr19:4662852 | C | G | 1 | a0001c0001t0001g0233 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.287+2024G>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4662852 | |||||||
chr19:4662926 | C | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0149 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.287+1950G>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4662926 | |||||||
chr19:4663024 | C | T | 1 | a0003c0007t0001g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.287+1852G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663024 | |||||||
chr19:4663034 | G | GTCCTCAT others(80): Show |
1 | a0001c0001t0001g0209 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.287+1841_287+1842i others(89): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663034 | |||||||
chr19:4663075 | T | C | 1 | a0001c0001t0001g0195 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.287+1801A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663075 | |||||||
chr19:4663076 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.287+1800G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663076 | |||||||
chr19:4663098 | G | A | 22 | a0001c0001t0001g0195 a0002c0003t0002g0007 a0002c0003t0002g0011 others(19): Show |
28 | HG01884.hp1 HG01891.hp1 HG02056.hp1 others(25): Show |
intron_variant | MODIFIER | c.287+1778C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663098 | |||||||
chr19:4663100 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.287+1776A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663100 | |||||||
chr19:4663105 | A | C | 1 | a0001c0001t0001g0195 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.287+1771T>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663105 | |||||||
chr19:4663106 | T | C | 1 | a0001c0001t0001g0195 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.287+1770A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663106 | |||||||
chr19:4663116 | A | G | 1 | a0001c0001t0001g0195 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.287+1760T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663116 | |||||||
chr19:4663117 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.287+1759G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663117 | |||||||
chr19:4663119 | T | C | 1 | a0001c0001t0001g0195 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.287+1757A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663119 | |||||||
chr19:4663119 | T | TCATCCTC others(124): Show |
7 | a0002c0002t0002g0026 a0002c0002t0002g0028 a0002c0002t0002g0081 others(4): Show |
9 | HG02257.hp2 HG02622.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.287+1756_287+1757i others(133): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663119 | |||||||
chr19:4663119 | T | TCATCCTC others(167): Show |
5 | a0002c0002t0002g0013 a0002c0002t0002g0087 a0002c0002t0002g0089 others(2): Show |
7 | HG01109.hp1 HG01167.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.287+1756_287+1757i others(176): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663119 | |||||||
chr19:4663119 | T | TCATCCTC others(341): Show |
1 | a0002c0002t0002g0074 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.287+1756_287+1757i others(350): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663119 | |||||||
chr19:4663119 | T | TCATCCTC others(570): Show |
1 | a0002c0002t0002g0094 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.287+1756_287+1757i others(579): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663119 | |||||||
chr19:4663119 | T | TCATCCTC others(615): Show |
5 | a0002c0002t0002g0090 a0002c0002t0002g0092 a0002c0002t0002g0093 others(2): Show |
5 | HG02109.hp2 HG02818.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.287+1756_287+1757i others(624): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663119 | |||||||
chr19:4663119 | T | TCATCCTC others(343): Show |
1 | a0002c0002t0002g0131 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.287+1756_287+1757i others(352): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663119 | |||||||
chr19:4663119 | T | TCATCCTC others(300): Show |
2 | a0002c0002t0002g0105 a0002c0002t0008g0106 |
2 | NA18974.hp1 NA19059.hp1 |
intron_variant | MODIFIER | c.287+1756_287+1757i others(309): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663119 | |||||||
chr19:4663119 | T | TCATCCTC others(255): Show |
10 | a0002c0002t0002g0029 a0002c0002t0002g0104 a0002c0002t0002g0109 others(7): Show |
11 | HG02040.hp2 HG02155.hp1 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.287+1756_287+1757i others(264): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663119 | |||||||
chr19:4663119 | T | TCATCCTC others(255): Show |
1 | a0002c0002t0002g0075 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.287+1756_287+1757i others(264): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663119 | |||||||
chr19:4663119 | T | TCATCCTC others(255): Show |
2 | a0002c0002t0002g0012 a0002c0002t0009g0072 |
4 | HG01891.hp2 HG02486.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.287+1756_287+1757i others(264): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663119 | |||||||
chr19:4663119 | T | TCATCCTC others(386): Show |
1 | a0002c0002t0002g0082 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.287+1756_287+1757i others(395): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663119 | |||||||
chr19:4663119 | T | TCATCCTC others(124): Show |
1 | a0002c0002t0002g0119 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.287+1756_287+1757i others(133): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663119 | |||||||
chr19:4663119 | T | TCATCCTC others(432): Show |
1 | a0002c0002t0002g0111 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.287+1756_287+1757i others(441): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663119 | |||||||
chr19:4663120 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.287+1756G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663120 | |||||||
chr19:4663121 | A | ATCCTCAT others(212): Show |
1 | a0001c0001t0001g0183 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.287+1754_287+1755i others(221): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663121 | |||||||
chr19:4663121 | A | G | 1 | a0001c0001t0001g0195 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.287+1755T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663121 | |||||||
chr19:4663131 | T | TACAGCCT others(38): Show |
1 | a0001c0001t0001g0237 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.287+1700_287+1744d others(47): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663131 | |||||||
chr19:4663131 | T | TACAGCCT others(38): Show |
1 | a0001c0001t0001g0140 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.287+1744_287+1745i others(47): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663131 | |||||||
chr19:4663131 | TACAGCCT others(38): Show |
T | 2 | a0001c0001t0001g0196 a0002c0002t0002g0121 |
2 | HG00609.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.287+1700_287+1744d others(47): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663131 | |||||||
chr19:4663136 | C | CCTCCAAT others(124): Show |
2 | a0002c0002t0002g0100 a0002c0002t0002g0101 |
2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.287+1739_287+1740i others(133): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663136 | |||||||
chr19:4663164 | G | GTCCTCAT others(388): Show |
1 | a0002c0002t0002g0091 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.287+1711_287+1712i others(397): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663164 | |||||||
chr19:4663164 | G | GTCCTCAT others(257): Show |
1 | a0002c0002t0002g0099 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.287+1711_287+1712i others(266): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663164 | |||||||
chr19:4663164 | G | GTCCTCAT others(384): Show |
1 | a0002c0002t0002g0098 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.287+1711_287+1712i others(393): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663164 | |||||||
chr19:4663176 | C | CACAGCCT others(36): Show |
2 | a0001c0001t0001g0195 a0001c0006t0001g0136 |
2 | NA19009.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.287+1699_287+1700i others(45): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663176 | |||||||
chr19:4663176 | C | CACAGCCT others(79): Show |
5 | a0002c0002t0002g0088 a0002c0003t0002g0046 a0002c0003t0002g0054 others(2): Show |
5 | HG02258.hp1 HG02273.hp1 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.287+1699_287+1700i others(88): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663176 | |||||||
chr19:4663176 | C | CACAGCCT others(210): Show |
3 | a0002c0002t0002g0114 a0002c0002t0002g0117 a0002c0002t0002g0128 |
3 | HG02015.hp2 HG02027.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.287+1699_287+1700i others(219): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663176 | |||||||
chr19:4663176 | C | CACAGCCT others(429): Show |
2 | a0002c0002t0002g0118 a0002c0002t0002g0126 |
2 | HG02132.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.287+1699_287+1700i others(438): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663176 | |||||||
chr19:4663181 | C | CCTCCAAT others(167): Show |
1 | a0002c0003t0002g0049 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.287+1694_287+1695i others(176): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663181 | |||||||
chr19:4663181 | C | CCTCCAAT others(124): Show |
14 | a0002c0003t0002g0007 a0002c0003t0002g0011 a0002c0003t0002g0021 others(11): Show |
20 | HG01884.hp1 HG01891.hp1 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.287+1694_287+1695i others(133): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663181 | |||||||
chr19:4663193 | C | CCTCCCCA others(432): Show |
1 | a0001c0001t0001g0172 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.287+1682_287+1683i others(441): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663193 | |||||||
chr19:4663200 | A | ATCCAC | 2 | a0002c0002t0002g0025 a0002c0002t0002g0112 |
3 | HG03453.hp1 HG03579.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.287+1675_287+1676i others(7): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663200 | |||||||
chr19:4663201 | C | T | 20 | a0002c0002t0002g0069 a0002c0002t0002g0073 a0002c0002t0002g0076 others(17): Show |
22 | HG01243.hp1 HG02145.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.287+1675G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663201 | |||||||
chr19:4663204 | G | A | 21 | a0001c0001t0001g0172 a0002c0002t0002g0069 a0002c0002t0002g0073 others(18): Show |
23 | HG01243.hp1 HG02145.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.287+1672C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663204 | |||||||
chr19:4663205 | T | C | 21 | a0001c0001t0001g0172 a0002c0002t0002g0069 a0002c0002t0002g0073 others(18): Show |
23 | HG01243.hp1 HG02145.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.287+1671A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663205 | |||||||
chr19:4663208 | T | C | 21 | a0001c0001t0001g0172 a0002c0002t0002g0069 a0002c0002t0002g0073 others(18): Show |
23 | HG01243.hp1 HG02145.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.287+1668A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663208 | |||||||
chr19:4663208 | T | TCATTCTA others(119): Show |
1 | a0002c0002t0002g0112 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.287+1667_287+1668i others(128): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663208 | |||||||
chr19:4663208 | T | TCATTCTA others(466): Show |
1 | a0002c0002t0002g0025 | 2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.287+1667_287+1668i others(475): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663208 | |||||||
chr19:4663209 | G | A | 4 | a0001c0001t0001g0172 a0002c0002t0002g0025 a0002c0002t0002g0112 others(1): Show |
