Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4907 |
| ensemblid | ENSG00000135318.12 |
| hgncid | 8021 |
| symbol | NT5E |
| name | 5'-nucleotidase ecto |
| refseq_nuc | NM_002526.4 |
| refseq_prot | NP_002517.1 |
| ensembl_nuc | ENST00000257770.8 |
| ensembl_prot | ENSP00000257770.3 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 85450083 |
| end | 85495784 |
| strand | + |
| ver | v1.2 |
| region | chr6:85450083-85495784 |
| region5000 | chr6:85445083-85500784 |
| regionname0 | NT5E_chr6_85450083_85495784 |
| regionname5000 | NT5E_chr6_85445083_85500784 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 574 | 218 | 52 | 33 | 104 | 5 | 24 | 80 | NT5E_chr6_85445083_85500784 | NT5E | MCPRA others(569): Show |
chr6 | 85445083 | 85500784 |
| a0002 | 1/1 | 574 | 72 | 1 | 6 | 53 | 5 | 5 | 42 | NT5E_chr6_85445083_85500784 | NT5E | MCPRA others(569): Show |
chr6 | 85445083 | 85500784 |
| a0003 | 0/0 | 574 | 46 | 31 | 3 | 11 | 0 | 1 | 8 | NT5E_chr6_85445083_85500784 | NT5E | MCPRA others(569): Show |
chr6 | 85445083 | 85500784 |
| a0004 | 0/0 | 574 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | MCPRA others(569): Show |
chr6 | 85445083 | 85500784 |
| a0005 | 0/0 | 574 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | MCPRA others(569): Show |
chr6 | 85445083 | 85500784 |
| a0006 | 0/0 | 574 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | MCPRA others(569): Show |
chr6 | 85445083 | 85500784 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1722 | 207 | 41 | 33 | 104 | 5 | 24 | NT5E_chr6_85445083_85500784 | NT5E | ATGTG others(1717): Show |
chr6 | 85445083 | 85500784 | ||
| a0001c0005 | 0/0 | 1722 | 7 | 7 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | ATGTG others(1717): Show |
chr6 | 85445083 | 85500784 | ||
| a0001c0006 | 0/0 | 1722 | 4 | 4 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | ATGTG others(1717): Show |
chr6 | 85445083 | 85500784 | ||
| a0002c0002 | 1/1 | 1722 | 72 | 1 | 6 | 53 | 5 | 5 | NT5E_chr6_85445083_85500784 | NT5E | ATGTG others(1717): Show |
chr6 | 85445083 | 85500784 | ||
| a0003c0003 | 0/0 | 1722 | 37 | 31 | 3 | 2 | 0 | 1 | NT5E_chr6_85445083_85500784 | NT5E | ATGTG others(1717): Show |
chr6 | 85445083 | 85500784 | ||
| a0003c0004 | 0/0 | 1722 | 9 | 0 | 0 | 9 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | ATGTG others(1717): Show |
chr6 | 85445083 | 85500784 | ||
| a0004c0007 | 0/0 | 1722 | 3 | 3 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | ATGTG others(1717): Show |
chr6 | 85445083 | 85500784 | ||
| a0005c0008 | 0/0 | 1722 | 2 | 0 | 0 | 0 | 2 | 0 | NT5E_chr6_85445083_85500784 | NT5E | ATGTG others(1717): Show |
chr6 | 85445083 | 85500784 | ||
| a0006c0009 | 0/0 | 1722 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | ATGTG others(1717): Show |
chr6 | 85445083 | 85500784 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3562 | 199 | 39 | 30 | 104 | 5 | 21 | NT5E_chr6_85445083_85500784 | NT5E | ACTCG others(3557): Show |
chr6 | 85445083 | 85500784 |
| a0001c0001t0002 | 0/0 | 3562 | 2 | 0 | 1 | 0 | 0 | 1 | NT5E_chr6_85445083_85500784 | NT5E | ACTCG others(3557): Show |
chr6 | 85445083 | 85500784 |
| a0001c0001t0004 | 0/0 | 3562 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | ACTCG others(3557): Show |
chr6 | 85445083 | 85500784 |
| a0001c0001t0008 | 0/0 | 3562 | 2 | 0 | 0 | 0 | 0 | 2 | NT5E_chr6_85445083_85500784 | NT5E | ACTCG others(3557): Show |
chr6 | 85445083 | 85500784 |
| a0001c0001t0012 | 0/0 | 3562 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | ACTCG others(3557): Show |
chr6 | 85445083 | 85500784 |
| a0001c0001t0013 | 0/0 | 3562 | 1 | 0 | 1 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | ACTCG others(3557): Show |
chr6 | 85445083 | 85500784 |
| a0001c0001t0014 | 0/0 | 3562 | 1 | 0 | 1 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | ACTCG others(3557): Show |
chr6 | 85445083 | 85500784 |
| a0001c0005t0001 | 0/0 | 3562 | 3 | 3 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | ACTCG others(3557): Show |
chr6 | 85445083 | 85500784 |
| a0001c0005t0004 | 0/0 | 3562 | 4 | 4 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | ACTCG others(3557): Show |
chr6 | 85445083 | 85500784 |
| a0001c0006t0001 | 0/0 | 3562 | 2 | 2 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | ACTCG others(3557): Show |
chr6 | 85445083 | 85500784 |
| a0001c0006t0009 | 0/0 | 3562 | 2 | 2 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | ACTCG others(3557): Show |
chr6 | 85445083 | 85500784 |
| a0002c0002t0002 | 1/1 | 3562 | 70 | 1 | 6 | 51 | 5 | 5 | NT5E_chr6_85445083_85500784 | NT5E | ACTCG others(3557): Show |
chr6 | 85445083 | 85500784 |
| a0002c0002t0007 | 0/0 | 3562 | 2 | 0 | 0 | 2 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | ACTCG others(3557): Show |
chr6 | 85445083 | 85500784 |
| a0003c0003t0001 | 0/0 | 3562 | 10 | 10 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | ACTCG others(3557): Show |
chr6 | 85445083 | 85500784 |
| a0003c0003t0003 | 0/0 | 3557 | 16 | 12 | 1 | 2 | 0 | 1 | NT5E_chr6_85445083_85500784 | NT5E | ACTCG others(3552): Show |
chr6 | 85445083 | 85500784 |
| a0003c0003t0005 | 0/0 | 3557 | 3 | 3 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | ACTCG others(3552): Show |
chr6 | 85445083 | 85500784 |
| a0003c0003t0006 | 0/0 | 3562 | 3 | 3 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | ACTCG others(3557): Show |
chr6 | 85445083 | 85500784 |
| a0003c0003t0010 | 0/0 | 3557 | 2 | 0 | 2 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | ACTCG others(3552): Show |
chr6 | 85445083 | 85500784 |
| a0003c0003t0011 | 0/0 | 3557 | 2 | 2 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | ACTCG others(3552): Show |
chr6 | 85445083 | 85500784 |
| a0003c0003t0015 | 0/0 | 3557 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | ACTCG others(3552): Show |
chr6 | 85445083 | 85500784 |
| a0003c0004t0003 | 0/0 | 3557 | 9 | 0 | 0 | 9 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | ACTCG others(3552): Show |
chr6 | 85445083 | 85500784 |
| a0004c0007t0001 | 0/0 | 3562 | 3 | 3 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | ACTCG others(3557): Show |
chr6 | 85445083 | 85500784 |
| a0005c0008t0001 | 0/0 | 3562 | 2 | 0 | 0 | 0 | 2 | 0 | NT5E_chr6_85445083_85500784 | NT5E | ACTCG others(3557): Show |
chr6 | 85445083 | 85500784 |
| a0006c0009t0001 | 0/0 | 3562 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | ACTCG others(3557): Show |
chr6 | 85445083 | 85500784 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 17 | 3 | 3 | 8 | 1 | 2 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0004 | 0/0 | 15 | 0 | 5 | 7 | 0 | 3 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0005 | 0/0 | 14 | 0 | 2 | 12 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0006 | 0/0 | 11 | 0 | 2 | 8 | 1 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 2 | 0 | 4 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0019 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0008g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0012g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0013g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0001t0014g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0005t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0005t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0005t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0005t0004g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0005t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0006t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0006t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0001c0006t0009g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0002c0002t0002g0001 | 0/0 | 32 | 0 | 2 | 27 | 2 | 1 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0002c0002t0002g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0002c0002t0002g0025 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0002c0002t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0002c0002t0002g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0002c0002t0002g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0002c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0002c0002t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0002c0002t0002g0055 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0002c0002t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0002c0002t0007g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0003c0003t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0003c0003t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0003c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0003c0003t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0003c0003t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0003c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0003c0003t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0003c0003t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0003c0003t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0003c0003t0003g0003 | 0/0 | 9 | 7 | 1 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0003c0003t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0003c0003t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0003c0003t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0003c0003t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0003c0003t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0003c0003t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0003c0003t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0003c0003t0005g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0003c0003t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0003c0003t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0003c0003t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0003c0003t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0003c0003t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0003c0003t0010g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0003c0003t0011g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0003c0003t0015g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0003c0004t0003g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0003c0004t0003g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0004c0007t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0005c0008t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| a0006c0009t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0001 | EUR | GBR | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0025 | EUR | FIN | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | FIN | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG00423 | hp2 | a0003 | c0004 | t0003 | g0010 | EAS | CHS | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG00544 | hp2 | a0003 | c0004 | t0003 | g0003 | EAS | CHS | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0121 | EAS | CHS | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG00639 | hp1 | a0001 | c0001 | t0013 | g0004 | AMR | PUR | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0118 | AMR | PUR | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01070 | hp1 | a0003 | c0003 | t0010 | g0015 | AMR | PUR | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01106 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01109 | hp1 | a0003 | c0003 | t0003 | g0003 | AMR | PUR | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0122 | AMR | PUR | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0135 | AMR | PUR | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0126 | AMR | CLM | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01358 | hp1 | a0001 | c0001 | t0014 | g0098 | AMR | CLM | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | CLM | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | IBS | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0028 | EUR | IBS | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01516 | hp1 | a0005 | c0008 | t0001 | g0022 | EUR | IBS | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0050 | EUR | IBS | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01517 | hp1 | a0005 | c0008 | t0001 | g0022 | EUR | IBS | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0028 | EUR | IBS | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01884 | hp1 | a0003 | c0003 | t0001 | g0040 | AFR | ACB | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01891 | hp1 | a0003 | c0003 | t0003 | g0003 | AFR | ACB | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01934 | hp2 | a0003 | c0003 | t0010 | g0015 | AMR | PEL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02027 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0186 | EAS | KHV | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02074 | hp1 | a0003 | c0004 | t0003 | g0010 | EAS | KHV | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CDX | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CDX | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02258 | hp1 | a0003 | c0003 | t0003 | g0051 | AFR | ACB | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02280 | hp2 | a0003 | c0003 | t0005 | g0148 | AFR | ACB | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0123 | EAS | KHV | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02622 | hp2 | a0003 | c0003 | t0003 | g0003 | AFR | GWD | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02630 | hp1 | a0001 | c0005 | t0001 | g0115 | AFR | GWD | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02630 | hp2 | a0001 | c0005 | t0004 | g0192 | AFR | GWD | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02647 | hp1 | a0003 | c0003 | t0001 | g0141 | AFR | GWD | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02647 | hp2 | a0001 | c0001 | t0012 | g0143 | AFR | GWD | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0053 | SAS | PJL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02818 | hp1 | a0004 | c0007 | t0001 | g0013 | AFR | GWD | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02818 | hp2 | a0003 | c0003 | t0003 | g0045 | AFR | GWD | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02886 | hp1 | a0006 | c0009 | t0001 | g0038 | AFR | GWD | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02895 | hp2 | a0003 | c0003 | t0006 | g0082 | AFR | GWD | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02896 | hp1 | a0001 | c0006 | t0001 | g0185 | AFR | GWD | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02896 | hp2 | a0003 | c0003 | t0003 | g0052 | AFR | GWD | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02897 | hp1 | a0003 | c0003 | t0003 | g0003 | AFR | GWD | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02965 | hp1 | a0003 | c0003 | t0001 | g0037 | AFR | ESN | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02965 | hp2 | a0003 | c0003 | t0006 | g0081 | AFR | ESN | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02970 | hp1 | a0001 | c0006 | t0009 | g0039 | AFR | ESN | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02976 | hp1 | a0001 | c0006 | t0009 | g0039 | AFR | ESN | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02976 | hp2 | a0003 | c0003 | t0001 | g0177 | AFR | ESN | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0056 | SAS | PJL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03041 | hp1 | a0003 | c0003 | t0001 | g0038 | AFR | GWD | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03041 | hp2 | a0003 | c0003 | t0011 | g0016 | AFR | GWD | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03098 | hp1 | a0004 | c0007 | t0001 | g0013 | AFR | MSL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03098 | hp2 | a0003 | c0003 | t0003 | g0003 | AFR | MSL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0116 | AFR | ESN | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03139 | hp1 | a0003 | c0003 | t0003 | g0003 | AFR | ESN | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03195 | hp1 | a0003 | c0003 | t0001 | g0041 | AFR | ESN | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03195 | hp2 | a0004 | c0007 | t0001 | g0013 | AFR | ESN | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03209 | hp1 | a0003 | c0003 | t0003 | g0044 | AFR | MSL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03225 | hp1 | a0003 | c0003 | t0005 | g0149 | AFR | MSL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03225 | hp2 | a0003 | c0003 | t0001 | g0037 | AFR | MSL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03453 | hp1 | a0003 | c0003 | t0011 | g0016 | AFR | MSL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03540 | hp1 | a0003 | c0003 | t0006 | g0158 | AFR | GWD | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03540 | hp2 | a0001 | c0006 | t0001 | g0035 | AFR | GWD | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03579 | hp1 | a0001 | c0005 | t0004 | g0014 | AFR | MSL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03654 | hp1 | a0001 | c0001 | t0008 | g0007 | SAS | PJL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | STU | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03688 | hp2 | a0001 | c0001 | t0008 | g0007 | SAS | STU | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03704 | hp1 | a0002 | c0002 | t0002 | g0027 | SAS | PJL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0027 | SAS | BEB | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG04115 | hp2 | a0003 | c0003 | t0003 | g0047 | SAS | STU | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0129 | SAS | BEB | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | STU | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18522 | hp1 | a0003 | c0003 | t0003 | g0003 | AFR | YRI | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CHB | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHB | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHB | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18906 | hp1 | a0003 | c0003 | t0001 | g0178 | AFR | YRI | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18906 | hp2 | a0003 | c0003 | t0015 | g0003 | AFR | YRI | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0131 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18946 | hp1 | a0002 | c0002 | t0007 | g0001 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18947 | hp1 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18948 | hp1 | a0003 | c0004 | t0003 | g0003 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18961 | hp1 | a0003 | c0004 | t0003 | g0003 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0127 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18965 | hp2 | a0003 | c0004 | t0003 | g0010 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18967 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18968 | hp1 | a0003 | c0004 | t0003 | g0003 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0113 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18974 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0125 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0120 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18984 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18985 | hp2 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0130 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18986 | hp2 | a0003 | c0004 | t0003 | g0003 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18990 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18992 | hp2 | a0003 | c0004 | t0003 | g0003 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18993 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19003 | hp1 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19030 | hp1 | a0001 | c0005 | t0004 | g0014 | AFR | LWK | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19030 | hp2 | a0001 | c0005 | t0001 | g0112 | AFR | LWK | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | LWK | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19043 | hp2 | a0003 | c0003 | t0003 | g0138 | AFR | LWK | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19055 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19064 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19068 | hp1 | a0002 | c0002 | t0007 | g0001 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0128 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19077 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19079 | hp2 | a0003 | c0003 | t0003 | g0133 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19080 | hp2 | a0002 | c0002 | t0002 | g0134 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19082 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0164 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0119 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19240 | hp1 | a0003 | c0003 | t0005 | g0157 | AFR | YRI | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA19240 | hp2 | a0003 | c0003 | t0001 | g0140 | AFR | YRI | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0001 | EUR | TSI | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0001 | SAS | GIH | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | GIH | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02109 | hp1 | a0001 | c0005 | t0004 | g0014 | AFR | ACB | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02559 | hp1 | a0001 | c0005 | t0001 | g0114 | AFR | ACB | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG02559 | hp2 | a0003 | c0003 | t0001 | g0139 | AFR | ACB | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG06807 | hp1 | a0002 | c0002 | t0002 | g0117 | AFR | USA | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | USA | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| NA20300 | hp2 | a0003 | c0003 | t0003 | g0003 | AFR | USA | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0002 | g0055 | REF | REF | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0002 | g0025 | REF | REF | NT5E_chr6_85445083_85500784 | NT5E | chr6 | 85445083 | 85500784 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:85471376 | G | C | 1 | a0006 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.702G>C | p.Arg234Ser | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/9 | 759/3562 | 702/1725 | 234/574 | chr6 | 85471376 | |||
| chr6:85485261 | G | T | 1 | a0005 | 2 | HG01516.hp1 HG01517.hp1 |
missense_variant | MODERATE | c.778G>T | p.Ala260Ser | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 4/9 | 835/3562 | 778/1725 | 260/574 | chr6 | 85485261 | |||
| chr6:85489515 | A | G | 5 | a0001 a0003 a0004 others(2): Show |
270 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(267): Show |
missense_variant | MODERATE | c.1126A>G | p.Thr376Ala | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 6/9 | 1183/3562 | 1126/1725 | 376/574 | chr6 | 85489515 | |||
| chr6:85489525 | T | C | 2 | a0003 a0006 |
47 | HG00423.hp2 HG00544.hp2 HG01070.hp1 others(44): Show |
missense_variant | MODERATE | c.1136T>C | p.Met379Thr | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 6/9 | 1193/3562 | 1136/1725 | 379/574 | chr6 | 85489525 | |||
| chr6:85493867 | A | G | 1 | a0004 | 3 | HG02818.hp1 HG03098.hp1 HG03195.hp2 |
missense_variant | MODERATE | c.1588A>G | p.Thr530Ala | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 9/9 | 1645/3562 | 1588/1725 | 530/574 | chr6 | 85493867 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:85467062 | A | G | 1 | a0001c0006 | 4 | HG02896.hp1 HG02970.hp1 HG02976.hp1 others(1): Show |
splice_region_variant&synonymous_variant | LOW | c.342A>G | p.Ala114Ala | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 2/9 | 399/3562 | 342/1725 | 114/574 | chr6 | 85467062 | |||
| chr6:85467248 | C | T | 1 | a0003c0004 | 9 | HG00423.hp2 HG00544.hp2 HG02074.hp1 others(6): Show |
synonymous_variant | LOW | c.528C>T | p.Tyr176Tyr | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 2/9 | 585/3562 | 528/1725 | 176/574 | chr6 | 85467248 | |||
| chr6:85485380 | C | T | 1 | a0001c0005 | 7 | HG02109.hp1 HG02559.hp1 HG02630.hp1 others(4): Show |
synonymous_variant | LOW | c.897C>T | p.Asn299Asn | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 4/9 | 954/3562 | 897/1725 | 299/574 | chr6 | 85485380 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:85494085 | T | G | 1 | a0002c0002t0007 | 2 | NA18946.hp1 NA19068.hp1 |
3_prime_UTR_variant | MODIFIER | c.*81T>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 9/9 | 81 | chr6 | 85494085 | ||||||
| chr6:85494245 | C | T | 5 | a0003c0003t0003 a0003c0003t0010 a0003c0003t0011 others(2): Show |
30 | HG00423.hp2 HG00544.hp2 HG01070.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*241C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 9/9 | 241 | chr6 | 85494245 | ||||||
| chr6:85494431 | C | T | 1 | a0003c0003t0006 | 3 | HG02895.hp2 HG02965.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*427C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 9/9 | 427 | chr6 | 85494431 | ||||||
| chr6:85494537 | C | G | 1 | a0003c0003t0015 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*533C>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 9/9 | 533 | chr6 | 85494537 | ||||||
| chr6:85494927 | C | A | 1 | a0003c0003t0010 | 2 | HG01070.hp1 HG01934.hp2 |
3_prime_UTR_variant | MODIFIER | c.*923C>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 9/9 | 923 | chr6 | 85494927 | ||||||
| chr6:85494938 | GTTATT | G | 6 | a0003c0003t0003 a0003c0003t0005 a0003c0003t0010 others(3): Show |
33 | HG00423.hp2 HG00544.hp2 HG01070.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*939_*943delTTTAT | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 9/9 | 939 | INFO_REALIGN_3_PRIME | chr6 | 85494938 | |||||
| chr6:85495030 | A | G | 1 | a0001c0006t0009 | 2 | HG02970.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1026A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 9/9 | 1026 | chr6 | 85495030 | ||||||
| chr6:85495099 | C | T | 1 | a0001c0001t0008 | 2 | HG03654.hp1 HG03688.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1095C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 9/9 | 1095 | chr6 | 85495099 | ||||||
| chr6:85495189 | A | T | 1 | a0003c0003t0006 | 3 | HG02895.hp2 HG02965.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1185A>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 9/9 | 1185 | chr6 | 85495189 | ||||||
| chr6:85495200 | T | C | 1 | a0001c0001t0012 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1196T>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 9/9 | 1196 | chr6 | 85495200 | ||||||
