Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4735 |
| ensemblid | ENSG00000168385.18 |
| hgncid | 7729 |
| symbol | SEPTIN2 |
| name | septin 2 |
| refseq_nuc | NM_004404.5 |
| refseq_prot | NP_004395.1 |
| ensembl_nuc | ENST00000391971.7 |
| ensembl_prot | ENSP00000375832.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 241315925 |
| end | 241354027 |
| strand | + |
| ver | v1.2 |
| region | chr2:241315925-241354027 |
| region5000 | chr2:241310925-241359027 |
| regionname0 | SEPTIN2_chr2_241315925_241354027 |
| regionname5000 | SEPTIN2_chr2_241310925_241359027 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 361 | 407 | 86 | 70 | 194 | 13 | 42 | 146 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | MSKQQ others(356): Show |
chr2 | 241310925 | 241359027 |
| a0002 | 0/0 | 361 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | MSKQQ others(356): Show |
chr2 | 241310925 | 241359027 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1083 | 404 | 86 | 69 | 192 | 13 | 42 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | ATGTC others(1078): Show |
chr2 | 241310925 | 241359027 | ||
| a0001c0002 | 0/0 | 1083 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | ATGTC others(1078): Show |
chr2 | 241310925 | 241359027 | ||
| a0001c0004 | 0/0 | 1083 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | ATGTC others(1078): Show |
chr2 | 241310925 | 241359027 | ||
| a0001c0005 | 0/0 | 1083 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | ATGTC others(1078): Show |
chr2 | 241310925 | 241359027 | ||
| a0002c0003 | 0/0 | 1083 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | ATGTC others(1078): Show |
chr2 | 241310925 | 241359027 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3251 | 98 | 7 | 10 | 67 | 4 | 10 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0001c0001t0002 | 0/0 | 3251 | 59 | 6 | 10 | 32 | 1 | 10 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0001c0001t0003 | 1/0 | 3251 | 49 | 16 | 6 | 16 | 1 | 9 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0001c0001t0004 | 0/0 | 3251 | 41 | 0 | 16 | 21 | 0 | 4 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0001c0001t0005 | 0/0 | 3251 | 34 | 0 | 0 | 32 | 2 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0001c0001t0006 | 0/0 | 3251 | 30 | 11 | 14 | 0 | 3 | 2 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0001c0001t0007 | 0/1 | 3251 | 29 | 1 | 6 | 15 | 1 | 5 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0001c0001t0008 | 0/0 | 3251 | 7 | 6 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0001c0001t0009 | 0/0 | 3247 | 5 | 0 | 0 | 5 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3242): Show |
chr2 | 241310925 | 241359027 |
| a0001c0001t0010 | 0/0 | 3251 | 5 | 5 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0001c0001t0011 | 0/0 | 3251 | 5 | 5 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0001c0001t0012 | 0/0 | 3251 | 5 | 2 | 3 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0001c0001t0013 | 0/0 | 3251 | 4 | 4 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0001c0001t0014 | 0/0 | 3251 | 4 | 4 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0001c0001t0015 | 0/0 | 3251 | 4 | 4 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0001c0001t0016 | 0/0 | 3251 | 4 | 4 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0001c0001t0017 | 0/0 | 3251 | 3 | 3 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0001c0001t0018 | 0/0 | 3251 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0001c0001t0019 | 0/0 | 3251 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0001c0001t0020 | 0/0 | 3251 | 2 | 0 | 1 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0001c0001t0021 | 0/0 | 3251 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0001c0001t0022 | 0/0 | 3251 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0001c0001t0023 | 0/0 | 3251 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0001c0001t0024 | 0/0 | 3251 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0001c0001t0025 | 0/0 | 3251 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0001c0001t0026 | 0/0 | 3251 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0001c0001t0027 | 0/0 | 3251 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0001c0001t0028 | 0/0 | 3251 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0001c0001t0029 | 0/0 | 3251 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0001c0001t0030 | 0/0 | 3251 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0001c0001t0031 | 0/0 | 3251 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0001c0002t0008 | 0/0 | 3251 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0001c0004t0002 | 0/0 | 3251 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0001c0005t0004 | 0/0 | 3251 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| a0002c0003t0002 | 0/0 | 3251 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | AGCGC others(3246): Show |
chr2 | 241310925 | 241359027 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 10 | 1 | 2 | 4 | 1 | 2 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0010 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0044 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0045 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0008 | 0/0 | 4 | 2 | 0 | 1 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0009 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0015 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0040 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0003 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0004g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0005g0004 | 0/0 | 6 | 0 | 0 | 5 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0005g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0005g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0005g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0005g0039 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0005g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0005g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0005g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0005g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0005g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0005g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0005g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0005g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0005g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0006g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0006g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0006g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0006g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0006g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0006g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0006g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0006g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0006g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0006g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0006g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0006g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0006g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0006g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0006g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0006g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0006g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0006g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0006g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0006g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0006g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0006g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0006g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0006g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0007g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0007g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0007g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0007g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0007g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0007g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0007g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0007g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0007g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0007g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0007g0180 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0007g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0007g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0007g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0007g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0007g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0007g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0007g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0007g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0007g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0007g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0007g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0007g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0008g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0008g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0008g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0008g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0008g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0009g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0009g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0009g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0009g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0009g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0010g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0010g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0010g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0010g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0011g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0011g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0011g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0011g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0012g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0012g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0013g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0013g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0013g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0013g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0014g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0014g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0014g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0014g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0015g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0015g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0015g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0016g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0016g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0016g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0017g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0017g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0017g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0018g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0018g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0019g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0019g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0020g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0020g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0021g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0021g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0022g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0023g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0024g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0025g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0026g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0027g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0028g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0029g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0030g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0001t0031g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0002t0008g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0004t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0001c0005t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| a0002c0003t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0006 | g0310 | EUR | GBR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00099 | hp2 | a0002 | c0003 | t0002 | g0059 | EUR | GBR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00140 | hp1 | a0001 | c0001 | t0029 | g0135 | EUR | GBR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00140 | hp2 | a0001 | c0001 | t0006 | g0309 | EUR | GBR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0039 | EUR | FIN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0255 | EUR | FIN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00323 | hp1 | a0001 | c0001 | t0005 | g0004 | EUR | FIN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0199 | EUR | FIN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0286 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00423 | hp1 | a0001 | c0001 | t0005 | g0208 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00423 | hp2 | a0001 | c0001 | t0007 | g0036 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00544 | hp1 | a0001 | c0001 | t0007 | g0005 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0226 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00597 | hp1 | a0001 | c0001 | t0009 | g0167 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00597 | hp2 | a0001 | c0001 | t0023 | g0284 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0163 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0279 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0035 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00639 | hp2 | a0001 | c0001 | t0007 | g0191 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00642 | hp1 | a0001 | c0001 | t0006 | g0300 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0220 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00741 | hp1 | a0001 | c0001 | t0012 | g0013 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0042 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01069 | hp1 | a0001 | c0001 | t0006 | g0311 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01069 | hp2 | a0001 | c0001 | t0012 | g0013 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01071 | hp1 | a0001 | c0001 | t0012 | g0013 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01074 | hp2 | a0001 | c0001 | t0006 | g0305 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01081 | hp1 | a0001 | c0001 | t0006 | g0050 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0166 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0277 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0252 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0242 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01109 | hp2 | a0001 | c0001 | t0006 | g0303 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01167 | hp2 | a0001 | c0001 | t0007 | g0174 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01168 | hp1 | a0001 | c0001 | t0006 | g0052 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0215 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01169 | hp2 | a0001 | c0001 | t0006 | g0052 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01175 | hp2 | a0001 | c0001 | t0026 | g0156 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01192 | hp1 | a0001 | c0001 | t0006 | g0253 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0282 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0312 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | CLM | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01256 | hp1 | a0001 | c0001 | t0006 | g0306 | AMR | CLM | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0164 | AMR | CLM | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01261 | hp1 | a0001 | c0001 | t0024 | g0193 | AMR | CLM | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01261 | hp2 | a0001 | c0001 | t0006 | g0050 | AMR | CLM | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01358 | hp1 | a0001 | c0001 | t0007 | g0037 | AMR | CLM | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01358 | hp2 | a0001 | c0001 | t0006 | g0302 | AMR | CLM | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0154 | AMR | CLM | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01433 | hp2 | a0001 | c0001 | t0006 | g0304 | AMR | CLM | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01496 | hp1 | a0001 | c0001 | t0008 | g0031 | AMR | CLM | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0015 | AMR | CLM | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | IBS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01516 | hp1 | a0001 | c0001 | t0007 | g0037 | EUR | IBS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01884 | hp1 | a0001 | c0001 | t0008 | g0032 | AFR | ACB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01884 | hp2 | a0001 | c0001 | t0016 | g0296 | AFR | ACB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0210 | AFR | ACB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01928 | hp2 | a0001 | c0001 | t0007 | g0186 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01934 | hp1 | a0001 | c0001 | t0020 | g0244 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01934 | hp2 | a0001 | c0002 | t0008 | g0149 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01975 | hp2 | a0001 | c0001 | t0007 | g0183 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01981 | hp1 | a0001 | c0001 | t0004 | g0314 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0159 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0082 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0165 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02027 | hp1 | a0001 | c0001 | t0007 | g0175 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02027 | hp2 | a0001 | c0001 | t0005 | g0039 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02056 | hp1 | a0001 | c0001 | t0005 | g0209 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0290 