Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 132001 |
| ensemblid | ENSG00000144559.11 |
| hgncid | 25187 |
| symbol | TAMM41 |
| name | TAM41 mitochondrial translocator assembly and maintenance homolog |
| refseq_nuc | NM_001284401.2 |
| refseq_prot | NP_001271330.1 |
| ensembl_nuc | ENST00000455809.6 |
| ensembl_prot | ENSP00000398596.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 11790442 |
| end | 11846885 |
| strand | - |
| ver | v1.2 |
| region | chr3:11790442-11846885 |
| region5000 | chr3:11785442-11851885 |
| regionname0 | TAMM41_chr3_11790442_11846885 |
| regionname5000 | TAMM41_chr3_11785442_11851885 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 337 | 282 | 71 | 54 | 119 | 11 | 26 | 88 | TAMM41_chr3_11785442_11851885 | TAMM41 | MALQT others(332): Show |
chr3 | 11785442 | 11851885 |
| a0002 | 0/0 | 337 | 73 | 14 | 11 | 33 | 3 | 12 | 27 | TAMM41_chr3_11785442_11851885 | TAMM41 | MALQT others(332): Show |
chr3 | 11785442 | 11851885 |
| a0003 | 0/1 | 337 | 10 | 0 | 3 | 2 | 3 | 1 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | MALQT others(332): Show |
chr3 | 11785442 | 11851885 |
| a0004 | 0/0 | 337 | 3 | 0 | 1 | 0 | 1 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | MALQT others(332): Show |
chr3 | 11785442 | 11851885 |
| a0005 | 0/0 | 337 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | MALQT others(332): Show |
chr3 | 11785442 | 11851885 |
| a0006 | 0/0 | 337 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | MALQT others(332): Show |
chr3 | 11785442 | 11851885 |
| a0007 | 0/0 | 337 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | MALQT others(332): Show |
chr3 | 11785442 | 11851885 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1011 | 193 | 40 | 31 | 100 | 4 | 17 | TAMM41_chr3_11785442_11851885 | TAMM41 | ATGGC others(1006): Show |
chr3 | 11785442 | 11851885 | ||
| a0001c0002 | 0/0 | 1011 | 86 | 29 | 23 | 18 | 7 | 9 | TAMM41_chr3_11785442_11851885 | TAMM41 | ATGGC others(1006): Show |
chr3 | 11785442 | 11851885 | ||
| a0001c0007 | 0/0 | 1011 | 2 | 2 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | ATGGC others(1006): Show |
chr3 | 11785442 | 11851885 | ||
| a0001c0012 | 0/0 | 1011 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | ATGGC others(1006): Show |
chr3 | 11785442 | 11851885 | ||
| a0002c0003 | 0/0 | 1011 | 43 | 5 | 2 | 26 | 1 | 9 | TAMM41_chr3_11785442_11851885 | TAMM41 | ATGGC others(1006): Show |
chr3 | 11785442 | 11851885 | ||
| a0002c0004 | 0/0 | 1011 | 30 | 9 | 9 | 7 | 2 | 3 | TAMM41_chr3_11785442_11851885 | TAMM41 | ATGGC others(1006): Show |
chr3 | 11785442 | 11851885 | ||
| a0003c0005 | 0/1 | 1011 | 8 | 0 | 2 | 2 | 3 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | ATGGC others(1006): Show |
chr3 | 11785442 | 11851885 | ||
| a0003c0008 | 0/0 | 1011 | 2 | 0 | 1 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | ATGGC others(1006): Show |
chr3 | 11785442 | 11851885 | ||
| a0004c0006 | 0/0 | 1011 | 3 | 0 | 1 | 0 | 1 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | ATGGC others(1006): Show |
chr3 | 11785442 | 11851885 | ||
| a0005c0009 | 0/0 | 1011 | 2 | 2 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | ATGGC others(1006): Show |
chr3 | 11785442 | 11851885 | ||
| a0006c0011 | 0/0 | 1011 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | ATGGC others(1006): Show |
chr3 | 11785442 | 11851885 | ||
| a0007c0010 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | ATGGC others(1006): Show |
chr3 | 11785442 | 11851885 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1326 | 167 | 36 | 18 | 95 | 2 | 15 | TAMM41_chr3_11785442_11851885 | TAMM41 | ACGGA others(1321): Show |
chr3 | 11785442 | 11851885 |
| a0001c0001t0003 | 0/0 | 1326 | 26 | 4 | 13 | 5 | 2 | 2 | TAMM41_chr3_11785442_11851885 | TAMM41 | ACGGA others(1321): Show |
chr3 | 11785442 | 11851885 |
| a0001c0002t0002 | 0/0 | 1326 | 71 | 27 | 15 | 17 | 5 | 7 | TAMM41_chr3_11785442_11851885 | TAMM41 | ACGGA others(1321): Show |
chr3 | 11785442 | 11851885 |
| a0001c0002t0004 | 0/0 | 1326 | 14 | 1 | 8 | 1 | 2 | 2 | TAMM41_chr3_11785442_11851885 | TAMM41 | ACGGA others(1321): Show |
chr3 | 11785442 | 11851885 |
| a0001c0002t0005 | 0/0 | 1326 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | ACGGA others(1321): Show |
chr3 | 11785442 | 11851885 |
| a0001c0007t0001 | 0/0 | 1326 | 2 | 2 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | ACGGA others(1321): Show |
chr3 | 11785442 | 11851885 |
| a0001c0012t0001 | 0/0 | 1326 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | ACGGA others(1321): Show |
chr3 | 11785442 | 11851885 |
| a0002c0003t0002 | 0/0 | 1326 | 20 | 3 | 2 | 10 | 0 | 5 | TAMM41_chr3_11785442_11851885 | TAMM41 | ACGGA others(1321): Show |
chr3 | 11785442 | 11851885 |
| a0002c0003t0003 | 0/0 | 1326 | 3 | 0 | 0 | 3 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | ACGGA others(1321): Show |
chr3 | 11785442 | 11851885 |
| a0002c0003t0004 | 0/0 | 1326 | 20 | 2 | 0 | 13 | 1 | 4 | TAMM41_chr3_11785442_11851885 | TAMM41 | ACGGA others(1321): Show |
chr3 | 11785442 | 11851885 |
| a0002c0004t0001 | 0/0 | 1326 | 15 | 8 | 2 | 5 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | ACGGA others(1321): Show |
chr3 | 11785442 | 11851885 |
| a0002c0004t0002 | 0/0 | 1326 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | ACGGA others(1321): Show |
chr3 | 11785442 | 11851885 |
| a0002c0004t0003 | 0/0 | 1326 | 14 | 0 | 7 | 2 | 2 | 3 | TAMM41_chr3_11785442_11851885 | TAMM41 | ACGGA others(1321): Show |
chr3 | 11785442 | 11851885 |
| a0003c0005t0001 | 0/0 | 1326 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | ACGGA others(1321): Show |
chr3 | 11785442 | 11851885 |
| a0003c0005t0003 | 0/1 | 1326 | 7 | 0 | 1 | 2 | 3 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | ACGGA others(1321): Show |
chr3 | 11785442 | 11851885 |
| a0003c0008t0004 | 0/0 | 1326 | 2 | 0 | 1 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | ACGGA others(1321): Show |
chr3 | 11785442 | 11851885 |
| a0004c0006t0004 | 0/0 | 1326 | 3 | 0 | 1 | 0 | 1 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | ACGGA others(1321): Show |
chr3 | 11785442 | 11851885 |
| a0005c0009t0002 | 0/0 | 1326 | 2 | 2 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | ACGGA others(1321): Show |
chr3 | 11785442 | 11851885 |
| a0006c0011t0004 | 0/0 | 1326 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | ACGGA others(1321): Show |
chr3 | 11785442 | 11851885 |
| a0007c0010t0001 | 0/0 | 1326 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | ACGGA others(1321): Show |
chr3 | 11785442 | 11851885 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0303 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0004g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0004g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0004g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0004g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0004g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0004g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0002t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0007t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0007t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0001c0012t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0003t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0003g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0003g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0002c0004t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0003c0005t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0003c0005t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0003c0005t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0003c0005t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0003c0005t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0003c0005t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0003c0005t0003g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0003c0005t0003g0301 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0003c0008t0004g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0003c0008t0004g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0004c0006t0004g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0004c0006t0004g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0004c0006t0004g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0005c0009t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0005c0009t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0006c0011t0004g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| a0007c0010t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0173 | EUR | GBR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00099 | hp2 | a0004 | c0006 | t0004 | g0142 | EUR | GBR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00140 | hp1 | a0003 | c0005 | t0003 | g0239 | EUR | GBR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00140 | hp2 | a0002 | c0003 | t0004 | g0113 | EUR | GBR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0130 | EUR | FIN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0175 | EUR | FIN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00323 | hp1 | a0002 | c0004 | t0003 | g0183 | EUR | FIN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00323 | hp2 | a0003 | c0005 | t0003 | g0300 | EUR | FIN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | CHS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0097 | EAS | CHS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00438 | hp2 | a0002 | c0003 | t0004 | g0050 | EAS | CHS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00544 | hp1 | a0002 | c0003 | t0004 | g0061 | EAS | CHS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0098 | EAS | CHS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | CHS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00639 | hp1 | a0003 | c0008 | t0004 | g0110 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0170 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0119 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0228 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | CHS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0176 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0118 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00738 | hp1 | a0006 | c0011 | t0004 | g0070 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0168 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0121 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01070 | hp2 | a0002 | c0004 | t0003 | g0184 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0116 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0139 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01099 | hp1 | a0002 | c0004 | t0001 | g0244 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0106 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0120 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01109 | hp1 | a0002 | c0004 | t0001 | g0247 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01109 | hp2 | a0002 | c0004 | t0003 | g0185 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0024 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0083 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01192 | hp1 | a0004 | c0006 | t0004 | g0141 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01192 | hp2 | a0002 | c0004 | t0003 | g0181 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0126 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01243 | hp2 | a0002 | c0003 | t0002 | g0093 | AMR | PUR | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | CLM | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01256 | hp2 | a0002 | c0004 | t0003 | g0011 | AMR | CLM | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0178 | AMR | CLM | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01257 | hp2 | a0002 | c0004 | t0003 | g0016 | AMR | CLM | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01258 | hp1 | a0002 | c0004 | t0003 | g0016 | AMR | CLM | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01258 | hp2 | a0002 | c0004 | t0003 | g0011 | AMR | CLM | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01261 | hp2 | a0003 | c0005 | t0003 | g0240 | AMR | CLM | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01358 | hp1 | a0001 | c0002 | t0004 | g0091 | AMR | CLM | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01358 | hp2 | a0003 | c0005 | t0001 | g0226 | AMR | CLM | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0166 | AMR | CLM | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0099 | EUR | IBS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0316 | EUR | IBS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01516 | hp1 | a0001 | c0002 | t0004 | g0010 | EUR | IBS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0180 | EUR | IBS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01517 | hp1 | a0001 | c0002 | t0004 | g0010 | EUR | IBS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0085 | EUR | IBS | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01884 | hp1 | a0002 | c0004 | t0001 | g0319 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01891 | hp1 | a0002 | c0003 | t0002 | g0037 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0101 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0177 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0077 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0023 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01975 | hp1 | a0001 | c0002 | t0004 | g0087 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0242 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01978 | hp2 | a0002 | c0003 | t0002 | g0066 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01981 | hp1 | a0001 | c0002 | t0004 | g0124 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02004 | hp2 | a0001 | c0002 | t0004 | g0094 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0076 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02027 | hp2 | a0001 | c0002 | t0004 | g0096 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0044 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02055 | hp2 | a0005 | c0009 | t0002 | g0036 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02071 | hp1 | a0002 | c0004 | t0001 | g0339 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02080 | hp1 | a0002 | c0003 | t0004 | g0075 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02080 | hp2 | a0003 | c0005 | t0003 | g0197 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02132 | hp2 | a0002 | c0003 | t0003 | g0149 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02145 | hp2 | a0001 | c0007 | t0001 | g0145 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02148 | hp2 | a0001 | c0002 | t0004 | g0089 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | CDX | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CDX | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | CDX | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02165 | hp2 | a0002 | c0004 | t0001 | g0217 | EAS | CDX | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02258 | hp1 | a0002 | c0004 | t0001 | g0305 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02258 | hp2 | a0001 | c0002 | t0005 | g0144 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02273 | hp2 | a0001 | c0002 | t0004 | g0088 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02280 | hp1 | a0002 | c0004 | t0001 | g0249 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02293 | hp2 | a0001 | c0002 | t0004 | g0048 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02300 | hp1 | a0001 | c0002 | t0004 | g0090 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0171 | AMR | PEL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0179 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0082 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | KHV | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0095 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0135 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02615 | hp2 | a0002 | c0004 | t0001 | g0306 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02622 | hp2 | a0002 | c0003 | t0002 | g0027 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0043 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0174 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0138 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0172 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0128 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02738 | hp1 | a0002 | c0003 | t0004 | g0064 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0340 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0034 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02818 | hp1 | a0002 | c0004 | t0002 | g0140 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0042 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0029 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0107 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0028 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | ESN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02922 | hp2 | a0002 | c0004 | t0001 | g0248 | AFR | ESN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0341 | AFR | ESN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | ESN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02976 | hp1 | a0002 | c0004 | t0001 | g0221 | AFR | ESN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0108 | AFR | ESN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03017 | hp1 | a0002 | c0003 | t0002 | g0069 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03017 | hp2 | a0002 | c0003 | t0002 | g0074 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03041 | hp2 | a0001 | c0002 | t0002 | g0030 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | MSL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | MSL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | ESN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0041 | AFR | ESN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0033 | AFR | ESN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0132 | AFR | ESN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0031 | AFR | ESN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03225 | hp1 | a0002 | c0004 | t0001 | g0250 | AFR | MSL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03225 | hp2 | a0001 | c0007 | t0001 | g0146 | AFR | MSL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03239 | hp2 | a0003 | c0008 | t0004 | g0047 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | MSL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | MSL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03486 | hp1 | a0005 | c0009 | t0002 | g0035 | AFR | MSL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | MSL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03490 | hp1 | a0002 | c0004 | t0003 | g0182 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0039 | AFR | ESN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0040 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0103 | AFR | GWD | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03579 | hp1 | a0002 | c0003 | t0002 | g0026 | AFR | MSL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03579 | hp2 | a0001 | c0002 | t0002 | g0136 | AFR | MSL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0081 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03654 | hp2 | a0002 | c0003 | t0002 | g0055 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03669 | hp1 | a0002 | c0003 | t0002 | g0067 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0127 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0114 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03710 | hp2 | a0002 | c0004 | t0003 | g0245 | SAS | PJL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0117 | SAS | BEB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | BEB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03927 | hp1 | a0001 | c0002 | t0004 | g0109 | SAS | BEB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03927 | hp2 | a0002 | c0003 | t0002 | g0073 | SAS | BEB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG04115 | hp1 | a0002 | c0003 | t0004 | g0053 | SAS | STU | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | STU | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | BEB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG04184 | hp2 | a0002 | c0003 | t0004 | g0056 | SAS | BEB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0131 | SAS | STU | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG04199 | hp2 | a0004 | c0006 | t0004 | g0143 | SAS | STU | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG04204 | hp1 | a0002 | c0003 | t0004 | g0112 | SAS | STU | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG04204 | hp2 | a0002 | c0004 | t0003 | g0164 | SAS | STU | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18522 | hp2 | a0001 | c0002 | t0004 | g0122 | AFR | YRI | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0282 | EAS | CHB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | YRI | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18906 | hp2 | a0002 | c0003 | t0004 | g0137 | AFR | YRI | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0123 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18943 | hp1 | a0002 | c0003 | t0002 | g0052 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18945 | hp2 | a0002 | c0003 | t0004 | g0006 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18946 | hp2 | a0002 | c0004 | t0001 | g0243 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18951 | hp2 | a0002 | c0004 | t0003 | g0194 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18953 | hp1 | a0002 | c0003 | t0003 | g0148 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18953 | hp2 | a0002 | c0003 | t0002 | g0072 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18954 | hp1 | a0002 | c0003 | t0002 | g0058 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0092 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18966 | hp1 | a0002 | c0003 | t0002 | g0051 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18966 | hp2 | a0002 | c0004 | t0001 | g0335 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0078 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18972 | hp2 | a0002 | c0004 | t0003 | g0204 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0295 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18974 | hp1 | a0002 | c0003 | t0004 | g0007 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18974 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18978 | hp1 | a0001 | c0002 | t0002 | g0115 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18982 | hp1 | a0002 | c0003 | t0002 | g0057 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18984 | hp1 | a0002 | c0004 | t0001 | g0203 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18986 | hp2 | a0002 | c0003 | t0002 | g0071 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18988 | hp1 | a0002 | c0003 | t0004 | g0059 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18990 | hp1 | a0002 | c0003 | t0002 | g0065 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18991 | hp1 | a0001 | c0012 | t0001 | g0210 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18991 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0125 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18994 | hp2 | a0002 | c0003 | t0002 | g0054 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18999 | hp1 | a0002 | c0003 | t0002 | g0049 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19001 | hp2 | a0002 | c0003 | t0004 | g0068 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19004 | hp2 | a0002 | c0003 | t0004 | g0105 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19006 | hp2 | a0001 | c0002 | t0002 | g0079 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19007 | hp2 | a0002 | c0003 | t0004 | g0063 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19009 | hp1 | a0002 | c0003 | t0004 | g0007 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0080 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0104 | AFR | LWK | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0134 | AFR | LWK | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | LWK | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19043 | hp2 | a0007 | c0010 | t0001 | g0147 | AFR | LWK | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19054 | hp2 | a0002 | c0003 | t0004 | g0062 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19067 | hp1 | a0001 | c0002 | t0002 | g0086 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19078 | hp1 | a0002 | c0003 | t0004 | g0060 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19080 | hp2 | a0002 | c0003 | t0003 | g0150 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19081 | hp2 | a0002 | c0003 | t0002 | g0100 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19083 | hp1 | a0002 | c0003 | t0004 | g0006 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0133 | AFR | YRI | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA19240 | hp2 | a0001 | c0002 | t0002 | g0102 | AFR | YRI | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0032 | AFR | ASW | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ASW | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0084 | EUR | TSI | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA20752 | hp2 | a0002 | c0004 | t0003 | g0151 | EUR | TSI | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA20805 | hp1 | a0003 | c0005 | t0003 | g0241 | EUR | TSI | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0129 | EUR | TSI | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA20905 | hp1 | a0001 | c0002 | t0004 | g0111 | SAS | GIH | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | GIH | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG02559 | hp2 | a0002 | c0003 | t0004 | g0025 | AFR | ACB | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | MSL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG06807 | hp1 | a0002 | c0004 | t0001 | g0246 | AFR | USA | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | USA | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA18955 | hp2 | a0003 | c0005 | t0003 | g0230 | EAS | JPT | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0238 | AFR | USA | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0038 | AFR | USA | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | LWK | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | LWK | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| homoSapiens | chm13v2 | a0003 | c0005 | t0003 | g0301 | REF | REF | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0303 | REF | REF | TAMM41_chr3_11785442_11851885 | TAMM41 | chr3 | 11785442 | 11851885 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:11829741 | T | C | 2 | a0003 a0006 |
10 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(7): Show |
missense_variant | MODERATE | c.535A>G | p.Ile179Val | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/8 | 784/1326 | 535/1014 | 179/337 | chr3 | 11829741 | |||
| chr3:11839286 | T | C | 2 | a0002 a0006 |
74 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(71): Show |
missense_variant | MODERATE | c.347A>G | p.Asn116Ser | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/8 | 596/1326 | 347/1014 | 116/337 | chr3 | 11839286 | |||
| chr3:11844075 | T | C | 1 | a0005 | 2 | HG02055.hp2 HG03486.hp1 |
missense_variant | MODERATE | c.272A>G | p.Tyr91Cys | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/8 | 521/1326 | 272/1014 | 91/337 | chr3 | 11844075 | |||
| chr3:11846519 | G | A | 1 | a0004 | 3 | HG00099.hp2 HG01192.hp1 HG04199.hp2 |
missense_variant | MODERATE | c.118C>T | p.Pro40Ser | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/8 | 367/1326 | 118/1014 | 40/337 | chr3 | 11846519 | |||
| chr3:11846599 | A | T | 1 | a0007 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.38T>A | p.Phe13Tyr | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/8 | 287/1326 | 38/1014 | 13/337 | chr3 | 11846599 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:11829769 | G | A | 1 | a0001c0012 | 1 | NA18991.hp1 | synonymous_variant | LOW | c.507C>T | p.Pro169Pro | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/8 | 756/1326 | 507/1014 | 169/337 | chr3 | 11829769 | |||
| chr3:11846517 | C | G | 6 | a0001c0002 a0002c0003 a0003c0008 others(3): Show |
137 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(134): Show |
synonymous_variant | LOW | c.120G>C | p.Pro40Pro | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/8 | 369/1326 | 120/1014 | 40/337 | chr3 | 11846517 | |||
| chr3:11846628 | C | T | 1 | a0001c0007 | 2 | HG02145.hp2 HG03225.hp2 |
synonymous_variant | LOW | c.9G>A | p.Leu3Leu | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/8 | 258/1326 | 9/1014 | 3/337 | chr3 | 11846628 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:11790479 | C | T | 9 | a0001c0001t0003 a0001c0002t0004 a0002c0003t0003 others(6): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*26G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 8/8 | 26 | chr3 | 11790479 | ||||||
| chr3:11846707 | T | C | 1 | a0001c0002t0005 | 1 | HG02258.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-71A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/8 | chr3 | 11846707 | |||||||
| chr3:11846785 | C | G | 10 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0005 others(7): Show |
135 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(132): Show |
5_prime_UTR_variant | MODIFIER | c.-149G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/8 | 149 | chr3 | 11846785 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:11790613 | T | C | 1 | a0001c0002t0002g0092 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.938-32A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11790613 | |||||||
| chr3:11790617 | G | A | 1 | a0002c0003t0003g0148 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.938-36C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11790617 | |||||||
| chr3:11790697 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0191 |
3 | HG02109.hp2 HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.938-116G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11790697 | |||||||
| chr3:11790894 | C | A | 1 | a0001c0002t0002g0031 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.938-313G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11790894 | |||||||
| chr3:11791106 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.938-525A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11791106 | |||||||
| chr3:11791124 | T | C | 1 | a0001c0001t0001g0251 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.938-543A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11791124 | |||||||
| chr3:11791130 | G | A | 1 | a0002c0003t0004g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.938-549C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11791130 | |||||||
| chr3:11791136 | G | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(104): Show |
122 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(119): Show |
intron_variant | MODIFIER | c.938-555C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11791136 | |||||||
| chr3:11791214 | C | T | 6 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0001c0001t0001g0309 others(3): Show |
6 | HG01884.hp2 HG02647.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.938-633G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11791214 | |||||||
| chr3:11791229 | C | T | 1 | a0001c0002t0002g0136 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.938-648G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11791229 | |||||||
| chr3:11791299 | G | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(245): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.938-718C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11791299 | |||||||
| chr3:11791324 | T | C | 1 | a0001c0001t0001g0162 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.938-743A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11791324 | |||||||
| chr3:11791721 | C | T | 74 | a0001c0001t0001g0167 a0001c0001t0001g0169 a0001c0001t0003g0012 others(71): Show |
81 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.938-1140G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11791721 | |||||||
| chr3:11791797 | C | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0191 a0002c0003t0004g0137 |
4 | HG02109.hp2 HG02280.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.938-1216G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11791797 | |||||||
| chr3:11791801 | T | G | 1 | a0001c0002t0002g0032 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.938-1220A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11791801 | |||||||
| chr3:11791819 | T | C | 1 | a0001c0001t0001g0263 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.938-1238A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11791819 | |||||||
| chr3:11791999 | C | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(180): Show |
205 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.938-1418G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11791999 | |||||||
| chr3:11792018 | A | G | 1 | a0001c0002t0002g0107 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.938-1437T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11792018 | |||||||
| chr3:11792058 | A | G | 2 | a0002c0004t0001g0305 a0002c0004t0001g0306 |
2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.938-1477T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11792058 | |||||||
| chr3:11792155 | G | A | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG02257.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.938-1574C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11792155 | |||||||
| chr3:11792163 | C | T | 8 | a0001c0001t0001g0315 a0001c0001t0001g0326 a0001c0002t0002g0041 others(5): Show |
8 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.938-1582G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11792163 | |||||||
| chr3:11792173 | A | AT | 108 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(105): Show |
124 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(121): Show |
intron_variant | MODIFIER | c.938-1593dupA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11792173 | |||||||
| chr3:11792183 | T | G | 9 | a0002c0003t0002g0066 a0002c0003t0002g0093 a0002c0004t0001g0221 others(6): Show |
9 | HG01109.hp1 HG01243.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.938-1602A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11792183 | |||||||
| chr3:11792185 | TG | T | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0002t0002g0032 |
3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.938-1605delC | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11792185 | |||||||
| chr3:11792186 | G | T | 1 | a0001c0002t0002g0133 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.938-1605C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11792186 | |||||||
| chr3:11792208 | C | T | 1 | a0001c0002t0002g0133 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.938-1627G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11792208 | |||||||
| chr3:11792486 | A | G | 2 | a0001c0001t0001g0236 a0001c0001t0001g0324 |
2 | HG02074.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.938-1905T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11792486 | |||||||
| chr3:11792705 | A | T | 1 | a0002c0003t0004g0007 | 2 | NA18974.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.938-2124T>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11792705 | |||||||
| chr3:11792815 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.938-2234T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11792815 | |||||||
| chr3:11792875 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.938-2294G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11792875 | |||||||
| chr3:11792955 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(83): Show |
99 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.938-2374C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11792955 | |||||||
| chr3:11793010 | G | A | 11 | a0001c0001t0001g0002 a0001c0001t0001g0198 a0001c0001t0001g0201 others(8): Show |
14 | NA18906.hp2 NA18943.hp1 NA18956.hp1 others(11): Show |
intron_variant | MODIFIER | c.938-2429C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793010 | |||||||
| chr3:11793018 | G | A | 1 | a0002c0003t0002g0051 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.938-2437C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793018 | |||||||
| chr3:11793059 | C | CA | 28 | a0001c0001t0001g0165 a0001c0001t0001g0187 a0001c0001t0001g0201 others(25): Show |
29 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.938-2479dupT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793059 | |||||||
| chr3:11793059 | C | CAA | 23 | a0001c0001t0001g0229 a0001c0001t0001g0258 a0001c0001t0001g0288 others(20): Show |
25 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.938-2480_938-2479d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793059 | |||||||
| chr3:11793059 | C | CAAA | 61 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(58): Show |
70 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.938-2481_938-2479d others(5): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793059 | |||||||
| chr3:11793059 | C | CAAAA | 30 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(27): Show |
35 | HG00621.hp2 HG01074.hp2 HG01361.hp1 others(32): Show |
intron_variant | MODIFIER | c.938-2482_938-2479d others(6): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793059 | |||||||
| chr3:11793059 | C | CAAAAAAA others(3): Show |
1 | a0001c0002t0002g0133 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.938-2488_938-2479d others(12): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793059 | |||||||
| chr3:11793059 | CA | C | 13 | a0001c0001t0001g0163 a0001c0001t0001g0186 a0001c0001t0001g0199 others(10): Show |
13 | HG00099.hp2 HG00642.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.938-2479delT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793059 | |||||||
| chr3:11793059 | CAA | C | 22 | a0001c0001t0001g0167 a0001c0001t0001g0169 a0001c0001t0001g0321 others(19): Show |
24 | HG00099.hp1 HG00733.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.938-2480_938-2479d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793059 | |||||||
| chr3:11793059 | CAAA | C | 51 | a0001c0001t0003g0022 a0001c0001t0003g0170 a0001c0001t0003g0242 others(48): Show |
56 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.938-2481_938-2479d others(5): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793059 | |||||||
| chr3:11793059 | CAAAAAAA others(1): Show |
C | 6 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(3): Show |
6 | HG02257.hp1 HG02647.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.938-2486_938-2479d others(10): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793059 | |||||||
| chr3:11793081 | A | AG | 4 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0331 others(1): Show |
4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.938-2501_938-2500i others(3): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793081 | |||||||
| chr3:11793083 | A | AAAAAAAA others(22): Show |
2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.938-2503_938-2502i others(31): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793083 | |||||||
| chr3:11793083 | A | AAAAAAAA others(9): Show |
1 | a0001c0002t0002g0032 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.938-2503_938-2502i others(18): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793083 | |||||||
| chr3:11793083 | A | G | 80 | a0001c0001t0001g0167 a0001c0001t0001g0169 a0001c0001t0001g0312 others(77): Show |
87 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.938-2502T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793083 | |||||||
| chr3:11793162 | A | G | 2 | a0001c0001t0001g0004 a0001c0001t0001g0212 |
4 | HG00558.hp1 NA18941.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.938-2581T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793162 | |||||||
| chr3:11793226 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.938-2645C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793226 | |||||||
| chr3:11793271 | A | G | 3 | a0001c0001t0001g0161 a0001c0002t0002g0038 a0001c0002t0002g0039 |
3 | HG02559.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.938-2690T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793271 | |||||||
| chr3:11793274 | T | A | 2 | a0003c0005t0003g0239 a0006c0011t0004g0070 |
2 | HG00140.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.938-2693A>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793274 | |||||||
| chr3:11793310 | A | G | 15 | a0001c0001t0001g0013 a0001c0001t0001g0155 a0001c0001t0001g0156 others(12): Show |
16 | HG01891.hp2 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.938-2729T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793310 | |||||||
| chr3:11793430 | CA | C | 4 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0331 others(1): Show |
4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.938-2850delT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793430 | |||||||
| chr3:11793580 | A | T | 1 | a0001c0002t0002g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.938-2999T>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793580 | |||||||
| chr3:11793583 | A | T | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0002t0002g0032 |
3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.938-3002T>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793583 | |||||||
| chr3:11793598 | C | G | 1 | a0001c0001t0001g0225 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.938-3017G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793598 | |||||||
| chr3:11793657 | A | G | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0002t0002g0032 |
3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.938-3076T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793657 | |||||||
| chr3:11793678 | A | G | 2 | a0001c0001t0001g0331 a0001c0001t0001g0332 |
2 | HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.938-3097T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793678 | |||||||
| chr3:11793687 | A | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(238): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.938-3106T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793687 | |||||||
| chr3:11793718 | G | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(118): Show |
137 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(134): Show |
intron_variant | MODIFIER | c.938-3137C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793718 | |||||||
| chr3:11793728 | G | A | 1 | a0001c0002t0002g0139 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.938-3147C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793728 | |||||||
| chr3:11793769 | C | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(106): Show |
125 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(122): Show |
intron_variant | MODIFIER | c.938-3188G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793769 | |||||||
| chr3:11793822 | C | T | 1 | a0002c0003t0004g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.938-3241G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11793822 | |||||||
| chr3:11794058 | A | C | 3 | a0001c0001t0001g0161 a0001c0002t0002g0038 a0001c0002t0002g0039 |
3 | HG02559.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.938-3477T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11794058 | |||||||
| chr3:11794059 | C | T | 1 | a0001c0001t0001g0341 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.938-3478G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11794059 | |||||||
| chr3:11794065 | C | T | 248 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(245): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.938-3484G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11794065 | |||||||
| chr3:11794148 | A | AT | 11 | a0001c0001t0001g0156 a0001c0001t0001g0201 a0001c0001t0001g0254 others(8): Show |
11 | HG02055.hp1 HG02055.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.938-3568dupA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11794148 | |||||||
| chr3:11794148 | A | ATT | 9 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0191 others(6): Show |
10 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.938-3569_938-3568d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11794148 | |||||||
| chr3:11794155 | T | TA | 120 | a0001c0001t0001g0162 a0001c0001t0001g0167 a0001c0001t0001g0169 others(117): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.938-3575_938-3574i others(3): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11794155 | |||||||
| chr3:11794161 | T | A | 41 | a0001c0001t0001g0162 a0001c0001t0001g0211 a0001c0001t0001g0236 others(38): Show |
41 | HG00099.hp2 HG00642.hp2 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.938-3580A>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11794161 | |||||||
| chr3:11794187 | A | G | 1 | a0002c0003t0004g0007 | 2 | NA18974.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.938-3606T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11794187 | |||||||
| chr3:11794229 | T | C | 1 | a0001c0001t0001g0265 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.938-3648A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11794229 | |||||||
| chr3:11794589 | T | TAAAAC | 4 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0331 others(1): Show |
4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.938-4009_938-4008i others(7): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11794589 | |||||||
