Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2342 |
| ensemblid | ENSG00000257365.8 |
| hgncid | 3785 |
| symbol | FNTB |
| name | farnesyltransferase, CAAX box, beta |
| refseq_nuc | NM_002028.4 |
| refseq_prot | NP_002019.1 |
| ensembl_nuc | ENST00000246166.3 |
| ensembl_prot | ENSP00000246166.2 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 64986895 |
| end | 65062650 |
| strand | + |
| ver | v1.2 |
| region | chr14:64986895-65062650 |
| region5000 | chr14:64981895-65067650 |
| regionname0 | FNTB_chr14_64986895_65062650 |
| regionname5000 | FNTB_chr14_64981895_65067650 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 437 | 357 | 86 | 66 | 153 | 10 | 40 | 110 | FNTB_chr14_64981895_65067650 | FNTB | MASPS others(432): Show |
chr14 | 64981895 | 65067650 |
| a0002 | 0/0 | 437 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | MASPS others(432): Show |
chr14 | 64981895 | 65067650 |
| a0003 | 0/0 | 437 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | MASPS others(432): Show |
chr14 | 64981895 | 65067650 |
| a0004 | 0/0 | 437 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | MASPS others(432): Show |
chr14 | 64981895 | 65067650 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1311 | 355 | 86 | 66 | 152 | 10 | 39 | FNTB_chr14_64981895_65067650 | FNTB | ATGGC others(1306): Show |
chr14 | 64981895 | 65067650 | ||
| a0001c0004 | 0/0 | 1311 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | ATGGC others(1306): Show |
chr14 | 64981895 | 65067650 | ||
| a0001c0005 | 0/0 | 1311 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | ATGGC others(1306): Show |
chr14 | 64981895 | 65067650 | ||
| a0002c0006 | 0/0 | 1311 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | ATGGC others(1306): Show |
chr14 | 64981895 | 65067650 | ||
| a0003c0003 | 0/0 | 1311 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | ATGGC others(1306): Show |
chr14 | 64981895 | 65067650 | ||
| a0004c0002 | 0/0 | 1311 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | ATGGC others(1306): Show |
chr14 | 64981895 | 65067650 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2711 | 239 | 30 | 52 | 118 | 8 | 29 | FNTB_chr14_64981895_65067650 | FNTB | AATGC others(2706): Show |
chr14 | 64981895 | 65067650 |
| a0001c0001t0002 | 0/0 | 2711 | 111 | 56 | 13 | 33 | 1 | 8 | FNTB_chr14_64981895_65067650 | FNTB | AATGC others(2706): Show |
chr14 | 64981895 | 65067650 |
| a0001c0001t0003 | 0/0 | 2711 | 2 | 0 | 0 | 0 | 0 | 2 | FNTB_chr14_64981895_65067650 | FNTB | AATGC others(2706): Show |
chr14 | 64981895 | 65067650 |
| a0001c0001t0004 | 0/0 | 2711 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | AATGC others(2706): Show |
chr14 | 64981895 | 65067650 |
| a0001c0001t0005 | 0/0 | 2711 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | AATGC others(2706): Show |
chr14 | 64981895 | 65067650 |
| a0001c0001t0006 | 0/0 | 2711 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | AATGC others(2706): Show |
chr14 | 64981895 | 65067650 |
| a0001c0004t0001 | 0/0 | 2711 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | AATGC others(2706): Show |
chr14 | 64981895 | 65067650 |
| a0001c0005t0002 | 0/0 | 2711 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | AATGC others(2706): Show |
chr14 | 64981895 | 65067650 |
| a0002c0006t0001 | 0/0 | 2711 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | AATGC others(2706): Show |
chr14 | 64981895 | 65067650 |
| a0003c0003t0001 | 0/0 | 2711 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | AATGC others(2706): Show |
chr14 | 64981895 | 65067650 |
| a0004c0002t0002 | 0/0 | 2711 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | AATGC others(2706): Show |
chr14 | 64981895 | 65067650 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0146 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0162 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0002g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0001t0006g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0004t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0001c0005t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0002c0006t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0003c0003t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| a0004c0002t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0264 | EUR | GBR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | GBR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | FIN | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0313 | EUR | FIN | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | CHS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0336 | EAS | CHS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | CHS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | CHS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | CHS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | CHS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | CHS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | CHS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0137 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0108 | EUR | IBS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | IBS | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02080 | hp2 | a0002 | c0006 | t0001 | g0215 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0328 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CDX | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CDX | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | CDX | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02258 | hp1 | a0003 | c0003 | t0001 | g0346 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0329 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02293 | hp2 | a0001 | c0001 | t0006 | g0145 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02602 | hp2 | a0001 | c0005 | t0002 | g0283 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0183 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0347 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0150 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0345 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | ESN | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | ESN | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0348 | AFR | ESN | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | ESN | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0070 | AFR | ESN | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | ESN | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0274 | AFR | ESN | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | MSL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | MSL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0234 | AFR | ESN | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | ESN | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | ESN | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | ESN | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | MSL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | MSL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0291 | AFR | MSL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | MSL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0087 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0341 | AFR | MSL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | MSL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | MSL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0044 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0042 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | GWD | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | MSL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0119 | SAS | BEB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | BEB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | STU | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | STU | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0270 | SAS | STU | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | STU | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | STU | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0080 | SAS | STU | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | STU | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | STU | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | YRI | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | YRI | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | CHB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | CHB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CHB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | YRI | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | YRI | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18979 | hp2 | a0001 | c0004 | t0001 | g0103 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | LWK | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | LWK | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | LWK | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19070 | hp2 | a0001 | c0001 | t0004 | g0325 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | YRI | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | YRI | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | ASW | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | ASW | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | TSI | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0043 | EUR | TSI | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0147 | EUR | TSI | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0255 | EUR | TSI | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | GIH | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | GIH | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | ACB | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | MSL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0335 | AFR | USA | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | USA | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | USA | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA20300 | hp2 | a0004 | c0002 | t0002 | g0015 | AFR | USA | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | LWK | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | LWK | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0162 | REF | REF | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0146 | REF | REF | FNTB_chr14_64981895_65067650 | FNTB | chr14 | 64981895 | 65067650 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:65027539 | A | T | 1 | a0002 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.461A>T | p.Tyr154Phe | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 5/12 | 520/2711 | 461/1314 | 154/437 | chr14 | 65027539 | |||
| chr14:65054660 | G | T | 1 | a0003 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.1153G>T | p.Val385Leu | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/12 | 1212/2711 | 1153/1314 | 385/437 | chr14 | 65054660 | |||
| chr14:65061259 | C | T | 1 | a0004 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.1261C>T | p.Pro421Ser | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 12/12 | 1320/2711 | 1261/1314 | 421/437 | chr14 | 65061259 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:65053323 | G | T | 1 | a0001c0005 | 1 | HG02602.hp2 | synonymous_variant | LOW | c.1041G>T | p.Ala347Ala | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/12 | 1100/2711 | 1041/1314 | 347/437 | chr14 | 65053323 | |||
| chr14:65054635 | C | T | 1 | a0001c0004 | 1 | NA18979.hp2 | synonymous_variant | LOW | c.1128C>T | p.Phe376Phe | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/12 | 1187/2711 | 1128/1314 | 376/437 | chr14 | 65054635 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:65061542 | C | T | 1 | a0001c0001t0006 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*230C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 12/12 | 230 | chr14 | 65061542 | ||||||
| chr14:65061671 | C | T | 1 | a0001c0001t0005 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*359C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 12/12 | 359 | chr14 | 65061671 | ||||||
| chr14:65062104 | C | T | 1 | a0001c0001t0004 | 1 | NA19070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*792C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 12/12 | 792 | chr14 | 65062104 | ||||||
| chr14:65062169 | A | T | 3 | a0001c0001t0002 a0001c0005t0002 a0004c0002t0002 |
113 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*857A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 12/12 | 857 | chr14 | 65062169 | ||||||
| chr14:65062174 | T | C | 3 | a0001c0001t0002 a0001c0005t0002 a0004c0002t0002 |
113 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*862T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 12/12 | 862 | chr14 | 65062174 | ||||||
| chr14:65062600 | C | T | 1 | a0001c0001t0003 | 2 | HG03490.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1288C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 12/12 | 1288 | chr14 | 65062600 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:64987138 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.144+41T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64987138 | |||||||
| chr14:64987465 | T | A | 5 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(2): Show |
5 | HG01081.hp2 HG02109.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.144+368T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64987465 | |||||||
| chr14:64987617 | C | G | 6 | a0001c0001t0001g0349 a0001c0001t0001g0350 a0001c0001t0001g0351 others(3): Show |
6 | HG02074.hp2 HG02083.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.144+520C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64987617 | |||||||
| chr14:64987681 | C | G | 63 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(60): Show |
64 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.144+584C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64987681 | |||||||
| chr14:64987997 | T | G | 1 | a0001c0001t0002g0014 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.144+900T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64987997 | |||||||
| chr14:64988302 | G | A | 2 | a0001c0001t0002g0009 a0001c0001t0002g0010 |
2 | HG01081.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.144+1205G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64988302 | |||||||
| chr14:64988368 | T | C | 1 | a0004c0002t0002g0015 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.144+1271T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64988368 | |||||||
| chr14:64988443 | C | CT | 20 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(17): Show |
20 | HG01192.hp1 HG01934.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.144+1367dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64988443 | ||||||
| chr14:64988443 | CT | C | 90 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(87): Show |
91 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.144+1367delT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64988443 | ||||||
| chr14:64988477 | C | T | 1 | a0001c0001t0001g0339 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.144+1380C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64988477 | |||||||
| chr14:64988477 | CG | C | 3 | a0001c0001t0002g0001 a0001c0001t0002g0051 a0001c0001t0002g0052 |
4 | HG02486.hp2 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+1381delG | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64988477 | |||||||
| chr14:64988530 | G | A | 1 | a0001c0001t0002g0053 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.144+1433G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64988530 | |||||||
| chr14:64988585 | C | T | 4 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
4 | HG01192.hp1 HG02273.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.144+1488C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64988585 | |||||||
| chr14:64988684 | G | A | 8 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(5): Show |
8 | HG03831.hp2 HG03927.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.144+1587G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64988684 | |||||||
| chr14:64988733 | G | A | 1 | a0001c0001t0001g0293 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.144+1636G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64988733 | |||||||
| chr14:64988914 | G | A | 1 | a0004c0002t0002g0015 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.144+1817G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64988914 | |||||||
| chr14:64988949 | T | C | 2 | a0001c0001t0002g0273 a0001c0001t0002g0274 |
2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.144+1852T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64988949 | |||||||
| chr14:64988974 | C | A | 1 | a0001c0001t0002g0006 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.144+1877C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64988974 | |||||||
| chr14:64989272 | C | CA | 39 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(36): Show |
40 | HG00597.hp2 HG00621.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.144+2197dupA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64989272 | ||||||
| chr14:64989304 | C | T | 1 | a0001c0001t0002g0291 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.144+2207C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64989304 | |||||||
| chr14:64989305 | G | A | 1 | a0001c0001t0001g0295 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.144+2208G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64989305 | |||||||
| chr14:64989313 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.144+2216A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64989313 | |||||||
| chr14:64989490 | AGCAAGAC others(4): Show |
A | 1 | a0001c0001t0002g0047 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.144+2394_144+2404d others(13): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64989490 | |||||||
| chr14:64989503 | G | T | 1 | a0001c0001t0002g0047 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.144+2406G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64989503 | |||||||
| chr14:64989521 | C | G | 75 | a0001c0001t0001g0022 a0001c0001t0001g0040 a0001c0001t0001g0041 others(72): Show |
76 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.144+2424C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64989521 | |||||||
| chr14:64989531 | T | TA | 75 | a0001c0001t0001g0022 a0001c0001t0001g0040 a0001c0001t0001g0041 others(72): Show |
76 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.144+2445dupA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64989531 | ||||||
| chr14:64989539 | AAAAC | A | 20 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0024 others(17): Show |
20 | HG00140.hp2 HG00642.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.144+2450_144+2453d others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64989539 | ||||||
| chr14:64989877 | A | T | 1 | a0001c0001t0002g0270 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.144+2780A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64989877 | |||||||
| chr14:64990090 | C | A | 1 | a0001c0001t0002g0087 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.144+2993C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64990090 | |||||||
| chr14:64990095 | G | A | 1 | a0004c0002t0002g0015 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.144+2998G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64990095 | |||||||
| chr14:64990338 | G | A | 1 | a0001c0001t0002g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.144+3241G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64990338 | |||||||
| chr14:64990347 | A | G | 1 | a0001c0001t0001g0338 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.144+3250A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64990347 | |||||||
| chr14:64990576 | G | A | 1 | a0001c0001t0002g0291 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.144+3479G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64990576 | |||||||
| chr14:64991019 | G | C | 3 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0291 |
3 | HG02615.hp2 HG02723.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.144+3922G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64991019 | |||||||
| chr14:64991175 | ATGGCATG others(15): Show |
A | 1 | a0001c0001t0002g0047 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.144+4088_144+4109d others(24): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64991175 | ||||||
| chr14:64991323 | C | G | 1 | a0001c0001t0001g0269 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.144+4226C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64991323 | |||||||
| chr14:64991464 | C | T | 1 | a0001c0001t0002g0268 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.144+4367C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64991464 | |||||||
| chr14:64991535 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.144+4438C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64991535 | |||||||
| chr14:64991553 | G | A | 12 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(9): Show |
12 | HG00140.hp2 HG00735.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.144+4456G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64991553 | |||||||
| chr14:64991636 | G | A | 26 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(23): Show |
27 | HG00140.hp2 HG00735.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.144+4539G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64991636 | |||||||
| chr14:64991704 | G | A | 1 | a0001c0001t0001g0296 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.144+4607G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64991704 | |||||||
| chr14:64991753 | G | C | 26 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(23): Show |
27 | HG00140.hp2 HG00735.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.144+4656G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64991753 | |||||||
| chr14:64991773 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.144+4676G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64991773 | |||||||
| chr14:64991833 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.144+4736G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64991833 | |||||||
| chr14:64992058 | G | A | 1 | a0001c0001t0002g0092 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.144+4961G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64992058 | |||||||
| chr14:64992207 | A | T | 51 | a0001c0001t0001g0005 a0001c0001t0001g0081 a0001c0001t0001g0082 others(48): Show |
52 | HG00140.hp1 HG00642.hp1 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.144+5110A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64992207 | |||||||
| chr14:64992241 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.144+5144A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64992241 | |||||||
| chr14:64992413 | T | A | 2 | a0001c0001t0001g0271 a0001c0001t0002g0093 |
2 | HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.144+5316T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64992413 | |||||||
| chr14:64992509 | A | G | 1 | a0001c0001t0002g0225 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.144+5412A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64992509 | |||||||
| chr14:64992720 | C | G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0090 |
4 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.144+5623C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64992720 | |||||||
| chr14:64992724 | G | C | 1 | a0001c0001t0002g0341 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.144+5627G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64992724 | |||||||
| chr14:64992776 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.144+5679G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64992776 | |||||||
| chr14:64992906 | A | G | 1 | a0001c0001t0002g0224 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.144+5809A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64992906 | |||||||
| chr14:64992982 | T | C | 1 | a0001c0001t0002g0094 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.144+5885T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64992982 | |||||||
| chr14:64993028 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.144+5931G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64993028 | |||||||
| chr14:64993071 | C | T | 2 | a0001c0001t0001g0271 a0001c0001t0002g0093 |
2 | HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.144+5974C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64993071 | |||||||
| chr14:64993111 | C | T | 2 | a0001c0001t0001g0271 a0001c0001t0002g0093 |
2 | HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.144+6014C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64993111 | |||||||
| chr14:64993133 | A | G | 1 | a0001c0001t0002g0080 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.144+6036A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64993133 | |||||||
| chr14:64993341 | A | T | 1 | a0001c0001t0001g0084 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.144+6244A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64993341 | |||||||
| chr14:64993421 | G | A | 2 | a0001c0001t0002g0095 a0001c0001t0002g0096 |
2 | NA18942.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.144+6324G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64993421 | |||||||
| chr14:64993442 | C | T | 1 | a0004c0002t0002g0015 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.144+6345C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64993442 | |||||||
| chr14:64993454 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.144+6357G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64993454 | |||||||
| chr14:64993512 | A | G | 1 | a0001c0001t0002g0047 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.144+6415A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64993512 | |||||||
| chr14:64993632 | G | A | 8 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(5): Show |
8 | HG03831.hp2 HG03927.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.144+6535G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64993632 | |||||||
| chr14:64993707 | C | G | 8 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(5): Show |
8 | HG03831.hp2 HG03927.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.144+6610C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64993707 | |||||||
| chr14:64993722 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.144+6625G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64993722 | |||||||
| chr14:64993838 | C | CT | 28 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(25): Show |
29 | HG00140.hp2 HG00735.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.144+6752dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64993838 | ||||||
| chr14:64993858 | A | C | 36 | a0001c0001t0001g0004 a0001c0001t0001g0077 a0001c0001t0001g0079 others(33): Show |
37 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.144+6761A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64993858 | |||||||
| chr14:64993933 | G | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0337 |
2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.144+6836G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64993933 | |||||||
| chr14:64994135 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0090 |
4 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.144+7038G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64994135 | |||||||
| chr14:64994194 | G | T | 7 | a0001c0001t0001g0345 a0001c0001t0001g0347 a0001c0001t0002g0038 others(4): Show |
7 | HG01891.hp1 HG02258.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.144+7097G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64994194 | |||||||
| chr14:64994226 | C | G | 1 | a0001c0001t0001g0195 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.144+7129C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64994226 | |||||||
| chr14:64994283 | C | T | 2 | a0001c0001t0002g0038 a0001c0001t0002g0196 |
2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.144+7186C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64994283 | |||||||
| chr14:64994655 | A | C | 13 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(10): Show |
13 | HG00140.hp2 HG00735.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.144+7558A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64994655 | |||||||
| chr14:64994656 | C | T | 1 | a0001c0001t0002g0336 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.144+7559C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64994656 | |||||||
| chr14:64994866 | C | T | 1 | a0001c0001t0002g0194 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.144+7769C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64994866 | |||||||
| chr14:64994935 | T | A | 2 | a0001c0001t0001g0297 a0004c0002t0002g0015 |
2 | NA18956.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.144+7838T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64994935 | |||||||
| chr14:64994954 | C | G | 1 | a0001c0001t0002g0047 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.144+7857C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64994954 | |||||||
| chr14:64995277 | A | G | 26 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(23): Show |
27 | HG00140.hp2 HG00735.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.144+8180A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64995277 | |||||||
| chr14:64995280 | T | G | 2 | a0001c0001t0002g0273 a0001c0001t0002g0274 |
2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.144+8183T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64995280 | |||||||
| chr14:64995463 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.144+8366A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64995463 | |||||||
| chr14:64995602 | C | T | 1 | a0001c0001t0002g0335 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.144+8505C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64995602 | |||||||
| chr14:64995727 | A | T | 1 | a0004c0002t0002g0015 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.145-8522A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64995727 | |||||||
| chr14:64995770 | CGTAT | C | 3 | a0001c0001t0001g0332 a0001c0001t0002g0030 a0001c0001t0002g0031 |