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0289 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02071 | hp2 | a0001 | c0001 | t0020 | g0245 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02074 | hp2 | a0001 | c0001 | t0005 | g0014 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02080 | hp1 | a0001 | c0001 | t0009 | g0168 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02080 | hp2 | a0001 | c0001 | t0007 | g0185 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02135 | hp2 | a0001 | c0001 | t0007 | g0036 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02145 | hp2 | a0001 | c0001 | t0008 | g0053 | AFR | ACB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | CDX | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CDX | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CDX | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CDX | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02257 | hp2 | a0001 | c0001 | t0017 | g0316 | AFR | ACB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0214 | AFR | ACB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0143 | AFR | ACB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0142 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0157 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02293 | hp2 | a0001 | c0001 | t0007 | g0178 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0035 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02300 | hp2 | a0001 | c0001 | t0004 | g0145 | AMR | PEL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02451 | hp1 | a0001 | c0001 | t0008 | g0148 | AFR | ACB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02451 | hp2 | a0001 | c0001 | t0011 | g0073 | AFR | ACB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02523 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0038 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02572 | hp2 | a0001 | c0001 | t0016 | g0298 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02615 | hp2 | a0001 | c0001 | t0011 | g0020 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0051 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02622 | hp2 | a0001 | c0001 | t0008 | g0032 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02630 | hp1 | a0001 | c0001 | t0019 | g0274 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02630 | hp2 | a0001 | c0001 | t0011 | g0071 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0251 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0283 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02717 | hp1 | a0001 | c0001 | t0015 | g0021 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0221 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02723 | hp1 | a0001 | c0001 | t0015 | g0076 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0198 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0045 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0038 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02818 | hp1 | a0001 | c0001 | t0019 | g0273 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02818 | hp2 | a0001 | c0001 | t0021 | g0223 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0307 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02896 | hp1 | a0001 | c0001 | t0018 | g0299 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02896 | hp2 | a0001 | c0001 | t0017 | g0077 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02897 | hp1 | a0001 | c0001 | t0018 | g0297 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02922 | hp1 | a0001 | c0001 | t0008 | g0146 | AFR | ESN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02922 | hp2 | a0001 | c0001 | t0013 | g0147 | AFR | ESN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0254 | AFR | ESN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02970 | hp1 | a0001 | c0001 | t0010 | g0022 | AFR | ESN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | ESN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0189 | AFR | ESN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03017 | hp1 | a0001 | c0001 | t0006 | g0301 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0212 | AFR | MSL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03098 | hp2 | a0001 | c0001 | t0014 | g0172 | AFR | MSL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03130 | hp1 | a0001 | c0001 | t0021 | g0007 | AFR | ESN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03130 | hp2 | a0001 | c0001 | t0013 | g0150 | AFR | ESN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0295 | AFR | ESN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03139 | hp2 | a0001 | c0001 | t0010 | g0072 | AFR | ESN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0213 | AFR | ESN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03195 | hp2 | a0001 | c0001 | t0013 | g0151 | AFR | ESN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03209 | hp1 | a0001 | c0001 | t0015 | g0021 | AFR | MSL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0292 | AFR | MSL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03453 | hp1 | a0001 | c0001 | t0022 | g0241 | AFR | MSL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03453 | hp2 | a0001 | c0001 | t0016 | g0049 | AFR | MSL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03486 | hp1 | a0001 | c0001 | t0011 | g0020 | AFR | MSL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | MSL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0040 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03516 | hp1 | a0001 | c0001 | t0015 | g0075 | AFR | ESN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03540 | hp1 | a0001 | c0001 | t0010 | g0080 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03540 | hp2 | a0001 | c0001 | t0012 | g0030 | AFR | GWD | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03579 | hp1 | a0001 | c0001 | t0010 | g0022 | AFR | MSL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0248 | AFR | MSL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03654 | hp2 | a0001 | c0001 | t0007 | g0188 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03669 | hp2 | a0001 | c0001 | t0027 | g0015 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | STU | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | STU | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0216 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0228 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03710 | hp2 | a0001 | c0001 | t0007 | g0278 | SAS | PJL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0280 | SAS | BEB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03831 | hp2 | a0001 | c0001 | t0007 | g0179 | SAS | BEB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0008 | SAS | BEB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0313 | SAS | BEB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03927 | hp1 | a0001 | c0001 | t0007 | g0182 | SAS | BEB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | BEB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03942 | hp1 | a0001 | c0001 | t0007 | g0192 | SAS | BEB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0281 | SAS | BEB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0227 | SAS | STU | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | STU | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | BEB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG04184 | hp2 | a0001 | c0001 | t0025 | g0028 | SAS | BEB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0263 | SAS | STU | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG04199 | hp2 | a0001 | c0001 | t0006 | g0308 | SAS | STU | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0285 | SAS | STU | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18522 | hp1 | a0001 | c0001 | t0013 | g0152 | AFR | YRI | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | YRI | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18612 | hp1 | a0001 | c0001 | t0007 | g0184 | EAS | CHB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | CHB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0195 | AFR | YRI | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18906 | hp2 | a0001 | c0001 | t0017 | g0078 | AFR | YRI | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18941 | hp2 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18943 | hp2 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18946 | hp2 | a0001 | c0001 | t0005 | g0016 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18950 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18951 | hp2 | a0001 | c0001 | t0009 | g0170 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18952 | hp1 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0162 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18954 | hp1 | a0001 | c0001 | t0030 | g0002 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18959 | hp2 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18961 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18962 | hp2 | a0001 | c0001 | t0005 | g0207 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18965 | hp1 | a0001 | c0001 | t0009 | g0153 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18966 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0161 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0171 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18970 | hp2 | a0001 | c0001 | t0005 | g0014 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18971 | hp2 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18977 | hp2 | a0001 | c0001 | t0005 | g0041 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18978 | hp1 | a0001 | c0001 | t0005 | g0041 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18981 | hp2 | a0001 | c0001 | t0009 | g0034 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18982 | hp1 | a0001 | c0001 | t0005 | g0230 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0144 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18984 | hp1 | a0001 | c0005 | t0004 | g0288 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18988 | hp1 | a0001 | c0001 | t0005 | g0014 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18988 | hp2 | a0001 | c0001 | t0004 | g0158 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18995 | hp1 | a0001 | c0001 | t0005 | g0233 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18998 | hp1 | a0001 | c0004 | t0002 | g0257 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19000 | hp1 | a0001 | c0001 | t0007 | g0190 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0155 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19006 | hp2 | a0001 | c0001 | t0005 | g0232 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0160 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19009 | hp2 | a0001 | c0001 | t0005 | g0202 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19010 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19010 | hp2 | a0001 | c0001 | t0007 | g0173 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19011 | hp1 | a0001 | c0001 | t0031 | g0120 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19012 | hp2 | a0001 | c0001 | t0007 | g0176 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19030 | hp1 | a0001 | c0001 | t0028 | g0211 | AFR | LWK | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19030 | hp2 | a0001 | c0001 | t0014 | g0200 | AFR | LWK | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0229 | AFR | LWK | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19043 | hp2 | a0001 | c0001 | t0012 | g0030 | AFR | LWK | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19054 | hp1 | a0001 | c0001 | t0005 | g0016 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19062 | hp1 | a0001 | c0001 | t0005 | g0231 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19063 | hp1 | a0001 | c0001 | t0005 | g0196 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19065 | hp1 | a0001 | c0001 | t0005 | g0243 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19067 | hp2 | a0001 | c0001 | t0005 | g0201 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19068 | hp2 | a0001 | c0001 | t0005 | g0016 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0169 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19070 | hp2 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19074 | hp1 | a0001 | c0001 | t0005 | g0206 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19076 | hp1 | a0001 | c0001 | t0007 | g0187 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0291 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19082 | hp1 | a0001 | c0001 | t0005 | g0204 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19083 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19084 | hp2 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19085 | hp1 | a0001 | c0001 | t0004 | g0287 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19087 | hp2 | a0001 | c0001 | t0005 | g0205 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19091 | hp2 | a0001 | c0001 | t0007 | g0177 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0051 | AFR | YRI | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA19240 | hp2 | a0001 | c0001 | t0008 | g0031 | AFR | YRI | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | ASW | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ASW | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | TSI | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA20805 | hp2 | a0001 | c0001 | t0006 | g0293 | EUR | TSI | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | GIH | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0197 | SAS | GIH | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01123 | hp1 | a0001 | c0001 | t0006 | g0294 | AMR | CLM | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | CLM | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0265 | AFR | ACB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02486 | hp2 | a0001 | c0001 | t0014 | g0240 | AFR | ACB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0194 | AFR | ACB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0218 | AFR | ACB | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0315 | AFR | MSL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG03471 | hp2 | a0001 | c0001 | t0016 | g0049 | AFR | MSL | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG06807 | hp1 | a0001 | c0001 | t0011 | g0074 | AFR | USA | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0219 | AFR | USA | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA20300 | hp1 | a0001 | c0001 | t0010 | g0079 | AFR | USA | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA20300 | hp2 | a0001 | c0001 | t0007 | g0181 | AFR | USA | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | LWK | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| NA21309 | hp2 | a0001 | c0001 | t0014 | g0246 | AFR | LWK | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0007 | g0180 | REF | REF | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0015 | REF | REF | SEPTIN2_chr2_241310925_241359027 | SEPTIN2 | chr2 | 241310925 | 241359027 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:241346222 | G | A | 1 | a0002 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.899G>A | p.Arg300His | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/13 | 974/3251 | 899/1086 | 300/361 | chr2 | 241346222 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:241337694 | G | A | 1 | a0001c0002 | 1 | HG01934.hp2 | synonymous_variant | LOW | c.498G>A | p.Ala166Ala | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/13 | 573/3251 | 498/1086 | 166/361 | chr2 | 241337694 | |||
| chr2:241343814 | C | T | 1 | a0001c0005 | 1 | NA18984.hp1 | synonymous_variant | LOW | c.759C>T | p.Val253Val | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/13 | 834/3251 | 759/1086 | 253/361 | chr2 | 241343814 | |||
| chr2:241350162 | G | A | 1 | a0001c0004 | 1 | NA18998.hp1 | synonymous_variant | LOW | c.1074G>A | p.Gly358Gly | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 12/13 | 1149/3251 | 1074/1086 | 358/361 | chr2 | 241350162 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:241315963 | G | A | 22 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(19): Show |
187 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
5_prime_UTR_variant | MODIFIER | c.-37G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/13 | 8270 | chr2 | 241315963 | ||||||
| chr2:241315964 | T | A | 1 | a0001c0001t0022 | 1 | HG03453.hp1 | 5_prime_UTR_variant | MODIFIER | c.-36T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/13 | 8269 | chr2 | 241315964 | ||||||
| chr2:241352200 | C | T | 1 | a0001c0001t0026 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*263C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 2026 | chr2 | 241352200 | ||||||
| chr2:241352328 | A | G | 6 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0025 others(3): Show |
107 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*391A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 2154 | chr2 | 241352328 | ||||||
| chr2:241352360 | C | T | 1 | a0001c0001t0028 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*423C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 2186 | chr2 | 241352360 | ||||||
| chr2:241352507 | G | A | 1 | a0001c0001t0018 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*570G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 2333 | chr2 | 241352507 | ||||||
| chr2:241352748 | C | T | 1 | a0001c0001t0011 | 5 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*811C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 2574 | chr2 | 241352748 | ||||||
| chr2:241352892 | T | C | 1 | a0001c0001t0007 | 28 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*955T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 2718 | chr2 | 241352892 | ||||||
| chr2:241352949 | G | T | 1 | a0001c0001t0021 | 2 | HG02818.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1012G>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 2775 | chr2 | 241352949 | ||||||
| chr2:241352963 | G | T | 19 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(16): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
3_prime_UTR_variant | MODIFIER | c.*1026G>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 2789 | chr2 | 241352963 | ||||||
| chr2:241353003 | C | A | 1 | a0001c0001t0012 | 5 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1066C>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 2829 | chr2 | 241353003 | ||||||