5 | HG02717.hp2 HG03453.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.287+1667C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663209 | |||||||
chr19:4663213 | T | A | 41 | a0001c0001t0001g0140 a0001c0001t0001g0148 a0002c0002t0002g0012 others(38): Show |
52 | HG01109.hp1 HG01167.hp2 HG01515.hp1 others(49): Show |
intron_variant | MODIFIER | c.287+1663A>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663213 | |||||||
chr19:4663213 | T | TCATTCTA others(38): Show |
21 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0031 others(18): Show |
28 | HG00733.hp1 HG01192.hp1 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.287+1662_287+1663i others(47): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663213 | |||||||
chr19:4663219 | TAC | T | 17 | a0002c0002t0002g0069 a0002c0002t0002g0076 a0002c0002t0002g0077 others(14): Show |
19 | HG01243.hp1 HG02145.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.287+1655_287+1656d others(4): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663219 | |||||||
chr19:4663221 | C | CACAGCCT others(36): Show |
1 | a0001c0001t0001g0254 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.287+1612_287+1654d others(45): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663221 | |||||||
chr19:4663221 | C | CAGCCTCC others(122): Show |
1 | a0002c0002t0002g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.287+1654_287+1655i others(131): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663221 | |||||||
chr19:4663221 | C | CAGCCTCC others(298): Show |
1 | a0002c0003t0002g0047 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.287+1654_287+1655i others(307): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663221 | |||||||
chr19:4663221 | C | CAGCCTCC others(77): Show |
1 | a0002c0002t0002g0073 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.287+1654_287+1655i others(86): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663221 | |||||||
chr19:4663223 | C | A | 1 | a0001c0001t0001g0172 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.287+1653G>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663223 | |||||||
chr19:4663226 | C | CCTCCAAT others(345): Show |
1 | a0004c0004t0002g0102 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.287+1649_287+1650i others(354): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663226 | |||||||
chr19:4663226 | C | CCTCCAAT others(124): Show |
1 | a0002c0003t0002g0053 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.287+1649_287+1650i others(133): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663226 | |||||||
chr19:4663226 | C | T | 68 | a0001c0001t0001g0195 a0002c0002t0002g0012 a0002c0002t0002g0013 others(65): Show |
82 | HG00597.hp1 HG01109.hp1 HG01167.hp2 others(79): Show |
intron_variant | MODIFIER | c.287+1650G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663226 | |||||||
chr19:4663245 | A | ACCCGTCC others(256): Show |
1 | a0002c0003t0002g0058 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.287+1630_287+1631i others(265): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663245 | |||||||
chr19:4663245 | A | ATCCACCC others(387): Show |
1 | a0002c0003t0002g0046 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.287+1630_287+1631i others(396): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663245 | |||||||
chr19:4663246 | C | CCCGTCCT others(127): Show |
1 | a0002c0002t0002g0088 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.287+1629_287+1630i others(136): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663246 | |||||||
chr19:4663246 | C | T | 1 | a0002c0002t0002g0121 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.287+1630G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663246 | |||||||
chr19:4663249 | A | G | 1 | a0001c0001t0001g0223 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.287+1627T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663249 | |||||||
chr19:4663250 | C | T | 1 | a0001c0001t0001g0223 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.287+1626G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663250 | |||||||
chr19:4663253 | C | T | 1 | a0001c0001t0001g0223 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.287+1623G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663253 | |||||||
chr19:4663254 | A | G | 1 | a0001c0001t0001g0223 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.287+1622T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663254 | |||||||
chr19:4663263 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.287+1613G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663263 | |||||||
chr19:4663266 | CAGCCTCC others(80): Show |
C | 1 | a0001c0001t0001g0223 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.287+1523_287+1609d others(89): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663266 | |||||||
chr19:4663272 | C | T | 1 | a0002c0002t0002g0121 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.287+1604G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663272 | |||||||
chr19:4663277 | CTG | C | 14 | a0002c0002t0002g0025 a0002c0002t0002g0076 a0002c0002t0002g0077 others(11): Show |
15 | HG00609.hp1 HG01243.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.287+1597_287+1598d others(4): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663277 | |||||||
chr19:4663281 | G | A | 14 | a0002c0002t0002g0025 a0002c0002t0002g0076 a0002c0002t0002g0077 others(11): Show |
15 | HG00609.hp1 HG01243.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.287+1595C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663281 | |||||||
chr19:4663286 | CTCCACCC others(37): Show |
C | 1 | a0002c0002t0002g0085 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.287+1546_287+1589d others(46): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663286 | |||||||
chr19:4663287 | T | C | 13 | a0002c0002t0002g0025 a0002c0002t0002g0076 a0002c0002t0002g0077 others(10): Show |
14 | HG00609.hp1 HG01243.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.287+1589A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663287 | |||||||
chr19:4663293 | C | T | 1 | a0002c0002t0002g0125 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.287+1583G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663293 | |||||||
chr19:4663294 | A | G | 7 | a0002c0002t0002g0086 a0002c0002t0002g0088 a0002c0002t0002g0091 others(4): Show |
7 | HG02630.hp2 HG02647.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.287+1582T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663294 | |||||||
chr19:4663295 | T | C | 10 | a0002c0002t0002g0025 a0002c0002t0002g0076 a0002c0002t0002g0077 others(7): Show |
11 | HG00609.hp1 HG01243.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.287+1581A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663295 | |||||||
chr19:4663298 | C | T | 5 | a0002c0002t0002g0086 a0002c0002t0002g0103 a0002c0002t0002g0107 others(2): Show |
5 | HG02647.hp2 NA18946.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.287+1578G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663298 | |||||||
chr19:4663299 | A | G | 5 | a0002c0002t0002g0086 a0002c0002t0002g0103 a0002c0002t0002g0107 others(2): Show |
5 | HG02647.hp2 NA18946.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.287+1577T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663299 | |||||||
chr19:4663300 | T | C | 1 | a0002c0002t0002g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.287+1576A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663300 | |||||||
chr19:4663328 | G | C | 6 | a0002c0002t0002g0083 a0002c0002t0002g0086 a0002c0002t0002g0103 others(3): Show |
6 | HG02647.hp2 HG02965.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.287+1548C>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663328 | |||||||
chr19:4663330 | T | TC | 6 | a0002c0002t0002g0083 a0002c0002t0002g0086 a0002c0002t0002g0103 others(3): Show |
6 | HG02647.hp2 HG02965.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.287+1545dupG | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663330 | |||||||
chr19:4663335 | T | C | 4 | a0002c0002t0002g0083 a0002c0002t0002g0085 a0002c0002t0002g0086 others(1): Show |
4 | HG02572.hp2 HG02647.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.287+1541A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663335 | |||||||
chr19:4663335 | T | TCCACCCC others(124): Show |
1 | a0002c0003t0002g0047 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.287+1540_287+1541i others(133): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663335 | |||||||
chr19:4663338 | A | G | 2 | a0002c0002t0002g0086 a0002c0002t0002g0130 |
2 | HG02647.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.287+1538T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663338 | |||||||
chr19:4663339 | C | T | 2 | a0002c0002t0002g0086 a0002c0002t0002g0130 |
2 | HG02647.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.287+1537G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663339 | |||||||
chr19:4663342 | C | T | 2 | a0002c0002t0002g0086 a0002c0002t0002g0130 |
2 | HG02647.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.287+1534G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663342 | |||||||
chr19:4663343 | A | G | 3 | a0002c0002t0002g0086 a0002c0002t0002g0107 a0002c0002t0002g0130 |
3 | HG02647.hp2 NA18946.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.287+1533T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663343 | |||||||
chr19:4663347 | T | A | 1 | a0002c0002t0002g0086 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.287+1529A>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663347 | |||||||
chr19:4663353 | T | TAC | 3 | a0001c0001t0001g0229 a0002c0002t0002g0086 a0002c0002t0002g0130 |
3 | HG02647.hp2 HG03492.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.287+1521_287+1522d others(4): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663353 | |||||||
chr19:4663358 | C | T | 2 | a0002c0002t0002g0086 a0002c0002t0002g0130 |
2 | HG02647.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.287+1518G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663358 | |||||||
chr19:4663359 | A | C | 9 | a0001c0001t0001g0223 a0001c0001t0001g0229 a0002c0002t0002g0083 others(6): Show |
9 | HG02572.hp2 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.287+1517T>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663359 | |||||||
chr19:4663361 | C | T | 2 | a0002c0002t0002g0103 a0002c0002t0002g0129 |
2 | NA18963.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.287+1515G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663361 | |||||||
chr19:4663370 | T | C | 9 | a0001c0001t0001g0223 a0001c0001t0001g0229 a0002c0002t0002g0083 others(6): Show |
9 | HG02572.hp2 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.287+1506A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663370 | |||||||
chr19:4663370 | T | TCTCCCCA others(36): Show |
1 | a0001c0001t0001g0164 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.287+1505_287+1506i others(45): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663370 | |||||||
chr19:4663370 | T | TCTCCCCA others(124): Show |
1 | a0002c0002t0002g0125 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.287+1505_287+1506i others(133): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663370 | |||||||
chr19:4663376 | CACCT | C | 19 | a0002c0002t0002g0027 a0002c0002t0002g0028 a0002c0002t0002g0104 others(16): Show |
21 | HG00609.hp1 HG02015.hp2 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.287+1496_287+1499d others(6): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663376 | |||||||
chr19:4663380 | T | C | 11 | a0001c0001t0001g0223 a0002c0002t0002g0083 a0002c0002t0002g0085 others(8): Show |
11 | HG02572.hp2 HG02647.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.287+1496A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663380 | |||||||