3 | HG01243.hp1 HG02895.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.145-8458_145-8455d others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64995770 | ||||||
| chr14:64995770 | CGTATGTA others(1): Show |
C | 82 | a0001c0001t0001g0002 a0001c0001t0001g0064 a0001c0001t0001g0071 others(79): Show |
83 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.145-8462_145-8455d others(10): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64995770 | ||||||
| chr14:64995771 | G | A | 8 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(5): Show |
8 | HG03831.hp2 HG03927.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.145-8478G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64995771 | |||||||
| chr14:64995774 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.145-8475T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64995774 | |||||||
| chr14:64995791 | G | A | 1 | a0001c0001t0001g0332 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.145-8458G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64995791 | |||||||
| chr14:64995903 | C | T | 7 | a0001c0001t0001g0033 a0001c0001t0002g0030 a0001c0001t0002g0031 others(4): Show |
7 | HG01192.hp2 HG01243.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.145-8346C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64995903 | |||||||
| chr14:64995906 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.145-8343G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64995906 | |||||||
| chr14:64995928 | G | A | 6 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0229 others(3): Show |
6 | HG00642.hp1 HG01081.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.145-8321G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64995928 | |||||||
| chr14:64995997 | C | T | 1 | a0001c0001t0002g0107 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.145-8252C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64995997 | |||||||
| chr14:64996037 | C | T | 12 | a0001c0001t0001g0022 a0001c0001t0001g0040 a0001c0001t0001g0041 others(9): Show |
13 | HG01106.hp2 HG01515.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.145-8212C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64996037 | |||||||
| chr14:64996083 | A | G | 1 | a0001c0001t0002g0107 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.145-8166A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64996083 | |||||||
| chr14:64996123 | C | CA | 20 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(17): Show |
21 | HG00140.hp2 HG00735.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.145-8109dupA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64996123 | ||||||
| chr14:64996123 | C | CAA | 9 | a0001c0001t0001g0023 a0001c0001t0001g0033 a0001c0001t0002g0030 others(6): Show |
9 | HG01192.hp2 HG01243.hp1 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.145-8110_145-8109d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64996123 | ||||||
| chr14:64996123 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0002g0047 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.145-8118_145-8109d others(12): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64996123 | ||||||
| chr14:64996141 | GAAAA | G | 7 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(4): Show |
7 | HG03927.hp2 NA18955.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.145-8105_145-8102d others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64996141 | ||||||
| chr14:64996145 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.145-8104A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64996145 | |||||||
| chr14:64996485 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.145-7764A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64996485 | |||||||
| chr14:64996766 | C | CT | 108 | a0001c0001t0001g0005 a0001c0001t0001g0071 a0001c0001t0001g0073 others(105): Show |
109 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.145-7462dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64996766 | ||||||
| chr14:64996766 | C | CTT | 7 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0264 others(4): Show |
7 | HG00140.hp1 HG01081.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.145-7463_145-7462d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64996766 | ||||||
| chr14:64996766 | CT | C | 17 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0016 others(14): Show |
17 | HG01515.hp1 HG01891.hp1 HG02723.hp1 others(14): Show |
intron_variant | MODIFIER | c.145-7462delT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64996766 | ||||||
| chr14:64996766 | CTT | C | 24 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0023 others(21): Show |
25 | HG00140.hp2 HG00735.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.145-7463_145-7462d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64996766 | ||||||
| chr14:64996987 | A | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0272 |
2 | HG01515.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.145-7262A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64996987 | |||||||
| chr14:64997019 | T | C | 1 | a0001c0001t0002g0047 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.145-7230T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64997019 | |||||||
| chr14:64997135 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.145-7114T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64997135 | |||||||
| chr14:64997286 | A | G | 38 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(35): Show |
40 | HG00140.hp2 HG00735.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.145-6963A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64997286 | |||||||
| chr14:64997458 | T | A | 13 | a0001c0001t0001g0022 a0001c0001t0001g0040 a0001c0001t0001g0041 others(10): Show |
14 | HG01106.hp2 HG01515.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.145-6791T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64997458 | |||||||
| chr14:64997584 | T | C | 110 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(107): Show |
113 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(110): Show |
intron_variant | MODIFIER | c.145-6665T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64997584 | |||||||
| chr14:64997643 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.145-6606C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64997643 | |||||||
| chr14:64998057 | T | C | 3 | a0001c0001t0001g0097 a0001c0001t0001g0109 a0001c0001t0001g0110 |
3 | NA18962.hp1 NA18993.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.145-6192T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64998057 | |||||||
| chr14:64998083 | TA | T | 7 | a0001c0001t0001g0345 a0001c0001t0001g0347 a0001c0001t0002g0038 others(4): Show |
7 | HG01891.hp1 HG02258.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.145-6162delA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64998083 | ||||||
| chr14:64998153 | G | A | 2 | a0001c0001t0002g0037 a0001c0001t0002g0111 |
2 | NA18942.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.145-6096G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64998153 | |||||||
| chr14:64998219 | A | G | 34 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(31): Show |
35 | HG00140.hp2 HG00735.hp2 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.145-6030A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64998219 | |||||||
| chr14:64998322 | G | A | 111 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(108): Show |
114 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(111): Show |
intron_variant | MODIFIER | c.145-5927G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64998322 | |||||||
| chr14:64998341 | A | G | 1 | a0001c0001t0002g0335 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.145-5908A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64998341 | |||||||
| chr14:64998409 | A | G | 1 | a0001c0001t0002g0047 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.145-5840A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64998409 | |||||||
| chr14:64998453 | CA | C | 45 | a0001c0001t0001g0005 a0001c0001t0001g0081 a0001c0001t0001g0082 others(42): Show |
46 | HG00140.hp1 HG00642.hp1 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.145-5794delA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 64998453 | ||||||
| chr14:64998504 | G | C | 13 | a0001c0001t0001g0022 a0001c0001t0001g0040 a0001c0001t0001g0041 others(10): Show |
14 | HG01106.hp2 HG01515.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.145-5745G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64998504 | |||||||
| chr14:64998657 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0090 |
4 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.145-5592C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64998657 | |||||||
| chr14:64998773 | A | G | 13 | a0001c0001t0001g0022 a0001c0001t0001g0040 a0001c0001t0001g0041 others(10): Show |
14 | HG01106.hp2 HG01515.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.145-5476A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64998773 | |||||||
| chr14:64998869 | G | A | 4 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(1): Show |
4 | HG00408.hp2 HG00609.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.145-5380G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64998869 | |||||||
| chr14:64998975 | T | G | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | NA18962.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.145-5274T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64998975 | |||||||
| chr14:64999007 | A | T | 39 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(36): Show |
41 | HG00140.hp2 HG00735.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.145-5242A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64999007 | |||||||
| chr14:64999087 | A | G | 1 | a0001c0001t0001g0338 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.145-5162A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64999087 | |||||||
| chr14:64999162 | G | A | 8 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(5): Show |
8 | HG03831.hp2 HG03927.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.145-5087G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64999162 | |||||||
| chr14:64999207 | G | T | 39 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(36): Show |
41 | HG00140.hp2 HG00735.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.145-5042G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64999207 | |||||||
| chr14:64999210 | T | C | 39 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(36): Show |
41 | HG00140.hp2 HG00735.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.145-5039T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64999210 | |||||||
| chr14:64999252 | G | A | 39 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(36): Show |
41 | HG00140.hp2 HG00735.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.145-4997G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64999252 | |||||||
| chr14:64999446 | A | G | 13 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(10): Show |
13 | HG00140.hp2 HG00735.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.145-4803A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64999446 | |||||||
| chr14:64999508 | G | C | 26 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(23): Show |
27 | HG00140.hp2 HG00735.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.145-4741G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64999508 | |||||||
| chr14:64999524 | G | A | 1 | a0001c0001t0002g0291 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.145-4725G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64999524 | |||||||
| chr14:64999607 | A | G | 2 | a0001c0001t0001g0229 a0001c0001t0001g0275 |
2 | HG01168.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.145-4642A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64999607 | |||||||
| chr14:64999687 | C | A | 1 | a0004c0002t0002g0015 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.145-4562C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64999687 | |||||||
| chr14:64999833 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.145-4416G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64999833 | |||||||
| chr14:64999941 | T | G | 1 | a0001c0001t0002g0080 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.145-4308T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64999941 | |||||||
| chr14:64999957 | G | A | 7 | a0001c0001t0001g0345 a0001c0001t0001g0347 a0001c0001t0002g0038 others(4): Show |
7 | HG01891.hp1 HG02258.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.145-4292G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64999957 | |||||||
| chr14:64999994 | C | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(5): Show |
8 | HG03831.hp2 HG03927.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.145-4255C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 64999994 | |||||||
| chr14:65000089 | G | T | 1 | a0001c0001t0001g0263 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.145-4160G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65000089 | |||||||
| chr14:65000229 | C | A | 1 | a0001c0001t0001g0116 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.145-4020C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65000229 | |||||||
| chr14:65000396 | G | T | 11 | a0001c0001t0001g0022 a0001c0001t0001g0040 a0001c0001t0001g0041 others(8): Show |
12 | HG01106.hp2 HG01515.hp2 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.145-3853G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65000396 | |||||||
| chr14:65000572 | G | A | 5 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0192 others(2): Show |
5 | HG00735.hp1 HG01109.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.145-3677G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65000572 | |||||||
| chr14:65000596 | A | C | 1 | a0001c0001t0001g0184 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.145-3653A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65000596 | |||||||
| chr14:65000616 | C | T | 1 | a0001c0001t0002g0183 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.145-3633C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65000616 | |||||||
| chr14:65000807 | C | T | 2 | a0001c0001t0001g0271 a0001c0001t0002g0093 |
2 | HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.145-3442C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65000807 | |||||||
| chr14:65000815 | C | CA | 21 | a0001c0001t0001g0041 a0001c0001t0001g0075 a0001c0001t0001g0122 others(18): Show |
21 | HG00544.hp2 HG01081.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.145-3408dupA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 65000815 | ||||||
| chr14:65000815 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0002g0047 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.145-3421_145-3408d others(16): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 65000815 | ||||||
| chr14:65000815 | CA | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0064 a0001c0001t0001g0071 others(90): Show |
94 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.145-3408delA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 65000815 | ||||||
| chr14:65000815 | CAA | C | 13 | a0001c0001t0001g0073 a0001c0001t0001g0264 a0001c0001t0001g0265 others(10): Show |
13 | HG00140.hp1 HG01175.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.145-3409_145-3408d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 65000815 | ||||||
| chr14:65000815 | CAAA | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(5): Show |
8 | HG03831.hp2 HG03927.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.145-3410_145-3408d others(5): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 65000815 | ||||||
| chr14:65000815 | CAAAAAAA others(2): Show |
C | 25 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(22): Show |
26 | HG00140.hp2 HG01169.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.145-3416_145-3408d others(11): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 65000815 | ||||||
| chr14:65000831 | A | G | 1 | a0001c0001t0002g0182 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.145-3418A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65000831 | |||||||
| chr14:65000838 | A | AAAAAAAA others(17): Show |
1 | a0001c0001t0001g0236 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.145-3408_145-3407i others(26): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 65000838 | ||||||
| chr14:65000838 | A | AAAAAAAA others(16): Show |
1 | a0001c0001t0001g0263 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.145-3408_145-3407i others(25): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 65000838 | ||||||
| chr14:65000838 | A | AAAAAAAA others(15): Show |
4 | a0001c0001t0001g0237 a0001c0001t0001g0288 a0001c0001t0001g0290 others(1): Show |
4 | HG02738.hp1 HG03017.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.145-3408_145-3407i others(24): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 65000838 | ||||||
| chr14:65000838 | A | AAAAAAAA others(14): Show |
4 | a0001c0001t0001g0227 a0001c0001t0001g0238 a0001c0001t0001g0239 others(1): Show |
4 | HG02698.hp1 NA18953.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.145-3408_145-3407i others(23): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 65000838 | ||||||
| chr14:65000838 | A | AAAAAAAA others(13): Show |
17 | a0001c0001t0001g0083 a0001c0001t0001g0232 a0001c0001t0001g0233 others(14): Show |
17 | HG02027.hp2 HG02083.hp2 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.145-3408_145-3407i others(22): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 65000838 | ||||||
| chr14:65000838 | A | AAAAAAAA others(12): Show |
12 | a0001c0001t0001g0005 a0001c0001t0001g0084 a0001c0001t0001g0228 others(9): Show |
13 | HG01099.hp2 HG01243.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.145-3408_145-3407i others(21): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 65000838 | ||||||
| chr14:65000838 | A | AAAAAAAA others(11): Show |
1 | a0001c0001t0001g0261 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.145-3408_145-3407i others(20): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 65000838 | ||||||
| chr14:65000838 | A | AG | 5 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0229 others(2): Show |
5 | HG00642.hp1 HG01081.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.145-3411_145-3410i others(3): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65000838 | |||||||
| chr14:65000838 | A | G | 5 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 others(2): Show |
5 | HG00140.hp1 HG01175.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.145-3411A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65000838 | |||||||
| chr14:65000863 | G | A | 39 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(36): Show |
41 | HG00140.hp2 HG00735.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.145-3386G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65000863 | |||||||
| chr14:65000893 | C | T | 1 | a0001c0005t0002g0283 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145-3356C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65000893 | |||||||
| chr14:65001017 | T | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(5): Show |
8 | HG03831.hp2 HG03927.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.145-3232T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65001017 | |||||||
| chr14:65001156 | C | T | 39 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(36): Show |
41 | HG00140.hp2 HG00735.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.145-3093C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65001156 | |||||||
| chr14:65001226 | A | T | 1 | a0001c0001t0002g0335 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.145-3023A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65001226 | |||||||
| chr14:65001874 | C | T | 1 | a0001c0001t0002g0107 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.145-2375C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65001874 | |||||||
| chr14:65002010 | A | G | 2 | a0001c0001t0001g0219 a0001c0001t0001g0220 |
2 | NA19001.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.145-2239A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65002010 | |||||||
| chr14:65002062 | G | A | 5 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0349 others(2): Show |
5 | HG02074.hp2 HG02083.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.145-2187G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65002062 | |||||||
| chr14:65002296 | T | G | 5 | a0001c0001t0001g0345 a0001c0001t0001g0347 a0001c0001t0002g0341 others(2): Show |
5 | HG02258.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.145-1953T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65002296 | |||||||
| chr14:65002312 | A | G | 1 | a0001c0001t0002g0218 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.145-1937A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65002312 | |||||||
| chr14:65002335 | G | A | 11 | a0001c0001t0001g0022 a0001c0001t0001g0040 a0001c0001t0001g0041 others(8): Show |
12 | HG01106.hp2 HG01515.hp2 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.145-1914G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65002335 | |||||||
| chr14:65002344 | C | T | 19 | a0001c0001t0001g0002 a0001c0001t0001g0064 a0001c0001t0001g0073 others(16): Show |
20 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.145-1905C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65002344 | |||||||
| chr14:65002398 | C | G | 2 | a0001c0001t0002g0038 a0001c0001t0002g0196 |
2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.145-1851C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65002398 | |||||||
| chr14:65002414 | G | C | 4 | a0001c0001t0001g0071 a0001c0001t0002g0099 a0001c0001t0002g0101 others(1): Show |
4 | HG01109.hp1 HG01884.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.145-1835G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65002414 | |||||||
| chr14:65002473 | G | C | 1 | a0001c0001t0001g0048 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.145-1776G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65002473 | |||||||
| chr14:65002483 | C | T | 26 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(23): Show |
27 | HG00140.hp2 HG00735.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.145-1766C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65002483 | |||||||
| chr14:65002561 | A | G | 1 | a0001c0001t0002g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.145-1688A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65002561 | |||||||
| chr14:65002626 | TA | T | 37 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(34): Show |
39 | HG00140.hp2 HG00735.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.145-1614delA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 65002626 | ||||||
| chr14:65002693 | G | A | 1 | a0001c0001t0001g0309 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.145-1556G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65002693 | |||||||
| chr14:65002721 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0058 |
3 | HG02723.hp1 HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.145-1528G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65002721 | |||||||
| chr14:65002931 | A | G | 51 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0293 others(48): Show |
51 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.145-1318A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65002931 | |||||||
| chr14:65003212 | G | A | 8 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(5): Show |
8 | HG03831.hp2 HG03927.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.145-1037G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65003212 | |||||||
| chr14:65003431 | C | G | 1 | a0001c0001t0001g0008 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.145-818C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65003431 | |||||||
| chr14:65003478 | A | G | 1 | a0001c0001t0001g0217 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.145-771A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65003478 | |||||||
| chr14:65003549 | T | C | 4 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0267 others(1): Show |
4 | HG00733.hp1 HG01261.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.145-700T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65003549 | |||||||
| chr14:65003731 | A | G | 17 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0022 others(14): Show |
18 | HG01106.hp2 HG01515.hp2 HG01981.hp1 others(15): Show |
intron_variant | MODIFIER | c.145-518A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65003731 | |||||||
| chr14:65003928 | C | T | 19 | a0001c0001t0001g0002 a0001c0001t0001g0064 a0001c0001t0001g0073 others(16): Show |
20 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.145-321C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65003928 | |||||||
| chr14:65004053 | C | T | 2 | a0001c0001t0001g0271 a0001c0001t0002g0093 |
2 | HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.145-196C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65004053 | |||||||
| chr14:65004102 | C | G | 2 | a0001c0001t0002g0341 a0001c0001t0002g0348 |
2 | HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.145-147C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65004102 | |||||||
| chr14:65004111 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.145-138C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65004111 | |||||||
| chr14:65004113 | A | G | 149 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
153 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.145-136A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65004113 | |||||||
| chr14:65004115 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.145-134C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65004115 | |||||||
| chr14:65004162 | T | C | 1 | a0001c0001t0001g0338 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.145-87T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 1/11 | chr14 | 65004162 | |||||||
| chr14:65004468 | C | T | 25 | a0001c0001t0001g0033 a0001c0001t0001g0079 a0001c0001t0001g0091 others(22): Show |
25 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.209+155C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65004468 | |||||||
| chr14:65004533 | A | G | 4 | a0001c0001t0001g0347 a0001c0001t0002g0206 a0001c0001t0002g0207 others(1): Show |
4 | HG01433.hp2 HG02258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.209+220A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65004533 | |||||||
| chr14:65004654 | T | C | 1 | a0001c0001t0001g0338 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.209+341T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65004654 | |||||||
| chr14:65004693 | G | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0058 |
2 | HG02723.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.209+380G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65004693 | |||||||
| chr14:65004745 | C | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0057 |
2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.209+432C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65004745 | |||||||
| chr14:65004772 | C | T | 1 | a0001c0001t0001g0338 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.209+459C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65004772 | |||||||
| chr14:65004823 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.209+510C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65004823 | |||||||
| chr14:65005202 | G | A | 24 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(21): Show |
24 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.209+889G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65005202 | |||||||
| chr14:65005417 | A | G | 1 | a0001c0001t0002g0087 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.209+1104A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65005417 | |||||||
| chr14:65005443 | CCTTTCTT others(6): Show |
C | 1 | a0001c0004t0001g0103 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.209+1139_209+1151d others(15): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005443 | ||||||
| chr14:65005449 | T | TTTTC | 50 | a0001c0001t0001g0008 a0001c0001t0001g0045 a0001c0001t0001g0057 others(47): Show |
50 | HG00323.hp1 HG00438.hp1 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.209+1198_209+1201d others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005449 | ||||||
| chr14:65005449 | T | TTTTCTTT others(1): Show |
12 | a0001c0001t0001g0122 a0001c0001t0001g0138 a0001c0001t0001g0151 others(9): Show |
12 | HG00544.hp2 HG01071.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.209+1194_209+1201d others(10): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005449 | ||||||
| chr14:65005449 | T | TTTTCTTT others(5): Show |
5 | a0001c0001t0001g0020 a0001c0001t0001g0139 a0001c0001t0001g0303 others(2): Show |
5 | HG00642.hp2 HG02698.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.209+1190_209+1201d others(14): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005449 | ||||||
| chr14:65005449 | T | TTTTCTTT others(9): Show |
1 | a0001c0001t0001g0097 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.209+1186_209+1201d others(18): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005449 | ||||||
| chr14:65005449 | TTTTC | T | 45 | a0001c0001t0001g0026 a0001c0001t0001g0056 a0001c0001t0001g0058 others(42): Show |
45 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.209+1198_209+1201d others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005449 | ||||||
| chr14:65005449 | TTTTCTTT others(1): Show |
T | 32 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(29): Show |
32 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.209+1194_209+1201d others(10): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005449 | ||||||
| chr14:65005449 | TTTTCTTT others(5): Show |
T | 18 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0024 others(15): Show |
19 | HG00733.hp1 HG00735.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.209+1190_209+1201d others(14): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005449 | ||||||
| chr14:65005449 | TTTTCTTT others(9): Show |
T | 2 | a0001c0001t0001g0116 a0001c0001t0002g0183 |
