Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23495 |
| ensemblid | ENSG00000240505.9 |
| hgncid | 18153 |
| symbol | TNFRSF13B |
| name | TNF receptor superfamily member 13B |
| refseq_nuc | NM_012452.3 |
| refseq_prot | NP_036584.1 |
| ensembl_nuc | ENST00000261652.7 |
| ensembl_prot | ENSP00000261652.2 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 16939081 |
| end | 16972118 |
| strand | - |
| ver | v1.2 |
| region | chr17:16939081-16972118 |
| region5000 | chr17:16934081-16977118 |
| regionname0 | TNFRSF13B_chr17_16939081_16972118 |
| regionname5000 | TNFRSF13B_chr17_16934081_16977118 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 293 | 296 | 71 | 58 | 122 | 12 | 31 | 99 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | MSGLG others(288): Show |
chr17 | 16934081 | 16977118 |
| a0002 | 0/0 | 293 | 97 | 15 | 10 | 58 | 1 | 13 | 41 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | MSGLG others(288): Show |
chr17 | 16934081 | 16977118 |
| a0003 | 0/0 | 293 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | MSGLG others(288): Show |
chr17 | 16934081 | 16977118 |
| a0004 | 0/0 | 293 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | MSGLG others(288): Show |
chr17 | 16934081 | 16977118 |
| a0005 | 0/0 | 293 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | MSGLG others(288): Show |
chr17 | 16934081 | 16977118 |
| a0006 | 0/0 | 293 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | MSGLG others(288): Show |
chr17 | 16934081 | 16977118 |
| a0007 | 0/0 | 293 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | MSGLG others(288): Show |
chr17 | 16934081 | 16977118 |
| a0008 | 0/0 | 293 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | MSGLG others(288): Show |
chr17 | 16934081 | 16977118 |
| a0009 | 0/0 | 211 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | MSGLG others(206): Show |
chr17 | 16934081 | 16977118 |
| a0010 | 0/0 | 293 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | MSDLG others(288): Show |
chr17 | 16934081 | 16977118 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 879 | 171 | 35 | 24 | 91 | 3 | 18 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | ATGAG others(874): Show |
chr17 | 16934081 | 16977118 | ||
| a0001c0002 | 0/0 | 879 | 101 | 35 | 23 | 31 | 6 | 6 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | ATGAG others(874): Show |
chr17 | 16934081 | 16977118 | ||
| a0001c0004 | 0/0 | 879 | 21 | 1 | 10 | 0 | 3 | 7 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | ATGAG others(874): Show |
chr17 | 16934081 | 16977118 | ||
| a0001c0005 | 1/1 | 879 | 3 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | ATGAG others(874): Show |
chr17 | 16934081 | 16977118 | ||
| a0002c0003 | 0/0 | 879 | 97 | 15 | 10 | 58 | 1 | 13 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | ATGAG others(874): Show |
chr17 | 16934081 | 16977118 | ||
| a0003c0007 | 0/0 | 879 | 2 | 1 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | ATGAG others(874): Show |
chr17 | 16934081 | 16977118 | ||
| a0003c0012 | 0/0 | 879 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | ATGAG others(874): Show |
chr17 | 16934081 | 16977118 | ||
| a0004c0006 | 0/0 | 879 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | ATGAG others(874): Show |
chr17 | 16934081 | 16977118 | ||
| a0005c0013 | 0/0 | 879 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | ATGAG others(874): Show |
chr17 | 16934081 | 16977118 | ||
| a0006c0014 | 0/0 | 879 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | ATGAG others(874): Show |
chr17 | 16934081 | 16977118 | ||
| a0007c0009 | 0/0 | 879 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | ATGAG others(874): Show |
chr17 | 16934081 | 16977118 | ||
| a0008c0010 | 0/0 | 879 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | ATGAG others(874): Show |
chr17 | 16934081 | 16977118 | ||
| a0009c0011 | 0/0 | 633 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | ATGAG others(628): Show |
chr17 | 16934081 | 16977118 | ||
| a0010c0008 | 0/0 | 879 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | ATGAG others(874): Show |
chr17 | 16934081 | 16977118 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1391 | 42 | 10 | 8 | 15 | 2 | 7 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | AAGCA others(1386): Show |
chr17 | 16934081 | 16977118 |
| a0001c0001t0002 | 0/0 | 1391 | 66 | 14 | 7 | 40 | 0 | 5 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | AAGCA others(1386): Show |
chr17 | 16934081 | 16977118 |
| a0001c0001t0003 | 0/0 | 1391 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | AAGCA others(1386): Show |
chr17 | 16934081 | 16977118 |
| a0001c0001t0004 | 0/0 | 1388 | 50 | 3 | 7 | 34 | 1 | 5 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | AAGCA others(1383): Show |
chr17 | 16934081 | 16977118 |
| a0001c0001t0006 | 0/0 | 1391 | 4 | 4 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | AAGCA others(1386): Show |
chr17 | 16934081 | 16977118 |
| a0001c0001t0007 | 0/0 | 1388 | 2 | 0 | 1 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | AAGCA others(1383): Show |
chr17 | 16934081 | 16977118 |
| a0001c0001t0008 | 0/0 | 1391 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | AAGCA others(1386): Show |
chr17 | 16934081 | 16977118 |
| a0001c0001t0009 | 0/0 | 1404 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | AAGCA others(1399): Show |
chr17 | 16934081 | 16977118 |
| a0001c0001t0010 | 0/0 | 1391 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | AAGCA others(1386): Show |
chr17 | 16934081 | 16977118 |
| a0001c0001t0012 | 0/0 | 1475 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | AAGCA others(1470): Show |
chr17 | 16934081 | 16977118 |
| a0001c0001t0013 | 0/0 | 1407 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | AAGCA others(1402): Show |
chr17 | 16934081 | 16977118 |
| a0001c0002t0001 | 0/0 | 1391 | 97 | 33 | 23 | 29 | 6 | 6 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | AAGCA others(1386): Show |
chr17 | 16934081 | 16977118 |
| a0001c0002t0002 | 0/0 | 1391 | 3 | 2 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | AAGCA others(1386): Show |
chr17 | 16934081 | 16977118 |
| a0001c0002t0014 | 0/0 | 1443 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | AAGCA others(1438): Show |
chr17 | 16934081 | 16977118 |
| a0001c0004t0001 | 0/0 | 1391 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | AAGCA others(1386): Show |
chr17 | 16934081 | 16977118 |
| a0001c0004t0002 | 0/0 | 1391 | 20 | 1 | 10 | 0 | 3 | 6 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | AAGCA others(1386): Show |
chr17 | 16934081 | 16977118 |
| a0001c0005t0001 | 1/1 | 1391 | 3 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | AAGCA others(1386): Show |
chr17 | 16934081 | 16977118 |
| a0002c0003t0001 | 0/0 | 1391 | 8 | 7 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | AAGCA others(1386): Show |
chr17 | 16934081 | 16977118 |
| a0002c0003t0002 | 0/0 | 1391 | 4 | 0 | 3 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | AAGCA others(1386): Show |
chr17 | 16934081 | 16977118 |
| a0002c0003t0003 | 0/0 | 1391 | 78 | 8 | 6 | 51 | 1 | 12 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | AAGCA others(1386): Show |
chr17 | 16934081 | 16977118 |
| a0002c0003t0005 | 0/0 | 1388 | 6 | 0 | 0 | 6 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | AAGCA others(1383): Show |
chr17 | 16934081 | 16977118 |
| a0002c0003t0011 | 0/0 | 1407 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | AAGCA others(1402): Show |
chr17 | 16934081 | 16977118 |
| a0003c0007t0002 | 0/0 | 1391 | 2 | 1 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | AAGCA others(1386): Show |
chr17 | 16934081 | 16977118 |
| a0003c0012t0001 | 0/0 | 1391 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | AAGCA others(1386): Show |
chr17 | 16934081 | 16977118 |
| a0004c0006t0002 | 0/0 | 1391 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | AAGCA others(1386): Show |
chr17 | 16934081 | 16977118 |
| a0004c0006t0004 | 0/0 | 1388 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | AAGCA others(1383): Show |
chr17 | 16934081 | 16977118 |
| a0005c0013t0001 | 0/0 | 1391 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | AAGCA others(1386): Show |
chr17 | 16934081 | 16977118 |
| a0006c0014t0003 | 0/0 | 1391 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | AAGCA others(1386): Show |
chr17 | 16934081 | 16977118 |
| a0007c0009t0001 | 0/0 | 1391 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | AAGCA others(1386): Show |
chr17 | 16934081 | 16977118 |
| a0008c0010t0001 | 0/0 | 1391 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | AAGCA others(1386): Show |
chr17 | 16934081 | 16977118 |
| a0009c0011t0002 | 0/0 | 1145 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | AAGCA others(1140): Show |
chr17 | 16934081 | 16977118 |
| a0010c0008t0002 | 0/0 | 1391 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | AAGCA others(1386): Show |
chr17 | 16934081 | 16977118 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0001g0054 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0001g0055 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0003 | 0/0 | 14 | 0 | 0 | 11 | 0 | 3 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0005 | 0/0 | 12 | 0 | 2 | 10 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0004g0002 | 0/0 | 17 | 0 | 1 | 16 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0004g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0004g0022 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0004g0026 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0004g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0004g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0006g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0007g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0007g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0008g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0009g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0010g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0012g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0001t0013g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0004 | 0/0 | 13 | 1 | 7 | 2 | 3 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0006 | 0/0 | 10 | 0 | 0 | 9 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0007 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0010 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0002t0014g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0004t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0004t0002g0012 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0004t0002g0013 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0004t0002g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0004t0002g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0004t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0004t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0004t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0004t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0004t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0004t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0004t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0004t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0005t0001g0172 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0005t0001g0183 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0001c0005t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0001g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0002g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0002g0048 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0001 | 0/0 | 19 | 1 | 1 | 14 | 0 | 3 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0051 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0052 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0053 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0005g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0005g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0005g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0002c0003t0011g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0003c0007t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0003c0007t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0003c0012t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0004c0006t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0004c0006t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0005c0013t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0006c0014t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0007c0009t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0008c0010t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0009c0011t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| a0010c0008t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0004 | EUR | GBR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00099 | hp2 | a0005 | c0013 | t0001 | g0185 | EUR | GBR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0004 | EUR | FIN | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0153 | EUR | FIN | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0099 | EUR | FIN | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0010 | EUR | FIN | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | CHS | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | CHS | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | CHS | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00423 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | CHS | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0129 | EAS | CHS | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0197 | EAS | CHS | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | CHS | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00558 | hp2 | a0002 | c0003 | t0003 | g0205 | EAS | CHS | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00597 | hp2 | a0002 | c0003 | t0003 | g0027 | EAS | CHS | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00609 | hp1 | a0002 | c0003 | t0003 | g0001 | EAS | CHS | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | CHS | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | CHS | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0097 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0157 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00642 | hp1 | a0001 | c0004 | t0002 | g0012 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00642 | hp2 | a0006 | c0014 | t0003 | g0237 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | CHS | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00673 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | CHS | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00733 | hp1 | a0002 | c0003 | t0002 | g0047 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00733 | hp2 | a0001 | c0004 | t0002 | g0013 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0095 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00738 | hp2 | a0001 | c0004 | t0002 | g0180 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0094 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0026 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0026 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01074 | hp1 | a0001 | c0004 | t0002 | g0012 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01081 | hp2 | a0001 | c0004 | t0002 | g0013 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01099 | hp2 | a0002 | c0003 | t0002 | g0048 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01106 | hp1 | a0007 | c0009 | t0001 | g0139 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01109 | hp2 | a0003 | c0007 | t0002 | g0118 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01167 | hp2 | a0002 | c0003 | t0003 | g0052 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01175 | hp2 | a0002 | c0003 | t0003 | g0053 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01192 | hp1 | a0002 | c0003 | t0001 | g0017 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0228 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01243 | hp2 | a0001 | c0004 | t0002 | g0187 | AMR | PUR | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01258 | hp2 | a0008 | c0010 | t0001 | g0189 | AMR | CLM | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | CLM | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01261 | hp2 | a0001 | c0004 | t0002 | g0179 | AMR | CLM | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01346 | hp1 | a0001 | c0004 | t0002 | g0175 | AMR | CLM | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0045 | AMR | CLM | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01361 | hp2 | a0001 | c0004 | t0002 | g0186 | AMR | CLM | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | CLM | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0090 | AMR | CLM | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0026 | EUR | IBS | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01515 | hp2 | a0001 | c0004 | t0002 | g0013 | EUR | IBS | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0054 | EUR | IBS | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01516 | hp2 | a0001 | c0004 | t0002 | g0181 | EUR | IBS | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0231 | EUR | IBS | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01517 | hp2 | a0001 | c0004 | t0002 | g0013 | EUR | IBS | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01891 | hp1 | a0001 | c0001 | t0010 | g0195 | AFR | ACB | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0109 | AFR | ACB | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0229 | AMR | PEL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01928 | hp2 | a0002 | c0003 | t0003 | g0001 | AMR | PEL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PEL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0158 | AMR | PEL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01952 | hp1 | a0001 | c0005 | t0001 | g0184 | AMR | PEL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01952 | hp2 | a0001 | c0001 | t0007 | g0154 | AMR | PEL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PEL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01981 | hp2 | a0002 | c0003 | t0002 | g0047 | AMR | PEL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01993 | hp1 | a0001 | c0001 | t0013 | g0131 | AMR | PEL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01993 | hp2 | a0001 | c0004 | t0002 | g0012 | AMR | PEL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02004 | hp1 | a0002 | c0003 | t0003 | g0064 | AMR | PEL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PEL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02015 | hp1 | a0002 | c0003 | t0003 | g0176 | EAS | KHV | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02015 | hp2 | a0001 | c0002 | t0014 | g0143 | EAS | KHV | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02027 | hp1 | a0002 | c0003 | t0003 | g0222 | EAS | KHV | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | KHV | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | KHV | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02040 | hp2 | a0002 | c0003 | t0003 | g0049 | EAS | KHV | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0194 | AFR | ACB | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | ACB | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02056 | hp1 | a0002 | c0003 | t0003 | g0219 | EAS | KHV | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02056 | hp2 | a0002 | c0003 | t0003 | g0220 | EAS | KHV | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02071 | hp1 | a0002 | c0003 | t0003 | g0049 | EAS | KHV | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | KHV | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02074 | hp1 | a0002 | c0003 | t0003 | g0177 | EAS | KHV | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | KHV | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02083 | hp1 | a0002 | c0003 | t0003 | g0009 | EAS | KHV | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | KHV | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0156 | EAS | KHV | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02145 | hp1 | a0002 | c0003 | t0001 | g0019 | AFR | ACB | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02145 | hp2 | a0004 | c0006 | t0004 | g0117 | AFR | ACB | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02148 | hp1 | a0002 | c0003 | t0003 | g0165 | AMR | PEL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0039 | AMR | PEL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | CDX | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | CDX | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CDX | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02165 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | CDX | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0036 | AFR | ACB | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | ACB | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02258 | hp1 | a0003 | c0012 | t0001 | g0120 | AFR | ACB | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | ACB | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02273 | hp1 | a0002 | c0003 | t0003 | g0166 | AMR | PEL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PEL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0171 | AFR | ACB | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0025 | AFR | ACB | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0096 | AMR | PEL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | ACB | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02451 | hp2 | a0002 | c0003 | t0003 | g0015 | AFR | ACB | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02523 | hp1 | a0002 | c0003 | t0003 | g0001 | EAS | KHV | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02523 | hp2 | a0002 | c0003 | t0003 | g0167 | EAS | KHV | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02602 | hp2 | a0002 | c0003 | t0003 | g0223 | SAS | PJL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02615 | hp1 | a0002 | c0003 | t0003 | g0213 | AFR | GWD | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02615 | hp2 | a0002 | c0003 | t0001 | g0019 | AFR | GWD | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | GWD | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02622 | hp2 | a0002 | c0003 | t0001 | g0017 | AFR | GWD | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0106 | AFR | GWD | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0071 | AFR | GWD | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | GWD | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | GWD | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0022 | SAS | PJL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02698 | hp2 | a0001 | c0004 | t0001 | g0182 | SAS | PJL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | GWD | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02723 | hp1 | a0002 | c0003 | t0003 | g0015 | AFR | GWD | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0007 | AFR | GWD | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0204 | SAS | PJL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0140 | SAS | PJL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02738 | hp1 | a0002 | c0003 | t0003 | g0053 | SAS | PJL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02738 | hp2 | a0002 | c0003 | t0003 | g0051 | SAS | PJL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | GWD | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02818 | hp1 | a0001 | c0004 | t0002 | g0012 | AFR | GWD | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0110 | AFR | GWD | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0100 | AFR | GWD | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0011 | AFR | GWD | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0011 | AFR | GWD | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02895 | hp2 | a0002 | c0003 | t0001 | g0104 | AFR | GWD | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0011 | AFR | GWD | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02897 | hp1 | a0001 | c0001 | t0006 | g0011 | AFR | GWD | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | ESN | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0073 | AFR | ESN | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0075 | AFR | ESN | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0190 | AFR | ESN | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | ESN | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03017 | hp1 | a0001 | c0004 | t0002 | g0178 | SAS | PJL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0006 | SAS | PJL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0036 | AFR | GWD | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | MSL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0105 | AFR | MSL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | ESN | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03130 | hp2 | a0002 | c0003 | t0003 | g0218 | AFR | ESN | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | ESN | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03139 | hp2 | a0003 | c0007 | t0002 | g0119 | AFR | ESN | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0007 | AFR | ESN | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0074 | AFR | MSL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03209 | hp2 | a0002 | c0003 | t0003 | g0001 | AFR | MSL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03225 | hp1 | a0002 | c0003 | t0001 | g0019 | AFR | MSL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0214 | AFR | MSL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03239 | hp1 | a0002 | c0003 | t0003 | g0001 | SAS | PJL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0057 | SAS | PJL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03453 | hp1 | a0002 | c0003 | t0001 | g0069 | AFR | MSL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | MSL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03490 | hp2 | a0001 | c0004 | t0002 | g0043 | SAS | PJL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03491 | hp2 | a0001 | c0004 | t0002 | g0044 | SAS | PJL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03492 | hp1 | a0001 | c0004 | t0002 | g0044 | SAS | PJL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03492 | hp2 | a0001 | c0004 | t0002 | g0043 | SAS | PJL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03516 | hp1 | a0004 | c0006 | t0002 | g0116 | AFR | ESN | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0112 | AFR | ESN | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03540 | hp2 | a0002 | c0003 | t0003 | g0203 | AFR | GWD | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | MSL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0111 | AFR | MSL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0233 | SAS | PJL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03669 | hp2 | a0002 | c0003 | t0003 | g0001 | SAS | PJL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03688 | hp1 | a0002 | c0003 | t0003 | g0093 | SAS | STU | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | STU | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0155 | SAS | PJL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03704 | hp2 | a0002 | c0003 | t0002 | g0048 | SAS | PJL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03710 | hp1 | a0002 | c0003 | t0003 | g0196 | SAS | PJL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0136 | SAS | PJL | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0098 | SAS | BEB | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0206 | SAS | BEB | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0170 | SAS | BEB | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03942 | hp1 | a0002 | c0003 | t0003 | g0230 | SAS | BEB | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG03942 | hp2 | a0001 | c0004 | t0002 | g0188 | SAS | BEB | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG04115 | hp1 | a0002 | c0003 | t0003 | g0234 | SAS | STU | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG04115 | hp2 | a0001 | c0001 | t0007 | g0198 | SAS | STU | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0200 | SAS | STU | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | STU | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | STU | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0092 | SAS | STU | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG04228 | hp1 | a0002 | c0003 | t0003 | g0209 | SAS | STU | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | STU | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | YRI | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | YRI | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18747 | hp1 | a0002 | c0003 | t0003 | g0009 | EAS | CHB | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18747 | hp2 | a0001 | c0001 | t0012 | g0077 | EAS | CHB | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | YRI | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | YRI | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0201 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18939 | hp2 | a0002 | c0003 | t0003 | g0174 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18944 | hp1 | a0001 | c0001 | t0009 | g0133 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18944 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18947 | hp2 | a0002 | c0003 | t0005 | g0016 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18948 | hp1 | a0002 | c0003 | t0003 | g0141 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0236 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0138 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18951 | hp2 | a0002 | c0003 | t0003 | g0226 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18954 | hp1 | a0009 | c0011 | t0002 | g0059 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18954 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18956 | hp2 | a0002 | c0003 | t0003 | g0146 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18960 | hp1 | a0002 | c0003 | t0003 | g0024 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18961 | hp1 | a0002 | c0003 | t0003 | g0159 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18964 | hp1 | a0002 | c0003 | t0005 | g0016 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18965 | hp1 | a0002 | c0003 | t0003 | g0217 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18966 | hp1 | a0002 | c0003 | t0003 | g0027 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18970 | hp2 | a0002 | c0003 | t0005 | g0016 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0127 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0163 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18977 | hp2 | a0002 | c0003 | t0003 | g0215 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18979 | hp1 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0132 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18980 | hp1 | a0002 | c0003 | t0011 | g0169 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18981 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18981 | hp2 | a0002 | c0003 | t0003 | g0208 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18983 | hp1 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0135 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18984 | hp2 | a0001 | c0001 | t0004 | g0134 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18985 | hp1 | a0002 | c0003 | t0003 | g0050 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18985 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18986 | hp1 | a0002 | c0003 | t0003 | g0024 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0130 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18994 | hp2 | a0002 | c0003 | t0003 | g0145 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0137 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18997 | hp2 | a0002 | c0003 | t0003 | g0211 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19001 | hp1 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19002 | hp1 | a0002 | c0003 | t0005 | g0016 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19004 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19009 | hp1 | a0002 | c0003 | t0003 | g0225 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19010 | hp1 | a0002 | c0003 | t0003 | g0009 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | LWK | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | LWK | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | LWK | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19043 | hp2 | a0002 | c0003 | t0001 | g0017 | AFR | LWK | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19057 | hp2 | a0002 | c0003 | t0003 | g0027 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19058 | hp1 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0149 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0199 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19062 | hp1 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19062 | hp2 | a0002 | c0003 | t0003 | g0216 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19063 | hp1 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19064 | hp2 | a0002 | c0003 | t0003 | g0212 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19067 | hp1 | a0010 | c0008 | t0002 | g0056 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19067 | hp2 | a0002 | c0003 | t0005 | g0207 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19074 | hp1 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19078 | hp1 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19079 | hp2 | a0002 | c0003 | t0005 | g0224 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19080 | hp1 | a0002 | c0003 | t0003 | g0050 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19081 | hp1 | a0002 | c0003 | t0003 | g0009 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19082 | hp2 | a0002 | c0003 | t0003 | g0227 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19084 | hp1 | a0002 | c0003 | t0003 | g0009 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19085 | hp2 | a0002 | c0003 | t0003 | g0024 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19087 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19087 | hp2 | a0002 | c0003 | t0003 | g0009 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | YRI | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | YRI | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0107 | AFR | ASW | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0039 | AFR | ASW | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0004 | EUR | TSI | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA20805 | hp2 | a0002 | c0003 | t0003 | g0052 | EUR | TSI | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA20905 | hp1 | a0002 | c0003 | t0003 | g0001 | SAS | GIH | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA20905 | hp2 | a0002 | c0003 | t0003 | g0051 | SAS | GIH | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | CLM | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0045 | AMR | CLM | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0235 | AFR | ACB | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0081 | AFR | ACB | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0072 | AFR | ACB | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG02559 | hp2 | a0002 | c0003 | t0003 | g0015 | AFR | ACB | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | USA | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0113 | AFR | USA | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18955 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA18955 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA20300 | hp1 | a0002 | c0003 | t0003 | g0015 | AFR | USA | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0148 | AFR | USA | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | LWK | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| homoSapiens | chm13v2 | a0001 | c0005 | t0001 | g0172 | REF | REF | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| homoSapiens | grch38p0 | a0001 | c0005 | t0001 | g0183 | REF | REF | TNFRSF13B_chr17_16934081_16977118 | TNFRSF13B | chr17 | 16934081 | 16977118 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:16939677 | G | A | 2 | a0002 a0006 |
98 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(95): Show |
missense_variant | MODERATE | c.752C>T | p.Pro251Leu | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 5/5 | 795/1391 | 752/882 | 251/293 | chr17 | 16939677 | |||
| chr17:16939770 | A | G | 1 | a0005 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.659T>C | p.Val220Ala | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 5/5 | 702/1391 | 659/882 | 220/293 | chr17 | 16939770 | |||
| chr17:16940389 | C | G | 1 | a0004 | 2 | HG02145.hp2 HG03516.hp1 |