chr19:4663381 | A | G | 1 | a0002c0002t0002g0085 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.287+1495T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663381 | |||||||
chr19:4663382 | C | T | 1 | a0002c0002t0002g0085 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.287+1494G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663382 | |||||||
chr19:4663385 | C | T | 1 | a0002c0002t0002g0085 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.287+1491G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663385 | |||||||
chr19:4663386 | A | G | 1 | a0002c0002t0002g0085 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.287+1490T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663386 | |||||||
chr19:4663387 | T | C | 1 | a0002c0002t0002g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.287+1489A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663387 | |||||||
chr19:4663396 | TAC | T | 6 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0002c0002t0002g0083 others(3): Show |
6 | HG02647.hp2 HG02683.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.287+1478_287+1479d others(4): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663396 | |||||||
chr19:4663397 | A | G | 1 | a0002c0002t0002g0125 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.287+1479T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663397 | |||||||
chr19:4663398 | C | CAGCCTCC others(169): Show |
1 | a0002c0002t0002g0103 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.287+1477_287+1478i others(178): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663398 | |||||||
chr19:4663398 | C | CAGCCTCC others(124): Show |
1 | a0002c0002t0002g0129 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.287+1477_287+1478i others(133): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663398 | |||||||
chr19:4663398 | C | CAGCCTCC others(255): Show |
1 | a0002c0002t0002g0107 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.287+1477_287+1478i others(264): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663398 | |||||||
chr19:4663404 | C | A | 1 | a0002c0005t0001g0108 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.287+1472G>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663404 | |||||||
chr19:4663410 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.287+1466A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663410 | |||||||
chr19:4663410 | T | TCTACCTT others(32): Show |
1 | a0002c0003t0002g0021 | 2 | NA19060.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.287+1465_287+1466i others(41): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663410 | |||||||
chr19:4663411 | CTG | C | 5 | a0001c0001t0001g0244 a0002c0002t0002g0083 a0002c0002t0002g0085 others(2): Show |
5 | HG02572.hp2 HG02965.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.287+1463_287+1464d others(4): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663411 | |||||||
chr19:4663415 | G | A | 5 | a0001c0001t0001g0244 a0002c0002t0002g0083 a0002c0002t0002g0085 others(2): Show |
5 | HG02572.hp2 HG02965.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.287+1461C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663415 | |||||||
chr19:4663417 | C | A | 2 | a0001c0001t0001g0222 a0002c0003t0002g0021 |
3 | HG02683.hp2 NA19060.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.287+1459G>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663417 | |||||||
chr19:4663417 | C | T | 1 | a0002c0005t0001g0108 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.287+1459G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663417 | |||||||
chr19:4663421 | T | C | 5 | a0001c0001t0001g0244 a0002c0002t0002g0083 a0002c0002t0002g0085 others(2): Show |
5 | HG02572.hp2 HG02965.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.287+1455A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663421 | |||||||
chr19:4663421 | T | TCCACCCA others(173): Show |
1 | a0001c0001t0001g0229 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.287+1454_287+1455i others(182): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663421 | |||||||
chr19:4663421 | T | TCCACCCA others(79): Show |
6 | a0002c0002t0002g0025 a0002c0002t0002g0076 a0002c0002t0002g0077 others(3): Show |
7 | HG01243.hp1 HG02280.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.287+1454_287+1455i others(88): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663421 | |||||||
chr19:4663427 | C | T | 2 | a0002c0002t0002g0107 a0002c0005t0001g0108 |
2 | NA18984.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.287+1449G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663427 | |||||||
chr19:4663428 | A | G | 1 | a0002c0002t0002g0085 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.287+1448T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663428 | |||||||
chr19:4663429 | C | T | 5 | a0001c0001t0001g0210 a0002c0002t0002g0085 a0002c0002t0002g0086 others(2): Show |
5 | HG02572.hp2 HG02647.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.287+1447G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663429 | |||||||
chr19:4663432 | C | T | 1 | a0002c0002t0002g0085 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.287+1444G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663432 | |||||||
chr19:4663433 | A | G | 1 | a0002c0002t0002g0085 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.287+1443T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663433 | |||||||
chr19:4663434 | TCCTCATT others(124): Show |
T | 4 | a0001c0001t0001g0193 a0001c0001t0001g0221 a0001c0001t0001g0222 others(1): Show |
4 | HG02523.hp2 HG02683.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.287+1311_287+1441d others(2): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663434 | |||||||
chr19:4663437 | T | A | 1 | a0002c0002t0002g0085 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.287+1439A>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663437 | |||||||
chr19:4663445 | C | CACAGCCT others(122): Show |
1 | a0001c0001t0001g0169 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.287+1430_287+1431i others(131): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663445 | |||||||
chr19:4663445 | C | CAGCCTCC others(944): Show |
1 | a0002c0002t0002g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.287+1430_287+1431i others(953): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663445 | |||||||
chr19:4663445 | C | CAGCCTCC others(80): Show |
1 | a0002c0002t0002g0081 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.287+1430_287+1431i others(89): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663445 | |||||||
chr19:4663450 | C | T | 2 | a0002c0002t0002g0085 a0002c0003t0002g0021 |
2 | HG02572.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.287+1426G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663450 | |||||||
chr19:4663451 | C | A | 1 | a0002c0002t0002g0081 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.287+1425G>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663451 | |||||||
chr19:4663451 | C | CTCCAATC others(35): Show |
3 | a0002c0002t0002g0107 a0002c0002t0002g0129 a0002c0002t0002g0130 |
3 | NA18946.hp2 NA18969.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.287+1424_287+1425i others(44): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663451 | |||||||
chr19:4663458 | C | CTG | 3 | a0002c0002t0002g0100 a0002c0002t0002g0101 a0002c0005t0001g0108 |
3 | HG02451.hp1 HG02622.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.287+1417_287+1418i others(4): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663458 | |||||||
chr19:4663460 | A | G | 3 | a0002c0002t0002g0100 a0002c0002t0002g0101 a0002c0005t0001g0108 |
3 | HG02451.hp1 HG02622.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.287+1416T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663460 | |||||||
chr19:4663461 | CCCTCCCC others(79): Show |
C | 2 | a0002c0002t0002g0027 a0002c0002t0002g0127 |
3 | NA18954.hp1 NA18977.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.287+1329_287+1414d others(88): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663461 | |||||||
chr19:4663462 | C | G | 2 | a0001c0001t0001g0210 a0002c0002t0002g0086 |
2 | HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.287+1414G>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663462 | |||||||
chr19:4663462 | C | T | 4 | a0002c0002t0002g0081 a0002c0002t0002g0107 a0002c0002t0002g0129 others(1): Show |
4 | HG02257.hp2 NA18946.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.287+1414G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663462 | |||||||
chr19:4663463 | C | T | 48 | a0001c0001t0001g0226 a0001c0001t0001g0247 a0002c0002t0002g0025 others(45): Show |
57 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(54): Show |
intron_variant | MODIFIER | c.287+1413G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663463 | |||||||
chr19:4663465 | C | CCCCA | 3 | a0002c0002t0002g0085 a0002c0002t0002g0125 a0002c0003t0002g0021 |
4 | HG02572.hp2 NA19060.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.287+1407_287+1410d others(6): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663465 | |||||||
chr19:4663465 | C | CTCCACCC others(44): Show |
1 | a0002c0002t0002g0101 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.287+1410_287+1411i others(53): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663465 | |||||||
chr19:4663472 | C | CACCCCAT others(81): Show |
1 | a0002c0002t0002g0114 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.287+1403_287+1404i others(90): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663472 | |||||||
chr19:4663475 | T | C | 1 | a0002c0003t0002g0021 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.287+1401A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663475 | |||||||
chr19:4663484 | T | TAC | 8 | a0002c0002t0002g0081 a0002c0002t0002g0100 a0002c0002t0002g0101 others(5): Show |
8 | HG02257.hp2 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.287+1390_287+1391d others(4): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663484 | |||||||
chr19:4663484 | T | TACAGCAT others(38): Show |
2 | a0001c0001t0001g0210 a0002c0002t0002g0086 |
2 | HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.287+1391_287+1392i others(47): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663484 | |||||||
chr19:4663495 | ACC | A | 4 | a0002c0002t0002g0083 a0002c0002t0002g0125 a0002c0003t0002g0021 others(1): Show |
4 | HG02965.hp1 NA19060.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.287+1379_287+1380d others(4): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663495 | |||||||
chr19:4663496 | C | T | 11 | a0001c0001t0001g0210 a0002c0002t0002g0081 a0002c0002t0002g0085 others(8): Show |
11 | HG02257.hp2 HG02451.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.287+1380G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663496 | |||||||
chr19:4663497 | C | CTACCCTC others(210): Show |
1 | a0002c0003t0002g0021 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.287+1378_287+1379i others(219): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663497 | |||||||
chr19:4663499 | G | C | 4 | a0002c0002t0002g0083 a0002c0002t0002g0125 a0002c0003t0002g0021 others(1): Show |
5 | HG02965.hp1 NA19060.hp1 NA19064.hp1 others(2): Show |
intron_variant | MODIFIER | c.287+1377C>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663499 | |||||||
chr19:4663501 | G | A | 4 | a0002c0002t0002g0083 a0002c0002t0002g0125 a0002c0003t0002g0021 others(1): Show |
5 | HG02965.hp1 NA19060.hp1 NA19064.hp1 others(2): Show |
intron_variant | MODIFIER | c.287+1375C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663501 | |||||||
chr19:4663503 | A | ACTCTCCA others(214): Show |
1 | a0001c0001t0001g0142 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.287+1372_287+1373i others(223): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663503 | |||||||