2 | HG02630.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.209+1186_209+1201d others(18): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005449 | ||||||
| chr14:65005449 | TTTTCTTT others(13): Show |
T | 2 | a0001c0001t0001g0216 a0001c0001t0001g0338 |
2 | HG02257.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.209+1182_209+1201d others(22): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005449 | ||||||
| chr14:65005449 | TTTTCTTT others(21): Show |
T | 1 | a0001c0001t0001g0050 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.209+1174_209+1201d others(30): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005449 | ||||||
| chr14:65005453 | C | CT | 4 | a0001c0001t0001g0285 a0001c0001t0001g0298 a0001c0001t0002g0088 others(1): Show |
4 | HG02523.hp1 HG02615.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.209+1143dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005453 | ||||||
| chr14:65005462 | TTTCTTTC others(4): Show |
T | 1 | a0001c0005t0002g0283 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.209+1152_209+1162d others(13): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005462 | ||||||
| chr14:65005482 | TTTCTTTC others(4): Show |
T | 4 | a0001c0001t0001g0240 a0001c0001t0001g0252 a0001c0001t0001g0288 others(1): Show |
4 | NA18939.hp2 NA18981.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.209+1172_209+1182d others(13): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005482 | ||||||
| chr14:65005491 | TTCTTTCT others(15): Show |
T | 3 | a0001c0001t0001g0105 a0001c0001t0001g0317 a0001c0001t0001g0344 |
3 | HG00544.hp1 NA19068.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.209+1182_209+1203d others(24): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005491 | ||||||
| chr14:65005491 | TTCTTTCT others(17): Show |
T | 1 | a0001c0001t0002g0121 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.209+1182_209+1205d others(26): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005491 | ||||||
| chr14:65005495 | TTCTTTCT others(11): Show |
T | 13 | a0001c0001t0001g0041 a0001c0001t0001g0104 a0001c0001t0001g0131 others(10): Show |
13 | HG02074.hp2 HG02083.hp1 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.209+1186_209+1203d others(20): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005495 | ||||||
| chr14:65005495 | TTCTTTCT others(13): Show |
T | 2 | a0001c0001t0002g0096 a0001c0001t0002g0120 |
2 | NA18945.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.209+1186_209+1205d others(22): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005495 | ||||||
| chr14:65005499 | TTCTTTCT others(7): Show |
T | 13 | a0001c0001t0001g0040 a0001c0001t0001g0193 a0001c0001t0001g0195 others(10): Show |
13 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(10): Show |
intron_variant | MODIFIER | c.209+1190_209+1203d others(16): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005499 | ||||||
| chr14:65005499 | TTCTTTCT others(9): Show |
T | 1 | a0001c0001t0002g0095 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.209+1190_209+1205d others(18): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005499 | ||||||
| chr14:65005503 | TTCTTTCT others(3): Show |
T | 23 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0198 others(20): Show |
23 | HG00323.hp2 HG00609.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.209+1194_209+1203d others(12): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005503 | ||||||
| chr14:65005503 | TTCTTTCT others(5): Show |
T | 1 | a0001c0001t0002g0311 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.209+1194_209+1205d others(14): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005503 | ||||||
| chr14:65005507 | TTCTTTC | T | 21 | a0001c0001t0001g0002 a0001c0001t0001g0201 a0001c0001t0001g0202 others(18): Show |
21 | HG01071.hp1 HG01081.hp2 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.209+1198_209+1203d others(8): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005507 | ||||||
| chr14:65005511 | T | C | 4 | a0001c0001t0001g0073 a0001c0001t0002g0078 a0001c0001t0002g0205 others(1): Show |
4 | HG01884.hp2 HG03041.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.209+1198T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65005511 | |||||||
| chr14:65005513 | C | CTT | 12 | a0001c0001t0001g0071 a0001c0001t0001g0090 a0001c0001t0001g0272 others(9): Show |
12 | HG01884.hp1 HG01981.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.209+1201_209+1202i others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005513 | ||||||
| chr14:65005515 | C | T | 2 | a0001c0001t0002g0101 a0001c0001t0002g0196 |
2 | HG01891.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.209+1202C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65005515 | |||||||
| chr14:65005519 | CTCTT | C | 3 | a0001c0001t0002g0038 a0001c0001t0002g0129 a0001c0005t0002g0283 |
3 | HG02602.hp2 HG02738.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.209+1210_209+1213d others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005519 | ||||||
| chr14:65005521 | CTT | C | 19 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(16): Show |
20 | HG00621.hp1 HG01106.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.209+1210_209+1211d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65005521 | ||||||
| chr14:65005523 | T | C | 215 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(212): Show |
216 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.209+1210T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65005523 | |||||||
| chr14:65005528 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.209+1215T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65005528 | |||||||
| chr14:65005639 | C | T | 3 | a0001c0001t0002g0078 a0001c0001t0002g0205 a0001c0001t0002g0222 |
3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.209+1326C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65005639 | |||||||
| chr14:65005756 | C | T | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0055 others(9): Show |
12 | HG02129.hp2 HG02723.hp1 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.209+1443C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65005756 | |||||||
| chr14:65005785 | A | T | 20 | a0001c0001t0002g0038 a0001c0001t0002g0053 a0001c0001t0002g0059 others(17): Show |
20 | HG01891.hp1 HG02280.hp2 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.209+1472A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65005785 | |||||||
| chr14:65005905 | C | T | 5 | a0001c0001t0001g0033 a0001c0001t0001g0045 a0001c0001t0001g0345 others(2): Show |
5 | HG01496.hp1 HG02258.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.209+1592C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65005905 | |||||||
| chr14:65005939 | C | T | 3 | a0001c0001t0002g0078 a0001c0001t0002g0205 a0001c0001t0002g0222 |
3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.209+1626C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65005939 | |||||||
| chr14:65006156 | C | CT | 207 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0016 others(204): Show |
209 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.209+1860dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65006156 | ||||||
| chr14:65006156 | C | CTT | 53 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0023 others(50): Show |
53 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.209+1859_209+1860d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65006156 | ||||||
| chr14:65006223 | G | A | 1 | a0003c0003t0001g0346 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.209+1910G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65006223 | |||||||
| chr14:65006369 | T | C | 1 | a0001c0001t0002g0006 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.209+2056T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65006369 | |||||||
| chr14:65006463 | C | G | 1 | a0001c0001t0001g0154 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.209+2150C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65006463 | |||||||
| chr14:65006478 | G | A | 240 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(237): Show |
243 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.209+2165G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65006478 | |||||||
| chr14:65006541 | G | C | 1 | a0004c0002t0002g0015 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.209+2228G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65006541 | |||||||
| chr14:65006575 | G | T | 1 | a0001c0001t0001g0174 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.209+2262G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65006575 | |||||||
| chr14:65006636 | G | T | 1 | a0001c0001t0002g0218 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.209+2323G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65006636 | |||||||
| chr14:65006639 | G | C | 20 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0197 others(17): Show |
20 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.209+2326G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65006639 | |||||||
| chr14:65006845 | A | T | 17 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(14): Show |
17 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.209+2532A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65006845 | |||||||
| chr14:65006921 | G | C | 4 | a0001c0001t0001g0064 a0001c0001t0001g0073 a0001c0001t0001g0077 others(1): Show |
4 | HG01884.hp2 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.209+2608G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65006921 | |||||||
| chr14:65006977 | T | A | 1 | a0001c0001t0001g0208 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.209+2664T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65006977 | |||||||
| chr14:65006978 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.209+2665T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65006978 | |||||||
| chr14:65007028 | A | G | 1 | a0001c0001t0002g0335 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.209+2715A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65007028 | |||||||
| chr14:65007157 | G | C | 239 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(236): Show |
242 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.209+2844G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65007157 | |||||||
| chr14:65007177 | A | C | 2 | a0001c0001t0001g0055 a0001c0001t0001g0057 |
2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.209+2864A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65007177 | |||||||
| chr14:65007338 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.209+3025A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65007338 | |||||||
| chr14:65007420 | G | C | 1 | a0001c0001t0002g0047 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.209+3107G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65007420 | |||||||
| chr14:65007456 | A | G | 1 | a0001c0001t0001g0338 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.209+3143A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65007456 | |||||||
| chr14:65007653 | G | C | 2 | a0001c0001t0002g0030 a0001c0001t0002g0031 |
2 | HG01243.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.209+3340G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65007653 | |||||||
| chr14:65007735 | C | T | 2 | a0001c0001t0001g0219 a0001c0001t0001g0220 |
2 | NA19001.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.209+3422C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65007735 | |||||||
| chr14:65007855 | A | G | 3 | a0001c0001t0002g0078 a0001c0001t0002g0205 a0001c0001t0002g0222 |
3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.209+3542A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65007855 | |||||||
| chr14:65007887 | T | C | 1 | a0001c0001t0002g0047 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.209+3574T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65007887 | |||||||
| chr14:65007905 | T | C | 2 | a0001c0001t0001g0055 a0001c0001t0001g0057 |
2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.209+3592T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65007905 | |||||||
| chr14:65008110 | C | T | 1 | a0001c0001t0002g0185 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.209+3797C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65008110 | |||||||
| chr14:65008180 | G | T | 6 | a0001c0001t0002g0062 a0001c0001t0002g0068 a0001c0001t0002g0069 others(3): Show |
6 | HG02280.hp2 HG02970.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.209+3867G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65008180 | |||||||
| chr14:65008292 | G | C | 73 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(70): Show |
74 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.209+3979G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65008292 | |||||||
| chr14:65008631 | T | G | 1 | a0001c0001t0001g0351 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.210-3686T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65008631 | |||||||
| chr14:65008649 | G | A | 3 | a0001c0001t0002g0078 a0001c0001t0002g0205 a0001c0001t0002g0222 |
3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.210-3668G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65008649 | |||||||
| chr14:65008670 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.210-3647A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65008670 | |||||||
| chr14:65008693 | A | G | 73 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(70): Show |
74 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.210-3624A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65008693 | |||||||
| chr14:65008822 | C | A | 236 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(233): Show |
239 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(236): Show |
intron_variant | MODIFIER | c.210-3495C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65008822 | |||||||
| chr14:65008990 | C | A | 17 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(14): Show |
17 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.210-3327C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65008990 | |||||||
| chr14:65009353 | C | CTGGCGCT | 3 | a0001c0001t0002g0078 a0001c0001t0002g0205 a0001c0001t0002g0222 |
3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.210-2963_210-2962i others(9): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65009353 | ||||||
| chr14:65009355 | A | C | 3 | a0001c0001t0002g0078 a0001c0001t0002g0205 a0001c0001t0002g0222 |
3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.210-2962A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65009355 | |||||||
| chr14:65009378 | C | G | 23 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0197 others(20): Show |
23 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.210-2939C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65009378 | |||||||
| chr14:65009411 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.210-2906C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65009411 | |||||||
| chr14:65009531 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0058 |
3 | HG02723.hp1 HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.210-2786C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65009531 | |||||||
| chr14:65009841 | C | A | 1 | a0001c0001t0001g0308 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.210-2476C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65009841 | |||||||
| chr14:65009857 | G | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0131 |
2 | NA18945.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.210-2460G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65009857 | |||||||
| chr14:65009893 | G | A | 20 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0197 others(17): Show |
20 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.210-2424G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65009893 | |||||||
| chr14:65009981 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.210-2336C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65009981 | |||||||
| chr14:65010160 | C | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0057 |
2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.210-2157C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65010160 | |||||||
| chr14:65010204 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.210-2113C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65010204 | |||||||
| chr14:65010268 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0058 |
3 | HG02723.hp1 HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.210-2049G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65010268 | |||||||
| chr14:65010277 | C | G | 20 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0197 others(17): Show |
20 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.210-2040C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65010277 | |||||||
| chr14:65010636 | C | T | 3 | a0001c0001t0002g0078 a0001c0001t0002g0205 a0001c0001t0002g0222 |
3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.210-1681C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65010636 | |||||||
| chr14:65010662 | C | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0058 |
3 | HG02723.hp1 HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.210-1655C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65010662 | |||||||
| chr14:65010672 | A | G | 22 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0038 others(19): Show |
22 | HG01243.hp1 HG01891.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.210-1645A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65010672 | |||||||
| chr14:65010681 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.210-1636A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65010681 | |||||||
| chr14:65010783 | C | T | 1 | a0001c0001t0001g0303 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.210-1534C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65010783 | |||||||
| chr14:65010807 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.210-1510C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65010807 | |||||||
| chr14:65010912 | T | G | 3 | a0001c0001t0002g0078 a0001c0001t0002g0205 a0001c0001t0002g0222 |
3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.210-1405T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65010912 | |||||||
| chr14:65010962 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.210-1355G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65010962 | |||||||
| chr14:65011018 | T | C | 3 | a0001c0001t0002g0078 a0001c0001t0002g0205 a0001c0001t0002g0222 |
3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.210-1299T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65011018 | |||||||
| chr14:65011024 | CCCTT | C | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(75): Show |
80 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.210-1292_210-1289d others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65011024 | |||||||
| chr14:65011193 | C | G | 20 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0197 others(17): Show |
20 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.210-1124C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65011193 | |||||||
| chr14:65011237 | G | A | 113 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(110): Show |
115 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.210-1080G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65011237 | |||||||
| chr14:65011312 | C | G | 1 | a0001c0001t0001g0321 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.210-1005C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65011312 | |||||||
| chr14:65011426 | C | G | 20 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0197 others(17): Show |
20 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.210-891C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65011426 | |||||||
| chr14:65011431 | G | GA | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0022 others(94): Show |
99 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.210-865dupA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65011431 | ||||||
| chr14:65011431 | G | GAA | 29 | a0001c0001t0001g0021 a0001c0001t0001g0272 a0001c0001t0001g0299 others(26): Show |
29 | HG00423.hp2 HG01243.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.210-866_210-865dup others(2): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65011431 | ||||||
| chr14:65011431 | GA | G | 23 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0057 others(20): Show |
23 | HG01099.hp1 HG01175.hp2 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.210-865delA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65011431 | ||||||
| chr14:65011431 | GAAAAAAA others(4): Show |
G | 1 | a0001c0001t0002g0190 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.210-875_210-865del others(11): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65011431 | ||||||
| chr14:65011453 | G | T | 1 | a0001c0001t0001g0040 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.210-864G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65011453 | |||||||
| chr14:65011457 | G | A | 3 | a0001c0001t0002g0078 a0001c0001t0002g0205 a0001c0001t0002g0222 |
3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.210-860G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65011457 | |||||||
| chr14:65011471 | A | C | 20 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0197 others(17): Show |
20 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.210-846A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65011471 | |||||||
| chr14:65011472 | C | T | 3 | a0001c0001t0002g0078 a0001c0001t0002g0205 a0001c0001t0002g0222 |
3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.210-845C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65011472 | |||||||
| chr14:65011637 | A | C | 5 | a0001c0001t0001g0033 a0001c0001t0001g0045 a0001c0001t0001g0345 others(2): Show |
5 | HG01496.hp1 HG02258.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.210-680A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65011637 | |||||||
| chr14:65011903 | C | T | 3 | a0001c0001t0002g0078 a0001c0001t0002g0205 a0001c0001t0002g0222 |
3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.210-414C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65011903 | |||||||
| chr14:65012059 | C | G | 2 | a0001c0001t0002g0152 a0001c0001t0002g0185 |
2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.210-258C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65012059 | |||||||
| chr14:65012065 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0058 |
3 | HG02723.hp1 HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.210-252C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65012065 | |||||||
| chr14:65012080 | G | A | 1 | a0001c0001t0002g0179 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.210-237G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65012080 | |||||||
| chr14:65012112 | A | T | 3 | a0001c0001t0001g0071 a0001c0001t0002g0099 a0001c0001t0002g0106 |
3 | HG01109.hp1 HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.210-205A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65012112 | |||||||
| chr14:65012205 | A | AG | 17 | a0001c0001t0002g0053 a0001c0001t0002g0059 a0001c0001t0002g0060 others(14): Show |
17 | HG02280.hp2 HG02572.hp2 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.210-107dupG | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 65012205 | ||||||
| chr14:65012212 | C | T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0002g0047 |
3 | HG01175.hp2 HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.210-105C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65012212 | |||||||
| chr14:65012230 | T | G | 54 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0023 others(51): Show |
54 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.210-87T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65012230 | |||||||
| chr14:65012247 | C | T | 1 | a0001c0001t0002g0080 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.210-70C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65012247 | |||||||
| chr14:65012248 | G | A | 6 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(3): Show |
6 | HG02129.hp2 HG02738.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.210-69G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65012248 | |||||||
| chr14:65012253 | C | G | 1 | a0001c0001t0001g0195 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.210-64C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65012253 | |||||||
| chr14:65012253 | C | T | 3 | a0001c0001t0002g0078 a0001c0001t0002g0205 a0001c0001t0002g0222 |
3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.210-64C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 2/11 | chr14 | 65012253 | |||||||
| chr14:65012395 | C | T | 1 | a0001c0001t0002g0011 | 1 | NA21309.hp1 | splice_region_variant&intron_variant | LOW | c.282+6C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65012395 | |||||||
| chr14:65012397 | C | A | 1 | a0001c0001t0002g0119 | 1 | HG03927.hp1 | splice_region_variant&intron_variant | LOW | c.282+8C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65012397 | |||||||
| chr14:65012583 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.282+194C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65012583 | |||||||
| chr14:65012628 | A | T | 3 | a0001c0001t0002g0078 a0001c0001t0002g0205 a0001c0001t0002g0222 |
3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.282+239A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65012628 | |||||||
| chr14:65012642 | A | G | 3 | a0001c0001t0002g0078 a0001c0001t0002g0205 a0001c0001t0002g0222 |
3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.282+253A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65012642 | |||||||
| chr14:65012733 | C | G | 2 | a0001c0001t0001g0029 a0001c0001t0001g0085 |
2 | HG00140.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.282+344C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65012733 | |||||||
| chr14:65012742 | C | T | 2 | a0001c0001t0002g0152 a0001c0001t0002g0185 |
2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.282+353C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65012742 | |||||||
| chr14:65012950 | G | A | 3 | a0001c0001t0002g0078 a0001c0001t0002g0205 a0001c0001t0002g0222 |
3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.282+561G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65012950 | |||||||
| chr14:65012953 | T | C | 1 | a0001c0001t0002g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.282+564T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65012953 | |||||||
| chr14:65013001 | C | T | 3 | a0001c0001t0002g0078 a0001c0001t0002g0205 a0001c0001t0002g0222 |
3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.282+612C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65013001 | |||||||
| chr14:65013248 | T | C | 3 | a0001c0001t0002g0078 a0001c0001t0002g0205 a0001c0001t0002g0222 |
3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.282+859T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65013248 | |||||||
| chr14:65013325 | C | CT | 237 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(234): Show |
240 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(237): Show |
intron_variant | MODIFIER | c.282+948dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 65013325 | ||||||
| chr14:65013365 | G | A | 4 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0243 others(1): Show |
4 | NA18970.hp2 NA18990.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+976G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65013365 | |||||||
| chr14:65013422 | T | C | 7 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(4): Show |
7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.282+1033T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65013422 | |||||||
| chr14:65013441 | C | T | 5 | a0001c0001t0001g0033 a0001c0001t0001g0045 a0001c0001t0001g0345 others(2): Show |
5 | HG01496.hp1 HG02258.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.282+1052C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65013441 | |||||||
| chr14:65013479 | C | T | 114 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(111): Show |
116 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.282+1090C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65013479 | |||||||
| chr14:65013490 | T | C | 109 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(106): Show |
110 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.282+1101T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65013490 | |||||||
| chr14:65013562 | A | G | 1 | a0001c0001t0001g0345 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.282+1173A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65013562 | |||||||
| chr14:65013580 | C | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0057 |
2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.282+1191C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65013580 | |||||||
| chr14:65013587 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.282+1198T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65013587 | |||||||
| chr14:65013737 | A | G | 3 | a0001c0001t0002g0078 a0001c0001t0002g0205 a0001c0001t0002g0222 |
3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.282+1348A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65013737 | |||||||
| chr14:65013768 | G | A | 19 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(16): Show |
19 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.282+1379G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65013768 | |||||||
| chr14:65013840 | G | A | 2 | a0001c0001t0001g0132 a0001c0001t0001g0192 |
2 | HG03942.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.282+1451G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65013840 | |||||||
| chr14:65013877 | A | G | 243 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(240): Show |
246 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.282+1488A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65013877 | |||||||
| chr14:65014089 | G | T | 1 | a0001c0001t0001g0177 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.283-1536G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65014089 | |||||||
| chr14:65014122 | C | CT | 7 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(4): Show |
