Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 138050 |
| ensemblid | ENSG00000165102.15 |
| hgncid | 26527 |
| symbol | HGSNAT |
| name | heparan-alpha-glucosaminide N-acetyltransferase |
| refseq_nuc | NM_152419.3 |
| refseq_prot | NP_689632.2 |
| ensembl_nuc | ENST00000379644.9 |
| ensembl_prot | ENSP00000368965.4 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 43140464 |
| end | 43202855 |
| strand | + |
| ver | v1.2 |
| region | chr8:43140464-43202855 |
| region5000 | chr8:43135464-43207855 |
| regionname0 | HGSNAT_chr8_43140464_43202855 |
| regionname5000 | HGSNAT_chr8_43135464_43207855 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 635 | 201 | 51 | 59 | 66 | 2 | 21 | 36 | HGSNAT_chr8_43135464_43207855 | HGSNAT | MSGAG others(630): Show |
chr8 | 43135464 | 43207855 |
| a0002 | 0/0 | 635 | 23 | 22 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | MSGAG others(630): Show |
chr8 | 43135464 | 43207855 |
| a0003 | 0/0 | 635 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | MSGAG others(630): Show |
chr8 | 43135464 | 43207855 |
| a0004 | 0/0 | 635 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | MSGAG others(630): Show |
chr8 | 43135464 | 43207855 |
| a0005 | 0/0 | 635 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | MSGAG others(630): Show |
chr8 | 43135464 | 43207855 |
| a0006 | 0/0 | 635 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | MSGAG others(630): Show |
chr8 | 43135464 | 43207855 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1905 | 196 | 48 | 58 | 66 | 2 | 21 | HGSNAT_chr8_43135464_43207855 | HGSNAT | ATGAG others(1900): Show |
chr8 | 43135464 | 43207855 | ||
| a0001c0004 | 1/0 | 1905 | 4 | 2 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | ATGAG others(1900): Show |
chr8 | 43135464 | 43207855 | ||
| a0001c0005 | 0/0 | 1905 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | ATGAG others(1900): Show |
chr8 | 43135464 | 43207855 | ||
| a0002c0002 | 0/0 | 1905 | 23 | 22 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | ATGAG others(1900): Show |
chr8 | 43135464 | 43207855 | ||
| a0003c0003 | 0/0 | 1905 | 7 | 6 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | ATGAG others(1900): Show |
chr8 | 43135464 | 43207855 | ||
| a0004c0007 | 0/0 | 1905 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | ATGAG others(1900): Show |
chr8 | 43135464 | 43207855 | ||
| a0005c0008 | 0/0 | 1905 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | ATGAG others(1900): Show |
chr8 | 43135464 | 43207855 | ||
| a0006c0006 | 0/0 | 1905 | 1 | 0 | 0 | 0 | 0 | 1 | HGSNAT_chr8_43135464_43207855 | HGSNAT | ATGAG others(1900): Show |
chr8 | 43135464 | 43207855 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5227 | 122 | 24 | 41 | 39 | 1 | 16 | HGSNAT_chr8_43135464_43207855 | HGSNAT | GGGCA others(5222): Show |
chr8 | 43135464 | 43207855 |
| a0001c0001t0002 | 0/0 | 5227 | 60 | 20 | 11 | 26 | 0 | 3 | HGSNAT_chr8_43135464_43207855 | HGSNAT | GGGCA others(5222): Show |
chr8 | 43135464 | 43207855 |
| a0001c0001t0006 | 0/0 | 5227 | 4 | 0 | 1 | 0 | 1 | 2 | HGSNAT_chr8_43135464_43207855 | HGSNAT | GGGCA others(5222): Show |
chr8 | 43135464 | 43207855 |
| a0001c0001t0007 | 0/0 | 5227 | 3 | 0 | 3 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | GGGCA others(5222): Show |
chr8 | 43135464 | 43207855 |
| a0001c0001t0008 | 0/0 | 5228 | 2 | 2 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | GGGCA others(5223): Show |
chr8 | 43135464 | 43207855 |
| a0001c0001t0011 | 0/0 | 5227 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | GGGCA others(5222): Show |
chr8 | 43135464 | 43207855 |
| a0001c0001t0012 | 0/0 | 5227 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | GGGCA others(5222): Show |
chr8 | 43135464 | 43207855 |
| a0001c0001t0013 | 0/0 | 5227 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | GGGCA others(5222): Show |
chr8 | 43135464 | 43207855 |
| a0001c0001t0014 | 0/0 | 5227 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | GGGCA others(5222): Show |
chr8 | 43135464 | 43207855 |
| a0001c0001t0015 | 0/0 | 5227 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | GGGCA others(5222): Show |
chr8 | 43135464 | 43207855 |
| a0001c0004t0002 | 1/0 | 5227 | 4 | 2 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | GGGCA others(5222): Show |
chr8 | 43135464 | 43207855 |
| a0001c0005t0001 | 0/0 | 5227 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | GGGCA others(5222): Show |
chr8 | 43135464 | 43207855 |
| a0002c0002t0003 | 0/0 | 5227 | 16 | 15 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | GGGCA others(5222): Show |
chr8 | 43135464 | 43207855 |
| a0002c0002t0005 | 0/0 | 5227 | 5 | 5 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | GGGCA others(5222): Show |
chr8 | 43135464 | 43207855 |
| a0002c0002t0009 | 0/0 | 5227 | 2 | 2 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | GGGCA others(5222): Show |
chr8 | 43135464 | 43207855 |
| a0003c0003t0004 | 0/0 | 5227 | 6 | 5 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | GGGCA others(5222): Show |
chr8 | 43135464 | 43207855 |
| a0003c0003t0010 | 0/0 | 5227 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | GGGCA others(5222): Show |
chr8 | 43135464 | 43207855 |
| a0004c0007t0001 | 0/0 | 5227 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | GGGCA others(5222): Show |
chr8 | 43135464 | 43207855 |
| a0005c0008t0003 | 0/0 | 5227 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | GGGCA others(5222): Show |
chr8 | 43135464 | 43207855 |
| a0006c0006t0001 | 0/0 | 5227 | 1 | 0 | 0 | 0 | 0 | 1 | HGSNAT_chr8_43135464_43207855 | HGSNAT | GGGCA others(5222): Show |
chr8 | 43135464 | 43207855 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 2 | 0 | 3 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0093 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0006g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0006g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0006g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0006g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0007g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0007g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0007g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0008g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0008g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0011g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0012g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0013g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0014g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0001t0015g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0004t0002g0008 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0004t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0004t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0001c0005t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0002c0002t0003g0001 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0002c0002t0003g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0002c0002t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0002c0002t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0002c0002t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0002c0002t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0002c0002t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0002c0002t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0002c0002t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0002c0002t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0002c0002t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0002c0002t0005g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0002c0002t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0002c0002t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0002c0002t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0002c0002t0009g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0002c0002t0009g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0003c0003t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0003c0003t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0003c0003t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0003c0003t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0003c0003t0004g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0003c0003t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0003c0003t0010g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0004c0007t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0005c0008t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| a0006c0006t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | GBR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG00099 | hp2 | a0001 | c0001 | t0006 | g0168 | EUR | GBR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | CHS | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | CHS | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | CHS | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | CHS | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01070 | hp2 | a0001 | c0001 | t0007 | g0061 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01071 | hp1 | a0001 | c0001 | t0006 | g0203 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01071 | hp2 | a0001 | c0001 | t0007 | g0062 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01109 | hp2 | a0001 | c0001 | t0011 | g0085 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01167 | hp2 | a0001 | c0004 | t0002 | g0055 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01175 | hp2 | a0001 | c0001 | t0007 | g0067 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01192 | hp2 | a0003 | c0003 | t0004 | g0199 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01243 | hp2 | a0002 | c0002 | t0003 | g0193 | AMR | PUR | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01928 | hp1 | a0001 | c0001 | t0015 | g0006 | AMR | PEL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01934 | hp1 | a0004 | c0007 | t0001 | g0107 | AMR | PEL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PEL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PEL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02055 | hp1 | a0002 | c0002 | t0005 | g0176 | AFR | ACB | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | KHV | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CDX | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | CDX | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | ACB | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | ACB | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | ACB | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02258 | hp2 | a0002 | c0002 | t0003 | g0136 | AFR | ACB | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | PEL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PEL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0073 | AFR | GWD | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | GWD | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02615 | hp2 | a0002 | c0002 | t0003 | g0016 | AFR | GWD | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02622 | hp2 | a0002 | c0002 | t0009 | g0181 | AFR | GWD | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02647 | hp1 | a0005 | c0008 | t0003 | g0180 | AFR | GWD | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | GWD | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02717 | hp2 | a0002 | c0002 | t0003 | g0001 | AFR | GWD | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02723 | hp2 | a0001 | c0005 | t0001 | g0195 | AFR | GWD | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02735 | hp2 | a0006 | c0006 | t0001 | g0086 | SAS | PJL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | GWD | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0151 | AFR | GWD | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02886 | hp2 | a0002 | c0002 | t0003 | g0001 | AFR | GWD | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02896 | hp1 | a0003 | c0003 | t0010 | g0200 | AFR | GWD | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02922 | hp1 | a0002 | c0002 | t0003 | g0001 | AFR | ESN | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02922 | hp2 | a0001 | c0004 | t0002 | g0054 | AFR | ESN | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02965 | hp2 | a0002 | c0002 | t0003 | g0135 | AFR | ESN | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03098 | hp1 | a0002 | c0002 | t0003 | g0192 | AFR | MSL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | MSL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03130 | hp2 | a0002 | c0002 | t0003 | g0189 | AFR | ESN | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03139 | hp1 | a0003 | c0003 | t0004 | g0173 | AFR | ESN | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03139 | hp2 | a0002 | c0002 | t0003 | g0191 | AFR | ESN | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03195 | hp1 | a0003 | c0003 | t0004 | g0197 | AFR | ESN | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03209 | hp1 | a0002 | c0002 | t0005 | g0175 | AFR | MSL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03209 | hp2 | a0002 | c0002 | t0003 | g0190 | AFR | MSL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | MSL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03225 | hp2 | a0003 | c0003 | t0004 | g0198 | AFR | MSL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | MSL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03453 | hp2 | a0002 | c0002 | t0003 | g0001 | AFR | MSL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03486 | hp2 | a0002 | c0002 | t0003 | g0016 | AFR | MSL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03516 | hp1 | a0003 | c0003 | t0004 | g0196 | AFR | ESN | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03516 | hp2 | a0002 | c0002 | t0003 | g0001 | AFR | ESN | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03540 | hp2 | a0001 | c0001 | t0014 | g0070 | AFR | GWD | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03579 | hp1 | a0003 | c0003 | t0004 | g0201 | AFR | MSL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03654 | hp2 | a0001 | c0001 | t0006 | g0204 | SAS | PJL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03669 | hp1 | a0001 | c0001 | t0006 | g0205 | SAS | PJL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0064 | SAS | PJL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | BEB | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | BEB | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0188 | SAS | BEB | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | STU | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | STU | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHB | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | CHB | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHB | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHB | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA18906 | hp2 | a0001 | c0001 | t0013 | g0202 | AFR | YRI | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA19011 | hp1 | a0001 | c0001 | t0012 | g0152 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA19043 | hp1 | a0001 | c0001 | t0008 | g0150 | AFR | LWK | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | LWK | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA19240 | hp1 | a0002 | c0002 | t0003 | g0001 | AFR | YRI | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | YRI | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA20129 | hp1 | a0002 | c0002 | t0005 | g0178 | AFR | ASW | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ASW | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | GIH | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | GIH | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02109 | hp1 | a0002 | c0002 | t0009 | g0174 | AFR | ACB | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02109 | hp2 | a0002 | c0002 | t0005 | g0179 | AFR | ACB | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | USA | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| HG06807 | hp2 | a0001 | c0004 | t0002 | g0008 | AFR | USA | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA20300 | hp1 | a0002 | c0002 | t0003 | g0206 | AFR | USA | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA20300 | hp2 | a0002 | c0002 | t0005 | g0177 | AFR | USA | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | LWK | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | LWK | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0093 | REF | REF | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| homoSapiens | grch38p0 | a0001 | c0004 | t0002 | g0008 | REF | REF | HGSNAT_chr8_43135464_43207855 | HGSNAT | chr8 | 43135464 | 43207855 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:43191595 | C | T | 1 | a0005 | 1 | HG02647.hp1 | missense_variant&splice_region_variant | MODERATE | c.1250C>T | p.Thr417Ile | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 12/18 | 1283/5227 | 1250/1908 | 417/635 | chr8 | 43191595 | |||
| chr8:43192428 | G | A | 1 | a0006 | 1 | HG02735.hp2 | missense_variant&splice_region_variant | MODERATE | c.1375G>A | p.Ala459Thr | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 13/18 | 1408/5227 | 1375/1908 | 459/635 | chr8 | 43192428 | |||
| chr8:43197696 | A | C | 2 | a0002 a0005 |
24 | HG01243.hp2 HG02055.hp1 HG02109.hp1 others(21): Show |
missense_variant | MODERATE | c.1567A>C | p.Lys523Gln | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 16/18 | 1600/5227 | 1567/1908 | 523/635 | chr8 | 43197696 | |||
| chr8:43199420 | G | A | 1 | a0005 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.1759G>A | p.Glu587Lys | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 18/18 | 1792/5227 | 1759/1908 | 587/635 | chr8 | 43199420 | |||
| chr8:43199501 | G | A | 1 | a0003 | 7 | HG01192.hp2 HG02896.hp1 HG03139.hp1 others(4): Show |
missense_variant | MODERATE | c.1840G>A | p.Val614Ile | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 18/18 | 1873/5227 | 1840/1908 | 614/635 | chr8 | 43199501 | |||
| chr8:43199504 | G | A | 1 | a0004 | 1 | HG01934.hp1 | missense_variant | MODERATE | c.1843G>A | p.Ala615Thr | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 18/18 | 1876/5227 | 1843/1908 | 615/635 | chr8 | 43199504 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:43140508 | G | A | 1 | a0001c0005 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.12G>A | p.Ala4Ala | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/18 | 45/5227 | 12/1908 | 4/635 | chr8 | 43140508 | |||
| chr8:43199410 | T | C | 7 | a0001c0001 a0001c0005 a0002c0002 others(4): Show |
229 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(226): Show |
synonymous_variant | LOW | c.1749T>C | p.Tyr583Tyr | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 18/18 | 1782/5227 | 1749/1908 | 583/635 | chr8 | 43199410 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:43200046 | G | A | 1 | a0001c0001t0008 | 2 | HG02886.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*477G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 18/18 | 477 | chr8 | 43200046 | ||||||
| chr8:43200154 | T | C | 2 | a0003c0003t0004 a0003c0003t0010 |
7 | HG01192.hp2 HG02896.hp1 HG03139.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*585T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 18/18 | 585 | chr8 | 43200154 | ||||||
| chr8:43200194 | A | G | 1 | a0001c0001t0015 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*625A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 18/18 | 625 | chr8 | 43200194 | ||||||
| chr8:43200302 | G | T | 1 | a0002c0002t0005 | 5 | HG02055.hp1 HG02109.hp2 HG03209.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*733G>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 18/18 | 733 | chr8 | 43200302 | ||||||
| chr8:43200537 | T | C | 1 | a0001c0001t0011 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*968T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 18/18 | 968 | chr8 | 43200537 | ||||||
| chr8:43200655 | G | C | 2 | a0002c0002t0005 a0002c0002t0009 |
7 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1086G>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 18/18 | 1086 | chr8 | 43200655 | ||||||
| chr8:43200785 | G | A | 4 | a0002c0002t0003 a0003c0003t0004 a0003c0003t0010 others(1): Show |
24 | HG01192.hp2 HG01243.hp2 HG02258.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1216G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 18/18 | 1216 | chr8 | 43200785 | ||||||
| chr8:43200800 | G | A | 4 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0009 others(1): Show |
24 | HG01243.hp2 HG02055.hp1 HG02109.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1231G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 18/18 | 1231 | chr8 | 43200800 | ||||||
| chr8:43201349 | C | T | 1 | a0001c0001t0006 | 4 | HG00099.hp2 HG01071.hp1 HG03654.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1780C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 18/18 | 1780 | chr8 | 43201349 | ||||||
| chr8:43201370 | T | C | 14 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0008 others(11): Show |
163 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*1801T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 18/18 | 1801 | chr8 | 43201370 | ||||||
| chr8:43201511 | A | G | 1 | a0001c0001t0008 | 2 | HG02886.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1942A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 18/18 | 1942 | chr8 | 43201511 | ||||||
