Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2799 |
| ensemblid | ENSG00000135677.11 |
| hgncid | 4422 |
| symbol | GNS |
| name | glucosamine (N-acetyl)-6-sulfatase |
| refseq_nuc | NM_002076.4 |
| refseq_prot | NP_002067.1 |
| ensembl_nuc | ENST00000258145.8 |
| ensembl_prot | ENSP00000258145.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 64713449 |
| end | 64759406 |
| strand | - |
| ver | v1.2 |
| region | chr12:64713449-64759406 |
| region5000 | chr12:64708449-64764406 |
| regionname0 | GNS_chr12_64713449_64759406 |
| regionname5000 | GNS_chr12_64708449_64764406 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 552 | 343 | 85 | 63 | 137 | 14 | 42 | 93 | GNS_chr12_64708449_64764406 | GNS | MRLLP others(547): Show |
chr12 | 64708449 | 64764406 |
| a0002 | 0/0 | 552 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | MRLLP others(547): Show |
chr12 | 64708449 | 64764406 |
| a0003 | 0/0 | 552 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | MRLLP others(547): Show |
chr12 | 64708449 | 64764406 |
| a0004 | 0/0 | 552 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | MRLLP others(547): Show |
chr12 | 64708449 | 64764406 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1656 | 243 | 67 | 37 | 101 | 9 | 28 | GNS_chr12_64708449_64764406 | GNS | ATGCG others(1651): Show |
chr12 | 64708449 | 64764406 | ||
| a0001c0002 | 1/0 | 1656 | 75 | 6 | 14 | 36 | 5 | 13 | GNS_chr12_64708449_64764406 | GNS | ATGCG others(1651): Show |
chr12 | 64708449 | 64764406 | ||
| a0001c0003 | 0/0 | 1656 | 13 | 0 | 12 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | ATGCG others(1651): Show |
chr12 | 64708449 | 64764406 | ||
| a0001c0004 | 0/0 | 1656 | 10 | 10 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | ATGCG others(1651): Show |
chr12 | 64708449 | 64764406 | ||
| a0001c0006 | 0/0 | 1656 | 2 | 2 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | ATGCG others(1651): Show |
chr12 | 64708449 | 64764406 | ||
| a0002c0005 | 0/0 | 1656 | 7 | 7 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | ATGCG others(1651): Show |
chr12 | 64708449 | 64764406 | ||
| a0003c0007 | 0/0 | 1656 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | ATGCG others(1651): Show |
chr12 | 64708449 | 64764406 | ||
| a0004c0008 | 0/0 | 1656 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | ATGCG others(1651): Show |
chr12 | 64708449 | 64764406 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5081 | 146 | 24 | 21 | 80 | 6 | 14 | GNS_chr12_64708449_64764406 | GNS | GTCTG others(5076): Show |
chr12 | 64708449 | 64764406 |
| a0001c0001t0003 | 0/0 | 5081 | 52 | 3 | 11 | 21 | 3 | 14 | GNS_chr12_64708449_64764406 | GNS | GTCTG others(5076): Show |
chr12 | 64708449 | 64764406 |
| a0001c0001t0004 | 0/0 | 5081 | 13 | 11 | 2 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | GTCTG others(5076): Show |
chr12 | 64708449 | 64764406 |
| a0001c0001t0006 | 0/0 | 5081 | 8 | 8 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | GTCTG others(5076): Show |
chr12 | 64708449 | 64764406 |
| a0001c0001t0007 | 0/0 | 5081 | 6 | 6 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | GTCTG others(5076): Show |
chr12 | 64708449 | 64764406 |
| a0001c0001t0008 | 0/0 | 5081 | 4 | 1 | 3 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | GTCTG others(5076): Show |
chr12 | 64708449 | 64764406 |
| a0001c0001t0009 | 0/0 | 5081 | 3 | 3 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | GTCTG others(5076): Show |
chr12 | 64708449 | 64764406 |
| a0001c0001t0010 | 0/0 | 5081 | 3 | 3 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | GTCTG others(5076): Show |
chr12 | 64708449 | 64764406 |
| a0001c0001t0011 | 0/0 | 5083 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | GTCTG others(5078): Show |
chr12 | 64708449 | 64764406 |
| a0001c0001t0013 | 0/0 | 5081 | 2 | 2 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | GTCTG others(5076): Show |
chr12 | 64708449 | 64764406 |
| a0001c0001t0014 | 0/0 | 5081 | 2 | 2 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | GTCTG others(5076): Show |
chr12 | 64708449 | 64764406 |
| a0001c0001t0015 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | GTCTG others(5076): Show |
chr12 | 64708449 | 64764406 |
| a0001c0001t0016 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | GTCTG others(5076): Show |
chr12 | 64708449 | 64764406 |
| a0001c0001t0021 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | GTCTG others(5076): Show |
chr12 | 64708449 | 64764406 |
| a0001c0002t0001 | 0/0 | 5081 | 6 | 2 | 0 | 0 | 0 | 4 | GNS_chr12_64708449_64764406 | GNS | GTCTG others(5076): Show |
chr12 | 64708449 | 64764406 |
| a0001c0002t0002 | 1/0 | 5081 | 62 | 3 | 12 | 33 | 5 | 8 | GNS_chr12_64708449_64764406 | GNS | GTCTG others(5076): Show |
chr12 | 64708449 | 64764406 |
| a0001c0002t0003 | 0/0 | 5081 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | GTCTG others(5076): Show |
chr12 | 64708449 | 64764406 |
| a0001c0002t0004 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | GTCTG others(5076): Show |
chr12 | 64708449 | 64764406 |
| a0001c0002t0012 | 0/0 | 5081 | 2 | 0 | 0 | 2 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | GTCTG others(5076): Show |
chr12 | 64708449 | 64764406 |
| a0001c0002t0017 | 0/0 | 5081 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | GTCTG others(5076): Show |
chr12 | 64708449 | 64764406 |
| a0001c0002t0018 | 0/0 | 5081 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | GTCTG others(5076): Show |
chr12 | 64708449 | 64764406 |
| a0001c0002t0020 | 0/0 | 5081 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | GTCTG others(5076): Show |
chr12 | 64708449 | 64764406 |
| a0001c0003t0002 | 0/0 | 5081 | 13 | 0 | 12 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | GTCTG others(5076): Show |
chr12 | 64708449 | 64764406 |
| a0001c0004t0005 | 0/0 | 5084 | 10 | 10 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | GTCTG others(5079): Show |
chr12 | 64708449 | 64764406 |
| a0001c0006t0011 | 0/0 | 5083 | 2 | 2 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | GTCTG others(5078): Show |
chr12 | 64708449 | 64764406 |
| a0002c0005t0004 | 0/0 | 5081 | 7 | 7 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | GTCTG others(5076): Show |
chr12 | 64708449 | 64764406 |
| a0003c0007t0019 | 0/0 | 5081 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | GTCTG others(5076): Show |
chr12 | 64708449 | 64764406 |
| a0004c0008t0003 | 0/0 | 5081 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | GTCTG others(5076): Show |
chr12 | 64708449 | 64764406 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0014 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0258 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0003 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0016 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0004g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0006g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0006g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0006g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0006g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0006g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0006g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0006g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0006g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0007g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0007g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0007g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0007g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0007g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0008g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0008g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0008g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0008g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0009g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0009g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0009g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0010g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0010g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0010g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0011g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0013g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0013g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0014g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0014g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0015g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0016g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0001t0021g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0086 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0012g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0012g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0017g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0018g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0002t0020g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0003t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0003t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0003t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0003t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0003t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0003t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0003t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0003t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0003t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0003t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0003t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0003t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0004t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0004t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0004t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0004t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0004t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0004t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0004t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0004t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0004t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0004t0005g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0006t0011g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0001c0006t0011g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0002c0005t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0002c0005t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0002c0005t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0002c0005t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0002c0005t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0002c0005t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0002c0005t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0003c0007t0019g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| a0004c0008t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0068 | EUR | GBR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0197 | EUR | GBR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0080 | EUR | FIN | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0282 | EUR | FIN | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0272 | EUR | FIN | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0204 | EUR | FIN | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0285 | EAS | CHS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00423 | hp2 | a0001 | c0002 | t0012 | g0083 | EAS | CHS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | CHS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | CHS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | CHS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0324 | EAS | CHS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0030 | EAS | CHS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00639 | hp1 | a0001 | c0003 | t0002 | g0056 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0020 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0199 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00733 | hp1 | a0001 | c0001 | t0008 | g0130 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00733 | hp2 | a0001 | c0003 | t0002 | g0089 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0038 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00738 | hp1 | a0001 | c0003 | t0002 | g0031 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0212 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0300 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0021 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0213 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01070 | hp1 | a0001 | c0003 | t0002 | g0077 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0029 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0092 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0306 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01081 | hp2 | a0001 | c0001 | t0008 | g0129 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01106 | hp1 | a0001 | c0003 | t0002 | g0055 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0153 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0193 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0104 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01175 | hp2 | a0001 | c0002 | t0020 | g0074 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0113 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0096 | AMR | PUR | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0149 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0191 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01256 | hp1 | a0001 | c0003 | t0002 | g0034 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01257 | hp2 | a0001 | c0003 | t0002 | g0006 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01258 | hp2 | a0001 | c0003 | t0002 | g0033 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01261 | hp2 | a0001 | c0003 | t0002 | g0053 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01346 | hp2 | a0001 | c0003 | t0002 | g0054 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01361 | hp1 | a0003 | c0007 | t0019 | g0064 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01361 | hp2 | a0001 | c0002 | t0017 | g0093 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0321 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01433 | hp2 | a0001 | c0003 | t0002 | g0006 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0060 | EUR | IBS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0146 | EUR | IBS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0098 | EUR | IBS | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01884 | hp1 | a0001 | c0001 | t0009 | g0133 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0143 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0045 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01891 | hp2 | a0001 | c0004 | t0005 | g0123 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0328 | AMR | PEL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0059 | AMR | PEL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0198 | AMR | PEL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0095 | AMR | PEL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0317 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0296 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0084 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0323 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0128 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02055 | hp2 | a0002 | c0005 | t0004 | g0101 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0032 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0048 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02132 | hp2 | a0001 | c0002 | t0012 | g0085 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02145 | hp1 | a0002 | c0005 | t0004 | g0100 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0057 | EAS | CDX | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | CDX | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CDX | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0103 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0148 | AMR | PEL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02280 | hp2 | a0001 | c0004 | t0005 | g0126 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PEL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0039 | AMR | PEL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02300 | hp2 | a0001 | c0001 | t0008 | g0131 | AMR | PEL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02451 | hp2 | a0001 | c0001 | t0015 | g0018 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0294 | EAS | KHV | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0107 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02572 | hp2 | a0001 | c0001 | t0007 | g0008 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0042 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0114 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02622 | hp2 | a0001 | c0001 | t0011 | g0106 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0079 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02630 | hp2 | a0001 | c0001 | t0013 | g0138 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0108 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0313 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0299 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0329 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0140 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0312 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0078 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0210 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0134 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0115 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0112 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02886 | hp2 | a0002 | c0005 | t0004 | g0110 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02895 | hp2 | a0001 | c0001 | t0009 | g0137 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02896 | hp2 | a0001 | c0001 | t0014 | g0065 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02897 | hp1 | a0001 | c0001 | t0014 | g0066 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02897 | hp2 | a0001 | c0001 | t0009 | g0141 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0142 | AFR | ESN | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | ESN | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0070 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0267 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03041 | hp1 | a0001 | c0004 | t0005 | g0120 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03041 | hp2 | a0001 | c0006 | t0011 | g0332 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03098 | hp1 | a0001 | c0001 | t0013 | g0135 | AFR | MSL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03098 | hp2 | a0002 | c0005 | t0004 | g0102 | AFR | MSL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03139 | hp1 | a0001 | c0001 | t0010 | g0187 | AFR | ESN | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0099 | AFR | ESN | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03195 | hp1 | a0001 | c0004 | t0005 | g0119 | AFR | ESN | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | ESN | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03209 | hp1 | a0001 | c0001 | t0010 | g0188 | AFR | MSL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03209 | hp2 | a0001 | c0001 | t0007 | g0117 | AFR | MSL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03225 | hp1 | a0001 | c0001 | t0021 | g0330 | AFR | MSL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03225 | hp2 | a0001 | c0004 | t0005 | g0292 | AFR | MSL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03239 | hp1 | a0001 | c0003 | t0002 | g0090 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0309 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03453 | hp1 | a0001 | c0004 | t0005 | g0125 | AFR | MSL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03453 | hp2 | a0002 | c0005 | t0004 | g0111 | AFR | MSL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03486 | hp1 | a0001 | c0004 | t0005 | g0121 | AFR | MSL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | MSL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0308 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0270 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0303 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0072 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0301 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0307 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0144 | AFR | ESN | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0139 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0116 | AFR | GWD | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0105 | AFR | MSL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03579 | hp2 | a0002 | c0005 | t0004 | g0063 | AFR | MSL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0087 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | STU | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0211 | SAS | STU | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0302 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0025 | SAS | BEB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0327 | SAS | BEB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0028 | SAS | BEB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | BEB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0035 | SAS | BEB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0194 | SAS | BEB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | BEB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0076 | SAS | BEB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | STU | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | STU | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | STU | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0041 | SAS | STU | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | STU | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | STU | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | STU | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0058 | SAS | STU | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | YRI | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CHB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0049 | EAS | CHB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | YRI | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18906 | hp2 | a0001 | c0004 | t0005 | g0124 | AFR | YRI | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18946 | hp2 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18948 | hp2 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18953 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18954 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18962 | hp2 | a0004 | c0008 | t0003 | g0318 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18966 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18967 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18969 | hp2 | a0001 | c0002 | t0018 | g0081 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0298 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18992 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18995 | hp1 | a0001 | c0002 | t0002 | g0147 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18997 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19001 | hp2 | a0001 | c0002 | t0002 | g0061 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0316 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0319 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19010 | hp1 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0305 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0118 | AFR | LWK | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | LWK | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19043 | hp1 | a0001 | c0001 | t0010 | g0289 | AFR | LWK | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | LWK | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0097 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0315 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0326 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19063 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0094 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0295 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19089 | hp1 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19090 | hp2 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19240 | hp1 | a0001 | c0001 | t0016 | g0017 | AFR | YRI | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0290 | AFR | YRI | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ASW | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA20129 | hp2 | a0001 | c0004 | t0005 | g0122 | AFR | ASW | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0201 | EUR | TSI | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0244 | EUR | TSI | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0320 | EUR | TSI | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0152 | EUR | TSI | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0314 | SAS | GIH | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA20905 | hp2 | a0001 | c0002 | t0003 | g0075 | SAS | GIH | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01123 | hp1 | a0001 | c0003 | t0002 | g0067 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0136 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02109 | hp2 | a0001 | c0004 | t0005 | g0127 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0036 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02559 | hp1 | a0001 | c0006 | t0011 | g0333 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG02559 | hp2 | a0002 | c0005 | t0004 | g0109 | AFR | ACB | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03471 | hp1 | a0001 | c0001 | t0007 | g0008 | AFR | MSL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | USA | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0145 | AFR | USA | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | USA | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0132 | AFR | USA | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | LWK | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| NA21309 | hp2 | a0001 | c0002 | t0004 | g0051 | AFR | LWK | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0258 | REF | REF | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0086 | REF | REF | GNS_chr12_64708449_64764406 | GNS | chr12 | 64708449 | 64764406 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:64716802 | C | T | 1 | a0002 | 7 | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
missense_variant | MODERATE | c.1598G>A | p.Arg533His | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 1728/5081 | 1598/1659 | 533/552 | chr12 | 64716802 | |||
| chr12:64720149 | G | C | 1 | a0003 | 1 | HG01361.hp1 | missense_variant | MODERATE | c.1453C>G | p.Pro485Ala | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/14 | 1583/5081 | 1453/1659 | 485/552 | chr12 | 64720149 | |||
| chr12:64745666 | T | C | 1 | a0004 | 1 | NA18962.hp2 | missense_variant | MODERATE | c.518A>G | p.Tyr173Cys | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 4/14 | 648/5081 | 518/1659 | 173/552 | chr12 | 64745666 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:64716750 | A | G | 1 | a0001c0004 | 10 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(7): Show |
synonymous_variant | LOW | c.1650T>C | p.His550His | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 1780/5081 | 1650/1659 | 550/552 | chr12 | 64716750 | |||
| chr12:64744875 | C | T | 1 | a0003c0007 | 1 | HG01361.hp1 | synonymous_variant | LOW | c.558G>A | p.Leu186Leu | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 5/14 | 688/5081 | 558/1659 | 186/552 | chr12 | 64744875 | |||
| chr12:64747808 | C | T | 1 | a0001c0003 | 13 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(10): Show |
synonymous_variant | LOW | c.363G>A | p.Lys121Lys | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 3/14 | 493/5081 | 363/1659 | 121/552 | chr12 | 64747808 | |||
| chr12:64752752 | C | T | 6 | a0001c0001 a0001c0004 a0001c0006 others(3): Show |
263 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(260): Show |
synonymous_variant | LOW | c.198G>A | p.Pro66Pro | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/14 | 328/5081 | 198/1659 | 66/552 | chr12 | 64752752 | |||
| chr12:64759256 | G | C | 1 | a0001c0006 | 2 | HG02559.hp1 HG03041.hp2 |
synonymous_variant | LOW | c.21C>G | p.Ala7Ala | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/14 | 151/5081 | 21/1659 | 7/552 | chr12 | 64759256 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:64713671 | T | TAA | 3 | a0001c0001t0011 a0001c0004t0005 a0001c0006t0011 |
13 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3068_*3069dupTT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 3069 | chr12 | 64713671 | ||||||
| chr12:64713900 | G | C | 1 | a0001c0001t0014 | 2 | HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2841C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 2841 | chr12 | 64713900 | ||||||
| chr12:64713932 | C | T | 2 | a0001c0001t0021 a0003c0007t0019 |
2 | HG01361.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2809G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 2809 | chr12 | 64713932 | ||||||
| chr12:64714117 | G | A | 1 | a0001c0001t0016 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2624C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 2624 | chr12 | 64714117 | ||||||
| chr12:64714129 | C | CA | 1 | a0001c0004t0005 | 10 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2611dupT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 2611 | chr12 | 64714129 | ||||||
| chr12:64714380 | G | C | 6 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0010 others(3): Show |
208 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(205): Show |
3_prime_UTR_variant | MODIFIER | c.*2361C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 2361 | chr12 | 64714380 | ||||||
| chr12:64714751 | T | C | 4 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0013 others(1): Show |
14 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1990A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 1990 | chr12 | 64714751 | ||||||
| chr12:64714858 | A | C | 1 | a0001c0002t0018 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1883T>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 1883 | chr12 | 64714858 | ||||||
| chr12:64715093 | G | A | 1 | a0001c0001t0007 | 6 | HG02572.hp2 HG02622.hp1 HG02818.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1648C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 1648 | chr12 | 64715093 | ||||||
| chr12:64715285 | G | A | 3 | a0001c0001t0007 a0001c0001t0011 a0001c0006t0011 |
9 | HG02559.hp1 HG02572.hp2 HG02622.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1456C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 1456 | chr12 | 64715285 | ||||||
| chr12:64715388 | C | T | 5 | a0001c0001t0001 a0001c0001t0003 a0001c0002t0001 others(2): Show |
205 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*1353G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 1353 | chr12 | 64715388 | ||||||
| chr12:64715513 | G | A | 1 | a0001c0001t0007 | 6 | HG02572.hp2 HG02622.hp1 HG02818.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1228C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 1228 | chr12 | 64715513 | ||||||
| chr12:64715799 | T | C | 7 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0008 others(4): Show |
25 | HG00733.hp1 HG01081.hp2 HG01884.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*942A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 942 | chr12 | 64715799 | ||||||
| chr12:64715882 | C | T | 1 | a0001c0002t0017 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*859G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 859 | chr12 | 64715882 | ||||||