missense_variant | MODERATE | c.568G>C | p.Gly190Arg | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 4/5 | 611/1391 | 568/882 | 190/293 | chr17 | 16940389 | |||
| chr17:16940394 | T | A | 1 | a0003 | 3 | HG01109.hp2 HG02258.hp1 HG03139.hp2 |
missense_variant | MODERATE | c.563A>T | p.Lys188Met | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 4/5 | 606/1391 | 563/882 | 188/293 | chr17 | 16940394 | |||
| chr17:16944838 | CAGGGAGC others(5564): Show |
C | 1 | a0009 | 1 | NA18954.hp1 | exon_loss_variant&splice_acceptor_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.200-1426_445+3899d others(2): Show |
TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/5 | chr17 | 16944838 | |||||||
| chr17:16948957 | C | A | 1 | a0001 | 1 | NA19009.hp2 | missense_variant | MODERATE | c.226G>T | p.Gly76Cys | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/5 | 269/1391 | 226/882 | 76/293 | chr17 | 16948957 | |||
| chr17:16952524 | C | G | 1 | a0008 | 1 | HG01258.hp2 | missense_variant | MODERATE | c.121G>C | p.Asp41His | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/5 | 164/1391 | 121/882 | 41/293 | chr17 | 16952524 | |||
| chr17:16952527 | A | G | 1 | a0007 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.118T>C | p.Trp40Arg | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/5 | 161/1391 | 118/882 | 40/293 | chr17 | 16952527 | |||
| chr17:16972018 | G | A | 1 | a0006 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.58C>T | p.Arg20Cys | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/5 | 101/1391 | 58/882 | 20/293 | chr17 | 16972018 | |||
| chr17:16972068 | C | T | 1 | a0010 | 1 | NA19067.hp1 | missense_variant | MODERATE | c.8G>A | p.Gly3Asp | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/5 | 51/1391 | 8/882 | 3/293 | chr17 | 16972068 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:16939598 | A | G | 9 | a0001c0001 a0001c0004 a0002c0003 others(6): Show |
297 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(294): Show |
synonymous_variant | LOW | c.831T>C | p.Ser277Ser | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 5/5 | 874/1391 | 831/882 | 277/293 | chr17 | 16939598 | |||
| chr17:16940339 | G | A | 1 | a0004c0006 | 2 | HG02145.hp2 HG03516.hp1 |
synonymous_variant | LOW | c.618C>T | p.Ala206Ala | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 4/5 | 661/1391 | 618/882 | 206/293 | chr17 | 16940339 | |||
| chr17:16948892 | A | C | 2 | a0001c0001 a0001c0002 |
9 | HG00621.hp2 HG00741.hp2 HG01192.hp2 others(6): Show |
synonymous_variant | LOW | c.291T>G | p.Pro97Pro | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/5 | 334/1391 | 291/882 | 97/293 | chr17 | 16948892 | |||
| chr17:16952564 | C | T | 11 | a0001c0001 a0001c0002 a0002c0003 others(8): Show |
379 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(376): Show |
synonymous_variant | LOW | c.81G>A | p.Thr27Thr | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/5 | 124/1391 | 81/882 | 27/293 | chr17 | 16952564 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:16939133 | C | T | 5 | a0001c0001t0003 a0002c0003t0003 a0002c0003t0005 others(2): Show |
88 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*414G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 5/5 | 414 | chr17 | 16939133 | ||||||
| chr17:16939272 | T | TCTCTCTG others(9): Show |
2 | a0001c0001t0013 a0002c0003t0011 |
2 | HG01993.hp1 NA18980.hp1 |
3_prime_UTR_variant | MODIFIER | c.*259_*274dupGGAGAG others(10): Show |
TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 5/5 | 274 | chr17 | 16939272 | ||||||
| chr17:16939272 | T | TCTCTCTG others(77): Show |
1 | a0001c0001t0012 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*191_*274dupGGAAAG others(78): Show |
TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 5/5 | 274 | chr17 | 16939272 | ||||||
| chr17:16939305 | C | CTCTCTGC others(9): Show |
1 | a0001c0001t0009 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*226_*241dupAGGAGA others(10): Show |
TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 5/5 | 241 | chr17 | 16939305 | ||||||
| chr17:16939324 | T | C | 1 | a0001c0002t0014 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*223A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 5/5 | 223 | chr17 | 16939324 | ||||||
| chr17:16939325 | C | T | 1 | a0001c0002t0014 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*222G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 5/5 | 222 | chr17 | 16939325 | ||||||
| chr17:16939327 | G | C | 1 | a0001c0002t0014 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*220C>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 5/5 | 220 | chr17 | 16939327 | ||||||
| chr17:16939328 | C | T | 1 | a0001c0002t0014 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*219G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 5/5 | 219 | chr17 | 16939328 | ||||||
| chr17:16939337 | T | C | 1 | a0001c0002t0014 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*210A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 5/5 | 210 | chr17 | 16939337 | ||||||
| chr17:16939339 | C | T | 1 | a0001c0002t0014 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*208G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 5/5 | 208 | chr17 | 16939339 | ||||||
| chr17:16939341 | T | C | 1 | a0001c0002t0014 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*206A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 5/5 | 206 | chr17 | 16939341 | ||||||
| chr17:16939353 | T | C | 1 | a0001c0002t0014 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*194A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 5/5 | 194 | chr17 | 16939353 | ||||||
| chr17:16939374 | C | T | 15 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(12): Show |
189 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(186): Show |
3_prime_UTR_variant | MODIFIER | c.*173G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 5/5 | 173 | chr17 | 16939374 | ||||||
| chr17:16939379 | G | C | 1 | a0001c0002t0014 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*168C>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 5/5 | 168 | chr17 | 16939379 | ||||||
| chr17:16939380 | T | TGCTTCCT others(45): Show |
1 | a0001c0002t0014 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*166_*167insGGAAGA others(46): Show |
TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 5/5 | 166 | chr17 | 16939380 | ||||||
| chr17:16939415 | C | T | 1 | a0001c0001t0010 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*132G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 5/5 | 132 | chr17 | 16939415 | ||||||
| chr17:16939424 | T | C | 1 | a0001c0002t0014 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*123A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 5/5 | 123 | chr17 | 16939424 | ||||||
| chr17:16939458 | CTCA | C | 5 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0009 others(2): Show |
60 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*86_*88delTGA | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 5/5 | 86 | chr17 | 16939458 | ||||||
| chr17:16939510 | A | G | 2 | a0001c0001t0006 a0001c0001t0008 |
5 | HG02886.hp2 HG02895.hp1 HG02896.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*37T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 5/5 | 37 | chr17 | 16939510 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:16939857 | A | G | 15 | a0001c0004t0001g0182 a0001c0004t0002g0012 a0001c0004t0002g0013 others(12): Show |
23 | HG00099.hp2 HG00642.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.632-60T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 4/4 | chr17 | 16939857 | |||||||
| chr17:16939883 | C | T | 12 | a0001c0001t0002g0005 a0001c0001t0002g0028 a0001c0001t0002g0046 others(9): Show |
25 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.632-86G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 4/4 | chr17 | 16939883 | |||||||
| chr17:16939936 | A | C | 15 | a0001c0004t0001g0182 a0001c0004t0002g0012 a0001c0004t0002g0013 others(12): Show |
23 | HG00099.hp2 HG00642.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.632-139T>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 4/4 | chr17 | 16939936 | |||||||
| chr17:16939942 | C | T | 1 | a0001c0001t0002g0076 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.632-145G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 4/4 | chr17 | 16939942 | |||||||
| chr17:16940034 | C | A | 1 | a0001c0002t0001g0171 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.632-237G>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 4/4 | chr17 | 16940034 | |||||||
| chr17:16940070 | G | T | 2 | a0001c0002t0002g0072 a0001c0002t0002g0190 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.631+256C>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 4/4 | chr17 | 16940070 | |||||||
| chr17:16940270 | C | T | 1 | a0001c0001t0007g0198 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.631+56G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 4/4 | chr17 | 16940270 | |||||||
| chr17:16940560 | G | A | 18 | a0001c0001t0002g0005 a0001c0001t0002g0028 a0001c0001t0002g0046 others(15): Show |
31 | HG00423.hp1 HG00597.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.446-49C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16940560 | |||||||
| chr17:16940597 | C | T | 4 | a0001c0001t0002g0032 a0001c0001t0002g0108 a0001c0001t0006g0011 others(1): Show |
8 | HG02809.hp1 HG02886.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.446-86G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16940597 | |||||||
| chr17:16940678 | G | A | 35 | a0001c0001t0002g0005 a0001c0001t0002g0028 a0001c0001t0002g0046 others(32): Show |
56 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.446-167C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16940678 | |||||||
| chr17:16940950 | A | G | 1 | a0002c0003t0003g0223 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.446-439T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16940950 | |||||||
| chr17:16940973 | G | A | 2 | a0001c0001t0004g0127 a0001c0001t0004g0138 |
2 | NA18951.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.446-462C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16940973 | |||||||
| chr17:16941180 | A | G | 58 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0058 others(55): Show |
98 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.446-669T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16941180 | |||||||
| chr17:16941199 | C | T | 1 | a0001c0002t0001g0057 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.446-688G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16941199 | |||||||
| chr17:16941549 | C | A | 35 | a0001c0001t0002g0005 a0001c0001t0002g0028 a0001c0001t0002g0046 others(32): Show |
56 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.446-1038G>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16941549 | |||||||
| chr17:16941562 | G | A | 35 | a0001c0001t0002g0005 a0001c0001t0002g0028 a0001c0001t0002g0046 others(32): Show |
56 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.446-1051C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16941562 | |||||||
| chr17:16941706 | G | A | 1 | a0001c0001t0002g0108 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.446-1195C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16941706 | |||||||
| chr17:16941853 | A | G | 55 | a0001c0001t0001g0168 a0001c0002t0001g0214 a0002c0003t0002g0047 others(52): Show |
95 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.446-1342T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16941853 | |||||||
| chr17:16941916 | A | G | 1 | a0001c0001t0002g0108 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.446-1405T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16941916 | |||||||
| chr17:16941974 | A | G | 22 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0035 others(19): Show |
31 | HG00741.hp2 HG01192.hp2 HG01516.hp1 others(28): Show |
intron_variant | MODIFIER | c.446-1463T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16941974 | |||||||
| chr17:16942048 | T | C | 41 | a0001c0001t0002g0005 a0001c0001t0002g0028 a0001c0001t0002g0032 others(38): Show |
66 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.446-1537A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16942048 | |||||||
| chr17:16942088 | T | A | 35 | a0001c0001t0002g0005 a0001c0001t0002g0028 a0001c0001t0002g0046 others(32): Show |
56 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.446-1577A>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16942088 | |||||||
| chr17:16942144 | G | A | 133 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0035 others(130): Show |
223 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(220): Show |
intron_variant | MODIFIER | c.446-1633C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16942144 | |||||||
| chr17:16942153 | T | C | 135 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0035 others(132): Show |
225 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(222): Show |
intron_variant | MODIFIER | c.446-1642A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16942153 | |||||||
| chr17:16942191 | C | T | 1 | a0001c0002t0001g0057 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.446-1680G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16942191 | |||||||
| chr17:16942267 | G | A | 1 | a0001c0001t0002g0037 | 2 | NA18980.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.446-1756C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16942267 | |||||||
| chr17:16942273 | C | T | 1 | a0001c0001t0004g0137 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.446-1762G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16942273 | |||||||
| chr17:16942311 | G | A | 2 | a0001c0002t0001g0214 a0002c0003t0003g0213 |
2 | HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.446-1800C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16942311 | |||||||
| chr17:16942325 | C | T | 1 | a0001c0004t0002g0012 | 4 | HG00642.hp1 HG01074.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.446-1814G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16942325 | |||||||
| chr17:16942532 | G | A | 1 | a0001c0001t0004g0021 | 3 | HG01069.hp1 HG01071.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.446-2021C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16942532 | |||||||
| chr17:16942681 | G | A | 4 | a0001c0002t0001g0153 a0001c0002t0001g0157 a0001c0002t0001g0158 others(1): Show |
4 | HG00280.hp2 HG00639.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.446-2170C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16942681 | |||||||
| chr17:16942699 | A | G | 1 | a0001c0001t0004g0132 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.446-2188T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16942699 | |||||||
| chr17:16942838 | A | C | 4 | a0001c0001t0002g0032 a0001c0001t0002g0108 a0001c0001t0006g0011 others(1): Show |
8 | HG02809.hp1 HG02886.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.446-2327T>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16942838 | |||||||
| chr17:16942841 | T | C | 174 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0031 others(171): Show |
291 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(288): Show |
intron_variant | MODIFIER | c.446-2330A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16942841 | |||||||
| chr17:16942862 | T | A | 174 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0031 others(171): Show |
291 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(288): Show |
intron_variant | MODIFIER | c.446-2351A>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16942862 | |||||||
| chr17:16942872 | G | T | 1 | a0001c0002t0001g0073 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.446-2361C>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16942872 | |||||||
| chr17:16942894 | G | A | 35 | a0001c0001t0002g0005 a0001c0001t0002g0028 a0001c0001t0002g0046 others(32): Show |
56 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.446-2383C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16942894 | |||||||
| chr17:16942984 | T | C | 178 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0031 others(175): Show |
298 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(295): Show |
intron_variant | MODIFIER | c.446-2473A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16942984 | |||||||
| chr17:16942992 | G | A | 2 | a0002c0003t0003g0159 a0002c0003t0003g0215 |
2 | NA18961.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.446-2481C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16942992 | |||||||
| chr17:16943033 | C | G | 16 | a0001c0001t0002g0003 a0001c0001t0002g0029 a0001c0001t0002g0037 others(13): Show |
32 | HG01070.hp1 HG01123.hp1 HG01934.hp1 others(29): Show |
intron_variant | MODIFIER | c.446-2522G>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16943033 | |||||||
| chr17:16943069 | CCCAGCAT others(4): Show |
C | 1 | a0001c0001t0002g0063 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.446-2569_446-2559d others(13): Show |
TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16943069 | |||||||
| chr17:16943098 | T | C | 1 | a0004c0006t0004g0117 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.446-2587A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16943098 | |||||||
| chr17:16943104 | C | T | 1 | a0001c0001t0002g0076 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.446-2593G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16943104 | |||||||
| chr17:16943152 | C | T | 2 | a0004c0006t0002g0116 a0004c0006t0004g0117 |
2 | HG02145.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.446-2641G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16943152 | |||||||
| chr17:16943449 | C | T | 4 | a0001c0002t0001g0025 a0001c0002t0001g0030 a0001c0002t0002g0072 others(1): Show |
7 | HG02280.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.446-2938G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16943449 | |||||||
| chr17:16943483 | T | C | 173 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0031 others(170): Show |
290 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(287): Show |
intron_variant | MODIFIER | c.446-2972A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16943483 | |||||||
| chr17:16943560 | C | T | 1 | a0001c0001t0013g0131 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.446-3049G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16943560 | |||||||