| chr8:43201827 | A | G | 1 | a0001c0001t0008 | 2 | HG02886.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2258A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 18/18 | 2258 | chr8 | 43201827 | ||||||
| chr8:43202031 | G | C | 1 | a0003c0003t0010 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2462G>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 18/18 | 2462 | chr8 | 43202031 | ||||||
| chr8:43202212 | G | A | 1 | a0001c0001t0012 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2643G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 18/18 | 2643 | chr8 | 43202212 | ||||||
| chr8:43202222 | A | AT | 1 | a0001c0001t0008 | 2 | HG02886.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2654dupT | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 18/18 | 2655 | INFO_REALIGN_3_PRIME | chr8 | 43202222 | |||||
| chr8:43202324 | C | T | 1 | a0001c0001t0008 | 2 | HG02886.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2755C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 18/18 | 2755 | chr8 | 43202324 | ||||||
| chr8:43202336 | C | T | 1 | a0001c0001t0013 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2767C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 18/18 | 2767 | chr8 | 43202336 | ||||||
| chr8:43202408 | T | C | 1 | a0001c0001t0014 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2839T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 18/18 | 2839 | chr8 | 43202408 | ||||||
| chr8:43202782 | T | A | 1 | a0001c0001t0007 | 3 | HG01070.hp2 HG01071.hp2 HG01175.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3213T>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 18/18 | 3213 | chr8 | 43202782 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:43140668 | C | T | 14 | a0001c0001t0001g0017 a0001c0001t0001g0194 a0001c0001t0006g0203 others(11): Show |
15 | HG01071.hp1 HG01192.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.118+54C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43140668 | |||||||
| chr8:43140683 | C | T | 7 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0189 others(4): Show |
13 | HG01243.hp2 HG02615.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.118+69C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43140683 | |||||||
| chr8:43140688 | C | G | 1 | a0001c0001t0002g0188 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.118+74C>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43140688 | |||||||
| chr8:43140775 | G | A | 1 | a0001c0001t0002g0188 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.118+161G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43140775 | |||||||
| chr8:43140785 | C | T | 1 | a0001c0001t0002g0187 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.118+171C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43140785 | |||||||
| chr8:43140835 | G | T | 2 | a0001c0001t0001g0017 a0002c0002t0003g0206 |
3 | HG02895.hp2 HG02897.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.118+221G>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43140835 | |||||||
| chr8:43140947 | C | T | 3 | a0001c0001t0006g0203 a0001c0001t0006g0204 a0001c0001t0006g0205 |
3 | HG01071.hp1 HG03654.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.118+333C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43140947 | |||||||
| chr8:43140948 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.118+334C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43140948 | |||||||
| chr8:43141143 | G | C | 2 | a0001c0001t0001g0017 a0002c0002t0003g0206 |
3 | HG02895.hp2 HG02897.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.118+529G>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43141143 | |||||||
| chr8:43141208 | G | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 |
3 | HG00738.hp2 HG00741.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.118+594G>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43141208 | |||||||
| chr8:43141240 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.118+626C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43141240 | |||||||
| chr8:43141288 | A | AGCC | 8 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(5): Show |
8 | HG00673.hp1 NA18612.hp2 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.118+696_118+698dup others(3): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr8 | 43141288 | ||||||
| chr8:43141288 | A | AGCCGCC | 3 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 |
3 | HG01192.hp1 HG02895.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.118+693_118+698dup others(6): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr8 | 43141288 | ||||||
| chr8:43141288 | A | AGCCGCCG others(5): Show |
3 | a0002c0002t0003g0001 a0002c0002t0003g0189 a0002c0002t0003g0190 |
8 | HG02717.hp2 HG02886.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.118+687_118+698dup others(12): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr8 | 43141288 | ||||||
| chr8:43141311 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.118+697C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43141311 | |||||||
| chr8:43141350 | C | G | 1 | a0001c0001t0001g0183 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.118+736C>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43141350 | |||||||
| chr8:43141351 | G | T | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.118+737G>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43141351 | |||||||
| chr8:43141354 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.118+740C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43141354 | |||||||
| chr8:43141412 | A | G | 15 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0189 others(12): Show |
21 | HG01243.hp2 HG02055.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.118+798A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43141412 | |||||||
| chr8:43141459 | C | G | 2 | a0001c0001t0002g0172 a0003c0003t0004g0173 |
2 | HG02615.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.118+845C>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43141459 | |||||||
| chr8:43141479 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.118+865A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43141479 | |||||||
| chr8:43141591 | T | C | 21 | a0001c0001t0001g0033 a0001c0001t0001g0047 a0001c0001t0002g0005 others(18): Show |
22 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(19): Show |
intron_variant | MODIFIER | c.118+977T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43141591 | |||||||
| chr8:43141863 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.118+1249C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43141863 | |||||||
| chr8:43141944 | C | T | 2 | a0001c0001t0002g0169 a0001c0001t0002g0170 |
2 | NA18942.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.118+1330C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43141944 | |||||||
| chr8:43142125 | C | T | 1 | a0001c0001t0006g0168 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.118+1511C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43142125 | |||||||
| chr8:43142519 | A | T | 1 | a0001c0001t0002g0167 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.118+1905A>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43142519 | |||||||
| chr8:43142601 | C | T | 15 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 others(12): Show |
15 | HG00408.hp2 HG01074.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.118+1987C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43142601 | |||||||
| chr8:43142644 | A | G | 1 | a0001c0001t0002g0048 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.118+2030A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43142644 | |||||||
| chr8:43142653 | C | G | 1 | a0001c0001t0002g0048 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.118+2039C>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43142653 | |||||||
| chr8:43143077 | AAG | A | 6 | a0001c0001t0002g0032 a0002c0002t0005g0175 a0002c0002t0005g0176 others(3): Show |
6 | HG00558.hp1 HG02055.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.118+2465_118+2466d others(4): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr8 | 43143077 | ||||||
| chr8:43143496 | A | G | 7 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0189 others(4): Show |
13 | HG01243.hp2 HG02615.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.118+2882A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43143496 | |||||||
| chr8:43143545 | T | C | 5 | a0002c0002t0005g0175 a0002c0002t0005g0176 a0002c0002t0005g0177 others(2): Show |
5 | HG02055.hp1 HG02109.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.118+2931T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43143545 | |||||||
| chr8:43143666 | T | A | 2 | a0001c0001t0006g0203 a0001c0001t0006g0204 |
2 | HG01071.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.118+3052T>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43143666 | |||||||
| chr8:43143704 | A | AT | 13 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0002g0172 others(10): Show |
13 | HG00438.hp2 HG00558.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.118+3104dupT | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr8 | 43143704 | ||||||
| chr8:43143704 | AT | A | 16 | a0001c0001t0001g0021 a0002c0002t0003g0001 a0002c0002t0003g0016 others(13): Show |
22 | HG01243.hp2 HG02055.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.118+3104delT | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr8 | 43143704 | ||||||
| chr8:43144062 | T | C | 1 | a0002c0002t0005g0179 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.119-2886T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43144062 | |||||||
| chr8:43144085 | C | T | 1 | a0002c0002t0005g0178 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.119-2863C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43144085 | |||||||
| chr8:43144324 | C | CA | 6 | a0001c0001t0001g0033 a0001c0001t0001g0049 a0001c0001t0001g0050 others(3): Show |
6 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(3): Show |
intron_variant | MODIFIER | c.119-2605dupA | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr8 | 43144324 | ||||||
| chr8:43144342 | A | T | 4 | a0002c0002t0005g0175 a0002c0002t0005g0176 a0002c0002t0005g0177 others(1): Show |
4 | HG02055.hp1 HG03209.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-2606A>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43144342 | |||||||
| chr8:43144343 | A | T | 4 | a0002c0002t0005g0175 a0002c0002t0005g0176 a0002c0002t0005g0177 others(1): Show |
4 | HG02055.hp1 HG03209.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-2605A>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43144343 | |||||||
| chr8:43144460 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.119-2488T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43144460 | |||||||
| chr8:43144516 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.119-2432C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43144516 | |||||||
| chr8:43144571 | A | T | 1 | a0001c0001t0002g0147 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.119-2377A>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43144571 | |||||||
| chr8:43144678 | G | A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0186 |
2 | HG03704.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.119-2270G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43144678 | |||||||
| chr8:43144807 | A | G | 1 | a0002c0002t0005g0179 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.119-2141A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43144807 | |||||||
| chr8:43144883 | C | T | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(141): Show |
164 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.119-2065C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43144883 | |||||||
| chr8:43145044 | T | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(108): Show |
124 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.119-1904T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43145044 | |||||||
| chr8:43145093 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.119-1855A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43145093 | |||||||
| chr8:43145651 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.119-1297T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43145651 | |||||||
| chr8:43145715 | C | T | 7 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.119-1233C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43145715 | |||||||
| chr8:43145736 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.119-1212G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43145736 | |||||||
| chr8:43146723 | CTGTGTGT others(17): Show |
C | 1 | a0001c0001t0002g0053 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.119-200_119-177del others(24): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr8 | 43146723 | ||||||
| chr8:43146762 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.119-186T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43146762 | |||||||
| chr8:43146783 | AT | A | 7 | a0001c0001t0013g0202 a0003c0003t0004g0196 a0003c0003t0004g0197 others(4): Show |
7 | HG01192.hp2 HG02896.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.119-164delT | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | chr8 | 43146783 | |||||||
| chr8:43146909 | CT | C | 10 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0154 others(7): Show |
10 | HG01074.hp2 HG01099.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.119-23delT | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr8 | 43146909 | ||||||
| chr8:43147104 | T | C | 1 | a0002c0002t0005g0179 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.234+41T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43147104 | |||||||
| chr8:43147394 | C | T | 7 | a0001c0001t0013g0202 a0003c0003t0004g0196 a0003c0003t0004g0197 others(4): Show |
7 | HG01192.hp2 HG02896.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.234+331C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43147394 | |||||||
| chr8:43147471 | C | G | 1 | a0001c0001t0001g0077 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.234+408C>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43147471 | |||||||
| chr8:43147697 | T | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG01261.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.234+634T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43147697 | |||||||
| chr8:43147706 | T | C | 4 | a0001c0001t0002g0172 a0001c0001t0008g0150 a0001c0001t0008g0151 others(1): Show |
4 | HG02615.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+643T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43147706 | |||||||
| chr8:43148229 | C | G | 1 | a0003c0003t0004g0201 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.234+1166C>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43148229 | |||||||
| chr8:43148323 | T | TATTTATA others(4): Show |
4 | a0001c0001t0002g0172 a0001c0001t0008g0150 a0001c0001t0008g0151 others(1): Show |
4 | HG02615.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+1270_234+1280d others(13): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr8 | 43148323 | ||||||
| chr8:43148333 | TAATTTAT others(4): Show |
T | 1 | a0001c0001t0001g0153 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.234+1286_234+1296d others(13): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr8 | 43148333 | ||||||
| chr8:43148401 | C | G | 2 | a0001c0001t0002g0010 a0001c0001t0002g0074 |
3 | HG02647.hp2 HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.234+1338C>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43148401 | |||||||
| chr8:43148750 | A | G | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(143): Show |
166 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.234+1687A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43148750 | |||||||
| chr8:43148780 | C | T | 2 | a0002c0002t0003g0135 a0002c0002t0003g0136 |
2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.234+1717C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43148780 | |||||||
| chr8:43148843 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.234+1780G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43148843 | |||||||
| chr8:43148882 | G | A | 7 | a0001c0001t0002g0004 a0001c0001t0002g0053 a0001c0001t0002g0056 others(4): Show |
9 | HG01106.hp1 HG02257.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.234+1819G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43148882 | |||||||
| chr8:43149040 | C | T | 4 | a0001c0001t0002g0172 a0001c0001t0008g0150 a0001c0001t0008g0151 others(1): Show |
4 | HG02615.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+1977C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43149040 | |||||||
| chr8:43149118 | A | AAAAT | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(114): Show |
136 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.234+2083_234+2086d others(6): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr8 | 43149118 | ||||||
| chr8:43149118 | A | AAAATAAA others(1): Show |
7 | a0001c0001t0001g0077 a0001c0001t0001g0130 a0001c0001t0001g0131 others(4): Show |
7 | HG00735.hp1 HG01978.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.234+2079_234+2086d others(10): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr8 | 43149118 | ||||||
| chr8:43149118 | A | AAAATAAA others(5): Show |
1 | a0001c0001t0001g0134 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.234+2075_234+2086d others(14): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr8 | 43149118 | ||||||
| chr8:43149163 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.234+2100C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43149163 | |||||||
| chr8:43149271 | G | A | 15 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0189 others(12): Show |
21 | HG01243.hp2 HG02055.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.234+2208G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43149271 | |||||||
| chr8:43149331 | T | C | 1 | a0001c0001t0001g0155 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.234+2268T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43149331 | |||||||
| chr8:43149370 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0184 |
2 | HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.234+2307C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43149370 | |||||||
| chr8:43149376 | C | CTG | 4 | a0001c0001t0002g0172 a0001c0001t0008g0150 a0001c0001t0008g0151 others(1): Show |
4 | HG02615.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+2314_234+2315i others(4): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr8 | 43149376 | ||||||
| chr8:43149586 | G | C | 4 | a0001c0001t0002g0172 a0001c0001t0008g0150 a0001c0001t0008g0151 others(1): Show |
4 | HG02615.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+2523G>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43149586 | |||||||
| chr8:43149616 | C | A | 1 | a0001c0001t0001g0080 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.234+2553C>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43149616 | |||||||
| chr8:43149660 | A | G | 7 | a0001c0001t0013g0202 a0003c0003t0004g0196 a0003c0003t0004g0197 others(4): Show |
7 | HG01192.hp2 HG02896.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.234+2597A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43149660 | |||||||
| chr8:43149699 | C | CA | 4 | a0001c0001t0001g0022 a0001c0001t0001g0075 a0001c0001t0002g0167 others(1): Show |
5 | HG02258.hp1 HG02615.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+2650dupA | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr8 | 43149699 | ||||||
| chr8:43149713 | A | T | 1 | a0001c0001t0001g0141 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.234+2650A>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43149713 | |||||||
| chr8:43149714 | T | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0081 a0001c0001t0001g0130 |
4 | HG00639.hp2 HG00738.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+2651T>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43149714 | |||||||
| chr8:43149897 | A | T | 1 | a0001c0001t0006g0204 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.234+2834A>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43149897 | |||||||
| chr8:43149954 | T | TTTTA | 3 | a0001c0001t0006g0203 a0001c0001t0006g0204 a0001c0001t0006g0205 |
3 | HG01071.hp1 HG03654.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.234+2907_234+2910d others(6): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr8 | 43149954 | ||||||
| chr8:43150019 | C | T | 5 | a0002c0002t0005g0175 a0002c0002t0005g0176 a0002c0002t0005g0177 others(2): Show |
5 | HG02055.hp1 HG02109.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.234+2956C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43150019 | |||||||
| chr8:43150082 | G | A | 2 | a0001c0001t0002g0010 a0001c0001t0002g0074 |
3 | HG02647.hp2 HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.234+3019G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43150082 | |||||||
| chr8:43150095 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.234+3032T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43150095 | |||||||
| chr8:43150103 | C | T | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(109): Show |
125 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.234+3040C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43150103 | |||||||
| chr8:43150230 | G | A | 1 | a0003c0003t0004g0196 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.234+3167G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43150230 | |||||||