| chr6:85495239 | A | T | 1 | a0001c0001t0014 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1235A>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 9/9 | 1235 | chr6 | 85495239 | ||||||
| chr6:85495605 | T | G | 21 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(18): Show |
268 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(265): Show |
3_prime_UTR_variant | MODIFIER | c.*1601T>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 9/9 | 1601 | chr6 | 85495605 | ||||||
| chr6:85495615 | G | T | 1 | a0001c0001t0013 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1611G>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 9/9 | 1611 | chr6 | 85495615 | ||||||
| chr6:85495657 | A | G | 2 | a0001c0001t0004 a0001c0005t0004 |
5 | HG02109.hp1 HG02630.hp2 HG03130.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1653A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 9/9 | 1653 | chr6 | 85495657 | ||||||
| chr6:85495673 | G | T | 1 | a0003c0003t0011 | 2 | HG03041.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1669G>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 9/9 | 1669 | chr6 | 85495673 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:85450491 | C | T | 2 | a0001c0005t0004g0014 a0001c0005t0004g0192 |
4 | HG02109.hp1 HG02630.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.339+13C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85450491 | |||||||
| chr6:85450499 | C | G | 1 | a0001c0001t0001g0191 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.339+21C>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85450499 | |||||||
| chr6:85450500 | G | C | 1 | a0001c0001t0001g0191 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.339+22G>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85450500 | |||||||
| chr6:85450581 | G | A | 2 | a0003c0003t0001g0040 a0003c0003t0001g0041 |
2 | HG01884.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.339+103G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85450581 | |||||||
| chr6:85450739 | A | G | 3 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 |
3 | HG02809.hp2 HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.339+261A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85450739 | |||||||
| chr6:85450861 | G | A | 4 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0003c0003t0003g0044 others(1): Show |
4 | HG02145.hp2 HG02486.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.339+383G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85450861 | |||||||
| chr6:85450869 | CTTTATCT others(8): Show |
C | 1 | a0001c0001t0001g0046 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.339+394_339+408del others(15): Show |
NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr6 | 85450869 | ||||||
| chr6:85450985 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.339+507C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85450985 | |||||||
| chr6:85451029 | C | T | 1 | a0002c0002t0002g0186 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.339+551C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85451029 | |||||||
| chr6:85451221 | G | GGAAA | 17 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(14): Show |
36 | HG00423.hp2 HG00544.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.339+758_339+761dup others(4): Show |
NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr6 | 85451221 | ||||||
| chr6:85451488 | A | G | 2 | a0001c0006t0001g0185 a0001c0006t0009g0039 |
3 | HG02896.hp1 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.339+1010A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85451488 | |||||||
| chr6:85451551 | A | G | 61 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(58): Show |
94 | HG00423.hp1 HG00735.hp2 HG01109.hp2 others(91): Show |
intron_variant | MODIFIER | c.339+1073A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85451551 | |||||||
| chr6:85451703 | G | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG01891.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.339+1225G>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85451703 | |||||||
| chr6:85451749 | A | G | 1 | a0001c0001t0001g0182 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.339+1271A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85451749 | |||||||
| chr6:85451751 | A | C | 5 | a0001c0001t0001g0142 a0001c0001t0001g0188 a0001c0001t0001g0189 others(2): Show |
5 | HG02647.hp2 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.339+1273A>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85451751 | |||||||
| chr6:85452016 | G | C | 2 | a0003c0003t0001g0040 a0003c0003t0001g0041 |
2 | HG01884.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.339+1538G>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85452016 | |||||||
| chr6:85452017 | T | A | 2 | a0003c0003t0001g0040 a0003c0003t0001g0041 |
2 | HG01884.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.339+1539T>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85452017 | |||||||
| chr6:85452088 | G | A | 2 | a0001c0001t0001g0057 a0002c0002t0002g0056 |
2 | HG03017.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.339+1610G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85452088 | |||||||
| chr6:85452283 | A | G | 1 | a0001c0001t0012g0143 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.339+1805A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85452283 | |||||||
| chr6:85452622 | C | G | 4 | a0003c0003t0001g0139 a0003c0003t0001g0140 a0003c0003t0001g0141 others(1): Show |
4 | HG02559.hp2 HG02647.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.339+2144C>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85452622 | |||||||
| chr6:85452658 | A | G | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | NA18943.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.339+2180A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85452658 | |||||||
| chr6:85453095 | C | G | 1 | a0001c0001t0001g0137 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.339+2617C>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85453095 | |||||||
| chr6:85453150 | G | A | 73 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(70): Show |
125 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.339+2672G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85453150 | |||||||
| chr6:85453229 | G | T | 1 | a0001c0001t0001g0179 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.339+2751G>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85453229 | |||||||
| chr6:85453361 | A | G | 5 | a0001c0001t0001g0142 a0001c0001t0001g0188 a0001c0001t0001g0189 others(2): Show |
5 | HG02647.hp2 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.339+2883A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85453361 | |||||||
| chr6:85453462 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.339+2984C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85453462 | |||||||
| chr6:85453494 | C | A | 17 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(14): Show |
36 | HG00423.hp2 HG00544.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.339+3016C>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85453494 | |||||||
| chr6:85453509 | C | T | 25 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(22): Show |
45 | HG00423.hp2 HG00544.hp2 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.339+3031C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85453509 | |||||||
| chr6:85453667 | G | T | 2 | a0001c0005t0004g0014 a0001c0005t0004g0192 |
4 | HG02109.hp1 HG02630.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.339+3189G>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85453667 | |||||||
| chr6:85453825 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.339+3347A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85453825 | |||||||
| chr6:85454005 | T | C | 6 | a0001c0001t0001g0142 a0001c0001t0001g0144 a0001c0001t0001g0188 others(3): Show |
6 | HG01109.hp2 HG02647.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.339+3527T>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85454005 | |||||||
| chr6:85454260 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.339+3782C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85454260 | |||||||
| chr6:85454268 | C | G | 1 | a0003c0003t0001g0178 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.339+3790C>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85454268 | |||||||
| chr6:85454298 | A | T | 4 | a0003c0003t0001g0037 a0003c0003t0001g0038 a0003c0003t0001g0177 others(1): Show |
5 | HG02886.hp1 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.339+3820A>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85454298 | |||||||
| chr6:85454325 | G | A | 4 | a0003c0003t0001g0139 a0003c0003t0001g0140 a0003c0003t0001g0141 others(1): Show |
4 | HG02559.hp2 HG02647.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.339+3847G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85454325 | |||||||
| chr6:85454413 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.339+3935T>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85454413 | |||||||
| chr6:85454443 | T | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
7 | HG02257.hp1 HG02717.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.339+3965T>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85454443 | |||||||
| chr6:85454865 | T | C | 1 | a0001c0005t0001g0112 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.339+4387T>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85454865 | |||||||
| chr6:85455078 | GAGTTATG others(11): Show |
G | 1 | a0002c0002t0002g0113 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.339+4603_339+4620d others(20): Show |
NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr6 | 85455078 | ||||||
| chr6:85455346 | A | G | 5 | a0001c0001t0001g0142 a0001c0001t0001g0188 a0001c0001t0001g0189 others(2): Show |
5 | HG02647.hp2 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.339+4868A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85455346 | |||||||
| chr6:85455516 | C | T | 1 | a0001c0005t0001g0112 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.339+5038C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85455516 | |||||||
| chr6:85455656 | C | G | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.339+5178C>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85455656 | |||||||
| chr6:85455672 | C | T | 3 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0002c0002t0002g0055 |
3 | HG01433.hp1 HG02698.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.339+5194C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85455672 | |||||||
| chr6:85455687 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.339+5209C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85455687 | |||||||
| chr6:85455700 | A | G | 2 | a0003c0003t0003g0044 a0003c0003t0003g0045 |
2 | HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.339+5222A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85455700 | |||||||
| chr6:85455749 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.339+5271G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85455749 | |||||||
| chr6:85455822 | T | A | 169 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(166): Show |
273 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(270): Show |
intron_variant | MODIFIER | c.339+5344T>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85455822 | |||||||
| chr6:85455824 | C | T | 18 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(15): Show |
37 | HG00423.hp2 HG00544.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.339+5346C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85455824 | |||||||
| chr6:85455913 | A | G | 75 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(72): Show |
127 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.339+5435A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85455913 | |||||||
| chr6:85456084 | C | T | 15 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(12): Show |
32 | HG00423.hp2 HG00544.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.339+5606C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85456084 | |||||||
| chr6:85456124 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.339+5646C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85456124 | |||||||
| chr6:85456142 | A | T | 1 | a0001c0001t0001g0184 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.339+5664A>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85456142 | |||||||
| chr6:85456314 | A | G | 1 | a0001c0001t0001g0175 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.339+5836A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85456314 | |||||||
| chr6:85456357 | A | G | 1 | a0001c0001t0004g0116 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.339+5879A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85456357 | |||||||
| chr6:85456365 | G | T | 1 | a0001c0001t0001g0109 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.339+5887G>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85456365 | |||||||
| chr6:85456425 | A | G | 2 | a0001c0005t0004g0014 a0001c0005t0004g0192 |
4 | HG02109.hp1 HG02630.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.339+5947A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85456425 | |||||||