| chr2:241353101 | G | C | 1 | a0001c0001t0029 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1164G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 2927 | chr2 | 241353101 | ||||||
| chr2:241353153 | C | T | 5 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0023 others(2): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1216C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 2979 | chr2 | 241353153 | ||||||
| chr2:241353229 | A | G | 1 | a0001c0001t0024 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1292A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 3055 | chr2 | 241353229 | ||||||
| chr2:241353355 | A | C | 1 | a0001c0001t0019 | 2 | HG02630.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1418A>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 3181 | chr2 | 241353355 | ||||||
| chr2:241353387 | A | T | 1 | a0001c0001t0027 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1450A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 3213 | chr2 | 241353387 | ||||||
| chr2:241353441 | A | G | 6 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0023 others(3): Show |
50 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1504A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 3267 | chr2 | 241353441 | ||||||
| chr2:241353444 | C | T | 1 | a0001c0001t0030 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1507C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 3270 | chr2 | 241353444 | ||||||
| chr2:241353529 | G | C | 3 | a0001c0001t0008 a0001c0001t0013 a0001c0002t0008 |
12 | HG01496.hp1 HG01884.hp1 HG01934.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1592G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 3355 | chr2 | 241353529 | ||||||
| chr2:241353606 | A | G | 7 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0015 others(4): Show |
111 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*1669A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 3432 | chr2 | 241353606 | ||||||
| chr2:241353606 | A | T | 1 | a0001c0001t0016 | 4 | HG01884.hp2 HG02572.hp2 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1669A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 3432 | chr2 | 241353606 | ||||||
| chr2:241353754 | A | T | 1 | a0001c0001t0023 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1817A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 3580 | chr2 | 241353754 | ||||||
| chr2:241353794 | C | A | 2 | a0001c0001t0005 a0001c0001t0020 |
36 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*1857C>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 3620 | chr2 | 241353794 | ||||||
| chr2:241353816 | G | A | 1 | a0001c0001t0013 | 4 | HG02922.hp2 HG03130.hp2 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1879G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 3642 | chr2 | 241353816 | ||||||
| chr2:241353891 | AATAG | A | 1 | a0001c0001t0009 | 5 | HG00597.hp1 HG02080.hp1 NA18951.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1958_*1961delGATA | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 3721 | INFO_REALIGN_3_PRIME | chr2 | 241353891 | |||||
| chr2:241353954 | T | G | 3 | a0001c0001t0010 a0001c0001t0011 a0001c0001t0017 |
13 | HG02257.hp2 HG02451.hp2 HG02615.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2017T>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 13/13 | 3780 | chr2 | 241353954 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:241315997 | G | A | 1 | a0001c0001t0008g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-18+15G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241315997 | |||||||
| chr2:241316175 | G | T | 1 | a0001c0001t0017g0316 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-18+193G>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241316175 | |||||||
| chr2:241316213 | C | T | 1 | a0001c0001t0002g0315 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-18+231C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241316213 | |||||||
| chr2:241316318 | C | T | 1 | a0001c0001t0002g0315 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-18+336C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241316318 | |||||||
| chr2:241316356 | G | GCCCGACA others(33): Show |
19 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0054 others(16): Show |
21 | HG00099.hp2 HG01123.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+376_-18+415dup others(40): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241316356 | ||||||
| chr2:241316356 | G | GCCCGACA others(33): Show |
1 | a0001c0001t0002g0313 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-18+382_-18+383ins others(40): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241316356 | ||||||
| chr2:241316357 | C | T | 1 | a0001c0001t0004g0314 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-18+375C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241316357 | |||||||
| chr2:241316415 | C | T | 26 | a0001c0001t0002g0017 a0001c0001t0006g0050 a0001c0001t0006g0051 others(23): Show |
32 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.-18+433C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241316415 | |||||||
| chr2:241316500 | G | A | 14 | a0001c0001t0010g0022 a0001c0001t0010g0072 a0001c0001t0010g0079 others(11): Show |
17 | HG02257.hp2 HG02451.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.-18+518G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241316500 | |||||||
| chr2:241316593 | A | G | 13 | a0001c0001t0004g0279 a0001c0001t0004g0280 a0001c0001t0004g0281 others(10): Show |
13 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.-18+611A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241316593 | |||||||
| chr2:241316594 | G | A | 1 | a0001c0001t0002g0081 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-18+612G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241316594 | |||||||
| chr2:241316714 | G | A | 1 | a0001c0001t0004g0279 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-18+732G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241316714 | |||||||
| chr2:241316846 | C | T | 1 | a0001c0001t0004g0003 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-18+864C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241316846 | |||||||
| chr2:241316942 | C | G | 1 | a0001c0001t0007g0278 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-18+960C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241316942 | |||||||
| chr2:241317136 | C | T | 1 | a0001c0001t0002g0070 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-18+1154C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241317136 | |||||||
| chr2:241317232 | C | T | 1 | a0001c0001t0003g0277 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-18+1250C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241317232 | |||||||
| chr2:241317239 | C | G | 1 | a0001c0001t0001g0276 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-18+1257C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241317239 | |||||||
| chr2:241317268 | G | A | 1 | a0001c0001t0004g0082 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-18+1286G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241317268 | |||||||
| chr2:241317303 | T | A | 2 | a0001c0001t0001g0083 a0001c0001t0001g0084 |
2 | NA18962.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.-18+1321T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241317303 | |||||||
| chr2:241317353 | G | A | 11 | a0001c0001t0001g0002 a0001c0001t0001g0085 a0001c0001t0001g0086 others(8): Show |
16 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.-18+1371G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241317353 | |||||||
| chr2:241317397 | G | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(71): Show |
100 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.-18+1415G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241317397 | |||||||
| chr2:241317535 | A | AT | 9 | a0001c0001t0001g0093 a0001c0001t0001g0141 a0001c0001t0001g0271 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18+1570dupT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241317535 | ||||||
| chr2:241317578 | C | G | 1 | a0001c0001t0004g0291 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-18+1596C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241317578 | |||||||
| chr2:241317749 | C | T | 52 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0044 others(49): Show |
59 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.-18+1767C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241317749 | |||||||
| chr2:241317750 | TTCCGG | T | 52 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0044 others(49): Show |
59 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.-18+1769_-18+1773d others(7): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241317750 | |||||||
| chr2:241317756 | G | A | 52 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0044 others(49): Show |
59 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.-18+1774G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241317756 | |||||||
| chr2:241317880 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-18+1898A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241317880 | |||||||
| chr2:241317943 | G | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(249): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.-18+1961G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241317943 | |||||||
| chr2:241318121 | G | GA | 8 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0002g0018 others(5): Show |
9 | HG01167.hp1 HG01169.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18+2150dupA | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241318121 | ||||||
| chr2:241318136 | GA | G | 20 | a0001c0001t0002g0048 a0001c0001t0002g0067 a0001c0001t0002g0068 others(17): Show |
24 | HG01123.hp2 HG01261.hp1 HG02004.hp1 others(21): Show |
intron_variant | MODIFIER | c.-18+2164delA | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241318136 | ||||||
| chr2:241318147 | G | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
5 | NA18953.hp1 NA19000.hp2 NA19082.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+2165G>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241318147 | |||||||
| chr2:241318170 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-18+2188G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241318170 | |||||||
| chr2:241318218 | T | C | 2 | a0001c0001t0019g0273 a0001c0001t0019g0274 |
2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-18+2236T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241318218 | |||||||
| chr2:241318420 | A | G | 23 | a0001c0001t0006g0189 a0001c0001t0007g0005 a0001c0001t0007g0036 others(20): Show |
29 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.-18+2438A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241318420 | |||||||
| chr2:241318444 | G | A | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(208): Show |
263 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.-18+2462G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241318444 | |||||||
| chr2:241318702 | C | CT | 57 | a0001c0001t0001g0092 a0001c0001t0001g0136 a0001c0001t0002g0066 others(54): Show |
66 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.-18+2737dupT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241318702 | ||||||
| chr2:241318702 | CT | C | 11 | a0001c0001t0001g0095 a0001c0001t0003g0197 a0001c0001t0005g0196 others(8): Show |
13 | HG01261.hp1 HG02559.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.-18+2737delT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241318702 | ||||||
| chr2:241318853 | A | G | 1 | a0001c0001t0007g0192 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-18+2871A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241318853 | |||||||
| chr2:241319232 | G | C | 1 | a0001c0001t0011g0074 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-18+3250G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241319232 | |||||||
| chr2:241319307 | A | G | 1 | a0001c0001t0008g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-18+3325A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241319307 | |||||||
| chr2:241319529 | A | G | 2 | a0001c0001t0004g0171 a0001c0001t0004g0282 |
2 | HG01192.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.-18+3547A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241319529 | |||||||
| chr2:241319547 | T | C | 1 | a0001c0001t0008g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-18+3565T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241319547 | |||||||
| chr2:241319557 | G | A | 1 | a0001c0001t0007g0174 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-18+3575G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241319557 | |||||||
| chr2:241319596 | C | T | 1 | a0001c0001t0007g0191 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-18+3614C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241319596 | |||||||
| chr2:241319737 | G | A | 2 | a0001c0001t0004g0142 a0001c0001t0004g0145 |
2 | HG02273.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-18+3755G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241319737 | |||||||
| chr2:241319792 | C | G | 67 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(64): Show |
80 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.-18+3810C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241319792 | |||||||
| chr2:241319820 | C | T | 2 | a0001c0001t0019g0273 a0001c0001t0019g0274 |
2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-18+3838C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241319820 | |||||||
| chr2:241320035 | C | CT | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(74): Show |
106 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-18+4054dupT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241320035 | ||||||
| chr2:241320114 | C | T | 3 | a0001c0001t0005g0016 a0001c0001t0020g0244 a0001c0001t0020g0245 |
5 | HG01934.hp1 HG02071.hp2 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-4102C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241320114 | |||||||
| chr2:241320199 | G | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(247): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.-17-4017G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241320199 | |||||||
| chr2:241320512 | G | A | 1 | a0001c0001t0006g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-17-3704G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241320512 | |||||||
| chr2:241320521 | C | T | 1 | a0001c0001t0011g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-17-3695C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241320521 | |||||||
| chr2:241320578 | G | C | 1 | a0001c0001t0006g0293 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-17-3638G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241320578 | |||||||
| chr2:241320724 | G | A | 2 | a0001c0001t0002g0266 a0001c0001t0002g0275 |
2 | NA18948.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.-17-3492G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241320724 | |||||||
| chr2:241320783 | C | T | 1 | a0001c0001t0005g0016 | 3 | NA18946.hp2 NA19054.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.-17-3433C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241320783 | |||||||
| chr2:241320925 | G | C | 23 | a0001c0001t0006g0189 a0001c0001t0007g0005 a0001c0001t0007g0036 others(20): Show |
29 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.-17-3291G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241320925 | |||||||
| chr2:241321030 | A | G | 1 | a0001c0001t0002g0065 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-17-3186A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241321030 | |||||||
| chr2:241321065 | T | G | 9 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0146 others(6): Show |
11 | HG01496.hp1 HG01884.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.-17-3151T>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241321065 | |||||||
| chr2:241321107 | A | C | 1 | a0001c0001t0007g0191 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-17-3109A>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241321107 | |||||||
| chr2:241321149 | A | G | 1 | a0001c0001t0002g0265 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-17-3067A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241321149 | |||||||
| chr2:241321247 | A | G | 52 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0044 others(49): Show |
59 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.-17-2969A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241321247 | |||||||
| chr2:241321282 | T | G | 5 | a0001c0001t0006g0038 a0001c0001t0006g0194 a0001c0001t0006g0195 others(2): Show |
6 | HG01261.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-2934T>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241321282 | |||||||
| chr2:241321341 | G | C | 67 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(64): Show |
80 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.-17-2875G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241321341 | |||||||
| chr2:241321516 | C | G | 5 | a0001c0001t0006g0038 a0001c0001t0006g0194 a0001c0001t0006g0195 others(2): Show |
6 | HG01261.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-2700C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241321516 | |||||||
| chr2:241321573 | G | GT | 8 | a0001c0001t0001g0091 a0001c0001t0001g0134 a0001c0001t0002g0056 others(5): Show |
8 | HG00438.hp1 HG00621.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17-2633dupT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241321573 | ||||||
| chr2:241321596 | C | T | 42 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(39): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.-17-2620C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241321596 | |||||||
| chr2:241321663 | T | C | 1 | a0001c0001t0008g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-17-2553T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241321663 | |||||||
| chr2:241321742 | C | G | 1 | a0001c0001t0005g0243 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-17-2474C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241321742 | |||||||
| chr2:241321748 | T | G | 1 | a0001c0001t0006g0294 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-17-2468T>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241321748 | |||||||