chr19:4663503 | A | C | 15 | a0001c0001t0001g0210 a0002c0002t0002g0073 a0002c0002t0002g0081 others(12): Show |
16 | HG02257.hp2 HG02451.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.287+1373T>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663503 | |||||||
chr19:4663503 | ACTCTCCA others(83): Show |
A | 1 | a0001c0001t0001g0001 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.287+1283_287+1372d others(92): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663503 | |||||||
chr19:4663507 | T | C | 4 | a0002c0002t0002g0083 a0002c0002t0002g0125 a0002c0003t0002g0021 others(1): Show |
5 | HG02965.hp1 NA19060.hp1 NA19064.hp1 others(2): Show |
intron_variant | MODIFIER | c.287+1369A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663507 | |||||||
chr19:4663507 | T | TCCACCCA others(38): Show |
2 | a0001c0001t0001g0001 a0002c0002t0002g0114 |
2 | HG00140.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.287+1368_287+1369i others(47): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663507 | |||||||
chr19:4663507 | T | TCCACCCA others(128): Show |
1 | a0001c0001t0001g0229 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.287+1368_287+1369i others(137): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663507 | |||||||
chr19:4663507 | T | TCCACCCA others(255): Show |
1 | a0002c0003t0001g0067 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.287+1368_287+1369i others(264): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663507 | |||||||
chr19:4663507 | T | TCCACCCA others(480): Show |
1 | a0001c0001t0001g0144 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.287+1368_287+1369i others(489): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663507 | |||||||
chr19:4663507 | T | TCCACCCA others(253): Show |
1 | a0001c0001t0001g0277 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.287+1368_287+1369i others(262): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663507 | |||||||
chr19:4663507 | T | TCCACCCA others(257): Show |
1 | a0001c0001t0001g0008 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.287+1368_287+1369i others(266): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663507 | |||||||
chr19:4663507 | T | TCCACCCA others(167): Show |
7 | a0001c0001t0001g0014 a0001c0001t0001g0139 a0001c0001t0001g0141 others(4): Show |
8 | HG00733.hp1 HG01928.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.287+1368_287+1369i others(176): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663507 | |||||||
chr19:4663507 | T | TCCACCCA others(345): Show |
1 | a0001c0001t0001g0278 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.287+1368_287+1369i others(354): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663507 | |||||||
chr19:4663507 | T | TCCACCCA others(257): Show |
1 | a0002c0003t0001g0063 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.287+1368_287+1369i others(266): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663507 | |||||||
chr19:4663507 | T | TCCACCCA others(343): Show |
1 | a0001c0001t0001g0008 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.287+1368_287+1369i others(352): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663507 | |||||||
chr19:4663515 | C | T | 2 | a0001c0001t0001g0252 a0002c0002t0002g0085 |
2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.287+1361G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663515 | |||||||
chr19:4663519 | A | ATCCTCAT others(36): Show |
1 | a0001c0001t0001g0198 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.287+1356_287+1357i others(45): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663519 | |||||||
chr19:4663520 | T | C | 1 | a0002c0002t0002g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.287+1356A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663520 | |||||||
chr19:4663520 | TCCTCATT others(38): Show |
T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(97): Show |
168 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.287+1311_287+1355d others(47): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663520 | |||||||
chr19:4663529 | TAC | T | 6 | a0001c0001t0001g0230 a0002c0002t0002g0025 a0002c0002t0002g0078 others(3): Show |
7 | HG01361.hp1 HG02273.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.287+1345_287+1346d others(4): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663529 | |||||||
chr19:4663531 | C | CACAGCCT others(36): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0178 |
2 | HG00140.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.287+1344_287+1345i others(45): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663531 | |||||||
chr19:4663531 | C | CACAGCCT others(122): Show |
1 | a0001c0006t0001g0136 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.287+1344_287+1345i others(131): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663531 | |||||||
chr19:4663531 | C | CACAGCCT others(165): Show |
1 | a0001c0001t0001g0002 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.287+1344_287+1345i others(174): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663531 | |||||||
chr19:4663531 | C | CACAGCCT others(480): Show |
1 | a0002c0003t0001g0066 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.287+1344_287+1345i others(489): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663531 | |||||||
chr19:4663531 | C | CACAGCCT others(122): Show |
2 | a0001c0001t0001g0008 a0001c0001t0001g0140 |
3 | HG03688.hp2 HG04199.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.287+1344_287+1345i others(131): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663531 | |||||||
chr19:4663531 | C | CACAGCCT others(208): Show |
1 | a0002c0003t0001g0068 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.287+1344_287+1345i others(217): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663531 | |||||||
chr19:4663531 | C | CACAGCCT others(165): Show |
2 | a0002c0003t0001g0022 a0002c0003t0001g0065 |
2 | HG02135.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.287+1344_287+1345i others(174): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663531 | |||||||
chr19:4663531 | C | CACAGCCT others(566): Show |
1 | a0002c0003t0001g0022 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.287+1344_287+1345i others(575): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663531 | |||||||
chr19:4663531 | C | CACAGCCT others(1082): Show |
1 | a0002c0003t0001g0064 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.287+1344_287+1345i others(1091): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663531 | |||||||
chr19:4663531 | C | CACAGCCT others(379): Show |
1 | a0002c0003t0002g0046 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.287+1344_287+1345i others(388): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663531 | |||||||
chr19:4663531 | C | CACAGCCT others(440): Show |
1 | a0002c0002t0002g0100 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.287+1344_287+1345i others(449): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663531 | |||||||
chr19:4663531 | C | CAGCCTCC others(333): Show |
1 | a0002c0003t0002g0058 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.287+1344_287+1345i others(342): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663531 | |||||||
chr19:4663531 | C | CAGCCTCC others(77): Show |
1 | a0001c0001t0001g0019 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.287+1344_287+1345i others(86): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663531 | |||||||
chr19:4663533 | C | CAGCCTCC others(167): Show |
1 | a0001c0001t0001g0044 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.287+1342_287+1343i others(176): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663533 | |||||||
chr19:4663543 | T | C | 1 | a0001c0001t0001g0019 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.287+1333A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663543 | |||||||
chr19:4663546 | A | ACGCTCCC others(82): Show |
1 | a0001c0001t0001g0252 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.287+1329_287+1330i others(91): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663546 | |||||||
chr19:4663546 | A | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0230 |
2 | HG01361.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.287+1330T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663546 | |||||||
chr19:4663547 | T | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(137): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.287+1329A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663547 | |||||||
chr19:4663547 | T | TCCTCCCC others(79): Show |
1 | a0001c0001t0001g0147 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.287+1328_287+1329i others(88): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663547 | |||||||
chr19:4663548 | C | A | 1 | a0001c0001t0001g0019 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.287+1328G>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663548 | |||||||
chr19:4663548 | C | CCTCCCCA others(34): Show |
5 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0167 others(2): Show |
7 | HG00639.hp2 HG01074.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.287+1327_287+1328i others(43): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663548 | |||||||
chr19:4663548 | C | T | 1 | a0002c0003t0002g0062 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.287+1328G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663548 | |||||||
chr19:4663552 | C | CCCACCCA others(79): Show |
1 | a0001c0001t0001g0204 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.287+1323_287+1324i others(88): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663552 | |||||||
chr19:4663552 | C | CCCACCCA others(210): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0002 |
2 | HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.287+1323_287+1324i others(219): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663552 | |||||||
chr19:4663552 | C | CCCACCCA others(522): Show |
1 | a0002c0002t0002g0109 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.287+1323_287+1324i others(531): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663552 | |||||||
chr19:4663552 | C | CCCACCCC others(34): Show |
10 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0146 others(7): Show |
10 | HG02300.hp2 HG02717.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.287+1323_287+1324i others(43): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663552 | |||||||
chr19:4663552 | C | CCCACCCC others(518): Show |
1 | a0001c0001t0001g0166 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.287+1323_287+1324i others(527): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663552 | |||||||
chr19:4663552 | C | CCCACCCC others(604): Show |
1 | a0001c0001t0001g0004 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.287+1323_287+1324i others(613): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663552 | |||||||
chr19:4663552 | C | CCCACCCC others(214): Show |
1 | a0001c0001t0001g0014 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.287+1323_287+1324i others(223): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663552 | |||||||
chr19:4663552 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0230 a0001c0001t0001g0252 |
3 | HG01361.hp1 HG01496.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.287+1324G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663552 | |||||||
chr19:4663556 | C | T | 1 | a0002c0002t0002g0085 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.287+1320G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663556 | |||||||
chr19:4663558 | C | T | 1 | a0002c0003t0002g0062 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.287+1318G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663558 | |||||||