| chr6:85456505 | T | G | 4 | a0003c0003t0001g0037 a0003c0003t0001g0038 a0003c0003t0001g0177 others(1): Show |
5 | HG02886.hp1 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.339+6027T>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85456505 | |||||||
| chr6:85456615 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.339+6137C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85456615 | |||||||
| chr6:85456760 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.339+6282G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85456760 | |||||||
| chr6:85456786 | T | C | 1 | a0003c0003t0001g0040 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.339+6308T>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85456786 | |||||||
| chr6:85456807 | G | T | 1 | a0001c0001t0001g0109 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.339+6329G>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85456807 | |||||||
| chr6:85457019 | C | G | 2 | a0003c0003t0001g0040 a0003c0003t0001g0041 |
2 | HG01884.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.339+6541C>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85457019 | |||||||
| chr6:85457091 | A | G | 7 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0005t0001g0112 others(4): Show |
7 | HG02145.hp2 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.339+6613A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85457091 | |||||||
| chr6:85457182 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.339+6704G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85457182 | |||||||
| chr6:85457305 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.339+6827C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85457305 | |||||||
| chr6:85457325 | C | T | 196 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(193): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(335): Show |
intron_variant | MODIFIER | c.339+6847C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85457325 | |||||||
| chr6:85457399 | T | C | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG01891.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.339+6921T>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85457399 | |||||||
| chr6:85457414 | C | T | 4 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(1): Show |
4 | HG02647.hp2 HG02809.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.339+6936C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85457414 | |||||||
| chr6:85457565 | C | A | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.339+7087C>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85457565 | |||||||
| chr6:85457747 | T | G | 1 | a0001c0001t0001g0152 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.339+7269T>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85457747 | |||||||
| chr6:85458025 | G | A | 1 | a0003c0003t0003g0047 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.339+7547G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85458025 | |||||||
| chr6:85458200 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.339+7722G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85458200 | |||||||
| chr6:85458391 | T | C | 4 | a0003c0003t0001g0037 a0003c0003t0001g0038 a0003c0003t0001g0177 others(1): Show |
5 | HG02886.hp1 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.339+7913T>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85458391 | |||||||
| chr6:85458504 | A | C | 1 | a0001c0001t0001g0150 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.339+8026A>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85458504 | |||||||
| chr6:85458546 | C | T | 15 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 others(12): Show |
34 | HG00099.hp1 HG00280.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.339+8068C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85458546 | |||||||
| chr6:85458547 | G | A | 20 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(17): Show |
36 | HG00423.hp2 HG00544.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.339+8069G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85458547 | |||||||
| chr6:85458583 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.339+8105C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85458583 | |||||||
| chr6:85458811 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.340-8249G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85458811 | |||||||
| chr6:85458816 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.340-8244C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85458816 | |||||||
| chr6:85458856 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.340-8204C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85458856 | |||||||
| chr6:85458903 | G | A | 3 | a0001c0001t0001g0147 a0003c0003t0001g0040 a0003c0003t0001g0041 |
3 | HG01884.hp1 HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.340-8157G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85458903 | |||||||
| chr6:85459142 | C | CAG | 5 | a0001c0001t0001g0150 a0001c0001t0004g0116 a0003c0003t0001g0139 others(2): Show |
5 | HG02280.hp2 HG02559.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.340-7905_340-7904d others(4): Show |
NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr6 | 85459142 | ||||||
| chr6:85459296 | T | C | 4 | a0003c0003t0001g0037 a0003c0003t0001g0038 a0003c0003t0001g0177 others(1): Show |
5 | HG02886.hp1 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.340-7764T>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85459296 | |||||||
| chr6:85459300 | T | G | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.340-7760T>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85459300 | |||||||
| chr6:85459487 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.340-7573G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85459487 | |||||||
| chr6:85459872 | C | T | 8 | a0001c0001t0001g0147 a0003c0003t0001g0037 a0003c0003t0001g0038 others(5): Show |
9 | HG01884.hp1 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.340-7188C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85459872 | |||||||
| chr6:85459919 | A | G | 15 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(12): Show |
31 | HG00423.hp2 HG00544.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.340-7141A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85459919 | |||||||
| chr6:85460153 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.340-6907G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85460153 | |||||||
| chr6:85460254 | C | A | 1 | a0001c0001t0001g0061 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.340-6806C>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85460254 | |||||||
| chr6:85460450 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.340-6610A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85460450 | |||||||
| chr6:85460507 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.340-6553G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85460507 | |||||||
| chr6:85460533 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.340-6527T>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85460533 | |||||||
| chr6:85460711 | A | C | 1 | a0001c0001t0014g0098 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.340-6349A>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85460711 | |||||||
| chr6:85460772 | T | G | 4 | a0003c0003t0001g0037 a0003c0003t0001g0038 a0003c0003t0001g0177 others(1): Show |
5 | HG02886.hp1 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.340-6288T>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85460772 | |||||||
| chr6:85460934 | G | A | 1 | a0001c0005t0001g0112 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.340-6126G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85460934 | |||||||
| chr6:85461085 | A | G | 1 | a0002c0002t0002g0031 | 2 | NA18947.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.340-5975A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85461085 | |||||||
| chr6:85461231 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.340-5829A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85461231 | |||||||
| chr6:85461307 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.340-5753A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85461307 | |||||||
| chr6:85461432 | C | G | 3 | a0001c0001t0001g0147 a0003c0003t0001g0040 a0003c0003t0001g0041 |
3 | HG01884.hp1 HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.340-5628C>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85461432 | |||||||
| chr6:85461473 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0005t0001g0112 |
3 | HG02145.hp2 HG02486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.340-5587C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85461473 | |||||||
| chr6:85461762 | G | A | 1 | a0001c0005t0001g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.340-5298G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85461762 | |||||||
| chr6:85461939 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.340-5121G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85461939 | |||||||
| chr6:85461985 | A | G | 1 | a0001c0005t0004g0192 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.340-5075A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85461985 | |||||||
| chr6:85462058 | C | T | 3 | a0003c0003t0003g0044 a0003c0003t0003g0045 a0003c0003t0011g0016 |
4 | HG02818.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.340-5002C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85462058 | |||||||
| chr6:85462185 | T | C | 1 | a0002c0002t0002g0119 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.340-4875T>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85462185 | |||||||
| chr6:85462225 | A | G | 21 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(18): Show |
40 | HG00423.hp2 HG00544.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.340-4835A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85462225 | |||||||
| chr6:85462520 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.340-4540G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85462520 | |||||||
| chr6:85462614 | T | A | 1 | a0001c0001t0001g0049 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.340-4446T>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85462614 | |||||||
| chr6:85462686 | A | C | 21 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(18): Show |
40 | HG00423.hp2 HG00544.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.340-4374A>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85462686 | |||||||
| chr6:85462734 | C | T | 30 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(27): Show |
50 | HG00423.hp2 HG00544.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.340-4326C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85462734 | |||||||
| chr6:85462859 | C | T | 3 | a0001c0001t0001g0060 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | HG02615.hp2 HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.340-4201C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85462859 | |||||||
| chr6:85463002 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.340-4058A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85463002 | |||||||
| chr6:85463156 | C | T | 1 | a0001c0001t0004g0116 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.340-3904C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85463156 | |||||||
| chr6:85463307 | A | C | 5 | a0003c0003t0001g0037 a0003c0003t0001g0038 a0003c0003t0001g0177 others(2): Show |
6 | HG02886.hp1 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.340-3753A>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85463307 | |||||||
| chr6:85463318 | G | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.340-3742G>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85463318 | |||||||
| chr6:85463386 | G | A | 8 | a0001c0001t0001g0147 a0003c0003t0001g0037 a0003c0003t0001g0038 others(5): Show |
9 | HG01884.hp1 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.340-3674G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85463386 | |||||||
| chr6:85463402 | C | A | 2 | a0001c0005t0004g0014 a0001c0005t0004g0192 |
4 | HG02109.hp1 HG02630.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.340-3658C>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85463402 | |||||||
| chr6:85463651 | T | A | 1 | a0003c0003t0011g0016 | 2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.340-3409T>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85463651 | |||||||
| chr6:85463684 | C | T | 1 | a0003c0003t0003g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.340-3376C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85463684 | |||||||
| chr6:85464024 | TG | T | 3 | a0001c0001t0001g0049 a0003c0003t0003g0047 a0003c0003t0010g0015 |
4 | HG01070.hp1 HG01358.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.340-3035delG | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85464024 | |||||||
| chr6:85464067 | A | AT | 49 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(46): Show |