7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.283-1502dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 65014122 | ||||||
| chr14:65014300 | G | A | 17 | a0001c0001t0002g0053 a0001c0001t0002g0059 a0001c0001t0002g0060 others(14): Show |
17 | HG02280.hp2 HG02572.hp2 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.283-1325G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65014300 | |||||||
| chr14:65014494 | C | T | 72 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(69): Show |
73 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.283-1131C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65014494 | |||||||
| chr14:65014675 | A | G | 1 | a0001c0001t0002g0080 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.283-950A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65014675 | |||||||
| chr14:65014691 | G | C | 3 | a0001c0001t0002g0078 a0001c0001t0002g0205 a0001c0001t0002g0222 |
3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.283-934G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65014691 | |||||||
| chr14:65014738 | C | T | 4 | a0001c0001t0001g0161 a0001c0001t0002g0125 a0001c0001t0002g0180 others(1): Show |
4 | NA18956.hp1 NA18990.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-887C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65014738 | |||||||
| chr14:65014826 | G | A | 51 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0023 others(48): Show |
51 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.283-799G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65014826 | |||||||
| chr14:65014933 | A | G | 3 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0269 |
3 | HG00735.hp1 HG01109.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.283-692A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65014933 | |||||||
| chr14:65014992 | C | G | 73 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(70): Show |
74 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.283-633C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65014992 | |||||||
| chr14:65015108 | CT | C | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(105): Show |
110 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.283-505delT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 65015108 | ||||||
| chr14:65015141 | C | T | 2 | a0001c0001t0002g0088 a0001c0001t0002g0089 |
2 | HG02615.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.283-484C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65015141 | |||||||
| chr14:65015303 | A | G | 3 | a0001c0001t0002g0078 a0001c0001t0002g0205 a0001c0001t0002g0222 |
3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.283-322A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65015303 | |||||||
| chr14:65015392 | C | T | 3 | a0001c0001t0002g0078 a0001c0001t0002g0205 a0001c0001t0002g0222 |
3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.283-233C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65015392 | |||||||
| chr14:65015410 | C | CT | 9 | a0001c0001t0001g0151 a0001c0001t0001g0159 a0001c0001t0001g0266 others(6): Show |
9 | HG01243.hp1 HG01255.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.283-191dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 65015410 | ||||||
| chr14:65015410 | C | CTT | 19 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(16): Show |
19 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.283-192_283-191dup others(2): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 65015410 | ||||||
| chr14:65015410 | CT | C | 98 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(95): Show |
99 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.283-191delT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 65015410 | ||||||
| chr14:65015410 | CTT | C | 10 | a0001c0001t0001g0254 a0001c0001t0001g0285 a0001c0001t0002g0063 others(7): Show |
10 | HG01943.hp1 HG02129.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.283-192_283-191del others(2): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 65015410 | ||||||
| chr14:65015410 | CTTTTTTT others(7): Show |
C | 3 | a0001c0001t0002g0078 a0001c0001t0002g0205 a0001c0001t0002g0222 |
3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.283-204_283-191del others(14): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 65015410 | ||||||
| chr14:65015417 | T | C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0058 |
3 | HG02723.hp1 HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.283-208T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 3/11 | chr14 | 65015417 | |||||||
| chr14:65016006 | C | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0058 |
3 | HG02723.hp1 HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.374+290C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65016006 | |||||||
| chr14:65016018 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.374+302A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65016018 | |||||||
| chr14:65016155 | C | G | 7 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(4): Show |
7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.374+439C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65016155 | |||||||
| chr14:65016203 | C | G | 1 | a0001c0001t0001g0260 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.374+487C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65016203 | |||||||
| chr14:65016461 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0058 |
3 | HG02723.hp1 HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.374+745C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65016461 | |||||||
| chr14:65016494 | T | G | 7 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(4): Show |
7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.374+778T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65016494 | |||||||
| chr14:65016570 | C | T | 7 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(4): Show |
7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.374+854C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65016570 | |||||||
| chr14:65016577 | GC | G | 7 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(4): Show |
7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.374+863delC | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65016577 | ||||||
| chr14:65016712 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.374+996G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65016712 | |||||||
| chr14:65016724 | A | G | 1 | a0004c0002t0002g0015 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.374+1008A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65016724 | |||||||
| chr14:65016764 | C | T | 83 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(80): Show |
85 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.374+1048C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65016764 | |||||||
| chr14:65016837 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.374+1121C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65016837 | |||||||
| chr14:65016920 | G | GT | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(186): Show |
192 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.374+1224dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65016920 | ||||||
| chr14:65016920 | G | GTT | 16 | a0001c0001t0001g0071 a0001c0001t0001g0090 a0001c0001t0001g0220 others(13): Show |
16 | HG00423.hp2 HG01109.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.374+1223_374+1224d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65016920 | ||||||
| chr14:65016920 | G | GTTTTT | 11 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(8): Show |
11 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.374+1220_374+1224d others(7): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65016920 | ||||||
| chr14:65016920 | G | GTTTTTT | 6 | a0001c0001t0001g0028 a0001c0001t0001g0048 a0001c0001t0001g0049 others(3): Show |
6 | HG01192.hp1 HG01358.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.374+1219_374+1224d others(8): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65016920 | ||||||
| chr14:65016920 | GT | G | 11 | a0001c0001t0001g0167 a0001c0001t0001g0312 a0001c0001t0001g0314 others(8): Show |
11 | HG00621.hp1 HG02965.hp1 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.374+1224delT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65016920 | ||||||
| chr14:65017002 | T | A | 7 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(4): Show |
7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.374+1286T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65017002 | |||||||
| chr14:65017083 | T | C | 349 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(346): Show |
355 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(352): Show |
intron_variant | MODIFIER | c.374+1367T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65017083 | |||||||
| chr14:65017084 | G | A | 1 | a0001c0001t0002g0051 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.374+1368G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65017084 | |||||||
| chr14:65017088 | A | C | 1 | a0001c0001t0002g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.374+1372A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65017088 | |||||||
| chr14:65017139 | T | G | 1 | a0001c0001t0001g0023 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.374+1423T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65017139 | |||||||
| chr14:65017169 | T | C | 243 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(240): Show |
246 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.374+1453T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65017169 | |||||||
| chr14:65017286 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.374+1570C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65017286 | |||||||
| chr14:65017449 | G | T | 21 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0116 others(18): Show |
21 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.374+1733G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65017449 | |||||||
| chr14:65017508 | T | C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0090 |
4 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.374+1792T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65017508 | |||||||
| chr14:65017680 | T | C | 7 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(4): Show |
7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.374+1964T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65017680 | |||||||
| chr14:65017706 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.374+1990A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65017706 | |||||||
| chr14:65017736 | A | G | 74 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(71): Show |
75 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.374+2020A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65017736 | |||||||
| chr14:65017757 | A | G | 21 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0116 others(18): Show |
21 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.374+2041A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65017757 | |||||||
| chr14:65017928 | C | T | 3 | a0001c0001t0002g0078 a0001c0001t0002g0205 a0001c0001t0002g0222 |
3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.374+2212C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65017928 | |||||||
| chr14:65018000 | A | T | 1 | a0001c0001t0001g0254 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.374+2284A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65018000 | |||||||
| chr14:65018084 | G | A | 1 | a0001c0001t0002g0307 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.374+2368G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65018084 | |||||||
| chr14:65018107 | C | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0057 |
2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.374+2391C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65018107 | |||||||
| chr14:65018109 | C | T | 1 | a0001c0001t0001g0002 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.374+2393C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65018109 | |||||||
| chr14:65018180 | A | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0090 |
4 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.374+2464A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65018180 | |||||||
| chr14:65018242 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.374+2526G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65018242 | |||||||
| chr14:65018369 | A | G | 21 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0116 others(18): Show |
21 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.374+2653A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65018369 | |||||||
| chr14:65018422 | C | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0057 |
2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.374+2706C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65018422 | |||||||
| chr14:65018718 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.374+3002G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65018718 | |||||||
| chr14:65018739 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.374+3023G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65018739 | |||||||
| chr14:65018809 | T | TA | 119 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(116): Show |
120 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.374+3112dupA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65018809 | ||||||
| chr14:65018809 | T | TAA | 11 | a0001c0001t0001g0054 a0001c0001t0001g0083 a0001c0001t0001g0230 others(8): Show |
11 | HG01106.hp1 HG02027.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.374+3111_374+3112d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65018809 | ||||||
| chr14:65018809 | TAA | T | 19 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0116 others(16): Show |
19 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.374+3111_374+3112d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65018809 | ||||||
| chr14:65018809 | TAAAA | T | 7 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(4): Show |
7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.374+3109_374+3112d others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65018809 | ||||||
| chr14:65018829 | G | T | 1 | a0001c0001t0001g0198 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.374+3113G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65018829 | |||||||
| chr14:65018843 | G | T | 1 | a0001c0001t0002g0199 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.374+3127G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65018843 | |||||||
| chr14:65018862 | G | C | 2 | a0001c0001t0002g0341 a0001c0001t0002g0348 |
2 | HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.374+3146G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65018862 | |||||||
| chr14:65018881 | T | C | 32 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0055 others(29): Show |
32 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.374+3165T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65018881 | |||||||
| chr14:65018900 | C | T | 2 | a0001c0001t0002g0030 a0001c0001t0002g0031 |
2 | HG01243.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.374+3184C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65018900 | |||||||
| chr14:65018923 | C | T | 1 | a0001c0001t0002g0119 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.374+3207C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65018923 | |||||||
| chr14:65019087 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.374+3371C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65019087 | |||||||
| chr14:65019097 | C | T | 70 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0040 others(67): Show |
71 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.374+3381C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65019097 | |||||||
| chr14:65019129 | C | T | 7 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(4): Show |
7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.374+3413C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65019129 | |||||||
| chr14:65019236 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0090 |
4 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.374+3520C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65019236 | |||||||
| chr14:65019262 | G | A | 1 | a0001c0001t0002g0093 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.374+3546G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65019262 | |||||||
| chr14:65019312 | C | A | 109 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(106): Show |
111 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.374+3596C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65019312 | |||||||
| chr14:65019503 | A | G | 5 | a0001c0001t0001g0033 a0001c0001t0001g0045 a0001c0001t0001g0345 others(2): Show |
5 | HG01496.hp1 HG02258.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.374+3787A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65019503 | |||||||
| chr14:65019508 | A | AT | 238 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(235): Show |
241 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.374+3800dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65019508 | ||||||
| chr14:65019572 | A | T | 1 | a0001c0001t0001g0337 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.374+3856A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65019572 | |||||||
| chr14:65019630 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.374+3914G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65019630 | |||||||
| chr14:65019737 | A | G | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG01081.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.374+4021A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65019737 | |||||||
| chr14:65019758 | G | A | 7 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(4): Show |
7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.374+4042G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65019758 | |||||||
| chr14:65019792 | G | A | 7 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(4): Show |
7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.374+4076G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65019792 | |||||||
| chr14:65019869 | A | G | 7 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(4): Show |
7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.374+4153A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65019869 | |||||||
| chr14:65019959 | G | A | 1 | a0001c0004t0001g0103 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.374+4243G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65019959 | |||||||
| chr14:65019981 | A | G | 18 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(15): Show |
18 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.374+4265A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65019981 | |||||||
| chr14:65019989 | T | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0057 |
2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.374+4273T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65019989 | |||||||
| chr14:65020072 | C | T | 1 | a0001c0001t0001g0322 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.374+4356C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65020072 | |||||||
| chr14:65020138 | G | A | 7 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(4): Show |
7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.374+4422G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65020138 | |||||||
| chr14:65020221 | G | A | 7 | a0001c0001t0001g0058 a0001c0001t0001g0064 a0001c0001t0001g0073 others(4): Show |
7 | HG01243.hp2 HG01884.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.374+4505G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65020221 | |||||||
| chr14:65020330 | C | T | 1 | a0001c0001t0002g0341 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.374+4614C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65020330 | |||||||
| chr14:65020434 | CCT | C | 5 | a0001c0001t0002g0032 a0001c0001t0002g0034 a0001c0001t0002g0039 others(2): Show |
5 | HG01074.hp2 HG01192.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.374+4721_374+4722d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65020434 | ||||||
| chr14:65020456 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.374+4740C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65020456 | |||||||
| chr14:65020472 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.374+4756C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65020472 | |||||||
| chr14:65020654 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.374+4938G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65020654 | |||||||
| chr14:65020733 | C | CT | 29 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(26): Show |
29 | HG00140.hp2 HG00323.hp1 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.374+5033dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65020733 | ||||||
| chr14:65020733 | C | CTT | 79 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(76): Show |
80 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.374+5032_374+5033d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65020733 | ||||||
| chr14:65020976 | T | C | 100 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(97): Show |
101 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.374+5260T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65020976 | |||||||
| chr14:65021019 | C | T | 21 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0116 others(18): Show |
21 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.374+5303C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65021019 | |||||||
| chr14:65021037 | C | T | 21 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0116 others(18): Show |
21 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.374+5321C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65021037 | |||||||
| chr14:65021078 | T | C | 243 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(240): Show |
246 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.374+5362T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65021078 | |||||||
| chr14:65021113 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.374+5397T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65021113 | |||||||
| chr14:65021479 | A | G | 1 | a0001c0001t0002g0031 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.374+5763A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65021479 | |||||||
| chr14:65021739 | G | A | 1 | a0001c0001t0001g0349 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.375-5714G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65021739 | |||||||
| chr14:65021742 | T | C | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0045 others(23): Show |
26 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.375-5711T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65021742 | |||||||
| chr14:65021749 | G | A | 3 | a0001c0001t0002g0078 a0001c0001t0002g0205 a0001c0001t0002g0222 |
3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.375-5704G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65021749 | |||||||
| chr14:65021873 | T | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0337 |
2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.375-5580T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65021873 | |||||||
| chr14:65021889 | G | A | 1 | a0001c0001t0002g0047 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.375-5564G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65021889 | |||||||
| chr14:65021921 | T | C | 1 | a0001c0001t0001g0338 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.375-5532T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65021921 | |||||||
| chr14:65021937 | C | T | 19 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(16): Show |
19 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.375-5516C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65021937 | |||||||
| chr14:65021942 | G | A | 1 | a0001c0001t0001g0338 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.375-5511G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65021942 | |||||||
| chr14:65022000 | A | G | 1 | a0001c0001t0002g0094 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.375-5453A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65022000 | |||||||
| chr14:65022055 | A | T | 1 | a0001c0001t0002g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.375-5398A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65022055 | |||||||
| chr14:65022116 | C | T | 1 | a0001c0001t0002g0291 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.375-5337C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65022116 | |||||||
| chr14:65022206 | C | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0055 others(2): Show |
5 | HG01175.hp2 HG02723.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.375-5247C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65022206 | |||||||
| chr14:65022232 | G | A | 2 | a0001c0001t0001g0091 a0001c0001t0001g0216 |
2 | HG00673.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.375-5221G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65022232 | |||||||
| chr14:65022284 | G | GT | 100 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(97): Show |
102 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.375-5156dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65022284 | ||||||
| chr14:65022284 | G | T | 1 | a0001c0001t0001g0290 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.375-5169G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65022284 | |||||||
| chr14:65022284 | GT | G | 31 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0055 others(28): Show |
32 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.375-5156delT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65022284 | ||||||
| chr14:65022284 | GTT | G | 7 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(4): Show |
7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.375-5157_375-5156d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65022284 | ||||||
| chr14:65022349 | G | C | 1 | a0001c0001t0002g0183 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.375-5104G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65022349 | |||||||
| chr14:65022647 | A | C | 1 | a0001c0001t0002g0047 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.375-4806A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65022647 | |||||||
| chr14:65022674 | T | TA | 7 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(4): Show |
7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.375-4766dupA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65022674 | ||||||
| chr14:65022675 | A | T | 1 | a0001c0001t0002g0006 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.375-4778A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65022675 | |||||||
| chr14:65022940 | G | C | 1 | a0001c0001t0001g0138 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.375-4513G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65022940 | |||||||
| chr14:65023001 | T | C | 4 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0230 others(1): Show |
4 | HG00642.hp1 HG01081.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.375-4452T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65023001 | |||||||
| chr14:65023169 | C | T | 18 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(15): Show |
18 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.375-4284C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65023169 | |||||||
| chr14:65023300 | C | G | 74 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(71): Show |
75 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.375-4153C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65023300 | |||||||
| chr14:65023347 | C | T | 7 | a0001c0001t0002g0062 a0001c0001t0002g0067 a0001c0001t0002g0068 others(4): Show |
7 | HG02280.hp2 HG02970.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.375-4106C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65023347 | |||||||
| chr14:65023435 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.375-4018G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65023435 | |||||||
| chr14:65023478 | A | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0057 |
2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.375-3975A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65023478 | |||||||
| chr14:65023590 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0272 |
2 | HG01515.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.375-3863G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65023590 | |||||||
| chr14:65023860 | G | A | 21 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0116 others(18): Show |
21 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.375-3593G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65023860 | |||||||
| chr14:65024009 | G | A | 10 | a0001c0001t0001g0022 a0001c0001t0001g0040 a0001c0001t0001g0041 others(7): Show |
10 | HG01106.hp2 HG01515.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.375-3444G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65024009 | |||||||
| chr14:65024103 | T | TA | 19 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(16): Show |
19 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.375-3335dupA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65024103 | ||||||
| chr14:65024162 | G | A | 1 | a0001c0001t0001g0331 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.375-3291G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65024162 | |||||||
| chr14:65024230 | T | C | 73 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(70): Show |
74 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.375-3223T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65024230 | |||||||
| chr14:65024240 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.375-3213G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65024240 | |||||||
| chr14:65024328 | A | AT | 76 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(73): Show |
77 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.375-3118dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65024328 | ||||||