chr19:4663559 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.287+1317T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663559 | |||||||
chr19:4663560 | C | T | 2 | a0001c0001t0001g0198 a0001c0001t0001g0230 |
2 | HG01361.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.287+1316G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663560 | |||||||
chr19:4663563 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.287+1313G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663563 | |||||||
chr19:4663564 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.287+1312T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663564 | |||||||
chr19:4663564 | ACCCTCAT others(120): Show |
A | 1 | a0002c0002t0002g0085 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.287+1185_287+1311d others(2): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663564 | |||||||
chr19:4663565 | C | CCCTCATT others(81): Show |
1 | a0002c0002t0003g0024 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.287+1310_287+1311i others(90): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663565 | |||||||
chr19:4663565 | C | CCCTCATT others(294): Show |
1 | a0002c0002t0009g0072 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.287+1310_287+1311i others(303): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663565 | |||||||
chr19:4663565 | C | CCCTCATT others(36): Show |
5 | a0001c0001t0001g0145 a0002c0002t0003g0024 a0002c0002t0003g0084 others(2): Show |
5 | HG01192.hp1 HG02145.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.287+1310_287+1311i others(45): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663565 | |||||||
chr19:4663565 | C | CCCTCATT others(79): Show |
1 | a0002c0003t0002g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.287+1310_287+1311i others(88): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663565 | |||||||
chr19:4663565 | C | CCCTCATT others(124): Show |
1 | a0002c0003t0002g0045 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.287+1310_287+1311i others(133): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663565 | |||||||
chr19:4663565 | C | CCCTCATT others(167): Show |
1 | a0001c0001t0001g0031 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.287+1310_287+1311i others(176): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663565 | |||||||
chr19:4663565 | C | CCCTCATT others(605): Show |
1 | a0001c0001t0001g0031 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.287+1310_287+1311i others(614): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663565 | |||||||
chr19:4663565 | C | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.287+1311G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663565 | |||||||
chr19:4663574 | TAC | T | 60 | a0001c0001t0001g0009 a0001c0001t0001g0032 a0001c0001t0001g0033 others(57): Show |
74 | HG00544.hp2 HG00609.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.287+1300_287+1301d others(4): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663574 | |||||||
chr19:4663576 | C | CACAGCCT others(169): Show |
1 | a0002c0002t0002g0122 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.287+1299_287+1300i others(178): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663576 | |||||||
chr19:4663576 | C | CACAGCCT others(1391): Show |
1 | a0002c0003t0002g0007 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.287+1299_287+1300i others(1400): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663576 | |||||||
chr19:4663576 | C | CACAGTCT others(81): Show |
1 | a0002c0002t0002g0116 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.287+1299_287+1300i others(90): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663576 | |||||||
chr19:4663576 | C | CACAGTCT others(171): Show |
1 | a0002c0002t0002g0124 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.287+1299_287+1300i others(180): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663576 | |||||||
chr19:4663576 | C | CAGCCTCC others(34): Show |
2 | a0002c0002t0002g0088 a0002c0002t0002g0099 |
2 | HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.287+1299_287+1300i others(43): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663576 | |||||||
chr19:4663576 | C | CAGCCTCC others(163): Show |
1 | a0002c0002t0002g0090 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.287+1299_287+1300i others(172): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663576 | |||||||
chr19:4663576 | C | CAGCCTCC others(378): Show |
1 | a0002c0003t0002g0050 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.287+1299_287+1300i others(387): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663576 | |||||||
chr19:4663576 | C | CAGCCTCC others(34): Show |
3 | a0002c0003t0002g0048 a0002c0003t0002g0049 a0002c0003t0002g0059 |
3 | HG02451.hp2 HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.287+1299_287+1300i others(43): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663576 | |||||||
chr19:4663576 | C | CAGCCTCC others(167): Show |
1 | a0002c0003t0002g0007 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.287+1299_287+1300i others(176): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663576 | |||||||
chr19:4663576 | C | CAGCCTCC others(122): Show |
1 | a0002c0003t0002g0062 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.287+1299_287+1300i others(131): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663576 | |||||||
chr19:4663576 | C | CAGCCTCC others(159): Show |
1 | a0002c0002t0002g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.287+1299_287+1300i others(168): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663576 | |||||||
chr19:4663576 | C | CAGCCTCC others(77): Show |
3 | a0002c0003t0002g0047 a0002c0003t0002g0055 a0002c0003t0002g0056 |
3 | HG02258.hp1 HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.287+1299_287+1300i others(86): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663576 | |||||||
chr19:4663576 | C | CAGCCTCC others(255): Show |
1 | a0002c0003t0002g0060 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.287+1299_287+1300i others(264): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663576 | |||||||
chr19:4663576 | C | CAGCCTCC others(120): Show |
5 | a0002c0003t0002g0007 a0002c0003t0002g0053 a0002c0003t0002g0054 others(2): Show |
5 | HG01884.hp1 HG02148.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.287+1299_287+1300i others(129): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663576 | |||||||
chr19:4663576 | C | CAGCCTCC others(210): Show |
1 | a0002c0003t0002g0007 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.287+1299_287+1300i others(219): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663576 | |||||||
chr19:4663576 | C | CAGCCTCC others(206): Show |
1 | a0002c0003t0002g0052 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.287+1299_287+1300i others(215): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663576 | |||||||
chr19:4663576 | C | CAGCCTCC others(393): Show |
1 | a0002c0002t0002g0101 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.287+1299_287+1300i others(402): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663576 | |||||||
chr19:4663576 | CACAGCCT others(36): Show |
C | 1 | a0001c0001t0001g0231 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.287+1257_287+1299d others(45): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663576 | |||||||
chr19:4663578 | C | CAGTCTCC others(255): Show |
1 | a0002c0002t0002g0028 | 2 | NA18974.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.287+1297_287+1298i others(264): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663578 | |||||||
chr19:4663593 | C | CCTCCCCA others(79): Show |
1 | a0001c0001t0001g0032 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.287+1282_287+1283i others(88): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663593 | |||||||
chr19:4663596 | CCCCA | C | 25 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0019 others(22): Show |
40 | HG00280.hp2 HG00544.hp2 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.287+1276_287+1279d others(6): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663596 | |||||||
chr19:4663597 | C | CCCACCCC others(34): Show |
2 | a0001c0001t0001g0230 a0001c0001t0001g0252 |
2 | HG01361.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.287+1278_287+1279i others(43): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663597 | |||||||
chr19:4663600 | A | ACCCACCC others(286): Show |
1 | a0001c0001t0001g0238 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.287+1275_287+1276i others(295): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663600 | |||||||
chr19:4663600 | A | ACCTCATC others(67): Show |
1 | a0001c0001t0001g0219 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.287+1275_287+1276i others(76): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663600 | |||||||
chr19:4663607 | C | T | 27 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0019 others(24): Show |
42 | HG00280.hp2 HG00544.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.287+1269G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663607 | |||||||
chr19:4663607 | CCATCCTC others(32): Show |
C | 1 | a0001c0001t0001g0206 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.287+1230_287+1268d others(41): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663607 | |||||||
chr19:4663610 | T | C | 17 | a0002c0002t0002g0026 a0002c0002t0002g0083 a0002c0002t0002g0086 others(14): Show |
18 | HG01109.hp1 HG02055.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.287+1266A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663610 | |||||||
chr19:4663619 | T | TAC | 29 | a0001c0001t0001g0147 a0001c0001t0001g0230 a0002c0002t0002g0026 others(26): Show |
34 | HG01109.hp1 HG01361.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.287+1255_287+1256d others(4): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663619 | |||||||
chr19:4663619 | T | TACACAGC others(920): Show |
1 | a0001c0001t0001g0207 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.287+1256_287+1257i others(929): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663619 | |||||||
chr19:4663619 | T | TACACAGC others(431): Show |
1 | a0002c0002t0003g0023 | 2 | HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.287+1256_287+1257i others(440): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663619 | |||||||
chr19:4663630 | A | G | 4 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0216 others(1): Show |
4 | HG00642.hp1 HG01070.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.287+1246T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663630 | |||||||
chr19:4663632 | C | A | 4 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0216 others(1): Show |
4 | HG00642.hp1 HG01070.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.287+1244G>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663632 | |||||||
chr19:4663639 | C | CCCCACCC others(478): Show |
1 | a0002c0002t0002g0093 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.287+1236_287+1237i others(487): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663639 | |||||||
chr19:4663639 | C | CCCCACCC others(568): Show |
1 | a0002c0002t0002g0095 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.287+1236_287+1237i others(577): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663639 | |||||||
chr19:4663639 | C | CCCCACCC others(650): Show |
1 | a0002c0002t0002g0094 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.287+1236_287+1237i others(659): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663639 | |||||||
chr19:4663639 | C | CCCCACCC others(214): Show |
1 | a0002c0002t0002g0097 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.287+1236_287+1237i others(223): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663639 | |||||||
chr19:4663639 | C | CCCCACCC others(126): Show |
1 | a0002c0003t0001g0067 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.287+1236_287+1237i others(135): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663639 | |||||||