96 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.340-2967dupT | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr6 | 85464067 | ||||||
| chr6:85464067 | A | ATT | 18 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0057 others(15): Show |
21 | HG00597.hp2 HG00741.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.340-2968_340-2967d others(4): Show |
NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr6 | 85464067 | ||||||
| chr6:85464067 | AT | A | 69 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(66): Show |
137 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.340-2967delT | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr6 | 85464067 | ||||||
| chr6:85464067 | ATT | A | 6 | a0001c0001t0001g0136 a0001c0001t0001g0169 a0001c0001t0001g0175 others(3): Show |
7 | HG03041.hp2 HG03453.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.340-2968_340-2967d others(4): Show |
NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr6 | 85464067 | ||||||
| chr6:85464067 | ATTT | A | 24 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(21): Show |
43 | HG00423.hp2 HG00544.hp2 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.340-2969_340-2967d others(5): Show |
NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr6 | 85464067 | ||||||
| chr6:85464138 | A | G | 3 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0137 |
3 | HG01243.hp1 HG02257.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.340-2922A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85464138 | |||||||
| chr6:85464250 | C | T | 2 | a0001c0005t0001g0114 a0001c0005t0001g0115 |
2 | HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.340-2810C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85464250 | |||||||
| chr6:85464277 | A | G | 1 | a0002c0002t0002g0119 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.340-2783A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85464277 | |||||||
| chr6:85464326 | C | T | 18 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(15): Show |
35 | HG00423.hp2 HG00544.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.340-2734C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85464326 | |||||||
| chr6:85464482 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.340-2578G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85464482 | |||||||
| chr6:85464515 | G | C | 1 | a0003c0003t0001g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.340-2545G>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85464515 | |||||||
| chr6:85464525 | A | G | 2 | a0003c0003t0001g0040 a0003c0003t0001g0041 |
2 | HG01884.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.340-2535A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85464525 | |||||||
| chr6:85464669 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.340-2391A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85464669 | |||||||
| chr6:85464732 | G | A | 18 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(15): Show |
35 | HG00423.hp2 HG00544.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.340-2328G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85464732 | |||||||
| chr6:85464898 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.340-2162A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85464898 | |||||||
| chr6:85464975 | G | A | 1 | a0003c0003t0011g0016 | 2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.340-2085G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85464975 | |||||||
| chr6:85465052 | C | T | 1 | a0001c0001t0014g0098 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.340-2008C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85465052 | |||||||
| chr6:85465127 | A | C | 159 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
262 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(259): Show |
intron_variant | MODIFIER | c.340-1933A>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85465127 | |||||||
| chr6:85465127 | A | G | 8 | a0001c0001t0001g0147 a0003c0003t0001g0037 a0003c0003t0001g0038 others(5): Show |
9 | HG01884.hp1 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.340-1933A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85465127 | |||||||
| chr6:85465142 | C | T | 18 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(15): Show |
35 | HG00423.hp2 HG00544.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.340-1918C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85465142 | |||||||
| chr6:85465147 | G | A | 2 | a0001c0005t0004g0014 a0001c0005t0004g0192 |
4 | HG02109.hp1 HG02630.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.340-1913G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85465147 | |||||||
| chr6:85465393 | A | G | 8 | a0001c0001t0001g0147 a0003c0003t0001g0037 a0003c0003t0001g0038 others(5): Show |
9 | HG01884.hp1 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.340-1667A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85465393 | |||||||
| chr6:85465422 | A | T | 1 | a0002c0002t0002g0134 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.340-1638A>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85465422 | |||||||
| chr6:85465481 | G | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG02071.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.340-1579G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85465481 | |||||||
| chr6:85465662 | T | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0087 |
2 | NA18984.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.340-1398T>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85465662 | |||||||
| chr6:85465718 | G | A | 8 | a0001c0001t0001g0147 a0003c0003t0001g0037 a0003c0003t0001g0038 others(5): Show |
9 | HG01884.hp1 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.340-1342G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85465718 | |||||||
| chr6:85465834 | G | C | 1 | a0001c0001t0001g0147 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.340-1226G>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85465834 | |||||||
| chr6:85465855 | G | C | 1 | a0003c0003t0003g0044 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.340-1205G>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85465855 | |||||||
| chr6:85465856 | G | A | 69 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(66): Show |
121 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.340-1204G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85465856 | |||||||
| chr6:85465968 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.340-1092G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85465968 | |||||||
| chr6:85465996 | G | T | 1 | a0001c0001t0001g0080 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.340-1064G>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85465996 | |||||||
| chr6:85466079 | G | A | 2 | a0003c0003t0001g0037 a0003c0003t0001g0177 |
3 | HG02965.hp1 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.340-981G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85466079 | |||||||
| chr6:85466174 | C | A | 17 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0001c0001t0001g0151 others(14): Show |
29 | HG00735.hp2 HG01884.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.340-886C>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85466174 | |||||||
| chr6:85466194 | G | A | 4 | a0003c0003t0001g0037 a0003c0003t0001g0038 a0003c0003t0001g0177 others(1): Show |
5 | HG02886.hp1 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.340-866G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85466194 | |||||||
| chr6:85466238 | A | G | 19 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(16): Show |
36 | HG00423.hp2 HG00544.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.340-822A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85466238 | |||||||
| chr6:85466278 | A | C | 1 | a0001c0001t0001g0175 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.340-782A>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85466278 | |||||||
| chr6:85466288 | C | G | 1 | a0001c0001t0001g0057 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.340-772C>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85466288 | |||||||
| chr6:85466377 | C | T | 1 | a0001c0001t0001g0021 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.340-683C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85466377 | |||||||
| chr6:85466656 | G | C | 2 | a0001c0001t0001g0069 a0001c0001t0001g0085 |
2 | HG01943.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.340-404G>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85466656 | |||||||
| chr6:85466693 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.340-367G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85466693 | |||||||
| chr6:85466776 | A | T | 1 | a0001c0001t0001g0105 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.340-284A>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85466776 | |||||||
| chr6:85466794 | T | C | 3 | a0003c0003t0003g0044 a0003c0003t0003g0045 a0003c0003t0011g0016 |
4 | HG02818.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.340-266T>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85466794 | |||||||
| chr6:85466829 | C | T | 5 | a0001c0001t0001g0142 a0001c0001t0001g0189 a0001c0001t0001g0190 others(2): Show |
5 | HG02647.hp2 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.340-231C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85466829 | |||||||
| chr6:85466907 | G | A | 28 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(25): Show |
48 | HG00423.hp2 HG00544.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.340-153G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85466907 | |||||||
| chr6:85467034 | C | G | 1 | a0001c0001t0001g0101 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.340-26C>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85467034 | |||||||
| chr6:85467046 | T | C | 1 | a0002c0002t0002g0135 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.340-14T>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 1/8 | chr6 | 85467046 | |||||||
| chr6:85467335 | C | T | 5 | a0001c0001t0001g0142 a0001c0001t0001g0189 a0001c0001t0001g0190 others(2): Show |
5 | HG02647.hp2 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.562+53C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 2/8 | chr6 | 85467335 | |||||||
| chr6:85467572 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.562+290G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 2/8 | chr6 | 85467572 | |||||||
| chr6:85467651 | G | A | 16 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0001c0001t0001g0151 others(13): Show |
28 | HG00735.hp2 HG02818.hp1 HG03017.hp1 others(25): Show |
intron_variant | MODIFIER | c.562+369G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 2/8 | chr6 | 85467651 | |||||||
| chr6:85467846 | A | G | 2 | a0001c0001t0001g0024 a0005c0008t0001g0022 |
4 | HG01175.hp2 HG01243.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.562+564A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 2/8 | chr6 | 85467846 | |||||||
| chr6:85468256 | G | A | 2 | a0001c0005t0004g0014 a0001c0005t0004g0192 |
4 | HG02109.hp1 HG02630.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.562+974G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 2/8 | chr6 | 85468256 | |||||||
| chr6:85468262 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.562+980G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 2/8 | chr6 | 85468262 | |||||||
| chr6:85468454 | C | T | 1 | a0001c0005t0004g0014 | 3 | HG02109.hp1 HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.562+1172C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 2/8 | chr6 | 85468454 | |||||||
| chr6:85468606 | G | T | 51 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0029 others(48): Show |
81 | HG00408.hp1 HG00423.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.562+1324G>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 2/8 | chr6 | 85468606 | |||||||
| chr6:85468656 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.562+1374T>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 2/8 | chr6 | 85468656 | |||||||
| chr6:85468786 | G | T | 1 | a0001c0001t0001g0067 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.562+1504G>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 2/8 | chr6 | 85468786 | |||||||
| chr6:85468792 | G | A | 2 | a0002c0002t0002g0120 a0002c0002t0002g0121 |
2 | HG00609.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.562+1510G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 2/8 | chr6 | 85468792 | |||||||
| chr6:85468944 | G | T | 16 | a0001c0001t0001g0049 a0001c0001t0002g0053 a0001c0001t0002g0054 others(13): Show |
33 | HG00423.hp2 HG00544.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.562+1662G>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 2/8 | chr6 | 85468944 | |||||||
| chr6:85468949 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.562+1667G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 2/8 | chr6 | 85468949 | |||||||
| chr6:85469037 | A | C | 1 | a0001c0001t0001g0042 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.562+1755A>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 2/8 | chr6 | 85469037 | |||||||