| chr2:241321825 | T | A | 23 | a0001c0001t0006g0189 a0001c0001t0007g0005 a0001c0001t0007g0036 others(20): Show |
29 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.-17-2391T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241321825 | |||||||
| chr2:241322019 | A | G | 15 | a0001c0001t0002g0017 a0001c0001t0006g0293 a0001c0001t0006g0300 others(12): Show |
17 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-2197A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322019 | |||||||
| chr2:241322090 | A | G | 1 | a0001c0001t0002g0264 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-17-2126A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322090 | |||||||
| chr2:241322099 | C | G | 1 | a0001c0001t0003g0242 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-17-2117C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322099 | |||||||
| chr2:241322167 | T | C | 1 | a0001c0001t0003g0198 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-17-2049T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322167 | |||||||
| chr2:241322387 | T | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(210): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.-17-1829T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322387 | |||||||
| chr2:241322449 | A | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(71): Show |
100 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.-17-1767A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322449 | |||||||
| chr2:241322464 | G | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(75): Show |
107 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-17-1752G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322464 | |||||||
| chr2:241322480 | G | A | 1 | a0001c0001t0007g0175 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-17-1736G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322480 | |||||||
| chr2:241322484 | G | C | 1 | a0001c0001t0003g0199 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-17-1732G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322484 | |||||||
| chr2:241322499 | C | T | 2 | a0001c0001t0002g0081 a0001c0001t0002g0263 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-17-1717C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322499 | |||||||
| chr2:241322500 | G | C | 1 | a0001c0001t0019g0273 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-17-1716G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322500 | |||||||
| chr2:241322526 | G | T | 51 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0044 others(48): Show |
58 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.-17-1690G>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322526 | |||||||
| chr2:241322603 | C | T | 1 | a0001c0001t0007g0190 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-17-1613C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322603 | |||||||
| chr2:241322664 | AT | A | 4 | a0001c0001t0002g0048 a0001c0001t0002g0268 a0001c0001t0002g0269 others(1): Show |
5 | NA18939.hp1 NA18954.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-1547delT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241322664 | ||||||
| chr2:241322700 | C | G | 1 | a0001c0001t0003g0198 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-17-1516C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322700 | |||||||
| chr2:241322720 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-17-1496C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322720 | |||||||
| chr2:241322896 | A | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(75): Show |
107 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-17-1320A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322896 | |||||||
| chr2:241322940 | C | T | 2 | a0001c0001t0014g0240 a0001c0001t0022g0241 |
2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-17-1276C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241322940 | |||||||
| chr2:241322991 | C | CAT | 29 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(26): Show |
36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.-17-1215_-17-1214d others(4): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241322991 | ||||||
| chr2:241323049 | T | C | 1 | a0001c0001t0024g0193 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-17-1167T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241323049 | |||||||
| chr2:241323124 | C | T | 6 | a0001c0001t0002g0258 a0001c0001t0002g0259 a0001c0001t0002g0260 others(3): Show |
6 | NA18949.hp1 NA18951.hp1 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17-1092C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241323124 | |||||||
| chr2:241323148 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-17-1068C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241323148 | |||||||
| chr2:241323160 | C | T | 1 | a0001c0001t0010g0072 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-17-1056C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241323160 | |||||||
| chr2:241323172 | T | A | 1 | a0001c0001t0001g0134 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-17-1044T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241323172 | |||||||
| chr2:241323174 | A | ATT | 7 | a0001c0001t0006g0293 a0001c0001t0006g0306 a0001c0001t0006g0307 others(4): Show |
7 | HG00099.hp1 HG00140.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-1027_-17-1026d others(4): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241323174 | ||||||
| chr2:241323174 | AT | A | 13 | a0001c0001t0001g0096 a0001c0001t0002g0268 a0001c0001t0004g0154 others(10): Show |
14 | HG01261.hp1 HG01433.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-17-1026delT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 241323174 | ||||||
| chr2:241323298 | G | A | 1 | a0001c0001t0014g0172 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-17-918G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241323298 | |||||||
| chr2:241323408 | G | A | 1 | a0001c0001t0014g0200 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-17-808G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241323408 | |||||||
| chr2:241323571 | G | A | 25 | a0001c0001t0002g0017 a0001c0001t0006g0050 a0001c0001t0006g0051 others(22): Show |
31 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.-17-645G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241323571 | |||||||
| chr2:241323596 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-17-620C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241323596 | |||||||
| chr2:241323808 | G | A | 22 | a0001c0001t0007g0005 a0001c0001t0007g0036 a0001c0001t0007g0037 others(19): Show |
28 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-408G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241323808 | |||||||
| chr2:241323857 | A | G | 1 | a0001c0001t0007g0174 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-17-359A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241323857 | |||||||
| chr2:241324021 | C | T | 5 | a0001c0001t0006g0038 a0001c0001t0006g0194 a0001c0001t0006g0195 others(2): Show |
6 | HG01261.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-195C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241324021 | |||||||
| chr2:241324039 | T | C | 3 | a0001c0001t0002g0044 a0001c0001t0002g0248 a0001c0001t0002g0249 |
4 | HG00642.hp2 HG01243.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-177T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241324039 | |||||||
| chr2:241324138 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-17-78C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241324138 | |||||||
| chr2:241324173 | T | C | 2 | a0001c0001t0004g0280 a0001c0001t0004g0283 |
2 | HG02698.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-17-43T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241324173 | |||||||
| chr2:241324200 | G | T | 1 | a0001c0001t0007g0192 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-17-16G>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 1/12 | chr2 | 241324200 | |||||||
| chr2:241324342 | A | G | 6 | a0001c0001t0003g0043 a0001c0001t0003g0235 a0001c0001t0003g0236 others(3): Show |
7 | HG00544.hp2 HG02129.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.9+101A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | chr2 | 241324342 | |||||||
| chr2:241324381 | T | C | 1 | a0001c0001t0010g0079 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.9+140T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | chr2 | 241324381 | |||||||
| chr2:241324388 | CT | C | 30 | a0001c0001t0001g0028 a0001c0001t0001g0130 a0001c0001t0001g0136 others(27): Show |
45 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.9+164delT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 241324388 | ||||||
| chr2:241324388 | CTT | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(234): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.9+163_9+164delTT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 241324388 | ||||||
| chr2:241324388 | CTTT | C | 10 | a0001c0001t0001g0097 a0001c0001t0001g0271 a0001c0001t0002g0054 others(7): Show |
11 | HG01167.hp1 HG01261.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.9+162_9+164delTTT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 241324388 | ||||||
| chr2:241324652 | T | C | 1 | a0001c0001t0010g0079 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.9+411T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | chr2 | 241324652 | |||||||
| chr2:241324776 | CTTAG | C | 6 | a0001c0001t0003g0043 a0001c0001t0003g0235 a0001c0001t0003g0236 others(3): Show |
7 | HG00544.hp2 HG02129.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.9+538_9+541delAGTT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 241324776 | ||||||
| chr2:241324834 | A | C | 13 | a0001c0001t0004g0279 a0001c0001t0004g0280 a0001c0001t0004g0281 others(10): Show |
13 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.9+593A>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | chr2 | 241324834 | |||||||
| chr2:241324856 | A | G | 1 | a0001c0001t0004g0281 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.9+615A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | chr2 | 241324856 | |||||||
| chr2:241324968 | G | GT | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(183): Show |
232 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.9+737dupT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 241324968 | ||||||
| chr2:241325075 | C | CA | 43 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0002g0017 others(40): Show |
52 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.9+844dupA | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 241325075 | ||||||
| chr2:241325211 | G | A | 48 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0045 others(45): Show |
54 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.10-782G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | chr2 | 241325211 | |||||||
| chr2:241325428 | A | G | 1 | a0001c0001t0002g0267 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.10-565A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | chr2 | 241325428 | |||||||
| chr2:241325500 | G | C | 6 | a0001c0001t0002g0018 a0001c0001t0002g0054 a0001c0001t0002g0055 others(3): Show |
7 | NA18939.hp2 NA18953.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.10-493G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | chr2 | 241325500 | |||||||
| chr2:241325709 | C | T | 1 | a0001c0001t0005g0014 | 3 | HG02074.hp2 NA18970.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.10-284C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | chr2 | 241325709 | |||||||
| chr2:241325718 | A | G | 1 | a0001c0001t0004g0154 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.10-275A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | chr2 | 241325718 | |||||||
| chr2:241325777 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.10-216A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | chr2 | 241325777 | |||||||
| chr2:241325858 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(210): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.10-135C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | chr2 | 241325858 | |||||||
| chr2:241325898 | C | A | 63 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0044 others(60): Show |
72 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.10-95C>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 2/12 | chr2 | 241325898 | |||||||
| chr2:241326248 | A | G | 4 | a0001c0001t0002g0048 a0001c0001t0002g0268 a0001c0001t0002g0269 others(1): Show |
5 | NA18939.hp1 NA18954.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.130+135A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241326248 | |||||||
| chr2:241326249 | T | C | 1 | a0001c0001t0002g0056 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.130+136T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241326249 | |||||||
| chr2:241326334 | T | C | 12 | a0001c0001t0001g0002 a0001c0001t0001g0085 a0001c0001t0001g0086 others(9): Show |
17 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.130+221T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241326334 | |||||||
| chr2:241326400 | TCCCTTCC others(142): Show |
T | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(249): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.130+438_130+586del | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 241326400 | ||||||
| chr2:241326648 | A | G | 1 | a0001c0001t0013g0152 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.130+535A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241326648 | |||||||
| chr2:241326664 | C | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(75): Show |
107 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.130+551C>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241326664 | |||||||
| chr2:241326925 | C | G | 9 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0146 others(6): Show |
11 | HG01496.hp1 HG01884.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.130+812C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241326925 | |||||||
| chr2:241326947 | A | G | 1 | a0001c0005t0004g0288 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.130+834A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241326947 | |||||||
| chr2:241327002 | C | T | 1 | a0001c0001t0006g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.130+889C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241327002 | |||||||
| chr2:241327050 | CA | C | 46 | a0001c0001t0001g0023 a0001c0001t0001g0087 a0001c0001t0001g0088 others(43): Show |
58 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.130+965delA | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 241327050 | ||||||
| chr2:241327050 | CAA | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(123): Show |
173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.130+964_130+965del others(2): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 241327050 | ||||||
| chr2:241327050 | CAAA | C | 101 | a0001c0001t0001g0084 a0001c0001t0001g0097 a0001c0001t0001g0125 others(98): Show |
117 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.130+963_130+965del others(3): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 241327050 | ||||||
| chr2:241327050 | CAAAA | C | 26 | a0001c0001t0001g0272 a0001c0001t0002g0064 a0001c0001t0002g0262 others(23): Show |
32 | HG00423.hp2 HG00544.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.130+962_130+965del others(4): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 241327050 | ||||||
| chr2:241327084 | G | A | 1 | a0001c0001t0002g0070 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.130+971G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241327084 | |||||||
| chr2:241327105 | C | T | 1 | a0001c0001t0006g0300 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.130+992C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241327105 | |||||||
| chr2:241327371 | G | A | 3 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0001t0007g0191 |
3 | HG00639.hp2 HG03927.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.130+1258G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241327371 | |||||||
| chr2:241327508 | C | CA | 47 | a0001c0001t0001g0101 a0001c0001t0002g0044 a0001c0001t0002g0248 others(44): Show |
58 | HG00423.hp2 HG00544.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.130+1407dupA | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 241327508 | ||||||
| chr2:241327508 | C | CAA | 48 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0045 others(45): Show |
54 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.130+1406_130+1407d others(4): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 241327508 | ||||||
| chr2:241327548 | G | C | 316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(313): Show |
402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.130+1435G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241327548 | |||||||
| chr2:241327820 | A | G | 2 | a0001c0001t0014g0240 a0001c0001t0022g0241 |
2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.130+1707A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241327820 | |||||||
| chr2:241327823 | G | C | 1 | a0001c0001t0006g0295 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.130+1710G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241327823 | |||||||
| chr2:241327898 | T | C | 1 | a0001c0001t0003g0235 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.130+1785T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241327898 | |||||||
| chr2:241328018 | G | A | 1 | a0001c0001t0008g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.130+1905G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241328018 | |||||||
| chr2:241328099 | G | A | 1 | a0001c0001t0001g0024 | 2 | HG02015.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.130+1986G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241328099 | |||||||
| chr2:241328202 | G | A | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(276): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.130+2089G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241328202 | |||||||
| chr2:241328219 | G | A | 2 | a0001c0001t0019g0273 a0001c0001t0019g0274 |
2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.130+2106G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241328219 | |||||||