chr19:4663639 | C | CCCCACCC others(44): Show |
1 | a0001c0001t0001g0159 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.287+1236_287+1237i others(53): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663639 | |||||||
chr19:4663646 | T | C | 9 | a0001c0001t0001g0032 a0001c0001t0001g0159 a0001c0001t0001g0192 others(6): Show |
10 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.287+1230A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663646 | |||||||
chr19:4663658 | T | TAC | 3 | a0001c0001t0001g0160 a0001c0001t0001g0207 a0001c0001t0001g0216 |
3 | HG01070.hp1 HG01074.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.287+1216_287+1217d others(4): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663658 | |||||||
chr19:4663660 | CAGCCTCC others(85): Show |
C | 1 | a0001c0001t0001g0191 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.287+1124_287+1215d others(94): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663660 | |||||||
chr19:4663663 | C | T | 2 | a0001c0001t0001g0160 a0001c0001t0001g0216 |
2 | HG01070.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.287+1213G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663663 | |||||||
chr19:4663669 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0159 a0001c0001t0001g0207 |
4 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.287+1207C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663669 | |||||||
chr19:4663669 | G | C | 2 | a0001c0001t0001g0160 a0001c0001t0001g0216 |
2 | HG01070.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.287+1207C>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663669 | |||||||
chr19:4663671 | A | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0159 a0001c0001t0001g0207 |
4 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.287+1205T>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663671 | |||||||
chr19:4663671 | A | G | 2 | a0001c0001t0001g0160 a0001c0001t0001g0216 |
2 | HG01070.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.287+1205T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663671 | |||||||
chr19:4663673 | A | G | 2 | a0001c0001t0001g0160 a0001c0001t0001g0216 |
2 | HG01070.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.287+1203T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663673 | |||||||
chr19:4663674 | C | T | 6 | a0002c0002t0002g0025 a0002c0002t0002g0076 a0002c0002t0002g0077 others(3): Show |
7 | HG01243.hp1 HG02280.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.287+1202G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663674 | |||||||
chr19:4663675 | C | T | 2 | a0001c0001t0001g0160 a0001c0001t0001g0216 |
2 | HG01070.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.287+1201G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663675 | |||||||
chr19:4663685 | C | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0184 |
3 | HG02647.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.287+1191G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663685 | |||||||
chr19:4663690 | T | C | 9 | a0001c0001t0001g0032 a0001c0001t0001g0159 a0001c0001t0001g0160 others(6): Show |
10 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.287+1186A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663690 | |||||||
chr19:4663691 | G | A | 9 | a0001c0001t0001g0032 a0001c0001t0001g0159 a0001c0001t0001g0160 others(6): Show |
10 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.287+1185C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663691 | |||||||
chr19:4663691 | G | GTCCTCAT others(314): Show |
1 | a0002c0002t0002g0091 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.287+1184_287+1185i others(323): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663691 | |||||||
chr19:4663691 | G | GTCCTCAT others(85): Show |
4 | a0002c0002t0002g0089 a0002c0002t0002g0090 a0002c0002t0002g0096 others(1): Show |
4 | HG02055.hp2 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.287+1093_287+1184d others(94): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663691 | |||||||
chr19:4663691 | G | GTCCTCAT others(314): Show |
1 | a0002c0002t0002g0099 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.287+1184_287+1185i others(323): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663691 | |||||||
chr19:4663691 | G | GTCCTCAT others(304): Show |
1 | a0002c0002t0002g0092 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.287+1184_287+1185i others(313): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663691 | |||||||
chr19:4663691 | GTCCTCAT others(85): Show |
G | 1 | a0002c0002t0002g0127 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.287+1093_287+1184d others(94): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663691 | |||||||
chr19:4663704 | A | G | 1 | a0002c0002t0002g0077 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.287+1172T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663704 | |||||||
chr19:4663705 | C | A | 3 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0216 |
3 | HG00642.hp1 HG01070.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.287+1171G>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663705 | |||||||
chr19:4663708 | T | C | 5 | a0001c0001t0001g0032 a0001c0001t0001g0159 a0001c0001t0001g0160 others(2): Show |
6 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.287+1168A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663708 | |||||||
chr19:4663716 | CTG | C | 4 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0207 others(1): Show |
4 | HG00642.hp1 HG01070.hp1 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.287+1158_287+1159d others(4): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663716 | |||||||
chr19:4663720 | G | A | 4 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0207 others(1): Show |
4 | HG00642.hp1 HG01070.hp1 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.287+1156C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663720 | |||||||
chr19:4663722 | T | C | 5 | a0001c0001t0001g0032 a0001c0001t0001g0159 a0001c0001t0001g0160 others(2): Show |
6 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.287+1154A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663722 | |||||||
chr19:4663722 | T | TCTCCCCA others(38): Show |
2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG03927.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.287+1109_287+1153d others(47): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663722 | |||||||
chr19:4663722 | TCTCCCCA others(38): Show |
T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0190 |
2 | HG02074.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.287+1109_287+1153d others(47): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663722 | |||||||
chr19:4663726 | C | T | 1 | a0001c0001t0001g0032 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.287+1150G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663726 | |||||||
chr19:4663731 | C | A | 1 | a0001c0001t0001g0246 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.287+1145G>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663731 | |||||||
chr19:4663747 | C | T | 1 | a0002c0003t0001g0064 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.287+1129G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663747 | |||||||
chr19:4663752 | A | AAGCCTCC others(38): Show |
1 | a0002c0003t0002g0046 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.287+1079_287+1123d others(47): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663752 | |||||||
chr19:4663752 | A | AAGCCTCC others(85): Show |
1 | a0002c0002t0002g0026 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.287+1123_287+1124i others(94): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663752 | |||||||
chr19:4663752 | A | AAGCCTCC others(432): Show |
1 | a0001c0001t0001g0186 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.287+1123_287+1124i others(441): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663752 | |||||||
chr19:4663752 | A | C | 9 | a0001c0001t0001g0032 a0001c0001t0001g0146 a0001c0001t0001g0149 others(6): Show |
10 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.287+1124T>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663752 | |||||||
chr19:4663763 | C | CTG | 4 | a0001c0001t0001g0032 a0001c0001t0001g0159 a0001c0001t0001g0216 others(1): Show |
5 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.287+1112_287+1113i others(4): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663763 | |||||||
chr19:4663765 | A | G | 4 | a0001c0001t0001g0032 a0001c0001t0001g0159 a0001c0001t0001g0216 others(1): Show |
5 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.287+1111T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663765 | |||||||
chr19:4663771 | C | CCCACCCA others(40): Show |
1 | a0001c0001t0001g0158 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.287+1058_287+1104d others(49): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663771 | |||||||
chr19:4663771 | C | CCCACCCA others(81): Show |
2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG01099.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.287+1104_287+1105i others(90): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663771 | |||||||
chr19:4663771 | C | CCCACCCA others(38): Show |
14 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0031 others(11): Show |
20 | HG00733.hp1 HG01192.hp1 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.287+1104_287+1105i others(47): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663771 | |||||||
chr19:4663771 | C | T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0159 a0001c0001t0001g0216 others(1): Show |
5 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.287+1105G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663771 | |||||||
chr19:4663793 | TAC | T | 43 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0027 others(40): Show |
50 | HG00597.hp1 HG00609.hp1 HG01167.hp2 others(47): Show |
intron_variant | MODIFIER | c.287+1081_287+1082d others(4): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663793 | |||||||
chr19:4663795 | C | CAAAGCCT others(81): Show |
1 | a0002c0002t0002g0081 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.287+1080_287+1081i others(90): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663795 | |||||||
chr19:4663795 | C | CACAGCCT others(120): Show |
1 | a0002c0002t0002g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.287+1080_287+1081i others(129): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663795 | |||||||
chr19:4663805 | A | C | 2 | a0002c0003t0002g0045 a0002c0003t0002g0051 |
2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.287+1071T>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663805 | |||||||
chr19:4663896 | C | T | 1 | a0001c0006t0001g0136 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.287+980G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663896 | |||||||
chr19:4663905 | G | A | 1 | a0001c0001t0001g0276 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.287+971C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4663905 | |||||||
chr19:4664026 | T | C | 97 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0025 others(94): Show |
114 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(111): Show |
intron_variant | MODIFIER | c.287+850A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4664026 | |||||||
chr19:4664041 | G | C | 8 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0154 others(5): Show |
11 | HG01070.hp2 HG01071.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.287+835C>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4664041 | |||||||
chr19:4664050 | T | C | 97 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0025 others(94): Show |
114 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(111): Show |