| chr3:11794591 | G | A | 4 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0331 others(1): Show |
4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.938-4010C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11794591 | |||||||
| chr3:11794621 | C | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(99): Show |
117 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.938-4040G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11794621 | |||||||
| chr3:11794823 | T | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(245): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.938-4242A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11794823 | |||||||
| chr3:11794912 | T | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(245): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.938-4331A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11794912 | |||||||
| chr3:11794944 | A | G | 1 | a0001c0001t0001g0318 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.938-4363T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11794944 | |||||||
| chr3:11794975 | T | C | 4 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0331 others(1): Show |
4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.938-4394A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11794975 | |||||||
| chr3:11795040 | G | A | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0002t0002g0032 |
3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.938-4459C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11795040 | |||||||
| chr3:11795112 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.938-4531T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11795112 | |||||||
| chr3:11795169 | T | G | 1 | a0001c0001t0001g0225 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.938-4588A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11795169 | |||||||
| chr3:11795208 | G | A | 3 | a0001c0001t0001g0236 a0001c0001t0001g0324 a0001c0001t0001g0333 |
3 | HG02074.hp1 HG02129.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.938-4627C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11795208 | |||||||
| chr3:11795299 | G | A | 5 | a0001c0001t0003g0177 a0001c0001t0003g0178 a0001c0001t0003g0179 others(2): Show |
5 | HG01192.hp1 HG01257.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.938-4718C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11795299 | |||||||
| chr3:11795588 | G | A | 1 | a0001c0002t0002g0133 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.938-5007C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11795588 | |||||||
| chr3:11795662 | T | C | 3 | a0001c0001t0001g0291 a0001c0001t0001g0293 a0001c0001t0001g0294 |
3 | HG00741.hp2 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.938-5081A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11795662 | |||||||
| chr3:11795730 | C | G | 1 | a0001c0002t0002g0133 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.938-5149G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11795730 | |||||||
| chr3:11795738 | T | G | 8 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0191 others(5): Show |
9 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.938-5157A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11795738 | |||||||
| chr3:11795923 | G | A | 7 | a0001c0002t0004g0087 a0001c0002t0004g0088 a0001c0002t0004g0089 others(4): Show |
7 | HG00438.hp2 HG01358.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.938-5342C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11795923 | |||||||
| chr3:11796035 | C | T | 3 | a0001c0001t0001g0214 a0001c0002t0002g0134 a0001c0002t0002g0135 |
3 | HG02615.hp1 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.938-5454G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11796035 | |||||||
| chr3:11796108 | G | A | 13 | a0001c0001t0001g0013 a0001c0001t0001g0155 a0001c0001t0001g0156 others(10): Show |
14 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.938-5527C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11796108 | |||||||
| chr3:11796538 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.938-5957G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11796538 | |||||||
| chr3:11796643 | G | A | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.938-6062C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11796643 | |||||||
| chr3:11796671 | G | C | 1 | a0001c0001t0003g0176 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.938-6090C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11796671 | |||||||
| chr3:11796710 | A | C | 15 | a0001c0001t0001g0013 a0001c0001t0001g0155 a0001c0001t0001g0156 others(12): Show |
16 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.938-6129T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11796710 | |||||||
| chr3:11796884 | C | CA | 248 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(245): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.938-6304dupT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11796884 | |||||||
| chr3:11797035 | T | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(99): Show |
117 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.938-6454A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11797035 | |||||||
| chr3:11797250 | T | A | 1 | a0001c0002t0002g0133 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.938-6669A>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11797250 | |||||||
| chr3:11797330 | G | A | 4 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0331 others(1): Show |
4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.938-6749C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11797330 | |||||||
| chr3:11797357 | T | G | 128 | a0001c0001t0001g0013 a0001c0001t0001g0162 a0001c0001t0001g0163 others(125): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.938-6776A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11797357 | |||||||
| chr3:11797456 | G | A | 2 | a0001c0001t0001g0318 a0002c0003t0004g0137 |
2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.938-6875C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11797456 | |||||||
| chr3:11797461 | T | C | 1 | a0002c0004t0003g0164 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.938-6880A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11797461 | |||||||
| chr3:11797484 | C | T | 4 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0331 others(1): Show |
4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.938-6903G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11797484 | |||||||
| chr3:11797525 | C | T | 1 | a0001c0001t0001g0325 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.938-6944G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11797525 | |||||||
| chr3:11797570 | TAAG | T | 4 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0331 others(1): Show |
4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.938-6992_938-6990d others(5): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11797570 | |||||||
| chr3:11797608 | G | A | 5 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(2): Show |
5 | HG02257.hp1 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.938-7027C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11797608 | |||||||
| chr3:11797769 | A | T | 1 | a0001c0001t0003g0238 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.938-7188T>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11797769 | |||||||
| chr3:11797896 | A | G | 1 | a0002c0004t0001g0243 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.938-7315T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11797896 | |||||||
| chr3:11798195 | A | G | 5 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(2): Show |
5 | HG02257.hp1 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.938-7614T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11798195 | |||||||
| chr3:11798292 | T | G | 2 | a0001c0001t0001g0224 a0001c0001t0001g0268 |
2 | HG03239.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.938-7711A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11798292 | |||||||
| chr3:11798418 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.938-7837T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11798418 | |||||||
| chr3:11798457 | C | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(116): Show |
134 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(131): Show |
intron_variant | MODIFIER | c.938-7876G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11798457 | |||||||
| chr3:11798492 | A | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(240): Show |
266 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.938-7911T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11798492 | |||||||
| chr3:11798568 | T | C | 2 | a0002c0003t0002g0073 a0002c0003t0002g0074 |
2 | HG03017.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.938-7987A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11798568 | |||||||
| chr3:11798726 | G | C | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG02257.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.938-8145C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11798726 | |||||||
| chr3:11798801 | A | G | 3 | a0001c0001t0001g0161 a0001c0002t0002g0038 a0001c0002t0002g0039 |
3 | HG02559.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.938-8220T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11798801 | |||||||
| chr3:11798811 | T | C | 1 | a0003c0005t0001g0226 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.938-8230A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11798811 | |||||||
| chr3:11798996 | C | T | 1 | a0002c0004t0001g0244 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.938-8415G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11798996 | |||||||
| chr3:11799042 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.938-8461G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11799042 | |||||||
| chr3:11799157 | C | T | 1 | a0001c0001t0001g0321 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.938-8576G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11799157 | |||||||
| chr3:11799203 | C | A | 34 | a0001c0001t0001g0162 a0001c0001t0001g0211 a0001c0001t0001g0236 others(31): Show |
34 | HG01099.hp1 HG01109.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.938-8622G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11799203 | |||||||
| chr3:11799238 | C | A | 1 | a0001c0002t0002g0133 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.937+8595G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11799238 | |||||||
| chr3:11799259 | A | AT | 41 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(38): Show |
45 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.937+8573_937+8574i others(3): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11799259 | |||||||
| chr3:11799345 | G | C | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0002t0002g0032 |
3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.937+8488C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11799345 | |||||||
| chr3:11799429 | A | G | 127 | a0001c0001t0001g0013 a0001c0001t0001g0162 a0001c0001t0001g0163 others(124): Show |
135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.937+8404T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11799429 | |||||||
| chr3:11799455 | C | T | 113 | a0001c0001t0001g0162 a0001c0001t0001g0167 a0001c0001t0001g0169 others(110): Show |
120 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.937+8378G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11799455 | |||||||
| chr3:11799504 | C | G | 1 | a0001c0001t0001g0318 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.937+8329G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11799504 | |||||||
| chr3:11799514 | C | A | 1 | a0001c0001t0001g0308 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.937+8319G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11799514 | |||||||
| chr3:11799594 | C | T | 10 | a0001c0001t0001g0196 a0001c0001t0001g0205 a0001c0001t0001g0327 others(7): Show |
10 | HG00423.hp2 HG00621.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.937+8239G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11799594 | |||||||
| chr3:11799608 | A | G | 6 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(3): Show |
6 | HG02257.hp1 HG02647.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.937+8225T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11799608 | |||||||
| chr3:11799609 | T | C | 1 | a0002c0004t0001g0217 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.937+8224A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11799609 | |||||||
| chr3:11799637 | G | C | 5 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(2): Show |
5 | HG02257.hp1 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.937+8196C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11799637 | |||||||
| chr3:11799685 | A | G | 4 | a0001c0001t0001g0020 a0001c0001t0001g0265 a0001c0001t0001g0286 others(1): Show |
5 | HG00621.hp2 HG02040.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.937+8148T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11799685 | |||||||
| chr3:11799970 | C | G | 239 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(236): Show |
262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.937+7863G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11799970 | |||||||
| chr3:11800337 | C | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(240): Show |
266 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.937+7496G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11800337 | |||||||
| chr3:11800475 | T | C | 2 | a0002c0003t0002g0026 a0002c0003t0002g0027 |
2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.937+7358A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11800475 | |||||||
| chr3:11800536 | T | A | 1 | a0001c0001t0001g0213 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.937+7297A>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11800536 | |||||||
| chr3:11800547 | TA | T | 79 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(76): Show |
87 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.937+7285delT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11800547 | |||||||
| chr3:11800547 | TAA | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(111): Show |
129 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(126): Show |
intron_variant | MODIFIER | c.937+7284_937+7285d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11800547 | |||||||
| chr3:11800547 | TAAA | T | 118 | a0001c0001t0001g0013 a0001c0001t0001g0162 a0001c0001t0001g0163 others(115): Show |
126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.937+7283_937+7285d others(5): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11800547 | |||||||
| chr3:11800547 | TAAAA | T | 9 | a0002c0003t0002g0037 a0002c0004t0001g0221 a0002c0004t0001g0244 others(6): Show |
9 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.937+7282_937+7285d others(6): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11800547 | |||||||
| chr3:11800729 | G | A | 240 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(237): Show |
262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.937+7104C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11800729 | |||||||
| chr3:11800763 | G | A | 34 | a0001c0001t0001g0162 a0001c0001t0001g0211 a0001c0001t0001g0236 others(31): Show |
34 | HG01099.hp1 HG01109.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.937+7070C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11800763 | |||||||
| chr3:11800880 | T | C | 124 | a0001c0001t0001g0013 a0001c0001t0001g0162 a0001c0001t0001g0163 others(121): Show |
132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.937+6953A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11800880 | |||||||
| chr3:11801098 | G | GA | 238 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(235): Show |
261 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.937+6734dupT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801098 | |||||||
| chr3:11801124 | C | T | 1 | a0002c0003t0002g0067 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.937+6709G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801124 | |||||||
| chr3:11801290 | T | C | 1 | a0002c0004t0003g0016 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.937+6543A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801290 | |||||||
| chr3:11801347 | CCT | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(107): Show |
125 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(122): Show |
intron_variant | MODIFIER | c.937+6484_937+6485d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801347 | |||||||
| chr3:11801381 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.937+6452A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801381 | |||||||
| chr3:11801386 | T | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(240): Show |
266 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.937+6447A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801386 | |||||||
| chr3:11801387 | A | C | 10 | a0001c0001t0001g0002 a0001c0001t0001g0198 a0001c0001t0001g0201 others(7): Show |
13 | NA18943.hp1 NA18956.hp1 NA18977.hp2 others(10): Show |
intron_variant | MODIFIER | c.937+6446T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801387 | |||||||
| chr3:11801400 | C | T | 3 | a0001c0001t0001g0161 a0001c0002t0002g0038 a0001c0002t0002g0039 |
3 | HG02559.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.937+6433G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801400 | |||||||
| chr3:11801401 | G | A | 1 | a0001c0002t0002g0133 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.937+6432C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801401 | |||||||
| chr3:11801408 | C | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(107): Show |
125 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(122): Show |
intron_variant | MODIFIER | c.937+6425G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801408 | |||||||
| chr3:11801409 | A | G | 237 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(234): Show |
260 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.937+6424T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801409 | |||||||
| chr3:11801493 | C | T | 1 | a0001c0001t0001g0257 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.937+6340G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801493 | |||||||
| chr3:11801538 | C | T | 2 | a0001c0002t0002g0003 a0001c0002t0002g0024 |
4 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.937+6295G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801538 | |||||||
| chr3:11801625 | C | T | 1 | a0001c0002t0002g0107 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.937+6208G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801625 | |||||||
| chr3:11801776 | T | C | 11 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0191 others(8): Show |
12 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.937+6057A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801776 | |||||||
| chr3:11801807 | G | A | 1 | a0001c0002t0002g0133 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.937+6026C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801807 | |||||||
| chr3:11801829 | A | G | 1 | a0001c0002t0002g0133 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.937+6004T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801829 | |||||||
| chr3:11801954 | C | T | 1 | a0001c0001t0001g0318 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.937+5879G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801954 | |||||||
| chr3:11801979 | G | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(83): Show |
99 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.937+5854C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801979 | |||||||
| chr3:11801980 | G | A | 4 | a0001c0001t0001g0196 a0001c0001t0001g0328 a0001c0001t0001g0329 others(1): Show |
4 | HG00621.hp1 NA18944.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.937+5853C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11801980 | |||||||
| chr3:11802205 | G | C | 3 | a0001c0001t0001g0161 a0001c0002t0002g0038 a0001c0002t0002g0039 |
3 | HG02559.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.937+5628C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11802205 | |||||||
| chr3:11802420 | A | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(103): Show |
121 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.937+5413T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11802420 | |||||||
| chr3:11802434 | A | G | 132 | a0001c0001t0001g0013 a0001c0001t0001g0155 a0001c0001t0001g0156 others(129): Show |
140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.937+5399T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11802434 | |||||||
| chr3:11802555 | T | C | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0002t0002g0032 |
3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.937+5278A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11802555 | |||||||
| chr3:11802623 | A | G | 1 | a0001c0002t0002g0092 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.937+5210T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11802623 | |||||||
| chr3:11802671 | G | A | 1 | a0001c0001t0001g0320 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.937+5162C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11802671 | |||||||
| chr3:11802703 | C | T | 3 | a0001c0001t0001g0161 a0001c0002t0002g0038 a0001c0002t0002g0039 |
3 | HG02559.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.937+5130G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11802703 | |||||||
| chr3:11802732 | G | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(99): Show |
117 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.937+5101C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11802732 | |||||||
| chr3:11802738 | A | C | 1 | a0001c0001t0001g0256 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.937+5095T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11802738 | |||||||
| chr3:11802880 | G | A | 1 | a0001c0002t0002g0133 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.937+4953C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11802880 | |||||||
| chr3:11802897 | T | C | 1 | a0001c0001t0001g0326 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.937+4936A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11802897 | |||||||
| chr3:11803007 | T | C | 1 | a0001c0001t0001g0328 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.937+4826A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11803007 | |||||||
| chr3:11803011 | C | A | 1 | a0001c0002t0002g0133 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.937+4822G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11803011 | |||||||