| chr2:241328277 | A | C | 1 | a0001c0001t0003g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.130+2164A>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241328277 | |||||||
| chr2:241328401 | T | G | 1 | a0001c0001t0008g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.130+2288T>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241328401 | |||||||
| chr2:241328483 | T | TCACAGCA others(10): Show |
2 | a0001c0001t0014g0240 a0001c0001t0022g0241 |
2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.130+2372_130+2388d others(19): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 241328483 | ||||||
| chr2:241328586 | T | C | 7 | a0001c0001t0003g0043 a0001c0001t0003g0217 a0001c0001t0003g0235 others(4): Show |
8 | HG00544.hp2 HG02074.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.130+2473T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241328586 | |||||||
| chr2:241328657 | A | C | 1 | a0001c0001t0004g0281 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.130+2544A>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241328657 | |||||||
| chr2:241328785 | G | A | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.130+2672G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241328785 | |||||||
| chr2:241328849 | C | T | 66 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(63): Show |
79 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.130+2736C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241328849 | |||||||
| chr2:241328862 | A | G | 10 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0053 others(7): Show |
12 | HG01496.hp1 HG01884.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.130+2749A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241328862 | |||||||
| chr2:241328866 | C | CA | 1 | a0001c0001t0001g0010 | 3 | HG03491.hp1 HG03492.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.130+2757dupA | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 241328866 | ||||||
| chr2:241328944 | C | T | 4 | a0001c0001t0006g0038 a0001c0001t0006g0194 a0001c0001t0006g0195 others(1): Show |
5 | HG01261.hp1 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+2831C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241328944 | |||||||
| chr2:241328960 | C | T | 2 | a0001c0001t0003g0227 a0001c0001t0003g0228 |
2 | HG03710.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.130+2847C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241328960 | |||||||
| chr2:241328976 | C | T | 4 | a0001c0001t0002g0047 a0001c0001t0002g0250 a0001c0001t0002g0256 others(1): Show |
5 | HG02132.hp2 NA18994.hp2 NA19075.hp2 others(2): Show |
intron_variant | MODIFIER | c.130+2863C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241328976 | |||||||
| chr2:241329007 | T | A | 18 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0048 others(15): Show |
21 | HG00609.hp1 HG01106.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.130+2894T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241329007 | |||||||
| chr2:241329021 | T | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(145): Show |
191 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.130+2908T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241329021 | |||||||
| chr2:241329095 | TTTG | T | 4 | a0001c0001t0002g0063 a0001c0001t0003g0214 a0001c0001t0006g0310 others(1): Show |
4 | HG00099.hp1 HG01069.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+2997_130+2999d others(5): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 241329095 | ||||||
| chr2:241329321 | G | T | 53 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0044 others(50): Show |
60 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.130+3208G>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241329321 | |||||||
| chr2:241329339 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.130+3226A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241329339 | |||||||
| chr2:241329363 | C | G | 1 | a0001c0005t0004g0288 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.130+3250C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241329363 | |||||||
| chr2:241329413 | TACAC | T | 4 | a0001c0001t0006g0038 a0001c0001t0006g0194 a0001c0001t0006g0195 others(1): Show |
5 | HG01261.hp1 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+3302_130+3305d others(6): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 241329413 | ||||||
| chr2:241329415 | C | A | 2 | a0001c0001t0005g0230 a0001c0001t0005g0233 |
2 | NA18982.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.130+3302C>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241329415 | |||||||
| chr2:241329416 | A | G | 1 | a0001c0001t0002g0251 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.130+3303A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241329416 | |||||||
| chr2:241329579 | T | C | 23 | a0001c0001t0006g0189 a0001c0001t0007g0005 a0001c0001t0007g0036 others(20): Show |
29 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.130+3466T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241329579 | |||||||
| chr2:241329581 | C | G | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.130+3468C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241329581 | |||||||
| chr2:241329593 | C | T | 41 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(38): Show |
48 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.130+3480C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241329593 | |||||||
| chr2:241329609 | A | G | 23 | a0001c0001t0006g0189 a0001c0001t0007g0005 a0001c0001t0007g0036 others(20): Show |
29 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.130+3496A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241329609 | |||||||
| chr2:241329719 | G | C | 1 | a0001c0001t0006g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.130+3606G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241329719 | |||||||
| chr2:241329888 | T | A | 70 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(67): Show |
84 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.130+3775T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241329888 | |||||||
| chr2:241329939 | C | T | 1 | a0001c0001t0006g0038 | 2 | HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.130+3826C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241329939 | |||||||
| chr2:241330060 | C | T | 7 | a0001c0001t0005g0006 a0001c0001t0005g0041 a0001c0001t0005g0201 others(4): Show |
11 | HG00423.hp1 HG02056.hp1 NA18941.hp2 others(8): Show |
intron_variant | MODIFIER | c.130+3947C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241330060 | |||||||
| chr2:241330086 | C | T | 1 | a0001c0001t0003g0203 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.130+3973C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241330086 | |||||||
| chr2:241330224 | A | G | 5 | a0001c0001t0006g0038 a0001c0001t0006g0194 a0001c0001t0006g0195 others(2): Show |
6 | HG01261.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.130+4111A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241330224 | |||||||
| chr2:241330373 | C | T | 1 | a0001c0001t0003g0216 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.130+4260C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241330373 | |||||||
| chr2:241330941 | T | G | 1 | a0001c0001t0005g0207 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.131-4185T>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241330941 | |||||||
| chr2:241330981 | C | A | 1 | a0001c0001t0001g0134 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.131-4145C>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241330981 | |||||||
| chr2:241331018 | A | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(71): Show |
100 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.131-4108A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241331018 | |||||||
| chr2:241331085 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.131-4041G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241331085 | |||||||
| chr2:241331175 | T | A | 1 | a0001c0001t0002g0058 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.131-3951T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241331175 | |||||||
| chr2:241331657 | C | T | 1 | a0001c0001t0006g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.131-3469C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241331657 | |||||||
| chr2:241331844 | G | A | 1 | a0001c0001t0005g0204 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.131-3282G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241331844 | |||||||
| chr2:241331920 | A | C | 1 | a0001c0001t0006g0052 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.131-3206A>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241331920 | |||||||
| chr2:241332129 | T | G | 1 | a0001c0001t0001g0103 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.131-2997T>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241332129 | |||||||
| chr2:241332151 | TTTC | T | 23 | a0001c0001t0006g0189 a0001c0001t0007g0005 a0001c0001t0007g0036 others(20): Show |
29 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.131-2972_131-2970d others(5): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 241332151 | ||||||
| chr2:241332212 | T | G | 26 | a0001c0001t0002g0017 a0001c0001t0006g0050 a0001c0001t0006g0051 others(23): Show |
32 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.131-2914T>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241332212 | |||||||
| chr2:241332275 | A | G | 5 | a0001c0001t0003g0203 a0001c0001t0003g0224 a0001c0001t0003g0225 others(2): Show |
5 | HG00558.hp1 NA18941.hp1 NA19006.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-2851A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241332275 | |||||||
| chr2:241332652 | A | G | 2 | a0001c0001t0019g0273 a0001c0001t0019g0274 |
2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.131-2474A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241332652 | |||||||
| chr2:241332709 | A | T | 4 | a0001c0001t0013g0147 a0001c0001t0013g0150 a0001c0001t0013g0151 others(1): Show |
4 | HG02922.hp2 HG03130.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-2417A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241332709 | |||||||
| chr2:241332751 | TG | T | 13 | a0001c0001t0004g0279 a0001c0001t0004g0280 a0001c0001t0004g0281 others(10): Show |
13 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.131-2374delG | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241332751 | |||||||
| chr2:241332952 | G | A | 1 | a0001c0001t0013g0150 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.131-2174G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241332952 | |||||||
| chr2:241332973 | A | G | 23 | a0001c0001t0006g0189 a0001c0001t0007g0005 a0001c0001t0007g0036 others(20): Show |
29 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.131-2153A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241332973 | |||||||
| chr2:241333071 | A | G | 1 | a0001c0001t0006g0189 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.131-2055A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333071 | |||||||
| chr2:241333073 | A | G | 1 | a0001c0001t0002g0056 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.131-2053A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333073 | |||||||
| chr2:241333107 | G | A | 1 | a0001c0001t0007g0184 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.131-2019G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333107 | |||||||
| chr2:241333200 | A | G | 51 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0044 others(48): Show |
58 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.131-1926A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333200 | |||||||
| chr2:241333226 | A | C | 1 | a0001c0001t0002g0068 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.131-1900A>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333226 | |||||||
| chr2:241333307 | T | C | 13 | a0001c0001t0004g0279 a0001c0001t0004g0280 a0001c0001t0004g0281 others(10): Show |
13 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.131-1819T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333307 | |||||||
| chr2:241333351 | G | A | 1 | a0001c0001t0003g0218 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.131-1775G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333351 | |||||||
| chr2:241333407 | C | G | 1 | a0001c0001t0006g0301 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.131-1719C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333407 | |||||||
| chr2:241333480 | C | G | 1 | a0001c0001t0005g0233 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.131-1646C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333480 | |||||||
| chr2:241333578 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0029g0135 |
3 | HG00140.hp1 HG01074.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.131-1548C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333578 | |||||||
| chr2:241333621 | T | TGCCTCA | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(147): Show |
193 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.131-1500_131-1499i others(8): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 241333621 | ||||||
| chr2:241333648 | C | T | 2 | a0001c0001t0012g0013 a0001c0001t0012g0030 |
5 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-1478C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333648 | |||||||
| chr2:241333649 | G | A | 1 | a0001c0001t0004g0159 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.131-1477G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333649 | |||||||
| chr2:241333661 | G | A | 3 | a0001c0001t0003g0224 a0001c0001t0003g0225 a0001c0001t0003g0234 |
3 | NA19006.hp1 NA19065.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.131-1465G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333661 | |||||||
| chr2:241333664 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.131-1462C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333664 | |||||||
| chr2:241333743 | T | A | 1 | a0001c0001t0004g0282 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.131-1383T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333743 | |||||||
| chr2:241333799 | G | A | 2 | a0001c0001t0001g0104 a0001c0001t0014g0172 |
2 | HG03098.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.131-1327G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333799 | |||||||
| chr2:241333931 | ATCTCTAA others(9): Show |
A | 1 | a0001c0001t0006g0308 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.131-1192_131-1177d others(18): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 241333931 | ||||||
| chr2:241333979 | T | C | 2 | a0001c0001t0019g0273 a0001c0001t0019g0274 |
2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.131-1147T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241333979 | |||||||
| chr2:241334027 | G | GT | 24 | a0001c0001t0001g0123 a0001c0001t0006g0189 a0001c0001t0007g0005 others(21): Show |
30 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.131-1091dupT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 241334027 | ||||||
| chr2:241334143 | G | A | 2 | a0001c0001t0003g0210 a0001c0001t0003g0219 |
2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.131-983G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241334143 | |||||||
| chr2:241334169 | C | G | 1 | a0001c0001t0003g0197 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.131-957C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241334169 | |||||||
| chr2:241334204 | C | A | 3 | a0001c0001t0002g0044 a0001c0001t0002g0248 a0001c0001t0002g0249 |
4 | HG00642.hp2 HG01243.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-922C>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241334204 | |||||||
| chr2:241334218 | T | A | 2 | a0001c0001t0010g0022 a0001c0001t0010g0079 |
3 | HG02970.hp1 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.131-908T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241334218 | |||||||
| chr2:241334412 | A | G | 1 | a0001c0001t0006g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.131-714A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241334412 | |||||||
| chr2:241334456 | C | T | 1 | a0001c0001t0008g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.131-670C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241334456 | |||||||
| chr2:241334497 | T | A | 2 | a0001c0001t0017g0077 a0001c0001t0017g0316 |
2 | HG02257.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.131-629T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241334497 | |||||||
| chr2:241334725 | C | A | 1 | a0001c0001t0006g0189 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.131-401C>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241334725 | |||||||
| chr2:241334727 | G | A | 42 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(39): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.131-399G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241334727 | |||||||
| chr2:241334738 | A | G | 1 | a0001c0001t0007g0179 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.131-388A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241334738 | |||||||
| chr2:241334895 | C | G | 2 | a0001c0001t0012g0013 a0001c0001t0012g0030 |
5 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-231C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241334895 | |||||||
| chr2:241335074 | G | C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(78): Show |
111 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.131-52G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 3/12 | chr2 | 241335074 | |||||||
| chr2:241335356 | G | A | 2 | a0001c0001t0010g0022 a0001c0001t0010g0079 |
3 | HG02970.hp1 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.217+144G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 4/12 | chr2 | 241335356 | |||||||
| chr2:241335367 | C | T | 4 | a0001c0001t0006g0038 a0001c0001t0006g0194 a0001c0001t0006g0195 others(1): Show |
5 | HG01261.hp1 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.217+155C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 4/12 | chr2 | 241335367 | |||||||
| chr2:241335406 | G | A | 2 | a0001c0001t0004g0158 a0001c0001t0004g0160 |
2 | NA18988.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.217+194G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 4/12 | chr2 | 241335406 | |||||||