| chr17:16943780 | G | T | 1 | a0001c0002t0001g0099 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.446-3269C>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16943780 | |||||||
| chr17:16943799 | G | A | 134 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0031 others(131): Show |
230 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(227): Show |
intron_variant | MODIFIER | c.446-3288C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16943799 | |||||||
| chr17:16943901 | G | C | 1 | a0001c0001t0002g0032 | 2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.446-3390C>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16943901 | |||||||
| chr17:16943997 | C | T | 1 | a0001c0001t0004g0130 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.446-3486G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16943997 | |||||||
| chr17:16944032 | C | T | 12 | a0001c0001t0001g0031 a0001c0001t0001g0083 a0001c0001t0001g0084 others(9): Show |
13 | HG00741.hp2 HG01192.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.446-3521G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16944032 | |||||||
| chr17:16944111 | C | T | 1 | a0004c0006t0002g0116 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.446-3600G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16944111 | |||||||
| chr17:16944116 | G | T | 36 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0058 others(33): Show |
62 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.446-3605C>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16944116 | |||||||
| chr17:16944161 | G | C | 1 | a0001c0001t0002g0076 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.446-3650C>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16944161 | |||||||
| chr17:16944227 | C | T | 1 | a0001c0004t0002g0179 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.446-3716G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16944227 | |||||||
| chr17:16944228 | G | A | 1 | a0001c0001t0002g0121 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.446-3717C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16944228 | |||||||
| chr17:16944283 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.446-3772G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16944283 | |||||||
| chr17:16944460 | A | G | 1 | a0001c0002t0001g0030 | 2 | HG02622.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.446-3949T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16944460 | |||||||
| chr17:16944546 | C | T | 1 | a0002c0003t0003g0166 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.446-4035G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16944546 | |||||||
| chr17:16944568 | G | T | 1 | a0001c0001t0002g0063 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.446-4057C>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16944568 | |||||||
| chr17:16944590 | G | C | 1 | a0001c0001t0002g0076 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.446-4079C>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16944590 | |||||||
| chr17:16944595 | T | C | 137 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0031 others(134): Show |
232 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(229): Show |
intron_variant | MODIFIER | c.446-4084A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16944595 | |||||||
| chr17:16945069 | G | A | 7 | a0001c0001t0004g0002 a0001c0001t0004g0022 a0001c0001t0004g0078 others(4): Show |
10 | HG00621.hp1 NA18939.hp1 NA18952.hp1 others(7): Show |
intron_variant | MODIFIER | c.445+3669C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16945069 | |||||||
| chr17:16945177 | A | G | 1 | a0001c0001t0002g0060 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.445+3561T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16945177 | |||||||
| chr17:16945251 | C | G | 56 | a0001c0001t0001g0168 a0001c0001t0002g0032 a0001c0002t0001g0214 others(53): Show |
97 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.445+3487G>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16945251 | |||||||
| chr17:16945264 | G | A | 3 | a0003c0007t0002g0118 a0003c0007t0002g0119 a0003c0012t0001g0120 |
3 | HG01109.hp2 HG02258.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.445+3474C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16945264 | |||||||
| chr17:16945275 | G | T | 2 | a0001c0002t0001g0007 a0001c0002t0001g0090 |
2 | HG01433.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.445+3463C>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16945275 | |||||||
| chr17:16945374 | A | G | 3 | a0002c0003t0003g0001 a0002c0003t0003g0053 a0002c0003t0003g0093 |
3 | HG02738.hp1 HG03669.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.445+3364T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16945374 | |||||||
| chr17:16945436 | C | T | 53 | a0001c0001t0001g0168 a0001c0001t0002g0032 a0001c0002t0001g0214 others(50): Show |
94 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.445+3302G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16945436 | |||||||
| chr17:16945578 | A | G | 1 | a0002c0003t0003g0216 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.445+3160T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16945578 | |||||||
| chr17:16945597 | A | C | 28 | a0001c0001t0001g0031 a0001c0001t0001g0083 a0001c0001t0001g0084 others(25): Show |
45 | HG00741.hp2 HG01070.hp1 HG01123.hp1 others(42): Show |
intron_variant | MODIFIER | c.445+3141T>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16945597 | |||||||
| chr17:16945606 | A | G | 135 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0031 others(132): Show |
230 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(227): Show |
intron_variant | MODIFIER | c.445+3132T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16945606 | |||||||
| chr17:16945618 | A | T | 1 | a0002c0003t0003g0208 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.445+3120T>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16945618 | |||||||
| chr17:16945630 | T | A | 1 | a0001c0001t0002g0202 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.445+3108A>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16945630 | |||||||
| chr17:16945825 | A | G | 65 | a0001c0001t0001g0058 a0001c0001t0001g0168 a0001c0001t0002g0005 others(62): Show |
118 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.445+2913T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16945825 | |||||||
| chr17:16946094 | C | T | 10 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(7): Show |
10 | HG00621.hp2 HG00741.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.445+2644G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16946094 | |||||||
| chr17:16946156 | G | C | 9 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(6): Show |
9 | HG00621.hp2 HG00741.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.445+2582C>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16946156 | |||||||
| chr17:16946165 | G | A | 26 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(23): Show |
42 | HG00621.hp2 HG00741.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.445+2573C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16946165 | |||||||
| chr17:16946499 | G | C | 57 | a0001c0001t0001g0020 a0001c0001t0001g0035 a0001c0001t0001g0040 others(54): Show |
89 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.445+2239C>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16946499 | |||||||
| chr17:16946559 | ATTATTTT others(5): Show |
A | 15 | a0001c0004t0001g0182 a0001c0004t0002g0012 a0001c0004t0002g0013 others(12): Show |
22 | HG00099.hp2 HG00642.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.445+2167_445+2178d others(14): Show |
TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16946559 | |||||||
| chr17:16946577 | T | A | 11 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(8): Show |
11 | HG00621.hp2 HG00741.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.445+2161A>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16946577 | |||||||
| chr17:16946580 | A | ATT | 3 | a0001c0001t0001g0124 a0001c0001t0004g0002 a0001c0001t0004g0163 |
3 | HG03490.hp1 NA18965.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.445+2156_445+2157d others(4): Show |
TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16946580 | |||||||
| chr17:16946580 | A | T | 11 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(8): Show |
11 | HG00621.hp2 HG00741.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.445+2158T>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16946580 | |||||||
| chr17:16946584 | A | T | 43 | a0001c0001t0001g0020 a0001c0001t0001g0035 a0001c0001t0001g0040 others(40): Show |
66 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.445+2154T>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16946584 | |||||||
| chr17:16946585 | T | TA | 30 | a0001c0001t0001g0020 a0001c0001t0001g0035 a0001c0001t0001g0040 others(27): Show |
52 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.445+2152_445+2153i others(3): Show |
TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16946585 | |||||||
| chr17:16946586 | T | A | 14 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(11): Show |
14 | HG00621.hp2 HG00741.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.445+2152A>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16946586 | |||||||
| chr17:16946586 | T | G | 3 | a0001c0004t0002g0179 a0001c0004t0002g0180 a0001c0004t0002g0181 |
3 | HG00738.hp2 HG01261.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.445+2152A>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16946586 | |||||||
| chr17:16946587 | T | A | 3 | a0001c0001t0001g0124 a0001c0001t0004g0002 a0001c0001t0004g0163 |
3 | HG03490.hp1 NA18965.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.445+2151A>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16946587 | |||||||
| chr17:16946588 | A | T | 16 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(13): Show |
17 | HG00621.hp2 HG00741.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.445+2150T>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16946588 | |||||||
| chr17:16946589 | T | A | 3 | a0001c0001t0004g0002 a0004c0006t0002g0116 a0004c0006t0004g0117 |
3 | HG02145.hp2 HG02273.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.445+2149A>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16946589 | |||||||
| chr17:16946591 | T | A | 2 | a0001c0001t0001g0128 a0001c0001t0004g0199 |
2 | HG02165.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.445+2147A>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16946591 | |||||||
| chr17:16946591 | TA | T | 3 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0013g0131 |
6 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.445+2146delT | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16946591 | |||||||
| chr17:16946592 | A | AT | 9 | a0001c0001t0001g0168 a0001c0001t0002g0076 a0001c0002t0001g0106 others(6): Show |
9 | HG00735.hp2 HG01175.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.445+2145dupA | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16946592 | |||||||
| chr17:16946592 | A | T | 32 | a0001c0001t0001g0020 a0001c0001t0001g0035 a0001c0001t0001g0040 others(29): Show |
52 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.445+2146T>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16946592 | |||||||
| chr17:16946595 | TA | T | 14 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(11): Show |
15 | HG00621.hp2 HG00741.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.445+2142delT | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16946595 | |||||||
| chr17:16946596 | A | AT | 4 | a0001c0002t0001g0007 a0001c0002t0001g0090 a0001c0002t0001g0105 others(1): Show |
6 | HG01433.hp2 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.445+2141dupA | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16946596 | |||||||
| chr17:16946596 | A | T | 114 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0035 others(111): Show |
194 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(191): Show |
intron_variant | MODIFIER | c.445+2142T>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16946596 | |||||||
| chr17:16946599 | T | A | 11 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(8): Show |
11 | HG00621.hp2 HG00741.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.445+2139A>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16946599 | |||||||
| chr17:16946600 | T | A | 19 | a0001c0001t0002g0003 a0001c0001t0002g0029 a0001c0001t0002g0037 others(16): Show |
35 | HG01070.hp1 HG01123.hp1 HG01934.hp1 others(32): Show |
intron_variant | MODIFIER | c.445+2138A>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16946600 | |||||||
| chr17:16946901 | AT | A | 11 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(8): Show |
11 | HG00621.hp2 HG00741.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.445+1836delA | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16946901 | |||||||
| chr17:16946953 | T | G | 1 | a0001c0002t0001g0010 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.445+1785A>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16946953 | |||||||
| chr17:16947009 | A | G | 169 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0031 others(166): Show |
283 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(280): Show |
intron_variant | MODIFIER | c.445+1729T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16947009 | |||||||
| chr17:16947186 | C | A | 4 | a0001c0001t0001g0089 a0001c0001t0012g0077 a0001c0002t0001g0088 others(1): Show |
4 | HG00621.hp2 HG01192.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.445+1552G>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16947186 | |||||||
| chr17:16947200 | A | G | 3 | a0001c0002t0001g0014 a0001c0002t0001g0110 a0001c0002t0001g0194 |
6 | HG02055.hp1 HG02717.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.445+1538T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16947200 | |||||||
| chr17:16947505 | A | C | 2 | a0002c0003t0003g0015 a0002c0003t0003g0203 |
5 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.445+1233T>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16947505 | |||||||
| chr17:16947505 | A | G | 20 | a0001c0001t0002g0003 a0001c0001t0002g0029 a0001c0001t0002g0037 others(17): Show |
36 | HG01070.hp1 HG01123.hp1 HG01934.hp1 others(33): Show |
intron_variant | MODIFIER | c.445+1233T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16947505 | |||||||
| chr17:16947593 | C | T | 1 | a0001c0002t0001g0228 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.445+1145G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16947593 | |||||||
| chr17:16947740 | G | A | 110 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0035 others(107): Show |
186 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.445+998C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16947740 | |||||||
| chr17:16947754 | G | A | 1 | a0001c0001t0007g0198 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.445+984C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16947754 | |||||||
| chr17:16947846 | G | A | 1 | a0002c0003t0003g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.445+892C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16947846 | |||||||
| chr17:16947872 | G | A | 108 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0035 others(105): Show |
184 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.445+866C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16947872 | |||||||
| chr17:16947897 | C | A | 2 | a0002c0003t0003g0196 a0002c0003t0003g0234 |
2 | HG03710.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.445+841G>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16947897 | |||||||
| chr17:16947964 | T | C | 1 | a0001c0001t0003g0081 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.445+774A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16947964 | |||||||
| chr17:16948028 | C | T | 125 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0035 others(122): Show |
209 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(206): Show |
intron_variant | MODIFIER | c.445+710G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16948028 | |||||||
| chr17:16948136 | G | A | 53 | a0001c0001t0001g0168 a0001c0001t0002g0032 a0001c0002t0001g0214 others(50): Show |
94 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.445+602C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16948136 | |||||||
| chr17:16948298 | A | G | 9 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(6): Show |
9 | HG00621.hp2 HG00741.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.445+440T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16948298 | |||||||
| chr17:16948308 | C | T | 33 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0123 others(30): Show |
57 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.445+430G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16948308 | |||||||
| chr17:16948336 | A | G | 1 | a0004c0006t0002g0116 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.445+402T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16948336 | |||||||
| chr17:16948520 | C | T | 114 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0035 others(111): Show |
198 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.445+218G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16948520 | |||||||
| chr17:16948594 | T | C | 15 | a0001c0004t0001g0182 a0001c0004t0002g0012 a0001c0004t0002g0013 others(12): Show |
23 | HG00099.hp2 HG00642.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.445+144A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16948594 | |||||||
| chr17:16948713 | T | G | 116 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0035 others(113): Show |
200 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.445+25A>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 3/4 | chr17 | 16948713 | |||||||
| chr17:16948997 | A | T | 1 | a0001c0002t0001g0006 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.200-14T>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16948997 | |||||||
| chr17:16948999 | T | C | 1 | a0001c0002t0001g0006 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.200-16A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16948999 | |||||||
| chr17:16949065 | TAA | T | 9 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(6): Show |
9 | HG00621.hp2 HG00741.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.200-84_200-83delTT | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16949065 | |||||||