intron_variant | MODIFIER | c.287+826A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4664050 | |||||||
chr19:4664062 | C | A | 97 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0025 others(94): Show |
114 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(111): Show |
intron_variant | MODIFIER | c.287+814G>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4664062 | |||||||
chr19:4664078 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.287+798G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4664078 | |||||||
chr19:4664113 | T | C | 2 | a0002c0002t0002g0077 a0002c0002t0002g0080 |
2 | HG03041.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.287+763A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4664113 | |||||||
chr19:4664134 | C | A | 1 | a0002c0002t0002g0073 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.287+742G>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4664134 | |||||||
chr19:4664181 | T | A | 1 | a0001c0001t0001g0231 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.287+695A>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4664181 | |||||||
chr19:4664207 | T | C | 1 | a0001c0001t0001g0265 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.287+669A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4664207 | |||||||
chr19:4664286 | G | C | 4 | a0002c0002t0003g0024 a0002c0002t0003g0084 a0002c0002t0004g0070 others(1): Show |
5 | HG02145.hp1 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.287+590C>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4664286 | |||||||
chr19:4664425 | G | C | 76 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0025 others(73): Show |
87 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(84): Show |
intron_variant | MODIFIER | c.287+451C>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4664425 | |||||||
chr19:4664489 | C | CA | 70 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0014 others(67): Show |
85 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.287+386dupT | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4664489 | |||||||
chr19:4664489 | C | CAA | 5 | a0001c0001t0001g0031 a0001c0001t0001g0278 a0002c0003t0001g0022 others(2): Show |
7 | HG02698.hp2 HG03669.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.287+385_287+386dup others(2): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4664489 | |||||||
chr19:4664596 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.287+280C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4664596 | |||||||
chr19:4664742 | G | A | 75 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0025 others(72): Show |
86 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(83): Show |
intron_variant | MODIFIER | c.287+134C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4664742 | |||||||
chr19:4664806 | C | T | 4 | a0002c0003t0002g0011 a0002c0003t0002g0047 a0002c0003t0002g0048 others(1): Show |
6 | HG01891.hp1 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.287+70G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4664806 | |||||||
chr19:4664846 | C | T | 1 | a0003c0007t0001g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.287+30G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 3/5 | chr19 | 4664846 | |||||||
chr19:4665005 | CT | C | 6 | a0002c0002t0002g0069 a0002c0002t0003g0023 a0002c0002t0003g0024 others(3): Show |
8 | HG02145.hp1 HG02630.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.226-69delA | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4665005 | |||||||
chr19:4665031 | T | C | 2 | a0002c0003t0002g0046 a0002c0003t0002g0058 |
2 | HG02300.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.226-94A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4665031 | |||||||
chr19:4665095 | G | A | 4 | a0002c0002t0002g0012 a0002c0002t0002g0074 a0002c0002t0002g0075 others(1): Show |
6 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.226-158C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4665095 | |||||||
chr19:4665103 | G | C | 28 | a0002c0003t0001g0022 a0002c0003t0001g0063 a0002c0003t0001g0064 others(25): Show |
35 | HG01884.hp1 HG01891.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.226-166C>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4665103 | |||||||
chr19:4665161 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.226-224A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4665161 | |||||||
chr19:4665213 | C | CTGTT | 6 | a0001c0001t0001g0176 a0001c0001t0001g0187 a0001c0001t0001g0188 others(3): Show |
6 | HG00639.hp1 HG02074.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.226-280_226-277dup others(4): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4665213 | |||||||
chr19:4665213 | CTGTT | C | 106 | a0001c0001t0001g0168 a0001c0001t0001g0239 a0002c0002t0002g0012 others(103): Show |
124 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(121): Show |
intron_variant | MODIFIER | c.226-280_226-277del others(4): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4665213 | |||||||
chr19:4665587 | C | T | 28 | a0002c0003t0001g0022 a0002c0003t0001g0063 a0002c0003t0001g0064 others(25): Show |
35 | HG01884.hp1 HG01891.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.226-650G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4665587 | |||||||
chr19:4665677 | C | T | 1 | a0002c0002t0009g0072 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.226-740G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4665677 | |||||||
chr19:4665684 | A | G | 105 | a0001c0006t0001g0136 a0002c0002t0002g0012 a0002c0002t0002g0013 others(102): Show |
123 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(120): Show |
intron_variant | MODIFIER | c.226-747T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4665684 | |||||||
chr19:4665694 | G | A | 6 | a0002c0002t0002g0025 a0002c0002t0002g0076 a0002c0002t0002g0077 others(3): Show |
7 | HG01243.hp1 HG02280.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.226-757C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4665694 | |||||||
chr19:4665722 | A | G | 106 | a0001c0001t0001g0258 a0001c0006t0001g0136 a0002c0002t0002g0012 others(103): Show |
124 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(121): Show |
intron_variant | MODIFIER | c.226-785T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4665722 | |||||||
chr19:4665738 | G | A | 2 | a0002c0002t0002g0069 a0002c0002t0002g0125 |
2 | HG03540.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.226-801C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4665738 | |||||||
chr19:4665795 | T | C | 1 | a0003c0007t0001g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.226-858A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4665795 | |||||||
chr19:4665804 | G | C | 1 | a0002c0003t0002g0058 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.226-867C>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4665804 | |||||||
chr19:4665820 | C | CA | 62 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(59): Show |
104 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.226-884dupT | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4665820 | |||||||
chr19:4665820 | C | CAA | 19 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0139 others(16): Show |
23 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.226-885_226-884dup others(2): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4665820 | |||||||
chr19:4665820 | C | CAAA | 11 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0140 others(8): Show |
15 | HG01358.hp2 HG01978.hp2 HG02293.hp1 others(12): Show |
intron_variant | MODIFIER | c.226-886_226-884dup others(3): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4665820 | |||||||
chr19:4665820 | CA | C | 8 | a0001c0001t0001g0035 a0001c0001t0001g0153 a0001c0001t0001g0184 others(5): Show |
9 | HG00323.hp2 HG01975.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.226-884delT | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4665820 | |||||||
chr19:4665820 | CAAAAAAA others(6): Show |
C | 15 | a0002c0002t0002g0025 a0002c0002t0002g0076 a0002c0002t0002g0078 others(12): Show |
16 | HG01243.hp1 HG02027.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.226-896_226-884del others(13): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4665820 | |||||||
chr19:4665820 | CAAAAAAA others(7): Show |
C | 87 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0026 others(84): Show |
104 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(101): Show |
intron_variant | MODIFIER | c.226-897_226-884del others(14): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4665820 | |||||||
chr19:4665820 | CAAAAAAA others(8): Show |
C | 3 | a0001c0001t0001g0252 a0002c0002t0002g0105 a0002c0002t0008g0106 |
3 | HG02965.hp2 NA18974.hp1 NA19059.hp1 |
intron_variant | MODIFIER | c.226-898_226-884del others(15): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4665820 | |||||||
chr19:4665881 | T | G | 105 | a0001c0006t0001g0136 a0002c0002t0002g0012 a0002c0002t0002g0013 others(102): Show |
123 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(120): Show |
intron_variant | MODIFIER | c.226-944A>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4665881 | |||||||
chr19:4665886 | A | G | 104 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0025 others(101): Show |
122 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(119): Show |
intron_variant | MODIFIER | c.226-949T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4665886 | |||||||
chr19:4665898 | A | C | 3 | a0002c0002t0002g0081 a0002c0002t0002g0100 a0002c0002t0002g0101 |
3 | HG02257.hp2 HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.226-961T>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4665898 | |||||||
chr19:4665967 | G | A | 28 | a0002c0003t0001g0022 a0002c0003t0001g0063 a0002c0003t0001g0064 others(25): Show |
35 | HG01884.hp1 HG01891.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.226-1030C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4665967 | |||||||
chr19:4666130 | C | A | 1 | a0001c0001t0001g0246 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.226-1193G>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4666130 | |||||||
chr19:4666144 | C | T | 18 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0031 others(15): Show |
24 | HG00733.hp1 HG01192.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.226-1207G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4666144 | |||||||
chr19:4666173 | C | A | 1 | a0001c0001t0001g0247 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.226-1236G>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4666173 | |||||||
chr19:4666185 | C | T | 1 | a0002c0002t0002g0129 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.226-1248G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4666185 | |||||||
chr19:4666269 | C | T | 16 | a0002c0002t0002g0026 a0002c0002t0002g0085 a0002c0002t0002g0086 others(13): Show |
17 | HG01109.hp1 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.226-1332G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4666269 | |||||||
chr19:4666277 | C | CT | 10 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0183 others(7): Show |
11 | HG01243.hp1 HG02273.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.226-1341dupA | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4666277 | |||||||
chr19:4666422 | C | A | 1 | a0001c0001t0001g0248 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.226-1485G>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4666422 | |||||||
chr19:4666422 | C | T | 76 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0025 others(73): Show |
87 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(84): Show |
intron_variant | MODIFIER | c.226-1485G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4666422 | |||||||