| chr8:43150361 | C | G | 2 | a0003c0003t0004g0199 a0003c0003t0010g0200 |
2 | HG01192.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.234+3298C>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43150361 | |||||||
| chr8:43150436 | G | A | 1 | a0001c0005t0001g0195 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.234+3373G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43150436 | |||||||
| chr8:43150516 | G | T | 1 | a0001c0001t0001g0071 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.234+3453G>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43150516 | |||||||
| chr8:43150572 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.234+3509A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43150572 | |||||||
| chr8:43150644 | C | T | 2 | a0001c0001t0002g0046 a0001c0005t0001g0195 |
2 | HG02165.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.234+3581C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43150644 | |||||||
| chr8:43150650 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.234+3587G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43150650 | |||||||
| chr8:43150777 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.234+3714A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43150777 | |||||||
| chr8:43150801 | T | C | 1 | a0005c0008t0003g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.234+3738T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43150801 | |||||||
| chr8:43150821 | G | T | 2 | a0001c0001t0002g0172 a0003c0003t0004g0173 |
2 | HG02615.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.234+3758G>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43150821 | |||||||
| chr8:43150834 | A | AAAAT | 2 | a0001c0001t0002g0010 a0001c0001t0002g0074 |
3 | HG02647.hp2 HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.234+3803_234+3806d others(6): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr8 | 43150834 | ||||||
| chr8:43150834 | A | AAAATAAA others(5): Show |
1 | a0001c0001t0002g0172 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.234+3795_234+3806d others(14): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr8 | 43150834 | ||||||
| chr8:43150834 | A | AAAATAAA others(9): Show |
5 | a0002c0002t0005g0175 a0002c0002t0005g0176 a0002c0002t0005g0177 others(2): Show |
5 | HG02055.hp1 HG03139.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.234+3791_234+3806d others(18): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr8 | 43150834 | ||||||
| chr8:43150834 | AAAAT | A | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(119): Show |
135 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.234+3803_234+3806d others(6): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr8 | 43150834 | ||||||
| chr8:43150834 | AAAATAAA others(1): Show |
A | 9 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0002c0002t0003g0001 others(6): Show |
15 | HG01243.hp2 HG01261.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.234+3799_234+3806d others(10): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr8 | 43150834 | ||||||
| chr8:43150866 | T | TAAATAAA others(9): Show |
1 | a0002c0002t0009g0174 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.234+3806_234+3807i others(18): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr8 | 43150866 | ||||||
| chr8:43150897 | CTA | C | 2 | a0001c0001t0002g0172 a0003c0003t0004g0173 |
2 | HG02615.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.234+3845_234+3846d others(4): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr8 | 43150897 | ||||||
| chr8:43150939 | A | ATATAT | 4 | a0001c0001t0002g0172 a0001c0001t0008g0150 a0001c0001t0008g0151 others(1): Show |
4 | HG02615.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+3879_234+3880i others(7): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr8 | 43150939 | ||||||
| chr8:43150991 | A | C | 1 | a0001c0001t0001g0153 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.234+3928A>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43150991 | |||||||
| chr8:43151086 | G | A | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(105): Show |
121 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.234+4023G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43151086 | |||||||
| chr8:43151163 | A | T | 1 | a0001c0001t0002g0004 | 3 | HG02572.hp2 HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.234+4100A>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43151163 | |||||||
| chr8:43151395 | G | C | 2 | a0001c0001t0002g0084 a0001c0001t0011g0085 |
2 | HG01109.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.234+4332G>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43151395 | |||||||
| chr8:43151411 | AGT | A | 2 | a0002c0002t0003g0191 a0002c0002t0003g0192 |
2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.234+4351_234+4352d others(4): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr8 | 43151411 | ||||||
| chr8:43151445 | C | T | 6 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0068 others(3): Show |
8 | HG02486.hp2 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.234+4382C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43151445 | |||||||
| chr8:43151482 | C | T | 2 | a0001c0001t0008g0150 a0001c0001t0008g0151 |
2 | HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.234+4419C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43151482 | |||||||
| chr8:43151576 | G | A | 2 | a0001c0001t0002g0172 a0003c0003t0004g0173 |
2 | HG02615.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.234+4513G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43151576 | |||||||
| chr8:43151844 | G | T | 1 | a0003c0003t0004g0196 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.234+4781G>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43151844 | |||||||
| chr8:43152028 | C | T | 1 | a0001c0001t0008g0151 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.234+4965C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43152028 | |||||||
| chr8:43152080 | G | A | 2 | a0001c0001t0002g0172 a0003c0003t0004g0173 |
2 | HG02615.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.234+5017G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43152080 | |||||||
| chr8:43152183 | T | C | 2 | a0001c0001t0002g0172 a0003c0003t0004g0173 |
2 | HG02615.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.234+5120T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43152183 | |||||||
| chr8:43152218 | T | G | 2 | a0001c0001t0002g0172 a0003c0003t0004g0173 |
2 | HG02615.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.234+5155T>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43152218 | |||||||
| chr8:43152487 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.234+5424T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43152487 | |||||||
| chr8:43152567 | C | T | 1 | a0001c0001t0007g0067 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.234+5504C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43152567 | |||||||
| chr8:43152904 | A | C | 2 | a0001c0001t0001g0017 a0002c0002t0003g0206 |
3 | HG02895.hp2 HG02897.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.235-5671A>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43152904 | |||||||
| chr8:43153131 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.235-5444A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43153131 | |||||||
| chr8:43153495 | T | G | 2 | a0001c0001t0001g0194 a0006c0006t0001g0086 |
2 | HG01261.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.235-5080T>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43153495 | |||||||
| chr8:43153499 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.235-5076C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43153499 | |||||||
| chr8:43153548 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.235-5027A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43153548 | |||||||
| chr8:43153741 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.235-4834T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43153741 | |||||||
| chr8:43153914 | A | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(108): Show |
124 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.235-4661A>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43153914 | |||||||
| chr8:43153937 | C | A | 1 | a0003c0003t0004g0196 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.235-4638C>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43153937 | |||||||
| chr8:43154052 | C | CT | 23 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0189 others(20): Show |
29 | HG01192.hp2 HG01243.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.235-4515dupT | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr8 | 43154052 | ||||||
| chr8:43154226 | G | A | 1 | a0001c0001t0002g0126 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.235-4349G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43154226 | |||||||
| chr8:43154237 | A | G | 1 | a0001c0001t0002g0126 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.235-4338A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43154237 | |||||||
| chr8:43154366 | C | T | 2 | a0001c0001t0008g0150 a0001c0001t0008g0151 |
2 | HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.235-4209C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43154366 | |||||||
| chr8:43154439 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.235-4136G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43154439 | |||||||
| chr8:43154525 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.235-4050C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43154525 | |||||||
| chr8:43154538 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.235-4037C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43154538 | |||||||
| chr8:43154544 | C | A | 7 | a0003c0003t0004g0173 a0003c0003t0004g0196 a0003c0003t0004g0197 others(4): Show |
7 | HG01192.hp2 HG02896.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.235-4031C>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43154544 | |||||||
| chr8:43154716 | A | G | 1 | a0001c0001t0002g0031 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.235-3859A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43154716 | |||||||
| chr8:43154769 | C | T | 2 | a0001c0001t0008g0150 a0001c0001t0008g0151 |
2 | HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.235-3806C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43154769 | |||||||
| chr8:43154983 | T | A | 16 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0189 others(13): Show |
22 | HG01243.hp2 HG02055.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.235-3592T>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43154983 | |||||||
| chr8:43155136 | A | G | 1 | a0003c0003t0004g0173 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.235-3439A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43155136 | |||||||
| chr8:43155161 | C | A | 1 | a0001c0001t0001g0017 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.235-3414C>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43155161 | |||||||
| chr8:43155412 | C | A | 1 | a0003c0003t0004g0196 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.235-3163C>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43155412 | |||||||
| chr8:43155424 | A | G | 1 | a0001c0001t0002g0066 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.235-3151A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43155424 | |||||||
| chr8:43155491 | T | C | 7 | a0003c0003t0004g0173 a0003c0003t0004g0196 a0003c0003t0004g0197 others(4): Show |
7 | HG01192.hp2 HG02896.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.235-3084T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43155491 | |||||||
| chr8:43155727 | G | C | 1 | a0001c0001t0002g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.235-2848G>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43155727 | |||||||
| chr8:43155785 | A | G | 1 | a0002c0002t0009g0174 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.235-2790A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43155785 | |||||||
| chr8:43155922 | C | G | 1 | a0001c0001t0002g0044 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.235-2653C>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43155922 | |||||||
| chr8:43156076 | G | A | 1 | a0005c0008t0003g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.235-2499G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43156076 | |||||||
| chr8:43156092 | G | A | 2 | a0001c0001t0001g0049 a0001c0001t0001g0060 |
2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.235-2483G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43156092 | |||||||
| chr8:43156159 | A | G | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(139): Show |
162 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.235-2416A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43156159 | |||||||
| chr8:43156375 | G | A | 4 | a0001c0001t0002g0188 a0001c0001t0007g0061 a0001c0001t0007g0062 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-2200G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43156375 | |||||||
| chr8:43156426 | C | T | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.235-2149C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43156426 | |||||||
| chr8:43156467 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.235-2108A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43156467 | |||||||
| chr8:43157302 | G | C | 8 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0189 others(5): Show |
14 | HG01243.hp2 HG02615.hp2 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.235-1273G>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43157302 | |||||||
| chr8:43157444 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.235-1131T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43157444 | |||||||
| chr8:43157491 | C | CT | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(108): Show |
124 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.235-1082dupT | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr8 | 43157491 | ||||||
| chr8:43157707 | G | A | 1 | a0005c0008t0003g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.235-868G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43157707 | |||||||
| chr8:43157994 | T | A | 1 | a0001c0001t0001g0194 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.235-581T>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43157994 | |||||||
| chr8:43158000 | C | G | 8 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0189 others(5): Show |
14 | HG01243.hp2 HG02615.hp2 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.235-575C>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43158000 | |||||||
| chr8:43158037 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.235-538T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43158037 | |||||||
| chr8:43158228 | A | G | 1 | a0001c0001t0001g0165 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.235-347A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43158228 | |||||||
| chr8:43158287 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.235-288A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43158287 | |||||||
| chr8:43158500 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.235-75G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 2/17 | chr8 | 43158500 | |||||||
| chr8:43158793 | C | T | 106 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(103): Show |
119 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.371+82C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 3/17 | chr8 | 43158793 | |||||||
| chr8:43159090 | G | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0075 a0001c0001t0001g0081 |
4 | HG00639.hp2 HG00738.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.493+46G>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 4/17 | chr8 | 43159090 | |||||||
| chr8:43159134 | C | T | 1 | a0001c0001t0001g0017 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.493+90C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 4/17 | chr8 | 43159134 | |||||||
| chr8:43159164 | G | A | 16 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0189 others(13): Show |
22 | HG01243.hp2 HG02055.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.493+120G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 4/17 | chr8 | 43159164 | |||||||
| chr8:43159372 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0091 |
4 | HG01070.hp1 HG01934.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.493+328G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 4/17 | chr8 | 43159372 | |||||||
| chr8:43159391 | G | A | 1 | a0001c0001t0002g0031 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.493+347G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 4/17 | chr8 | 43159391 | |||||||
| chr8:43159731 | T | C | 1 | a0001c0001t0001g0017 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.493+687T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 4/17 | chr8 | 43159731 | |||||||
| chr8:43159880 | G | A | 3 | a0003c0003t0004g0197 a0003c0003t0004g0199 a0003c0003t0010g0200 |
3 | HG01192.hp2 HG02896.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.493+836G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 4/17 | chr8 | 43159880 | |||||||
| chr8:43160538 | ATAGTTT | A | 8 | a0002c0002t0003g0193 a0003c0003t0004g0173 a0003c0003t0004g0196 others(5): Show |
8 | HG01192.hp2 HG01243.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.494-896_494-891del others(6): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr8 | 43160538 | ||||||
| chr8:43160687 | C | T | 1 | a0005c0008t0003g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.494-751C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 4/17 | chr8 | 43160687 | |||||||
| chr8:43161017 | G | C | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(199): Show |
228 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.494-421G>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 4/17 | chr8 | 43161017 | |||||||
| chr8:43161557 | C | T | 7 | a0003c0003t0004g0173 a0003c0003t0004g0196 a0003c0003t0004g0197 others(4): Show |
7 | HG01192.hp2 HG02896.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.563+50C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43161557 | |||||||
| chr8:43161803 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.563+296C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43161803 | |||||||
| chr8:43161865 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.563+358C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43161865 | |||||||
| chr8:43162038 | G | A | 7 | a0003c0003t0004g0173 a0003c0003t0004g0196 a0003c0003t0004g0197 others(4): Show |
7 | HG01192.hp2 HG02896.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.563+531G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43162038 | |||||||
| chr8:43162144 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.563+637A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43162144 | |||||||
| chr8:43162453 | C | A | 1 | a0001c0001t0002g0035 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.563+946C>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43162453 | |||||||
| chr8:43162554 | A | AT | 5 | a0001c0001t0006g0168 a0001c0001t0006g0203 a0001c0001t0006g0204 others(2): Show |
5 | HG00099.hp2 HG01071.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.563+1061dupT | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr8 | 43162554 | ||||||
| chr8:43162577 | G | A | 1 | a0002c0002t0003g0193 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.563+1070G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43162577 | |||||||
| chr8:43162741 | T | C | 4 | a0001c0001t0006g0168 a0001c0001t0006g0203 a0001c0001t0006g0204 others(1): Show |
4 | HG00099.hp2 HG01071.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.563+1234T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43162741 | |||||||
| chr8:43162770 | A | G | 2 | a0001c0001t0007g0061 a0001c0001t0007g0062 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.563+1263A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43162770 | |||||||
| chr8:43162881 | C | T | 1 | a0002c0002t0003g0193 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.563+1374C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43162881 | |||||||
| chr8:43163099 | G | T | 7 | a0003c0003t0004g0173 a0003c0003t0004g0196 a0003c0003t0004g0197 others(4): Show |
7 | HG01192.hp2 HG02896.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.563+1592G>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43163099 | |||||||
| chr8:43163196 | A | G | 7 | a0003c0003t0004g0173 a0003c0003t0004g0196 a0003c0003t0004g0197 others(4): Show |
7 | HG01192.hp2 HG02896.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.563+1689A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43163196 | |||||||
| chr8:43163215 | C | A | 1 | a0001c0001t0001g0092 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.563+1708C>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43163215 | |||||||
| chr8:43163216 | A | T | 3 | a0003c0003t0004g0197 a0003c0003t0004g0199 a0003c0003t0010g0200 |
3 | HG01192.hp2 HG02896.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.563+1709A>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43163216 | |||||||
| chr8:43163521 | CT | C | 7 | a0003c0003t0004g0173 a0003c0003t0004g0196 a0003c0003t0004g0197 others(4): Show |