| chr6:85469192 | T | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.562+1910T>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 2/8 | chr6 | 85469192 | |||||||
| chr6:85469268 | C | G | 4 | a0001c0001t0001g0150 a0003c0003t0001g0139 a0003c0003t0005g0148 others(1): Show |
4 | HG02280.hp2 HG02559.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.563-1969C>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 2/8 | chr6 | 85469268 | |||||||
| chr6:85469388 | T | C | 8 | a0001c0001t0001g0147 a0003c0003t0001g0037 a0003c0003t0001g0038 others(5): Show |
9 | HG01884.hp1 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.563-1849T>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 2/8 | chr6 | 85469388 | |||||||
| chr6:85469493 | G | A | 1 | a0003c0003t0005g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.563-1744G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 2/8 | chr6 | 85469493 | |||||||
| chr6:85469688 | A | G | 102 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(99): Show |
175 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.563-1549A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 2/8 | chr6 | 85469688 | |||||||
| chr6:85470117 | T | C | 17 | a0001c0001t0001g0049 a0001c0001t0002g0053 a0001c0001t0002g0054 others(14): Show |
34 | HG00423.hp2 HG00544.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.563-1120T>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 2/8 | chr6 | 85470117 | |||||||
| chr6:85470148 | C | A | 5 | a0001c0001t0001g0142 a0001c0001t0001g0189 a0001c0001t0001g0190 others(2): Show |
5 | HG02647.hp2 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.563-1089C>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 2/8 | chr6 | 85470148 | |||||||
| chr6:85470458 | T | A | 1 | a0003c0003t0011g0016 | 2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.563-779T>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 2/8 | chr6 | 85470458 | |||||||
| chr6:85470532 | C | G | 2 | a0003c0003t0001g0040 a0003c0003t0001g0041 |
2 | HG01884.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.563-705C>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 2/8 | chr6 | 85470532 | |||||||
| chr6:85470536 | C | T | 1 | a0002c0002t0002g0131 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.563-701C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 2/8 | chr6 | 85470536 | |||||||
| chr6:85470582 | C | G | 1 | a0002c0002t0002g0130 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.563-655C>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 2/8 | chr6 | 85470582 | |||||||
| chr6:85470860 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.563-377G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 2/8 | chr6 | 85470860 | |||||||
| chr6:85470954 | A | G | 1 | a0001c0001t0001g0059 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.563-283A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 2/8 | chr6 | 85470954 | |||||||
| chr6:85471014 | A | C | 79 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(76): Show |
134 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.563-223A>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 2/8 | chr6 | 85471014 | |||||||
| chr6:85471043 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.563-194T>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 2/8 | chr6 | 85471043 | |||||||
| chr6:85471208 | A | G | 80 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(77): Show |
135 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.563-29A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 2/8 | chr6 | 85471208 | |||||||
| chr6:85471749 | T | A | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.751+324T>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85471749 | |||||||
| chr6:85471848 | A | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.751+423A>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85471848 | |||||||
| chr6:85471959 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.751+534G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85471959 | |||||||
| chr6:85472100 | G | T | 1 | a0002c0002t0002g0129 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.751+675G>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85472100 | |||||||
| chr6:85472125 | C | A | 1 | a0001c0001t0001g0175 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.751+700C>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85472125 | |||||||
| chr6:85472130 | A | G | 3 | a0003c0003t0003g0044 a0003c0003t0003g0045 a0003c0003t0011g0016 |
4 | HG02818.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.751+705A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85472130 | |||||||
| chr6:85472153 | A | C | 1 | a0001c0001t0001g0162 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.751+728A>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85472153 | |||||||
| chr6:85472213 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(91): Show |
166 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.751+788A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85472213 | |||||||
| chr6:85472470 | T | C | 1 | a0002c0002t0002g0122 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.751+1045T>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85472470 | |||||||
| chr6:85472808 | A | C | 5 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0005t0001g0112 others(2): Show |
5 | HG02145.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.751+1383A>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85472808 | |||||||
| chr6:85472919 | G | T | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.751+1494G>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85472919 | |||||||
| chr6:85472923 | G | A | 1 | a0002c0002t0002g0123 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.751+1498G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85472923 | |||||||
| chr6:85472961 | A | C | 1 | a0001c0001t0001g0092 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.751+1536A>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85472961 | |||||||
| chr6:85473050 | T | C | 8 | a0001c0001t0001g0147 a0003c0003t0001g0037 a0003c0003t0001g0038 others(5): Show |
9 | HG01884.hp1 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.751+1625T>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85473050 | |||||||
| chr6:85473104 | G | C | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.751+1679G>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85473104 | |||||||
| chr6:85473269 | G | A | 5 | a0003c0003t0001g0037 a0003c0003t0001g0038 a0003c0003t0001g0177 others(2): Show |
6 | HG02886.hp1 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.751+1844G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85473269 | |||||||
| chr6:85473287 | C | A | 13 | a0001c0001t0001g0049 a0001c0001t0002g0053 a0001c0001t0002g0054 others(10): Show |
29 | HG00423.hp2 HG00544.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.751+1862C>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85473287 | |||||||
| chr6:85473303 | A | T | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.751+1878A>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85473303 | |||||||
| chr6:85473305 | G | T | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.751+1880G>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85473305 | |||||||
| chr6:85473350 | G | A | 5 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0005t0001g0112 others(2): Show |
5 | HG02145.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.751+1925G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85473350 | |||||||
| chr6:85473375 | A | G | 1 | a0001c0001t0001g0059 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.751+1950A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85473375 | |||||||
| chr6:85473413 | A | G | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.751+1988A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85473413 | |||||||
| chr6:85473922 | G | T | 1 | a0001c0001t0001g0161 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.751+2497G>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85473922 | |||||||
| chr6:85473972 | C | A | 1 | a0001c0001t0004g0116 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.751+2547C>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85473972 | |||||||
| chr6:85474067 | G | A | 2 | a0001c0005t0004g0014 a0001c0005t0004g0192 |
4 | HG02109.hp1 HG02630.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.751+2642G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85474067 | |||||||
| chr6:85474147 | A | G | 2 | a0001c0001t0001g0097 a0001c0001t0001g0188 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.751+2722A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85474147 | |||||||
| chr6:85474235 | T | C | 5 | a0003c0003t0001g0139 a0003c0003t0001g0140 a0003c0003t0001g0141 others(2): Show |
5 | HG02559.hp2 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.751+2810T>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85474235 | |||||||
| chr6:85474254 | G | A | 8 | a0001c0001t0001g0147 a0003c0003t0001g0037 a0003c0003t0001g0038 others(5): Show |
9 | HG01884.hp1 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.751+2829G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85474254 | |||||||
| chr6:85474294 | A | G | 3 | a0001c0001t0001g0150 a0003c0003t0005g0148 a0003c0003t0005g0149 |
3 | HG02280.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.751+2869A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85474294 | |||||||
| chr6:85474665 | A | G | 7 | a0003c0003t0001g0037 a0003c0003t0001g0038 a0003c0003t0001g0040 others(4): Show |
8 | HG01884.hp1 HG02886.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.751+3240A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85474665 | |||||||
| chr6:85474732 | C | T | 1 | a0001c0001t0001g0032 | 2 | NA19054.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.751+3307C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85474732 | |||||||
| chr6:85474733 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.751+3308G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85474733 | |||||||
| chr6:85474744 | G | C | 8 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0190 others(5): Show |
10 | HG02109.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.751+3319G>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85474744 | |||||||
| chr6:85474774 | A | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.751+3349A>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85474774 | |||||||
| chr6:85474802 | C | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0188 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.751+3377C>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85474802 | |||||||
| chr6:85475064 | G | A | 1 | a0001c0001t0001g0008 | 4 | HG02257.hp1 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.751+3639G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85475064 | |||||||
| chr6:85475086 | C | T | 3 | a0003c0003t0003g0044 a0003c0003t0003g0045 a0003c0003t0011g0016 |
4 | HG02818.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.751+3661C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85475086 | |||||||
| chr6:85475093 | A | G | 2 | a0001c0001t0001g0024 a0005c0008t0001g0022 |
4 | HG01175.hp2 HG01243.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.751+3668A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85475093 | |||||||
| chr6:85475172 | G | A | 168 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(165): Show |
270 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.751+3747G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85475172 | |||||||
| chr6:85475173 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.751+3748C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85475173 | |||||||
| chr6:85475223 | G | T | 8 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0190 others(5): Show |
10 | HG02109.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.751+3798G>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85475223 | |||||||
| chr6:85475238 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.751+3813A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85475238 | |||||||
| chr6:85475561 | A | C | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.751+4136A>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85475561 | |||||||
| chr6:85475625 | C | G | 169 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(166): Show |
271 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.751+4200C>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85475625 | |||||||
| chr6:85476066 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.751+4641C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85476066 | |||||||
| chr6:85476161 | T | C | 18 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0021 others(15): Show |
30 | HG00597.hp2 HG01069.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.751+4736T>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85476161 | |||||||
| chr6:85476455 | C | T | 3 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0137 |
3 | HG01243.hp1 HG02257.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.751+5030C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85476455 | |||||||