| chr2:241335577 | C | T | 1 | a0001c0001t0006g0305 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.217+365C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 4/12 | chr2 | 241335577 | |||||||
| chr2:241335583 | C | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(71): Show |
100 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.217+371C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 4/12 | chr2 | 241335583 | |||||||
| chr2:241335652 | C | T | 1 | a0001c0001t0002g0265 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.218-323C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 4/12 | chr2 | 241335652 | |||||||
| chr2:241335653 | T | C | 1 | a0001c0001t0002g0265 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.218-322T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 4/12 | chr2 | 241335653 | |||||||
| chr2:241335847 | C | A | 19 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0142 others(16): Show |
25 | HG00609.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.218-128C>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 4/12 | chr2 | 241335847 | |||||||
| chr2:241336136 | C | G | 14 | a0001c0001t0010g0022 a0001c0001t0010g0072 a0001c0001t0010g0079 others(11): Show |
17 | HG02257.hp2 HG02451.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.341+38C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 5/12 | chr2 | 241336136 | |||||||
| chr2:241336164 | G | A | 23 | a0001c0001t0006g0189 a0001c0001t0007g0005 a0001c0001t0007g0036 others(20): Show |
29 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.341+66G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 5/12 | chr2 | 241336164 | |||||||
| chr2:241336376 | G | A | 2 | a0001c0001t0002g0044 a0001c0001t0002g0248 |
3 | HG00642.hp2 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.341+278G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 5/12 | chr2 | 241336376 | |||||||
| chr2:241336529 | C | T | 42 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(39): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.341+431C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 5/12 | chr2 | 241336529 | |||||||
| chr2:241336746 | A | G | 1 | a0001c0001t0006g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.342-636A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 5/12 | chr2 | 241336746 | |||||||
| chr2:241336747 | T | C | 1 | a0001c0001t0007g0185 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.342-635T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 5/12 | chr2 | 241336747 | |||||||
| chr2:241336748 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0134 |
2 | HG00438.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.342-634G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 5/12 | chr2 | 241336748 | |||||||
| chr2:241336829 | C | T | 42 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(39): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.342-553C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 5/12 | chr2 | 241336829 | |||||||
| chr2:241336834 | G | T | 2 | a0001c0001t0019g0273 a0001c0001t0019g0274 |
2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.342-548G>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 5/12 | chr2 | 241336834 | |||||||
| chr2:241336957 | G | A | 1 | a0001c0001t0006g0194 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.342-425G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 5/12 | chr2 | 241336957 | |||||||
| chr2:241337026 | A | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(149): Show |
196 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.342-356A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 5/12 | chr2 | 241337026 | |||||||
| chr2:241337051 | G | A | 1 | a0001c0001t0002g0063 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.342-331G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 5/12 | chr2 | 241337051 | |||||||
| chr2:241337060 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.342-322C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 5/12 | chr2 | 241337060 | |||||||
| chr2:241337093 | C | CA | 29 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(26): Show |
36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.342-278dupA | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 241337093 | ||||||
| chr2:241337093 | CA | C | 24 | a0001c0001t0002g0249 a0001c0001t0006g0189 a0001c0001t0007g0005 others(21): Show |
30 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.342-278delA | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 241337093 | ||||||
| chr2:241337108 | C | A | 23 | a0001c0001t0006g0189 a0001c0001t0007g0005 a0001c0001t0007g0036 others(20): Show |
29 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.342-274C>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 5/12 | chr2 | 241337108 | |||||||
| chr2:241337614 | A | G | 10 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0053 others(7): Show |
12 | HG01496.hp1 HG01884.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.477-59A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 6/12 | chr2 | 241337614 | |||||||
| chr2:241338029 | C | T | 1 | a0001c0001t0006g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.594+239C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338029 | |||||||
| chr2:241338246 | G | A | 1 | a0001c0001t0004g0161 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.594+456G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338246 | |||||||
| chr2:241338300 | G | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(74): Show |
104 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.594+510G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338300 | |||||||
| chr2:241338402 | C | T | 1 | a0001c0001t0029g0135 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.594+612C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338402 | |||||||
| chr2:241338417 | C | T | 2 | a0001c0001t0012g0013 a0001c0001t0012g0030 |
5 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.594+627C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338417 | |||||||
| chr2:241338418 | C | T | 23 | a0001c0001t0006g0189 a0001c0001t0007g0005 a0001c0001t0007g0036 others(20): Show |
29 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.594+628C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338418 | |||||||
| chr2:241338459 | G | T | 1 | a0001c0001t0009g0168 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.594+669G>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338459 | |||||||
| chr2:241338590 | AAT | A | 41 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(38): Show |
48 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.594+813_594+814del others(2): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338590 | ||||||
| chr2:241338592 | T | A | 25 | a0001c0001t0002g0017 a0001c0001t0006g0050 a0001c0001t0006g0051 others(22): Show |
31 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.594+802T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338592 | |||||||
| chr2:241338594 | T | A | 2 | a0001c0001t0012g0013 a0001c0001t0012g0030 |
5 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.594+804T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338594 | |||||||
| chr2:241338597 | A | G | 1 | a0001c0001t0005g0243 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.594+807A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338597 | |||||||
| chr2:241338603 | A | T | 23 | a0001c0001t0006g0189 a0001c0001t0007g0005 a0001c0001t0007g0036 others(20): Show |
29 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.594+813A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338603 | |||||||
| chr2:241338624 | A | G | 4 | a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(1): Show |
4 | NA18992.hp2 NA18998.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+834A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338624 | |||||||
| chr2:241338649 | T | C | 4 | a0001c0001t0006g0038 a0001c0001t0006g0194 a0001c0001t0006g0195 others(1): Show |
5 | HG01261.hp1 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.594+859T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338649 | |||||||
| chr2:241338668 | T | C | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.594+878T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338668 | |||||||
| chr2:241338687 | G | A | 42 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(39): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.594+897G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338687 | |||||||
| chr2:241338702 | T | TTTATATT others(23): Show |
1 | a0001c0001t0001g0027 | 2 | HG01074.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.594+928_594+957dup others(30): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338702 | ||||||
| chr2:241338713 | TATATA | T | 26 | a0001c0001t0002g0017 a0001c0001t0006g0050 a0001c0001t0006g0051 others(23): Show |
32 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.594+929_594+933del others(5): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338713 | ||||||
| chr2:241338719 | ATATAT | A | 21 | a0001c0001t0003g0043 a0001c0001t0003g0217 a0001c0001t0003g0235 others(18): Show |
22 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.594+935_594+939del others(5): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338719 | ||||||
| chr2:241338721 | ATAT | A | 28 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(25): Show |
35 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.594+935_594+937del others(3): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338721 | ||||||
| chr2:241338728 | A | G | 1 | a0001c0001t0009g0153 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.594+938A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338728 | |||||||
| chr2:241338767 | T | TATATATA others(24): Show |
1 | a0001c0001t0016g0298 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.594+981_594+1011du others(32): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338767 | ||||||
| chr2:241338767 | T | TATATATA others(110): Show |
2 | a0001c0001t0019g0273 a0001c0001t0019g0274 |
2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.594+1011_594+1012i others(119): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338767 | ||||||
| chr2:241338771 | T | TATATATA others(23): Show |
1 | a0001c0001t0001g0092 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.594+985_594+986ins others(30): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338771 | ||||||
| chr2:241338771 | T | TATATATT others(21): Show |
8 | a0001c0001t0001g0002 a0001c0001t0001g0085 a0001c0001t0001g0087 others(5): Show |
13 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.594+985_594+986ins others(28): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338771 | ||||||
| chr2:241338771 | T | TATATTAT others(20): Show |
2 | a0001c0001t0016g0049 a0001c0001t0016g0296 |
3 | HG01884.hp2 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.594+999_594+1000in others(28): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338771 | ||||||
| chr2:241338771 | T | TATATTAT others(24): Show |
90 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(87): Show |
121 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.594+1012_594+1042d others(33): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338771 | ||||||
| chr2:241338771 | T | TATATTTA others(19): Show |
2 | a0001c0001t0001g0086 a0001c0001t0001g0090 |
2 | NA18955.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.594+986_594+987ins others(26): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338771 | ||||||
| chr2:241338771 | T | TATTATAT others(22): Show |
1 | a0001c0001t0001g0130 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.594+983_594+984ins others(29): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338771 | ||||||
| chr2:241338771 | T | TTATATTT others(20): Show |
1 | a0001c0001t0001g0129 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.594+981_594+982ins others(27): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338771 | |||||||
| chr2:241338772 | ATATT | A | 2 | a0001c0001t0010g0022 a0001c0001t0010g0079 |
3 | HG02970.hp1 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.594+983_594+986del others(4): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338772 | |||||||
| chr2:241338802 | C | CATATATT others(52): Show |
41 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(38): Show |
48 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.594+1016_594+1017i others(61): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338802 | ||||||
| chr2:241338802 | C | CATATATT others(83): Show |
1 | a0001c0001t0004g0166 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.594+1016_594+1017i others(92): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338802 | ||||||
| chr2:241338802 | C | CATATTAT others(24): Show |
76 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0019 others(73): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.594+1017_594+1047d others(33): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338802 | ||||||
| chr2:241338802 | C | T | 5 | a0001c0001t0016g0049 a0001c0001t0016g0296 a0001c0001t0016g0298 others(2): Show |
6 | HG01884.hp2 HG02572.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.594+1012C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338802 | |||||||
| chr2:241338806 | T | TTATATTT others(21): Show |
1 | a0001c0001t0001g0106 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.594+1042_594+1043i others(30): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338806 | ||||||
| chr2:241338820 | T | TTTATATA others(20): Show |
4 | a0001c0001t0006g0038 a0001c0001t0006g0194 a0001c0001t0006g0195 others(1): Show |
5 | HG01261.hp1 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.594+1047_594+1048i others(29): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338820 | ||||||
| chr2:241338821 | TTATATAT others(76): Show |
T | 8 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0146 others(5): Show |
10 | HG01496.hp1 HG01884.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.594+1038_594+1120d others(85): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338821 | ||||||
| chr2:241338830 | A | ATATATAT others(24): Show |
1 | a0001c0001t0002g0251 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.594+1047_594+1048i others(33): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338830 | ||||||
| chr2:241338838 | A | T | 1 | a0001c0001t0006g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.594+1048A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338838 | |||||||
| chr2:241338840 | T | TATTTATA others(13): Show |
1 | a0001c0001t0006g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.594+1051_594+1052i others(22): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338840 | ||||||
| chr2:241338842 | A | T | 1 | a0001c0001t0006g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.594+1052A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338842 | |||||||
| chr2:241338853 | T | C | 1 | a0002c0003t0002g0059 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.594+1063T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338853 | |||||||
| chr2:241338854 | A | G | 2 | a0001c0001t0012g0013 a0001c0001t0012g0030 |
5 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.594+1064A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338854 | |||||||
| chr2:241338857 | TAA | T | 2 | a0001c0001t0002g0047 a0001c0001t0002g0256 |
3 | NA19075.hp2 NA19086.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.594+1071_594+1072d others(4): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338857 | ||||||
| chr2:241338859 | A | T | 2 | a0001c0001t0014g0240 a0001c0001t0022g0241 |
2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.594+1069A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338859 | |||||||
| chr2:241338861 | AAT | A | 5 | a0001c0001t0001g0088 a0001c0001t0006g0038 a0001c0001t0006g0194 others(2): Show |
6 | HG01261.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.594+1080_594+1081d others(4): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338861 | ||||||
| chr2:241338866 | A | AT | 42 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(39): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.594+1077dupT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338866 | ||||||
| chr2:241338881 | C | CTATAATA others(118): Show |
1 | a0001c0001t0006g0189 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.594+1128_594+1129i others(127): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338881 | ||||||
| chr2:241338889 | T | C | 1 | a0001c0001t0005g0004 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.594+1099T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338889 | |||||||
| chr2:241338890 | A | C | 1 | a0001c0001t0001g0139 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.594+1100A>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338890 | |||||||
| chr2:241338910 | AAT | A | 30 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0002g0017 others(27): Show |
36 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.594+1128_594+1129d others(4): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338910 | ||||||
| chr2:241338921 | TTG | T | 23 | a0001c0001t0006g0189 a0001c0001t0007g0005 a0001c0001t0007g0036 others(20): Show |
29 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.594+1133_594+1134d others(4): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338921 | ||||||
| chr2:241338944 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.594+1154A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338944 | |||||||
| chr2:241338945 | TTA | T | 5 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0006g0292 others(2): Show |
5 | HG02257.hp1 HG03017.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.594+1164_594+1165d others(4): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338945 | ||||||
| chr2:241338951 | A | T | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.594+1161A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338951 | |||||||
| chr2:241338954 | T | A | 23 | a0001c0001t0006g0189 a0001c0001t0007g0005 a0001c0001t0007g0036 others(20): Show |
29 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.594+1164T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338954 | |||||||
| chr2:241338955 | A | T | 25 | a0001c0001t0006g0189 a0001c0001t0007g0005 a0001c0001t0007g0036 others(22): Show |