| chr12:64715927 | A | G | 1 | a0001c0001t0007 | 6 | HG02572.hp2 HG02622.hp1 HG02818.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*814T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 814 | chr12 | 64715927 | ||||||
| chr12:64716088 | T | G | 1 | a0001c0001t0013 | 2 | HG02630.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*653A>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 653 | chr12 | 64716088 | ||||||
| chr12:64716175 | T | C | 4 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0013 others(1): Show |
14 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*566A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 566 | chr12 | 64716175 | ||||||
| chr12:64716330 | C | T | 7 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0008 others(4): Show |
25 | HG00733.hp1 HG01081.hp2 HG01884.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*411G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 411 | chr12 | 64716330 | ||||||
| chr12:64716361 | G | A | 15 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(12): Show |
245 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*380C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 380 | chr12 | 64716361 | ||||||
| chr12:64716472 | G | A | 4 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0020 others(1): Show |
55 | HG00140.hp2 HG00408.hp2 HG00609.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*269C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 269 | chr12 | 64716472 | ||||||
| chr12:64716500 | G | A | 1 | a0001c0001t0021 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*241C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 241 | chr12 | 64716500 | ||||||
| chr12:64716580 | C | T | 2 | a0001c0001t0009 a0001c0002t0012 |
5 | HG00423.hp2 HG01884.hp1 HG02132.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*161G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 161 | chr12 | 64716580 | ||||||
| chr12:64716682 | C | T | 1 | a0001c0001t0015 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*59G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 14/14 | 59 | chr12 | 64716682 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:64716903 | G | C | 19 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0205 others(16): Show |
19 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.1581-84C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64716903 | |||||||
| chr12:64716972 | C | T | 1 | a0001c0002t0004g0051 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1581-153G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64716972 | |||||||
| chr12:64716975 | C | G | 4 | a0001c0001t0003g0298 a0001c0001t0003g0310 a0001c0001t0003g0319 others(1): Show |
4 | NA18962.hp2 NA18969.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.1581-156G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64716975 | |||||||
| chr12:64717028 | G | A | 24 | a0001c0001t0006g0118 a0001c0001t0006g0132 a0001c0001t0006g0134 others(21): Show |
25 | HG00733.hp1 HG01081.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.1581-209C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64717028 | |||||||
| chr12:64717114 | G | T | 1 | a0001c0004t0005g0120 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1581-295C>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64717114 | |||||||
| chr12:64717249 | T | C | 3 | a0001c0001t0004g0143 a0001c0001t0004g0144 a0001c0001t0004g0145 |
3 | HG01884.hp2 HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1581-430A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64717249 | |||||||
| chr12:64717511 | C | G | 1 | a0001c0001t0001g0185 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1581-692G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64717511 | |||||||
| chr12:64717518 | A | AT | 27 | a0001c0001t0004g0113 a0001c0001t0004g0144 a0001c0001t0006g0132 others(24): Show |
28 | HG01106.hp1 HG01175.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1581-700dupA | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64717518 | |||||||
| chr12:64717518 | AT | A | 8 | a0001c0001t0004g0099 a0001c0001t0004g0104 a0001c0001t0004g0105 others(5): Show |
8 | HG01081.hp2 HG01109.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.1581-700delA | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64717518 | |||||||
| chr12:64717518 | ATTTTTTT others(1): Show |
A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(187): Show |
204 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.1581-707_1581-700d others(10): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64717518 | |||||||
| chr12:64717563 | A | G | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG00621.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1581-744T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64717563 | |||||||
| chr12:64717697 | A | C | 1 | a0001c0001t0003g0297 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1581-878T>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64717697 | |||||||
| chr12:64717799 | G | A | 5 | a0001c0001t0007g0008 a0001c0001t0007g0114 a0001c0001t0007g0115 others(2): Show |
6 | HG02572.hp2 HG02622.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1581-980C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64717799 | |||||||
| chr12:64717825 | T | A | 3 | a0001c0001t0004g0143 a0001c0001t0004g0144 a0001c0001t0004g0145 |
3 | HG01884.hp2 HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1581-1006A>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64717825 | |||||||
| chr12:64717918 | G | A | 1 | a0001c0001t0016g0017 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1581-1099C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64717918 | |||||||
| chr12:64718146 | C | CAACAGGC others(81): Show |
1 | a0001c0001t0004g0143 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1581-1415_1581-132 others(92): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64718146 | |||||||
| chr12:64718240 | G | A | 1 | a0001c0001t0003g0320 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1581-1421C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64718240 | |||||||
| chr12:64718319 | T | G | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(252): Show |
271 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.1581-1500A>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64718319 | |||||||
| chr12:64718788 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1580+1234C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64718788 | |||||||
| chr12:64718856 | C | G | 3 | a0001c0002t0002g0022 a0001c0002t0002g0026 a0001c0002t0002g0071 |
3 | NA18943.hp1 NA18953.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.1580+1166G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64718856 | |||||||
| chr12:64718894 | A | G | 1 | a0001c0001t0008g0128 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1580+1128T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64718894 | |||||||
| chr12:64719046 | G | C | 14 | a0001c0001t0006g0118 a0001c0001t0006g0132 a0001c0001t0006g0134 others(11): Show |
14 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1580+976C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64719046 | |||||||
| chr12:64719383 | G | C | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(277): Show |
297 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.1580+639C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64719383 | |||||||
| chr12:64719516 | A | G | 2 | a0001c0001t0003g0267 a0001c0001t0003g0270 |
2 | HG03017.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1580+506T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64719516 | |||||||
| chr12:64719699 | G | A | 4 | a0001c0001t0003g0298 a0001c0001t0003g0310 a0001c0001t0003g0319 others(1): Show |
4 | NA18962.hp2 NA18969.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.1580+323C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64719699 | |||||||
| chr12:64719809 | G | A | 14 | a0001c0001t0006g0118 a0001c0001t0006g0132 a0001c0001t0006g0134 others(11): Show |
14 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1580+213C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 13/13 | chr12 | 64719809 | |||||||
| chr12:64720285 | TA | T | 18 | a0001c0001t0001g0287 a0001c0001t0004g0007 a0001c0001t0004g0099 others(15): Show |
19 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1420-104delT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 12/13 | chr12 | 64720285 | |||||||
| chr12:64720319 | C | T | 1 | a0001c0002t0002g0084 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1420-137G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 12/13 | chr12 | 64720319 | |||||||
| chr12:64720406 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1420-224A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 12/13 | chr12 | 64720406 | |||||||
| chr12:64720461 | G | C | 1 | a0001c0001t0003g0317 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1420-279C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 12/13 | chr12 | 64720461 | |||||||
| chr12:64720855 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1420-673C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 12/13 | chr12 | 64720855 | |||||||
| chr12:64720866 | C | G | 3 | a0001c0001t0003g0191 a0001c0001t0003g0193 a0001c0001t0003g0313 |
3 | HG01109.hp1 HG01255.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1420-684G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 12/13 | chr12 | 64720866 | |||||||
| chr12:64720875 | TTA | T | 3 | a0001c0001t0008g0129 a0001c0001t0008g0130 a0001c0001t0008g0131 |
3 | HG00733.hp1 HG01081.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1420-695_1420-694d others(4): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 12/13 | chr12 | 64720875 | |||||||
| chr12:64720983 | T | G | 13 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0029 others(10): Show |
13 | HG00280.hp1 HG00639.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.1419+612A>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 12/13 | chr12 | 64720983 | |||||||
| chr12:64721020 | T | C | 1 | a0001c0001t0003g0210 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1419+575A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 12/13 | chr12 | 64721020 | |||||||
| chr12:64721150 | T | A | 1 | a0001c0001t0001g0184 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1419+445A>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 12/13 | chr12 | 64721150 | |||||||
| chr12:64721215 | C | G | 1 | a0001c0001t0003g0198 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1419+380G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 12/13 | chr12 | 64721215 | |||||||
| chr12:64721322 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1419+273T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 12/13 | chr12 | 64721322 | |||||||
| chr12:64722008 | TC | T | 14 | a0001c0001t0006g0118 a0001c0001t0006g0132 a0001c0001t0006g0134 others(11): Show |
14 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1309-304delG | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 11/13 | chr12 | 64722008 | |||||||
| chr12:64722064 | G | T | 31 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0158 others(28): Show |
33 | HG00323.hp1 HG00408.hp1 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.1309-359C>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 11/13 | chr12 | 64722064 | |||||||
| chr12:64722117 | C | T | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1309-412G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 11/13 | chr12 | 64722117 | |||||||
| chr12:64722174 | C | T | 1 | a0001c0001t0003g0316 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1309-469G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 11/13 | chr12 | 64722174 | |||||||
| chr12:64722327 | C | T | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(223): Show |
241 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.1309-622G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 11/13 | chr12 | 64722327 | |||||||
| chr12:64722532 | A | G | 1 | a0001c0002t0018g0081 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1308+474T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 11/13 | chr12 | 64722532 | |||||||
| chr12:64722624 | C | T | 2 | a0001c0001t0004g0107 a0001c0001t0004g0108 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1308+382G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 11/13 | chr12 | 64722624 | |||||||
| chr12:64722667 | C | G | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(221): Show |
239 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1308+339G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 11/13 | chr12 | 64722667 | |||||||
| chr12:64722766 | G | A | 1 | a0001c0002t0002g0039 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1308+240C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 11/13 | chr12 | 64722766 | |||||||
| chr12:64722816 | T | A | 1 | a0001c0001t0001g0262 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1308+190A>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 11/13 | chr12 | 64722816 | |||||||
| chr12:64722817 | C | G | 1 | a0001c0001t0001g0262 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1308+189G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 11/13 | chr12 | 64722817 | |||||||
| chr12:64723218 | C | G | 1 | a0001c0001t0004g0144 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1201-105G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64723218 | |||||||
| chr12:64723308 | C | T | 14 | a0001c0001t0006g0118 a0001c0001t0006g0132 a0001c0001t0006g0134 others(11): Show |
14 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1201-195G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64723308 | |||||||
| chr12:64723561 | A | G | 1 | a0001c0001t0016g0017 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1201-448T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64723561 | |||||||
| chr12:64723609 | T | C | 2 | a0001c0003t0002g0053 a0001c0003t0002g0056 |
2 | HG00639.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1201-496A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64723609 | |||||||
| chr12:64723893 | T | C | 3 | a0001c0001t0011g0106 a0001c0006t0011g0332 a0001c0006t0011g0333 |
3 | HG02559.hp1 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1201-780A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64723893 | |||||||
| chr12:64723943 | C | T | 1 | a0001c0004t0005g0125 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1201-830G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64723943 | |||||||
| chr12:64724373 | T | C | 3 | a0001c0001t0010g0187 a0001c0001t0010g0188 a0001c0001t0010g0289 |
3 | HG03139.hp1 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1201-1260A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64724373 | |||||||
| chr12:64724452 | A | C | 5 | a0001c0001t0001g0186 a0001c0001t0001g0230 a0001c0001t0001g0233 others(2): Show |
5 | HG02015.hp2 HG02080.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.1201-1339T>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64724452 | |||||||
| chr12:64724487 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1201-1374G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64724487 | |||||||
| chr12:64724490 | G | C | 1 | a0001c0001t0016g0017 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1201-1377C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64724490 | |||||||
| chr12:64724501 | A | G | 1 | a0001c0001t0006g0118 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1201-1388T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64724501 | |||||||
| chr12:64724513 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1201-1400G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64724513 | |||||||
| chr12:64724523 | C | T | 1 | a0001c0001t0007g0116 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1201-1410G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64724523 | |||||||
| chr12:64724543 | C | G | 129 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(126): Show |