| chr6:85476596 | G | A | 2 | a0001c0001t0001g0086 a0001c0001t0001g0093 |
2 | HG01243.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.751+5171G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85476596 | |||||||
| chr6:85476757 | A | G | 168 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(165): Show |
270 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.751+5332A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85476757 | |||||||
| chr6:85476775 | G | C | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.751+5350G>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85476775 | |||||||
| chr6:85476784 | G | A | 8 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0190 others(5): Show |
10 | HG02109.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.751+5359G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85476784 | |||||||
| chr6:85476901 | G | A | 2 | a0001c0001t0001g0136 a0003c0003t0001g0139 |
2 | HG02559.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.751+5476G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85476901 | |||||||
| chr6:85476911 | G | A | 3 | a0001c0001t0001g0147 a0002c0002t0002g0009 a0002c0002t0002g0164 |
6 | HG02109.hp2 NA18968.hp2 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.751+5486G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85476911 | |||||||
| chr6:85477008 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.751+5583A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85477008 | |||||||
| chr6:85477055 | C | T | 1 | a0002c0002t0002g0129 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.751+5630C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85477055 | |||||||
| chr6:85477077 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.751+5652G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85477077 | |||||||
| chr6:85477078 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.751+5653C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85477078 | |||||||
| chr6:85477240 | G | A | 1 | a0003c0003t0011g0016 | 2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.751+5815G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85477240 | |||||||
| chr6:85477259 | CA | C | 4 | a0003c0003t0001g0037 a0003c0003t0001g0038 a0003c0003t0001g0177 others(1): Show |
5 | HG02886.hp1 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.751+5835delA | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85477259 | |||||||
| chr6:85477267 | T | G | 4 | a0001c0001t0001g0150 a0003c0003t0001g0139 a0003c0003t0005g0148 others(1): Show |
4 | HG02280.hp2 HG02559.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.751+5842T>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85477267 | |||||||
| chr6:85477377 | G | C | 1 | a0001c0001t0001g0067 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.751+5952G>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85477377 | |||||||
| chr6:85477592 | A | C | 1 | a0001c0001t0001g0176 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.751+6167A>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85477592 | |||||||
| chr6:85478026 | C | CA | 72 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0019 others(69): Show |
118 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.751+6618dupA | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 85478026 | ||||||
| chr6:85478045 | G | T | 16 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0001c0001t0001g0151 others(13): Show |
25 | HG00735.hp2 HG02818.hp1 HG02895.hp1 others(22): Show |
intron_variant | MODIFIER | c.751+6620G>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85478045 | |||||||
| chr6:85478219 | A | C | 1 | a0002c0002t0002g0028 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.751+6794A>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85478219 | |||||||
| chr6:85478269 | A | T | 1 | a0001c0001t0001g0073 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.751+6844A>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85478269 | |||||||
| chr6:85478275 | C | T | 4 | a0001c0001t0001g0150 a0003c0003t0001g0139 a0003c0003t0005g0148 others(1): Show |
4 | HG02280.hp2 HG02559.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.751+6850C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85478275 | |||||||
| chr6:85478674 | T | C | 1 | a0001c0001t0001g0071 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.752-6561T>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85478674 | |||||||
| chr6:85478732 | T | C | 1 | a0002c0002t0002g0126 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.752-6503T>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85478732 | |||||||
| chr6:85478747 | A | G | 2 | a0002c0002t0002g0027 a0002c0002t0002g0129 |
3 | HG03704.hp1 HG03831.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.752-6488A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85478747 | |||||||
| chr6:85478829 | A | C | 2 | a0001c0001t0001g0136 a0003c0004t0003g0010 |
4 | HG00423.hp2 HG02074.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.752-6406A>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85478829 | |||||||
| chr6:85478832 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.752-6403T>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85478832 | |||||||
| chr6:85478910 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.752-6325C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85478910 | |||||||
| chr6:85478974 | C | T | 1 | a0001c0005t0004g0192 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.752-6261C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85478974 | |||||||
| chr6:85479017 | G | T | 1 | a0002c0002t0002g0056 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.752-6218G>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85479017 | |||||||
| chr6:85479126 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.752-6109T>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85479126 | |||||||
| chr6:85479372 | C | A | 1 | a0001c0001t0001g0190 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.752-5863C>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85479372 | |||||||
| chr6:85479802 | T | C | 75 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(72): Show |
130 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.752-5433T>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85479802 | |||||||
| chr6:85479829 | C | T | 3 | a0001c0001t0001g0142 a0001c0001t0001g0189 a0001c0001t0012g0143 |
3 | HG02647.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.752-5406C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85479829 | |||||||
| chr6:85479892 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.752-5343A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85479892 | |||||||
| chr6:85480769 | T | TAAAC | 7 | a0003c0003t0001g0037 a0003c0003t0001g0038 a0003c0003t0001g0041 others(4): Show |
8 | HG02258.hp1 HG02886.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.752-4441_752-4438d others(6): Show |
NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 85480769 | ||||||
| chr6:85480909 | C | T | 4 | a0001c0001t0001g0142 a0001c0001t0001g0189 a0001c0001t0004g0116 others(1): Show |
4 | HG02647.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.752-4326C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85480909 | |||||||
| chr6:85481012 | T | G | 1 | a0002c0002t0002g0027 | 2 | HG03704.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.752-4223T>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85481012 | |||||||
| chr6:85481066 | T | A | 4 | a0001c0001t0001g0142 a0001c0001t0001g0189 a0001c0001t0004g0116 others(1): Show |
4 | HG02647.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.752-4169T>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85481066 | |||||||
| chr6:85481067 | G | T | 4 | a0001c0001t0001g0142 a0001c0001t0001g0189 a0001c0001t0004g0116 others(1): Show |
4 | HG02647.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.752-4168G>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85481067 | |||||||
| chr6:85481248 | A | C | 1 | a0001c0001t0001g0072 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.752-3987A>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85481248 | |||||||
| chr6:85481334 | T | C | 4 | a0001c0001t0001g0142 a0001c0001t0001g0189 a0001c0001t0004g0116 others(1): Show |
4 | HG02647.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.752-3901T>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85481334 | |||||||
| chr6:85481422 | C | G | 5 | a0001c0001t0001g0150 a0003c0003t0005g0148 a0003c0003t0005g0149 others(2): Show |
5 | HG02280.hp2 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.752-3813C>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85481422 | |||||||
| chr6:85481496 | G | T | 1 | a0001c0001t0001g0074 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.752-3739G>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85481496 | |||||||
| chr6:85482001 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.752-3234G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85482001 | |||||||
| chr6:85482171 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.752-3064G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85482171 | |||||||
| chr6:85482265 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.752-2970C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85482265 | |||||||
| chr6:85482539 | G | A | 12 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0003c0003t0003g0003 others(9): Show |
28 | HG00423.hp2 HG00544.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.752-2696G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85482539 | |||||||
| chr6:85482740 | G | T | 1 | a0002c0002t0002g0131 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.752-2495G>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85482740 | |||||||
| chr6:85482902 | A | G | 15 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0003c0003t0003g0003 others(12): Show |
32 | HG00423.hp2 HG00544.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.752-2333A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85482902 | |||||||
| chr6:85483231 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.752-2004C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85483231 | |||||||
| chr6:85483300 | C | A | 1 | a0001c0006t0009g0039 | 2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.752-1935C>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85483300 | |||||||
| chr6:85483535 | A | G | 1 | a0001c0001t0001g0008 | 4 | HG02257.hp1 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.752-1700A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85483535 | |||||||
| chr6:85483893 | G | A | 1 | a0001c0001t0001g0011 | 3 | HG00609.hp1 HG02155.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.752-1342G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85483893 | |||||||
| chr6:85484104 | C | T | 7 | a0003c0003t0001g0037 a0003c0003t0001g0038 a0003c0003t0001g0040 others(4): Show |
8 | HG01884.hp1 HG02886.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.752-1131C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85484104 | |||||||
| chr6:85484112 | G | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0188 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.752-1123G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85484112 | |||||||
| chr6:85484124 | T | C | 1 | a0001c0001t0001g0165 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.752-1111T>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85484124 | |||||||
| chr6:85484128 | T | C | 1 | a0001c0001t0004g0116 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.752-1107T>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85484128 | |||||||
| chr6:85484428 | C | T | 12 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0003c0003t0003g0003 others(9): Show |
28 | HG00423.hp2 HG00544.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.752-807C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85484428 | |||||||
| chr6:85484547 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.752-688G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85484547 | |||||||
| chr6:85484711 | T | G | 8 | a0001c0001t0001g0147 a0003c0003t0001g0037 a0003c0003t0001g0038 others(5): Show |
9 | HG01884.hp1 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.752-524T>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85484711 | |||||||
| chr6:85484923 | G | A | 2 | a0001c0001t0001g0024 a0005c0008t0001g0022 |
4 | HG01175.hp2 HG01243.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.752-312G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85484923 | |||||||
| chr6:85484952 | C | T | 1 | a0003c0003t0001g0141 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.752-283C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85484952 | |||||||
| chr6:85484956 | G | A | 3 | a0003c0003t0003g0044 a0003c0003t0003g0045 a0003c0003t0011g0016 |
4 | HG02818.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.752-279G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85484956 | |||||||