| chr3:11803062 | A | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(103): Show |
121 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.937+4771T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11803062 | |||||||
| chr3:11803216 | G | A | 1 | a0004c0006t0004g0143 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.937+4617C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11803216 | |||||||
| chr3:11803281 | G | A | 105 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(102): Show |
120 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.937+4552C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11803281 | |||||||
| chr3:11803288 | G | A | 1 | a0001c0001t0001g0334 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.937+4545C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11803288 | |||||||
| chr3:11803536 | A | G | 4 | a0002c0003t0002g0066 a0002c0003t0002g0093 a0002c0004t0001g0335 others(1): Show |
4 | HG01243.hp2 HG01978.hp2 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.937+4297T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11803536 | |||||||
| chr3:11803577 | A | G | 238 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(235): Show |
261 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.937+4256T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11803577 | |||||||
| chr3:11803623 | G | A | 1 | a0001c0001t0001g0195 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.937+4210C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11803623 | |||||||
| chr3:11803685 | A | G | 1 | a0001c0001t0001g0260 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.937+4148T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11803685 | |||||||
| chr3:11803714 | A | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(99): Show |
117 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.937+4119T>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11803714 | |||||||
| chr3:11803732 | C | CA | 4 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0331 others(1): Show |
4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.937+4100dupT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11803732 | |||||||
| chr3:11803774 | T | A | 1 | a0002c0003t0004g0113 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.937+4059A>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11803774 | |||||||
| chr3:11803811 | G | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(239): Show |
264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.937+4022C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11803811 | |||||||
| chr3:11804016 | G | T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(102): Show |
120 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.937+3817C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11804016 | |||||||
| chr3:11804442 | C | G | 1 | a0001c0001t0001g0318 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.937+3391G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11804442 | |||||||
| chr3:11804824 | C | T | 1 | a0001c0001t0001g0310 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.937+3009G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11804824 | |||||||
| chr3:11804858 | T | C | 11 | a0001c0001t0001g0162 a0001c0001t0001g0211 a0001c0001t0001g0236 others(8): Show |
11 | HG02074.hp1 HG02129.hp1 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.937+2975A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11804858 | |||||||
| chr3:11804868 | A | AT | 9 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0341 others(6): Show |
9 | HG02965.hp1 HG03098.hp2 HG03471.hp2 others(6): Show |
intron_variant | MODIFIER | c.937+2964dupA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11804868 | |||||||
| chr3:11804868 | AT | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(99): Show |
117 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.937+2964delA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11804868 | |||||||
| chr3:11804996 | C | CT | 69 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0153 others(66): Show |
72 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.937+2836dupA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11804996 | |||||||
| chr3:11804996 | C | CTT | 7 | a0001c0001t0001g0189 a0001c0001t0001g0207 a0001c0001t0001g0324 others(4): Show |
7 | HG02074.hp1 HG02698.hp1 NA18991.hp1 others(4): Show |
intron_variant | MODIFIER | c.937+2835_937+2836d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11804996 | |||||||
| chr3:11804996 | CT | C | 10 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0216 others(7): Show |
11 | HG00544.hp1 HG02071.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.937+2836delA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11804996 | |||||||
| chr3:11804996 | CTTTTTTT others(4): Show |
C | 1 | a0002c0003t0004g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.937+2826_937+2836d others(13): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11804996 | |||||||
| chr3:11804999 | T | TTG | 8 | a0001c0001t0001g0253 a0001c0001t0001g0278 a0001c0001t0001g0312 others(5): Show |
8 | HG01981.hp2 HG02257.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.937+2833_937+2834i others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11804999 | |||||||
| chr3:11805000 | T | TG | 98 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(95): Show |
113 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.937+2832_937+2833i others(3): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805000 | |||||||
| chr3:11805001 | T | G | 2 | a0001c0001t0001g0215 a0001c0001t0001g0298 |
2 | HG01256.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.937+2832A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805001 | |||||||
| chr3:11805002 | T | G | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0002t0002g0032 |
3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.937+2831A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805002 | |||||||
| chr3:11805003 | T | G | 2 | a0001c0001t0001g0216 a0001c0002t0002g0032 |
2 | HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.937+2830A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805003 | |||||||
| chr3:11805009 | T | G | 3 | a0001c0001t0001g0253 a0001c0001t0001g0278 a0001c0001t0001g0326 |
3 | HG01981.hp2 HG06807.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.937+2824A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805009 | |||||||
| chr3:11805010 | T | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(99): Show |
117 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.937+2823A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805010 | |||||||
| chr3:11805011 | T | G | 1 | a0001c0001t0001g0298 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.937+2822A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805011 | |||||||
| chr3:11805012 | T | G | 4 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0331 others(1): Show |
4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.937+2821A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805012 | |||||||
| chr3:11805053 | A | G | 239 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(236): Show |
262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.937+2780T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805053 | |||||||
| chr3:11805062 | G | A | 1 | a0001c0002t0002g0102 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.937+2771C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805062 | |||||||
| chr3:11805124 | C | T | 2 | a0001c0002t0002g0038 a0001c0002t0002g0039 |
2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.937+2709G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805124 | |||||||
| chr3:11805150 | T | C | 5 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0331 others(2): Show |
5 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.937+2683A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805150 | |||||||
| chr3:11805244 | T | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(121): Show |
140 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(137): Show |
intron_variant | MODIFIER | c.937+2589A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805244 | |||||||
| chr3:11805338 | T | C | 1 | a0002c0003t0002g0066 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.937+2495A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805338 | |||||||
| chr3:11805519 | G | A | 1 | a0001c0002t0004g0087 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.937+2314C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805519 | |||||||
| chr3:11805564 | G | A | 2 | a0001c0001t0001g0187 a0001c0002t0002g0131 |
2 | HG02602.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.937+2269C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805564 | |||||||
| chr3:11805607 | C | T | 111 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(108): Show |
126 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(123): Show |
intron_variant | MODIFIER | c.937+2226G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805607 | |||||||
| chr3:11805656 | T | C | 1 | a0002c0004t0003g0204 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.937+2177A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805656 | |||||||
| chr3:11805728 | G | A | 4 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0331 others(1): Show |
4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.937+2105C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805728 | |||||||
| chr3:11805730 | T | A | 4 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0331 others(1): Show |
4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.937+2103A>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805730 | |||||||
| chr3:11805731 | C | A | 4 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0331 others(1): Show |
4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.937+2102G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805731 | |||||||
| chr3:11805747 | C | T | 106 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(103): Show |
121 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.937+2086G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805747 | |||||||
| chr3:11805776 | C | A | 1 | a0001c0001t0003g0174 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.937+2057G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805776 | |||||||
| chr3:11805825 | C | G | 132 | a0001c0001t0001g0013 a0001c0001t0001g0155 a0001c0001t0001g0156 others(129): Show |
140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.937+2008G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805825 | |||||||
| chr3:11805930 | T | C | 10 | a0001c0001t0001g0227 a0001c0001t0001g0253 a0001c0001t0001g0284 others(7): Show |
10 | HG01256.hp1 HG01515.hp2 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.937+1903A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11805930 | |||||||
| chr3:11806063 | G | C | 4 | a0001c0001t0001g0196 a0001c0001t0001g0328 a0001c0001t0001g0329 others(1): Show |
4 | HG00621.hp1 NA18944.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.937+1770C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11806063 | |||||||
| chr3:11806223 | C | T | 1 | a0002c0003t0004g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.937+1610G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11806223 | |||||||
| chr3:11806338 | T | C | 1 | a0002c0004t0001g0306 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.937+1495A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11806338 | |||||||
| chr3:11806377 | C | T | 1 | a0001c0002t0002g0115 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.937+1456G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11806377 | |||||||
| chr3:11806466 | AAG | A | 5 | a0001c0001t0003g0228 a0001c0002t0004g0122 a0001c0002t0004g0124 others(2): Show |
5 | HG00099.hp2 HG00642.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.937+1365_937+1366d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11806466 | |||||||
| chr3:11806468 | G | C | 1 | a0002c0004t0001g0247 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.937+1365C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11806468 | |||||||
| chr3:11806488 | T | G | 2 | a0001c0002t0002g0028 a0001c0002t0002g0029 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.937+1345A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11806488 | |||||||
| chr3:11806705 | T | C | 5 | a0001c0001t0001g0015 a0001c0001t0001g0259 a0001c0001t0001g0261 others(2): Show |
6 | HG02074.hp2 HG03834.hp2 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.937+1128A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11806705 | |||||||
| chr3:11807059 | C | T | 4 | a0001c0001t0001g0161 a0001c0002t0002g0038 a0001c0002t0002g0039 others(1): Show |
4 | HG02559.hp1 HG03516.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.937+774G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11807059 | |||||||
| chr3:11807107 | C | T | 1 | a0001c0002t0002g0081 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.937+726G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11807107 | |||||||
| chr3:11807110 | C | A | 1 | a0001c0002t0002g0133 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.937+723G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11807110 | |||||||
| chr3:11807162 | C | G | 1 | a0002c0003t0004g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.937+671G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11807162 | |||||||
| chr3:11807338 | C | A | 4 | a0001c0001t0001g0161 a0001c0002t0002g0038 a0001c0002t0002g0039 others(1): Show |
4 | HG02559.hp1 HG03516.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.937+495G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11807338 | |||||||
| chr3:11807366 | T | C | 1 | a0007c0010t0001g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.937+467A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11807366 | |||||||
| chr3:11807388 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.937+445G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11807388 | |||||||
| chr3:11807400 | G | C | 41 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(38): Show |
44 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.937+433C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11807400 | |||||||
| chr3:11807404 | C | T | 3 | a0001c0001t0001g0161 a0001c0002t0002g0038 a0001c0002t0002g0039 |
3 | HG02559.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.937+429G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11807404 | |||||||
| chr3:11807449 | CCACT | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(99): Show |
117 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.937+380_937+383del others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11807449 | |||||||
| chr3:11807611 | A | G | 3 | a0001c0001t0001g0161 a0001c0002t0002g0038 a0001c0002t0002g0039 |
3 | HG02559.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.937+222T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 7/7 | chr3 | 11807611 | |||||||
| chr3:11807910 | C | A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0191 others(5): Show |
9 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.875-15G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11807910 | |||||||
| chr3:11808070 | G | C | 3 | a0001c0001t0001g0161 a0001c0002t0002g0038 a0001c0002t0002g0039 |
3 | HG02559.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.875-175C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808070 | |||||||
| chr3:11808075 | C | T | 1 | a0001c0002t0002g0098 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.875-180G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808075 | |||||||
| chr3:11808102 | G | A | 5 | a0002c0003t0002g0055 a0002c0003t0002g0067 a0002c0003t0002g0069 others(2): Show |
5 | HG03017.hp1 HG03017.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.875-207C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808102 | |||||||
| chr3:11808141 | C | T | 4 | a0001c0001t0001g0165 a0001c0002t0002g0083 a0001c0002t0002g0085 others(1): Show |
4 | HG00735.hp2 HG01175.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.875-246G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808141 | |||||||
| chr3:11808270 | C | T | 7 | a0001c0001t0001g0161 a0001c0001t0001g0312 a0001c0001t0001g0313 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.875-375G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808270 | |||||||
| chr3:11808303 | G | A | 9 | a0001c0001t0003g0012 a0001c0001t0003g0017 a0001c0001t0003g0170 others(6): Show |
11 | HG00639.hp2 HG01069.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.875-408C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808303 | |||||||
| chr3:11808333 | A | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(240): Show |
266 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.875-438T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808333 | |||||||
| chr3:11808436 | T | C | 75 | a0001c0001t0001g0167 a0001c0001t0001g0169 a0001c0001t0001g0175 others(72): Show |
82 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.875-541A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808436 | |||||||
| chr3:11808437 | A | T | 75 | a0001c0001t0001g0167 a0001c0001t0001g0169 a0001c0001t0001g0175 others(72): Show |
82 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.875-542T>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808437 | |||||||
| chr3:11808438 | AAC | A | 75 | a0001c0001t0001g0167 a0001c0001t0001g0169 a0001c0001t0001g0175 others(72): Show |
82 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.875-545_875-544del others(2): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808438 | |||||||
| chr3:11808501 | G | T | 79 | a0001c0001t0001g0167 a0001c0001t0001g0169 a0001c0001t0001g0175 others(76): Show |
86 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.875-606C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808501 | |||||||
| chr3:11808518 | C | T | 4 | a0001c0001t0001g0161 a0001c0002t0002g0038 a0001c0002t0002g0039 others(1): Show |
4 | HG02559.hp1 HG03516.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.875-623G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808518 | |||||||
| chr3:11808530 | C | T | 3 | a0001c0001t0001g0161 a0001c0002t0002g0038 a0001c0002t0002g0039 |
3 | HG02559.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.875-635G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808530 | |||||||
| chr3:11808589 | T | C | 4 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0331 others(1): Show |
4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.875-694A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808589 | |||||||
| chr3:11808749 | T | C | 3 | a0001c0001t0001g0161 a0001c0002t0002g0038 a0001c0002t0002g0039 |
3 | HG02559.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.874+768A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808749 | |||||||
| chr3:11808801 | T | C | 3 | a0001c0001t0001g0161 a0001c0002t0002g0038 a0001c0002t0002g0039 |
3 | HG02559.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.874+716A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808801 | |||||||
| chr3:11808893 | G | T | 239 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(236): Show |
262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.874+624C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808893 | |||||||
| chr3:11808918 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.874+599C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11808918 | |||||||
| chr3:11809077 | G | A | 8 | a0002c0003t0002g0037 a0002c0004t0001g0221 a0002c0004t0001g0244 others(5): Show |
8 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.874+440C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11809077 | |||||||
| chr3:11809079 | G | A | 35 | a0001c0001t0001g0162 a0001c0001t0001g0211 a0001c0001t0001g0236 others(32): Show |
35 | HG01099.hp1 HG01109.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.874+438C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11809079 | |||||||
| chr3:11809092 | G | C | 1 | a0001c0001t0001g0321 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.874+425C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11809092 | |||||||
| chr3:11809513 | G | A | 1 | a0002c0004t0001g0339 | 1 | HG02071.hp1 | splice_region_variant&intron_variant | LOW | c.874+4C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 6/7 | chr3 | 11809513 | |||||||
| chr3:11809742 | C | A | 3 | a0001c0001t0001g0161 a0001c0001t0001g0318 a0001c0002t0002g0133 |
3 | HG02559.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.709-60G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11809742 | |||||||
| chr3:11810004 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.709-322A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11810004 | |||||||
| chr3:11810023 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.709-341G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11810023 | |||||||
| chr3:11810067 | T | C | 1 | a0001c0001t0001g0267 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.709-385A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11810067 | |||||||
| chr3:11810258 | A | G | 1 | a0003c0005t0003g0300 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.709-576T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11810258 | |||||||
| chr3:11810285 | C | T | 11 | a0001c0001t0001g0162 a0001c0001t0001g0211 a0001c0001t0001g0236 others(8): Show |
11 | HG02074.hp1 HG02129.hp1 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.709-603G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11810285 | |||||||
| chr3:11810467 | A | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(238): Show |
264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.709-785T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11810467 | |||||||
| chr3:11810641 | G | A | 1 | a0001c0001t0003g0283 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.709-959C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11810641 | |||||||
| chr3:11810644 | G | C | 4 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0331 others(1): Show |
4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.709-962C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11810644 | |||||||
| chr3:11810894 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.709-1212C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11810894 | |||||||
| chr3:11810902 | G | GA | 36 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(33): Show |
43 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.709-1221dupT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11810902 | |||||||
| chr3:11810902 | GA | G | 41 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(38): Show |
41 | HG01099.hp1 HG01109.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.709-1221delT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11810902 | |||||||