31 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.594+1165A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338955 | |||||||
| chr2:241338961 | TA | T | 23 | a0001c0001t0006g0189 a0001c0001t0007g0005 a0001c0001t0007g0036 others(20): Show |
29 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.594+1172delA | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338961 | |||||||
| chr2:241338962 | A | ATTATAAA others(18): Show |
1 | a0001c0001t0027g0015 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.594+1184_594+1208d others(27): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338962 | ||||||
| chr2:241338967 | AAATAT | A | 23 | a0001c0001t0006g0189 a0001c0001t0007g0005 a0001c0001t0007g0036 others(20): Show |
29 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.594+1184_594+1188d others(7): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338967 | ||||||
| chr2:241338971 | A | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(74): Show |
104 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.594+1181A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241338971 | |||||||
| chr2:241338984 | ATATT | A | 2 | a0001c0001t0012g0013 a0001c0001t0012g0030 |
5 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.594+1198_594+1201d others(6): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338984 | ||||||
| chr2:241338991 | TA | T | 6 | a0001c0001t0006g0038 a0001c0001t0006g0194 a0001c0001t0006g0195 others(3): Show |
7 | HG01261.hp1 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.594+1204delA | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338991 | ||||||
| chr2:241338992 | AAAT | A | 42 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(39): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.594+1204_594+1206d others(5): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241338992 | ||||||
| chr2:241339034 | ATAT | A | 52 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0044 others(49): Show |
59 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.594+1248_594+1250d others(5): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241339034 | ||||||
| chr2:241339132 | G | A | 26 | a0001c0001t0002g0017 a0001c0001t0006g0050 a0001c0001t0006g0051 others(23): Show |
32 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.594+1342G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241339132 | |||||||
| chr2:241339144 | T | A | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(276): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.594+1354T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241339144 | |||||||
| chr2:241339156 | G | C | 1 | a0001c0001t0014g0172 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.594+1366G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241339156 | |||||||
| chr2:241339192 | G | A | 1 | a0001c0001t0007g0278 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.594+1402G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241339192 | |||||||
| chr2:241339264 | G | T | 10 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0053 others(7): Show |
12 | HG01496.hp1 HG01884.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.594+1474G>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241339264 | |||||||
| chr2:241339291 | G | C | 1 | a0001c0001t0003g0198 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.594+1501G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241339291 | |||||||
| chr2:241339357 | A | AG | 26 | a0001c0001t0002g0017 a0001c0001t0006g0050 a0001c0001t0006g0051 others(23): Show |
32 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.594+1568dupG | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241339357 | ||||||
| chr2:241339370 | C | G | 1 | a0001c0001t0001g0122 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.594+1580C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241339370 | |||||||
| chr2:241339375 | G | GA | 24 | a0001c0001t0006g0189 a0001c0001t0007g0005 a0001c0001t0007g0036 others(21): Show |
30 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.594+1597dupA | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241339375 | ||||||
| chr2:241339703 | G | A | 29 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(26): Show |
36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.594+1913G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241339703 | |||||||
| chr2:241339898 | G | C | 1 | a0001c0001t0002g0057 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.594+2108G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241339898 | |||||||
| chr2:241339942 | G | A | 1 | a0001c0001t0014g0200 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.594+2152G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241339942 | |||||||
| chr2:241340027 | G | A | 2 | a0001c0001t0001g0109 a0001c0001t0001g0122 |
2 | HG00733.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.594+2237G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241340027 | |||||||
| chr2:241340150 | C | T | 1 | a0001c0001t0021g0223 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.594+2360C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241340150 | |||||||
| chr2:241340324 | C | T | 1 | a0001c0001t0006g0052 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.594+2534C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241340324 | |||||||
| chr2:241340338 | T | C | 1 | a0001c0001t0016g0296 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.594+2548T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241340338 | |||||||
| chr2:241340565 | T | G | 15 | a0001c0001t0002g0017 a0001c0001t0006g0293 a0001c0001t0006g0300 others(12): Show |
17 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.595-2427T>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241340565 | |||||||
| chr2:241340568 | T | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(238): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.595-2424T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241340568 | |||||||
| chr2:241340656 | T | C | 2 | a0001c0001t0002g0259 a0001c0001t0002g0260 |
2 | NA18949.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.595-2336T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241340656 | |||||||
| chr2:241340696 | A | C | 1 | a0001c0001t0001g0133 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.595-2296A>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241340696 | |||||||
| chr2:241340735 | C | G | 1 | a0001c0001t0001g0108 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.595-2257C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241340735 | |||||||
| chr2:241340937 | T | C | 1 | a0001c0001t0005g0208 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.595-2055T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241340937 | |||||||
| chr2:241341111 | T | C | 1 | a0001c0001t0002g0315 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.595-1881T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241341111 | |||||||
| chr2:241341134 | C | T | 1 | a0001c0001t0001g0026 | 2 | HG01070.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.595-1858C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241341134 | |||||||
| chr2:241341393 | T | G | 2 | a0001c0001t0007g0181 a0001c0001t0007g0182 |
2 | HG03927.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.595-1599T>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241341393 | |||||||
| chr2:241341394 | TACTA | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(78): Show |
111 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.595-1594_595-1591d others(6): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241341394 | ||||||
| chr2:241341410 | A | G | 26 | a0001c0001t0002g0017 a0001c0001t0006g0050 a0001c0001t0006g0051 others(23): Show |
32 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.595-1582A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241341410 | |||||||
| chr2:241341420 | C | T | 26 | a0001c0001t0002g0017 a0001c0001t0006g0050 a0001c0001t0006g0051 others(23): Show |
32 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.595-1572C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241341420 | |||||||
| chr2:241341508 | C | T | 4 | a0001c0001t0004g0035 a0001c0001t0004g0082 a0001c0001t0004g0157 others(1): Show |
5 | HG00639.hp1 HG01981.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.595-1484C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241341508 | |||||||
| chr2:241341509 | G | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(78): Show |
111 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.595-1483G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241341509 | |||||||
| chr2:241341569 | A | T | 1 | a0001c0001t0006g0195 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.595-1423A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241341569 | |||||||
| chr2:241341688 | T | C | 1 | a0001c0001t0002g0249 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.595-1304T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241341688 | |||||||
| chr2:241342000 | C | A | 1 | a0001c0001t0001g0134 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.595-992C>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241342000 | |||||||
| chr2:241342023 | T | A | 23 | a0001c0001t0006g0189 a0001c0001t0007g0005 a0001c0001t0007g0036 others(20): Show |
29 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.595-969T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241342023 | |||||||
| chr2:241342028 | T | C | 1 | a0001c0002t0008g0149 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.595-964T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241342028 | |||||||
| chr2:241342185 | T | C | 29 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(26): Show |
36 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.595-807T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241342185 | |||||||
| chr2:241342225 | C | T | 1 | a0001c0001t0006g0052 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.595-767C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241342225 | |||||||
| chr2:241342314 | C | G | 2 | a0001c0001t0012g0013 a0001c0001t0012g0030 |
5 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.595-678C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241342314 | |||||||
| chr2:241342319 | G | T | 42 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(39): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.595-673G>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241342319 | |||||||
| chr2:241342373 | T | G | 1 | a0001c0001t0001g0110 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.595-619T>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241342373 | |||||||
| chr2:241342534 | A | AT | 43 | a0001c0001t0002g0061 a0001c0001t0002g0066 a0001c0001t0002g0252 others(40): Show |
53 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.595-434dupT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241342534 | ||||||
| chr2:241342534 | A | ATT | 30 | a0001c0001t0002g0017 a0001c0001t0003g0203 a0001c0001t0003g0225 others(27): Show |
36 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.595-435_595-434dup others(2): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241342534 | ||||||
| chr2:241342534 | AT | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(109): Show |
148 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.595-434delT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 241342534 | ||||||
| chr2:241342564 | G | A | 1 | a0001c0001t0002g0259 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.595-428G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241342564 | |||||||
| chr2:241342577 | G | A | 1 | a0001c0001t0006g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.595-415G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241342577 | |||||||
| chr2:241342788 | G | A | 10 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0053 others(7): Show |
12 | HG01496.hp1 HG01884.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.595-204G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241342788 | |||||||
| chr2:241342832 | G | A | 2 | a0001c0001t0019g0273 a0001c0001t0019g0274 |
2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.595-160G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241342832 | |||||||
| chr2:241342947 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.595-45A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241342947 | |||||||
| chr2:241342950 | C | A | 1 | a0001c0001t0003g0215 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.595-42C>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 7/12 | chr2 | 241342950 | |||||||
| chr2:241343167 | G | T | 1 | a0001c0001t0001g0133 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.696+74G>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 8/12 | chr2 | 241343167 | |||||||
| chr2:241343207 | T | A | 1 | a0001c0001t0005g0208 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.696+114T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 8/12 | chr2 | 241343207 | |||||||
| chr2:241343308 | G | A | 1 | a0001c0001t0007g0036 | 2 | HG00423.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.696+215G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 8/12 | chr2 | 241343308 | |||||||
| chr2:241343431 | A | G | 1 | a0001c0001t0011g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.697-321A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 8/12 | chr2 | 241343431 | |||||||
| chr2:241343497 | CA | C | 12 | a0001c0001t0001g0083 a0001c0001t0001g0118 a0001c0001t0008g0031 others(9): Show |
14 | HG01496.hp1 HG01884.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.697-241delA | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 241343497 | ||||||
| chr2:241343542 | A | T | 67 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(64): Show |
80 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.697-210A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 8/12 | chr2 | 241343542 | |||||||
| chr2:241343656 | C | T | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(249): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.697-96C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 8/12 | chr2 | 241343656 | |||||||
| chr2:241343679 | A | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(238): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.697-73A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 8/12 | chr2 | 241343679 | |||||||
| chr2:241343708 | G | T | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.697-44G>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 8/12 | chr2 | 241343708 | |||||||
| chr2:241343730 | T | A | 1 | a0001c0001t0001g0111 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.697-22T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 8/12 | chr2 | 241343730 | |||||||
| chr2:241343936 | G | A | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.842+39G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241343936 | |||||||
| chr2:241343937 | T | C | 2 | a0001c0001t0001g0083 a0001c0001t0001g0084 |
2 | NA18962.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.842+40T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241343937 | |||||||
| chr2:241344007 | C | T | 1 | a0001c0001t0007g0187 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.842+110C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344007 | |||||||
| chr2:241344008 | G | A | 6 | a0001c0001t0002g0018 a0001c0001t0002g0054 a0001c0001t0002g0055 others(3): Show |
7 | NA18939.hp2 NA18953.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.842+111G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344008 | |||||||
| chr2:241344139 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.842+242C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344139 | |||||||
| chr2:241344158 | C | T | 1 | a0001c0001t0003g0238 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.842+261C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344158 | |||||||
| chr2:241344264 | T | C | 1 | a0001c0001t0004g0145 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.842+367T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344264 | |||||||
| chr2:241344381 | A | G | 1 | a0001c0001t0002g0264 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.842+484A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344381 | |||||||
| chr2:241344391 | T | C | 1 | a0001c0001t0028g0211 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.842+494T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344391 | |||||||
| chr2:241344411 | T | C | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.842+514T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344411 | |||||||
| chr2:241344507 | A | C | 1 | a0001c0001t0006g0253 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.842+610A>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344507 | |||||||
| chr2:241344518 | G | A | 2 | a0001c0001t0019g0273 a0001c0001t0019g0274 |
2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.842+621G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344518 | |||||||
| chr2:241344562 | C | T | 2 | a0001c0001t0014g0240 a0001c0001t0022g0241 |
2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.842+665C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344562 | |||||||
| chr2:241344576 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.842+679C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344576 | |||||||
| chr2:241344600 | G | C | 26 | a0001c0001t0002g0017 a0001c0001t0006g0050 a0001c0001t0006g0051 others(23): Show |
32 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.842+703G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344600 | |||||||
| chr2:241344633 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.842+736G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344633 | |||||||
| chr2:241344751 | T | C | 52 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0044 others(49): Show |
59 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.842+854T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344751 | |||||||
| chr2:241344811 | C | T | 1 | a0001c0001t0012g0013 | 3 | HG00741.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.842+914C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344811 | |||||||
| chr2:241344878 | T | TGACATGG others(16): Show |
2 | a0001c0001t0019g0273 a0001c0001t0019g0274 |