137 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.1201-1430G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64724543 | |||||||
| chr12:64724627 | G | A | 17 | a0001c0001t0004g0007 a0001c0001t0004g0099 a0001c0001t0004g0103 others(14): Show |
18 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1201-1514C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64724627 | |||||||
| chr12:64724667 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1201-1554C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64724667 | |||||||
| chr12:64725449 | A | G | 1 | a0001c0001t0001g0184 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1201-2336T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64725449 | |||||||
| chr12:64725928 | G | A | 1 | a0001c0002t0002g0087 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1201-2815C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64725928 | |||||||
| chr12:64725995 | C | CA | 17 | a0001c0001t0004g0144 a0001c0001t0006g0118 a0001c0001t0006g0132 others(14): Show |
17 | HG00733.hp1 HG01081.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1201-2883dupT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64725995 | |||||||
| chr12:64725995 | CA | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(192): Show |
209 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.1201-2883delT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64725995 | |||||||
| chr12:64725995 | CAA | C | 17 | a0001c0001t0001g0157 a0001c0001t0001g0163 a0001c0001t0001g0208 others(14): Show |
18 | HG01109.hp2 HG01243.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1201-2884_1201-288 others(6): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64725995 | |||||||
| chr12:64726204 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1200+2752C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64726204 | |||||||
| chr12:64726297 | C | T | 10 | a0001c0004t0005g0119 a0001c0004t0005g0120 a0001c0004t0005g0121 others(7): Show |
10 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1200+2659G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64726297 | |||||||
| chr12:64726532 | C | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(249): Show |
268 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.1200+2424G>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64726532 | |||||||
| chr12:64726578 | T | G | 1 | a0001c0001t0003g0198 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1200+2378A>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64726578 | |||||||
| chr12:64726597 | C | T | 1 | a0001c0001t0003g0199 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1200+2359G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64726597 | |||||||
| chr12:64726928 | T | TA | 15 | a0001c0001t0006g0118 a0001c0001t0006g0132 a0001c0001t0006g0134 others(12): Show |
15 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1200+2027dupT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64726928 | |||||||
| chr12:64726928 | TA | T | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(219): Show |
237 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.1200+2027delT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64726928 | |||||||
| chr12:64727119 | T | C | 1 | a0001c0001t0006g0142 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1200+1837A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64727119 | |||||||
| chr12:64727139 | C | T | 1 | a0001c0001t0001g0286 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1200+1817G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64727139 | |||||||
| chr12:64727212 | T | C | 7 | a0002c0005t0004g0063 a0002c0005t0004g0100 a0002c0005t0004g0101 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1200+1744A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64727212 | |||||||
| chr12:64727270 | T | TA | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(186): Show |
203 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.1200+1685dupT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64727270 | |||||||
| chr12:64727367 | CTGAGG | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(220): Show |
238 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.1200+1584_1200+158 others(9): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64727367 | |||||||
| chr12:64727373 | C | G | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(220): Show |
238 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.1200+1583G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64727373 | |||||||
| chr12:64727375 | GCAGT | G | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(220): Show |
238 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.1200+1577_1200+158 others(8): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64727375 | |||||||
| chr12:64727514 | G | A | 1 | a0001c0001t0006g0142 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1200+1442C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64727514 | |||||||
| chr12:64727584 | G | A | 3 | a0001c0002t0002g0024 a0001c0002t0002g0025 a0001c0002t0002g0046 |
3 | HG03831.hp1 NA18956.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.1200+1372C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64727584 | |||||||
| chr12:64727640 | G | A | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(222): Show |
240 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.1200+1316C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64727640 | |||||||
| chr12:64727829 | G | C | 7 | a0002c0005t0004g0063 a0002c0005t0004g0100 a0002c0005t0004g0101 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1200+1127C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64727829 | |||||||
| chr12:64728024 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1200+932T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64728024 | |||||||
| chr12:64728090 | G | T | 1 | a0001c0004t0005g0125 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1200+866C>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64728090 | |||||||
| chr12:64728205 | C | T | 1 | a0001c0004t0005g0127 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1200+751G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64728205 | |||||||
| chr12:64728217 | C | T | 1 | a0001c0002t0002g0024 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1200+739G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64728217 | |||||||
| chr12:64728383 | T | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(249): Show |
268 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.1200+573A>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64728383 | |||||||
| chr12:64728415 | T | C | 3 | a0001c0002t0002g0062 a0001c0002t0012g0083 a0001c0002t0012g0085 |
3 | HG00423.hp2 HG00558.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.1200+541A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64728415 | |||||||
| chr12:64728491 | T | C | 1 | a0001c0001t0003g0306 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1200+465A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64728491 | |||||||
| chr12:64728516 | G | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(190): Show |
207 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1200+440C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64728516 | |||||||
| chr12:64728556 | G | C | 1 | a0001c0001t0006g0140 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1200+400C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64728556 | |||||||
| chr12:64728582 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0154 a0001c0001t0001g0185 |
4 | HG02257.hp1 HG02258.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1200+374C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64728582 | |||||||
| chr12:64728838 | C | T | 1 | a0001c0001t0016g0017 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1200+118G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 10/13 | chr12 | 64728838 | |||||||
| chr12:64729185 | T | A | 1 | a0001c0002t0002g0084 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1099-128A>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64729185 | |||||||
| chr12:64729197 | T | A | 1 | a0001c0001t0003g0309 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1099-140A>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64729197 | |||||||
| chr12:64729356 | T | C | 2 | a0001c0001t0003g0285 a0001c0001t0003g0296 |
2 | HG00408.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.1099-299A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64729356 | |||||||
| chr12:64729478 | A | G | 11 | a0001c0001t0006g0132 a0001c0001t0006g0134 a0001c0001t0006g0136 others(8): Show |
11 | HG01884.hp1 HG02109.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1099-421T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64729478 | |||||||
| chr12:64729865 | T | C | 1 | a0001c0001t0001g0176 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1099-808A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64729865 | |||||||
| chr12:64730140 | G | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(190): Show |
207 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1099-1083C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64730140 | |||||||
| chr12:64730230 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1099-1173A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64730230 | |||||||
| chr12:64730240 | A | G | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(225): Show |
243 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.1099-1183T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64730240 | |||||||
| chr12:64730309 | C | T | 1 | a0001c0002t0002g0072 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1099-1252G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64730309 | |||||||
| chr12:64730419 | T | C | 1 | a0001c0001t0003g0312 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1099-1362A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64730419 | |||||||
| chr12:64730434 | C | CA | 33 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0177 others(30): Show |
33 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1099-1378dupT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64730434 | |||||||
| chr12:64730434 | CA | C | 82 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0158 others(79): Show |
88 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1099-1378delT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64730434 | |||||||
| chr12:64730434 | CAA | C | 7 | a0001c0001t0003g0199 a0001c0001t0003g0320 a0001c0001t0003g0321 others(4): Show |
7 | HG00642.hp1 HG00733.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.1099-1379_1099-137 others(6): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64730434 | |||||||
| chr12:64730512 | G | A | 7 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0029 others(4): Show |
7 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1099-1455C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64730512 | |||||||
| chr12:64730544 | A | T | 1 | a0001c0002t0004g0051 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1099-1487T>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64730544 | |||||||
| chr12:64730577 | T | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(249): Show |
268 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.1099-1520A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64730577 | |||||||
| chr12:64730918 | A | T | 1 | a0001c0002t0002g0043 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1099-1861T>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64730918 | |||||||
| chr12:64730922 | C | T | 10 | a0001c0001t0007g0008 a0001c0001t0007g0114 a0001c0001t0007g0115 others(7): Show |
11 | HG00733.hp1 HG01081.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1099-1865G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64730922 | |||||||
| chr12:64731319 | C | T | 2 | a0001c0001t0021g0330 a0003c0007t0019g0064 |
2 | HG01361.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1099-2262G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64731319 | |||||||
| chr12:64731413 | A | T | 1 | a0001c0001t0004g0108 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1099-2356T>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64731413 | |||||||
| chr12:64731430 | T | C | 1 | a0003c0007t0019g0064 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1099-2373A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64731430 | |||||||
| chr12:64731910 | T | C | 17 | a0001c0001t0004g0007 a0001c0001t0004g0099 a0001c0001t0004g0103 others(14): Show |
18 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1099-2853A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64731910 | |||||||
| chr12:64731954 | G | A | 3 | a0001c0001t0008g0129 a0001c0001t0008g0130 a0001c0001t0008g0131 |
3 | HG00733.hp1 HG01081.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1099-2897C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64731954 | |||||||
| chr12:64732065 | C | A | 1 | a0001c0001t0003g0300 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1099-3008G>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732065 | |||||||
| chr12:64732153 | A | ATTT | 6 | a0001c0001t0001g0248 a0001c0001t0001g0275 a0001c0001t0001g0282 others(3): Show |
6 | HG00280.hp2 HG02004.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099-3099_1099-309 others(7): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732153 | |||||||
| chr12:64732153 | A | ATTTT | 30 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(27): Show |
36 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.1099-3100_1099-309 others(8): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732153 | |||||||
| chr12:64732153 | A | ATTTTT | 59 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(56): Show |
63 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1099-3101_1099-309 others(9): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732153 | |||||||
| chr12:64732153 | A | ATTTTTT | 52 | a0001c0001t0001g0013 a0001c0001t0001g0155 a0001c0001t0001g0159 others(49): Show |
55 | HG00140.hp2 HG00323.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.1099-3102_1099-309 others(10): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732153 | |||||||
| chr12:64732153 | A | ATTTTTTT | 34 | a0001c0001t0001g0014 a0001c0001t0001g0165 a0001c0001t0001g0183 others(31): Show |
36 | HG00408.hp1 HG00408.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.1099-3103_1099-309 others(11): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732153 | |||||||
| chr12:64732153 | A | ATTTTTTT others(1): Show |
12 | a0001c0001t0001g0158 a0001c0001t0001g0166 a0001c0001t0001g0218 others(9): Show |
12 | HG01109.hp1 HG02523.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1099-3104_1099-309 others(12): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732153 | |||||||
| chr12:64732153 | A | ATTTTTTT others(2): Show |
8 | a0001c0001t0001g0156 a0001c0001t0001g0170 a0001c0001t0001g0207 others(5): Show |
8 | HG00544.hp1 HG01109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1099-3105_1099-309 others(13): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732153 | |||||||
| chr12:64732153 | A | ATTTTTTT others(3): Show |
5 | a0001c0001t0001g0182 a0001c0001t0001g0327 a0001c0001t0003g0210 others(2): Show |
5 | HG00741.hp2 HG02738.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.1099-3106_1099-309 others(14): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732153 | |||||||
| chr12:64732153 | A | ATTTTTTT others(4): Show |
5 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0003g0303 others(2): Show |
5 | HG03195.hp1 HG03491.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.1099-3107_1099-309 others(15): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732153 | |||||||
| chr12:64732153 | A | ATTTTTTT others(5): Show |
2 | a0001c0001t0003g0295 a0001c0001t0003g0301 |
2 | HG03492.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1099-3108_1099-309 others(16): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732153 | |||||||