| chr3:11810914 | G | C | 2 | a0001c0001t0001g0321 a0001c0002t0002g0132 |
2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.709-1232C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11810914 | |||||||
| chr3:11811004 | G | A | 45 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(42): Show |
45 | HG01099.hp1 HG01109.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.709-1322C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11811004 | |||||||
| chr3:11811023 | G | C | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0002t0002g0032 |
3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.709-1341C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11811023 | |||||||
| chr3:11811236 | T | C | 1 | a0002c0003t0004g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.709-1554A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11811236 | |||||||
| chr3:11811415 | A | G | 1 | a0001c0001t0001g0314 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.709-1733T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11811415 | |||||||
| chr3:11811512 | A | T | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.709-1830T>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11811512 | |||||||
| chr3:11811567 | T | C | 1 | a0001c0002t0002g0133 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.709-1885A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11811567 | |||||||
| chr3:11811596 | G | A | 2 | a0002c0003t0002g0054 a0002c0003t0002g0100 |
2 | NA18994.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.709-1914C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11811596 | |||||||
| chr3:11811653 | T | C | 1 | a0001c0002t0002g0133 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.709-1971A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11811653 | |||||||
| chr3:11811693 | T | C | 128 | a0001c0001t0001g0013 a0001c0001t0001g0155 a0001c0001t0001g0156 others(125): Show |
136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.709-2011A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11811693 | |||||||
| chr3:11811788 | G | A | 1 | a0002c0004t0001g0244 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.709-2106C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11811788 | |||||||
| chr3:11811789 | A | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(107): Show |
125 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(122): Show |
intron_variant | MODIFIER | c.709-2107T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11811789 | |||||||
| chr3:11811962 | C | G | 235 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(232): Show |
258 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.709-2280G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11811962 | |||||||
| chr3:11811989 | G | A | 1 | a0001c0002t0002g0086 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.709-2307C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11811989 | |||||||
| chr3:11811990 | C | T | 1 | a0002c0003t0002g0055 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.709-2308G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11811990 | |||||||
| chr3:11812073 | G | A | 4 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0331 others(1): Show |
4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.709-2391C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11812073 | |||||||
| chr3:11812164 | C | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(240): Show |
266 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.709-2482G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11812164 | |||||||
| chr3:11812242 | G | A | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0002t0002g0032 |
3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.709-2560C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11812242 | |||||||
| chr3:11812324 | C | T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(102): Show |
120 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.709-2642G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11812324 | |||||||
| chr3:11812372 | C | T | 4 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(1): Show |
4 | HG01884.hp2 HG02647.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.709-2690G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11812372 | |||||||
| chr3:11812423 | G | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(107): Show |
125 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(122): Show |
intron_variant | MODIFIER | c.709-2741C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11812423 | |||||||
| chr3:11812462 | G | A | 1 | a0001c0002t0004g0089 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.709-2780C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11812462 | |||||||
| chr3:11812617 | C | T | 34 | a0001c0001t0001g0162 a0001c0001t0001g0211 a0001c0001t0001g0236 others(31): Show |
34 | HG01099.hp1 HG01109.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.709-2935G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11812617 | |||||||
| chr3:11812900 | G | T | 1 | a0001c0001t0001g0318 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.709-3218C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11812900 | |||||||
| chr3:11812909 | G | A | 1 | a0001c0001t0001g0320 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.709-3227C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11812909 | |||||||
| chr3:11813029 | T | C | 1 | a0002c0003t0004g0063 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.709-3347A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813029 | |||||||
| chr3:11813043 | T | G | 10 | a0001c0001t0001g0229 a0001c0001t0001g0322 a0001c0001t0001g0340 others(7): Show |
12 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.709-3361A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813043 | |||||||
| chr3:11813146 | C | T | 2 | a0001c0007t0001g0145 a0001c0007t0001g0146 |
2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.709-3464G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813146 | |||||||
| chr3:11813177 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.709-3495T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813177 | |||||||
| chr3:11813203 | C | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(99): Show |
117 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.709-3521G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813203 | |||||||
| chr3:11813385 | C | T | 1 | a0001c0002t0004g0109 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.709-3703G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813385 | |||||||
| chr3:11813488 | C | T | 3 | a0003c0005t0003g0240 a0003c0005t0003g0241 a0003c0005t0003g0300 |
3 | HG00323.hp2 HG01261.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.708+3704G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813488 | |||||||
| chr3:11813729 | G | A | 1 | a0001c0002t0002g0133 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.708+3463C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813729 | |||||||
| chr3:11813828 | A | ATG | 58 | a0001c0001t0001g0159 a0001c0001t0001g0175 a0001c0001t0001g0187 others(55): Show |
64 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.708+3362_708+3363d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813828 | |||||||
| chr3:11813828 | A | ATGTG | 30 | a0001c0001t0001g0161 a0001c0001t0001g0167 a0001c0001t0001g0169 others(27): Show |
32 | HG00099.hp1 HG00639.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.708+3360_708+3363d others(6): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813828 | |||||||
| chr3:11813828 | A | ATGTGTG | 14 | a0001c0001t0001g0163 a0001c0001t0003g0022 a0001c0001t0003g0171 others(11): Show |
15 | HG00140.hp1 HG00639.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.708+3358_708+3363d others(8): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813828 | |||||||
| chr3:11813828 | A | ATGTGTGT others(1): Show |
30 | a0001c0001t0001g0013 a0001c0001t0001g0162 a0001c0001t0001g0191 others(27): Show |
31 | HG01099.hp1 HG01109.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.708+3356_708+3363d others(10): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813828 | |||||||
| chr3:11813828 | A | ATGTGTGT others(3): Show |
5 | a0001c0002t0002g0103 a0002c0003t0002g0057 a0002c0003t0002g0058 others(2): Show |
5 | HG02071.hp1 HG03017.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.708+3354_708+3363d others(12): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813828 | |||||||
| chr3:11813828 | A | ATGTGTGT others(5): Show |
10 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(7): Show |
10 | HG01891.hp2 HG01978.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.708+3352_708+3363d others(14): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813828 | |||||||
| chr3:11813828 | A | G | 2 | a0003c0005t0003g0241 a0003c0005t0003g0300 |
2 | HG00323.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.708+3364T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813828 | |||||||
| chr3:11813828 | ATG | A | 6 | a0001c0001t0001g0289 a0001c0001t0001g0299 a0001c0002t0002g0045 others(3): Show |
6 | HG03491.hp2 NA18991.hp2 NA19001.hp2 others(3): Show |
intron_variant | MODIFIER | c.708+3362_708+3363d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813828 | |||||||
| chr3:11813850 | GTGTGTGT others(1): Show |
G | 4 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0331 others(1): Show |
4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.708+3334_708+3341d others(10): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813850 | |||||||
| chr3:11813852 | GTGTGTA | G | 4 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0002t0002g0032 others(1): Show |
4 | HG03098.hp2 HG03471.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.708+3334_708+3339d others(8): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813852 | |||||||
| chr3:11813858 | A | G | 5 | a0001c0001t0001g0321 a0001c0001t0003g0176 a0001c0002t0002g0038 others(2): Show |
5 | HG00733.hp2 HG02630.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.708+3334T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813858 | |||||||
| chr3:11813862 | A | G | 1 | a0001c0001t0001g0321 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.708+3330T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813862 | |||||||
| chr3:11813866 | A | G | 1 | a0001c0001t0001g0321 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.708+3326T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813866 | |||||||
| chr3:11813866 | ATATATAT others(1): Show |
A | 3 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0329 |
3 | HG01070.hp1 HG01071.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.708+3318_708+3325d others(10): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813866 | |||||||
| chr3:11813868 | A | G | 3 | a0001c0002t0002g0038 a0001c0002t0002g0039 a0001c0002t0002g0132 |
3 | HG03195.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.708+3324T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813868 | |||||||
| chr3:11813870 | A | G | 1 | a0001c0001t0001g0321 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.708+3322T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813870 | |||||||
| chr3:11813870 | ATATG | A | 3 | a0001c0002t0002g0038 a0001c0002t0002g0039 a0001c0002t0002g0132 |
3 | HG03195.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.708+3318_708+3321d others(6): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813870 | |||||||
| chr3:11813888 | A | ATGTGTAT others(13): Show |
1 | a0001c0001t0001g0324 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.708+3284_708+3303d others(22): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813888 | |||||||
| chr3:11813904 | A | G | 2 | a0001c0001t0001g0152 a0001c0001t0001g0186 |
2 | HG00733.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.708+3288T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813904 | |||||||
| chr3:11813904 | ATATG | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(99): Show |
117 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.708+3284_708+3287d others(6): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813904 | |||||||
| chr3:11813920 | GTA | G | 5 | a0001c0001t0001g0312 a0001c0001t0001g0331 a0001c0002t0002g0009 others(2): Show |
6 | HG00438.hp1 HG00673.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.708+3270_708+3271d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813920 | |||||||
| chr3:11813924 | ATATG | A | 7 | a0001c0001t0001g0211 a0002c0003t0002g0054 a0002c0003t0002g0057 others(4): Show |
7 | HG02165.hp2 NA18948.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.708+3264_708+3267d others(6): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813924 | |||||||
| chr3:11813991 | T | TAC | 78 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(75): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.708+3199_708+3200d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813991 | |||||||
| chr3:11813991 | T | TACAC | 15 | a0001c0001t0001g0161 a0001c0002t0002g0039 a0001c0002t0004g0087 others(12): Show |
15 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.708+3197_708+3200d others(6): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813991 | |||||||
| chr3:11813991 | TAC | T | 31 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(28): Show |
34 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.708+3199_708+3200d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813991 | |||||||
| chr3:11813991 | TACAC | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0191 a0001c0002t0002g0032 others(1): Show |
5 | HG02109.hp2 HG02280.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.708+3197_708+3200d others(6): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813991 | |||||||
| chr3:11813991 | TACACAC | T | 5 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0318 others(2): Show |
5 | HG02257.hp2 HG03098.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.708+3195_708+3200d others(8): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11813991 | |||||||
| chr3:11814302 | C | T | 1 | a0001c0001t0001g0341 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.708+2890G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11814302 | |||||||
| chr3:11814494 | G | A | 8 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0312 others(5): Show |
8 | HG02257.hp2 HG03098.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.708+2698C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11814494 | |||||||
| chr3:11814524 | G | A | 1 | a0001c0001t0003g0171 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.708+2668C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11814524 | |||||||
| chr3:11814688 | C | T | 2 | a0001c0001t0001g0321 a0001c0002t0002g0132 |
2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.708+2504G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11814688 | |||||||
| chr3:11814689 | G | A | 1 | a0001c0002t0002g0133 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.708+2503C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11814689 | |||||||
| chr3:11814782 | G | A | 1 | a0001c0001t0001g0015 | 2 | NA18945.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.708+2410C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11814782 | |||||||
| chr3:11814806 | C | T | 1 | a0002c0004t0002g0140 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.708+2386G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11814806 | |||||||
| chr3:11814955 | C | T | 2 | a0001c0007t0001g0145 a0001c0007t0001g0146 |
2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.708+2237G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11814955 | |||||||
| chr3:11815045 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(111): Show |
130 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(127): Show |
intron_variant | MODIFIER | c.708+2147T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11815045 | |||||||
| chr3:11815096 | A | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(242): Show |
268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.708+2096T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11815096 | |||||||
| chr3:11815106 | T | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(111): Show |
130 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(127): Show |
intron_variant | MODIFIER | c.708+2086A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11815106 | |||||||
| chr3:11815197 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(111): Show |
130 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(127): Show |
intron_variant | MODIFIER | c.708+1995T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11815197 | |||||||
| chr3:11815247 | C | T | 5 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0331 others(2): Show |
5 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.708+1945G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11815247 | |||||||
| chr3:11815248 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.708+1944C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11815248 | |||||||
| chr3:11815673 | T | G | 2 | a0001c0002t0002g0038 a0001c0002t0002g0039 |
2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.708+1519A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11815673 | |||||||
| chr3:11815728 | T | TA | 102 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(99): Show |
117 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.708+1463dupT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11815728 | |||||||
| chr3:11815820 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.708+1372T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11815820 | |||||||
| chr3:11815899 | G | A | 4 | a0001c0001t0001g0196 a0001c0001t0001g0328 a0001c0001t0001g0329 others(1): Show |
4 | HG00621.hp1 NA18944.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.708+1293C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11815899 | |||||||
| chr3:11815962 | G | A | 6 | a0002c0003t0002g0055 a0002c0003t0002g0065 a0002c0003t0002g0067 others(3): Show |
6 | HG03017.hp1 HG03017.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.708+1230C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11815962 | |||||||
| chr3:11815986 | C | A | 1 | a0001c0002t0002g0119 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.708+1206G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11815986 | |||||||
| chr3:11816137 | C | T | 6 | a0001c0001t0001g0225 a0001c0002t0002g0082 a0001c0002t0002g0126 others(3): Show |
6 | HG00280.hp1 HG01243.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.708+1055G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816137 | |||||||
| chr3:11816154 | C | T | 5 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0331 others(2): Show |
5 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.708+1038G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816154 | |||||||
| chr3:11816217 | G | GA | 39 | a0001c0001t0001g0018 a0001c0001t0001g0162 a0001c0001t0001g0234 others(36): Show |
40 | HG01099.hp1 HG01109.hp1 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.708+974dupT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816217 | |||||||
| chr3:11816299 | G | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(99): Show |
117 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.708+893C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816299 | |||||||
| chr3:11816344 | TAAAC | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(82): Show |
98 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.708+844_708+847del others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816344 | |||||||
| chr3:11816356 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.708+836C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816356 | |||||||
| chr3:11816384 | T | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(111): Show |
130 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(127): Show |
intron_variant | MODIFIER | c.708+808A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816384 | |||||||
| chr3:11816390 | C | T | 2 | a0002c0004t0001g0305 a0002c0004t0001g0306 |
2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.708+802G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816390 | |||||||
| chr3:11816398 | T | C | 1 | a0001c0001t0001g0298 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.708+794A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816398 | |||||||
| chr3:11816521 | T | C | 2 | a0001c0001t0001g0278 a0001c0001t0001g0279 |
2 | HG01978.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.708+671A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816521 | |||||||
| chr3:11816678 | A | C | 2 | a0001c0002t0002g0003 a0001c0002t0002g0024 |
4 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.708+514T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816678 | |||||||
| chr3:11816750 | G | GC | 5 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0331 others(2): Show |
5 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.708+441_708+442ins others(1): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816750 | |||||||
| chr3:11816775 | A | C | 1 | a0001c0002t0004g0122 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.708+417T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816775 | |||||||
| chr3:11816791 | AC | A | 6 | a0001c0001t0001g0219 a0001c0001t0001g0312 a0001c0001t0001g0313 others(3): Show |
6 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.708+400delG | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816791 | |||||||
| chr3:11816792 | C | A | 105 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(102): Show |
120 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.708+400G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816792 | |||||||
| chr3:11816851 | G | A | 1 | a0002c0004t0003g0011 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.708+341C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816851 | |||||||
| chr3:11816926 | T | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(110): Show |
129 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(126): Show |
intron_variant | MODIFIER | c.708+266A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 5/7 | chr3 | 11816926 | |||||||
| chr3:11817414 | T | C | 1 | a0002c0003t0004g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.563-77A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11817414 | |||||||
| chr3:11817731 | T | C | 1 | a0002c0003t0002g0067 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.563-394A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11817731 | |||||||
| chr3:11817857 | A | G | 8 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0191 others(5): Show |