| chr6:85485010 | G | C | 1 | a0001c0001t0001g0023 | 2 | HG00280.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.752-225G>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 3/8 | chr6 | 85485010 | |||||||
| chr6:85485475 | G | C | 1 | a0002c0002t0002g0027 | 2 | HG03704.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.949+43G>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 4/8 | chr6 | 85485475 | |||||||
| chr6:85485530 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.949+98A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 4/8 | chr6 | 85485530 | |||||||
| chr6:85485580 | A | G | 104 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(101): Show |
177 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.949+148A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 4/8 | chr6 | 85485580 | |||||||
| chr6:85485734 | A | G | 5 | a0001c0005t0001g0112 a0001c0005t0001g0114 a0001c0005t0001g0115 others(2): Show |
7 | HG02109.hp1 HG02559.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.949+302A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 4/8 | chr6 | 85485734 | |||||||
| chr6:85485933 | T | G | 1 | a0001c0001t0001g0103 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.949+501T>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 4/8 | chr6 | 85485933 | |||||||
| chr6:85486079 | A | G | 168 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(165): Show |
270 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.949+647A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 4/8 | chr6 | 85486079 | |||||||
| chr6:85486337 | G | T | 1 | a0001c0001t0001g0104 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.949+905G>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 4/8 | chr6 | 85486337 | |||||||
| chr6:85486495 | C | A | 1 | a0002c0002t0002g0055 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.950-840C>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 4/8 | chr6 | 85486495 | |||||||
| chr6:85486501 | C | T | 1 | a0001c0005t0001g0112 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.950-834C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 4/8 | chr6 | 85486501 | |||||||
| chr6:85486577 | T | C | 1 | a0001c0001t0001g0021 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.950-758T>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 4/8 | chr6 | 85486577 | |||||||
| chr6:85486588 | G | T | 24 | a0001c0001t0001g0136 a0001c0001t0001g0147 a0001c0001t0002g0053 others(21): Show |
42 | HG00423.hp2 HG00544.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.950-747G>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 4/8 | chr6 | 85486588 | |||||||
| chr6:85486694 | A | G | 1 | a0002c0002t0002g0026 | 2 | NA18985.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.950-641A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 4/8 | chr6 | 85486694 | |||||||
| chr6:85486891 | G | A | 2 | a0001c0005t0001g0114 a0001c0005t0001g0115 |
2 | HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.950-444G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 4/8 | chr6 | 85486891 | |||||||
| chr6:85487104 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.950-231G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 4/8 | chr6 | 85487104 | |||||||
| chr6:85487109 | G | T | 1 | a0003c0003t0001g0139 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.950-226G>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 4/8 | chr6 | 85487109 | |||||||
| chr6:85487126 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.950-209T>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 4/8 | chr6 | 85487126 | |||||||
| chr6:85487249 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.950-86G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 4/8 | chr6 | 85487249 | |||||||
| chr6:85487272 | C | G | 28 | a0001c0001t0001g0147 a0001c0001t0002g0053 a0001c0001t0002g0054 others(25): Show |
46 | HG00423.hp2 HG00544.hp2 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.950-63C>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 4/8 | chr6 | 85487272 | |||||||
| chr6:85487535 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1104+46G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 5/8 | chr6 | 85487535 | |||||||
| chr6:85487661 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1104+172G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 5/8 | chr6 | 85487661 | |||||||
| chr6:85487793 | T | A | 1 | a0001c0001t0001g0136 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1104+304T>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 5/8 | chr6 | 85487793 | |||||||
| chr6:85487863 | C | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0168 |
3 | HG02258.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1104+374C>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 5/8 | chr6 | 85487863 | |||||||
| chr6:85488083 | C | G | 1 | a0001c0001t0001g0162 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1104+594C>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 5/8 | chr6 | 85488083 | |||||||
| chr6:85488555 | T | TTTTA | 10 | a0001c0001t0001g0018 a0001c0001t0001g0065 a0001c0001t0001g0072 others(7): Show |
11 | HG00597.hp2 HG02027.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1105-922_1105-919d others(6): Show |
NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 85488555 | ||||||
| chr6:85488572 | TTTAA | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0065 a0001c0001t0001g0072 others(2): Show |
6 | HG00597.hp2 HG02027.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1105-911_1105-908d others(6): Show |
NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 85488572 | ||||||
| chr6:85488576 | A | T | 2 | a0001c0001t0001g0071 a0003c0003t0006g0082 |
2 | HG02895.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1105-918A>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 5/8 | chr6 | 85488576 | |||||||
| chr6:85488583 | A | T | 33 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0033 others(30): Show |
51 | HG00408.hp1 HG00423.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.1105-911A>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 5/8 | chr6 | 85488583 | |||||||
| chr6:85488587 | T | A | 9 | a0001c0001t0001g0189 a0001c0005t0004g0192 a0003c0003t0001g0040 others(6): Show |
9 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1105-907T>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 5/8 | chr6 | 85488587 | |||||||
| chr6:85488620 | G | A | 1 | a0002c0002t0002g0031 | 2 | NA18947.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1105-874G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 5/8 | chr6 | 85488620 | |||||||
| chr6:85488662 | C | A | 8 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0061 others(5): Show |
11 | HG00609.hp1 HG02040.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1105-832C>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 5/8 | chr6 | 85488662 | |||||||
| chr6:85488667 | G | A | 1 | a0003c0003t0003g0044 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1105-827G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 5/8 | chr6 | 85488667 | |||||||
| chr6:85488881 | C | CT | 14 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0046 others(11): Show |
18 | HG00408.hp1 HG01109.hp2 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.1105-595dupT | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 85488881 | ||||||
| chr6:85488881 | CT | C | 22 | a0001c0001t0001g0033 a0001c0001t0001g0145 a0001c0001t0001g0147 others(19): Show |
40 | HG00423.hp2 HG00544.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.1105-595delT | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 85488881 | ||||||
| chr6:85489009 | G | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1105-485G>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 5/8 | chr6 | 85489009 | |||||||
| chr6:85489377 | A | G | 3 | a0003c0003t0005g0148 a0003c0003t0005g0149 a0003c0003t0005g0157 |
3 | HG02280.hp2 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1105-117A>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 5/8 | chr6 | 85489377 | |||||||
| chr6:85489444 | TAAGG | T | 47 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0029 others(44): Show |
74 | HG00408.hp1 HG00423.hp1 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.1105-46_1105-43del others(4): Show |
NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 85489444 | ||||||
| chr6:85489611 | G | C | 122 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
204 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.1210+12G>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 6/8 | chr6 | 85489611 | |||||||
| chr6:85489625 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1210+26G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 6/8 | chr6 | 85489625 | |||||||
| chr6:85489837 | G | T | 1 | a0002c0002t0002g0127 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1210+238G>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 6/8 | chr6 | 85489837 | |||||||
| chr6:85490137 | C | T | 5 | a0001c0005t0001g0112 a0001c0005t0001g0114 a0001c0005t0001g0115 others(2): Show |
7 | HG02109.hp1 HG02559.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1211-371C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 6/8 | chr6 | 85490137 | |||||||
| chr6:85490429 | A | T | 2 | a0001c0005t0001g0114 a0001c0005t0001g0115 |
2 | HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1211-79A>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 6/8 | chr6 | 85490429 | |||||||
| chr6:85490431 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1211-77C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 6/8 | chr6 | 85490431 | |||||||
| chr6:85490987 | T | A | 1 | a0001c0001t0001g0156 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1360+330T>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 7/8 | chr6 | 85490987 | |||||||
| chr6:85491784 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1361-193C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 7/8 | chr6 | 85491784 | |||||||
| chr6:85491844 | C | T | 1 | a0003c0003t0001g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1361-133C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 7/8 | chr6 | 85491844 | |||||||
| chr6:85491942 | T | A | 1 | a0003c0003t0003g0047 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1361-35T>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 7/8 | chr6 | 85491942 | |||||||
| chr6:85492577 | T | G | 2 | a0003c0003t0001g0038 a0006c0009t0001g0038 |
2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1561+400T>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 8/8 | chr6 | 85492577 | |||||||
| chr6:85492605 | G | A | 8 | a0001c0001t0001g0147 a0003c0003t0001g0037 a0003c0003t0001g0038 others(5): Show |
9 | HG01884.hp1 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1561+428G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 8/8 | chr6 | 85492605 | |||||||
| chr6:85492674 | C | G | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1561+497C>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 8/8 | chr6 | 85492674 | |||||||
| chr6:85492697 | A | T | 3 | a0001c0001t0001g0147 a0003c0003t0001g0040 a0003c0003t0001g0041 |
3 | HG01884.hp1 HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1561+520A>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 8/8 | chr6 | 85492697 | |||||||
| chr6:85492832 | G | C | 1 | a0003c0003t0001g0177 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1561+655G>C | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 8/8 | chr6 | 85492832 | |||||||
| chr6:85492913 | G | A | 8 | a0001c0001t0001g0147 a0003c0003t0001g0037 a0003c0003t0001g0038 others(5): Show |
9 | HG01884.hp1 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1561+736G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 8/8 | chr6 | 85492913 | |||||||
| chr6:85492985 | C | T | 13 | a0003c0003t0003g0003 a0003c0003t0003g0044 a0003c0003t0003g0045 others(10): Show |
30 | HG00423.hp2 HG00544.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1561+808C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 8/8 | chr6 | 85492985 | |||||||
| chr6:85493130 | G | A | 2 | a0001c0005t0001g0114 a0001c0005t0001g0115 |
2 | HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1562-711G>A | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 8/8 | chr6 | 85493130 | |||||||
| chr6:85493243 | C | G | 3 | a0001c0001t0001g0049 a0001c0006t0001g0185 a0001c0006t0009g0039 |
4 | HG01358.hp2 HG02896.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1562-598C>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 8/8 | chr6 | 85493243 | |||||||
| chr6:85493544 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1562-297C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 8/8 | chr6 | 85493544 | |||||||
| chr6:85493623 | C | G | 8 | a0003c0003t0001g0040 a0003c0003t0001g0041 a0003c0003t0001g0139 others(5): Show |
8 | HG01884.hp1 HG02559.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1562-218C>G | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 8/8 | chr6 | 85493623 | |||||||
| chr6:85493652 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1562-189C>T | NT5E | ENSG00000135318.12 | transcript | ENST00000257770.8 | protein_coding | 8/8 | chr6 | 85493652 |