7 | HG01192.hp2 HG02647.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.563+2029delT | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr8 | 43163521 | ||||||
| chr8:43163631 | A | G | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.563+2124A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43163631 | |||||||
| chr8:43163650 | C | G | 1 | a0001c0001t0001g0120 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.563+2143C>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43163650 | |||||||
| chr8:43163722 | T | C | 11 | a0001c0001t0001g0033 a0001c0001t0001g0153 a0001c0001t0001g0155 others(8): Show |
11 | HG00597.hp1 HG02129.hp1 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.563+2215T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43163722 | |||||||
| chr8:43163969 | G | C | 1 | a0001c0001t0001g0182 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.563+2462G>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43163969 | |||||||
| chr8:43164293 | T | C | 2 | a0001c0001t0001g0128 a0001c0001t0001g0184 |
2 | HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.563+2786T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43164293 | |||||||
| chr8:43164647 | G | A | 1 | a0001c0001t0002g0048 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.563+3140G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43164647 | |||||||
| chr8:43164722 | C | T | 2 | a0001c0001t0008g0150 a0001c0001t0008g0151 |
2 | HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.563+3215C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43164722 | |||||||
| chr8:43164736 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.563+3229C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43164736 | |||||||
| chr8:43164862 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.563+3355T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43164862 | |||||||
| chr8:43164894 | GAATA | G | 3 | a0001c0001t0001g0076 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01099.hp2 HG01361.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.563+3388_563+3391d others(6): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43164894 | |||||||
| chr8:43165044 | A | AT | 22 | a0001c0001t0001g0033 a0001c0001t0001g0049 a0001c0001t0001g0071 others(19): Show |
24 | HG00438.hp1 HG00597.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.563+3564dupT | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr8 | 43165044 | ||||||
| chr8:43165044 | AT | A | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(111): Show |
132 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.563+3564delT | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr8 | 43165044 | ||||||
| chr8:43165044 | ATT | A | 14 | a0001c0001t0001g0013 a0001c0001t0001g0137 a0001c0001t0001g0146 others(11): Show |
15 | HG00099.hp2 HG01071.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.563+3563_563+3564d others(4): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr8 | 43165044 | ||||||
| chr8:43165185 | C | T | 1 | a0001c0001t0002g0043 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.563+3678C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43165185 | |||||||
| chr8:43165285 | G | C | 7 | a0003c0003t0004g0173 a0003c0003t0004g0196 a0003c0003t0004g0197 others(4): Show |
7 | HG01192.hp2 HG02896.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.563+3778G>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43165285 | |||||||
| chr8:43165441 | G | A | 7 | a0003c0003t0004g0173 a0003c0003t0004g0196 a0003c0003t0004g0197 others(4): Show |
7 | HG01192.hp2 HG02896.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.564-3732G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43165441 | |||||||
| chr8:43165656 | G | T | 1 | a0001c0001t0001g0013 | 2 | NA18747.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.564-3517G>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43165656 | |||||||
| chr8:43165912 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.564-3261G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43165912 | |||||||
| chr8:43165963 | A | G | 2 | a0001c0001t0002g0169 a0001c0001t0002g0170 |
2 | NA18942.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.564-3210A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43165963 | |||||||
| chr8:43166286 | T | G | 14 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0034 others(11): Show |
15 | HG01074.hp1 HG01081.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.564-2887T>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43166286 | |||||||
| chr8:43166425 | A | G | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(108): Show |
124 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.564-2748A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43166425 | |||||||
| chr8:43166558 | T | C | 1 | a0001c0001t0001g0017 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.564-2615T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43166558 | |||||||
| chr8:43166565 | T | C | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(139): Show |
162 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.564-2608T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43166565 | |||||||
| chr8:43166583 | T | G | 1 | a0002c0002t0005g0179 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.564-2590T>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43166583 | |||||||
| chr8:43166715 | C | T | 1 | a0001c0001t0002g0167 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.564-2458C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43166715 | |||||||
| chr8:43166781 | C | T | 4 | a0001c0001t0002g0188 a0001c0001t0007g0061 a0001c0001t0007g0062 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.564-2392C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43166781 | |||||||
| chr8:43166966 | G | A | 1 | a0002c0002t0009g0174 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.564-2207G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43166966 | |||||||
| chr8:43167184 | A | G | 1 | a0001c0001t0001g0017 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.564-1989A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43167184 | |||||||
| chr8:43167240 | G | A | 7 | a0001c0001t0001g0094 a0001c0001t0001g0137 a0001c0001t0001g0138 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.564-1933G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43167240 | |||||||
| chr8:43167360 | C | T | 8 | a0002c0002t0003g0193 a0003c0003t0004g0173 a0003c0003t0004g0196 others(5): Show |
8 | HG01192.hp2 HG01243.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.564-1813C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43167360 | |||||||
| chr8:43167511 | T | A | 1 | a0001c0001t0006g0204 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.564-1662T>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43167511 | |||||||
| chr8:43167628 | T | C | 11 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(8): Show |
14 | HG00423.hp1 HG02015.hp1 HG02129.hp2 others(11): Show |
intron_variant | MODIFIER | c.564-1545T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43167628 | |||||||
| chr8:43167672 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.564-1501A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43167672 | |||||||
| chr8:43167698 | G | A | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(105): Show |
121 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.564-1475G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43167698 | |||||||
| chr8:43167754 | A | G | 1 | a0001c0001t0001g0017 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.564-1419A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43167754 | |||||||
| chr8:43168089 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.564-1084T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43168089 | |||||||
| chr8:43168249 | C | A | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.564-924C>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43168249 | |||||||
| chr8:43168304 | T | A | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(105): Show |
121 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.564-869T>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43168304 | |||||||
| chr8:43168323 | C | A | 1 | a0001c0001t0001g0095 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.564-850C>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43168323 | |||||||
| chr8:43168384 | C | CT | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(109): Show |
125 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.564-764dupT | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr8 | 43168384 | ||||||
| chr8:43168384 | C | CTT | 34 | a0001c0001t0001g0017 a0001c0001t0001g0075 a0001c0001t0001g0083 others(31): Show |
41 | HG00408.hp1 HG00408.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.564-765_564-764dup others(2): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr8 | 43168384 | ||||||
| chr8:43168384 | C | CTTT | 6 | a0002c0002t0003g0192 a0002c0002t0005g0179 a0002c0002t0009g0174 others(3): Show |
6 | HG02109.hp1 HG02109.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.564-766_564-764dup others(3): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr8 | 43168384 | ||||||
| chr8:43168422 | C | T | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.564-751C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43168422 | |||||||
| chr8:43168476 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.564-697T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43168476 | |||||||
| chr8:43168523 | A | T | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | HG00597.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.564-650A>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43168523 | |||||||
| chr8:43168541 | C | T | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.564-632C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43168541 | |||||||
| chr8:43168656 | C | A | 1 | a0003c0003t0004g0199 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.564-517C>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | chr8 | 43168656 | |||||||
| chr8:43169057 | TTTAA | T | 7 | a0003c0003t0004g0173 a0003c0003t0004g0196 a0003c0003t0004g0197 others(4): Show |
7 | HG01192.hp2 HG02896.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.564-112_564-109del others(4): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr8 | 43169057 | ||||||
| chr8:43169262 | G | C | 1 | a0001c0001t0012g0152 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.633+20G>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 6/17 | chr8 | 43169262 | |||||||
| chr8:43169366 | C | T | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.633+124C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 6/17 | chr8 | 43169366 | |||||||
| chr8:43169370 | T | A | 1 | a0001c0001t0002g0024 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.633+128T>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 6/17 | chr8 | 43169370 | |||||||
| chr8:43169452 | G | A | 8 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0189 others(5): Show |
14 | HG01243.hp2 HG02615.hp2 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.633+210G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 6/17 | chr8 | 43169452 | |||||||
| chr8:43169466 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.633+224C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 6/17 | chr8 | 43169466 | |||||||
| chr8:43169482 | T | G | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(109): Show |
125 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.633+240T>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 6/17 | chr8 | 43169482 | |||||||
| chr8:43169689 | G | C | 2 | a0001c0001t0008g0150 a0001c0001t0008g0151 |
2 | HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.633+447G>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 6/17 | chr8 | 43169689 | |||||||
| chr8:43169764 | A | C | 1 | a0001c0001t0001g0133 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.633+522A>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 6/17 | chr8 | 43169764 | |||||||
| chr8:43170203 | C | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 |
3 | HG01192.hp1 HG02895.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.634-382C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 6/17 | chr8 | 43170203 | |||||||
| chr8:43170209 | C | T | 1 | a0001c0001t0002g0029 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.634-376C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 6/17 | chr8 | 43170209 | |||||||
| chr8:43170343 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.634-242G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 6/17 | chr8 | 43170343 | |||||||
| chr8:43170409 | G | A | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.634-176G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 6/17 | chr8 | 43170409 | |||||||
| chr8:43170942 | C | G | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.743+248C>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 7/17 | chr8 | 43170942 | |||||||
| chr8:43170977 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.743+283G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 7/17 | chr8 | 43170977 | |||||||
| chr8:43171053 | A | G | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.743+359A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 7/17 | chr8 | 43171053 | |||||||
| chr8:43171760 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.744-550C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 7/17 | chr8 | 43171760 | |||||||
| chr8:43171841 | T | A | 8 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0189 others(5): Show |
14 | HG01243.hp2 HG02615.hp2 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.744-469T>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 7/17 | chr8 | 43171841 | |||||||
| chr8:43171867 | G | A | 109 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(106): Show |
122 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.744-443G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 7/17 | chr8 | 43171867 | |||||||
| chr8:43172236 | A | C | 1 | a0003c0003t0004g0196 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.744-74A>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 7/17 | chr8 | 43172236 | |||||||
| chr8:43172509 | C | T | 16 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0189 others(13): Show |
22 | HG01243.hp2 HG02055.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.820+123C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 8/17 | chr8 | 43172509 | |||||||
| chr8:43173171 | G | A | 1 | a0003c0003t0004g0196 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.821-542G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 8/17 | chr8 | 43173171 | |||||||
| chr8:43173186 | C | G | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.821-527C>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 8/17 | chr8 | 43173186 | |||||||
| chr8:43173437 | G | A | 15 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0189 others(12): Show |
21 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.821-276G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 8/17 | chr8 | 43173437 | |||||||
| chr8:43173478 | T | A | 3 | a0003c0003t0004g0197 a0003c0003t0004g0199 a0003c0003t0010g0200 |
3 | HG01192.hp2 HG02896.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.821-235T>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 8/17 | chr8 | 43173478 | |||||||
| chr8:43173512 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.821-201G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 8/17 | chr8 | 43173512 | |||||||
| chr8:43173607 | C | G | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.821-106C>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 8/17 | chr8 | 43173607 | |||||||
| chr8:43173953 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.851+210C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 9/17 | chr8 | 43173953 | |||||||
| chr8:43174613 | A | AT | 7 | a0003c0003t0004g0173 a0003c0003t0004g0196 a0003c0003t0004g0197 others(4): Show |
7 | HG01192.hp2 HG02896.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.851+876dupT | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr8 | 43174613 | ||||||
| chr8:43174744 | C | T | 2 | a0001c0001t0002g0041 a0001c0001t0002g0043 |
2 | HG00438.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.851+1001C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 9/17 | chr8 | 43174744 | |||||||
| chr8:43174997 | A | AACATGTG others(12): Show |
140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(137): Show |
160 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.851+1259_851+1260i others(21): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr8 | 43174997 | ||||||
| chr8:43175052 | C | G | 7 | a0003c0003t0004g0173 a0003c0003t0004g0196 a0003c0003t0004g0197 others(4): Show |
7 | HG01192.hp2 HG02896.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.851+1309C>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 9/17 | chr8 | 43175052 | |||||||
| chr8:43175557 | C | CT | 25 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0050 others(22): Show |
26 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.851+1839dupT | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr8 | 43175557 | ||||||
| chr8:43175557 | CT | C | 10 | a0001c0001t0001g0143 a0001c0001t0002g0025 a0001c0001t0002g0036 others(7): Show |
10 | HG01192.hp2 HG02004.hp1 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.851+1839delT | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr8 | 43175557 | ||||||
| chr8:43175580 | T | C | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.851+1837T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 9/17 | chr8 | 43175580 | |||||||
| chr8:43175627 | A | G | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.851+1884A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 9/17 | chr8 | 43175627 | |||||||
| chr8:43175661 | G | A | 1 | a0001c0001t0001g0017 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.851+1918G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 9/17 | chr8 | 43175661 | |||||||
| chr8:43175690 | C | T | 1 | a0001c0001t0001g0017 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.851+1947C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 9/17 | chr8 | 43175690 | |||||||
| chr8:43176058 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0021 a0001c0001t0001g0022 others(2): Show |
6 | HG01192.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.852-2016C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 9/17 | chr8 | 43176058 | |||||||
| chr8:43176229 | A | G | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(139): Show |
162 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.852-1845A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 9/17 | chr8 | 43176229 | |||||||
| chr8:43176248 | G | C | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.852-1826G>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 9/17 | chr8 | 43176248 | |||||||
| chr8:43176403 | T | C | 4 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0104 others(1): Show |
4 | HG01243.hp1 HG01433.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.852-1671T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 9/17 | chr8 | 43176403 | |||||||
| chr8:43176429 | A | G | 1 | a0001c0001t0001g0080 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.852-1645A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 9/17 | chr8 | 43176429 | |||||||
| chr8:43176603 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.852-1471A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 9/17 | chr8 | 43176603 | |||||||
| chr8:43176780 | T | A | 1 | a0001c0001t0002g0056 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.852-1294T>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 9/17 | chr8 | 43176780 | |||||||
| chr8:43176978 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG00738.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.852-1096G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 9/17 | chr8 | 43176978 | |||||||
| chr8:43177280 | G | A | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.852-794G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 9/17 | chr8 | 43177280 | |||||||
| chr8:43177347 | T | C | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.852-727T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 9/17 | chr8 | 43177347 | |||||||
| chr8:43177367 | C | T | 1 | a0001c0001t0006g0204 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.852-707C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 9/17 | chr8 | 43177367 | |||||||
| chr8:43177431 | A | G | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.852-643A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 9/17 | chr8 | 43177431 | |||||||
| chr8:43177508 | A | T | 3 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0162 |
3 | NA18939.hp1 NA18970.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.852-566A>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 9/17 | chr8 | 43177508 | |||||||
| chr8:43177557 | CA | C | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(119): Show |
141 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.852-496delA | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr8 | 43177557 | ||||||
| chr8:43177557 | CAA | C | 13 | a0001c0001t0001g0099 a0001c0001t0001g0103 a0002c0002t0005g0175 others(10): Show |
13 | HG01192.hp2 HG02055.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.852-497_852-496del others(2): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr8 | 43177557 | ||||||