9 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.563-520T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11817857 | |||||||
| chr3:11817871 | T | G | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.563-534A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11817871 | |||||||
| chr3:11817956 | C | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(99): Show |
117 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.563-619G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11817956 | |||||||
| chr3:11817971 | G | A | 1 | a0002c0003t0002g0069 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.563-634C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11817971 | |||||||
| chr3:11817990 | C | A | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.563-653G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11817990 | |||||||
| chr3:11818179 | G | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(239): Show |
265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.563-842C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818179 | |||||||
| chr3:11818241 | A | G | 1 | a0001c0001t0001g0318 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.563-904T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818241 | |||||||
| chr3:11818242 | A | T | 1 | a0001c0001t0001g0318 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.563-905T>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818242 | |||||||
| chr3:11818248 | T | A | 1 | a0001c0001t0001g0318 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.563-911A>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818248 | |||||||
| chr3:11818311 | G | A | 3 | a0001c0001t0003g0172 a0001c0001t0003g0173 a0001c0001t0003g0180 |
3 | HG00099.hp1 HG01516.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.563-974C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818311 | |||||||
| chr3:11818322 | T | C | 1 | a0001c0001t0001g0318 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.563-985A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818322 | |||||||
| chr3:11818360 | T | A | 4 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(1): Show |
4 | HG02148.hp1 HG02293.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.563-1023A>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818360 | |||||||
| chr3:11818415 | C | G | 1 | a0002c0003t0004g0056 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.563-1078G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818415 | |||||||
| chr3:11818635 | A | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(240): Show |
266 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.563-1298T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818635 | |||||||
| chr3:11818663 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.563-1326C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818663 | |||||||
| chr3:11818703 | T | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(116): Show |
135 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(132): Show |
intron_variant | MODIFIER | c.563-1366A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818703 | |||||||
| chr3:11818746 | A | C | 2 | a0002c0003t0002g0026 a0002c0003t0002g0027 |
2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.563-1409T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818746 | |||||||
| chr3:11818746 | A | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(116): Show |
135 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(132): Show |
intron_variant | MODIFIER | c.563-1409T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818746 | |||||||
| chr3:11818833 | G | C | 1 | a0001c0001t0001g0315 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.563-1496C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818833 | |||||||
| chr3:11818893 | A | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(116): Show |
135 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(132): Show |
intron_variant | MODIFIER | c.563-1556T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818893 | |||||||
| chr3:11818897 | C | CA | 117 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(114): Show |
133 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(130): Show |
intron_variant | MODIFIER | c.563-1561dupT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11818897 | |||||||
| chr3:11819023 | A | G | 1 | a0006c0011t0004g0070 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.563-1686T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11819023 | |||||||
| chr3:11819033 | T | C | 1 | a0001c0001t0001g0255 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.563-1696A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11819033 | |||||||
| chr3:11819050 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.563-1713T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11819050 | |||||||
| chr3:11819067 | T | G | 1 | a0001c0001t0001g0296 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.563-1730A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11819067 | |||||||
| chr3:11819141 | A | G | 5 | a0002c0003t0002g0066 a0002c0003t0002g0093 a0002c0003t0004g0053 others(2): Show |
5 | HG01243.hp2 HG01978.hp2 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.563-1804T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11819141 | |||||||
| chr3:11819183 | C | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(110): Show |
129 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(126): Show |
intron_variant | MODIFIER | c.563-1846G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11819183 | |||||||
| chr3:11819208 | A | G | 1 | a0002c0004t0001g0305 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.563-1871T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11819208 | |||||||
| chr3:11819290 | T | G | 2 | a0001c0001t0003g0282 a0001c0001t0003g0283 |
2 | NA18612.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.563-1953A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11819290 | |||||||
| chr3:11819296 | G | C | 4 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(1): Show |
4 | HG02257.hp1 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.563-1959C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11819296 | |||||||
| chr3:11819384 | A | T | 1 | a0001c0001t0001g0271 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.563-2047T>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11819384 | |||||||
| chr3:11819461 | T | C | 1 | a0001c0002t0002g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.563-2124A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11819461 | |||||||
| chr3:11819466 | C | T | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(298): Show |
331 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.563-2129G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11819466 | |||||||
| chr3:11819693 | G | A | 2 | a0001c0002t0002g0038 a0001c0002t0002g0039 |
2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.563-2356C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11819693 | |||||||
| chr3:11819712 | T | C | 1 | a0002c0003t0004g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.563-2375A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11819712 | |||||||
| chr3:11819986 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.563-2649G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11819986 | |||||||
| chr3:11820160 | T | C | 1 | a0001c0001t0003g0174 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.563-2823A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11820160 | |||||||
| chr3:11820176 | C | T | 2 | a0003c0005t0003g0239 a0006c0011t0004g0070 |
2 | HG00140.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.563-2839G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11820176 | |||||||
| chr3:11820241 | G | A | 1 | a0001c0002t0002g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.563-2904C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11820241 | |||||||
| chr3:11820386 | T | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(100): Show |
118 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.563-3049A>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11820386 | |||||||
| chr3:11820424 | A | C | 3 | a0001c0001t0001g0225 a0001c0002t0002g0127 a0001c0002t0002g0128 |
3 | HG02683.hp2 HG02735.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.563-3087T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11820424 | |||||||
| chr3:11820492 | G | A | 34 | a0001c0001t0001g0162 a0001c0001t0001g0211 a0001c0001t0001g0236 others(31): Show |
34 | HG01099.hp1 HG01109.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.563-3155C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11820492 | |||||||
| chr3:11820558 | A | G | 6 | a0001c0002t0004g0087 a0001c0002t0004g0088 a0001c0002t0004g0089 others(3): Show |
6 | HG01358.hp1 HG01975.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.563-3221T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11820558 | |||||||
| chr3:11820947 | T | C | 1 | a0001c0002t0004g0111 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.563-3610A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11820947 | |||||||
| chr3:11820969 | C | T | 1 | a0007c0010t0001g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.563-3632G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11820969 | |||||||
| chr3:11821242 | T | G | 1 | a0001c0001t0001g0205 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.563-3905A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11821242 | |||||||
| chr3:11821365 | G | T | 1 | a0002c0003t0004g0105 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.563-4028C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11821365 | |||||||
| chr3:11821499 | A | G | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG02257.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.563-4162T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11821499 | |||||||
| chr3:11821511 | T | C | 1 | a0002c0004t0001g0243 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.563-4174A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11821511 | |||||||
| chr3:11821589 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.563-4252C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11821589 | |||||||
| chr3:11821666 | G | A | 5 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0331 others(2): Show |
5 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.563-4329C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11821666 | |||||||
| chr3:11821732 | T | C | 1 | a0003c0005t0003g0241 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.563-4395A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11821732 | |||||||
| chr3:11821891 | T | C | 2 | a0001c0001t0001g0321 a0001c0002t0002g0132 |
2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.563-4554A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11821891 | |||||||
| chr3:11821952 | G | A | 2 | a0001c0001t0001g0321 a0001c0002t0002g0132 |
2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.563-4615C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11821952 | |||||||
| chr3:11822006 | T | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(108): Show |
126 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(123): Show |
intron_variant | MODIFIER | c.563-4669A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11822006 | |||||||
| chr3:11822461 | A | G | 3 | a0002c0003t0002g0026 a0002c0003t0002g0027 a0002c0004t0002g0140 |
3 | HG02622.hp2 HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.563-5124T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11822461 | |||||||
| chr3:11822559 | G | A | 1 | a0001c0002t0002g0031 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.563-5222C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11822559 | |||||||
| chr3:11822758 | T | C | 1 | a0001c0002t0002g0131 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.563-5421A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11822758 | |||||||
| chr3:11822846 | G | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(100): Show |
118 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.563-5509C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11822846 | |||||||
| chr3:11822953 | G | A | 243 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(240): Show |
266 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.563-5616C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11822953 | |||||||
| chr3:11823038 | T | G | 1 | a0001c0001t0001g0158 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.563-5701A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823038 | |||||||
| chr3:11823127 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(104): Show |
122 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(119): Show |
intron_variant | MODIFIER | c.563-5790G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823127 | |||||||
| chr3:11823254 | G | GT | 16 | a0001c0001t0001g0021 a0001c0001t0001g0161 a0001c0001t0001g0201 others(13): Show |
17 | HG00738.hp2 HG00741.hp1 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.563-5918dupA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823254 | |||||||
| chr3:11823256 | T | TG | 5 | a0001c0001t0001g0196 a0001c0001t0001g0214 a0001c0001t0001g0270 others(2): Show |
5 | HG00621.hp1 HG03516.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.563-5920_563-5919i others(3): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823256 | |||||||
| chr3:11823257 | T | G | 90 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(87): Show |
103 | HG00423.hp2 HG00438.hp1 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.563-5920A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823257 | |||||||
| chr3:11823260 | T | G | 19 | a0001c0001t0001g0020 a0001c0001t0001g0195 a0001c0001t0001g0215 others(16): Show |
20 | HG00621.hp2 HG02027.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.563-5923A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823260 | |||||||
| chr3:11823406 | C | A | 4 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0331 others(1): Show |
4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.563-6069G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823406 | |||||||
| chr3:11823448 | G | T | 1 | a0007c0010t0001g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.563-6111C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823448 | |||||||
| chr3:11823660 | C | CT | 101 | a0001c0001t0001g0013 a0001c0001t0001g0161 a0001c0001t0001g0163 others(98): Show |
109 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.562+6053dupA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823660 | |||||||
| chr3:11823660 | C | CTT | 9 | a0001c0001t0001g0167 a0001c0001t0001g0215 a0001c0001t0001g0216 others(6): Show |
9 | HG01361.hp2 HG01433.hp1 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.562+6052_562+6053d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823660 | |||||||
| chr3:11823678 | T | G | 2 | a0002c0003t0002g0026 a0002c0003t0002g0027 |
2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.562+6036A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823678 | |||||||
| chr3:11823701 | C | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(99): Show |
117 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.562+6013G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823701 | |||||||
| chr3:11823795 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.562+5919C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823795 | |||||||
| chr3:11823825 | C | T | 2 | a0001c0001t0001g0309 a0001c0001t0001g0311 |
2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.562+5889G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823825 | |||||||
| chr3:11823829 | C | CT | 160 | a0001c0001t0001g0013 a0001c0001t0001g0155 a0001c0001t0001g0156 others(157): Show |
169 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.562+5884dupA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823829 | |||||||
| chr3:11823829 | C | CTT | 8 | a0001c0001t0001g0215 a0001c0001t0001g0288 a0001c0001t0001g0333 others(5): Show |
8 | HG01109.hp2 HG01361.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.562+5883_562+5884d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823829 | |||||||
| chr3:11823829 | C | CTTT | 97 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(94): Show |
112 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(109): Show |
intron_variant | MODIFIER | c.562+5882_562+5884d others(5): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823829 | |||||||
| chr3:11823862 | G | T | 248 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(245): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.562+5852C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11823862 | |||||||
| chr3:11824213 | C | CA | 4 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0331 others(1): Show |
4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.562+5500dupT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11824213 | |||||||
| chr3:11824240 | G | C | 4 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0331 others(1): Show |
4 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.562+5474C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11824240 | |||||||
| chr3:11824357 | A | AT | 148 | a0001c0001t0001g0013 a0001c0001t0001g0162 a0001c0001t0001g0163 others(145): Show |
158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.562+5356dupA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11824357 | |||||||
| chr3:11824357 | A | ATT | 10 | a0001c0001t0001g0161 a0001c0001t0003g0280 a0001c0002t0002g0101 others(7): Show |
10 | HG00544.hp1 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.562+5355_562+5356d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11824357 | |||||||
| chr3:11824357 | AT | A | 8 | a0001c0001t0001g0218 a0001c0001t0001g0270 a0001c0001t0001g0294 others(5): Show |
9 | HG01070.hp1 HG01106.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.562+5356delA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11824357 | |||||||
| chr3:11824481 | A | G | 4 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(1): Show |
4 | HG02257.hp1 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.562+5233T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11824481 | |||||||
| chr3:11824785 | A | T | 1 | a0001c0001t0001g0155 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.562+4929T>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11824785 | |||||||
| chr3:11824793 | T | G | 2 | a0001c0002t0002g0003 a0001c0002t0002g0024 |
4 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.562+4921A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11824793 | |||||||
| chr3:11824807 | C | T | 1 | a0001c0002t0002g0133 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.562+4907G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11824807 | |||||||
| chr3:11824919 | A | G | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0002t0002g0032 |
3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.562+4795T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11824919 | |||||||
| chr3:11825083 | C | G | 1 | a0001c0002t0002g0133 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.562+4631G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11825083 | |||||||
| chr3:11825092 | C | T | 1 | a0001c0001t0003g0176 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.562+4622G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11825092 | |||||||
| chr3:11825141 | A | G | 1 | a0001c0001t0001g0318 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.562+4573T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11825141 | |||||||
| chr3:11825320 | G | A | 2 | a0001c0007t0001g0145 a0001c0007t0001g0146 |
2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.562+4394C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11825320 | |||||||
| chr3:11825345 | C | T | 106 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(103): Show |
121 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.562+4369G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11825345 | |||||||
| chr3:11825362 | C | T | 1 | a0001c0002t0002g0132 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.562+4352G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11825362 | |||||||
| chr3:11825560 | A | C | 3 | a0001c0001t0001g0214 a0001c0002t0002g0134 a0001c0002t0002g0135 |
3 | HG02615.hp1 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.562+4154T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11825560 | |||||||
| chr3:11825705 | G | A | 4 | a0001c0001t0001g0196 a0001c0001t0001g0328 a0001c0001t0001g0329 others(1): Show |
4 | HG00621.hp1 NA18944.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.562+4009C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11825705 | |||||||
| chr3:11826027 | C | T | 1 | a0004c0006t0004g0142 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.562+3687G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11826027 | |||||||
| chr3:11826251 | C | A | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.562+3463G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11826251 | |||||||
| chr3:11826260 | G | A | 1 | a0001c0001t0003g0238 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.562+3454C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11826260 | |||||||
| chr3:11826304 | C | T | 1 | a0001c0002t0002g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.562+3410G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11826304 | |||||||
| chr3:11826354 | G | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(99): Show |
117 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.562+3360C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11826354 | |||||||
| chr3:11826397 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(98): Show |
116 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.562+3317G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11826397 | |||||||
| chr3:11826433 | G | A | 1 | a0001c0002t0002g0133 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.562+3281C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11826433 | |||||||
| chr3:11826530 | C | CA | 182 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(179): Show |
205 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.562+3183dupT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11826530 | |||||||
| chr3:11826530 | C | CAA | 58 | a0001c0001t0001g0162 a0001c0001t0001g0175 a0001c0001t0001g0211 others(55): Show |
58 | HG00280.hp2 HG00323.hp2 HG01099.hp1 others(55): Show |
intron_variant | MODIFIER | c.562+3182_562+3183d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11826530 | |||||||
| chr3:11826574 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.562+3140C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11826574 | |||||||