| chr17:16949145 | A | G | 1 | a0001c0001t0002g0076 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.200-162T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16949145 | |||||||
| chr17:16949174 | T | A | 2 | a0001c0002t0001g0214 a0002c0003t0003g0213 |
2 | HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.200-191A>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16949174 | |||||||
| chr17:16949491 | A | G | 1 | a0001c0001t0004g0130 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.200-508T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16949491 | |||||||
| chr17:16949654 | ATTATC | A | 9 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0054 others(6): Show |
17 | HG01516.hp1 HG01517.hp1 HG03453.hp2 others(14): Show |
intron_variant | MODIFIER | c.200-676_200-672del others(5): Show |
TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16949654 | |||||||
| chr17:16949678 | T | A | 2 | a0001c0001t0004g0075 a0001c0001t0010g0195 |
2 | HG01891.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.200-695A>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16949678 | |||||||
| chr17:16949686 | A | ATT | 14 | a0001c0004t0001g0182 a0001c0004t0002g0012 a0001c0004t0002g0013 others(11): Show |
18 | HG00099.hp2 HG00642.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.200-705_200-704dup others(2): Show |
TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16949686 | |||||||
| chr17:16949686 | AT | A | 7 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0054 others(4): Show |
7 | HG01167.hp1 HG02258.hp2 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.200-704delA | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16949686 | |||||||
| chr17:16949727 | C | T | 2 | a0004c0006t0002g0116 a0004c0006t0004g0117 |
2 | HG02145.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.200-744G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16949727 | |||||||
| chr17:16949844 | C | A | 9 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(6): Show |
9 | HG00621.hp2 HG00741.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.200-861G>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16949844 | |||||||
| chr17:16949962 | A | G | 1 | a0004c0006t0004g0117 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.200-979T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16949962 | |||||||
| chr17:16949979 | G | A | 1 | a0002c0003t0003g0222 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.200-996C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16949979 | |||||||
| chr17:16950009 | A | T | 1 | a0001c0001t0002g0202 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.200-1026T>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16950009 | |||||||
| chr17:16950080 | G | T | 1 | a0001c0002t0001g0162 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.200-1097C>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16950080 | |||||||
| chr17:16950146 | A | G | 1 | a0001c0002t0001g0073 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.200-1163T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16950146 | |||||||
| chr17:16950157 | A | G | 1 | a0001c0001t0010g0195 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.200-1174T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16950157 | |||||||
| chr17:16950158 | C | A | 1 | a0001c0001t0010g0195 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.200-1175G>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16950158 | |||||||
| chr17:16950352 | C | T | 2 | a0002c0003t0001g0017 a0002c0003t0001g0069 |
4 | HG01192.hp1 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.200-1369G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16950352 | |||||||
| chr17:16950386 | C | T | 2 | a0002c0003t0003g0159 a0002c0003t0003g0215 |
2 | NA18961.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.200-1403G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16950386 | |||||||
| chr17:16950565 | C | A | 1 | a0001c0001t0002g0155 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.200-1582G>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16950565 | |||||||
| chr17:16950566 | C | A | 1 | a0001c0001t0002g0155 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.200-1583G>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16950566 | |||||||
| chr17:16950589 | A | C | 9 | a0002c0003t0003g0027 a0002c0003t0003g0050 a0002c0003t0003g0167 others(6): Show |
15 | HG00558.hp2 HG00597.hp2 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.200-1606T>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16950589 | |||||||
| chr17:16950719 | ACCCTCCC others(15): Show |
A | 1 | a0001c0001t0002g0076 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.199+1705_199+1726d others(24): Show |
TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16950719 | |||||||
| chr17:16950764 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.199+1682G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16950764 | |||||||
| chr17:16950886 | A | G | 4 | a0001c0004t0001g0182 a0001c0004t0002g0179 a0001c0004t0002g0180 others(1): Show |
4 | HG00738.hp2 HG01261.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+1560T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16950886 | |||||||
| chr17:16951028 | G | A | 1 | a0001c0001t0002g0067 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.199+1418C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16951028 | |||||||
| chr17:16951071 | T | C | 24 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(21): Show |
32 | HG00099.hp2 HG00621.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.199+1375A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16951071 | |||||||
| chr17:16951166 | G | A | 53 | a0001c0001t0001g0168 a0001c0001t0002g0032 a0001c0002t0001g0214 others(50): Show |
94 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.199+1280C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16951166 | |||||||
| chr17:16951232 | G | T | 173 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0031 others(170): Show |
290 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(287): Show |
intron_variant | MODIFIER | c.199+1214C>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16951232 | |||||||
| chr17:16951251 | G | T | 1 | a0001c0001t0001g0034 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.199+1195C>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16951251 | |||||||
| chr17:16951323 | A | G | 1 | a0001c0001t0002g0076 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.199+1123T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16951323 | |||||||
| chr17:16951523 | A | G | 2 | a0001c0001t0002g0029 a0001c0001t0002g0070 |
3 | HG03041.hp1 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.199+923T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16951523 | |||||||
| chr17:16951626 | C | T | 1 | a0002c0003t0003g0213 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.199+820G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16951626 | |||||||
| chr17:16951763 | C | T | 1 | a0002c0003t0003g0165 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.199+683G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16951763 | |||||||
| chr17:16951816 | C | T | 190 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0031 others(187): Show |
333 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(330): Show |
intron_variant | MODIFIER | c.199+630G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16951816 | |||||||
| chr17:16951901 | TA | T | 89 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0058 others(86): Show |
156 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.199+544delT | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16951901 | |||||||
| chr17:16951908 | A | T | 89 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0058 others(86): Show |
156 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.199+538T>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16951908 | |||||||
| chr17:16951936 | A | G | 1 | a0001c0001t0010g0195 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.199+510T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16951936 | |||||||
| chr17:16952007 | A | T | 19 | a0001c0001t0001g0058 a0001c0001t0001g0123 a0001c0001t0001g0124 others(16): Show |
32 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.199+439T>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16952007 | |||||||
| chr17:16952056 | G | A | 9 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(6): Show |
9 | HG00621.hp2 HG00741.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.199+390C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16952056 | |||||||
| chr17:16952258 | C | T | 1 | a0001c0002t0001g0025 | 3 | HG02280.hp2 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.199+188G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 2/4 | chr17 | 16952258 | |||||||
| chr17:16952740 | A | T | 1 | a0001c0002t0001g0099 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.62-157T>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16952740 | |||||||
| chr17:16952757 | C | A | 5 | a0002c0003t0003g0146 a0002c0003t0003g0216 a0002c0003t0003g0226 others(2): Show |
5 | HG00642.hp2 NA18951.hp2 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.62-174G>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16952757 | |||||||
| chr17:16952878 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.62-295G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16952878 | |||||||
| chr17:16953006 | T | A | 2 | a0001c0001t0001g0086 a0001c0002t0001g0090 |
2 | HG01433.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.62-423A>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16953006 | |||||||
| chr17:16953049 | C | G | 1 | a0002c0003t0003g0166 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.62-466G>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16953049 | |||||||
| chr17:16953209 | C | A | 1 | a0001c0001t0001g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.62-626G>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16953209 | |||||||
| chr17:16953222 | A | G | 2 | a0002c0003t0003g0226 a0002c0003t0003g0227 |
2 | NA18951.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.62-639T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16953222 | |||||||
| chr17:16953226 | C | T | 1 | a0001c0004t0002g0043 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.62-643G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16953226 | |||||||
| chr17:16953264 | A | G | 191 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0031 others(188): Show |
334 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(331): Show |
intron_variant | MODIFIER | c.62-681T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16953264 | |||||||
| chr17:16953291 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.62-708C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16953291 | |||||||
| chr17:16953495 | C | T | 1 | a0001c0001t0010g0195 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.62-912G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16953495 | |||||||
| chr17:16953548 | A | T | 53 | a0001c0001t0001g0168 a0001c0001t0002g0032 a0001c0002t0001g0214 others(50): Show |
94 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.62-965T>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16953548 | |||||||
| chr17:16953572 | G | A | 1 | a0002c0003t0003g0217 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.62-989C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16953572 | |||||||
| chr17:16953655 | A | G | 220 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0031 others(217): Show |
379 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(376): Show |
intron_variant | MODIFIER | c.62-1072T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16953655 | |||||||
| chr17:16953774 | C | CT | 10 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(7): Show |
11 | HG00621.hp2 HG01192.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.62-1192dupA | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16953774 | |||||||
| chr17:16953778 | T | C | 18 | a0001c0001t0004g0042 a0001c0002t0001g0006 a0001c0002t0001g0023 others(15): Show |
31 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.62-1195A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16953778 | |||||||
| chr17:16953825 | G | A | 1 | a0002c0003t0003g0174 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.62-1242C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16953825 | |||||||
| chr17:16953830 | T | C | 191 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0031 others(188): Show |
334 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(331): Show |
intron_variant | MODIFIER | c.62-1247A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16953830 | |||||||
| chr17:16953863 | G | A | 53 | a0001c0001t0001g0168 a0001c0001t0002g0032 a0001c0002t0001g0214 others(50): Show |
94 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.62-1280C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16953863 | |||||||
| chr17:16954008 | G | A | 1 | a0002c0003t0003g0217 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.62-1425C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16954008 | |||||||
| chr17:16954017 | G | A | 1 | a0002c0003t0003g0208 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.62-1434C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16954017 | |||||||
| chr17:16954111 | G | A | 72 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0058 others(69): Show |
125 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.62-1528C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16954111 | |||||||
| chr17:16954150 | T | G | 1 | a0002c0003t0003g0146 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.62-1567A>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16954150 | |||||||
| chr17:16954256 | G | A | 1 | a0001c0002t0001g0030 | 2 | HG02622.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.62-1673C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16954256 | |||||||
| chr17:16954256 | G | T | 1 | a0001c0001t0002g0028 | 2 | NA18945.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.62-1673C>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16954256 | |||||||
| chr17:16954404 | G | A | 1 | a0001c0002t0001g0073 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.62-1821C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16954404 | |||||||
| chr17:16954471 | C | G | 19 | a0001c0001t0002g0003 a0001c0001t0002g0029 a0001c0001t0002g0037 others(16): Show |
35 | HG01070.hp1 HG01123.hp1 HG01934.hp1 others(32): Show |
intron_variant | MODIFIER | c.62-1888G>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16954471 | |||||||
| chr17:16954473 | T | C | 190 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0031 others(187): Show |
333 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(330): Show |
intron_variant | MODIFIER | c.62-1890A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16954473 | |||||||
| chr17:16954845 | G | A | 1 | a0005c0013t0001g0185 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.62-2262C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16954845 | |||||||
| chr17:16954859 | C | T | 9 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(6): Show |
9 | HG00621.hp2 HG01192.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.62-2276G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16954859 | |||||||
| chr17:16955029 | G | A | 1 | a0002c0003t0003g0218 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.62-2446C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16955029 | |||||||
| chr17:16955145 | A | T | 19 | a0001c0001t0002g0003 a0001c0001t0002g0029 a0001c0001t0002g0037 others(16): Show |
35 | HG01070.hp1 HG01123.hp1 HG01934.hp1 others(32): Show |
intron_variant | MODIFIER | c.62-2562T>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16955145 | |||||||
| chr17:16955296 | C | T | 1 | a0002c0003t0003g0212 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.62-2713G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16955296 | |||||||
| chr17:16955329 | C | G | 10 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(7): Show |
10 | HG00621.hp2 HG01192.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.62-2746G>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16955329 | |||||||
| chr17:16955381 | A | G | 9 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(6): Show |
9 | HG00621.hp2 HG01192.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.62-2798T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16955381 | |||||||
| chr17:16955428 | T | C | 34 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0123 others(31): Show |
58 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.62-2845A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16955428 | |||||||
| chr17:16955464 | T | C | 2 | a0002c0003t0003g0050 a0002c0003t0003g0211 |
3 | NA18985.hp1 NA18997.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.62-2881A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16955464 | |||||||
| chr17:16955554 | C | T | 1 | a0001c0001t0004g0127 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.62-2971G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16955554 | |||||||
| chr17:16955740 | C | T | 9 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(6): Show |
9 | HG00621.hp2 HG01192.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.62-3157G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16955740 | |||||||
| chr17:16955935 | G | A | 12 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0054 others(9): Show |
20 | HG00741.hp2 HG01516.hp1 HG01517.hp1 others(17): Show |
intron_variant | MODIFIER | c.62-3352C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16955935 | |||||||
| chr17:16956042 | C | T | 1 | a0004c0006t0004g0117 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.62-3459G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16956042 | |||||||
| chr17:16956101 | T | A | 9 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(6): Show |
9 | HG00621.hp2 HG01192.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.62-3518A>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16956101 | |||||||
| chr17:16956400 | A | ACCC | 10 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(7): Show |
10 | HG00621.hp2 HG00741.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.62-3818_62-3817ins others(3): Show |
TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16956400 | |||||||
| chr17:16956403 | C | T | 10 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(7): Show |
10 | HG00621.hp2 HG00741.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.62-3820G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16956403 | |||||||
| chr17:16956404 | A | G | 10 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(7): Show |
10 | HG00621.hp2 HG00741.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.62-3821T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16956404 | |||||||
| chr17:16956405 | G | C | 10 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(7): Show |
10 | HG00621.hp2 HG00741.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.62-3822C>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16956405 | |||||||
| chr17:16956406 | A | C | 10 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(7): Show |
10 | HG00621.hp2 HG00741.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.62-3823T>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16956406 | |||||||
| chr17:16956437 | A | G | 15 | a0001c0001t0002g0003 a0001c0001t0002g0029 a0001c0001t0002g0037 others(12): Show |
31 | HG01070.hp1 HG01123.hp1 HG01934.hp1 others(28): Show |
intron_variant | MODIFIER | c.62-3854T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16956437 | |||||||
| chr17:16956466 | A | G | 1 | a0001c0001t0002g0061 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.62-3883T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16956466 | |||||||
| chr17:16956515 | G | A | 19 | a0001c0001t0002g0003 a0001c0001t0002g0029 a0001c0001t0002g0037 others(16): Show |
35 | HG01070.hp1 HG01123.hp1 HG01934.hp1 others(32): Show |
intron_variant | MODIFIER | c.62-3932C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16956515 | |||||||
| chr17:16956582 | G | GT | 19 | a0001c0001t0002g0003 a0001c0001t0002g0029 a0001c0001t0002g0037 others(16): Show |
35 | HG01070.hp1 HG01123.hp1 HG01934.hp1 others(32): Show |
intron_variant | MODIFIER | c.62-4000dupA | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16956582 | |||||||
| chr17:16956740 | A | G | 2 | a0002c0003t0002g0047 a0002c0003t0002g0048 |
4 | HG00733.hp1 HG01099.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-4157T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16956740 | |||||||
| chr17:16956769 | C | A | 2 | a0001c0001t0002g0060 a0001c0001t0002g0063 |
2 | NA19003.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.62-4186G>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16956769 | |||||||
| chr17:16956877 | G | A | 19 | a0001c0001t0002g0003 a0001c0001t0002g0029 a0001c0001t0002g0037 others(16): Show |
35 | HG01070.hp1 HG01123.hp1 HG01934.hp1 others(32): Show |
intron_variant | MODIFIER | c.62-4294C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16956877 | |||||||
| chr17:16956943 | C | T | 14 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0054 others(11): Show |
25 | HG00741.hp2 HG01516.hp1 HG01517.hp1 others(22): Show |
intron_variant | MODIFIER | c.62-4360G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16956943 | |||||||
| chr17:16957094 | C | CG | 9 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(6): Show |
9 | HG00621.hp2 HG01192.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.62-4512dupC | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16957094 | |||||||
| chr17:16957095 | G | C | 19 | a0001c0001t0002g0003 a0001c0001t0002g0029 a0001c0001t0002g0037 others(16): Show |
35 | HG01070.hp1 HG01123.hp1 HG01934.hp1 others(32): Show |
intron_variant | MODIFIER | c.62-4512C>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16957095 | |||||||
| chr17:16957177 | C | CT | 74 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0031 others(71): Show |
123 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.62-4595dupA | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16957177 | |||||||
| chr17:16957177 | C | CTT | 19 | a0001c0001t0001g0173 a0001c0001t0001g0192 a0001c0001t0001g0193 others(16): Show |
35 | HG01952.hp2 HG02074.hp2 HG02622.hp1 others(32): Show |
intron_variant | MODIFIER | c.62-4596_62-4595dup others(2): Show |
TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16957177 | |||||||
| chr17:16957308 | C | T | 1 | a0001c0002t0001g0107 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.62-4725G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16957308 | |||||||
| chr17:16957384 | A | G | 1 | a0001c0001t0001g0192 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.62-4801T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16957384 | |||||||
| chr17:16957726 | C | T | 1 | a0001c0001t0002g0076 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.62-5143G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16957726 | |||||||
| chr17:16957730 | C | A | 1 | a0001c0001t0002g0076 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.62-5147G>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16957730 | |||||||
| chr17:16957749 | A | T | 1 | a0001c0001t0002g0032 | 2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.62-5166T>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16957749 | |||||||
| chr17:16957756 | A | G | 9 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(6): Show |
9 | HG00621.hp2 HG01192.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.62-5173T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16957756 | |||||||
| chr17:16957784 | A | C | 37 | a0001c0001t0002g0003 a0001c0001t0002g0029 a0001c0001t0002g0037 others(34): Show |
66 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.62-5201T>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16957784 | |||||||
| chr17:16957881 | A | T | 1 | a0001c0001t0001g0101 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.62-5298T>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16957881 | |||||||
| chr17:16957889 | C | T | 14 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0054 others(11): Show |
25 | HG00741.hp2 HG01516.hp1 HG01517.hp1 others(22): Show |
intron_variant | MODIFIER | c.62-5306G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16957889 | |||||||
| chr17:16958018 | G | A | 46 | a0001c0001t0001g0034 a0001c0001t0002g0067 a0001c0001t0002g0068 others(43): Show |
86 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.62-5435C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16958018 | |||||||
| chr17:16958019 | G | A | 1 | a0001c0001t0002g0122 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.62-5436C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16958019 | |||||||
| chr17:16958045 | C | G | 32 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0123 others(29): Show |
56 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.62-5462G>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16958045 | |||||||
| chr17:16958142 | C | G | 37 | a0001c0001t0002g0003 a0001c0001t0002g0029 a0001c0001t0002g0037 others(34): Show |
66 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.62-5559G>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16958142 | |||||||
| chr17:16958193 | T | C | 3 | a0002c0003t0003g0009 a0002c0003t0003g0220 a0002c0003t0003g0225 |
8 | HG02056.hp2 HG02083.hp1 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.62-5610A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16958193 | |||||||
| chr17:16958412 | TA | T | 40 | a0001c0001t0001g0085 a0001c0001t0001g0101 a0001c0001t0002g0003 others(37): Show |
69 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.62-5830delT | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16958412 | |||||||
| chr17:16958425 | T | G | 1 | a0001c0001t0010g0195 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.62-5842A>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16958425 | |||||||
| chr17:16958492 | TA | T | 14 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0054 others(11): Show |
25 | HG00741.hp2 HG01516.hp1 HG01517.hp1 others(22): Show |
intron_variant | MODIFIER | c.62-5910delT | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16958492 | |||||||
| chr17:16958530 | C | T | 1 | a0001c0002t0001g0018 | 3 | NA18975.hp1 NA19056.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.62-5947G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16958530 | |||||||
| chr17:16958625 | T | C | 3 | a0001c0002t0001g0014 a0001c0002t0001g0110 a0001c0002t0001g0194 |
6 | HG02055.hp1 HG02717.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.62-6042A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16958625 | |||||||
| chr17:16958655 | C | A | 4 | a0001c0002t0001g0023 a0001c0002t0001g0142 a0001c0002t0001g0144 others(1): Show |
6 | HG00408.hp2 HG00673.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.62-6072G>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16958655 | |||||||
| chr17:16958761 | A | T | 1 | a0001c0001t0010g0195 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.62-6178T>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16958761 | |||||||
| chr17:16958779 | T | A | 2 | a0001c0001t0002g0029 a0001c0001t0002g0066 |
3 | HG01934.hp1 HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.62-6196A>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16958779 | |||||||
| chr17:16958916 | C | G | 222 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0031 others(219): Show |
381 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(378): Show |
intron_variant | MODIFIER | c.62-6333G>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16958916 | |||||||
| chr17:16958984 | C | T | 1 | a0002c0003t0003g0174 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.62-6401G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16958984 | |||||||
| chr17:16959061 | A | G | 1 | a0002c0003t0003g0211 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.62-6478T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16959061 | |||||||
| chr17:16959135 | T | G | 37 | a0001c0001t0002g0003 a0001c0001t0002g0029 a0001c0001t0002g0037 others(34): Show |
66 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.62-6552A>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16959135 | |||||||
| chr17:16959432 | T | TAGA | 37 | a0001c0001t0002g0003 a0001c0001t0002g0029 a0001c0001t0002g0037 others(34): Show |
66 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.62-6852_62-6850dup others(3): Show |
TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16959432 | |||||||
| chr17:16959478 | T | G | 37 | a0001c0001t0002g0003 a0001c0001t0002g0029 a0001c0001t0002g0037 others(34): Show |
66 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.62-6895A>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16959478 | |||||||
| chr17:16959617 | A | G | 2 | a0001c0001t0002g0080 a0001c0001t0002g0091 |
2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.62-7034T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16959617 | |||||||
| chr17:16959833 | T | A | 37 | a0001c0001t0002g0003 a0001c0001t0002g0029 a0001c0001t0002g0037 others(34): Show |
66 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.62-7250A>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16959833 | |||||||
| chr17:16959858 | C | T | 37 | a0001c0001t0002g0003 a0001c0001t0002g0029 a0001c0001t0002g0037 others(34): Show |
66 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.62-7275G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16959858 | |||||||
| chr17:16959933 | C | T | 37 | a0001c0001t0002g0003 a0001c0001t0002g0029 a0001c0001t0002g0037 others(34): Show |
66 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.62-7350G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16959933 | |||||||
| chr17:16959941 | A | G | 37 | a0001c0001t0002g0003 a0001c0001t0002g0029 a0001c0001t0002g0037 others(34): Show |
66 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.62-7358T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16959941 | |||||||
| chr17:16959994 | T | C | 37 | a0001c0001t0002g0003 a0001c0001t0002g0029 a0001c0001t0002g0037 others(34): Show |
66 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.62-7411A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16959994 | |||||||
| chr17:16960018 | G | A | 1 | a0001c0004t0002g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.62-7435C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16960018 | |||||||
| chr17:16960048 | A | G | 209 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0031 others(206): Show |
368 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(365): Show |
intron_variant | MODIFIER | c.62-7465T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16960048 | |||||||
| chr17:16960163 | T | A | 209 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0031 others(206): Show |
368 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(365): Show |
intron_variant | MODIFIER | c.62-7580A>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16960163 | |||||||
| chr17:16960324 | C | G | 52 | a0001c0001t0001g0168 a0001c0002t0001g0214 a0002c0003t0002g0047 others(49): Show |
92 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.62-7741G>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16960324 | |||||||
| chr17:16960360 | T | C | 220 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0031 others(217): Show |
379 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(376): Show |
intron_variant | MODIFIER | c.62-7777A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16960360 | |||||||
| chr17:16960373 | C | G | 1 | a0001c0002t0001g0153 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.62-7790G>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16960373 | |||||||
| chr17:16960420 | A | G | 37 | a0001c0001t0002g0003 a0001c0001t0002g0029 a0001c0001t0002g0037 others(34): Show |
66 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.62-7837T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16960420 | |||||||
| chr17:16960422 | C | A | 32 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0123 others(29): Show |
56 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.62-7839G>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16960422 | |||||||
| chr17:16960431 | A | G | 37 | a0001c0001t0002g0003 a0001c0001t0002g0029 a0001c0001t0002g0037 others(34): Show |
66 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.62-7848T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16960431 | |||||||
| chr17:16960440 | C | A | 1 | a0001c0002t0001g0158 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.62-7857G>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16960440 | |||||||
| chr17:16960469 | C | T | 2 | a0004c0006t0002g0116 a0004c0006t0004g0117 |
2 | HG02145.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.62-7886G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16960469 | |||||||
| chr17:16960628 | T | G | 37 | a0001c0001t0002g0003 a0001c0001t0002g0029 a0001c0001t0002g0037 others(34): Show |
66 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.62-8045A>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16960628 | |||||||
| chr17:16960727 | A | G | 11 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0054 others(8): Show |
19 | HG01516.hp1 HG01517.hp1 HG03453.hp2 others(16): Show |
intron_variant | MODIFIER | c.62-8144T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16960727 | |||||||
| chr17:16960786 | A | C | 1 | a0001c0001t0001g0126 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.62-8203T>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16960786 | |||||||
| chr17:16960992 | C | T | 9 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(6): Show |
9 | HG00621.hp2 HG01192.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.62-8409G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16960992 | |||||||
| chr17:16961105 | C | G | 107 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0058 others(104): Show |
188 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.62-8522G>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16961105 | |||||||
| chr17:16961106 | G | A | 107 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0058 others(104): Show |
188 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.62-8523C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16961106 | |||||||
| chr17:16961245 | C | T | 209 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0031 others(206): Show |
368 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(365): Show |
intron_variant | MODIFIER | c.62-8662G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16961245 | |||||||
| chr17:16961441 | A | G | 1 | a0001c0002t0001g0097 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.62-8858T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16961441 | |||||||
| chr17:16961651 | T | C | 2 | a0001c0001t0004g0039 a0001c0001t0004g0148 |
3 | HG02148.hp2 NA20129.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.62-9068A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16961651 | |||||||
| chr17:16961696 | G | A | 220 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0031 others(217): Show |
379 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(376): Show |
intron_variant | MODIFIER | c.62-9113C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16961696 | |||||||
| chr17:16961873 | T | C | 3 | a0001c0002t0001g0014 a0001c0002t0001g0110 a0001c0002t0001g0194 |
6 | HG02055.hp1 HG02717.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.62-9290A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16961873 | |||||||
| chr17:16962035 | G | A | 1 | a0001c0001t0002g0029 | 2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.62-9452C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16962035 | |||||||
| chr17:16962109 | T | C | 18 | a0001c0001t0002g0108 a0001c0001t0004g0075 a0001c0002t0001g0007 others(15): Show |
32 | HG01192.hp1 HG01891.hp2 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.62-9526A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16962109 | |||||||
| chr17:16962162 | A | G | 2 | a0001c0002t0001g0106 a0001c0002t0001g0113 |
2 | HG02630.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.62-9579T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16962162 | |||||||
| chr17:16962242 | C | T | 1 | a0001c0004t0002g0180 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.62-9659G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16962242 | |||||||
| chr17:16962276 | G | A | 10 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(7): Show |