| chr12:64732153 | A | ATTTTTTT others(9): Show |
1 | a0001c0001t0003g0195 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1099-3097_1099-309 others(20): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732153 | |||||||
| chr12:64732154 | TTTTTTTT others(8): Show |
T | 1 | a0001c0001t0001g0225 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1099-3112_1099-309 others(19): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732154 | |||||||
| chr12:64732163 | T | G | 6 | a0001c0001t0006g0118 a0001c0001t0015g0018 a0001c0002t0002g0035 others(3): Show |
7 | HG01175.hp2 HG01257.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.1099-3106A>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732163 | |||||||
| chr12:64732166 | G | T | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(221): Show |
240 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.1099-3109C>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732166 | |||||||
| chr12:64732169 | G | T | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(219): Show |
237 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.1099-3112C>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732169 | |||||||
| chr12:64732169 | GT | G | 25 | a0001c0001t0006g0118 a0001c0001t0006g0132 a0001c0001t0006g0134 others(22): Show |
26 | HG00733.hp1 HG01081.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1099-3113delA | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732169 | |||||||
| chr12:64732170 | T | G | 4 | a0001c0001t0004g0143 a0001c0001t0004g0144 a0001c0001t0004g0145 others(1): Show |
4 | HG01361.hp1 HG01884.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-3113A>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732170 | |||||||
| chr12:64732175 | T | G | 7 | a0001c0001t0007g0008 a0001c0001t0007g0114 a0001c0001t0007g0115 others(4): Show |
8 | HG01361.hp1 HG02572.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1099-3118A>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732175 | |||||||
| chr12:64732191 | G | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(190): Show |
207 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1099-3134C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732191 | |||||||
| chr12:64732216 | G | T | 1 | a0001c0001t0001g0160 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1099-3159C>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732216 | |||||||
| chr12:64732255 | C | T | 30 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0150 others(27): Show |
33 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.1099-3198G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732255 | |||||||
| chr12:64732260 | C | T | 17 | a0001c0001t0004g0007 a0001c0001t0004g0099 a0001c0001t0004g0103 others(14): Show |
18 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1099-3203G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732260 | |||||||
| chr12:64732308 | C | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(200): Show |
217 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.1099-3251G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732308 | |||||||
| chr12:64732359 | G | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(190): Show |
207 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1099-3302C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732359 | |||||||
| chr12:64732404 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1099-3347C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732404 | |||||||
| chr12:64732437 | G | A | 17 | a0001c0001t0004g0007 a0001c0001t0004g0099 a0001c0001t0004g0103 others(14): Show |
18 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1099-3380C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732437 | |||||||
| chr12:64732460 | G | A | 4 | a0001c0001t0001g0152 a0001c0001t0011g0106 a0001c0006t0011g0332 others(1): Show |
4 | HG02559.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1099-3403C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732460 | |||||||
| chr12:64732907 | A | G | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(227): Show |
246 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.1099-3850T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64732907 | |||||||
| chr12:64733044 | G | C | 1 | a0001c0001t0003g0306 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1098+3960C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64733044 | |||||||
| chr12:64733104 | G | A | 4 | a0001c0001t0008g0128 a0001c0001t0008g0129 a0001c0001t0008g0130 others(1): Show |
4 | HG00733.hp1 HG01081.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+3900C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64733104 | |||||||
| chr12:64733144 | A | T | 1 | a0001c0001t0021g0330 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1098+3860T>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64733144 | |||||||
| chr12:64733297 | C | CA | 92 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0014 others(89): Show |
96 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.1098+3706dupT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64733297 | |||||||
| chr12:64733297 | C | CAA | 20 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0001g0185 others(17): Show |
20 | HG00140.hp2 HG00280.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.1098+3705_1098+370 others(6): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64733297 | |||||||
| chr12:64733297 | CA | C | 25 | a0001c0001t0001g0162 a0001c0001t0001g0175 a0001c0001t0001g0186 others(22): Show |
25 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.1098+3706delT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64733297 | |||||||
| chr12:64733297 | CAA | C | 10 | a0001c0001t0004g0104 a0001c0001t0004g0108 a0001c0001t0007g0008 others(7): Show |
11 | HG00733.hp1 HG01081.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1098+3705_1098+370 others(6): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64733297 | |||||||
| chr12:64733297 | CAAA | C | 10 | a0001c0001t0004g0007 a0001c0001t0004g0099 a0001c0001t0004g0103 others(7): Show |
11 | HG01243.hp1 HG02257.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1098+3704_1098+370 others(7): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64733297 | |||||||
| chr12:64733297 | CAAAA | C | 6 | a0001c0002t0004g0051 a0002c0005t0004g0063 a0002c0005t0004g0100 others(3): Show |
6 | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1098+3703_1098+370 others(8): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64733297 | |||||||
| chr12:64733329 | T | A | 1 | a0001c0001t0001g0257 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1098+3675A>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64733329 | |||||||
| chr12:64733589 | G | C | 1 | a0001c0001t0001g0233 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1098+3415C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64733589 | |||||||
| chr12:64733745 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1098+3259C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64733745 | |||||||
| chr12:64733894 | T | C | 1 | a0001c0002t0012g0085 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1098+3110A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64733894 | |||||||
| chr12:64734066 | C | T | 9 | a0001c0001t0004g0007 a0001c0001t0004g0099 a0001c0001t0004g0103 others(6): Show |
10 | HG01109.hp2 HG01243.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1098+2938G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64734066 | |||||||
| chr12:64734072 | T | C | 13 | a0001c0001t0011g0106 a0001c0004t0005g0119 a0001c0004t0005g0120 others(10): Show |
13 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1098+2932A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64734072 | |||||||
| chr12:64734275 | A | T | 1 | a0001c0001t0003g0309 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1098+2729T>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64734275 | |||||||
| chr12:64734400 | G | A | 5 | a0001c0001t0007g0008 a0001c0001t0007g0114 a0001c0001t0007g0115 others(2): Show |
6 | HG02572.hp2 HG02622.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1098+2604C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64734400 | |||||||
| chr12:64734452 | C | T | 1 | a0001c0002t0002g0032 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1098+2552G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64734452 | |||||||
| chr12:64734570 | C | T | 1 | a0001c0003t0002g0006 | 2 | HG01257.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1098+2434G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64734570 | |||||||
| chr12:64734839 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1098+2165C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64734839 | |||||||
| chr12:64734929 | C | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(190): Show |
207 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1098+2075G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64734929 | |||||||
| chr12:64735188 | G | A | 17 | a0001c0001t0004g0007 a0001c0001t0004g0099 a0001c0001t0004g0103 others(14): Show |
18 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1098+1816C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64735188 | |||||||
| chr12:64735640 | C | G | 1 | a0001c0001t0001g0151 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1098+1364G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64735640 | |||||||
| chr12:64736062 | T | A | 1 | a0001c0001t0016g0017 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1098+942A>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64736062 | |||||||
| chr12:64736110 | T | C | 1 | a0001c0001t0003g0192 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1098+894A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64736110 | |||||||
| chr12:64736115 | A | T | 2 | a0001c0001t0021g0330 a0003c0007t0019g0064 |
2 | HG01361.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1098+889T>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64736115 | |||||||
| chr12:64736122 | G | T | 2 | a0001c0001t0003g0307 a0001c0001t0003g0308 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1098+882C>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64736122 | |||||||
| chr12:64736159 | C | A | 1 | a0001c0003t0002g0054 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1098+845G>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64736159 | |||||||
| chr12:64736202 | C | T | 5 | a0001c0001t0007g0008 a0001c0001t0007g0114 a0001c0001t0007g0115 others(2): Show |
6 | HG02572.hp2 HG02622.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1098+802G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64736202 | |||||||
| chr12:64736469 | G | C | 3 | a0001c0001t0008g0129 a0001c0001t0008g0130 a0001c0001t0008g0131 |
3 | HG00733.hp1 HG01081.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1098+535C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64736469 | |||||||
| chr12:64736643 | T | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(249): Show |
268 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.1098+361A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64736643 | |||||||
| chr12:64736940 | G | C | 1 | a0001c0001t0001g0154 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1098+64C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 9/13 | chr12 | 64736940 | |||||||
| chr12:64737930 | C | T | 1 | a0001c0001t0021g0330 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.995-823G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64737930 | |||||||
| chr12:64738036 | G | T | 1 | a0001c0001t0001g0173 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.995-929C>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64738036 | |||||||
| chr12:64738135 | G | A | 3 | a0001c0001t0011g0106 a0001c0006t0011g0332 a0001c0006t0011g0333 |
3 | HG02559.hp1 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.995-1028C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64738135 | |||||||
| chr12:64738156 | T | A | 1 | a0001c0001t0006g0118 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.995-1049A>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64738156 | |||||||
| chr12:64738353 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.994+1028G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64738353 | |||||||
| chr12:64738359 | T | C | 1 | a0001c0001t0003g0317 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.994+1022A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64738359 | |||||||
| chr12:64738539 | C | T | 14 | a0001c0001t0006g0118 a0001c0001t0006g0132 a0001c0001t0006g0134 others(11): Show |
14 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.994+842G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64738539 | |||||||
| chr12:64738674 | G | A | 1 | a0001c0002t0004g0051 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.994+707C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64738674 | |||||||
| chr12:64738761 | C | T | 2 | a0001c0001t0021g0330 a0003c0007t0019g0064 |
2 | HG01361.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.994+620G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64738761 | |||||||
| chr12:64738815 | C | T | 4 | a0001c0001t0001g0206 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | HG02027.hp2 NA18747.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.994+566G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64738815 | |||||||
| chr12:64738825 | C | CA | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(205): Show |
223 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.994+555_994+556ins others(1): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64738825 | |||||||
| chr12:64738826 | C | A | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(206): Show |
224 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.994+555G>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64738826 | |||||||
| chr12:64738826 | C | CA | 26 | a0001c0001t0001g0165 a0001c0001t0001g0234 a0001c0001t0001g0327 others(23): Show |
26 | HG00280.hp1 HG00639.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.994+554dupT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64738826 | |||||||
| chr12:64738827 | A | C | 1 | a0001c0001t0006g0142 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.994+554T>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64738827 | |||||||
| chr12:64738847 | T | C | 3 | a0001c0001t0004g0143 a0001c0001t0004g0144 a0001c0001t0004g0145 |
3 | HG01884.hp2 HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.994+534A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64738847 | |||||||
| chr12:64738946 | A | G | 1 | a0001c0001t0001g0241 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.994+435T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64738946 | |||||||
| chr12:64739181 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0274 |
2 | NA18960.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.994+200C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64739181 | |||||||
| chr12:64739197 | T | A | 1 | a0001c0001t0003g0300 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.994+184A>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64739197 | |||||||
| chr12:64739202 | C | T | 17 | a0001c0001t0004g0007 a0001c0001t0004g0099 a0001c0001t0004g0103 others(14): Show |
18 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.994+179G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64739202 | |||||||
| chr12:64739228 | T | C | 2 | a0001c0001t0021g0330 a0003c0007t0019g0064 |
2 | HG01361.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.994+153A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 8/13 | chr12 | 64739228 | |||||||
| chr12:64739502 | G | A | 1 | a0001c0001t0016g0017 | 1 | NA19240.hp1 | splice_region_variant&intron_variant | LOW | c.876-3C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 7/13 | chr12 | 64739502 | |||||||
| chr12:64739564 | C | CA | 18 | a0001c0001t0001g0154 a0001c0001t0001g0160 a0001c0001t0001g0172 others(15): Show |