2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.842+1005_842+1027d others(25): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 241344878 | ||||||
| chr2:241344882 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.842+985A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344882 | |||||||
| chr2:241344989 | C | T | 2 | a0001c0001t0010g0022 a0001c0001t0010g0079 |
3 | HG02970.hp1 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.842+1092C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344989 | |||||||
| chr2:241344990 | G | A | 23 | a0001c0001t0006g0189 a0001c0001t0007g0005 a0001c0001t0007g0036 others(20): Show |
29 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.842+1093G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241344990 | |||||||
| chr2:241345077 | C | T | 1 | a0001c0001t0010g0080 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.843-1089C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241345077 | |||||||
| chr2:241345230 | C | T | 26 | a0001c0001t0002g0017 a0001c0001t0006g0050 a0001c0001t0006g0051 others(23): Show |
32 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.843-936C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241345230 | |||||||
| chr2:241345231 | G | A | 10 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0053 others(7): Show |
12 | HG01496.hp1 HG01884.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.843-935G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241345231 | |||||||
| chr2:241345365 | A | G | 1 | a0001c0001t0002g0057 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.843-801A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241345365 | |||||||
| chr2:241345409 | G | A | 71 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(68): Show |
85 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.843-757G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241345409 | |||||||
| chr2:241345437 | GACTTT | G | 26 | a0001c0001t0002g0017 a0001c0001t0006g0050 a0001c0001t0006g0051 others(23): Show |
32 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.843-722_843-718del others(5): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 241345437 | ||||||
| chr2:241345606 | A | T | 1 | a0001c0001t0006g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.843-560A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241345606 | |||||||
| chr2:241345607 | T | A | 3 | a0001c0001t0003g0210 a0001c0001t0003g0219 a0001c0001t0028g0211 |
3 | HG01891.hp1 HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.843-559T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241345607 | |||||||
| chr2:241345735 | A | G | 1 | a0001c0001t0002g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.843-431A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241345735 | |||||||
| chr2:241345736 | T | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG01515.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.843-430T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241345736 | |||||||
| chr2:241345769 | G | A | 2 | a0001c0001t0019g0273 a0001c0001t0019g0274 |
2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.843-397G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241345769 | |||||||
| chr2:241345836 | T | G | 1 | a0001c0001t0001g0089 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.843-330T>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241345836 | |||||||
| chr2:241345873 | T | C | 4 | a0001c0001t0002g0081 a0001c0001t0002g0252 a0001c0001t0002g0263 others(1): Show |
4 | HG01106.hp2 HG01192.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.843-293T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241345873 | |||||||
| chr2:241345958 | C | T | 1 | a0001c0001t0007g0178 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.843-208C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241345958 | |||||||
| chr2:241346007 | G | A | 1 | a0001c0001t0003g0227 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.843-159G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241346007 | |||||||
| chr2:241346086 | T | C | 42 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(39): Show |
49 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.843-80T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241346086 | |||||||
| chr2:241346102 | T | C | 7 | a0001c0001t0003g0043 a0001c0001t0003g0217 a0001c0001t0003g0235 others(4): Show |
8 | HG00544.hp2 HG02074.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.843-64T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241346102 | |||||||
| chr2:241346125 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.843-41T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241346125 | |||||||
| chr2:241346130 | A | G | 52 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0044 others(49): Show |
59 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.843-36A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 9/12 | chr2 | 241346130 | |||||||
| chr2:241346528 | T | A | 1 | a0001c0001t0001g0115 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.926+279T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241346528 | |||||||
| chr2:241346592 | T | A | 52 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0044 others(49): Show |
59 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.926+343T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241346592 | |||||||
| chr2:241346592 | TA | T | 24 | a0001c0001t0004g0164 a0001c0001t0005g0206 a0001c0001t0006g0189 others(21): Show |
29 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.926+356delA | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 241346592 | ||||||
| chr2:241346725 | C | T | 2 | a0001c0001t0002g0252 a0001c0001t0006g0253 |
2 | HG01106.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.926+476C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241346725 | |||||||
| chr2:241346829 | G | T | 1 | a0001c0001t0006g0309 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.926+580G>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241346829 | |||||||
| chr2:241346933 | C | T | 1 | a0001c0001t0006g0195 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.926+684C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241346933 | |||||||
| chr2:241346934 | G | A | 2 | a0001c0001t0004g0280 a0001c0001t0004g0283 |
2 | HG02698.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.926+685G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241346934 | |||||||
| chr2:241346959 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.926+710C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241346959 | |||||||
| chr2:241346967 | A | C | 1 | a0001c0001t0001g0094 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.926+718A>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241346967 | |||||||
| chr2:241346982 | C | A | 1 | a0001c0001t0006g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.926+733C>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241346982 | |||||||
| chr2:241347028 | G | A | 2 | a0001c0001t0003g0212 a0001c0001t0003g0221 |
2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.926+779G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241347028 | |||||||
| chr2:241347053 | G | C | 1 | a0001c0001t0014g0172 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.926+804G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241347053 | |||||||
| chr2:241347082 | T | G | 1 | a0001c0001t0001g0130 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.926+833T>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241347082 | |||||||
| chr2:241347176 | G | A | 1 | a0001c0001t0006g0303 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.926+927G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241347176 | |||||||
| chr2:241347253 | A | G | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.927-881A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241347253 | |||||||
| chr2:241347332 | A | G | 64 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0044 others(61): Show |
73 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.927-802A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241347332 | |||||||
| chr2:241347419 | G | C | 1 | a0001c0001t0003g0203 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.927-715G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241347419 | |||||||
| chr2:241347459 | C | T | 3 | a0001c0001t0006g0038 a0001c0001t0006g0194 a0001c0001t0024g0193 |
4 | HG01261.hp1 HG02559.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.927-675C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241347459 | |||||||
| chr2:241347560 | A | G | 1 | a0002c0003t0002g0059 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.927-574A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241347560 | |||||||
| chr2:241347612 | A | G | 2 | a0001c0001t0004g0162 a0001c0001t0004g0169 |
2 | NA18952.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.927-522A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241347612 | |||||||
| chr2:241347625 | G | A | 2 | a0001c0001t0012g0013 a0001c0001t0012g0030 |
5 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.927-509G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241347625 | |||||||
| chr2:241347668 | A | G | 6 | a0001c0001t0002g0046 a0001c0001t0002g0048 a0001c0001t0002g0247 others(3): Show |
8 | HG00609.hp1 HG02129.hp1 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.927-466A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241347668 | |||||||
| chr2:241347697 | G | T | 1 | a0001c0001t0006g0189 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.927-437G>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241347697 | |||||||
| chr2:241347778 | T | C | 1 | a0001c0001t0028g0211 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.927-356T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241347778 | |||||||
| chr2:241347885 | C | T | 1 | a0001c0001t0002g0068 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.927-249C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241347885 | |||||||
| chr2:241347920 | T | C | 1 | a0001c0001t0008g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.927-214T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241347920 | |||||||
| chr2:241348072 | T | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(145): Show |
191 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.927-62T>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 10/12 | chr2 | 241348072 | |||||||
| chr2:241348475 | C | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(70): Show |
100 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.984+284C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | chr2 | 241348475 | |||||||
| chr2:241348626 | TGAG | T | 2 | a0001c0001t0016g0049 a0001c0001t0016g0296 |
3 | HG01884.hp2 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.984+441_984+443del others(3): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 241348626 | ||||||
| chr2:241348745 | CAATTT | C | 5 | a0001c0001t0010g0072 a0001c0001t0011g0020 a0001c0001t0011g0071 others(2): Show |
6 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.984+556_984+560del others(5): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 241348745 | ||||||
| chr2:241349020 | C | G | 2 | a0001c0001t0014g0240 a0001c0001t0022g0241 |
2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.984+829C>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | chr2 | 241349020 | |||||||
| chr2:241349049 | A | G | 1 | a0001c0001t0003g0220 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.984+858A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | chr2 | 241349049 | |||||||
| chr2:241349235 | G | A | 2 | a0001c0001t0002g0266 a0001c0001t0002g0275 |
2 | NA18948.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.985-838G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | chr2 | 241349235 | |||||||
| chr2:241349368 | C | CT | 3 | a0001c0001t0001g0110 a0001c0001t0001g0127 a0001c0001t0001g0276 |
3 | HG00438.hp2 HG02015.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.985-702dupT | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 241349368 | ||||||
| chr2:241349371 | T | TA | 6 | a0001c0001t0001g0125 a0001c0001t0007g0036 a0001c0001t0007g0179 others(3): Show |
7 | HG00140.hp1 HG00423.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.985-689dupA | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 241349371 | ||||||
| chr2:241349381 | A | AT | 33 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0025 others(30): Show |
42 | HG00597.hp1 HG00735.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.985-692_985-691ins others(1): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | chr2 | 241349381 | |||||||
| chr2:241349381 | A | T | 54 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0044 others(51): Show |
63 | HG00099.hp2 HG00609.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.985-692A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | chr2 | 241349381 | |||||||
| chr2:241349383 | A | AT | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(71): Show |
102 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.985-690_985-689ins others(1): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | chr2 | 241349383 | |||||||
| chr2:241349383 | A | T | 142 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0025 others(139): Show |
169 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.985-690A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | chr2 | 241349383 | |||||||
| chr2:241349385 | T | A | 1 | a0001c0001t0003g0222 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.985-688T>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | chr2 | 241349385 | |||||||
| chr2:241349604 | C | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0129 |
2 | NA18943.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.985-469C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | chr2 | 241349604 | |||||||
| chr2:241349636 | T | C | 22 | a0001c0001t0007g0005 a0001c0001t0007g0036 a0001c0001t0007g0037 others(19): Show |
28 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.985-437T>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | chr2 | 241349636 | |||||||
| chr2:241349649 | C | T | 1 | a0001c0001t0002g0017 | 3 | HG01070.hp2 HG01071.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.985-424C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | chr2 | 241349649 | |||||||
| chr2:241349650 | G | A | 8 | a0001c0001t0010g0022 a0001c0001t0010g0072 a0001c0001t0010g0079 others(5): Show |
10 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.985-423G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | chr2 | 241349650 | |||||||
| chr2:241349736 | G | A | 4 | a0001c0001t0006g0038 a0001c0001t0006g0194 a0001c0001t0006g0195 others(1): Show |
5 | HG01261.hp1 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.985-337G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | chr2 | 241349736 | |||||||
| chr2:241350004 | A | G | 43 | a0001c0001t0004g0003 a0001c0001t0004g0033 a0001c0001t0004g0034 others(40): Show |
50 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.985-69A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 11/12 | chr2 | 241350004 | |||||||
| chr2:241350248 | C | CATT | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(250): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.*29+46_*29+48dupAT others(1): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 241350248 | ||||||
| chr2:241350410 | G | C | 34 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(31): Show |
45 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.*29+207G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 12/12 | chr2 | 241350410 | |||||||
| chr2:241350428 | A | T | 52 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0044 others(49): Show |
59 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.*29+225A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 12/12 | chr2 | 241350428 | |||||||
| chr2:241350476 | C | CTAAGCTT others(3): Show |
1 | a0001c0001t0002g0275 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.*29+274_*29+283dup others(10): Show |
SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 241350476 | ||||||
| chr2:241350632 | C | A | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.*29+429C>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 12/12 | chr2 | 241350632 | |||||||
| chr2:241350632 | C | T | 3 | a0001c0001t0009g0153 a0001c0001t0009g0167 a0001c0001t0009g0170 |
3 | HG00597.hp1 NA18951.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.*29+429C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 12/12 | chr2 | 241350632 | |||||||
| chr2:241350633 | A | G | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.*29+430A>G | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 12/12 | chr2 | 241350633 | |||||||
| chr2:241350723 | G | A | 1 | a0001c0001t0014g0200 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.*29+520G>A | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 12/12 | chr2 | 241350723 | |||||||
| chr2:241350913 | A | C | 1 | a0001c0001t0002g0069 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.*29+710A>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 12/12 | chr2 | 241350913 | |||||||
| chr2:241350970 | G | C | 1 | a0001c0001t0005g0196 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.*29+767G>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 12/12 | chr2 | 241350970 | |||||||
| chr2:241351059 | C | T | 1 | a0001c0001t0002g0249 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.*29+856C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 12/12 | chr2 | 241351059 | |||||||
| chr2:241351339 | A | T | 1 | a0001c0001t0001g0088 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.*30-628A>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 12/12 | chr2 | 241351339 | |||||||
| chr2:241351342 | C | T | 2 | a0001c0001t0019g0273 a0001c0001t0019g0274 |
2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.*30-625C>T | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 12/12 | chr2 | 241351342 | |||||||
| chr2:241351752 | A | C | 4 | a0001c0001t0004g0279 a0001c0001t0004g0282 a0001c0001t0004g0289 others(1): Show |
4 | HG00621.hp1 HG01192.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.*30-215A>C | SEPTIN2 | ENSG00000168385.18 | transcript | ENST00000391971.7 | protein_coding | 12/12 | chr2 | 241351752 |