10 | HG00621.hp2 HG01192.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.62-9693C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16962276 | |||||||
| chr17:16962298 | G | A | 1 | a0001c0002t0001g0144 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.62-9715C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16962298 | |||||||
| chr17:16962450 | C | T | 1 | a0001c0001t0003g0071 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.61+9565G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16962450 | |||||||
| chr17:16962500 | C | T | 1 | a0001c0001t0004g0204 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.61+9515G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16962500 | |||||||
| chr17:16962511 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.61+9504G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16962511 | |||||||
| chr17:16962513 | CAAAAAAA others(8): Show |
C | 1 | a0001c0002t0001g0096 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.61+9487_61+9501del others(15): Show |
TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16962513 | |||||||
| chr17:16962514 | A | C | 1 | a0001c0001t0010g0195 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.61+9501T>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16962514 | |||||||
| chr17:16962591 | A | G | 1 | a0001c0002t0001g0102 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.61+9424T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16962591 | |||||||
| chr17:16962682 | T | C | 1 | a0001c0002t0001g0036 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.61+9333A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16962682 | |||||||
| chr17:16962703 | G | A | 37 | a0001c0001t0002g0003 a0001c0001t0002g0029 a0001c0001t0002g0037 others(34): Show |
66 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.61+9312C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16962703 | |||||||
| chr17:16962761 | C | A | 173 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0031 others(170): Show |
303 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.61+9254G>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16962761 | |||||||
| chr17:16962790 | G | A | 1 | a0002c0003t0001g0069 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.61+9225C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16962790 | |||||||
| chr17:16962799 | G | GCAGC | 1 | a0001c0001t0004g0021 | 3 | HG01069.hp1 HG01071.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.61+9212_61+9215dup others(4): Show |
TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16962799 | |||||||
| chr17:16962850 | C | T | 210 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0031 others(207): Show |
369 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(366): Show |
intron_variant | MODIFIER | c.61+9165G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16962850 | |||||||
| chr17:16962929 | C | A | 1 | a0001c0001t0004g0075 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.61+9086G>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16962929 | |||||||
| chr17:16962940 | G | A | 37 | a0001c0001t0002g0003 a0001c0001t0002g0029 a0001c0001t0002g0037 others(34): Show |
66 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.61+9075C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16962940 | |||||||
| chr17:16962967 | C | T | 37 | a0001c0001t0002g0003 a0001c0001t0002g0029 a0001c0001t0002g0037 others(34): Show |
66 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.61+9048G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16962967 | |||||||
| chr17:16963068 | T | C | 32 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0123 others(29): Show |
56 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.61+8947A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16963068 | |||||||
| chr17:16963249 | A | G | 4 | a0001c0001t0001g0034 a0001c0002t0001g0010 a0001c0002t0001g0094 others(1): Show |
9 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.61+8766T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16963249 | |||||||
| chr17:16963344 | G | A | 1 | a0001c0001t0004g0075 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.61+8671C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16963344 | |||||||
| chr17:16963414 | C | T | 2 | a0001c0001t0001g0173 a0001c0001t0001g0192 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.61+8601G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16963414 | |||||||
| chr17:16963463 | C | G | 78 | a0001c0001t0001g0031 a0001c0001t0001g0058 a0001c0001t0001g0083 others(75): Show |
136 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.61+8552G>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16963463 | |||||||
| chr17:16963528 | G | GTTTTGT | 37 | a0001c0001t0002g0003 a0001c0001t0002g0029 a0001c0001t0002g0037 others(34): Show |
66 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.61+8481_61+8486dup others(6): Show |
TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16963528 | |||||||
| chr17:16963531 | T | TTG | 9 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(6): Show |
9 | HG00621.hp2 HG01192.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.61+8482_61+8483dup others(2): Show |
TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16963531 | |||||||
| chr17:16963544 | T | C | 1 | a0001c0001t0010g0195 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.61+8471A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16963544 | |||||||
| chr17:16963550 | TG | T | 5 | a0001c0002t0001g0007 a0001c0002t0001g0105 a0001c0002t0001g0106 others(2): Show |
11 | HG02630.hp1 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.61+8464delC | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16963550 | |||||||
| chr17:16963560 | G | A | 9 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(6): Show |
9 | HG00621.hp2 HG01192.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.61+8455C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16963560 | |||||||
| chr17:16963619 | G | A | 3 | a0001c0004t0002g0043 a0001c0004t0002g0044 a0001c0004t0002g0178 |
5 | HG03017.hp1 HG03490.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+8396C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16963619 | |||||||
| chr17:16963629 | A | C | 1 | a0004c0006t0002g0116 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.61+8386T>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16963629 | |||||||
| chr17:16963738 | G | A | 1 | a0002c0003t0003g0203 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.61+8277C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16963738 | |||||||
| chr17:16963785 | C | T | 3 | a0003c0007t0002g0118 a0003c0007t0002g0119 a0003c0012t0001g0120 |
3 | HG01109.hp2 HG02258.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.61+8230G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16963785 | |||||||
| chr17:16963797 | G | A | 2 | a0001c0005t0001g0184 a0005c0013t0001g0185 |
2 | HG00099.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.61+8218C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16963797 | |||||||
| chr17:16963802 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.61+8213C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16963802 | |||||||
| chr17:16963845 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.61+8170G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16963845 | |||||||
| chr17:16963886 | A | G | 19 | a0001c0001t0001g0058 a0001c0001t0002g0005 a0001c0001t0002g0028 others(16): Show |
32 | HG00423.hp1 HG00597.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.61+8129T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16963886 | |||||||
| chr17:16963908 | T | C | 1 | a0004c0006t0004g0117 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.61+8107A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16963908 | |||||||
| chr17:16964013 | A | C | 1 | a0001c0001t0002g0152 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.61+8002T>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16964013 | |||||||
| chr17:16964129 | A | G | 1 | a0001c0004t0002g0179 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.61+7886T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16964129 | |||||||
| chr17:16964156 | A | G | 1 | a0001c0002t0001g0095 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.61+7859T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16964156 | |||||||
| chr17:16964237 | A | C | 1 | a0002c0003t0003g0209 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.61+7778T>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16964237 | |||||||
| chr17:16964337 | C | CT | 11 | a0001c0001t0001g0035 a0001c0001t0001g0054 a0001c0001t0001g0231 others(8): Show |
13 | HG01516.hp1 HG01517.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.61+7677dupA | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16964337 | |||||||
| chr17:16964337 | C | CTT | 8 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(5): Show |
8 | HG00621.hp2 HG01192.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.61+7676_61+7677dup others(2): Show |
TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16964337 | |||||||
| chr17:16964337 | CT | C | 95 | a0001c0001t0001g0034 a0001c0001t0001g0083 a0001c0001t0001g0164 others(92): Show |
177 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.61+7677delA | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16964337 | |||||||
| chr17:16964337 | CTT | C | 6 | a0001c0001t0004g0075 a0001c0002t0001g0097 a0001c0002t0001g0111 others(3): Show |
6 | HG00639.hp1 HG02056.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.61+7676_61+7677del others(2): Show |
TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16964337 | |||||||
| chr17:16964469 | A | G | 2 | a0001c0002t0002g0072 a0001c0002t0002g0190 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.61+7546T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16964469 | |||||||
| chr17:16964480 | T | C | 1 | a0001c0001t0004g0136 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.61+7535A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16964480 | |||||||
| chr17:16964632 | C | T | 4 | a0001c0001t0002g0076 a0001c0002t0001g0073 a0001c0002t0002g0072 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+7383G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16964632 | |||||||
| chr17:16964819 | C | T | 2 | a0001c0001t0001g0191 a0001c0002t0001g0073 |
2 | HG00741.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.61+7196G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16964819 | |||||||
| chr17:16964820 | G | A | 1 | a0001c0002t0001g0098 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.61+7195C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16964820 | |||||||
| chr17:16964917 | A | C | 18 | a0001c0001t0002g0108 a0001c0001t0004g0075 a0001c0002t0001g0007 others(15): Show |
32 | HG01192.hp1 HG01891.hp2 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.61+7098T>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16964917 | |||||||
| chr17:16964940 | C | G | 1 | a0001c0001t0008g0074 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.61+7075G>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16964940 | |||||||
| chr17:16965045 | G | T | 1 | a0001c0002t0001g0105 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.61+6970C>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16965045 | |||||||
| chr17:16965093 | T | C | 4 | a0001c0001t0002g0076 a0001c0002t0001g0073 a0001c0002t0002g0072 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+6922A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16965093 | |||||||
| chr17:16965247 | C | T | 125 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0034 others(122): Show |
219 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.61+6768G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16965247 | |||||||
| chr17:16965328 | C | T | 2 | a0001c0002t0002g0072 a0001c0002t0002g0190 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.61+6687G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16965328 | |||||||
| chr17:16965362 | C | T | 25 | a0001c0001t0001g0034 a0001c0001t0002g0067 a0001c0001t0002g0068 others(22): Show |
46 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.61+6653G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16965362 | |||||||
| chr17:16965701 | A | G | 1 | a0001c0002t0001g0150 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.61+6314T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16965701 | |||||||
| chr17:16965983 | G | A | 2 | a0001c0001t0002g0076 a0001c0002t0001g0073 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.61+6032C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16965983 | |||||||
| chr17:16965984 | G | A | 1 | a0001c0001t0004g0135 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.61+6031C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16965984 | |||||||
| chr17:16966115 | A | C | 1 | a0001c0001t0002g0066 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.61+5900T>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16966115 | |||||||
| chr17:16966126 | C | T | 74 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0035 others(71): Show |
137 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.61+5889G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16966126 | |||||||
| chr17:16966203 | G | A | 1 | a0001c0002t0001g0099 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.61+5812C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16966203 | |||||||
| chr17:16966231 | G | A | 2 | a0002c0003t0003g0051 a0002c0003t0003g0223 |
3 | HG02602.hp2 HG02738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.61+5784C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16966231 | |||||||
| chr17:16966265 | C | A | 20 | a0001c0001t0002g0076 a0001c0001t0002g0108 a0001c0001t0004g0075 others(17): Show |
32 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.61+5750G>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16966265 | |||||||
| chr17:16966266 | A | C | 19 | a0001c0001t0002g0076 a0001c0001t0002g0108 a0001c0001t0004g0075 others(16): Show |
31 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(28): Show |
intron_variant | MODIFIER | c.61+5749T>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16966266 | |||||||
| chr17:16966333 | C | A | 1 | a0001c0001t0001g0221 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.61+5682G>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16966333 | |||||||
| chr17:16966435 | G | C | 16 | a0001c0001t0002g0108 a0001c0001t0004g0075 a0001c0002t0001g0007 others(13): Show |
28 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.61+5580C>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16966435 | |||||||
| chr17:16966545 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.61+5470A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16966545 | |||||||
| chr17:16966704 | C | G | 1 | a0001c0002t0001g0036 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.61+5311G>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16966704 | |||||||
| chr17:16966764 | AT | A | 39 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0054 others(36): Show |
60 | HG00621.hp2 HG00741.hp2 HG01192.hp2 others(57): Show |
intron_variant | MODIFIER | c.61+5250delA | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16966764 | |||||||
| chr17:16966810 | G | T | 3 | a0001c0001t0001g0123 a0001c0001t0002g0079 a0001c0002t0001g0102 |
3 | HG02135.hp2 HG02451.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.61+5205C>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16966810 | |||||||
| chr17:16966836 | T | C | 2 | a0001c0001t0002g0037 a0001c0001t0002g0121 |
3 | HG01070.hp1 NA18980.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.61+5179A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16966836 | |||||||
| chr17:16966836 | TTTC | T | 130 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0034 others(127): Show |
225 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.61+5176_61+5178del others(3): Show |
TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16966836 | |||||||
| chr17:16966837 | TTC | T | 80 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0035 others(77): Show |
136 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.61+5176_61+5177del others(2): Show |
TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16966837 | |||||||
| chr17:16966838 | TC | T | 5 | a0001c0001t0001g0035 a0001c0001t0001g0055 a0001c0001t0004g0138 others(2): Show |
5 | HG01934.hp2 NA18951.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+5176delG | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16966838 | |||||||
| chr17:16966839 | CT | C | 8 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(5): Show |
8 | HG00621.hp2 HG01192.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.61+5175delA | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16966839 | |||||||
| chr17:16966841 | T | C | 5 | a0001c0001t0002g0067 a0001c0001t0002g0076 a0001c0002t0001g0073 others(2): Show |
5 | HG02258.hp2 HG02559.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+5174A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16966841 | |||||||
| chr17:16966847 | T | C | 4 | a0001c0001t0002g0076 a0001c0002t0001g0073 a0001c0002t0002g0072 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+5168A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16966847 | |||||||
| chr17:16966879 | C | CA | 9 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(6): Show |
9 | HG00621.hp2 HG01192.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.61+5135_61+5136ins others(1): Show |
TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16966879 | |||||||
| chr17:16966913 | A | G | 9 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(6): Show |
9 | HG00621.hp2 HG01192.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.61+5102T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16966913 | |||||||
| chr17:16966978 | A | G | 3 | a0001c0001t0004g0026 a0001c0001t0004g0204 a0001c0002t0001g0206 |
5 | HG01070.hp2 HG01071.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+5037T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16966978 | |||||||
| chr17:16966995 | T | A | 2 | a0001c0001t0006g0011 a0001c0001t0008g0074 |
5 | HG02886.hp2 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+5020A>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16966995 | |||||||