| chr3:11826576 | A | T | 1 | a0001c0002t0004g0111 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.562+3138T>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11826576 | |||||||
| chr3:11827011 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.562+2703A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11827011 | |||||||
| chr3:11827309 | CT | C | 240 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(237): Show |
263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.562+2404delA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11827309 | |||||||
| chr3:11827335 | A | G | 1 | a0001c0001t0003g0166 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.562+2379T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11827335 | |||||||
| chr3:11827556 | G | T | 1 | a0001c0002t0002g0133 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.562+2158C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11827556 | |||||||
| chr3:11827636 | G | GA | 16 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0191 others(13): Show |
17 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.562+2077dupT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11827636 | |||||||
| chr3:11827636 | GA | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(104): Show |
121 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.562+2077delT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11827636 | |||||||
| chr3:11827667 | G | A | 1 | a0007c0010t0001g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.562+2047C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11827667 | |||||||
| chr3:11827691 | A | G | 2 | a0001c0001t0001g0015 a0002c0003t0002g0051 |
3 | NA18945.hp1 NA18966.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.562+2023T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11827691 | |||||||
| chr3:11827908 | G | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(100): Show |
118 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.562+1806C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11827908 | |||||||
| chr3:11827913 | G | A | 1 | a0001c0002t0002g0133 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.562+1801C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11827913 | |||||||
| chr3:11828058 | G | A | 4 | a0001c0001t0001g0196 a0001c0001t0001g0328 a0001c0001t0001g0329 others(1): Show |
4 | HG00621.hp1 NA18944.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.562+1656C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11828058 | |||||||
| chr3:11828075 | C | G | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0002t0002g0032 |
3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.562+1639G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11828075 | |||||||
| chr3:11828108 | C | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(97): Show |
113 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.562+1606G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11828108 | |||||||
| chr3:11828177 | C | G | 1 | a0002c0003t0004g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.562+1537G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11828177 | |||||||
| chr3:11828188 | G | T | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0002t0002g0032 |
3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.562+1526C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11828188 | |||||||
| chr3:11828216 | A | G | 1 | a0002c0003t0004g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.562+1498T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11828216 | |||||||
| chr3:11828343 | T | C | 1 | a0001c0001t0001g0287 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.562+1371A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11828343 | |||||||
| chr3:11828483 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.562+1231G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11828483 | |||||||
| chr3:11828640 | A | G | 2 | a0001c0002t0002g0028 a0001c0002t0002g0029 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.562+1074T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11828640 | |||||||
| chr3:11828801 | A | G | 1 | a0001c0001t0001g0254 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.562+913T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11828801 | |||||||
| chr3:11828849 | G | A | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0002t0002g0032 |
3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.562+865C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11828849 | |||||||
| chr3:11829023 | T | C | 5 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0331 others(2): Show |
5 | HG02257.hp2 HG03453.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.562+691A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11829023 | |||||||
| chr3:11829312 | G | A | 37 | a0001c0001t0001g0167 a0001c0001t0001g0169 a0001c0001t0001g0175 others(34): Show |
40 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.562+402C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11829312 | |||||||
| chr3:11829332 | A | G | 2 | a0001c0001t0001g0321 a0001c0002t0002g0132 |
2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.562+382T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11829332 | |||||||
| chr3:11829447 | T | C | 1 | a0001c0001t0003g0022 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.562+267A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11829447 | |||||||
| chr3:11829541 | G | A | 1 | a0002c0004t0001g0249 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.562+173C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 4/7 | chr3 | 11829541 | |||||||
| chr3:11829908 | G | A | 1 | a0001c0001t0001g0275 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.412-44C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11829908 | |||||||
| chr3:11829965 | T | C | 1 | a0001c0002t0002g0081 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.412-101A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11829965 | |||||||
| chr3:11830212 | C | T | 1 | a0001c0001t0001g0218 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.412-348G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11830212 | |||||||
| chr3:11830234 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.412-370A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11830234 | |||||||
| chr3:11830424 | T | C | 116 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(113): Show |
122 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.412-560A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11830424 | |||||||
| chr3:11830510 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.412-646G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11830510 | |||||||
| chr3:11830813 | G | C | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0002t0002g0032 |
3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.412-949C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11830813 | |||||||
| chr3:11830881 | C | CA | 92 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(89): Show |
103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.412-1018dupT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11830881 | |||||||
| chr3:11830881 | C | CAA | 192 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(189): Show |
211 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(208): Show |
intron_variant | MODIFIER | c.412-1019_412-1018d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11830881 | |||||||
| chr3:11830881 | C | CAAA | 8 | a0001c0001t0001g0276 a0001c0001t0001g0289 a0001c0001t0001g0317 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.412-1020_412-1018d others(5): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11830881 | |||||||
| chr3:11830908 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(242): Show |
267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.412-1044A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11830908 | |||||||
| chr3:11831162 | G | A | 2 | a0002c0003t0002g0026 a0002c0003t0002g0027 |
2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.412-1298C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11831162 | |||||||
| chr3:11831257 | C | T | 2 | a0001c0002t0002g0038 a0001c0002t0002g0039 |
2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.412-1393G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11831257 | |||||||
| chr3:11831302 | T | C | 1 | a0001c0001t0001g0220 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.412-1438A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11831302 | |||||||
| chr3:11831428 | C | T | 3 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0002t0002g0079 |
3 | NA19006.hp1 NA19006.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.412-1564G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11831428 | |||||||
| chr3:11831511 | T | G | 1 | a0001c0001t0001g0318 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.412-1647A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11831511 | |||||||
| chr3:11831644 | C | A | 5 | a0001c0001t0003g0177 a0001c0001t0003g0178 a0001c0001t0003g0179 others(2): Show |
5 | HG01192.hp1 HG01257.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.412-1780G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11831644 | |||||||
| chr3:11831906 | T | C | 1 | a0002c0003t0002g0069 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.412-2042A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11831906 | |||||||
| chr3:11831940 | G | A | 1 | a0002c0003t0002g0055 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.412-2076C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11831940 | |||||||
| chr3:11832280 | AAAC | A | 7 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(4): Show |
7 | HG02257.hp1 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.412-2419_412-2417d others(5): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11832280 | |||||||
| chr3:11832281 | AAC | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(217): Show |
241 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.412-2419_412-2418d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11832281 | |||||||
| chr3:11832282 | AC | A | 16 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0191 others(13): Show |
17 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.412-2419delG | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11832282 | |||||||
| chr3:11832385 | C | T | 8 | a0001c0001t0001g0013 a0001c0001t0001g0191 a0001c0001t0001g0341 others(5): Show |
9 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.412-2521G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11832385 | |||||||
| chr3:11832717 | G | C | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0002t0002g0032 |
3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.412-2853C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11832717 | |||||||
| chr3:11833103 | T | C | 9 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0191 others(6): Show |
10 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.412-3239A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833103 | |||||||
| chr3:11833105 | G | C | 1 | a0001c0002t0002g0130 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.412-3241C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833105 | |||||||
| chr3:11833138 | A | G | 1 | a0001c0002t0002g0114 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.412-3274T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833138 | |||||||
| chr3:11833157 | A | G | 1 | a0001c0001t0001g0252 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.412-3293T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833157 | |||||||
| chr3:11833211 | C | A | 1 | a0002c0003t0002g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.412-3347G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833211 | |||||||
| chr3:11833214 | C | T | 1 | a0001c0001t0003g0242 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.412-3350G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833214 | |||||||
| chr3:11833221 | A | C | 1 | a0002c0003t0004g0056 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.412-3357T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833221 | |||||||
| chr3:11833256 | G | A | 1 | a0001c0002t0002g0121 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.412-3392C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833256 | |||||||
| chr3:11833288 | G | A | 37 | a0001c0001t0001g0167 a0001c0001t0001g0169 a0001c0001t0001g0175 others(34): Show |
40 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.412-3424C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833288 | |||||||
| chr3:11833350 | C | G | 4 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0315 others(1): Show |
4 | HG02622.hp1 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.412-3486G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833350 | |||||||
| chr3:11833404 | A | G | 2 | a0001c0002t0002g0116 a0001c0002t0002g0126 |
2 | HG01074.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.412-3540T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833404 | |||||||
| chr3:11833465 | C | T | 1 | a0001c0002t0002g0133 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.412-3601G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833465 | |||||||
| chr3:11833797 | T | C | 24 | a0001c0001t0001g0165 a0001c0001t0001g0187 a0001c0001t0001g0225 others(21): Show |
25 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.412-3933A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833797 | |||||||
| chr3:11833860 | T | C | 2 | a0001c0001t0001g0187 a0001c0002t0002g0131 |
2 | HG02602.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.412-3996A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833860 | |||||||
| chr3:11833879 | A | C | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0002t0002g0032 |
3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.412-4015T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833879 | |||||||
| chr3:11833966 | G | C | 1 | a0001c0002t0002g0114 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.412-4102C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833966 | |||||||
| chr3:11833970 | A | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(242): Show |
268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.412-4106T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833970 | |||||||
| chr3:11833980 | T | C | 2 | a0001c0001t0001g0278 a0001c0001t0001g0279 |
2 | HG01978.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.412-4116A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11833980 | |||||||
| chr3:11834167 | C | A | 1 | a0003c0005t0003g0300 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.412-4303G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11834167 | |||||||
| chr3:11834345 | A | T | 10 | a0001c0001t0001g0229 a0001c0001t0001g0322 a0001c0001t0001g0340 others(7): Show |
12 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.412-4481T>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11834345 | |||||||
| chr3:11834369 | C | T | 8 | a0001c0002t0002g0114 a0001c0002t0002g0116 a0001c0002t0002g0117 others(5): Show |
9 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.412-4505G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11834369 | |||||||
| chr3:11834495 | A | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(100): Show |
118 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.412-4631T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11834495 | |||||||
| chr3:11834718 | G | A | 3 | a0002c0003t0002g0037 a0002c0004t0001g0319 a0002c0004t0002g0140 |
3 | HG01884.hp1 HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.411+4504C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11834718 | |||||||
| chr3:11834833 | C | T | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(239): Show |
264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.411+4389G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11834833 | |||||||
| chr3:11834908 | G | A | 5 | a0001c0002t0002g0041 a0001c0002t0002g0042 a0001c0002t0002g0043 others(2): Show |
5 | HG02055.hp1 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.411+4314C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11834908 | |||||||
| chr3:11835038 | A | C | 1 | a0002c0003t0002g0100 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.411+4184T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11835038 | |||||||
| chr3:11835116 | G | T | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0002t0002g0032 |
3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.411+4106C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11835116 | |||||||
| chr3:11835128 | A | G | 1 | a0002c0003t0002g0051 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.411+4094T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11835128 | |||||||
| chr3:11835248 | T | G | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.411+3974A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11835248 | |||||||
| chr3:11835399 | T | C | 1 | a0001c0002t0002g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.411+3823A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11835399 | |||||||
| chr3:11835615 | C | A | 1 | a0001c0001t0003g0180 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.411+3607G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11835615 | |||||||
| chr3:11835990 | C | CT | 116 | a0001c0001t0001g0013 a0001c0001t0001g0162 a0001c0001t0001g0163 others(113): Show |
124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.411+3231dupA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11835990 | |||||||
| chr3:11835990 | C | CTT | 12 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(9): Show |
12 | HG02080.hp1 HG02257.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.411+3230_411+3231d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11835990 | |||||||
| chr3:11836020 | C | T | 1 | a0001c0002t0002g0133 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.411+3202G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11836020 | |||||||
| chr3:11836045 | G | A | 3 | a0001c0001t0001g0284 a0001c0002t0002g0038 a0001c0002t0002g0039 |
3 | HG03516.hp1 NA18959.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.411+3177C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11836045 | |||||||
| chr3:11836126 | G | A | 5 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(2): Show |
5 | HG02257.hp1 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.411+3096C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11836126 | |||||||
| chr3:11836142 | C | T | 122 | a0001c0001t0001g0013 a0001c0001t0001g0155 a0001c0001t0001g0156 others(119): Show |
129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.411+3080G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11836142 | |||||||
| chr3:11836172 | G | T | 1 | a0001c0001t0001g0299 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.411+3050C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11836172 | |||||||
| chr3:11836260 | G | A | 1 | a0001c0001t0001g0315 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.411+2962C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11836260 | |||||||
| chr3:11836427 | C | G | 3 | a0001c0001t0001g0004 a0001c0001t0001g0212 a0001c0001t0001g0218 |
5 | HG00558.hp1 NA18941.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.411+2795G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11836427 | |||||||
| chr3:11836620 | C | T | 1 | a0001c0001t0001g0296 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.411+2602G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11836620 | |||||||
| chr3:11836711 | G | A | 115 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(112): Show |
122 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.411+2511C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11836711 | |||||||
| chr3:11836711 | G | T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0212 |
4 | HG00558.hp1 NA18941.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.411+2511C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11836711 | |||||||
| chr3:11836753 | A | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(113): Show |
131 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(128): Show |
intron_variant | MODIFIER | c.411+2469T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11836753 | |||||||
| chr3:11837006 | T | C | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0002t0002g0032 |
3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.411+2216A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11837006 | |||||||
| chr3:11837208 | T | C | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0002t0002g0032 |
3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.411+2014A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11837208 | |||||||
| chr3:11837214 | C | T | 114 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(111): Show |
120 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.411+2008G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11837214 | |||||||
| chr3:11837258 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(242): Show |
268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.411+1964A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11837258 | |||||||
| chr3:11837330 | T | C | 1 | a0001c0001t0003g0242 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.411+1892A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11837330 | |||||||
| chr3:11837405 | G | GA | 9 | a0001c0001t0001g0020 a0001c0001t0001g0195 a0001c0001t0001g0285 others(6): Show |
10 | HG00438.hp1 HG00621.hp2 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.411+1816dupT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11837405 | |||||||
| chr3:11837521 | G | C | 2 | a0002c0003t0002g0073 a0002c0003t0002g0074 |
2 | HG03017.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.411+1701C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11837521 | |||||||
| chr3:11837615 | A | C | 1 | a0007c0010t0001g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.411+1607T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11837615 | |||||||
| chr3:11837638 | T | G | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0002t0002g0032 |
3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.411+1584A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11837638 | |||||||
| chr3:11837730 | C | T | 3 | a0001c0002t0002g0032 a0003c0005t0003g0197 a0003c0005t0003g0230 |
3 | HG02080.hp2 NA18955.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.411+1492G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11837730 | |||||||
| chr3:11837760 | C | T | 1 | a0001c0001t0001g0222 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.411+1462G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11837760 | |||||||
| chr3:11837861 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.411+1361A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11837861 | |||||||