| chr14:65024328 | AT | A | 7 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(4): Show |
7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.375-3118delT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 65024328 | ||||||
| chr14:65024537 | A | G | 246 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(243): Show |
250 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(247): Show |
intron_variant | MODIFIER | c.375-2916A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65024537 | |||||||
| chr14:65024565 | A | G | 83 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(80): Show |
85 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.375-2888A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65024565 | |||||||
| chr14:65024574 | G | A | 20 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(17): Show |
20 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.375-2879G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65024574 | |||||||
| chr14:65024594 | T | G | 73 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0040 others(70): Show |
74 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.375-2859T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65024594 | |||||||
| chr14:65024768 | C | G | 19 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(16): Show |
19 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.375-2685C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65024768 | |||||||
| chr14:65024791 | T | C | 2 | a0001c0001t0001g0055 a0001c0001t0001g0057 |
2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.375-2662T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65024791 | |||||||
| chr14:65024908 | T | C | 1 | a0004c0002t0002g0015 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.375-2545T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65024908 | |||||||
| chr14:65024929 | G | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG03490.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.375-2524G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65024929 | |||||||
| chr14:65025022 | A | G | 1 | a0001c0001t0001g0255 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.375-2431A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65025022 | |||||||
| chr14:65025035 | A | G | 3 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0234 |
3 | HG02615.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.375-2418A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65025035 | |||||||
| chr14:65025086 | C | T | 21 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0116 others(18): Show |
21 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.375-2367C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65025086 | |||||||
| chr14:65025197 | G | C | 6 | a0001c0001t0002g0166 a0001c0001t0002g0182 a0001c0001t0002g0190 others(3): Show |
6 | HG02165.hp2 NA18950.hp1 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.375-2256G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65025197 | |||||||
| chr14:65025226 | A | G | 1 | a0001c0001t0001g0334 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.375-2227A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65025226 | |||||||
| chr14:65025484 | C | A | 1 | a0001c0001t0002g0123 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.375-1969C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65025484 | |||||||
| chr14:65025636 | G | A | 2 | a0001c0001t0002g0030 a0001c0001t0002g0031 |
2 | HG01243.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.375-1817G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65025636 | |||||||
| chr14:65025982 | T | C | 33 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0055 others(30): Show |
33 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.375-1471T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65025982 | |||||||
| chr14:65026238 | A | G | 1 | a0001c0001t0002g0078 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.375-1215A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026238 | |||||||
| chr14:65026273 | G | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0057 |
2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.375-1180G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026273 | |||||||
| chr14:65026408 | T | C | 1 | a0001c0001t0002g0235 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.375-1045T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026408 | |||||||
| chr14:65026420 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.375-1033G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026420 | |||||||
| chr14:65026429 | T | G | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | NA18984.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.375-1024T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026429 | |||||||
| chr14:65026462 | G | A | 1 | a0001c0001t0002g0047 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.375-991G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026462 | |||||||
| chr14:65026522 | G | A | 1 | a0001c0001t0002g0336 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.375-931G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026522 | |||||||
| chr14:65026568 | T | G | 1 | a0001c0001t0001g0091 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.375-885T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026568 | |||||||
| chr14:65026608 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.375-845C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026608 | |||||||
| chr14:65026617 | G | T | 6 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(3): Show |
6 | HG02129.hp2 HG02738.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.375-836G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026617 | |||||||
| chr14:65026618 | C | G | 1 | a0001c0001t0001g0347 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.375-835C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026618 | |||||||
| chr14:65026646 | G | C | 1 | a0001c0001t0001g0040 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.375-807G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026646 | |||||||
| chr14:65026696 | A | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0057 |
2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.375-757A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026696 | |||||||
| chr14:65026726 | A | G | 3 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0234 |
3 | HG02615.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.375-727A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026726 | |||||||
| chr14:65026735 | G | A | 18 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(15): Show |
18 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.375-718G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026735 | |||||||
| chr14:65026873 | C | A | 6 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(3): Show |
6 | HG02129.hp2 HG02738.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.375-580C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026873 | |||||||
| chr14:65026881 | C | A | 6 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(3): Show |
6 | HG02129.hp2 HG02738.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.375-572C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65026881 | |||||||
| chr14:65027205 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.375-248T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65027205 | |||||||
| chr14:65027231 | G | A | 1 | a0001c0001t0001g0312 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.375-222G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65027231 | |||||||
| chr14:65027416 | C | G | 1 | a0001c0001t0001g0144 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.375-37C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 4/11 | chr14 | 65027416 | |||||||
| chr14:65027856 | AGGAACAT others(4): Show |
A | 1 | a0001c0001t0002g0166 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.605+78_605+88delAA others(9): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 65027856 | ||||||
| chr14:65028059 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.605+278A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65028059 | |||||||
| chr14:65028060 | T | A | 1 | a0001c0001t0001g0269 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.605+279T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65028060 | |||||||
| chr14:65028179 | T | C | 1 | a0001c0001t0001g0321 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.605+398T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65028179 | |||||||
| chr14:65028236 | G | A | 1 | a0001c0001t0005g0043 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.605+455G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65028236 | |||||||
| chr14:65028278 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.605+497C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65028278 | |||||||
| chr14:65028611 | C | T | 2 | a0001c0001t0003g0042 a0001c0001t0003g0044 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.605+830C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65028611 | |||||||
| chr14:65028907 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.605+1126A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65028907 | |||||||
| chr14:65028908 | CTAAGAT | C | 3 | a0001c0001t0002g0078 a0001c0001t0002g0205 a0001c0001t0002g0222 |
3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.605+1130_605+1135d others(8): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 65028908 | ||||||
| chr14:65029092 | C | T | 1 | a0001c0001t0002g0291 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.605+1311C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65029092 | |||||||
| chr14:65029098 | A | G | 262 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(259): Show |
266 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.605+1317A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65029098 | |||||||
| chr14:65029255 | A | AC | 4 | a0001c0001t0001g0259 a0001c0001t0001g0306 a0001c0001t0001g0351 others(1): Show |
4 | HG01891.hp1 HG01934.hp2 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.605+1478dupC | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 65029255 | ||||||
| chr14:65029266 | A | G | 7 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(4): Show |
7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.605+1485A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65029266 | |||||||
| chr14:65029523 | A | G | 1 | a0001c0001t0002g0189 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.605+1742A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65029523 | |||||||
| chr14:65029570 | A | G | 1 | a0001c0001t0001g0331 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.605+1789A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65029570 | |||||||
| chr14:65029648 | G | T | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | HG01433.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.605+1867G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65029648 | |||||||
| chr14:65029730 | A | C | 4 | a0001c0001t0001g0276 a0001c0001t0002g0037 a0001c0001t0002g0111 others(1): Show |
4 | NA18942.hp2 NA18955.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.605+1949A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65029730 | |||||||
| chr14:65030084 | C | G | 7 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(4): Show |
7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.605+2303C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65030084 | |||||||
| chr14:65030091 | C | G | 1 | a0001c0001t0002g0335 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.605+2310C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65030091 | |||||||
| chr14:65030145 | G | A | 20 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0197 others(17): Show |
20 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.605+2364G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65030145 | |||||||
| chr14:65030207 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.606-2403G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65030207 | |||||||
| chr14:65030279 | A | C | 1 | a0001c0001t0002g0182 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.606-2331A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65030279 | |||||||
| chr14:65030492 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.606-2118A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65030492 | |||||||
| chr14:65030598 | C | T | 1 | a0004c0002t0002g0015 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.606-2012C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65030598 | |||||||
| chr14:65030722 | A | G | 7 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(4): Show |
7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.606-1888A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65030722 | |||||||
| chr14:65030747 | A | G | 7 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(4): Show |
7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.606-1863A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65030747 | |||||||
| chr14:65030793 | C | G | 1 | a0001c0001t0001g0313 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.606-1817C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65030793 | |||||||
| chr14:65030806 | C | A | 167 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(164): Show |
169 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.606-1804C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65030806 | |||||||
| chr14:65030829 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.606-1781A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65030829 | |||||||
| chr14:65030955 | G | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.606-1655G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65030955 | |||||||
| chr14:65031004 | C | T | 11 | a0001c0001t0001g0022 a0001c0001t0001g0040 a0001c0001t0001g0041 others(8): Show |
11 | HG01106.hp2 HG01515.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.606-1606C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65031004 | |||||||
| chr14:65031467 | G | A | 6 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0230 others(3): Show |
6 | HG00642.hp1 HG01081.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.606-1143G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65031467 | |||||||
| chr14:65031638 | A | T | 1 | a0001c0001t0002g0093 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.606-972A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65031638 | |||||||
| chr14:65031695 | T | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
168 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.606-915T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65031695 | |||||||
| chr14:65031696 | G | T | 20 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(17): Show |
20 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.606-914G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65031696 | |||||||
| chr14:65031775 | G | A | 1 | a0001c0001t0001g0295 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.606-835G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65031775 | |||||||
| chr14:65031778 | A | G | 21 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0116 others(18): Show |
21 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.606-832A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65031778 | |||||||
| chr14:65031794 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.606-816G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65031794 | |||||||
| chr14:65031900 | G | A | 1 | a0001c0001t0002g0335 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.606-710G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65031900 | |||||||
| chr14:65031979 | C | CGT | 74 | a0001c0001t0001g0005 a0001c0001t0001g0045 a0001c0001t0001g0046 others(71): Show |
76 | HG00140.hp1 HG00597.hp1 HG01071.hp1 others(73): Show |
intron_variant | MODIFIER | c.606-592_606-591dup others(2): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 65031979 | ||||||
| chr14:65031979 | C | CGTGT | 16 | a0001c0001t0001g0082 a0001c0001t0001g0113 a0001c0001t0001g0114 others(13): Show |
16 | HG00609.hp1 HG00642.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.606-594_606-591dup others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 65031979 | ||||||
| chr14:65031979 | C | CGTGTGT | 8 | a0001c0001t0001g0020 a0001c0001t0001g0064 a0001c0001t0001g0073 others(5): Show |
8 | HG00408.hp2 HG00642.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.606-596_606-591dup others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 65031979 | ||||||
| chr14:65031979 | C | CGTGTGTG others(1): Show |
3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0174 |
3 | HG02056.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.606-598_606-591dup others(8): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 65031979 | ||||||
| chr14:65031979 | C | CGTGTGTG others(3): Show |
1 | a0001c0001t0001g0278 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.606-600_606-591dup others(10): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 65031979 | ||||||
| chr14:65031979 | C | CGTGTGTG others(5): Show |
1 | a0001c0001t0002g0335 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.606-602_606-591dup others(12): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 65031979 | ||||||
| chr14:65031979 | C | CGTGTGTG others(13): Show |
1 | a0001c0001t0002g0222 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.606-610_606-591dup others(20): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 65031979 | ||||||
| chr14:65031979 | C | CGTGTGTG others(15): Show |
1 | a0001c0001t0002g0205 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.606-612_606-591dup others(22): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 65031979 | ||||||
| chr14:65031979 | C | CGTGTGTG others(17): Show |
1 | a0001c0001t0002g0078 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.606-614_606-591dup others(24): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 65031979 | ||||||
| chr14:65031979 | C | CGTGTGTG others(29): Show |
1 | a0001c0001t0002g0047 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.606-626_606-591dup others(36): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 65031979 | ||||||
| chr14:65031979 | CGT | C | 51 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0033 others(48): Show |
53 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.606-592_606-591del others(2): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 65031979 | ||||||
| chr14:65031979 | CGTGTGT | C | 27 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(24): Show |
27 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.606-596_606-591del others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 65031979 | ||||||
| chr14:65031979 | CGTGTGTG others(7): Show |
C | 1 | a0001c0001t0001g0109 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.606-604_606-591del others(14): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 65031979 | ||||||
| chr14:65032307 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.606-303C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65032307 | |||||||
| chr14:65032499 | A | G | 8 | a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0067 others(5): Show |
8 | HG02280.hp2 HG02970.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.606-111A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65032499 | |||||||
| chr14:65032573 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.606-37G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 6/11 | chr14 | 65032573 | |||||||
| chr14:65032730 | G | A | 1 | a0001c0001t0001g0313 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.692+34G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65032730 | |||||||
| chr14:65032732 | G | A | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
122 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.692+36G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65032732 | |||||||
| chr14:65032736 | A | G | 1 | a0001c0001t0002g0335 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.692+40A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65032736 | |||||||
| chr14:65032745 | C | T | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
122 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.692+49C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65032745 | |||||||
| chr14:65032859 | C | A | 1 | a0001c0001t0001g0262 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.692+163C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65032859 | |||||||
| chr14:65032910 | T | TA | 76 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(73): Show |
77 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.692+220dupA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65032910 | ||||||
| chr14:65033000 | C | T | 5 | a0001c0001t0002g0108 a0001c0001t0002g0130 a0001c0001t0002g0135 others(2): Show |
5 | HG00733.hp2 HG01099.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.692+304C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65033000 | |||||||
| chr14:65033038 | C | T | 10 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0236 others(7): Show |
10 | HG00140.hp1 HG01123.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.692+342C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65033038 | |||||||
| chr14:65033191 | T | G | 246 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(243): Show |
250 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(247): Show |
intron_variant | MODIFIER | c.692+495T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65033191 | |||||||
| chr14:65033358 | G | A | 3 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0235 |
3 | HG02145.hp2 HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.692+662G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65033358 | |||||||
| chr14:65033431 | G | A | 69 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0040 others(66): Show |
70 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.692+735G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65033431 | |||||||
| chr14:65033454 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.692+758A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65033454 | |||||||
| chr14:65033679 | C | A | 246 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(243): Show |
250 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(247): Show |
intron_variant | MODIFIER | c.692+983C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65033679 | |||||||
| chr14:65033745 | T | A | 22 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0116 others(19): Show |
22 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.692+1049T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65033745 | |||||||
| chr14:65033750 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.692+1054G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65033750 | |||||||
| chr14:65033754 | A | G | 1 | a0001c0001t0002g0234 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.692+1058A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65033754 | |||||||
| chr14:65033788 | C | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0132 |
2 | HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.692+1092C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65033788 | |||||||
| chr14:65033887 | A | C | 2 | a0001c0001t0001g0055 a0001c0001t0001g0057 |
2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.692+1191A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65033887 | |||||||
| chr14:65034017 | A | G | 263 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(260): Show |
268 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.692+1321A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65034017 | |||||||
| chr14:65034311 | C | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0055 others(2): Show |
5 | HG01175.hp2 HG02723.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.692+1615C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65034311 | |||||||
| chr14:65034353 | T | G | 1 | a0001c0001t0001g0316 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.692+1657T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65034353 | |||||||
| chr14:65034462 | TTGGCAA | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0002g0047 |
3 | HG01175.hp2 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.692+1770_692+1775d others(8): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65034462 | ||||||
| chr14:65034811 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.692+2115C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65034811 | |||||||
| chr14:65035222 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.692+2526G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65035222 | |||||||
| chr14:65035283 | A | G | 1 | a0001c0001t0001g0338 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.692+2587A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65035283 | |||||||
| chr14:65035284 | G | C | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(105): Show |
110 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.692+2588G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65035284 | |||||||
| chr14:65035294 | G | A | 18 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(15): Show |
18 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.692+2598G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65035294 | |||||||
| chr14:65035363 | C | T | 4 | a0001c0001t0001g0002 a0001c0001t0001g0345 a0001c0001t0001g0347 others(1): Show |
5 | HG02258.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.692+2667C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65035363 | |||||||
| chr14:65035375 | G | A | 22 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0116 others(19): Show |
22 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.692+2679G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65035375 | |||||||
| chr14:65035402 | G | C | 17 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(14): Show |
17 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.692+2706G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65035402 | |||||||
| chr14:65035521 | G | A | 262 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(259): Show |
267 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.692+2825G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65035521 | |||||||
| chr14:65035530 | TTCTC | T | 3 | a0001c0001t0002g0078 a0001c0001t0002g0205 a0001c0001t0002g0222 |
3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.692+2838_692+2841d others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65035530 | ||||||
| chr14:65035553 | C | A | 245 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(242): Show |
249 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.692+2857C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65035553 | |||||||
| chr14:65035634 | A | G | 6 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(3): Show |
6 | HG02129.hp2 HG02738.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.692+2938A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65035634 | |||||||
| chr14:65035667 | C | G | 6 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(3): Show |
6 | HG02129.hp2 HG02738.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.692+2971C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65035667 | |||||||
| chr14:65035713 | T | A | 1 | a0001c0001t0002g0335 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.692+3017T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65035713 | |||||||
| chr14:65035856 | A | G | 1 | a0001c0001t0001g0097 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.692+3160A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65035856 | |||||||
| chr14:65036196 | T | C | 2 | a0001c0001t0001g0305 a0001c0001t0001g0342 |
2 | HG00423.hp2 HG00438.hp2 |
intron_variant | MODIFIER | c.692+3500T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65036196 | |||||||
| chr14:65036211 | G | A | 1 | a0001c0001t0001g0297 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.692+3515G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65036211 | |||||||
| chr14:65036243 | T | A | 11 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(8): Show |
11 | HG01981.hp2 HG02129.hp2 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.692+3547T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65036243 | |||||||
| chr14:65036429 | G | T | 43 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0116 others(40): Show |
43 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.692+3733G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65036429 | |||||||
| chr14:65036590 | C | T | 2 | a0001c0001t0001g0240 a0001c0001t0001g0288 |
2 | NA19067.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.692+3894C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65036590 | |||||||
| chr14:65036607 | G | A | 8 | a0001c0001t0001g0161 a0001c0001t0002g0124 a0001c0001t0002g0125 others(5): Show |
8 | HG01981.hp2 NA18956.hp1 NA18975.hp1 others(5): Show |
intron_variant | MODIFIER | c.692+3911G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65036607 | |||||||
| chr14:65036687 | C | T | 4 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0345 others(1): Show |
5 | HG01496.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.692+3991C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65036687 | |||||||
| chr14:65036699 | ATTC | A | 10 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0236 others(7): Show |
10 | HG00140.hp1 HG01123.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.692+4006_692+4008d others(5): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65036699 | ||||||
| chr14:65036754 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | NA18954.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.693-4036C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65036754 | |||||||
| chr14:65036755 | G | A | 76 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(73): Show |
77 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.693-4035G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65036755 | |||||||
| chr14:65037077 | C | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0090 others(1): Show |