chr19:4666569 | C | T | 104 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0025 others(101): Show |
122 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(119): Show |
intron_variant | MODIFIER | c.226-1632G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4666569 | |||||||
chr19:4666744 | C | T | 105 | a0001c0006t0001g0136 a0002c0002t0002g0012 a0002c0002t0002g0013 others(102): Show |
123 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(120): Show |
intron_variant | MODIFIER | c.226-1807G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4666744 | |||||||
chr19:4666758 | A | C | 1 | a0001c0001t0001g0142 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.226-1821T>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4666758 | |||||||
chr19:4666764 | T | C | 2 | a0001c0001t0001g0181 a0001c0001t0001g0249 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.226-1827A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4666764 | |||||||
chr19:4666790 | C | T | 1 | a0002c0002t0002g0076 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.225+1805G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4666790 | |||||||
chr19:4666791 | A | G | 104 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0025 others(101): Show |
122 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(119): Show |
intron_variant | MODIFIER | c.225+1804T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4666791 | |||||||
chr19:4666831 | C | T | 28 | a0002c0003t0001g0022 a0002c0003t0001g0063 a0002c0003t0001g0064 others(25): Show |
35 | HG01884.hp1 HG01891.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.225+1764G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4666831 | |||||||
chr19:4666841 | T | C | 123 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0031 others(120): Show |
147 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(144): Show |
intron_variant | MODIFIER | c.225+1754A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4666841 | |||||||
chr19:4666887 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.225+1708C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4666887 | |||||||
chr19:4667054 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.225+1541C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4667054 | |||||||
chr19:4667121 | C | CT | 31 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0033 others(28): Show |
40 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.225+1473dupA | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4667121 | |||||||
chr19:4667121 | CT | C | 53 | a0001c0001t0001g0138 a0001c0001t0001g0252 a0001c0001t0001g0253 others(50): Show |
60 | HG00597.hp1 HG00609.hp1 HG01074.hp1 others(57): Show |
intron_variant | MODIFIER | c.225+1473delA | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4667121 | |||||||
chr19:4667121 | CTT | C | 24 | a0002c0002t0002g0026 a0002c0002t0002g0083 a0002c0002t0002g0085 others(21): Show |
27 | HG01109.hp1 HG01891.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.225+1472_225+1473d others(4): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4667121 | |||||||
chr19:4667121 | CTTT | C | 21 | a0002c0003t0001g0022 a0002c0003t0001g0064 a0002c0003t0001g0065 others(18): Show |
26 | HG01884.hp1 HG02080.hp1 HG02135.hp1 others(23): Show |
intron_variant | MODIFIER | c.225+1471_225+1473d others(5): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4667121 | |||||||
chr19:4667168 | G | A | 1 | a0001c0006t0001g0136 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.225+1427C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4667168 | |||||||
chr19:4667222 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.225+1373C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4667222 | |||||||
chr19:4667277 | C | T | 45 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0027 others(42): Show |
52 | HG00597.hp1 HG00609.hp1 HG01167.hp2 others(49): Show |
intron_variant | MODIFIER | c.225+1318G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4667277 | |||||||
chr19:4667330 | G | A | 1 | a0001c0001t0001g0263 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.225+1265C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4667330 | |||||||
chr19:4667375 | G | A | 1 | a0001c0006t0001g0136 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.225+1220C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4667375 | |||||||
chr19:4667382 | C | T | 6 | a0002c0002t0002g0069 a0002c0002t0003g0023 a0002c0002t0003g0024 others(3): Show |
8 | HG02145.hp1 HG02630.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.225+1213G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4667382 | |||||||
chr19:4667383 | C | A | 1 | a0001c0001t0001g0264 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.225+1212G>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4667383 | |||||||
chr19:4667555 | AGCCACTG others(1): Show |
A | 6 | a0002c0002t0002g0069 a0002c0002t0003g0023 a0002c0002t0003g0024 others(3): Show |
8 | HG02145.hp1 HG02630.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.225+1032_225+1039d others(10): Show |
MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4667555 | |||||||
chr19:4667714 | CT | C | 97 | a0001c0001t0001g0265 a0002c0002t0002g0012 a0002c0002t0002g0013 others(94): Show |
114 | HG00597.hp1 HG00609.hp1 HG00639.hp1 others(111): Show |
intron_variant | MODIFIER | c.225+880delA | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4667714 | |||||||
chr19:4667794 | C | T | 5 | a0002c0002t0003g0023 a0002c0002t0003g0024 a0002c0002t0003g0084 others(2): Show |
7 | HG02145.hp1 HG02630.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.225+801G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4667794 | |||||||
chr19:4667846 | C | T | 5 | a0002c0002t0003g0023 a0002c0002t0003g0024 a0002c0002t0003g0084 others(2): Show |
7 | HG02145.hp1 HG02630.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.225+749G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4667846 | |||||||
chr19:4668044 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.225+551G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4668044 | |||||||
chr19:4668118 | A | G | 105 | a0001c0006t0001g0136 a0002c0002t0002g0012 a0002c0002t0002g0013 others(102): Show |
123 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(120): Show |
intron_variant | MODIFIER | c.225+477T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4668118 | |||||||
chr19:4668298 | T | C | 2 | a0002c0002t0002g0100 a0002c0002t0002g0101 |
2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.225+297A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4668298 | |||||||
chr19:4668345 | TG | T | 6 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0159 others(3): Show |
10 | HG00642.hp1 HG01070.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.225+249delC | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4668345 | |||||||
chr19:4668405 | A | G | 105 | a0001c0006t0001g0136 a0002c0002t0002g0012 a0002c0002t0002g0013 others(102): Show |
123 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(120): Show |
intron_variant | MODIFIER | c.225+190T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 2/5 | chr19 | 4668405 | |||||||
chr19:4668707 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.175-62C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 1/5 | chr19 | 4668707 | |||||||
chr19:4668746 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.175-101T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 1/5 | chr19 | 4668746 | |||||||
chr19:4668836 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0156 a0001c0001t0001g0157 |
4 | HG01070.hp2 HG01071.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.175-191G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 1/5 | chr19 | 4668836 | |||||||
chr19:4668849 | A | AT | 101 | a0001c0001t0001g0139 a0001c0001t0001g0151 a0001c0001t0001g0152 others(98): Show |
119 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.175-205dupA | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 1/5 | chr19 | 4668849 | |||||||
chr19:4668849 | AT | A | 14 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0044 others(11): Show |
21 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.175-205delA | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 1/5 | chr19 | 4668849 | |||||||
chr19:4668936 | C | T | 1 | a0002c0002t0002g0069 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.175-291G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 1/5 | chr19 | 4668936 | |||||||
chr19:4668937 | G | A | 1 | a0002c0002t0003g0084 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.175-292C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 1/5 | chr19 | 4668937 | |||||||
chr19:4669102 | T | C | 16 | a0002c0002t0002g0026 a0002c0002t0002g0085 a0002c0002t0002g0086 others(13): Show |
17 | HG01109.hp1 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.175-457A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 1/5 | chr19 | 4669102 | |||||||
chr19:4669120 | C | A | 1 | a0003c0007t0001g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.175-475G>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 1/5 | chr19 | 4669120 | |||||||
chr19:4669663 | A | G | 122 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0031 others(119): Show |
146 | HG00597.hp1 HG00609.hp1 HG00733.hp1 others(143): Show |
intron_variant | MODIFIER | c.174+498T>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 1/5 | chr19 | 4669663 | |||||||
chr19:4669699 | C | A | 1 | a0002c0002t0002g0134 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.174+462G>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 1/5 | chr19 | 4669699 | |||||||
chr19:4669787 | C | T | 97 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0025 others(94): Show |
114 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(111): Show |
intron_variant | MODIFIER | c.174+374G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 1/5 | chr19 | 4669787 | |||||||
chr19:4669828 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0137 a0001c0001t0001g0138 |
4 | HG00642.hp2 HG01358.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+333C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 1/5 | chr19 | 4669828 | |||||||
chr19:4669829 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0137 a0001c0001t0001g0138 |
4 | HG00642.hp2 HG01358.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+332G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 1/5 | chr19 | 4669829 | |||||||
chr19:4669934 | G | C | 2 | a0002c0002t0002g0100 a0002c0002t0002g0101 |
2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.174+227C>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 1/5 | chr19 | 4669934 | |||||||
chr19:4669957 | T | C | 1 | a0002c0002t0002g0135 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.174+204A>G | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 1/5 | chr19 | 4669957 | |||||||
chr19:4669991 | C | T | 1 | a0002c0003t0002g0045 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.174+170G>A | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 1/5 | chr19 | 4669991 | |||||||
chr19:4670062 | C | G | 1 | a0001c0006t0001g0136 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.174+99G>C | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 1/5 | chr19 | 4670062 | |||||||
chr19:4670127 | G | A | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG03927.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.174+34C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 1/5 | chr19 | 4670127 | |||||||
chr19:4670153 | G | A | 38 | a0002c0002t0002g0013 a0002c0002t0002g0027 a0002c0002t0002g0028 others(35): Show |
43 | HG00597.hp1 HG00609.hp1 HG01167.hp2 others(40): Show |
splice_region_variant&intron_variant | LOW | c.174+8C>T | MYDGF | ENSG00000074842.8 | transcript | ENST00000262947.8 | protein_coding | 1/5 | chr19 | 4670153 |