| chr8:43177741 | T | A | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.852-333T>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 9/17 | chr8 | 43177741 | |||||||
| chr8:43177862 | A | T | 1 | a0001c0001t0001g0052 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.852-212A>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 9/17 | chr8 | 43177862 | |||||||
| chr8:43178342 | A | G | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1012+108A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43178342 | |||||||
| chr8:43178362 | T | C | 1 | a0001c0001t0001g0033 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1012+128T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43178362 | |||||||
| chr8:43178579 | GATTTCAT others(2650): Show |
G | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1012+361_1013-894d others(2): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43178579 | ||||||
| chr8:43178587 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1012+353C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43178587 | |||||||
| chr8:43178594 | C | CT | 10 | a0001c0001t0001g0130 a0001c0001t0002g0024 a0001c0001t0002g0025 others(7): Show |
10 | HG01978.hp1 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1012+380dupT | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43178594 | ||||||
| chr8:43178594 | C | CTT | 7 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0189 others(4): Show |
13 | HG02615.hp2 HG02717.hp2 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.1012+379_1012+380d others(4): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43178594 | ||||||
| chr8:43178594 | CT | C | 19 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0076 others(16): Show |
20 | HG01099.hp2 HG01167.hp2 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.1012+380delT | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43178594 | ||||||
| chr8:43178655 | T | TTCTCGCA others(4): Show |
7 | a0003c0003t0004g0173 a0003c0003t0004g0196 a0003c0003t0004g0197 others(4): Show |
7 | HG01192.hp2 HG02896.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1012+421_1012+422i others(13): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43178655 | |||||||
| chr8:43178750 | C | T | 4 | a0001c0001t0006g0168 a0001c0001t0006g0203 a0001c0001t0006g0204 others(1): Show |
4 | HG00099.hp2 HG01071.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1012+516C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43178750 | |||||||
| chr8:43178911 | A | G | 1 | a0002c0002t0009g0181 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1012+677A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43178911 | |||||||
| chr8:43179230 | C | T | 2 | a0002c0002t0005g0179 a0002c0002t0009g0181 |
2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1012+996C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43179230 | |||||||
| chr8:43179293 | C | A | 1 | a0001c0001t0001g0002 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1012+1059C>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43179293 | |||||||
| chr8:43179348 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1012+1114C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43179348 | |||||||
| chr8:43179361 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1012+1127G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43179361 | |||||||
| chr8:43179532 | C | T | 14 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0189 others(11): Show |
20 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1012+1298C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43179532 | |||||||
| chr8:43179534 | A | AC | 27 | a0001c0001t0001g0003 a0001c0001t0001g0033 a0001c0001t0001g0075 others(24): Show |
29 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.1012+1308dupC | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43179534 | ||||||
| chr8:43179540 | C | A | 1 | a0001c0001t0001g0002 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1012+1306C>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43179540 | |||||||
| chr8:43179540 | C | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0021 a0001c0001t0001g0022 others(2): Show |
6 | HG01192.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1012+1306C>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43179540 | |||||||
| chr8:43179543 | A | C | 7 | a0003c0003t0004g0173 a0003c0003t0004g0196 a0003c0003t0004g0197 others(4): Show |
7 | HG01192.hp2 HG02896.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1012+1309A>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43179543 | |||||||
| chr8:43179556 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1012+1322C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43179556 | |||||||
| chr8:43179557 | G | A | 2 | a0001c0001t0008g0150 a0001c0001t0008g0151 |
2 | HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1012+1323G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43179557 | |||||||
| chr8:43179576 | A | G | 7 | a0003c0003t0004g0173 a0003c0003t0004g0196 a0003c0003t0004g0197 others(4): Show |
7 | HG01192.hp2 HG02896.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1012+1342A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43179576 | |||||||
| chr8:43179595 | TCCAGTAG others(169): Show |
T | 4 | a0001c0001t0006g0168 a0001c0001t0006g0203 a0001c0001t0006g0204 others(1): Show |
4 | HG00099.hp2 HG01071.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1012+1404_1012+157 others(4): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43179595 | ||||||
| chr8:43179595 | TCCAGTAG others(564): Show |
T | 1 | a0005c0008t0003g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1012+1386_1013-195 others(4): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43179595 | ||||||
| chr8:43179639 | G | T | 1 | a0001c0001t0002g0063 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1012+1405G>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43179639 | |||||||
| chr8:43179652 | A | AGGCGGGG others(144): Show |
1 | a0003c0003t0004g0199 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1012+1427_1012+142 others(155): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43179652 | ||||||
| chr8:43179666 | T | C | 1 | a0003c0003t0004g0199 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1012+1432T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43179666 | |||||||
| chr8:43179666 | T | TCCCCCCA others(92): Show |
1 | a0001c0001t0001g0112 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1012+1449_1012+145 others(103): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43179666 | ||||||
| chr8:43179666 | T | TCCCCCCA others(93): Show |
1 | a0001c0001t0001g0156 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1012+1452_1012+145 others(104): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43179666 | ||||||
| chr8:43179666 | T | TCCCCCCA others(42): Show |
2 | a0001c0001t0001g0182 a0001c0001t0002g0005 |
2 | HG02015.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.1012+1452_1012+145 others(53): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43179666 | ||||||
| chr8:43179666 | T | TCCCCCCA others(143): Show |
1 | a0003c0003t0004g0173 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1012+1452_1012+145 others(154): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43179666 | ||||||
| chr8:43179666 | T | TCCCCCCA others(142): Show |
4 | a0003c0003t0004g0196 a0003c0003t0004g0197 a0003c0003t0004g0198 others(1): Show |
4 | HG02896.hp1 HG03195.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1012+1452_1012+145 others(153): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43179666 | ||||||
| chr8:43179666 | T | TCCCCCCA others(92): Show |
169 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(166): Show |
189 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.1012+1452_1012+145 others(103): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43179666 | ||||||
| chr8:43179666 | T | TCCCCCCA others(93): Show |
3 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0082 |
3 | HG01192.hp1 HG02809.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1012+1452_1012+145 others(104): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43179666 | ||||||
| chr8:43179666 | T | TCCCCCCA others(93): Show |
1 | a0001c0001t0002g0043 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1012+1452_1012+145 others(104): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43179666 | ||||||
| chr8:43179666 | T | TCCCCCCA others(93): Show |
1 | a0001c0001t0002g0024 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1012+1452_1012+145 others(104): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43179666 | ||||||
| chr8:43179666 | T | TCCCCCCA others(143): Show |
1 | a0003c0003t0004g0201 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1012+1452_1012+145 others(154): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43179666 | ||||||
| chr8:43179666 | T | TCCCCCCA others(93): Show |
8 | a0001c0001t0001g0002 a0001c0001t0001g0139 a0001c0001t0001g0140 others(5): Show |
8 | HG01167.hp1 HG01261.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.1012+1452_1012+145 others(104): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43179666 | ||||||
| chr8:43179666 | T | TCCCCCCA others(93): Show |
2 | a0001c0001t0001g0002 a0001c0001t0001g0130 |
2 | HG01978.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1012+1452_1012+145 others(104): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43179666 | ||||||
| chr8:43179666 | T | TCCCCCCA others(94): Show |
1 | a0001c0001t0002g0038 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1012+1452_1012+145 others(105): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43179666 | ||||||
| chr8:43179666 | T | TCCCCCCA others(93): Show |
1 | a0001c0001t0002g0007 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1012+1452_1012+145 others(104): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43179666 | ||||||
| chr8:43179684 | G | GGACGGGG others(92): Show |
1 | a0001c0001t0002g0007 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1012+1452_1012+145 others(103): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43179684 | ||||||
| chr8:43179687 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1012+1453T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43179687 | |||||||
| chr8:43179692 | C | CGGCTGGC others(96): Show |
1 | a0001c0001t0001g0124 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1012+1466_1012+146 others(107): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43179692 | ||||||
| chr8:43179736 | C | G | 1 | a0001c0001t0002g0188 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1012+1502C>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43179736 | |||||||
| chr8:43179757 | G | A | 1 | a0001c0001t0002g0024 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1012+1523G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43179757 | |||||||
| chr8:43179786 | C | T | 8 | a0001c0001t0001g0183 a0003c0003t0004g0173 a0003c0003t0004g0196 others(5): Show |
8 | HG01192.hp2 HG01496.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1012+1552C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43179786 | |||||||
| chr8:43179866 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1012+1632G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43179866 | |||||||
| chr8:43179907 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1012+1673C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43179907 | |||||||
| chr8:43179916 | C | T | 1 | a0001c0001t0001g0014 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1012+1682C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43179916 | |||||||
| chr8:43179924 | C | T | 14 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0189 others(11): Show |
20 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1012+1690C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43179924 | |||||||
| chr8:43179967 | TCTGGCCG others(164): Show |
T | 1 | a0001c0001t0008g0151 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1012+1801_1013-194 others(4): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43179967 | ||||||
| chr8:43180035 | A | G | 22 | a0001c0001t0008g0150 a0002c0002t0003g0001 a0002c0002t0003g0016 others(19): Show |
28 | HG01192.hp2 HG02055.hp1 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1012+1801A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43180035 | |||||||
| chr8:43180038 | C | T | 14 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0189 others(11): Show |
20 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1012+1804C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43180038 | |||||||
| chr8:43180040 | G | C | 5 | a0003c0003t0004g0197 a0003c0003t0004g0198 a0003c0003t0004g0199 others(2): Show |
5 | HG01192.hp2 HG02896.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1012+1806G>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43180040 | |||||||
| chr8:43180051 | C | G | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(105): Show |
121 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.1012+1817C>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43180051 | |||||||
| chr8:43180093 | G | T | 1 | a0001c0001t0001g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1012+1859G>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43180093 | |||||||
| chr8:43180102 | A | AC | 71 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(68): Show |
73 | HG00423.hp2 HG00558.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.1012+1879dupC | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43180102 | ||||||
| chr8:43180102 | A | ACC | 82 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(79): Show |
88 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1012+1878_1012+187 others(6): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43180102 | ||||||
| chr8:43180110 | C | CG | 5 | a0003c0003t0004g0196 a0003c0003t0004g0197 a0003c0003t0004g0198 others(2): Show |
5 | HG02896.hp1 HG03195.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1012+1876_1012+187 others(5): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43180110 | |||||||
| chr8:43180113 | C | T | 7 | a0003c0003t0004g0173 a0003c0003t0004g0196 a0003c0003t0004g0197 others(4): Show |
7 | HG01192.hp2 HG02896.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1012+1879C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43180113 | |||||||
| chr8:43180124 | TC | T | 14 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0189 others(11): Show |
20 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1012+1893delC | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43180124 | ||||||
| chr8:43180214 | T | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(136): Show |
159 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1013-1931T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43180214 | |||||||
| chr8:43180222 | C | T | 1 | a0001c0001t0002g0038 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1013-1923C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43180222 | |||||||
| chr8:43180255 | C | T | 1 | a0001c0001t0008g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1013-1890C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43180255 | |||||||
| chr8:43180299 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1013-1846C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43180299 | |||||||
| chr8:43180312 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1013-1833G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43180312 | |||||||
| chr8:43180388 | C | T | 2 | a0001c0001t0001g0137 a0001c0001t0001g0139 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1013-1757C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43180388 | |||||||
| chr8:43180389 | G | T | 1 | a0001c0001t0001g0013 | 2 | NA18747.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.1013-1756G>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43180389 | |||||||
| chr8:43180439 | A | G | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(137): Show |
160 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1013-1706A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43180439 | |||||||
| chr8:43180493 | C | T | 15 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0189 others(12): Show |
21 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1013-1652C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43180493 | |||||||
| chr8:43180504 | C | T | 5 | a0002c0002t0005g0175 a0002c0002t0005g0176 a0002c0002t0005g0177 others(2): Show |
5 | HG02055.hp1 HG02109.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1013-1641C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43180504 | |||||||
| chr8:43180575 | G | T | 1 | a0001c0001t0001g0171 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1013-1570G>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43180575 | |||||||
| chr8:43180679 | CTTCCCAG others(6): Show |
C | 1 | a0001c0001t0012g0152 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1013-1464_1013-145 others(17): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43180679 | ||||||
| chr8:43180700 | T | C | 3 | a0001c0001t0001g0017 a0001c0001t0008g0150 a0001c0001t0008g0151 |
4 | HG02886.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1013-1445T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43180700 | |||||||
| chr8:43180852 | AGGCCGAG others(7): Show |
A | 1 | a0001c0001t0002g0025 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1013-1291_1013-127 others(18): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43180852 | ||||||
| chr8:43180911 | C | T | 1 | a0001c0001t0002g0064 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1013-1234C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43180911 | |||||||
| chr8:43180912 | G | A | 2 | a0001c0001t0008g0150 a0001c0001t0008g0151 |
2 | HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1013-1233G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43180912 | |||||||
| chr8:43180928 | C | CA | 14 | a0001c0001t0001g0014 a0001c0001t0001g0109 a0001c0001t0001g0110 others(11): Show |
14 | HG00597.hp2 HG00673.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.1013-1209dupA | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43180928 | ||||||
| chr8:43180933 | A | G | 1 | a0001c0001t0002g0063 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1013-1212A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43180933 | |||||||
| chr8:43180937 | C | A | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(198): Show |
227 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.1013-1208C>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43180937 | |||||||
| chr8:43180958 | C | T | 1 | a0001c0001t0002g0032 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1013-1187C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43180958 | |||||||
| chr8:43180965 | C | T | 2 | a0001c0001t0008g0150 a0001c0001t0008g0151 |
2 | HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1013-1180C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43180965 | |||||||
| chr8:43180996 | G | A | 1 | a0001c0001t0001g0002 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1013-1149G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43180996 | |||||||
| chr8:43181030 | C | T | 2 | a0001c0001t0008g0150 a0001c0001t0008g0151 |
2 | HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1013-1115C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181030 | |||||||
| chr8:43181081 | T | TGGAGGGA others(27): Show |
2 | a0001c0001t0001g0002 a0001c0001t0002g0007 |
2 | HG02129.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1013-1059_1013-102 others(38): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181081 | ||||||
| chr8:43181081 | T | TGGAGGGA others(33): Show |
2 | a0001c0001t0001g0003 a0001c0001t0001g0157 |
2 | HG01993.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.1013-1059_1013-102 others(44): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181081 | ||||||
| chr8:43181081 | T | TGGAGGGA others(39): Show |
1 | a0001c0001t0002g0038 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1013-1059_1013-101 others(50): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181081 | ||||||
| chr8:43181081 | T | TGGAGGGA others(45): Show |
1 | a0001c0001t0002g0005 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1013-1059_1013-100 others(56): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181081 | ||||||
| chr8:43181082 | G | GGAGGGAG others(5): Show |
1 | a0001c0001t0001g0091 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1013-921_1013-910d others(14): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181082 | ||||||
| chr8:43181082 | G | GGAGGGAG others(11): Show |
1 | a0003c0003t0010g0200 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1013-927_1013-910d others(20): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181082 | ||||||
| chr8:43181082 | G | GGAGGGAG others(17): Show |
3 | a0001c0001t0001g0109 a0001c0001t0001g0146 a0001c0001t0006g0205 |
3 | HG03491.hp2 HG03669.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.1013-933_1013-910d others(26): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181082 | ||||||
| chr8:43181082 | G | GGAGGGAG others(23): Show |
3 | a0001c0001t0001g0162 a0001c0001t0001g0165 a0003c0003t0004g0198 |
3 | HG03225.hp2 NA18970.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1013-939_1013-910d others(32): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181082 | ||||||