5 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.693-3713C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037077 | |||||||
| chr14:65037261 | G | A | 26 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0038 others(23): Show |
26 | HG01243.hp1 HG01891.hp1 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.693-3529G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037261 | |||||||
| chr14:65037287 | AG | A | 3 | a0001c0001t0001g0071 a0001c0001t0002g0099 a0001c0001t0002g0106 |
3 | HG01109.hp1 HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.693-3502delG | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037287 | |||||||
| chr14:65037346 | G | A | 2 | a0001c0001t0002g0078 a0001c0001t0002g0205 |
2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.693-3444G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037346 | |||||||
| chr14:65037395 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.693-3395G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037395 | |||||||
| chr14:65037402 | C | CT | 11 | a0001c0001t0001g0046 a0001c0001t0001g0147 a0001c0001t0001g0195 others(8): Show |
11 | HG01515.hp2 HG02280.hp2 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.693-3388_693-3387i others(3): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | C | CTT | 9 | a0001c0001t0001g0022 a0001c0001t0001g0272 a0001c0001t0002g0053 others(6): Show |
9 | HG01106.hp2 HG01109.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.693-3388_693-3387i others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | C | CTTCTTTT others(1): Show |
5 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0026 others(2): Show |
5 | HG00735.hp2 HG01169.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.693-3388_693-3387i others(10): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | C | CTTCTTTT others(3): Show |
2 | a0001c0001t0001g0027 a0001c0001t0002g0014 |
2 | HG02148.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.693-3388_693-3387i others(12): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | C | CTTCTTTT others(4): Show |
1 | a0001c0001t0001g0085 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.693-3388_693-3387i others(13): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | C | CTTCTTTT others(5): Show |
1 | a0001c0001t0001g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.693-3388_693-3387i others(14): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | C | CTTCTTTT others(9): Show |
1 | a0001c0001t0002g0035 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.693-3388_693-3387i others(18): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | C | CTTCTTTT others(20): Show |
1 | a0001c0001t0001g0050 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.693-3388_693-3387i others(29): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | C | CTTCTTTT others(26): Show |
1 | a0001c0001t0001g0292 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.693-3388_693-3387i others(35): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | C | CTTT | 3 | a0001c0001t0001g0040 a0001c0001t0001g0293 a0001c0001t0002g0160 |
3 | HG02630.hp2 HG03654.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.693-3388_693-3387i others(5): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | C | CTTTTT | 3 | a0001c0001t0001g0299 a0001c0001t0002g0060 a0001c0001t0002g0102 |
3 | HG03098.hp2 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.693-3388_693-3387i others(7): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | C | CTTTTTTT others(7): Show |
3 | a0001c0001t0002g0063 a0001c0001t0002g0067 a0001c0001t0002g0107 |
3 | HG03195.hp2 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.693-3388_693-3387i others(16): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | C | CTTTTTTT others(10): Show |
1 | a0001c0001t0002g0291 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.693-3388_693-3387i others(19): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0001g0298 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.693-3388_693-3387i others(21): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | C | CTTTTTTT others(13): Show |
1 | a0001c0001t0002g0069 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.693-3388_693-3387i others(22): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | CCT | C | 5 | a0001c0001t0001g0134 a0001c0001t0001g0188 a0001c0001t0002g0123 others(2): Show |
5 | HG00438.hp1 HG01361.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.693-3387_693-3386d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | CCTT | C | 20 | a0001c0001t0001g0074 a0001c0001t0001g0133 a0001c0001t0001g0149 others(17): Show |
21 | HG00735.hp1 HG01123.hp2 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.693-3387_693-3385d others(5): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | CCTTT | C | 50 | a0001c0001t0001g0020 a0001c0001t0001g0075 a0001c0001t0001g0097 others(47): Show |
50 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.693-3387_693-3384d others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | CCTTTT | C | 43 | a0001c0001t0001g0036 a0001c0001t0001g0109 a0001c0001t0001g0110 others(40): Show |
43 | HG00323.hp1 HG00733.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.693-3387_693-3383d others(7): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | CCTTTTT | C | 36 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(33): Show |
37 | HG00609.hp1 HG01081.hp1 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.693-3387_693-3382d others(8): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | CCTTTTTT | C | 17 | a0001c0001t0001g0058 a0001c0001t0001g0082 a0001c0001t0001g0126 others(14): Show |
17 | HG00140.hp1 HG00642.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.693-3387_693-3381d others(9): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | CCTTTTTT others(1): Show |
C | 10 | a0001c0001t0001g0029 a0001c0001t0001g0049 a0001c0001t0001g0064 others(7): Show |
10 | HG00140.hp2 HG01074.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.693-3387_693-3380d others(10): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | CCTTTTTT others(3): Show |
C | 1 | a0001c0001t0002g0205 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.693-3387_693-3378d others(12): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | CCTTTTTT others(4): Show |
C | 4 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0030 others(1): Show |
4 | HG01081.hp2 HG01175.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.693-3387_693-3377d others(13): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | CCTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0008 a0001c0001t0002g0031 a0001c0001t0002g0194 |
3 | HG01243.hp1 HG01361.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.693-3387_693-3376d others(14): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | CCTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0007 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.693-3387_693-3375d others(15): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | CCTTTTTT others(7): Show |
C | 3 | a0001c0001t0002g0089 a0001c0001t0002g0234 a0004c0002t0002g0015 |
3 | HG02615.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.693-3387_693-3374d others(16): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | CCTTTTTT others(8): Show |
C | 28 | a0001c0001t0001g0003 a0001c0001t0001g0090 a0001c0001t0001g0198 others(25): Show |
29 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.693-3387_693-3373d others(17): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | CCTTTTTT others(9): Show |
C | 35 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0076 others(32): Show |
36 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.693-3387_693-3372d others(18): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | CCTTTTTT others(10): Show |
C | 3 | a0001c0001t0001g0055 a0001c0001t0002g0039 a0001c0001t0002g0341 |
3 | HG03453.hp1 HG03927.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.693-3387_693-3371d others(19): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | CCTTTTTT others(11): Show |
C | 1 | a0001c0001t0001g0057 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.693-3387_693-3370d others(20): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | CCTTTTTT others(12): Show |
C | 2 | a0001c0001t0001g0322 a0001c0001t0002g0006 |
3 | HG02015.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.693-3387_693-3369d others(21): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | CCTTTTTT others(13): Show |
C | 3 | a0001c0001t0001g0045 a0001c0001t0001g0131 a0001c0001t0002g0080 |
3 | HG02970.hp1 HG04204.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.693-3387_693-3368d others(22): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | CCTTTTTT others(14): Show |
C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0209 others(3): Show |
7 | HG01496.hp1 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.693-3387_693-3367d others(23): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | CCTTTTTT others(15): Show |
C | 23 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0116 others(20): Show |
23 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.693-3387_693-3366d others(24): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | CCTTTTTT others(16): Show |
C | 2 | a0001c0001t0001g0136 a0001c0001t0002g0335 |
2 | HG06807.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.693-3387_693-3365d others(25): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037402 | CCTTTTTT others(18): Show |
C | 1 | a0001c0001t0005g0043 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.693-3387_693-3363d others(27): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037402 | |||||||
| chr14:65037403 | C | T | 52 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(49): Show |
52 | HG00735.hp2 HG01106.hp2 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.693-3387C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037403 | |||||||
| chr14:65037410 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.693-3380T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037410 | |||||||
| chr14:65037413 | T | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0049 |
2 | HG00140.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.693-3377T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037413 | |||||||
| chr14:65037417 | T | C | 1 | a0001c0001t0002g0194 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.693-3373T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037417 | |||||||
| chr14:65037606 | G | A | 6 | a0001c0001t0002g0166 a0001c0001t0002g0182 a0001c0001t0002g0190 others(3): Show |
6 | HG02165.hp2 NA18950.hp1 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.693-3184G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037606 | |||||||
| chr14:65037676 | C | T | 26 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0116 others(23): Show |
26 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.693-3114C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037676 | |||||||
| chr14:65037677 | G | A | 7 | a0001c0001t0001g0201 a0001c0001t0002g0095 a0001c0001t0002g0096 others(4): Show |
7 | HG01943.hp2 HG02129.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.693-3113G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037677 | |||||||
| chr14:65037704 | T | C | 1 | a0001c0001t0001g0002 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.693-3086T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037704 | |||||||
| chr14:65037726 | C | CTTAT | 10 | a0001c0001t0001g0164 a0001c0001t0001g0233 a0001c0001t0001g0240 others(7): Show |
10 | HG01891.hp2 HG02622.hp2 NA18949.hp2 others(7): Show |
intron_variant | MODIFIER | c.693-3050_693-3047d others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037726 | ||||||
| chr14:65037726 | CTTATTTA others(8): Show |
C | 1 | a0001c0001t0001g0184 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.693-3046_693-3032d others(17): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037726 | ||||||
| chr14:65037726 | CTTATTTA others(12): Show |
C | 1 | a0001c0001t0001g0033 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.693-3046_693-3028d others(21): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037726 | ||||||
| chr14:65037730 | TTTATTTA others(4): Show |
T | 29 | a0001c0001t0001g0026 a0001c0001t0001g0055 a0001c0001t0001g0057 others(26): Show |
29 | HG00323.hp2 HG00544.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.693-3046_693-3036d others(13): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037730 | ||||||
| chr14:65037734 | TTTATTTA | T | 46 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0023 others(43): Show |
46 | HG00423.hp1 HG00673.hp1 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.693-3046_693-3040d others(9): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037734 | ||||||
| chr14:65037737 | ATTTATTA others(5): Show |
A | 1 | a0001c0001t0001g0331 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.693-3050_693-3039d others(14): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037737 | ||||||
| chr14:65037738 | TTTA | T | 47 | a0001c0001t0001g0025 a0001c0001t0001g0064 a0001c0001t0001g0073 others(44): Show |
48 | HG00323.hp1 HG00597.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.693-3046_693-3044d others(5): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037738 | ||||||
| chr14:65037741 | A | AT | 10 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0049 others(7): Show |
10 | HG00140.hp2 HG00733.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.693-3047dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037741 | ||||||
| chr14:65037741 | ATTAT | A | 21 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0021 others(18): Show |
22 | HG00642.hp2 HG01255.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.693-2995_693-2992d others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037741 | ||||||
| chr14:65037741 | ATTATTTA others(1): Show |
A | 19 | a0001c0001t0001g0149 a0001c0001t0001g0284 a0001c0001t0001g0294 others(16): Show |
19 | HG00597.hp2 HG01433.hp2 HG01928.hp1 others(16): Show |
intron_variant | MODIFIER | c.693-2999_693-2992d others(10): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037741 | ||||||
| chr14:65037741 | ATTATTTA others(5): Show |
A | 53 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0040 others(50): Show |
54 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.693-3003_693-2992d others(14): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037741 | ||||||
| chr14:65037741 | ATTATTTA others(9): Show |
A | 3 | a0001c0001t0001g0329 a0001c0001t0001g0334 a0001c0001t0002g0107 |
3 | HG02293.hp1 NA18522.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.693-3007_693-2992d others(18): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037741 | ||||||
| chr14:65037741 | ATTATTTA others(13): Show |
A | 8 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0300 others(5): Show |
8 | HG01891.hp1 HG02615.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.693-3011_693-2992d others(22): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037741 | ||||||
| chr14:65037744 | A | T | 108 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(105): Show |
111 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.693-3046A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037744 | |||||||
| chr14:65037745 | T | A | 101 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(98): Show |
104 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.693-3045T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037745 | |||||||
| chr14:65037745 | T | TTTA | 3 | a0001c0001t0001g0048 a0001c0001t0001g0267 a0001c0001t0001g0347 |
3 | HG00733.hp1 HG02300.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.693-3042_693-3040d others(5): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037745 | ||||||
| chr14:65037748 | A | T | 58 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(55): Show |
59 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.693-3042A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037748 | |||||||
| chr14:65037748 | AT | A | 45 | a0001c0001t0001g0029 a0001c0001t0001g0049 a0001c0001t0001g0050 others(42): Show |
46 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.693-3039delT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037748 | ||||||
| chr14:65037751 | TA | T | 6 | a0001c0001t0001g0083 a0001c0001t0001g0232 a0001c0001t0001g0248 others(3): Show |
6 | HG02055.hp2 HG02083.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.693-3038delA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037751 | |||||||
| chr14:65037752 | A | T | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | HG01433.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.693-3038A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037752 | |||||||
| chr14:65037752 | AT | A | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0025 others(18): Show |
21 | HG00733.hp2 HG01071.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.693-3035delT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037752 | ||||||
| chr14:65037756 | AT | A | 52 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(49): Show |
52 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.693-3031delT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037756 | ||||||
| chr14:65037760 | AT | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0184 a0001c0001t0002g0119 |
3 | HG01169.hp1 HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.693-3027delT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65037760 | ||||||
| chr14:65037863 | T | C | 2 | a0001c0001t0002g0030 a0001c0001t0002g0031 |
2 | HG01243.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.693-2927T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037863 | |||||||
| chr14:65037875 | G | C | 1 | a0001c0001t0002g0341 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.693-2915G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037875 | |||||||
| chr14:65037882 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0002g0047 |
3 | HG01175.hp2 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.693-2908C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037882 | |||||||
| chr14:65037883 | G | A | 15 | a0001c0001t0001g0076 a0001c0001t0001g0178 a0001c0001t0001g0301 others(12): Show |
15 | HG00323.hp2 HG00609.hp2 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.693-2907G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65037883 | |||||||
| chr14:65038055 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0002g0047 |
3 | HG01175.hp2 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.693-2735G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65038055 | |||||||
| chr14:65038186 | G | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0045 others(2): Show |
6 | HG01496.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.693-2604G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65038186 | |||||||
| chr14:65038192 | C | T | 1 | a0001c0001t0001g0350 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.693-2598C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65038192 | |||||||
| chr14:65038343 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.693-2447G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65038343 | |||||||
| chr14:65038359 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0054 others(1): Show |
4 | NA18964.hp1 NA18978.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.693-2431G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65038359 | |||||||
| chr14:65038501 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.693-2289C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65038501 | |||||||
| chr14:65038605 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.693-2185G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65038605 | |||||||
| chr14:65038761 | G | A | 1 | a0001c0001t0001g0255 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.693-2029G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65038761 | |||||||
| chr14:65038809 | T | C | 24 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0116 others(21): Show |
24 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.693-1981T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65038809 | |||||||
| chr14:65038927 | T | C | 18 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(15): Show |
18 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.693-1863T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65038927 | |||||||
| chr14:65038979 | C | G | 26 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0116 others(23): Show |
26 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.693-1811C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65038979 | |||||||
| chr14:65039115 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.693-1675G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65039115 | |||||||
| chr14:65039143 | G | A | 2 | a0001c0001t0001g0253 a0001c0001t0001g0261 |
2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.693-1647G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65039143 | |||||||
| chr14:65039211 | G | A | 4 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0243 others(1): Show |
4 | NA18970.hp2 NA18990.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.693-1579G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65039211 | |||||||
| chr14:65039310 | A | G | 2 | a0001c0001t0001g0074 a0001c0001t0002g0087 |
2 | HG03239.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.693-1480A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65039310 | |||||||
| chr14:65039336 | G | A | 84 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(81): Show |
86 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.693-1454G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65039336 | |||||||
| chr14:65039346 | T | A | 26 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0116 others(23): Show |
26 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.693-1444T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65039346 | |||||||
| chr14:65039352 | C | T | 18 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(15): Show |
18 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.693-1438C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65039352 | |||||||
| chr14:65039460 | G | A | 1 | a0001c0001t0002g0183 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.693-1330G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65039460 | |||||||
| chr14:65039603 | C | A | 1 | a0001c0001t0002g0006 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.693-1187C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65039603 | |||||||
| chr14:65039791 | T | A | 8 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(5): Show |
8 | HG00642.hp1 HG01081.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.693-999T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65039791 | |||||||
| chr14:65039931 | G | A | 17 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(14): Show |
17 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.693-859G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65039931 | |||||||
| chr14:65039999 | G | T | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | HG01433.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.693-791G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65039999 | |||||||
| chr14:65040011 | A | G | 18 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(15): Show |
18 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.693-779A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040011 | |||||||
| chr14:65040016 | C | G | 1 | a0001c0001t0002g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.693-774C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040016 | |||||||
| chr14:65040043 | G | A | 3 | a0001c0001t0002g0078 a0001c0001t0002g0205 a0001c0001t0002g0222 |
3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.693-747G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040043 | |||||||
| chr14:65040155 | C | T | 1 | a0001c0001t0004g0325 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.693-635C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040155 | |||||||
| chr14:65040208 | C | T | 18 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(15): Show |
18 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.693-582C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040208 | |||||||
| chr14:65040210 | A | G | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
122 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.693-580A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040210 | |||||||
| chr14:65040224 | T | G | 26 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0116 others(23): Show |
26 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.693-566T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040224 | |||||||
| chr14:65040247 | C | A | 26 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0116 others(23): Show |
26 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.693-543C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040247 | |||||||
| chr14:65040257 | A | ATGTATAT others(17): Show |
1 | a0001c0001t0002g0335 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.693-521_693-498dup others(24): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65040257 | ||||||
| chr14:65040257 | A | G | 56 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0023 others(53): Show |
56 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.693-533A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040257 | |||||||
| chr14:65040271 | ATATATAT others(5): Show |
A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0057 |
2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.693-511_693-500del others(12): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65040271 | ||||||
| chr14:65040283 | G | A | 3 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0004t0001g0103 |
3 | NA18979.hp2 NA18981.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.693-507G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040283 | |||||||
| chr14:65040283 | GTA | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0002g0047 |
3 | HG01175.hp2 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.693-495_693-494del others(2): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65040283 | ||||||
| chr14:65040285 | A | ATATATAT others(23): Show |
1 | a0001c0001t0001g0091 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.693-494_693-493ins others(30): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65040285 | ||||||
| chr14:65040285 | A | ATATATAT others(21): Show |
25 | a0001c0001t0001g0079 a0001c0001t0001g0116 a0001c0001t0001g0122 others(22): Show |
25 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.693-480_693-479ins others(28): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65040285 | ||||||
| chr14:65040285 | A | G | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | HG01433.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.693-505A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040285 | |||||||
| chr14:65040329 | A | G | 3 | a0001c0001t0001g0294 a0001c0001t0001g0332 a0001c0001t0001g0353 |
3 | HG00597.hp2 NA19001.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.693-461A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040329 | |||||||
| chr14:65040400 | T | A | 3 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0001c0001t0001g0293 |
3 | HG02683.hp1 HG03239.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.693-390T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040400 | |||||||
| chr14:65040416 | G | A | 7 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(4): Show |
7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.693-374G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040416 | |||||||
| chr14:65040483 | C | T | 21 | a0001c0001t0001g0005 a0001c0001t0001g0112 a0001c0001t0001g0113 others(18): Show |
22 | HG00408.hp2 HG00609.hp1 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.693-307C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040483 | |||||||
| chr14:65040525 | C | T | 1 | a0001c0001t0001g0316 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.693-265C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040525 | |||||||
| chr14:65040561 | C | T | 1 | a0001c0001t0002g0006 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.693-229C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040561 | |||||||
| chr14:65040604 | C | CT | 133 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0040 others(130): Show |
134 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.693-166dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65040604 | ||||||
| chr14:65040604 | C | CTT | 11 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(8): Show |
13 | HG01496.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.693-167_693-166dup others(2): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65040604 | ||||||
| chr14:65040604 | CT | C | 23 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0024 others(20): Show |
23 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.693-166delT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 65040604 | ||||||
| chr14:65040662 | T | C | 1 | a0001c0001t0001g0164 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.693-128T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 7/11 | chr14 | 65040662 | |||||||
| chr14:65040936 | C | T | 18 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(15): Show |
18 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.822+17C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65040936 | |||||||
| chr14:65040958 | G | C | 1 | a0004c0002t0002g0015 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.822+39G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65040958 | |||||||
| chr14:65040991 | G | C | 1 | a0001c0001t0001g0084 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.822+72G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65040991 | |||||||
| chr14:65041137 | C | T | 1 | a0001c0001t0002g0335 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.822+218C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65041137 | |||||||
| chr14:65041173 | A | G | 7 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(4): Show |