18 | HG00639.hp1 HG01106.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.876-66dupT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 7/13 | chr12 | 64739564 | |||||||
| chr12:64739585 | A | C | 3 | a0001c0002t0002g0022 a0001c0002t0002g0026 a0001c0002t0002g0071 |
3 | NA18943.hp1 NA18953.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.876-86T>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 7/13 | chr12 | 64739585 | |||||||
| chr12:64739681 | C | T | 13 | a0001c0001t0011g0106 a0001c0004t0005g0119 a0001c0004t0005g0120 others(10): Show |
13 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.876-182G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 7/13 | chr12 | 64739681 | |||||||
| chr12:64739849 | G | A | 3 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0322 |
3 | HG02280.hp1 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.876-350C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 7/13 | chr12 | 64739849 | |||||||
| chr12:64739864 | C | G | 122 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(119): Show |
130 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.876-365G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 7/13 | chr12 | 64739864 | |||||||
| chr12:64740089 | G | A | 17 | a0001c0001t0004g0007 a0001c0001t0004g0099 a0001c0001t0004g0103 others(14): Show |
18 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.875+517C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 7/13 | chr12 | 64740089 | |||||||
| chr12:64740485 | C | T | 1 | a0001c0001t0021g0330 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.875+121G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 7/13 | chr12 | 64740485 | |||||||
| chr12:64740756 | C | G | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(244): Show |
262 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.793-68G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64740756 | |||||||
| chr12:64741047 | TAGAAAAT others(169): Show |
T | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(249): Show |
268 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.793-535_793-360del | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64741047 | |||||||
| chr12:64741268 | T | C | 3 | a0001c0001t0003g0301 a0001c0001t0003g0302 a0001c0001t0003g0303 |
3 | HG03491.hp1 HG03492.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.793-580A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64741268 | |||||||
| chr12:64741320 | C | T | 1 | a0001c0001t0004g0143 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.793-632G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64741320 | |||||||
| chr12:64741354 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.793-666G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64741354 | |||||||
| chr12:64741407 | A | G | 2 | a0001c0001t0021g0330 a0003c0007t0019g0064 |
2 | HG01361.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.793-719T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64741407 | |||||||
| chr12:64741491 | C | T | 1 | a0001c0001t0003g0305 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.793-803G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64741491 | |||||||
| chr12:64741590 | T | C | 1 | a0001c0002t0018g0081 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.793-902A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64741590 | |||||||
| chr12:64741742 | C | T | 1 | a0003c0007t0019g0064 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.793-1054G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64741742 | |||||||
| chr12:64742057 | G | A | 1 | a0001c0002t0002g0039 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.792+1084C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742057 | |||||||
| chr12:64742114 | G | A | 2 | a0001c0001t0014g0065 a0001c0001t0014g0066 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.792+1027C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742114 | |||||||
| chr12:64742158 | G | C | 1 | a0001c0002t0004g0051 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.792+983C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742158 | |||||||
| chr12:64742210 | T | C | 2 | a0001c0001t0004g0144 a0001c0001t0004g0145 |
2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.792+931A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742210 | |||||||
| chr12:64742216 | T | G | 3 | a0001c0001t0008g0129 a0001c0001t0008g0130 a0001c0001t0008g0131 |
3 | HG00733.hp1 HG01081.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.792+925A>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742216 | |||||||
| chr12:64742221 | T | C | 2 | a0001c0001t0001g0254 a0001c0001t0001g0304 |
2 | HG00673.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.792+920A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742221 | |||||||
| chr12:64742242 | A | G | 4 | a0001c0001t0001g0257 a0001c0001t0004g0144 a0001c0001t0004g0145 others(1): Show |
4 | HG01256.hp2 HG03225.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.792+899T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742242 | |||||||
| chr12:64742255 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.792+886G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742255 | |||||||
| chr12:64742261 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.792+880A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742261 | |||||||
| chr12:64742266 | C | G | 5 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0004t0005g0120 others(2): Show |
5 | HG02717.hp1 HG02809.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.792+875G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742266 | |||||||
| chr12:64742271 | T | C | 1 | a0003c0007t0019g0064 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.792+870A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742271 | |||||||
| chr12:64742299 | C | T | 2 | a0001c0003t0002g0067 a0001c0003t0002g0090 |
2 | HG01123.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.792+842G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742299 | |||||||
| chr12:64742300 | A | G | 5 | a0001c0001t0008g0129 a0001c0001t0008g0130 a0001c0001t0008g0131 others(2): Show |
5 | HG00733.hp1 HG01081.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.792+841T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742300 | |||||||
| chr12:64742312 | G | A | 1 | a0001c0002t0020g0074 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.792+829C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742312 | |||||||
| chr12:64742413 | T | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(131): Show |
143 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.792+728A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742413 | |||||||
| chr12:64742415 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.792+726A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742415 | |||||||
| chr12:64742743 | C | G | 1 | a0001c0001t0003g0244 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.792+398G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742743 | |||||||
| chr12:64742774 | C | T | 2 | a0001c0001t0014g0065 a0001c0001t0014g0066 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.792+367G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742774 | |||||||
| chr12:64742847 | G | A | 2 | a0001c0001t0014g0065 a0001c0001t0014g0066 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.792+294C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64742847 | |||||||
| chr12:64743062 | G | A | 1 | a0001c0003t0002g0054 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.792+79C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64743062 | |||||||
| chr12:64743087 | C | G | 2 | a0001c0003t0002g0077 a0001c0003t0002g0089 |
2 | HG00733.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.792+54G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64743087 | |||||||
| chr12:64743116 | G | C | 3 | a0001c0001t0004g0143 a0001c0001t0004g0144 a0001c0001t0004g0145 |
3 | HG01884.hp2 HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.792+25C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64743116 | |||||||
| chr12:64743125 | T | C | 2 | a0001c0001t0021g0330 a0003c0007t0019g0064 |
2 | HG01361.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.792+16A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 6/13 | chr12 | 64743125 | |||||||
| chr12:64743356 | G | A | 10 | a0001c0001t0004g0007 a0001c0001t0004g0099 a0001c0001t0004g0103 others(7): Show |
11 | HG01109.hp2 HG01243.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.625-48C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 5/13 | chr12 | 64743356 | |||||||
| chr12:64743385 | G | T | 8 | a0001c0001t0004g0007 a0001c0001t0004g0099 a0001c0001t0004g0103 others(5): Show |
9 | HG01109.hp2 HG01243.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.625-77C>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 5/13 | chr12 | 64743385 | |||||||
| chr12:64743626 | A | T | 17 | a0001c0001t0004g0007 a0001c0001t0004g0099 a0001c0001t0004g0103 others(14): Show |
18 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.625-318T>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 5/13 | chr12 | 64743626 | |||||||
| chr12:64743631 | G | A | 1 | a0001c0001t0016g0017 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.625-323C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 5/13 | chr12 | 64743631 | |||||||
| chr12:64743673 | A | G | 1 | a0001c0001t0001g0173 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.625-365T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 5/13 | chr12 | 64743673 | |||||||
| chr12:64743731 | T | C | 2 | a0001c0001t0014g0065 a0001c0001t0014g0066 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.625-423A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 5/13 | chr12 | 64743731 | |||||||
| chr12:64743921 | C | T | 2 | a0001c0001t0001g0160 a0001c0001t0001g0243 |
2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.625-613G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 5/13 | chr12 | 64743921 | |||||||
| chr12:64744201 | G | A | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(242): Show |
261 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.624+608C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 5/13 | chr12 | 64744201 | |||||||
| chr12:64744352 | A | G | 1 | a0001c0002t0003g0075 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.624+457T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 5/13 | chr12 | 64744352 | |||||||
| chr12:64744474 | T | C | 1 | a0001c0001t0001g0209 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.624+335A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 5/13 | chr12 | 64744474 | |||||||
| chr12:64744501 | A | G | 1 | a0001c0001t0001g0242 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.624+308T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 5/13 | chr12 | 64744501 | |||||||
| chr12:64744542 | TC | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(185): Show |
202 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.624+266delG | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 5/13 | chr12 | 64744542 | |||||||
| chr12:64744555 | A | T | 1 | a0001c0001t0001g0162 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.624+254T>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 5/13 | chr12 | 64744555 | |||||||
| chr12:64745032 | A | G | 1 | a0001c0002t0002g0020 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.526-125T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 4/13 | chr12 | 64745032 | |||||||
| chr12:64745136 | C | G | 2 | a0001c0002t0002g0048 a0001c0002t0002g0049 |
2 | HG02071.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.526-229G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 4/13 | chr12 | 64745136 | |||||||
| chr12:64745164 | G | A | 17 | a0001c0001t0004g0007 a0001c0001t0004g0099 a0001c0001t0004g0103 others(14): Show |
18 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.526-257C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 4/13 | chr12 | 64745164 | |||||||
| chr12:64745204 | CT | C | 65 | a0001c0001t0001g0154 a0001c0001t0001g0163 a0001c0001t0001g0215 others(62): Show |
67 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.526-298delA | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 4/13 | chr12 | 64745204 | |||||||
| chr12:64745204 | CTT | C | 62 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0170 others(59): Show |
62 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.526-299_526-298del others(2): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 4/13 | chr12 | 64745204 | |||||||
| chr12:64745204 | CTTT | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(162): Show |
181 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.526-300_526-298del others(3): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 4/13 | chr12 | 64745204 | |||||||
| chr12:64745204 | CTTTT | C | 9 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(6): Show |
9 | HG00280.hp2 HG00544.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-301_526-298del others(4): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 4/13 | chr12 | 64745204 | |||||||
| chr12:64745204 | CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0008g0129 a0001c0001t0008g0130 a0001c0001t0008g0131 |
3 | HG00733.hp1 HG01081.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.526-307_526-298del others(10): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 4/13 | chr12 | 64745204 | |||||||
| chr12:64745204 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0001g0287 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.526-312_526-298del others(15): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 4/13 | chr12 | 64745204 | |||||||
| chr12:64745218 | T | G | 3 | a0001c0001t0004g0143 a0001c0001t0004g0144 a0001c0001t0004g0145 |
3 | HG01884.hp2 HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.526-311A>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 4/13 | chr12 | 64745218 | |||||||
| chr12:64745314 | G | A | 2 | a0001c0001t0004g0144 a0001c0001t0004g0145 |
2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.525+345C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 4/13 | chr12 | 64745314 | |||||||
| chr12:64745484 | T | C | 1 | a0001c0001t0011g0106 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.525+175A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 4/13 | chr12 | 64745484 | |||||||
| chr12:64745625 | C | T | 17 | a0001c0001t0004g0007 a0001c0001t0004g0099 a0001c0001t0004g0103 others(14): Show |
18 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.525+34G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 4/13 | chr12 | 64745625 | |||||||
| chr12:64746004 | A | G | 2 | a0001c0006t0011g0332 a0001c0006t0011g0333 |
2 | HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.460-280T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 3/13 | chr12 | 64746004 | |||||||
| chr12:64746212 | TCCACACA others(7): Show |
T | 23 | a0001c0001t0006g0118 a0001c0001t0006g0132 a0001c0001t0006g0134 others(20): Show |
23 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.460-502_460-489del others(14): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 3/13 | chr12 | 64746212 | |||||||
| chr12:64746340 | G | A | 2 | a0001c0006t0011g0332 a0001c0006t0011g0333 |
2 | HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.460-616C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 3/13 | chr12 | 64746340 | |||||||
| chr12:64747021 | G | C | 23 | a0001c0001t0006g0118 a0001c0001t0006g0132 a0001c0001t0006g0134 others(20): Show |
23 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.459+691C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 3/13 | chr12 | 64747021 | |||||||
| chr12:64747076 | G | T | 1 | a0001c0001t0001g0226 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.459+636C>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 3/13 | chr12 | 64747076 | |||||||
| chr12:64747186 | C | T | 10 | a0001c0004t0005g0119 a0001c0004t0005g0120 a0001c0004t0005g0121 others(7): Show |