| chr8:43181082 | G | GGAGGGAG others(29): Show |
1 | a0001c0001t0001g0131 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1013-945_1013-910d others(38): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181082 | ||||||
| chr8:43181082 | G | GGAGGGAG others(58): Show |
1 | a0001c0001t0001g0160 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1013-1017_1013-101 others(69): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181082 | ||||||
| chr8:43181082 | G | GGAGGGAG others(41): Show |
1 | a0003c0003t0004g0199 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1013-957_1013-910d others(50): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181082 | ||||||
| chr8:43181082 | G | GGAGGGAG others(53): Show |
1 | a0001c0001t0001g0120 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1013-969_1013-910d others(62): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181082 | ||||||
| chr8:43181082 | G | GGAGGGAG others(59): Show |
1 | a0003c0003t0004g0197 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1013-975_1013-910d others(68): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181082 | ||||||
| chr8:43181082 | G | GGAGGGAG others(71): Show |
1 | a0001c0001t0001g0149 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1013-987_1013-910d others(80): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181082 | ||||||
| chr8:43181082 | G | GGAGGGAG others(51): Show |
3 | a0001c0001t0001g0002 a0001c0001t0002g0036 a0001c0001t0002g0041 |
3 | HG02132.hp1 HG02293.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.1013-1014_1013-101 others(62): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181082 | ||||||
| chr8:43181082 | G | GGAGGGAG others(39): Show |
4 | a0001c0001t0001g0099 a0001c0001t0002g0034 a0001c0001t0002g0126 others(1): Show |
4 | HG01074.hp1 HG02273.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1013-1020_1013-101 others(50): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181082 | ||||||
| chr8:43181082 | G | GGAGGGAG others(51): Show |
1 | a0001c0001t0002g0045 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1013-1020_1013-101 others(62): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181082 | ||||||
| chr8:43181082 | G | GGAGGGAG others(39): Show |
1 | a0001c0001t0002g0065 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1013-1026_1013-102 others(50): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181082 | ||||||
| chr8:43181082 | G | GGAGGGAG others(51): Show |
2 | a0001c0001t0007g0061 a0001c0001t0007g0062 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1013-1026_1013-102 others(62): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181082 | ||||||
| chr8:43181082 | G | GGAGGGAG others(63): Show |
1 | a0001c0001t0001g0156 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1013-1026_1013-102 others(74): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181082 | ||||||
| chr8:43181082 | GGAGGGAG others(5): Show |
G | 2 | a0001c0001t0001g0145 a0001c0001t0006g0203 |
2 | HG01071.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1013-921_1013-910d others(14): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181082 | ||||||
| chr8:43181082 | GGAGGGAG others(17): Show |
G | 1 | a0001c0001t0001g0129 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1013-933_1013-910d others(26): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181082 | ||||||
| chr8:43181082 | GGAGGGAG others(29): Show |
G | 1 | a0003c0003t0004g0196 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1013-945_1013-910d others(38): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181082 | ||||||
| chr8:43181082 | GGAGGGAG others(59): Show |
G | 1 | a0003c0003t0004g0173 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1013-975_1013-910d others(68): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181082 | ||||||
| chr8:43181082 | GGAGGGAG others(91): Show |
G | 1 | a0001c0001t0001g0017 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1013-1061_1013-964 others(101): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181082 | ||||||
| chr8:43181088 | A | AGAGGGAG others(21): Show |
2 | a0001c0001t0001g0105 a0001c0001t0001g0153 |
2 | HG03540.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1013-1053_1013-102 others(32): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181088 | ||||||
| chr8:43181088 | A | AGAGGGAG others(27): Show |
3 | a0001c0001t0002g0037 a0001c0001t0002g0072 a0001c0001t0002g0187 |
3 | HG00423.hp1 HG01168.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1013-1053_1013-102 others(38): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181088 | ||||||
| chr8:43181088 | A | AGAGGGAG others(33): Show |
3 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0002g0006 |
3 | HG01361.hp2 HG02273.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.1013-1053_1013-101 others(44): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181088 | ||||||
| chr8:43181088 | A | AGAGGGAG others(42): Show |
1 | a0001c0001t0012g0152 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1013-1056_1013-100 others(53): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181088 | ||||||
| chr8:43181088 | A | AGAGGGAG others(127): Show |
1 | a0001c0001t0002g0042 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1013-1014_1013-101 others(138): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181088 | ||||||
| chr8:43181092 | GGAGAGGG others(49): Show |
G | 1 | a0001c0001t0001g0092 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1013-1049_1013-994 others(59): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181092 | ||||||
| chr8:43181094 | A | AGAGGGAG others(15): Show |
1 | a0001c0001t0007g0067 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1013-1047_1013-102 others(26): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181094 | ||||||
| chr8:43181094 | A | AGAGGGAG others(21): Show |
5 | a0001c0001t0001g0079 a0001c0001t0001g0121 a0001c0001t0001g0127 others(2): Show |
5 | HG00735.hp2 HG01109.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1013-1047_1013-102 others(32): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181094 | ||||||
| chr8:43181094 | A | AGAGGGAG others(27): Show |
1 | a0001c0001t0001g0012 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1013-1047_1013-101 others(38): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181094 | ||||||
| chr8:43181094 | A | AGAGGGAG others(33): Show |
2 | a0001c0001t0001g0014 a0001c0001t0001g0112 |
2 | HG01169.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.1013-1047_1013-100 others(44): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181094 | ||||||
| chr8:43181094 | A | AGAGGGAG others(32): Show |
1 | a0001c0001t0001g0113 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1013-1020_1013-101 others(43): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181094 | ||||||
| chr8:43181098 | GGAGAGGG others(49): Show |
G | 1 | a0002c0002t0009g0181 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1013-1043_1013-988 others(59): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181098 | ||||||
| chr8:43181098 | GGAGAGGG others(55): Show |
G | 5 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0008g0151 others(2): Show |
5 | HG00738.hp2 HG01081.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1013-1043_1013-982 others(65): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181098 | ||||||
| chr8:43181098 | GGAGAGGG others(61): Show |
G | 7 | a0001c0001t0001g0020 a0001c0001t0008g0150 a0002c0002t0005g0175 others(4): Show |
7 | HG00741.hp2 HG02055.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1013-1043_1013-976 others(71): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181098 | ||||||
| chr8:43181100 | A | AGAGGGAG others(9): Show |
2 | a0001c0001t0001g0182 a0001c0001t0002g0007 |
2 | HG02015.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.1013-1041_1013-102 others(20): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181100 | ||||||
| chr8:43181100 | A | AGAGGGAG others(15): Show |
3 | a0001c0001t0001g0123 a0001c0001t0001g0183 a0001c0001t0011g0085 |
3 | HG01109.hp2 HG01496.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1013-1041_1013-102 others(26): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181100 | ||||||
| chr8:43181100 | A | AGAGGGAG others(27): Show |
2 | a0001c0001t0001g0014 a0001c0001t0002g0035 |
2 | HG01168.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1013-1041_1013-100 others(38): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181100 | ||||||
| chr8:43181100 | A | AGAGGGAG others(33): Show |
1 | a0001c0001t0001g0155 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1013-1041_1013-100 others(44): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181100 | ||||||
| chr8:43181100 | AGAGGGAG others(60): Show |
A | 6 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0189 others(3): Show |
12 | HG02615.hp2 HG02717.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.1013-1044_1013-978 others(70): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181100 | |||||||
| chr8:43181100 | AGAGGGAG others(66): Show |
A | 1 | a0002c0002t0003g0191 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1013-1044_1013-972 others(76): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181100 | |||||||
| chr8:43181104 | GGAGAGGG others(43): Show |
G | 1 | a0001c0001t0002g0167 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1013-1037_1013-988 others(53): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181104 | ||||||
| chr8:43181106 | A | AGAGGGAG others(3): Show |
3 | a0001c0001t0001g0158 a0001c0001t0002g0066 a0001c0001t0015g0006 |
3 | HG01928.hp1 HG03831.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.1013-1035_1013-102 others(14): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181106 | ||||||
| chr8:43181106 | A | AGAGGGAG others(9): Show |
5 | a0001c0001t0001g0003 a0001c0001t0002g0056 a0001c0001t0002g0078 others(2): Show |
5 | HG01993.hp1 HG02257.hp1 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.1013-1035_1013-102 others(20): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181106 | ||||||
| chr8:43181106 | A | AGAGGGAG others(15): Show |
6 | a0001c0001t0001g0003 a0001c0001t0001g0081 a0001c0001t0001g0100 others(3): Show |
6 | HG00639.hp2 HG01106.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.1013-1035_1013-101 others(26): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181106 | ||||||
| chr8:43181106 | A | AGAGGGAG others(21): Show |
5 | a0001c0001t0001g0013 a0001c0001t0001g0033 a0001c0001t0002g0044 others(2): Show |
6 | HG00597.hp1 HG01081.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.1013-1035_1013-100 others(32): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181106 | ||||||
| chr8:43181106 | A | AGAGGGAG others(27): Show |
1 | a0001c0001t0001g0164 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1013-1035_1013-100 others(38): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181106 | ||||||
| chr8:43181110 | GGAGAGGG others(19): Show |
G | 2 | a0001c0001t0001g0049 a0001c0001t0002g0064 |
2 | HG03710.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1013-1031_1013-100 others(30): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181110 | ||||||
| chr8:43181110 | GGAGAGGG others(25): Show |
G | 1 | a0001c0001t0001g0060 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1013-1031_1013-100 others(36): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181110 | ||||||
| chr8:43181110 | GGAGAGGG others(31): Show |
G | 2 | a0001c0001t0001g0071 a0001c0001t0002g0030 |
2 | HG01358.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1013-1031_1013-994 others(41): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181110 | ||||||
| chr8:43181112 | A | AGAGGGAG others(3): Show |
7 | a0001c0001t0001g0023 a0001c0001t0001g0133 a0001c0001t0001g0134 others(4): Show |
7 | HG01192.hp1 HG01978.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.1013-1029_1013-102 others(14): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181112 | ||||||
| chr8:43181112 | A | AGAGGGAG others(9): Show |
4 | a0001c0001t0001g0051 a0001c0001t0001g0154 a0001c0001t0002g0046 others(1): Show |
4 | HG01074.hp2 HG02165.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1013-1029_1013-101 others(20): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181112 | ||||||
| chr8:43181112 | A | AGAGGGAG others(15): Show |
4 | a0001c0001t0001g0050 a0001c0001t0001g0095 a0001c0001t0001g0122 others(1): Show |
4 | HG00741.hp1 HG01934.hp2 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1013-1029_1013-100 others(26): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181112 | ||||||
| chr8:43181112 | A | AGAGGGAG others(3): Show |
1 | a0001c0001t0002g0031 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1013-1026_1013-102 others(14): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181112 | ||||||
| chr8:43181114 | A | G | 1 | a0001c0001t0002g0025 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1013-1031A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181114 | |||||||
| chr8:43181116 | GGAGAGGG others(7): Show |
G | 3 | a0001c0001t0001g0194 a0001c0001t0002g0028 a0001c0001t0002g0169 |
3 | HG01261.hp2 NA18939.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.1013-1025_1013-101 others(18): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181116 | ||||||
| chr8:43181116 | GGAGAGGG others(13): Show |
G | 1 | a0001c0001t0002g0029 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1013-1025_1013-100 others(24): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181116 | ||||||
| chr8:43181116 | GGAGAGGG others(37): Show |
G | 1 | a0001c0001t0001g0142 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1013-1025_1013-982 others(47): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181116 | ||||||
| chr8:43181118 | A | AGAGG | 5 | a0001c0001t0001g0089 a0001c0001t0001g0098 a0001c0001t0002g0010 others(2): Show |
5 | HG00099.hp1 HG01243.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1013-1023_1013-102 others(8): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181118 | ||||||
| chr8:43181118 | A | AGAGGGAG others(9): Show |
3 | a0001c0001t0001g0097 a0001c0001t0001g0103 a0001c0001t0001g0186 |
3 | HG03654.hp1 HG03704.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1013-1023_1013-100 others(20): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181118 | ||||||
| chr8:43181118 | A | AGAGGGAG others(15): Show |
2 | a0001c0001t0002g0048 a0001c0001t0002g0073 |
2 | HG02572.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.1013-1023_1013-100 others(26): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181118 | ||||||
| chr8:43181120 | A | G | 1 | a0001c0001t0002g0025 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1013-1025A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181120 | |||||||
| chr8:43181122 | G | A | 1 | a0002c0002t0003g0135 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1013-1023G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181122 | |||||||
| chr8:43181122 | GGAGAGGG others(1): Show |
G | 6 | a0001c0001t0001g0015 a0001c0001t0001g0077 a0001c0001t0001g0111 others(3): Show |
7 | HG00673.hp2 HG02809.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1013-1019_1013-101 others(12): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181122 | ||||||
| chr8:43181122 | GGAGAGGG others(7): Show |
G | 3 | a0001c0001t0001g0088 a0001c0001t0001g0104 a0001c0001t0001g0132 |
3 | HG01433.hp2 HG03471.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.1013-1019_1013-100 others(18): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181122 | ||||||
| chr8:43181122 | GGAGAGGG others(13): Show |
G | 1 | a0001c0001t0001g0114 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1013-1019_1013-100 others(24): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181122 | ||||||
| chr8:43181122 | GGAGAGGG others(19): Show |
G | 2 | a0001c0001t0001g0102 a0001c0001t0002g0009 |
2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1013-1019_1013-994 others(29): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181122 | ||||||
| chr8:43181122 | GGAGAGGG others(25): Show |
G | 2 | a0001c0001t0001g0139 a0001c0001t0002g0009 |
2 | HG01167.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1013-1019_1013-988 others(35): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181122 | ||||||
| chr8:43181122 | GGAGAGGG others(31): Show |
G | 3 | a0001c0001t0001g0002 a0001c0001t0001g0076 a0001c0001t0001g0137 |
3 | HG01099.hp2 HG01169.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1013-1019_1013-982 others(41): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181122 | ||||||
| chr8:43181124 | A | AGAGG | 6 | a0001c0001t0001g0022 a0001c0001t0001g0117 a0001c0001t0001g0171 others(3): Show |
6 | HG02071.hp2 HG02723.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1013-1017_1013-101 others(8): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181124 | ||||||
| chr8:43181124 | A | AGAGGGAG others(3): Show |
5 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0128 others(2): Show |
5 | HG00639.hp1 HG00738.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.1013-1017_1013-100 others(14): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181124 | ||||||
| chr8:43181124 | A | AGAGGGAG others(92): Show |
1 | a0001c0001t0002g0043 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1013-1014_1013-101 others(103): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181124 | ||||||
| chr8:43181124 | A | AGGGAGAG others(91): Show |
1 | a0001c0001t0002g0040 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1013-1020_1013-101 others(102): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181124 | ||||||
| chr8:43181124 | A | G | 2 | a0001c0001t0002g0026 a0001c0001t0002g0170 |
2 | NA18612.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.1013-1021A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181124 | |||||||
| chr8:43181124 | AGAGGGAG others(3): Show |
A | 1 | a0001c0001t0002g0025 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1013-1017_1013-100 others(14): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181124 | ||||||
| chr8:43181128 | GGAGAGGG others(7): Show |
G | 2 | a0001c0001t0001g0082 a0004c0007t0001g0107 |
2 | HG01934.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1013-1013_1013-100 others(18): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181128 | ||||||
| chr8:43181128 | GGAGAGGG others(13): Show |
G | 2 | a0001c0001t0001g0116 a0001c0001t0002g0004 |
2 | HG02572.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.1013-1013_1013-994 others(23): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181128 | ||||||
| chr8:43181128 | GGAGAGGG others(19): Show |
G | 2 | a0001c0001t0001g0119 a0001c0001t0001g0144 |
2 | HG00423.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1013-1013_1013-988 others(29): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181128 | ||||||
| chr8:43181128 | GGAGAGGG others(25): Show |
G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0087 a0001c0001t0001g0090 others(2): Show |
6 | HG01346.hp2 HG01928.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.1013-1013_1013-982 others(35): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181128 | ||||||
| chr8:43181128 | GGAGAGGG others(31): Show |
G | 1 | a0001c0001t0001g0140 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1013-1013_1013-976 others(41): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181128 | ||||||
| chr8:43181130 | A | AGAGG | 3 | a0001c0001t0001g0021 a0001c0001t0001g0115 a0001c0001t0001g0148 |
3 | HG00558.hp2 HG02486.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1013-1011_1013-100 others(8): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181130 | ||||||
| chr8:43181130 | A | G | 1 | a0001c0001t0002g0026 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1013-1015A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181130 | |||||||
| chr8:43181134 | GGAGAGGG others(7): Show |
G | 1 | a0001c0001t0001g0096 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1013-1007_1013-994 others(17): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181134 | ||||||
| chr8:43181134 | GGAGAGGG others(13): Show |
G | 2 | a0001c0001t0001g0075 a0001c0001t0001g0083 |
2 | HG00408.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1013-1007_1013-988 others(23): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181134 | ||||||
| chr8:43181134 | GGAGAGGG others(25): Show |
G | 1 | a0001c0001t0001g0101 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1013-1007_1013-976 others(35): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181134 | ||||||
| chr8:43181136 | A | AGAGG | 2 | a0001c0001t0001g0052 a0001c0001t0001g0118 |
2 | HG03491.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1013-1005_1013-100 others(8): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181136 | ||||||
| chr8:43181136 | A | AGAGGGAG others(15): Show |
1 | a0001c0001t0001g0184 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1013-1005_1013-984 others(25): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181136 | ||||||
| chr8:43181136 | A | G | 5 | a0001c0001t0001g0194 a0001c0001t0002g0025 a0001c0001t0002g0026 others(2): Show |
5 | HG01261.hp2 NA18612.hp2 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.1013-1009A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181136 | |||||||
| chr8:43181140 | GGAGAGGG others(13): Show |