| chr17:16967140 | A | G | 4 | a0001c0001t0002g0076 a0001c0002t0001g0073 a0001c0002t0002g0072 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+4875T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16967140 | |||||||
| chr17:16967258 | A | G | 1 | a0001c0001t0002g0070 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.61+4757T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16967258 | |||||||
| chr17:16967285 | G | A | 2 | a0001c0001t0001g0089 a0001c0002t0001g0088 |
2 | HG00621.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.61+4730C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16967285 | |||||||
| chr17:16967322 | CAAAAAT | C | 2 | a0001c0001t0001g0040 a0001c0001t0004g0136 |
3 | HG02602.hp1 HG03710.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.61+4687_61+4692del others(6): Show |
TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16967322 | |||||||
| chr17:16967433 | C | A | 1 | a0002c0003t0003g0052 | 2 | HG01167.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.61+4582G>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16967433 | |||||||
| chr17:16967502 | C | T | 1 | a0002c0003t0003g0205 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.61+4513G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16967502 | |||||||
| chr17:16967518 | G | T | 1 | a0001c0004t0002g0178 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.61+4497C>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16967518 | |||||||
| chr17:16967533 | T | C | 1 | a0002c0003t0003g0223 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.61+4482A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16967533 | |||||||
| chr17:16967593 | A | T | 4 | a0001c0001t0002g0076 a0001c0002t0001g0073 a0001c0002t0002g0072 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+4422T>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16967593 | |||||||
| chr17:16967594 | A | T | 3 | a0001c0002t0001g0073 a0001c0002t0002g0072 a0001c0002t0002g0190 |
3 | HG02559.hp1 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.61+4421T>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16967594 | |||||||
| chr17:16967684 | G | T | 1 | a0001c0002t0001g0142 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.61+4331C>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16967684 | |||||||
| chr17:16967709 | G | A | 1 | a0003c0007t0002g0118 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.61+4306C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16967709 | |||||||
| chr17:16967751 | C | A | 4 | a0001c0001t0002g0076 a0001c0002t0001g0073 a0001c0002t0002g0072 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+4264G>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16967751 | |||||||
| chr17:16967751 | C | CA | 79 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0035 others(76): Show |
123 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.61+4263dupT | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16967751 | |||||||
| chr17:16967751 | C | CAA | 7 | a0001c0001t0004g0022 a0001c0001t0004g0137 a0001c0001t0004g0138 others(4): Show |
12 | HG01192.hp2 HG01433.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.61+4262_61+4263dup others(2): Show |
TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16967751 | |||||||
| chr17:16967751 | CA | C | 7 | a0001c0001t0002g0029 a0001c0001t0002g0041 a0001c0001t0002g0066 others(4): Show |
9 | HG01069.hp2 HG01934.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.61+4263delT | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16967751 | |||||||
| chr17:16967769 | A | G | 2 | a0002c0003t0003g0015 a0002c0003t0003g0203 |
5 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+4246T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16967769 | |||||||
| chr17:16967877 | C | T | 1 | a0001c0001t0002g0067 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.61+4138G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16967877 | |||||||
| chr17:16967963 | G | T | 1 | a0002c0003t0003g0141 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.61+4052C>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16967963 | |||||||
| chr17:16967973 | T | TA | 17 | a0001c0001t0002g0108 a0001c0002t0001g0007 a0001c0002t0001g0014 others(14): Show |
29 | HG01106.hp1 HG01891.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.61+4041dupT | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16967973 | |||||||
| chr17:16968154 | AAAG | A | 39 | a0001c0001t0001g0034 a0001c0001t0001g0173 a0001c0001t0001g0192 others(36): Show |
62 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.61+3858_61+3860del others(3): Show |
TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16968154 | |||||||
| chr17:16968155 | AAG | A | 124 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0035 others(121): Show |
215 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.61+3858_61+3859del others(2): Show |
TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16968155 | |||||||
| chr17:16968156 | AG | A | 40 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0035 others(37): Show |
56 | HG00423.hp1 HG00597.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.61+3858delC | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16968156 | |||||||
| chr17:16968157 | G | A | 35 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(32): Show |
44 | HG00621.hp2 HG01192.hp2 HG01433.hp2 others(41): Show |
intron_variant | MODIFIER | c.61+3858C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16968157 | |||||||
| chr17:16968159 | A | G | 1 | a0001c0001t0002g0076 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.61+3856T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16968159 | |||||||
| chr17:16968451 | T | C | 135 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0035 others(132): Show |
242 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(239): Show |
intron_variant | MODIFIER | c.61+3564A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16968451 | |||||||
| chr17:16968632 | T | A | 1 | a0001c0001t0010g0195 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.61+3383A>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16968632 | |||||||
| chr17:16968744 | T | C | 2 | a0002c0003t0003g0226 a0002c0003t0003g0227 |
2 | NA18951.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.61+3271A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16968744 | |||||||
| chr17:16968763 | A | G | 64 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0123 others(61): Show |
115 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.61+3252T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16968763 | |||||||
| chr17:16968768 | C | A | 1 | a0001c0002t0001g0073 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.61+3247G>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16968768 | |||||||
| chr17:16968796 | T | G | 4 | a0001c0001t0002g0076 a0001c0002t0001g0073 a0001c0002t0002g0072 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+3219A>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16968796 | |||||||
| chr17:16968829 | T | C | 14 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0054 others(11): Show |
26 | HG00741.hp2 HG01516.hp1 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.61+3186A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16968829 | |||||||
| chr17:16968957 | T | C | 2 | a0001c0002t0001g0102 a0001c0002t0001g0103 |
2 | NA19077.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.61+3058A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16968957 | |||||||
| chr17:16969004 | C | A | 206 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0031 others(203): Show |
365 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(362): Show |
intron_variant | MODIFIER | c.61+3011G>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16969004 | |||||||
| chr17:16969027 | G | C | 10 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(7): Show |
10 | HG00621.hp2 HG01192.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.61+2988C>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16969027 | |||||||
| chr17:16969194 | G | A | 1 | a0001c0001t0004g0148 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.61+2821C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16969194 | |||||||
| chr17:16969227 | T | C | 1 | a0001c0001t0004g0149 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.61+2788A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16969227 | |||||||
| chr17:16969441 | G | A | 1 | a0001c0001t0002g0037 | 2 | NA18980.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.61+2574C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16969441 | |||||||
| chr17:16969500 | A | G | 1 | a0002c0003t0003g0196 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.61+2515T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16969500 | |||||||
| chr17:16969506 | T | C | 1 | a0001c0001t0002g0091 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.61+2509A>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16969506 | |||||||
| chr17:16969726 | G | C | 41 | a0001c0001t0001g0008 a0001c0001t0001g0034 a0001c0001t0001g0035 others(38): Show |
73 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.61+2289C>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16969726 | |||||||
| chr17:16969788 | G | C | 2 | a0001c0002t0001g0102 a0001c0002t0001g0103 |
2 | NA19077.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.61+2227C>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16969788 | |||||||
| chr17:16969926 | T | A | 2 | a0004c0006t0002g0116 a0004c0006t0004g0117 |
2 | HG02145.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.61+2089A>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16969926 | |||||||
| chr17:16969964 | C | G | 33 | a0001c0001t0001g0031 a0001c0001t0001g0083 a0001c0001t0001g0084 others(30): Show |
44 | HG00621.hp2 HG01109.hp2 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.61+2051G>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16969964 | |||||||
| chr17:16969994 | T | G | 26 | a0001c0001t0001g0031 a0001c0001t0001g0083 a0001c0001t0001g0084 others(23): Show |
32 | HG00621.hp2 HG01243.hp1 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.61+2021A>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16969994 | |||||||
| chr17:16970111 | C | T | 4 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0231 others(1): Show |
6 | HG01516.hp1 HG01517.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.61+1904G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16970111 | |||||||
| chr17:16970142 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.61+1873T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16970142 | |||||||
| chr17:16970310 | G | A | 1 | a0001c0001t0004g0075 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.61+1705C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16970310 | |||||||
| chr17:16970349 | C | T | 1 | a0001c0002t0001g0025 | 3 | HG02280.hp2 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.61+1666G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16970349 | |||||||
| chr17:16970459 | CG | C | 26 | a0001c0001t0001g0031 a0001c0001t0001g0083 a0001c0001t0001g0084 others(23): Show |
32 | HG00621.hp2 HG01243.hp1 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.61+1555delC | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16970459 | |||||||
| chr17:16970461 | G | A | 26 | a0001c0001t0001g0031 a0001c0001t0001g0083 a0001c0001t0001g0084 others(23): Show |
32 | HG00621.hp2 HG01243.hp1 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.61+1554C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16970461 | |||||||
| chr17:16970643 | G | A | 1 | a0001c0001t0002g0065 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.61+1372C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16970643 | |||||||
| chr17:16970680 | C | CG | 71 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0123 others(68): Show |
125 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.61+1334dupC | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16970680 | |||||||
| chr17:16970754 | G | T | 73 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0123 others(70): Show |
127 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.61+1261C>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16970754 | |||||||
| chr17:16970758 | C | T | 63 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0034 others(60): Show |
110 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.61+1257G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16970758 | |||||||
| chr17:16970923 | G | A | 1 | a0001c0001t0002g0076 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.61+1092C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16970923 | |||||||
| chr17:16971052 | G | A | 73 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0123 others(70): Show |
127 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.61+963C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16971052 | |||||||
| chr17:16971064 | C | T | 10 | a0001c0001t0001g0058 a0001c0001t0002g0005 a0001c0001t0002g0028 others(7): Show |
22 | HG00423.hp1 HG00597.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.61+951G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16971064 | |||||||
| chr17:16971071 | G | C | 66 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0034 others(63): Show |
118 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.61+944C>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16971071 | |||||||
| chr17:16971071 | G | T | 1 | a0001c0002t0001g0092 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.61+944C>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16971071 | |||||||
| chr17:16971076 | C | T | 1 | a0002c0003t0003g0176 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.61+939G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16971076 | |||||||
| chr17:16971163 | C | T | 11 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0173 others(8): Show |
15 | HG00741.hp2 HG01516.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.61+852G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16971163 | |||||||
| chr17:16971206 | G | A | 6 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0231 others(3): Show |
8 | HG01516.hp1 HG01517.hp1 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.61+809C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16971206 | |||||||
| chr17:16971210 | G | A | 30 | a0001c0001t0001g0164 a0001c0001t0001g0168 a0001c0001t0002g0003 others(27): Show |
58 | HG00280.hp2 HG00639.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.61+805C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16971210 | |||||||
| chr17:16971280 | C | T | 2 | a0001c0001t0002g0070 a0001c0001t0003g0071 |
2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.61+735G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16971280 | |||||||
| chr17:16971295 | G | A | 71 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0123 others(68): Show |
125 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.61+720C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16971295 | |||||||
| chr17:16971308 | C | T | 1 | a0001c0002t0001g0038 | 2 | NA18990.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.61+707G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16971308 | |||||||
| chr17:16971314 | A | C | 1 | a0001c0001t0002g0037 | 2 | NA18980.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.61+701T>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16971314 | |||||||
| chr17:16971342 | C | G | 1 | a0001c0001t0002g0115 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.61+673G>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16971342 | |||||||
| chr17:16971361 | C | CAA | 33 | a0001c0001t0001g0008 a0001c0001t0001g0034 a0001c0001t0001g0035 others(30): Show |
68 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.61+652_61+653dupTT | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16971361 | |||||||
| chr17:16971361 | C | CAAAAACA others(1): Show |
184 | a0001c0001t0001g0020 a0001c0001t0001g0031 a0001c0001t0001g0040 others(181): Show |
307 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(304): Show |
intron_variant | MODIFIER | c.61+646_61+653dupTT others(6): Show |
TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16971361 | |||||||
| chr17:16971384 | A | AC | 76 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0034 others(73): Show |
132 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.61+630_61+631insG | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16971384 | |||||||
| chr17:16971428 | GA | G | 16 | a0001c0001t0001g0058 a0001c0001t0002g0005 a0001c0001t0002g0028 others(13): Show |
31 | HG00423.hp1 HG00597.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.61+586delT | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16971428 | |||||||
| chr17:16971537 | C | T | 2 | a0002c0003t0003g0176 a0002c0003t0003g0177 |
2 | HG02015.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.61+478G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16971537 | |||||||
| chr17:16971592 | G | C | 1 | a0001c0002t0001g0171 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.61+423C>G | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16971592 | |||||||
| chr17:16971667 | C | T | 149 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0031 others(146): Show |
259 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.61+348G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16971667 | |||||||
| chr17:16971711 | C | T | 1 | a0001c0004t0002g0175 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.61+304G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16971711 | |||||||
| chr17:16971747 | A | G | 151 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0031 others(148): Show |
261 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.61+268T>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16971747 | |||||||
| chr17:16971782 | T | G | 1 | a0001c0002t0001g0235 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.61+233A>C | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16971782 | |||||||
| chr17:16971815 | C | T | 1 | a0001c0002t0001g0057 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.61+200G>A | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16971815 | |||||||
| chr17:16971848 | G | A | 1 | a0001c0001t0004g0236 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.61+167C>T | TNFRSF13B | ENSG00000240505.9 | transcript | ENST00000261652.7 | protein_coding | 1/4 | chr17 | 16971848 |