10 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.459+526G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 3/13 | chr12 | 64747186 | |||||||
| chr12:64747340 | T | C | 1 | a0001c0001t0015g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.459+372A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 3/13 | chr12 | 64747340 | |||||||
| chr12:64747531 | T | C | 1 | a0001c0001t0001g0284 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.459+181A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 3/13 | chr12 | 64747531 | |||||||
| chr12:64747571 | G | A | 3 | a0001c0001t0003g0198 a0001c0001t0003g0285 a0001c0001t0003g0296 |
3 | HG00408.hp2 HG01978.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.459+141C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 3/13 | chr12 | 64747571 | |||||||
| chr12:64747698 | A | G | 8 | a0001c0001t0004g0007 a0001c0001t0004g0099 a0001c0001t0004g0103 others(5): Show |
9 | HG01109.hp2 HG01243.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.459+14T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 3/13 | chr12 | 64747698 | |||||||
| chr12:64747942 | C | T | 1 | a0001c0001t0016g0017 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.253-24G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64747942 | |||||||
| chr12:64747989 | A | G | 4 | a0001c0001t0008g0128 a0001c0001t0008g0129 a0001c0001t0008g0130 others(1): Show |
4 | HG00733.hp1 HG01081.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.253-71T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64747989 | |||||||
| chr12:64748034 | C | T | 23 | a0001c0001t0006g0118 a0001c0001t0006g0132 a0001c0001t0006g0134 others(20): Show |
23 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.253-116G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64748034 | |||||||
| chr12:64748191 | G | A | 35 | a0001c0001t0006g0118 a0001c0001t0006g0132 a0001c0001t0006g0134 others(32): Show |
36 | HG00733.hp1 HG01081.hp2 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.253-273C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64748191 | |||||||
| chr12:64748199 | AGTT | A | 17 | a0001c0001t0004g0007 a0001c0001t0004g0099 a0001c0001t0004g0103 others(14): Show |
18 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.253-284_253-282del others(3): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64748199 | |||||||
| chr12:64748417 | C | T | 1 | a0001c0001t0006g0142 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.253-499G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64748417 | |||||||
| chr12:64748634 | A | C | 1 | a0001c0001t0001g0225 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.253-716T>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64748634 | |||||||
| chr12:64748700 | T | C | 1 | a0001c0001t0006g0142 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.253-782A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64748700 | |||||||
| chr12:64748771 | A | G | 1 | a0001c0001t0001g0205 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.253-853T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64748771 | |||||||
| chr12:64748844 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0154 a0001c0001t0001g0185 |
4 | HG02257.hp1 HG02258.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.253-926C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64748844 | |||||||
| chr12:64748960 | G | A | 4 | a0001c0001t0008g0128 a0001c0001t0008g0129 a0001c0001t0008g0130 others(1): Show |
4 | HG00733.hp1 HG01081.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.253-1042C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64748960 | |||||||
| chr12:64748962 | T | G | 35 | a0001c0001t0006g0118 a0001c0001t0006g0132 a0001c0001t0006g0134 others(32): Show |
36 | HG00733.hp1 HG01081.hp2 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.253-1044A>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64748962 | |||||||
| chr12:64748964 | G | A | 4 | a0001c0001t0008g0128 a0001c0001t0008g0129 a0001c0001t0008g0130 others(1): Show |
4 | HG00733.hp1 HG01081.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.253-1046C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64748964 | |||||||
| chr12:64748970 | C | T | 1 | a0001c0001t0016g0017 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.253-1052G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64748970 | |||||||
| chr12:64748980 | C | T | 2 | a0001c0002t0002g0068 a0001c0002t0002g0096 |
2 | HG00140.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.253-1062G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64748980 | |||||||
| chr12:64749001 | G | A | 1 | a0001c0002t0001g0028 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.253-1083C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749001 | |||||||
| chr12:64749033 | G | A | 3 | a0001c0001t0006g0132 a0001c0001t0006g0136 a0001c0001t0006g0140 |
3 | HG02109.hp1 HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.253-1115C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749033 | |||||||
| chr12:64749089 | G | A | 1 | a0001c0002t0002g0149 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.253-1171C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749089 | |||||||
| chr12:64749182 | A | G | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(261): Show |
280 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.253-1264T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749182 | |||||||
| chr12:64749248 | C | CT | 16 | a0001c0001t0001g0154 a0001c0001t0001g0165 a0001c0001t0001g0166 others(13): Show |
16 | HG00423.hp1 HG01255.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.253-1331dupA | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749248 | |||||||
| chr12:64749248 | CT | C | 76 | a0001c0001t0001g0159 a0001c0001t0001g0164 a0001c0001t0004g0007 others(73): Show |
79 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.253-1331delA | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749248 | |||||||
| chr12:64749248 | CTT | C | 56 | a0001c0002t0001g0028 a0001c0002t0001g0041 a0001c0002t0001g0042 others(53): Show |
58 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.253-1332_253-1331d others(4): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749248 | |||||||
| chr12:64749336 | T | C | 2 | a0001c0006t0011g0332 a0001c0006t0011g0333 |
2 | HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.253-1418A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749336 | |||||||
| chr12:64749363 | C | T | 5 | a0001c0001t0007g0008 a0001c0001t0007g0114 a0001c0001t0007g0115 others(2): Show |
6 | HG02572.hp2 HG02622.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.253-1445G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749363 | |||||||
| chr12:64749366 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.253-1448G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749366 | |||||||
| chr12:64749409 | C | T | 9 | a0001c0001t0001g0222 a0001c0001t0004g0007 a0001c0001t0004g0099 others(6): Show |
10 | HG01109.hp2 HG01243.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.253-1491G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749409 | |||||||
| chr12:64749410 | G | A | 5 | a0001c0001t0007g0008 a0001c0001t0007g0114 a0001c0001t0007g0115 others(2): Show |
6 | HG02572.hp2 HG02622.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.253-1492C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749410 | |||||||
| chr12:64749551 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.253-1633G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749551 | |||||||
| chr12:64749602 | A | G | 143 | a0001c0001t0004g0007 a0001c0001t0004g0099 a0001c0001t0004g0103 others(140): Show |
148 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.253-1684T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749602 | |||||||
| chr12:64749623 | C | T | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG00423.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.253-1705G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749623 | |||||||
| chr12:64749668 | G | A | 1 | a0001c0004t0005g0127 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.253-1750C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749668 | |||||||
| chr12:64749729 | A | G | 1 | a0001c0001t0021g0330 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.253-1811T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749729 | |||||||
| chr12:64749776 | T | C | 2 | a0001c0006t0011g0332 a0001c0006t0011g0333 |
2 | HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.253-1858A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749776 | |||||||
| chr12:64749873 | A | AT | 125 | a0001c0001t0001g0162 a0001c0001t0001g0327 a0001c0001t0004g0143 others(122): Show |
129 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.253-1956dupA | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749873 | |||||||
| chr12:64749921 | G | A | 1 | a0001c0001t0001g0286 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.253-2003C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64749921 | |||||||
| chr12:64750028 | C | A | 1 | a0001c0001t0001g0287 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.253-2110G>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64750028 | |||||||
| chr12:64750187 | T | C | 6 | a0001c0001t0001g0186 a0001c0001t0007g0008 a0001c0001t0007g0114 others(3): Show |
7 | HG02572.hp2 HG02622.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.253-2269A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64750187 | |||||||
| chr12:64750196 | G | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(185): Show |
202 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.253-2278C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64750196 | |||||||
| chr12:64750255 | G | C | 1 | a0001c0001t0001g0288 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.253-2337C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64750255 | |||||||
| chr12:64750384 | T | C | 1 | a0001c0001t0015g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.252+2314A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64750384 | |||||||
| chr12:64750495 | A | T | 142 | a0001c0001t0004g0007 a0001c0001t0004g0099 a0001c0001t0004g0103 others(139): Show |
147 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.252+2203T>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64750495 | |||||||
| chr12:64750631 | C | T | 4 | a0001c0001t0008g0128 a0001c0001t0008g0129 a0001c0001t0008g0130 others(1): Show |
4 | HG00733.hp1 HG01081.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+2067G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64750631 | |||||||
| chr12:64750658 | A | G | 1 | a0003c0007t0019g0064 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.252+2040T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64750658 | |||||||
| chr12:64750679 | G | A | 35 | a0001c0001t0006g0118 a0001c0001t0006g0132 a0001c0001t0006g0134 others(32): Show |
36 | HG00733.hp1 HG01081.hp2 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.252+2019C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64750679 | |||||||
| chr12:64750704 | A | G | 23 | a0001c0001t0006g0118 a0001c0001t0006g0132 a0001c0001t0006g0134 others(20): Show |
23 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.252+1994T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64750704 | |||||||
| chr12:64750811 | C | T | 4 | a0001c0001t0004g0143 a0001c0001t0004g0144 a0001c0001t0004g0145 others(1): Show |
4 | HG01884.hp2 HG03516.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+1887G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64750811 | |||||||
| chr12:64750812 | G | A | 23 | a0001c0001t0006g0118 a0001c0001t0006g0132 a0001c0001t0006g0134 others(20): Show |
23 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.252+1886C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64750812 | |||||||
| chr12:64750855 | T | C | 1 | a0001c0002t0002g0087 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.252+1843A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64750855 | |||||||
| chr12:64750955 | C | T | 2 | a0001c0001t0014g0065 a0001c0001t0014g0066 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.252+1743G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64750955 | |||||||
| chr12:64750984 | G | T | 1 | a0001c0001t0001g0010 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.252+1714C>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64750984 | |||||||
| chr12:64751132 | G | A | 5 | a0001c0001t0007g0008 a0001c0001t0007g0114 a0001c0001t0007g0115 others(2): Show |
6 | HG02572.hp2 HG02622.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.252+1566C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64751132 | |||||||
| chr12:64751343 | C | A | 10 | a0001c0001t0004g0007 a0001c0001t0004g0099 a0001c0001t0004g0103 others(7): Show |
11 | HG01109.hp2 HG01243.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.252+1355G>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64751343 | |||||||
| chr12:64751375 | A | G | 1 | a0001c0002t0003g0075 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.252+1323T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64751375 | |||||||
| chr12:64751444 | G | A | 4 | a0001c0001t0008g0128 a0001c0001t0008g0129 a0001c0001t0008g0130 others(1): Show |
4 | HG00733.hp1 HG01081.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+1254C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64751444 | |||||||
| chr12:64751599 | C | T | 33 | a0001c0002t0001g0028 a0001c0002t0001g0041 a0001c0002t0001g0042 others(30): Show |
34 | HG01175.hp2 HG01361.hp2 HG01515.hp1 others(31): Show |
intron_variant | MODIFIER | c.252+1099G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64751599 | |||||||
| chr12:64751637 | C | T | 1 | a0003c0007t0019g0064 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.252+1061G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64751637 | |||||||
| chr12:64751660 | T | C | 3 | a0001c0002t0002g0005 a0001c0002t0002g0057 a0001c0002t0002g0091 |
4 | HG02155.hp1 NA18966.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+1038A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64751660 | |||||||
| chr12:64751787 | G | A | 17 | a0001c0001t0004g0007 a0001c0001t0004g0099 a0001c0001t0004g0103 others(14): Show |
18 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.252+911C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64751787 | |||||||
| chr12:64751951 | C | CA | 27 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0325 others(24): Show |
30 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.252+746dupT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64751951 | |||||||
| chr12:64751951 | CA | C | 10 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0003g0294 others(7): Show |
10 | HG00140.hp1 HG00639.hp2 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.252+746delT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64751951 | |||||||
| chr12:64752102 | TTAAA | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(185): Show |
202 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.252+592_252+595del others(4): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64752102 | |||||||
| chr12:64752324 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.252+374T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64752324 | |||||||
| chr12:64752507 | T | C | 1 | a0001c0001t0001g0291 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.252+191A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64752507 | |||||||
| chr12:64752511 | C | T | 2 | a0001c0006t0011g0332 a0001c0006t0011g0333 |
2 | HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.252+187G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 2/13 | chr12 | 64752511 | |||||||
| chr12:64752896 | T | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(185): Show |
202 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.193-139A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64752896 | |||||||