7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+254A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65041173 | |||||||
| chr14:65041202 | A | T | 1 | a0001c0001t0001g0027 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.822+283A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65041202 | |||||||
| chr14:65041414 | A | G | 1 | a0001c0001t0002g0093 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.822+495A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65041414 | |||||||
| chr14:65041489 | A | T | 1 | a0001c0001t0001g0117 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.822+570A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65041489 | |||||||
| chr14:65041640 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.822+721G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65041640 | |||||||
| chr14:65041871 | A | T | 1 | a0001c0001t0001g0033 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.822+952A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65041871 | |||||||
| chr14:65042268 | C | T | 351 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(348): Show |
357 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(354): Show |
intron_variant | MODIFIER | c.822+1349C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65042268 | |||||||
| chr14:65042351 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.822+1432C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65042351 | |||||||
| chr14:65042426 | G | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG01081.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.822+1507G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65042426 | |||||||
| chr14:65042621 | C | A | 1 | a0001c0001t0002g0335 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.823-1690C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65042621 | |||||||
| chr14:65042658 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.823-1653T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65042658 | |||||||
| chr14:65042828 | T | A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0345 others(1): Show |
5 | HG01496.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.823-1483T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65042828 | |||||||
| chr14:65042901 | A | G | 2 | a0001c0001t0001g0081 a0001c0001t0001g0082 |
2 | HG00642.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.823-1410A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65042901 | |||||||
| chr14:65043002 | T | C | 1 | a0001c0001t0001g0271 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.823-1309T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043002 | |||||||
| chr14:65043160 | C | T | 248 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(245): Show |
252 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.823-1151C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043160 | |||||||
| chr14:65043161 | G | A | 8 | a0001c0001t0001g0074 a0001c0001t0001g0164 a0001c0001t0001g0165 others(5): Show |
8 | HG03239.hp2 HG03831.hp1 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.823-1150G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043161 | |||||||
| chr14:65043307 | G | A | 17 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(14): Show |
17 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.823-1004G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043307 | |||||||
| chr14:65043354 | C | T | 1 | a0001c0001t0001g0342 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.823-957C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043354 | |||||||
| chr14:65043459 | C | G | 1 | a0001c0001t0002g0291 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.823-852C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043459 | |||||||
| chr14:65043618 | C | T | 25 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0122 others(22): Show |
25 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.823-693C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043618 | |||||||
| chr14:65043641 | T | C | 20 | a0001c0001t0002g0053 a0001c0001t0002g0059 a0001c0001t0002g0060 others(17): Show |
20 | HG02280.hp2 HG02572.hp2 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.823-670T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043641 | |||||||
| chr14:65043668 | A | G | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
253 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.823-643A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043668 | |||||||
| chr14:65043691 | G | A | 1 | a0004c0002t0002g0015 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.823-620G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043691 | |||||||
| chr14:65043715 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0002g0047 |
3 | HG01175.hp2 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.823-596G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043715 | |||||||
| chr14:65043779 | G | A | 1 | a0001c0001t0001g0323 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.823-532G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043779 | |||||||
| chr14:65043802 | C | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0090 |
4 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-509C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043802 | |||||||
| chr14:65043808 | G | A | 1 | a0001c0001t0002g0335 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.823-503G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043808 | |||||||
| chr14:65043815 | C | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0184 |
2 | HG03704.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.823-496C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043815 | |||||||
| chr14:65043823 | C | T | 1 | a0003c0003t0001g0346 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.823-488C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043823 | |||||||
| chr14:65043828 | C | CA | 42 | a0001c0001t0001g0020 a0001c0001t0001g0097 a0001c0001t0001g0109 others(39): Show |
42 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.823-451dupA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 65043828 | ||||||
| chr14:65043828 | C | CAA | 10 | a0001c0001t0001g0133 a0001c0001t0001g0167 a0001c0001t0001g0347 others(7): Show |
11 | HG02572.hp1 HG02622.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.823-452_823-451dup others(2): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 65043828 | ||||||
| chr14:65043828 | C | CAAA | 7 | a0001c0001t0001g0159 a0001c0001t0001g0281 a0001c0001t0002g0013 others(4): Show |
7 | HG01074.hp2 HG01192.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.823-453_823-451dup others(3): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 65043828 | ||||||
| chr14:65043828 | C | CAAAAAAA others(12): Show |
1 | a0001c0001t0001g0008 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.823-469_823-451dup others(19): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 65043828 | ||||||
| chr14:65043828 | CA | C | 10 | a0001c0001t0001g0033 a0001c0001t0001g0055 a0001c0001t0001g0057 others(7): Show |
10 | HG00323.hp1 HG01123.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.823-451delA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 65043828 | ||||||
| chr14:65043828 | CAA | C | 19 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0045 others(16): Show |
19 | HG01099.hp2 HG01243.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.823-452_823-451del others(2): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 65043828 | ||||||
| chr14:65043828 | CAAA | C | 54 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(51): Show |
55 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.823-453_823-451del others(3): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 65043828 | ||||||
| chr14:65043828 | CAAAAAAA | C | 7 | a0001c0001t0001g0079 a0001c0001t0002g0095 a0001c0001t0002g0096 others(4): Show |
7 | HG00621.hp2 HG02129.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.823-457_823-451del others(7): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 65043828 | ||||||
| chr14:65043828 | CAAAAAAA others(1): Show |
C | 24 | a0001c0001t0001g0091 a0001c0001t0001g0116 a0001c0001t0001g0122 others(21): Show |
24 | HG00423.hp1 HG00544.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.823-458_823-451del others(8): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 65043828 | ||||||
| chr14:65043828 | CAAAAAAA others(4): Show |
C | 11 | a0001c0001t0001g0027 a0001c0001t0001g0040 a0001c0001t0001g0071 others(8): Show |
11 | HG01123.hp1 HG01884.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.823-461_823-451del others(11): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 65043828 | ||||||
| chr14:65043828 | CAAAAAAA others(5): Show |
C | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(95): Show |
100 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.823-462_823-451del others(12): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 65043828 | ||||||
| chr14:65043828 | CAAAAAAA others(6): Show |
C | 3 | a0001c0001t0001g0204 a0001c0001t0002g0038 a0001c0001t0002g0101 |
3 | HG01169.hp2 HG02896.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.823-463_823-451del others(13): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 65043828 | ||||||
| chr14:65043828 | CAAAAAAA others(7): Show |
C | 17 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(14): Show |
17 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.823-464_823-451del others(14): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 65043828 | ||||||
| chr14:65043854 | A | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0057 |
2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.823-457A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043854 | |||||||
| chr14:65043860 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.823-451A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043860 | |||||||
| chr14:65043964 | T | G | 1 | a0001c0001t0001g0041 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.823-347T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65043964 | |||||||
| chr14:65044115 | T | C | 3 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0234 |
3 | HG02615.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.823-196T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65044115 | |||||||
| chr14:65044248 | T | C | 26 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0116 others(23): Show |
26 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.823-63T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65044248 | |||||||
| chr14:65044253 | C | T | 17 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(14): Show |
17 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.823-58C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 8/11 | chr14 | 65044253 | |||||||
| chr14:65044457 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0090 |
4 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.955+14G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65044457 | |||||||
| chr14:65044525 | T | C | 3 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0269 |
3 | HG00735.hp1 HG01109.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.955+82T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65044525 | |||||||
| chr14:65044700 | G | A | 6 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(3): Show |
6 | HG02129.hp2 HG02738.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.955+257G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65044700 | |||||||
| chr14:65044703 | G | T | 3 | a0001c0001t0001g0128 a0001c0001t0001g0237 a0001c0001t0001g0245 |
3 | HG01261.hp1 HG03017.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.955+260G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65044703 | |||||||
| chr14:65044711 | G | A | 26 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0116 others(23): Show |
26 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.955+268G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65044711 | |||||||
| chr14:65044726 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0002g0047 |
3 | HG01175.hp2 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.955+283G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65044726 | |||||||
| chr14:65045126 | TTCTC | T | 6 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(3): Show |
6 | HG02129.hp2 HG02738.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.955+689_955+692del others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 65045126 | ||||||
| chr14:65045180 | T | C | 1 | a0001c0001t0002g0348 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.955+737T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65045180 | |||||||
| chr14:65045329 | A | G | 6 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(3): Show |
6 | HG02129.hp2 HG02738.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.955+886A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65045329 | |||||||
| chr14:65045409 | G | A | 19 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0023 others(16): Show |
20 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.955+966G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65045409 | |||||||
| chr14:65045424 | C | T | 1 | a0001c0001t0001g0351 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.955+981C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65045424 | |||||||
| chr14:65045434 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.955+991G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65045434 | |||||||
| chr14:65045659 | G | A | 17 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(14): Show |
17 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.955+1216G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65045659 | |||||||
| chr14:65045711 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0002g0129 |
3 | HG02723.hp1 HG02738.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.955+1268C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65045711 | |||||||
| chr14:65045777 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0002g0047 |
3 | HG01175.hp2 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.955+1334C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65045777 | |||||||
| chr14:65045840 | G | A | 1 | a0001c0001t0002g0189 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.955+1397G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65045840 | |||||||
| chr14:65046031 | A | C | 1 | a0001c0001t0001g0287 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.955+1588A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65046031 | |||||||
| chr14:65046134 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0002g0047 |
3 | HG01175.hp2 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.955+1691G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65046134 | |||||||
| chr14:65046196 | G | A | 3 | a0001c0001t0002g0078 a0001c0001t0002g0205 a0001c0001t0002g0222 |
3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.955+1753G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65046196 | |||||||
| chr14:65046217 | C | G | 1 | a0001c0001t0001g0176 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.955+1774C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65046217 | |||||||
| chr14:65046219 | G | C | 1 | a0001c0001t0002g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.955+1776G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65046219 | |||||||
| chr14:65046470 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.955+2027G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65046470 | |||||||
| chr14:65046548 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.955+2105G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65046548 | |||||||
| chr14:65046748 | G | T | 1 | a0001c0001t0001g0240 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.955+2305G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65046748 | |||||||
| chr14:65046795 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.955+2352G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65046795 | |||||||
| chr14:65046852 | G | GCTT | 251 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(248): Show |
255 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(252): Show |
intron_variant | MODIFIER | c.955+2412_955+2414d others(5): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 65046852 | ||||||
| chr14:65047117 | T | C | 18 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(15): Show |
18 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.955+2674T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65047117 | |||||||
| chr14:65047378 | C | G | 1 | a0001c0001t0001g0298 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.955+2935C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65047378 | |||||||
| chr14:65047450 | A | C | 27 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0159 others(24): Show |
27 | HG00438.hp1 HG01981.hp2 HG02074.hp1 others(24): Show |
intron_variant | MODIFIER | c.955+3007A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65047450 | |||||||
| chr14:65047872 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.955+3429G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65047872 | |||||||
| chr14:65047978 | A | AT | 28 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0083 others(25): Show |
28 | HG00673.hp2 HG01243.hp1 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.955+3562dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 65047978 | ||||||
| chr14:65047978 | AT | A | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0020 others(198): Show |
205 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(202): Show |
intron_variant | MODIFIER | c.955+3562delT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 65047978 | ||||||
| chr14:65047978 | ATT | A | 13 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0057 others(10): Show |
14 | HG00323.hp1 HG00408.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.955+3561_955+3562d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 65047978 | ||||||
| chr14:65047978 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0331 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.955+3552_955+3562d others(13): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 65047978 | ||||||
| chr14:65048082 | A | G | 1 | a0001c0001t0001g0302 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.955+3639A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65048082 | |||||||
| chr14:65048127 | G | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0054 others(1): Show |
4 | NA18964.hp1 NA18978.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.955+3684G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65048127 | |||||||
| chr14:65048197 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.955+3754G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65048197 | |||||||
| chr14:65048325 | T | TA | 106 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(103): Show |
107 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.955+3895dupA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 65048325 | ||||||
| chr14:65048560 | G | A | 1 | a0001c0001t0002g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.955+4117G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65048560 | |||||||
| chr14:65048663 | G | A | 25 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0122 others(22): Show |
25 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.955+4220G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65048663 | |||||||
| chr14:65048678 | G | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0057 |
2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.955+4235G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65048678 | |||||||
| chr14:65048710 | C | G | 1 | a0001c0001t0001g0227 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.955+4267C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65048710 | |||||||
| chr14:65048865 | G | T | 1 | a0001c0001t0002g0013 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.956-4373G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65048865 | |||||||
| chr14:65048866 | C | G | 1 | a0001c0001t0002g0013 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.956-4372C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65048866 | |||||||
| chr14:65049040 | T | C | 2 | a0001c0001t0001g0055 a0001c0001t0001g0057 |
2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.956-4198T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65049040 | |||||||
| chr14:65049059 | G | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0057 |
2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.956-4179G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65049059 | |||||||
| chr14:65049084 | G | A | 6 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(3): Show |
6 | HG02129.hp2 HG02738.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.956-4154G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65049084 | |||||||
| chr14:65049125 | TA | T | 243 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(240): Show |
246 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.956-4097delA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 65049125 | ||||||
| chr14:65049125 | TAA | T | 6 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0045 others(3): Show |
7 | HG01496.hp1 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.956-4098_956-4097d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 65049125 | ||||||
| chr14:65049146 | T | G | 1 | a0001c0001t0002g0160 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.956-4092T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65049146 | |||||||
| chr14:65049207 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.956-4031A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65049207 | |||||||
| chr14:65049411 | C | T | 1 | a0001c0001t0002g0335 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.956-3827C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65049411 | |||||||
| chr14:65049462 | T | G | 3 | a0001c0001t0002g0078 a0001c0001t0002g0205 a0001c0001t0002g0222 |
3 | HG03041.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.956-3776T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65049462 | |||||||
| chr14:65049911 | A | C | 1 | a0001c0001t0001g0026 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.956-3327A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65049911 | |||||||
| chr14:65050081 | A | G | 1 | a0001c0001t0001g0347 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.956-3157A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65050081 | |||||||
| chr14:65050148 | T | G | 1 | a0001c0001t0001g0020 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.956-3090T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65050148 | |||||||
| chr14:65050318 | G | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0057 |
2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.956-2920G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65050318 | |||||||
| chr14:65050388 | C | T | 79 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(76): Show |
80 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.956-2850C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65050388 | |||||||
| chr14:65050497 | A | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0045 others(2): Show |
6 | HG01496.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.956-2741A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65050497 | |||||||
| chr14:65050570 | G | A | 1 | a0001c0001t0002g0222 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.956-2668G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65050570 | |||||||
| chr14:65050711 | G | A | 17 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(14): Show |
17 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.956-2527G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65050711 | |||||||
| chr14:65050824 | C | T | 24 | a0001c0001t0002g0038 a0001c0001t0002g0053 a0001c0001t0002g0059 others(21): Show |
24 | HG01891.hp1 HG02280.hp2 HG02572.hp2 others(21): Show |
intron_variant | MODIFIER | c.956-2414C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65050824 | |||||||
| chr14:65051007 | T | C | 1 | a0001c0001t0002g0053 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.956-2231T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65051007 | |||||||
| chr14:65051015 | C | CAGGTGAG others(5): Show |
1 | a0001c0001t0001g0238 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.956-2222_956-2211d others(14): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 65051015 | ||||||
| chr14:65051113 | T | C | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG01081.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.956-2125T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65051113 | |||||||
| chr14:65051165 | C | T | 7 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(4): Show |
7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.956-2073C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65051165 | |||||||
| chr14:65051338 | G | A | 1 | a0001c0001t0001g0271 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.956-1900G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65051338 | |||||||
| chr14:65051559 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.956-1679C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65051559 | |||||||
| chr14:65051567 | T | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0090 |
4 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.956-1671T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65051567 | |||||||
| chr14:65051588 | G | A | 1 | a0001c0001t0002g0273 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.956-1650G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65051588 | |||||||
| chr14:65051797 | A | AT | 21 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(18): Show |
21 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.956-1426dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 65051797 | ||||||
| chr14:65051857 | T | A | 3 | a0001c0001t0002g0038 a0001c0001t0002g0101 a0001c0001t0002g0196 |
3 | HG01891.hp1 HG02896.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.956-1381T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65051857 | |||||||
| chr14:65051887 | T | C | 3 | a0001c0001t0001g0002 a0001c0001t0001g0345 a0001c0001t0001g0347 |
4 | HG02647.hp2 HG02717.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.956-1351T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65051887 | |||||||
| chr14:65051895 | C | T | 1 | a0001c0001t0001g0257 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.956-1343C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65051895 | |||||||
| chr14:65051940 | G | A | 5 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0129 others(2): Show |
5 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.956-1298G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65051940 | |||||||
| chr14:65051949 | C | T | 1 | a0001c0001t0002g0070 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.956-1289C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65051949 | |||||||
| chr14:65051986 | A | G | 4 | a0001c0001t0001g0002 a0001c0001t0001g0260 a0001c0001t0001g0345 others(1): Show |
5 | HG02647.hp2 HG02717.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.956-1252A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65051986 | |||||||
| chr14:65052075 | A | G | 2 | a0001c0001t0002g0235 a0001c0001t0002g0335 |
2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.956-1163A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65052075 | |||||||
| chr14:65052077 | A | G | 2 | a0001c0001t0002g0235 a0001c0001t0002g0335 |
2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.956-1161A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65052077 | |||||||
| chr14:65052325 | T | G | 1 | a0001c0001t0002g0123 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.956-913T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65052325 | |||||||
| chr14:65052350 | G | T | 1 | a0001c0001t0002g0080 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.956-888G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65052350 | |||||||
| chr14:65052384 | T | A | 12 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0055 others(9): Show |
13 | HG02129.hp2 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.956-854T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65052384 | |||||||
| chr14:65052385 | A | T | 20 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0116 others(17): Show |
20 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.956-853A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65052385 | |||||||
| chr14:65052418 | A | C | 1 | a0001c0001t0001g0161 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.956-820A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65052418 | |||||||
| chr14:65052436 | T | C | 3 | a0001c0001t0002g0047 a0001c0001t0002g0235 a0001c0001t0002g0335 |
3 | HG01175.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.956-802T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65052436 | |||||||
| chr14:65052451 | G | A | 207 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(204): Show |
210 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.956-787G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65052451 | |||||||
| chr14:65052517 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0347 |
3 | HG02647.hp2 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.956-721G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65052517 | |||||||
| chr14:65052703 | A | T | 1 | a0001c0005t0002g0283 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.956-535A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65052703 | |||||||
| chr14:65052708 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.956-530C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65052708 | |||||||
| chr14:65052717 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.956-521G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65052717 | |||||||
| chr14:65052722 | A | G | 2 | a0001c0001t0002g0012 a0001c0001t0002g0100 |