G | 1 | a0001c0001t0001g0124 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1013-1001_1013-982 others(23): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181140 | ||||||
| chr8:43181140 | GGAGAGGG others(19): Show |
G | 1 | a0001c0001t0001g0080 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1013-1001_1013-976 others(29): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181140 | ||||||
| chr8:43181142 | A | G | 7 | a0001c0001t0001g0049 a0001c0001t0001g0194 a0001c0001t0002g0026 others(4): Show |
7 | HG01261.hp2 HG03710.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.1013-1003A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181142 | |||||||
| chr8:43181148 | A | G | 4 | a0001c0001t0001g0049 a0001c0001t0001g0060 a0001c0001t0002g0029 others(1): Show |
4 | HG03710.hp2 HG03831.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.1013-997A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181148 | |||||||
| chr8:43181154 | A | G | 4 | a0001c0001t0001g0060 a0001c0001t0001g0071 a0001c0001t0001g0092 others(1): Show |
4 | HG01346.hp1 HG01358.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.1013-991A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181154 | |||||||
| chr8:43181160 | A | AGAGG | 2 | a0001c0001t0002g0040 a0001c0001t0002g0042 |
2 | HG02132.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.1013-981_1013-978d others(6): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181160 | ||||||
| chr8:43181160 | A | G | 5 | a0001c0001t0001g0071 a0001c0001t0001g0092 a0001c0001t0002g0030 others(2): Show |
5 | HG01346.hp1 HG01358.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1013-985A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181160 | |||||||
| chr8:43181163 | G | GGGAGAGG others(32): Show |
1 | a0001c0001t0001g0003 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1013-969_1013-968i others(41): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181163 | ||||||
| chr8:43181166 | A | G | 9 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(6): Show |
9 | HG00738.hp2 HG01081.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.1013-979A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181166 | |||||||
| chr8:43181171 | GA | G | 6 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0189 others(3): Show |
12 | HG02615.hp2 HG02717.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.1013-973delA | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181171 | |||||||
| chr8:43181172 | A | G | 14 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(11): Show |
14 | HG00738.hp2 HG00741.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.1013-973A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181172 | |||||||
| chr8:43181178 | A | G | 20 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(17): Show |
26 | HG00738.hp2 HG00741.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.1013-967A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181178 | |||||||
| chr8:43181184 | A | G | 21 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(18): Show |
28 | HG00738.hp2 HG00741.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.1013-961A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181184 | |||||||
| chr8:43181190 | A | G | 14 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(11): Show |
21 | HG00738.hp2 HG00741.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.1013-955A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181190 | |||||||
| chr8:43181196 | A | G | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
8 | HG00738.hp2 HG00741.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.1013-949A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181196 | |||||||
| chr8:43181202 | A | G | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(2): Show |
6 | HG00738.hp2 HG00741.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.1013-943A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181202 | |||||||
| chr8:43181208 | A | G | 4 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(1): Show |
5 | HG00738.hp2 HG00741.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.1013-937A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181208 | |||||||
| chr8:43181209 | G | C | 1 | a0003c0003t0004g0173 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1013-936G>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181209 | |||||||
| chr8:43181214 | A | G | 4 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(1): Show |
5 | HG00738.hp2 HG00741.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.1013-931A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181214 | |||||||
| chr8:43181218 | G | C | 1 | a0001c0001t0001g0077 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1013-927G>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181218 | |||||||
| chr8:43181220 | A | G | 4 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(1): Show |
5 | HG00738.hp2 HG00741.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.1013-925A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181220 | |||||||
| chr8:43181221 | G | C | 1 | a0003c0003t0004g0173 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1013-924G>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181221 | |||||||
| chr8:43181226 | A | G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 |
3 | HG00738.hp2 HG00741.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.1013-919A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181226 | |||||||
| chr8:43181228 | A | AGGGAGAG others(53): Show |
1 | a0001c0001t0001g0130 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1013-910_1013-909i others(62): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr8 | 43181228 | ||||||
| chr8:43181230 | G | C | 2 | a0001c0001t0001g0015 a0001c0001t0002g0028 |
3 | HG02896.hp2 HG02897.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.1013-915G>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181230 | |||||||
| chr8:43181286 | T | C | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1013-859T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181286 | |||||||
| chr8:43181554 | G | C | 2 | a0001c0001t0008g0150 a0001c0001t0008g0151 |
2 | HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1013-591G>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181554 | |||||||
| chr8:43181629 | G | A | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1013-516G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181629 | |||||||
| chr8:43181702 | C | T | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1013-443C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 10/17 | chr8 | 43181702 | |||||||
| chr8:43182395 | C | T | 1 | a0001c0001t0002g0125 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1128+135C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43182395 | |||||||
| chr8:43182732 | C | T | 2 | a0001c0001t0008g0150 a0001c0001t0008g0151 |
2 | HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1128+472C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43182732 | |||||||
| chr8:43182741 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1128+481C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43182741 | |||||||
| chr8:43182863 | C | A | 1 | a0001c0001t0001g0182 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1128+603C>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43182863 | |||||||
| chr8:43183063 | C | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(131): Show |
154 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.1128+803C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43183063 | |||||||
| chr8:43183279 | A | G | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(138): Show |
161 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.1128+1019A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43183279 | |||||||
| chr8:43183373 | C | T | 4 | a0001c0001t0006g0168 a0001c0001t0006g0203 a0001c0001t0006g0204 others(1): Show |
4 | HG00099.hp2 HG01071.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128+1113C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43183373 | |||||||
| chr8:43183393 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1128+1133C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43183393 | |||||||
| chr8:43183425 | C | T | 1 | a0001c0001t0002g0053 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1128+1165C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43183425 | |||||||
| chr8:43183443 | A | G | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1128+1183A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43183443 | |||||||
| chr8:43183469 | A | AT | 5 | a0001c0001t0001g0033 a0001c0001t0002g0024 a0001c0001t0006g0204 others(2): Show |
5 | HG00597.hp1 HG03098.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.1128+1223dupT | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr8 | 43183469 | ||||||
| chr8:43183586 | T | A | 1 | a0001c0001t0001g0111 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1128+1326T>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43183586 | |||||||
| chr8:43183615 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1128+1355C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43183615 | |||||||
| chr8:43183646 | T | A | 7 | a0001c0001t0002g0004 a0001c0001t0002g0053 a0001c0001t0002g0056 others(4): Show |
9 | HG01106.hp1 HG02257.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1128+1386T>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43183646 | |||||||
| chr8:43183717 | T | C | 1 | a0001c0001t0002g0073 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1128+1457T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43183717 | |||||||
| chr8:43183800 | A | C | 16 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0189 others(13): Show |
22 | HG01243.hp2 HG02055.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1128+1540A>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43183800 | |||||||
| chr8:43183820 | G | A | 1 | a0001c0001t0002g0073 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1128+1560G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43183820 | |||||||
| chr8:43183826 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1128+1566C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43183826 | |||||||
| chr8:43183861 | C | A | 1 | a0001c0001t0002g0125 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1128+1601C>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43183861 | |||||||
| chr8:43183898 | T | C | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1128+1638T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43183898 | |||||||
| chr8:43184098 | G | A | 2 | a0002c0002t0003g0135 a0002c0002t0003g0136 |
2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1128+1838G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43184098 | |||||||
| chr8:43184113 | T | C | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1128+1853T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43184113 | |||||||
| chr8:43184209 | A | G | 16 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0189 others(13): Show |
22 | HG01243.hp2 HG02055.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1128+1949A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43184209 | |||||||
| chr8:43184224 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1128+1964A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43184224 | |||||||
| chr8:43184241 | C | T | 107 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(104): Show |
120 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.1128+1981C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43184241 | |||||||
| chr8:43184295 | CTGT | C | 2 | a0002c0002t0005g0179 a0002c0002t0009g0181 |
2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1128+2040_1128+204 others(7): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr8 | 43184295 | ||||||
| chr8:43184429 | G | A | 1 | a0005c0008t0003g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1128+2169G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43184429 | |||||||
| chr8:43184469 | T | A | 1 | a0001c0001t0002g0025 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1128+2209T>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43184469 | |||||||
| chr8:43184492 | C | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0081 |
3 | HG00639.hp2 HG00738.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1128+2232C>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43184492 | |||||||
| chr8:43184556 | G | T | 1 | a0003c0003t0004g0196 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1128+2296G>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43184556 | |||||||
| chr8:43184640 | G | A | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1128+2380G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43184640 | |||||||
| chr8:43184813 | A | G | 1 | a0002c0002t0005g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1128+2553A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43184813 | |||||||
| chr8:43184833 | T | C | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1128+2573T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43184833 | |||||||
| chr8:43184934 | A | G | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1128+2674A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43184934 | |||||||
| chr8:43185288 | T | C | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1128+3028T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43185288 | |||||||
| chr8:43185340 | G | A | 1 | a0001c0001t0008g0151 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1128+3080G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43185340 | |||||||
| chr8:43185377 | G | C | 4 | a0001c0001t0006g0168 a0001c0001t0006g0203 a0001c0001t0006g0204 others(1): Show |
4 | HG00099.hp2 HG01071.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128+3117G>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43185377 | |||||||
| chr8:43185560 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1128+3300A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43185560 | |||||||
| chr8:43186062 | G | A | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1128+3802G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43186062 | |||||||
| chr8:43186248 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1128+3988G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43186248 | |||||||
| chr8:43186517 | G | T | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1128+4257G>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43186517 | |||||||
| chr8:43186527 | C | T | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1128+4267C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43186527 | |||||||
| chr8:43186580 | A | G | 2 | a0001c0001t0008g0150 a0001c0001t0008g0151 |
2 | HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1128+4320A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43186580 | |||||||
| chr8:43186940 | A | G | 1 | a0002c0002t0005g0179 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1129-4534A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43186940 | |||||||
| chr8:43187088 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1129-4386C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43187088 | |||||||
| chr8:43187089 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1129-4385A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43187089 | |||||||
| chr8:43187109 | G | C | 1 | a0001c0001t0002g0028 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1129-4365G>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43187109 | |||||||
| chr8:43187124 | T | G | 4 | a0001c0001t0006g0168 a0001c0001t0006g0203 a0001c0001t0006g0204 others(1): Show |
4 | HG00099.hp2 HG01071.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1129-4350T>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43187124 | |||||||
| chr8:43187127 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1129-4347A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43187127 | |||||||
| chr8:43187153 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1129-4321C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43187153 | |||||||
| chr8:43187161 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1129-4313T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43187161 | |||||||
| chr8:43187162 | G | T | 1 | a0001c0001t0001g0141 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1129-4312G>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43187162 | |||||||
| chr8:43187165 | G | T | 1 | a0001c0001t0001g0141 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1129-4309G>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43187165 | |||||||
| chr8:43187182 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1129-4292A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43187182 | |||||||
| chr8:43187183 | T | G | 1 | a0001c0001t0001g0141 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1129-4291T>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43187183 | |||||||
| chr8:43187291 | G | T | 109 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(106): Show |
122 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1129-4183G>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43187291 | |||||||
| chr8:43187425 | T | G | 1 | a0001c0001t0001g0087 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1129-4049T>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43187425 | |||||||
| chr8:43187470 | C | T | 7 | a0003c0003t0004g0173 a0003c0003t0004g0196 a0003c0003t0004g0197 others(4): Show |
7 | HG01192.hp2 HG02896.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1129-4004C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43187470 | |||||||
| chr8:43187520 | T | G | 7 | a0003c0003t0004g0173 a0003c0003t0004g0196 a0003c0003t0004g0197 others(4): Show |
7 | HG01192.hp2 HG02896.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1129-3954T>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43187520 | |||||||
| chr8:43187543 | C | T | 1 | a0005c0008t0003g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1129-3931C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43187543 | |||||||
| chr8:43187661 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1129-3813A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43187661 | |||||||
| chr8:43187689 | C | T | 8 | a0001c0001t0001g0017 a0002c0002t0003g0001 a0002c0002t0003g0016 others(5): Show |
15 | HG02615.hp2 HG02717.hp2 HG02886.hp2 others(12): Show |
intron_variant | MODIFIER | c.1129-3785C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43187689 | |||||||
| chr8:43187958 | T | G | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1129-3516T>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43187958 | |||||||
| chr8:43188048 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1129-3426T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43188048 | |||||||
| chr8:43188461 | C | T | 1 | a0004c0007t0001g0107 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1129-3013C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43188461 | |||||||
| chr8:43188581 | G | A | 1 | a0001c0001t0001g0017 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1129-2893G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43188581 | |||||||
| chr8:43188585 | A | G | 26 | a0001c0001t0001g0017 a0001c0001t0008g0150 a0001c0001t0008g0151 others(23): Show |
33 | HG01192.hp2 HG02055.hp1 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1129-2889A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43188585 | |||||||
| chr8:43188729 | G | A | 1 | a0001c0001t0002g0064 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1129-2745G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43188729 | |||||||
| chr8:43188747 | C | G | 1 | a0001c0001t0001g0047 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1129-2727C>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43188747 | |||||||
| chr8:43189052 | G | A | 1 | a0003c0003t0004g0173 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1129-2422G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43189052 | |||||||
| chr8:43189054 | G | A | 1 | a0003c0003t0004g0196 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1129-2420G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43189054 | |||||||
| chr8:43189133 | C | T | 15 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0189 others(12): Show |
21 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1129-2341C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43189133 | |||||||
| chr8:43189202 | C | T | 1 | a0001c0001t0002g0025 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1129-2272C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43189202 | |||||||
| chr8:43189207 | A | G | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1129-2267A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43189207 | |||||||
| chr8:43189220 | C | T | 15 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0189 others(12): Show |
21 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1129-2254C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43189220 | |||||||
| chr8:43189242 | C | T | 1 | a0001c0001t0002g0147 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1129-2232C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43189242 | |||||||
| chr8:43189315 | T | A | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1129-2159T>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43189315 | |||||||