| chr12:64753009 | G | T | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | NA18747.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.193-252C>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64753009 | |||||||
| chr12:64753079 | G | A | 4 | a0001c0002t0002g0038 a0001c0002t0002g0058 a0001c0002t0002g0092 others(1): Show |
4 | HG00735.hp2 HG01074.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-322C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64753079 | |||||||
| chr12:64753591 | T | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(207): Show |
225 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.193-834A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64753591 | |||||||
| chr12:64753600 | G | T | 1 | a0001c0004t0005g0119 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.193-843C>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64753600 | |||||||
| chr12:64753633 | T | C | 2 | a0001c0001t0006g0118 a0001c0001t0006g0142 |
2 | HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.193-876A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64753633 | |||||||
| chr12:64753778 | A | T | 1 | a0001c0001t0009g0133 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.193-1021T>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64753778 | |||||||
| chr12:64753902 | T | C | 1 | a0001c0001t0003g0319 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.193-1145A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64753902 | |||||||
| chr12:64753921 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(185): Show |
202 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.193-1164T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64753921 | |||||||
| chr12:64753976 | G | A | 4 | a0001c0001t0008g0128 a0001c0001t0008g0129 a0001c0001t0008g0130 others(1): Show |
4 | HG00733.hp1 HG01081.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-1219C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64753976 | |||||||
| chr12:64754209 | T | C | 10 | a0001c0001t0006g0132 a0001c0001t0006g0134 a0001c0001t0006g0136 others(7): Show |
10 | HG01884.hp1 HG02109.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.193-1452A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64754209 | |||||||
| chr12:64754333 | T | C | 5 | a0001c0002t0002g0039 a0001c0002t0002g0059 a0001c0002t0002g0094 others(2): Show |
5 | HG01361.hp2 HG01975.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.193-1576A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64754333 | |||||||
| chr12:64754691 | C | T | 2 | a0001c0006t0011g0332 a0001c0006t0011g0333 |
2 | HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.193-1934G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64754691 | |||||||
| chr12:64754734 | T | C | 1 | a0001c0002t0002g0060 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.193-1977A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64754734 | |||||||
| chr12:64754805 | T | C | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(244): Show |
263 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.193-2048A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64754805 | |||||||
| chr12:64754813 | C | G | 1 | a0001c0001t0001g0293 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.193-2056G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64754813 | |||||||
| chr12:64754890 | C | CA | 53 | a0001c0001t0001g0293 a0001c0001t0001g0304 a0001c0001t0001g0311 others(50): Show |
56 | HG00140.hp2 HG00609.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.193-2134dupT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64754890 | |||||||
| chr12:64754902 | AAAG | A | 17 | a0001c0001t0004g0007 a0001c0001t0004g0099 a0001c0001t0004g0103 others(14): Show |
18 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.193-2148_193-2146d others(5): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64754902 | |||||||
| chr12:64755077 | T | C | 1 | a0001c0002t0002g0096 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.193-2320A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64755077 | |||||||
| chr12:64755317 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.193-2560G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64755317 | |||||||
| chr12:64755331 | C | A | 33 | a0001c0001t0006g0118 a0001c0001t0006g0134 a0001c0001t0006g0136 others(30): Show |
34 | HG00733.hp1 HG01081.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.193-2574G>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64755331 | |||||||
| chr12:64755439 | G | A | 1 | a0003c0007t0019g0064 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.193-2682C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64755439 | |||||||
| chr12:64755532 | C | T | 1 | a0001c0001t0021g0330 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.193-2775G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64755532 | |||||||
| chr12:64755577 | C | CA | 7 | a0001c0001t0001g0160 a0001c0001t0001g0214 a0001c0001t0004g0144 others(4): Show |
7 | HG00558.hp2 HG01175.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-2821dupT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64755577 | |||||||
| chr12:64755577 | CA | C | 11 | a0001c0001t0006g0118 a0001c0001t0006g0134 a0001c0001t0006g0136 others(8): Show |
11 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.193-2821delT | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64755577 | |||||||
| chr12:64755678 | A | AT | 39 | a0001c0001t0001g0009 a0001c0001t0001g0154 a0001c0001t0001g0155 others(36): Show |
41 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.193-2922dupA | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64755678 | |||||||
| chr12:64755752 | C | T | 1 | a0001c0001t0006g0118 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.193-2995G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64755752 | |||||||
| chr12:64755755 | T | C | 1 | a0001c0002t0002g0032 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.193-2998A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64755755 | |||||||
| chr12:64755845 | A | AT | 9 | a0001c0004t0005g0119 a0001c0004t0005g0120 a0001c0004t0005g0121 others(6): Show |
9 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.193-3089dupA | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64755845 | |||||||
| chr12:64755866 | G | A | 3 | a0001c0001t0003g0199 a0001c0001t0003g0320 a0001c0001t0003g0321 |
3 | HG00642.hp1 HG01433.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.193-3109C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64755866 | |||||||
| chr12:64755997 | T | C | 17 | a0001c0001t0004g0007 a0001c0001t0004g0099 a0001c0001t0004g0103 others(14): Show |
18 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.192+3088A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64755997 | |||||||
| chr12:64756064 | A | T | 1 | a0001c0001t0006g0132 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.192+3021T>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64756064 | |||||||
| chr12:64756232 | A | T | 1 | a0001c0001t0006g0132 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.192+2853T>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64756232 | |||||||
| chr12:64756393 | G | A | 1 | a0001c0001t0001g0322 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.192+2692C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64756393 | |||||||
| chr12:64756458 | T | G | 12 | a0001c0001t0007g0008 a0001c0001t0007g0114 a0001c0001t0007g0115 others(9): Show |
13 | HG00733.hp1 HG01081.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.192+2627A>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64756458 | |||||||
| chr12:64756562 | G | A | 2 | a0001c0001t0003g0323 a0001c0001t0003g0324 |
2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.192+2523C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64756562 | |||||||
| chr12:64756705 | C | T | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(244): Show |
263 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.192+2380G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64756705 | |||||||
| chr12:64756746 | G | A | 22 | a0001c0001t0006g0118 a0001c0001t0006g0132 a0001c0001t0006g0134 others(19): Show |
22 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.192+2339C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64756746 | |||||||
| chr12:64756898 | T | C | 1 | a0001c0002t0002g0098 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.192+2187A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64756898 | |||||||
| chr12:64756982 | C | T | 2 | a0001c0001t0014g0065 a0001c0001t0014g0066 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.192+2103G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64756982 | |||||||
| chr12:64757082 | G | C | 1 | a0001c0001t0016g0017 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.192+2003C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64757082 | |||||||
| chr12:64757146 | T | C | 1 | a0001c0001t0003g0200 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.192+1939A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64757146 | |||||||
| chr12:64757194 | G | C | 10 | a0001c0001t0004g0007 a0001c0001t0004g0099 a0001c0001t0004g0103 others(7): Show |
11 | HG01109.hp2 HG01243.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.192+1891C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64757194 | |||||||
| chr12:64757222 | A | T | 1 | a0001c0001t0015g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.192+1863T>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64757222 | |||||||
| chr12:64757293 | C | T | 1 | a0003c0007t0019g0064 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.192+1792G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64757293 | |||||||
| chr12:64757785 | C | T | 2 | a0001c0003t0002g0033 a0001c0003t0002g0034 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.192+1300G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64757785 | |||||||
| chr12:64757847 | C | A | 9 | a0001c0004t0005g0119 a0001c0004t0005g0120 a0001c0004t0005g0121 others(6): Show |
9 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.192+1238G>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64757847 | |||||||
| chr12:64757911 | C | T | 1 | a0001c0001t0003g0153 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.192+1174G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64757911 | |||||||
| chr12:64758073 | G | A | 1 | a0001c0002t0002g0149 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.192+1012C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758073 | |||||||
| chr12:64758162 | C | T | 5 | a0001c0001t0001g0152 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG00323.hp2 HG01346.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.192+923G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758162 | |||||||
| chr12:64758204 | C | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(205): Show |
223 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.192+881G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758204 | |||||||
| chr12:64758230 | G | A | 1 | a0001c0001t0004g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.192+855C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758230 | |||||||
| chr12:64758309 | C | CT | 32 | a0001c0002t0001g0036 a0001c0002t0001g0041 a0001c0002t0001g0042 others(29): Show |
34 | HG00558.hp2 HG00639.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.192+775dupA | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758309 | |||||||
| chr12:64758309 | C | CTT | 14 | a0001c0002t0001g0028 a0001c0002t0002g0019 a0001c0002t0002g0020 others(11): Show |
14 | HG00621.hp2 HG00639.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.192+774_192+775dup others(2): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758309 | |||||||
| chr12:64758309 | CTTTT | C | 50 | a0001c0001t0001g0152 a0001c0001t0001g0154 a0001c0001t0001g0155 others(47): Show |
50 | HG00140.hp2 HG00438.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.192+772_192+775del others(4): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758309 | |||||||
| chr12:64758309 | CTTTTT | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(141): Show |
158 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.192+771_192+775del others(5): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758309 | |||||||
| chr12:64758309 | CTTTTTT | C | 8 | a0001c0001t0001g0325 a0001c0001t0003g0326 a0001c0001t0004g0007 others(5): Show |
9 | HG01243.hp1 HG02080.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.192+770_192+775del others(6): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758309 | |||||||
| chr12:64758309 | CTTTTTTT others(4): Show |
C | 5 | a0001c0001t0007g0008 a0001c0001t0007g0114 a0001c0001t0007g0115 others(2): Show |
6 | HG02572.hp2 HG02622.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.192+765_192+775del others(11): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758309 | |||||||
| chr12:64758309 | CTTTTTTT others(5): Show |
C | 11 | a0001c0001t0001g0327 a0001c0001t0006g0118 a0001c0004t0005g0119 others(8): Show |
11 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.192+764_192+775del others(12): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758309 | |||||||
| chr12:64758309 | CTTTTTTT others(6): Show |
C | 15 | a0001c0001t0006g0132 a0001c0001t0006g0134 a0001c0001t0006g0136 others(12): Show |
15 | HG00733.hp1 HG01081.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.192+763_192+775del others(13): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758309 | |||||||
| chr12:64758309 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0015g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.192+762_192+775del others(14): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758309 | |||||||
| chr12:64758309 | CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0004g0143 a0001c0001t0004g0144 |
2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.192+761_192+775del others(15): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758309 | |||||||
| chr12:64758309 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0004g0145 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.192+760_192+775del others(16): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758309 | |||||||
| chr12:64758309 | CTTTTTTT others(10): Show |
C | 5 | a0001c0002t0002g0146 a0001c0002t0002g0147 a0001c0002t0002g0148 others(2): Show |
5 | HG01255.hp1 HG01515.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+759_192+775del others(17): Show |
GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758309 | |||||||
| chr12:64758386 | G | A | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(186): Show |
203 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.192+699C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758386 | |||||||
| chr12:64758716 | C | G | 1 | a0001c0002t0002g0328 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.192+369G>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758716 | |||||||
| chr12:64758717 | T | G | 1 | a0001c0002t0002g0328 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.192+368A>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758717 | |||||||
| chr12:64758734 | A | G | 1 | a0001c0001t0015g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.192+351T>C | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758734 | |||||||
| chr12:64758776 | G | C | 1 | a0001c0002t0002g0329 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.192+309C>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758776 | |||||||
| chr12:64758918 | T | C | 1 | a0001c0001t0021g0330 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.192+167A>G | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758918 | |||||||
| chr12:64758972 | C | T | 1 | a0001c0001t0016g0017 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.192+113G>A | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64758972 | |||||||
| chr12:64759005 | G | A | 1 | a0001c0001t0001g0331 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.192+80C>T | GNS | ENSG00000135677.11 | transcript | ENST00000258145.8 | protein_coding | 1/13 | chr12 | 64759005 |