| chr3:11837875 | G | T | 1 | a0001c0001t0001g0337 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.411+1347C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11837875 | |||||||
| chr3:11837968 | C | T | 1 | a0002c0003t0004g0050 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.411+1254G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11837968 | |||||||
| chr3:11838003 | T | C | 1 | a0001c0001t0001g0337 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.411+1219A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11838003 | |||||||
| chr3:11838225 | T | C | 1 | a0002c0004t0001g0250 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.411+997A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11838225 | |||||||
| chr3:11838251 | G | A | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | NA18954.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.411+971C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11838251 | |||||||
| chr3:11838276 | G | A | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0002t0002g0032 |
3 | HG03098.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.411+946C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11838276 | |||||||
| chr3:11838289 | A | G | 1 | a0001c0002t0002g0114 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.411+933T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11838289 | |||||||
| chr3:11838349 | G | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0212 a0001c0001t0001g0218 |
5 | HG00558.hp1 NA18941.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.411+873C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11838349 | |||||||
| chr3:11838373 | G | A | 2 | a0001c0001t0001g0331 a0001c0001t0001g0332 |
2 | HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.411+849C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11838373 | |||||||
| chr3:11838422 | T | C | 1 | a0002c0003t0004g0075 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.411+800A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11838422 | |||||||
| chr3:11838461 | G | A | 1 | a0001c0001t0001g0299 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.411+761C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11838461 | |||||||
| chr3:11838528 | T | G | 1 | a0002c0003t0004g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.411+694A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11838528 | |||||||
| chr3:11838641 | C | T | 1 | a0001c0001t0001g0307 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.411+581G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11838641 | |||||||
| chr3:11838647 | T | C | 6 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0315 others(3): Show |
6 | HG02622.hp1 HG02622.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.411+575A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11838647 | |||||||
| chr3:11838702 | C | CT | 103 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(100): Show |
118 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.411+519dupA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 3/7 | chr3 | 11838702 | |||||||
| chr3:11839342 | C | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(183): Show |
203 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.319-28G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11839342 | |||||||
| chr3:11839557 | A | G | 1 | a0007c0010t0001g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.319-243T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11839557 | |||||||
| chr3:11839671 | A | G | 1 | a0001c0002t0002g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.319-357T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11839671 | |||||||
| chr3:11840027 | C | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG02109.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.319-713G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11840027 | |||||||
| chr3:11840190 | C | A | 7 | a0001c0001t0001g0214 a0001c0001t0001g0340 a0001c0002t0002g0041 others(4): Show |
7 | HG02055.hp1 HG02258.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.319-876G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11840190 | |||||||
| chr3:11840236 | A | AT | 146 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0167 others(143): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.319-923dupA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11840236 | |||||||
| chr3:11840236 | AT | A | 7 | a0001c0001t0001g0213 a0001c0002t0002g0101 a0001c0002t0002g0102 others(4): Show |
7 | HG00323.hp2 HG01891.hp2 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.319-923delA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11840236 | |||||||
| chr3:11840319 | G | A | 8 | a0001c0001t0001g0214 a0001c0001t0001g0340 a0001c0002t0002g0040 others(5): Show |
8 | HG02055.hp1 HG02258.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.319-1005C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11840319 | |||||||
| chr3:11840380 | G | A | 1 | a0001c0001t0001g0333 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.319-1066C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11840380 | |||||||
| chr3:11840391 | T | A | 1 | a0001c0001t0001g0334 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.319-1077A>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11840391 | |||||||
| chr3:11840530 | C | T | 1 | a0001c0001t0001g0015 | 2 | NA18945.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.319-1216G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11840530 | |||||||
| chr3:11840646 | T | A | 2 | a0001c0002t0002g0038 a0001c0002t0002g0039 |
2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.319-1332A>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11840646 | |||||||
| chr3:11840806 | G | C | 1 | a0001c0001t0001g0302 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.319-1492C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11840806 | |||||||
| chr3:11840822 | C | G | 1 | a0002c0004t0001g0305 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.319-1508G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11840822 | |||||||
| chr3:11841067 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.319-1753T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841067 | |||||||
| chr3:11841073 | A | AT | 19 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(16): Show |
19 | HG00741.hp2 HG01175.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.319-1760dupA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841073 | |||||||
| chr3:11841073 | A | ATT | 36 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(33): Show |
39 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.319-1761_319-1760d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841073 | |||||||
| chr3:11841073 | A | ATTT | 10 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(7): Show |
11 | HG00558.hp1 HG00673.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.319-1762_319-1760d others(5): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841073 | |||||||
| chr3:11841073 | AT | A | 12 | a0001c0001t0001g0273 a0001c0001t0001g0302 a0001c0001t0001g0318 others(9): Show |
13 | HG01993.hp2 HG02055.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.319-1760delA | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841073 | |||||||
| chr3:11841073 | ATT | A | 7 | a0001c0002t0002g0045 a0001c0002t0002g0115 a0001c0002t0002g0131 others(4): Show |
7 | HG01358.hp1 HG04184.hp2 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.319-1761_319-1760d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841073 | |||||||
| chr3:11841073 | ATTT | A | 87 | a0001c0001t0001g0341 a0001c0002t0002g0008 a0001c0002t0002g0009 others(84): Show |
91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.319-1762_319-1760d others(5): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841073 | |||||||
| chr3:11841073 | ATTTT | A | 12 | a0001c0001t0001g0187 a0001c0002t0002g0086 a0001c0002t0002g0114 others(9): Show |
13 | HG00642.hp1 HG00735.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.319-1763_319-1760d others(6): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841073 | |||||||
| chr3:11841073 | ATTTTT | A | 29 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0175 others(26): Show |
30 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.319-1764_319-1760d others(7): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841073 | |||||||
| chr3:11841073 | ATTTTTT | A | 20 | a0001c0001t0001g0169 a0001c0001t0001g0320 a0001c0001t0001g0321 others(17): Show |
20 | HG00423.hp2 HG01099.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.319-1765_319-1760d others(8): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841073 | |||||||
| chr3:11841073 | ATTTTTTT | A | 6 | a0001c0002t0002g0028 a0001c0002t0002g0029 a0001c0002t0002g0030 others(3): Show |
6 | HG02622.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.319-1766_319-1760d others(9): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841073 | |||||||
| chr3:11841073 | ATTTTTTT others(3): Show |
A | 10 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0001c0001t0001g0309 others(7): Show |
10 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.319-1769_319-1760d others(12): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841073 | |||||||
| chr3:11841170 | C | A | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.319-1856G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841170 | |||||||
| chr3:11841240 | A | G | 105 | a0001c0001t0001g0341 a0001c0002t0002g0008 a0001c0002t0002g0009 others(102): Show |
110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.319-1926T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841240 | |||||||
| chr3:11841471 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0193 |
3 | HG00423.hp1 HG00673.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.319-2157G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841471 | |||||||
| chr3:11841632 | G | A | 2 | a0001c0002t0002g0033 a0001c0002t0002g0034 |
2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.319-2318C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841632 | |||||||
| chr3:11841748 | C | T | 2 | a0001c0001t0001g0318 a0001c0001t0003g0022 |
3 | HG02965.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.318+2281G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841748 | |||||||
| chr3:11841754 | T | C | 3 | a0001c0002t0002g0134 a0001c0002t0002g0135 a0001c0002t0002g0136 |
3 | HG02615.hp1 HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.318+2275A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841754 | |||||||
| chr3:11841795 | G | T | 3 | a0001c0002t0002g0038 a0001c0002t0002g0039 a0002c0003t0002g0037 |
3 | HG01891.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.318+2234C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841795 | |||||||
| chr3:11841893 | C | T | 18 | a0001c0001t0001g0013 a0001c0001t0001g0191 a0001c0001t0001g0192 others(15): Show |
21 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.318+2136G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841893 | |||||||
| chr3:11841971 | G | A | 191 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(188): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.318+2058C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11841971 | |||||||
| chr3:11842124 | T | C | 192 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(189): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.318+1905A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842124 | |||||||
| chr3:11842314 | A | G | 1 | a0002c0004t0003g0164 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.318+1715T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842314 | |||||||
| chr3:11842318 | T | C | 191 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(188): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.318+1711A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842318 | |||||||
| chr3:11842327 | G | A | 1 | a0004c0006t0004g0143 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.318+1702C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842327 | |||||||
| chr3:11842353 | C | A | 104 | a0001c0001t0001g0341 a0001c0002t0002g0008 a0001c0002t0002g0009 others(101): Show |
109 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.318+1676G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842353 | |||||||
| chr3:11842394 | CA | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(140): Show |
160 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(157): Show |
intron_variant | MODIFIER | c.318+1634delT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842394 | |||||||
| chr3:11842394 | CAA | C | 192 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(189): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.318+1633_318+1634d others(4): Show |
TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842394 | |||||||
| chr3:11842420 | C | A | 7 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(4): Show |
7 | HG02109.hp1 HG02145.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.318+1609G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842420 | |||||||
| chr3:11842428 | G | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0218 a0002c0004t0001g0217 |
5 | HG00558.hp1 HG02165.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.318+1601C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842428 | |||||||
| chr3:11842464 | T | C | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 |
3 | HG02109.hp1 HG02559.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.318+1565A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842464 | |||||||
| chr3:11842509 | C | T | 1 | a0001c0002t0002g0106 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.318+1520G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842509 | |||||||
| chr3:11842514 | C | T | 1 | a0007c0010t0001g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.318+1515G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842514 | |||||||
| chr3:11842555 | G | A | 247 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(244): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.318+1474C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842555 | |||||||
| chr3:11842594 | T | A | 2 | a0001c0001t0001g0318 a0001c0001t0003g0022 |
3 | HG02965.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.318+1435A>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842594 | |||||||
| chr3:11842707 | G | GA | 105 | a0001c0001t0001g0316 a0001c0001t0001g0341 a0001c0002t0002g0008 others(102): Show |
110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.318+1321dupT | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842707 | |||||||
| chr3:11842796 | G | A | 1 | a0001c0001t0001g0317 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.318+1233C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842796 | |||||||
| chr3:11842877 | A | G | 16 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(13): Show |
17 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.318+1152T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11842877 | |||||||
| chr3:11843073 | G | A | 1 | a0002c0003t0004g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.318+956C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11843073 | |||||||
| chr3:11843075 | G | A | 2 | a0001c0001t0001g0219 a0001c0001t0001g0220 |
2 | NA18951.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.318+954C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11843075 | |||||||
| chr3:11843092 | G | T | 1 | a0007c0010t0001g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.318+937C>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11843092 | |||||||
| chr3:11843104 | T | C | 4 | a0001c0001t0001g0336 a0001c0001t0001g0337 a0001c0001t0001g0338 others(1): Show |
4 | NA18941.hp2 NA18966.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+925A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11843104 | |||||||
| chr3:11843213 | A | T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(187): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.318+816T>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11843213 | |||||||
| chr3:11843278 | G | A | 20 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0001t0001g0322 others(17): Show |
20 | HG00423.hp2 HG01884.hp1 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.318+751C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11843278 | |||||||
| chr3:11843388 | A | AG | 18 | a0001c0001t0001g0013 a0001c0001t0001g0191 a0001c0001t0001g0192 others(15): Show |
21 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.318+640dupC | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11843388 | |||||||
| chr3:11843435 | C | T | 3 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 |
3 | HG02683.hp1 HG02698.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.318+594G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11843435 | |||||||
| chr3:11843562 | C | A | 2 | a0001c0001t0001g0318 a0001c0001t0003g0022 |
3 | HG02965.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.318+467G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11843562 | |||||||
| chr3:11843666 | C | T | 25 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0169 others(22): Show |
26 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.318+363G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11843666 | |||||||
| chr3:11843825 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.318+204T>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11843825 | |||||||
| chr3:11843903 | G | A | 4 | a0001c0002t0002g0101 a0001c0002t0002g0102 a0001c0002t0002g0103 others(1): Show |
4 | HG01891.hp2 HG03540.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.318+126C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11843903 | |||||||
| chr3:11843946 | C | G | 1 | a0001c0002t0002g0045 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.318+83G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 2/7 | chr3 | 11843946 | |||||||
| chr3:11844246 | T | G | 23 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0001t0001g0322 others(20): Show |
23 | HG00423.hp2 HG01884.hp1 HG02074.hp1 others(20): Show |
intron_variant | MODIFIER | c.136-35A>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11844246 | |||||||
| chr3:11844341 | T | C | 119 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(116): Show |
124 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.136-130A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11844341 | |||||||
| chr3:11844442 | C | T | 4 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0007t0001g0145 others(1): Show |
4 | HG02145.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-231G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11844442 | |||||||
| chr3:11844605 | C | A | 1 | a0002c0003t0004g0105 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.136-394G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11844605 | |||||||
| chr3:11844642 | C | T | 1 | a0002c0004t0003g0151 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.136-431G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11844642 | |||||||
| chr3:11844742 | C | T | 105 | a0001c0001t0001g0341 a0001c0002t0002g0008 a0001c0002t0002g0009 others(102): Show |
110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.136-531G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11844742 | |||||||
| chr3:11844744 | C | A | 2 | a0001c0002t0002g0138 a0001c0002t0002g0139 |
2 | HG01074.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.136-533G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11844744 | |||||||
| chr3:11844891 | T | C | 108 | a0001c0001t0001g0341 a0001c0002t0002g0008 a0001c0002t0002g0009 others(105): Show |
113 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.136-680A>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11844891 | |||||||
| chr3:11844977 | G | A | 39 | a0001c0001t0001g0341 a0001c0002t0002g0106 a0001c0002t0002g0107 others(36): Show |
40 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(37): Show |
intron_variant | MODIFIER | c.136-766C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11844977 | |||||||
| chr3:11845176 | G | C | 7 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(4): Show |
7 | HG02109.hp1 HG02145.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-965C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11845176 | |||||||
| chr3:11845270 | C | G | 7 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(4): Show |
7 | HG02109.hp1 HG02145.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-1059G>C | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11845270 | |||||||
| chr3:11845277 | G | A | 108 | a0001c0001t0001g0341 a0001c0002t0002g0008 a0001c0002t0002g0009 others(105): Show |
113 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.136-1066C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11845277 | |||||||
| chr3:11845515 | C | T | 1 | a0002c0004t0002g0140 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.135+987G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11845515 | |||||||
| chr3:11845570 | A | T | 117 | a0001c0001t0001g0340 a0001c0001t0001g0341 a0001c0002t0002g0008 others(114): Show |
122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.135+932T>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11845570 | |||||||
| chr3:11845575 | G | A | 117 | a0001c0001t0001g0340 a0001c0001t0001g0341 a0001c0002t0002g0008 others(114): Show |
122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.135+927C>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11845575 | |||||||
| chr3:11845591 | C | A | 117 | a0001c0001t0001g0340 a0001c0001t0001g0341 a0001c0002t0002g0008 others(114): Show |
122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.135+911G>T | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11845591 | |||||||
| chr3:11845651 | G | C | 117 | a0001c0001t0001g0340 a0001c0001t0001g0341 a0001c0002t0002g0008 others(114): Show |
122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.135+851C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11845651 | |||||||
| chr3:11845756 | C | T | 4 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(1): Show |
4 | HG02257.hp1 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+746G>A | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11845756 | |||||||
| chr3:11845877 | G | C | 132 | a0001c0001t0001g0340 a0001c0001t0001g0341 a0001c0002t0002g0003 others(129): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.135+625C>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11845877 | |||||||
| chr3:11846020 | A | C | 5 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(2): Show |
6 | HG00733.hp1 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.135+482T>G | TAMM41 | ENSG00000144559.11 | transcript | ENST00000455809.6 | protein_coding | 1/7 | chr3 | 11846020 |