| chr8:43189343 | T | C | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1129-2131T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43189343 | |||||||
| chr8:43189364 | C | T | 7 | a0003c0003t0004g0173 a0003c0003t0004g0196 a0003c0003t0004g0197 others(4): Show |
7 | HG01192.hp2 HG02896.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1129-2110C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43189364 | |||||||
| chr8:43189374 | T | C | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1129-2100T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43189374 | |||||||
| chr8:43189418 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1129-2056G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43189418 | |||||||
| chr8:43189437 | A | G | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1129-2037A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43189437 | |||||||
| chr8:43189578 | C | G | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1129-1896C>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43189578 | |||||||
| chr8:43189648 | G | A | 1 | a0001c0001t0006g0168 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1129-1826G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43189648 | |||||||
| chr8:43189730 | G | A | 1 | a0001c0001t0002g0125 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1129-1744G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43189730 | |||||||
| chr8:43189752 | C | T | 7 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0189 others(4): Show |
13 | HG02615.hp2 HG02717.hp2 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.1129-1722C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43189752 | |||||||
| chr8:43189817 | C | T | 5 | a0001c0001t0002g0025 a0001c0001t0002g0027 a0001c0001t0002g0029 others(2): Show |
5 | HG00673.hp1 NA18946.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.1129-1657C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43189817 | |||||||
| chr8:43189844 | T | C | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1129-1630T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43189844 | |||||||
| chr8:43189872 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1129-1602C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43189872 | |||||||
| chr8:43190422 | G | A | 6 | a0003c0003t0004g0173 a0003c0003t0004g0196 a0003c0003t0004g0197 others(3): Show |
6 | HG01192.hp2 HG03139.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1129-1052G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43190422 | |||||||
| chr8:43190594 | G | A | 1 | a0002c0002t0005g0179 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1129-880G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43190594 | |||||||
| chr8:43190595 | C | T | 1 | a0002c0002t0005g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1129-879C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43190595 | |||||||
| chr8:43190596 | G | A | 1 | a0001c0001t0002g0031 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1129-878G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43190596 | |||||||
| chr8:43190628 | A | G | 8 | a0001c0001t0013g0202 a0003c0003t0004g0173 a0003c0003t0004g0196 others(5): Show |
8 | HG01192.hp2 HG02896.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.1129-846A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43190628 | |||||||
| chr8:43190816 | T | C | 7 | a0003c0003t0004g0173 a0003c0003t0004g0196 a0003c0003t0004g0197 others(4): Show |
7 | HG01192.hp2 HG02896.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1129-658T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43190816 | |||||||
| chr8:43190837 | G | A | 106 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(103): Show |
119 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.1129-637G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43190837 | |||||||
| chr8:43191150 | A | G | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1129-324A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43191150 | |||||||
| chr8:43191201 | A | G | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1129-273A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43191201 | |||||||
| chr8:43191252 | G | A | 107 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(104): Show |
120 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.1129-222G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43191252 | |||||||
| chr8:43191287 | A | G | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1129-187A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 11/17 | chr8 | 43191287 | |||||||
| chr8:43191602 | G | A | 1 | a0001c0001t0002g0167 | 1 | HG02258.hp1 | splice_region_variant&intron_variant | LOW | c.1250+7G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 12/17 | chr8 | 43191602 | |||||||
| chr8:43191668 | G | T | 1 | a0001c0001t0002g0084 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1250+73G>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 12/17 | chr8 | 43191668 | |||||||
| chr8:43191927 | G | GT | 18 | a0001c0001t0001g0049 a0001c0001t0001g0060 a0001c0001t0001g0071 others(15): Show |
18 | HG00673.hp1 HG00735.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.1250+342dupT | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr8 | 43191927 | ||||||
| chr8:43191968 | G | A | 2 | a0002c0002t0005g0179 a0002c0002t0009g0181 |
2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1251-336G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 12/17 | chr8 | 43191968 | |||||||
| chr8:43191976 | A | T | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1251-328A>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 12/17 | chr8 | 43191976 | |||||||
| chr8:43192013 | G | C | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(134): Show |
156 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.1251-291G>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 12/17 | chr8 | 43192013 | |||||||
| chr8:43192015 | G | A | 7 | a0003c0003t0004g0173 a0003c0003t0004g0196 a0003c0003t0004g0197 others(4): Show |
7 | HG01192.hp2 HG02896.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1251-289G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 12/17 | chr8 | 43192015 | |||||||
| chr8:43192084 | A | G | 13 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0189 others(10): Show |
19 | HG01243.hp2 HG02055.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1251-220A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 12/17 | chr8 | 43192084 | |||||||
| chr8:43192174 | C | T | 7 | a0003c0003t0004g0173 a0003c0003t0004g0196 a0003c0003t0004g0197 others(4): Show |
7 | HG01192.hp2 HG02896.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1251-130C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 12/17 | chr8 | 43192174 | |||||||
| chr8:43192257 | C | T | 7 | a0003c0003t0004g0173 a0003c0003t0004g0196 a0003c0003t0004g0197 others(4): Show |
7 | HG01192.hp2 HG02896.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1251-47C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 12/17 | chr8 | 43192257 | |||||||
| chr8:43192450 | G | A | 27 | a0001c0001t0001g0002 a0001c0001t0001g0076 a0001c0001t0001g0080 others(24): Show |
31 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.1377+20G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 13/17 | chr8 | 43192450 | |||||||
| chr8:43192859 | T | C | 4 | a0001c0001t0006g0168 a0001c0001t0006g0203 a0001c0001t0006g0204 others(1): Show |
4 | HG00099.hp2 HG01071.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1377+429T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 13/17 | chr8 | 43192859 | |||||||
| chr8:43192906 | G | A | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1377+476G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 13/17 | chr8 | 43192906 | |||||||
| chr8:43192910 | T | C | 7 | a0001c0001t0002g0004 a0001c0001t0002g0053 a0001c0001t0002g0056 others(4): Show |
9 | HG01106.hp1 HG02257.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1377+480T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 13/17 | chr8 | 43192910 | |||||||
| chr8:43193018 | C | CG | 7 | a0001c0001t0001g0112 a0001c0001t0001g0130 a0001c0001t0001g0161 others(4): Show |
7 | HG01106.hp1 HG01978.hp1 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.1377+592dupG | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr8 | 43193018 | ||||||
| chr8:43193044 | A | G | 7 | a0003c0003t0004g0173 a0003c0003t0004g0196 a0003c0003t0004g0197 others(4): Show |
7 | HG01192.hp2 HG02896.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1377+614A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 13/17 | chr8 | 43193044 | |||||||
| chr8:43193092 | G | A | 4 | a0001c0001t0006g0168 a0001c0001t0006g0203 a0001c0001t0006g0204 others(1): Show |
4 | HG00099.hp2 HG01071.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1377+662G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 13/17 | chr8 | 43193092 | |||||||
| chr8:43193123 | T | C | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(138): Show |
161 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.1378-634T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 13/17 | chr8 | 43193123 | |||||||
| chr8:43193707 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1378-50G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 13/17 | chr8 | 43193707 | |||||||
| chr8:43193988 | G | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG01261.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1464+145G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | chr8 | 43193988 | |||||||
| chr8:43194006 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1464+163C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | chr8 | 43194006 | |||||||
| chr8:43194052 | C | CA | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(108): Show |
124 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.1464+216dupA | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr8 | 43194052 | ||||||
| chr8:43194187 | C | T | 2 | a0001c0001t0006g0203 a0001c0001t0006g0204 |
2 | HG01071.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1464+344C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | chr8 | 43194187 | |||||||
| chr8:43194600 | G | T | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(138): Show |
161 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.1464+757G>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | chr8 | 43194600 | |||||||
| chr8:43194938 | G | A | 1 | a0001c0001t0002g0042 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1464+1095G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | chr8 | 43194938 | |||||||
| chr8:43195268 | G | T | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1464+1425G>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | chr8 | 43195268 | |||||||
| chr8:43195344 | C | T | 2 | a0001c0001t0008g0150 a0001c0001t0008g0151 |
2 | HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1464+1501C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | chr8 | 43195344 | |||||||
| chr8:43195366 | G | T | 1 | a0001c0001t0001g0023 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1464+1523G>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | chr8 | 43195366 | |||||||
| chr8:43195369 | A | G | 1 | a0005c0008t0003g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1464+1526A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | chr8 | 43195369 | |||||||
| chr8:43195415 | A | C | 1 | a0005c0008t0003g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1465-1533A>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | chr8 | 43195415 | |||||||
| chr8:43195480 | TAGG | T | 1 | a0001c0001t0001g0017 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1465-1459_1465-145 others(7): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr8 | 43195480 | ||||||
| chr8:43195492 | A | G | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(137): Show |
159 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1465-1456A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | chr8 | 43195492 | |||||||
| chr8:43195514 | A | G | 1 | a0001c0001t0002g0065 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1465-1434A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | chr8 | 43195514 | |||||||
| chr8:43195515 | G | A | 1 | a0001c0001t0002g0065 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1465-1433G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | chr8 | 43195515 | |||||||
| chr8:43195518 | AGAAGAGG others(2): Show |
A | 1 | a0001c0001t0001g0014 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1465-1418_1465-141 others(13): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr8 | 43195518 | ||||||
| chr8:43195521 | A | AGAG | 8 | a0001c0001t0013g0202 a0003c0003t0004g0173 a0003c0003t0004g0196 others(5): Show |
8 | HG01192.hp2 HG02896.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.1465-1421_1465-141 others(7): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr8 | 43195521 | ||||||
| chr8:43195528 | G | GAGA | 2 | a0001c0001t0008g0150 a0001c0001t0008g0151 |
2 | HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1465-1419_1465-141 others(7): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr8 | 43195528 | ||||||
| chr8:43195572 | G | GGGGGTGG others(47): Show |
1 | a0001c0001t0001g0071 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1465-1350_1465-129 others(58): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr8 | 43195572 | ||||||
| chr8:43195655 | T | TGGAGGAG others(14): Show |
135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(132): Show |
155 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.1465-1278_1465-127 others(25): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr8 | 43195655 | ||||||
| chr8:43195655 | T | TGGAGGAG others(10): Show |
1 | a0001c0001t0012g0152 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1465-1280_1465-127 others(21): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr8 | 43195655 | ||||||
| chr8:43195656 | G | GGAGGAGG others(11): Show |
2 | a0001c0001t0008g0150 a0001c0001t0008g0151 |
2 | HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1465-1278_1465-127 others(22): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr8 | 43195656 | ||||||
| chr8:43195738 | G | A | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1465-1210G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | chr8 | 43195738 | |||||||
| chr8:43195746 | AGAG | A | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(131): Show |
154 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.1465-1191_1465-118 others(7): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr8 | 43195746 | ||||||
| chr8:43195761 | G | A | 1 | a0005c0008t0003g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1465-1187G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | chr8 | 43195761 | |||||||
| chr8:43195849 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1465-1099G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | chr8 | 43195849 | |||||||
| chr8:43196050 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1465-898C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | chr8 | 43196050 | |||||||
| chr8:43196134 | C | T | 5 | a0001c0001t0001g0079 a0001c0001t0001g0102 a0001c0001t0001g0106 others(2): Show |
5 | HG02055.hp2 HG02622.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1465-814C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | chr8 | 43196134 | |||||||
| chr8:43196184 | G | A | 10 | a0001c0001t0008g0150 a0001c0001t0008g0151 a0001c0001t0013g0202 others(7): Show |
10 | HG01192.hp2 HG02886.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.1465-764G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | chr8 | 43196184 | |||||||
| chr8:43196414 | C | T | 1 | a0001c0001t0001g0017 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1465-534C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | chr8 | 43196414 | |||||||
| chr8:43196527 | C | T | 2 | a0001c0001t0008g0150 a0001c0001t0008g0151 |
2 | HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1465-421C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | chr8 | 43196527 | |||||||
| chr8:43196568 | C | A | 7 | a0003c0003t0004g0173 a0003c0003t0004g0196 a0003c0003t0004g0197 others(4): Show |
7 | HG01192.hp2 HG02896.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1465-380C>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | chr8 | 43196568 | |||||||
| chr8:43196574 | C | G | 17 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0135 others(14): Show |
23 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1465-374C>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 14/17 | chr8 | 43196574 | |||||||
| chr8:43197045 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1542+20C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 15/17 | chr8 | 43197045 | |||||||
| chr8:43197598 | A | G | 6 | a0002c0002t0005g0175 a0002c0002t0005g0176 a0002c0002t0005g0177 others(3): Show |
6 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1543-74A>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 15/17 | chr8 | 43197598 | |||||||
| chr8:43198235 | T | C | 1 | a0003c0003t0004g0196 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1726+283T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 17/17 | chr8 | 43198235 | |||||||
| chr8:43198244 | G | A | 1 | a0001c0001t0002g0065 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1726+292G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 17/17 | chr8 | 43198244 | |||||||
| chr8:43198280 | C | CT | 25 | a0001c0001t0001g0033 a0001c0001t0001g0101 a0001c0001t0001g0106 others(22): Show |
25 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.1726+353dupT | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr8 | 43198280 | ||||||
| chr8:43198280 | CT | C | 17 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0002g0046 others(14): Show |
23 | HG00673.hp2 HG01167.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.1726+353delT | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr8 | 43198280 | ||||||
| chr8:43198280 | CTT | C | 5 | a0001c0001t0006g0168 a0001c0001t0006g0203 a0001c0001t0006g0204 others(2): Show |
5 | HG00099.hp2 HG01071.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1726+352_1726+353d others(4): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr8 | 43198280 | ||||||
| chr8:43198280 | CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0008g0150 a0001c0001t0008g0151 |
2 | HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1726+343_1726+353d others(13): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr8 | 43198280 | ||||||
| chr8:43198280 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1726+342_1726+353d others(14): Show |
HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr8 | 43198280 | ||||||
| chr8:43198301 | T | C | 1 | a0001c0001t0013g0202 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1726+349T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 17/17 | chr8 | 43198301 | |||||||
| chr8:43198380 | C | G | 1 | a0001c0001t0011g0085 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1726+428C>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 17/17 | chr8 | 43198380 | |||||||
| chr8:43198418 | G | A | 1 | a0003c0003t0004g0196 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1726+466G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 17/17 | chr8 | 43198418 | |||||||
| chr8:43198432 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1726+480C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 17/17 | chr8 | 43198432 | |||||||
| chr8:43198497 | T | C | 1 | a0001c0005t0001g0195 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1726+545T>C | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 17/17 | chr8 | 43198497 | |||||||
| chr8:43198516 | C | T | 1 | a0005c0008t0003g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1726+564C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 17/17 | chr8 | 43198516 | |||||||
| chr8:43198523 | G | A | 1 | a0001c0001t0001g0015 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1726+571G>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 17/17 | chr8 | 43198523 | |||||||
| chr8:43198666 | G | T | 10 | a0001c0001t0008g0150 a0001c0001t0008g0151 a0001c0001t0013g0202 others(7): Show |
10 | HG01192.hp2 HG02886.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.1726+714G>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 17/17 | chr8 | 43198666 | |||||||
| chr8:43198751 | C | A | 18 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0135 others(15): Show |
24 | HG01243.hp2 HG02055.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1727-637C>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 17/17 | chr8 | 43198751 | |||||||
| chr8:43198930 | C | T | 1 | a0003c0003t0004g0198 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1727-458C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 17/17 | chr8 | 43198930 | |||||||
| chr8:43199199 | C | A | 1 | a0001c0001t0001g0094 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1727-189C>A | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 17/17 | chr8 | 43199199 | |||||||
| chr8:43199236 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1727-152C>T | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 17/17 | chr8 | 43199236 | |||||||
| chr8:43199282 | T | G | 1 | a0001c0001t0001g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1727-106T>G | HGSNAT | ENSG00000165102.15 | transcript | ENST00000379644.9 | protein_coding | 17/17 | chr8 | 43199282 |