2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.956-516A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65052722 | |||||||
| chr14:65052908 | C | T | 3 | a0001c0001t0002g0006 a0001c0001t0002g0341 a0001c0001t0002g0348 |
4 | HG02965.hp1 HG03453.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.956-330C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65052908 | |||||||
| chr14:65052971 | T | C | 3 | a0001c0001t0002g0038 a0001c0001t0002g0101 a0001c0001t0002g0196 |
3 | HG01891.hp1 HG02896.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.956-267T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65052971 | |||||||
| chr14:65053113 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.956-125A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65053113 | |||||||
| chr14:65053122 | G | C | 1 | a0001c0001t0001g0036 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.956-116G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 9/11 | chr14 | 65053122 | |||||||
| chr14:65053369 | G | A | 3 | a0001c0001t0002g0014 a0001c0001t0002g0035 a0001c0001t0002g0194 |
3 | HG01361.hp2 HG01928.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.1067+20G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65053369 | |||||||
| chr14:65053377 | G | C | 1 | a0001c0001t0001g0154 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1067+28G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65053377 | |||||||
| chr14:65053528 | T | C | 276 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(273): Show |
282 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(279): Show |
intron_variant | MODIFIER | c.1067+179T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65053528 | |||||||
| chr14:65053608 | G | T | 1 | a0001c0001t0002g0119 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1067+259G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65053608 | |||||||
| chr14:65053625 | T | TAAAAAAA others(8): Show |
5 | a0001c0001t0002g0014 a0001c0001t0002g0035 a0001c0001t0002g0099 others(2): Show |
5 | HG01109.hp1 HG01361.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.1067+276_1067+277i others(17): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65053625 | |||||||
| chr14:65053625 | T | TAAAAAAA others(9): Show |
4 | a0001c0001t0002g0047 a0001c0001t0002g0107 a0001c0001t0002g0291 others(1): Show |
4 | HG01175.hp2 HG03225.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1067+276_1067+277i others(18): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65053625 | |||||||
| chr14:65053625 | T | TAAAAAAA others(7): Show |
8 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0119 others(5): Show |
8 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1067+276_1067+277i others(16): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65053625 | |||||||
| chr14:65053625 | T | TAAAAAAA others(8): Show |
34 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(31): Show |
34 | HG01081.hp2 HG01243.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.1067+276_1067+277i others(17): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65053625 | |||||||
| chr14:65053626 | T | A | 129 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0025 others(126): Show |
130 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.1067+277T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65053626 | |||||||
| chr14:65053634 | A | C | 1 | a0001c0001t0001g0153 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1067+285A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65053634 | |||||||
| chr14:65053635 | C | A | 83 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(80): Show |
84 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1067+286C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65053635 | |||||||
| chr14:65053690 | T | C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0090 |
4 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1067+341T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65053690 | |||||||
| chr14:65053898 | G | A | 201 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(198): Show |
205 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(202): Show |
intron_variant | MODIFIER | c.1067+549G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65053898 | |||||||
| chr14:65054001 | A | G | 51 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(48): Show |
51 | HG01081.hp2 HG01109.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.1068-574A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65054001 | |||||||
| chr14:65054388 | G | A | 58 | a0001c0001t0001g0171 a0001c0001t0002g0001 a0001c0001t0002g0006 others(55): Show |
60 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(57): Show |
intron_variant | MODIFIER | c.1068-187G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65054388 | |||||||
| chr14:65054440 | A | C | 51 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(48): Show |
51 | HG01081.hp2 HG01109.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.1068-135A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65054440 | |||||||
| chr14:65054443 | A | G | 1 | a0001c0001t0001g0320 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1068-132A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | chr14 | 65054443 | |||||||
| chr14:65054468 | TG | T | 51 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(48): Show |
51 | HG01081.hp2 HG01109.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.1068-99delG | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 65054468 | ||||||
| chr14:65054832 | C | T | 7 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(4): Show |
7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1182+143C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65054832 | |||||||
| chr14:65054833 | G | A | 4 | a0001c0001t0002g0014 a0001c0001t0002g0035 a0001c0001t0002g0119 others(1): Show |
4 | HG01361.hp2 HG01928.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1182+144G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65054833 | |||||||
| chr14:65054862 | G | A | 1 | a0001c0001t0002g0311 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1182+173G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65054862 | |||||||
| chr14:65054910 | A | C | 1 | a0001c0001t0001g0317 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1182+221A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65054910 | |||||||
| chr14:65055020 | A | G | 3 | a0001c0001t0001g0002 a0001c0001t0001g0345 a0001c0001t0001g0347 |
4 | HG02647.hp2 HG02717.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1182+331A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65055020 | |||||||
| chr14:65055022 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1182+333G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65055022 | |||||||
| chr14:65055025 | C | T | 51 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(48): Show |
51 | HG01081.hp2 HG01109.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.1182+336C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65055025 | |||||||
| chr14:65055160 | G | T | 1 | a0001c0001t0001g0134 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1182+471G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65055160 | |||||||
| chr14:65055194 | ATG | A | 84 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(81): Show |
85 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.1182+511_1182+512d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65055194 | ||||||
| chr14:65055243 | G | T | 1 | a0001c0001t0001g0236 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1182+554G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65055243 | |||||||
| chr14:65055497 | T | C | 2 | a0001c0001t0002g0094 a0001c0001t0002g0123 |
2 | HG02074.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.1182+808T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65055497 | |||||||
| chr14:65055504 | A | T | 9 | a0001c0001t0001g0116 a0001c0001t0001g0131 a0001c0001t0001g0294 others(6): Show |
9 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(6): Show |
intron_variant | MODIFIER | c.1182+815A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65055504 | |||||||
| chr14:65055505 | T | A | 203 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(200): Show |
207 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(204): Show |
intron_variant | MODIFIER | c.1182+816T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65055505 | |||||||
| chr14:65055506 | T | A | 3 | a0001c0001t0002g0038 a0001c0001t0002g0101 a0001c0001t0002g0196 |
3 | HG01891.hp1 HG02896.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1182+817T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65055506 | |||||||
| chr14:65055588 | C | G | 1 | a0001c0001t0002g0087 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1182+899C>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65055588 | |||||||
| chr14:65055696 | T | C | 71 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0027 others(68): Show |
72 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1182+1007T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65055696 | |||||||
| chr14:65055841 | A | C | 5 | a0001c0001t0002g0108 a0001c0001t0002g0130 a0001c0001t0002g0135 others(2): Show |
5 | HG00733.hp2 HG01099.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.1182+1152A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65055841 | |||||||
| chr14:65055944 | A | G | 1 | a0001c0001t0001g0033 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1182+1255A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65055944 | |||||||
| chr14:65055985 | GT | G | 7 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(4): Show |
7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1182+1304delT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65055985 | ||||||
| chr14:65056046 | C | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG01081.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1182+1357C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65056046 | |||||||
| chr14:65056228 | CAT | C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0090 others(3): Show |
7 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1182+1540_1182+154 others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65056228 | |||||||
| chr14:65056269 | A | G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0090 |
4 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1182+1580A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65056269 | |||||||
| chr14:65056277 | A | G | 51 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(48): Show |
51 | HG01081.hp2 HG01109.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.1182+1588A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65056277 | |||||||
| chr14:65056297 | G | A | 200 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(197): Show |
204 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.1182+1608G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65056297 | |||||||
| chr14:65056523 | A | G | 20 | a0001c0001t0002g0053 a0001c0001t0002g0059 a0001c0001t0002g0060 others(17): Show |
20 | HG02280.hp2 HG02572.hp2 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.1182+1834A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65056523 | |||||||
| chr14:65056544 | A | G | 7 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(4): Show |
7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1182+1855A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65056544 | |||||||
| chr14:65056577 | T | C | 110 | a0001c0001t0001g0071 a0001c0001t0002g0001 a0001c0001t0002g0006 others(107): Show |
112 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(109): Show |
intron_variant | MODIFIER | c.1182+1888T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65056577 | |||||||
| chr14:65056619 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1182+1930T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65056619 | |||||||
| chr14:65056635 | TCTGCCAG others(16): Show |
T | 1 | a0001c0001t0001g0315 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1182+1947_1182+196 others(27): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65056635 | |||||||
| chr14:65056674 | G | A | 69 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0012 others(66): Show |
71 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(68): Show |
intron_variant | MODIFIER | c.1182+1985G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65056674 | |||||||
| chr14:65056703 | T | C | 2 | a0001c0001t0001g0159 a0001c0001t0001g0281 |
2 | NA18969.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1182+2014T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65056703 | |||||||
| chr14:65056859 | T | C | 1 | a0001c0001t0002g0011 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1182+2170T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65056859 | |||||||
| chr14:65057282 | G | A | 109 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0009 others(106): Show |
111 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(108): Show |
intron_variant | MODIFIER | c.1182+2593G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65057282 | |||||||
| chr14:65057614 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1182+2925G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65057614 | |||||||
| chr14:65057752 | A | G | 3 | a0001c0001t0001g0002 a0001c0001t0001g0345 a0001c0001t0001g0347 |
4 | HG02647.hp2 HG02717.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1182+3063A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65057752 | |||||||
| chr14:65057776 | T | TA | 3 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0090 |
4 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1182+3089dupA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65057776 | ||||||
| chr14:65057782 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1182+3093A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65057782 | |||||||
| chr14:65057809 | A | G | 4 | a0001c0001t0002g0032 a0001c0001t0002g0034 a0001c0001t0002g0039 others(1): Show |
4 | HG01192.hp2 HG02055.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1182+3120A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65057809 | |||||||
| chr14:65057866 | T | TG | 3 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0090 |
4 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1182+3178dupG | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65057866 | ||||||
| chr14:65057936 | G | A | 1 | a0001c0001t0001g0327 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1183-3245G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65057936 | |||||||
| chr14:65058110 | CT | C | 50 | a0001c0001t0001g0025 a0001c0001t0001g0064 a0001c0001t0001g0073 others(47): Show |
50 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(47): Show |
intron_variant | MODIFIER | c.1183-3059delT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65058110 | ||||||
| chr14:65058146 | A | G | 40 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(37): Show |
40 | HG01081.hp2 HG01109.hp1 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.1183-3035A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65058146 | |||||||
| chr14:65058201 | TTTTC | T | 59 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0012 others(56): Show |
61 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.1183-2976_1183-297 others(8): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65058201 | ||||||
| chr14:65058230 | T | A | 1 | a0001c0001t0001g0217 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1183-2951T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65058230 | |||||||
| chr14:65058268 | T | C | 4 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0235 others(1): Show |
4 | HG01081.hp2 HG02109.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1183-2913T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65058268 | |||||||
| chr14:65058268 | T | TC | 36 | a0001c0001t0002g0011 a0001c0001t0002g0030 a0001c0001t0002g0031 others(33): Show |
36 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.1183-2912dupC | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65058268 | ||||||
| chr14:65058270 | G | A | 67 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0012 others(64): Show |
69 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(66): Show |
intron_variant | MODIFIER | c.1183-2911G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65058270 | |||||||
| chr14:65058270 | G | T | 2 | a0001c0001t0002g0182 a0001c0001t0002g0224 |
2 | HG02165.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1183-2911G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65058270 | |||||||
| chr14:65058325 | C | A | 1 | a0001c0001t0001g0333 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1183-2856C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65058325 | |||||||
| chr14:65058448 | C | T | 7 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0120 others(4): Show |
7 | HG02129.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1183-2733C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65058448 | |||||||
| chr14:65058523 | G | C | 109 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0009 others(106): Show |
111 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(108): Show |
intron_variant | MODIFIER | c.1183-2658G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65058523 | |||||||
| chr14:65058540 | A | G | 111 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0009 others(108): Show |
113 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(110): Show |
intron_variant | MODIFIER | c.1183-2641A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65058540 | |||||||
| chr14:65058546 | G | C | 1 | a0001c0001t0001g0079 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1183-2635G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65058546 | |||||||
| chr14:65058612 | A | G | 1 | a0001c0001t0002g0080 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1183-2569A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65058612 | |||||||
| chr14:65058892 | T | C | 40 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(37): Show |
40 | HG01081.hp2 HG01109.hp1 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.1183-2289T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65058892 | |||||||
| chr14:65058895 | T | C | 1 | a0001c0001t0001g0177 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1183-2286T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65058895 | |||||||
| chr14:65059076 | A | G | 201 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(198): Show |
205 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(202): Show |
intron_variant | MODIFIER | c.1183-2105A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65059076 | |||||||
| chr14:65059302 | G | A | 61 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0012 others(58): Show |
63 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(60): Show |
intron_variant | MODIFIER | c.1183-1879G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65059302 | |||||||
| chr14:65059304 | G | A | 111 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0009 others(108): Show |
113 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(110): Show |
intron_variant | MODIFIER | c.1183-1877G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65059304 | |||||||
| chr14:65059334 | T | C | 111 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0009 others(108): Show |
113 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(110): Show |
intron_variant | MODIFIER | c.1183-1847T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65059334 | |||||||
| chr14:65059495 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0090 |
4 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1183-1686G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65059495 | |||||||
| chr14:65059662 | G | A | 8 | a0001c0001t0002g0078 a0001c0001t0002g0099 a0001c0001t0002g0106 others(5): Show |
8 | HG01109.hp1 HG02280.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.1183-1519G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65059662 | |||||||
| chr14:65059738 | A | G | 6 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(3): Show |
6 | HG00408.hp2 HG00609.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.1183-1443A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65059738 | |||||||
| chr14:65059810 | T | TACATATT others(3): Show |
1 | a0001c0001t0001g0315 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1183-1370_1183-136 others(14): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65059810 | ||||||
| chr14:65059837 | C | CT | 57 | a0001c0001t0001g0071 a0001c0001t0001g0136 a0001c0001t0001g0154 others(54): Show |
57 | HG01081.hp2 HG01109.hp1 HG01175.hp2 others(54): Show |
intron_variant | MODIFIER | c.1183-1328dupT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65059837 | ||||||
| chr14:65059837 | C | CTT | 58 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0012 others(55): Show |
60 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(57): Show |
intron_variant | MODIFIER | c.1183-1329_1183-132 others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65059837 | ||||||
| chr14:65059837 | CT | C | 66 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0022 others(63): Show |
68 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1183-1328delT | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65059837 | ||||||
| chr14:65059855 | A | G | 1 | a0001c0001t0001g0271 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1183-1326A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65059855 | |||||||
| chr14:65059919 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1183-1262C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65059919 | |||||||
| chr14:65059958 | C | T | 1 | a0001c0001t0002g0199 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1183-1223C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65059958 | |||||||
| chr14:65060056 | C | T | 1 | a0001c0001t0001g0343 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1183-1125C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060056 | |||||||
| chr14:65060230 | A | C | 1 | a0001c0001t0001g0143 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-951A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060230 | |||||||
| chr14:65060231 | T | A | 1 | a0001c0001t0001g0143 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-950T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060231 | |||||||
| chr14:65060233 | A | T | 1 | a0001c0001t0001g0143 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-948A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060233 | |||||||
| chr14:65060234 | A | T | 1 | a0001c0001t0001g0143 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-947A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060234 | |||||||
| chr14:65060236 | A | C | 1 | a0001c0001t0001g0143 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-945A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060236 | |||||||
| chr14:65060241 | G | T | 1 | a0001c0001t0001g0143 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-940G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060241 | |||||||
| chr14:65060242 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-939G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060242 | |||||||
| chr14:65060250 | A | T | 1 | a0001c0001t0001g0143 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-931A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060250 | |||||||
| chr14:65060251 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-930C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060251 | |||||||
| chr14:65060253 | A | T | 1 | a0001c0001t0001g0143 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-928A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060253 | |||||||
| chr14:65060254 | T | G | 1 | a0001c0001t0001g0143 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-927T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060254 | |||||||
| chr14:65060256 | T | A | 1 | a0001c0001t0001g0143 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-925T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060256 | |||||||
| chr14:65060258 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-923T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060258 | |||||||
| chr14:65060259 | G | C | 1 | a0001c0001t0001g0143 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-922G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060259 | |||||||
| chr14:65060261 | T | A | 1 | a0001c0001t0001g0143 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-920T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060261 | |||||||
| chr14:65060269 | T | A | 1 | a0001c0001t0001g0143 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-912T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060269 | |||||||
| chr14:65060273 | T | A | 1 | a0001c0001t0001g0143 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-908T>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060273 | |||||||
| chr14:65060274 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-907C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060274 | |||||||
| chr14:65060276 | C | A | 1 | a0001c0001t0001g0143 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-905C>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060276 | |||||||
| chr14:65060278 | G | C | 1 | a0001c0001t0001g0143 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-903G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060278 | |||||||
| chr14:65060279 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-902G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060279 | |||||||
| chr14:65060279 | G | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0090 |
4 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1183-902G>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060279 | |||||||
| chr14:65060281 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-900A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060281 | |||||||
| chr14:65060282 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-899C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060282 | |||||||
| chr14:65060284 | A | T | 1 | a0001c0001t0001g0143 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1183-897A>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060284 | |||||||
| chr14:65060348 | G | C | 1 | a0001c0001t0002g0273 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1183-833G>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060348 | |||||||
| chr14:65060359 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1183-822C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060359 | |||||||
| chr14:65060404 | C | T | 88 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(85): Show |
89 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.1183-777C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060404 | |||||||
| chr14:65060417 | T | C | 1 | a0001c0001t0002g0189 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1183-764T>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060417 | |||||||
| chr14:65060426 | TAAAAATA others(277): Show |
T | 111 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0009 others(108): Show |
113 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(110): Show |
intron_variant | MODIFIER | c.1183-740_1183-457d others(2): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65060426 | ||||||
| chr14:65060559 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1183-622A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060559 | |||||||
| chr14:65060560 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1183-621G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060560 | |||||||
| chr14:65060564 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1183-617C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060564 | |||||||
| chr14:65060565 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1183-616G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060565 | |||||||
| chr14:65060697 | C | CAAAAAAA others(1): Show |
66 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(63): Show |
67 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.1183-473_1183-466d others(10): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65060697 | ||||||
| chr14:65060697 | C | CAAAAAAA others(2): Show |
21 | a0001c0001t0001g0019 a0001c0001t0001g0054 a0001c0001t0001g0064 others(18): Show |
21 | HG00609.hp1 HG01256.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.1183-474_1183-466d others(11): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65060697 | ||||||
| chr14:65060697 | CA | C | 68 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0027 others(65): Show |
69 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.1183-466delA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65060697 | ||||||
| chr14:65060718 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0090 others(1): Show |
5 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1183-463C>T | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060718 | |||||||
| chr14:65060766 | A | G | 1 | a0001c0001t0002g0189 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1183-415A>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060766 | |||||||
| chr14:65060810 | T | G | 1 | a0001c0001t0001g0271 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1183-371T>G | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060810 | |||||||
| chr14:65060870 | C | CA | 11 | a0001c0001t0001g0024 a0001c0001t0001g0048 a0001c0001t0001g0079 others(8): Show |
11 | HG00621.hp2 HG00735.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1183-286dupA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65060870 | ||||||
| chr14:65060870 | CA | C | 10 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0027 others(7): Show |
11 | HG00438.hp2 HG01106.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.1183-286delA | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65060870 | ||||||
| chr14:65060870 | CAA | C | 62 | a0001c0001t0001g0004 a0001c0001t0001g0040 a0001c0001t0001g0041 others(59): Show |
63 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.1183-287_1183-286d others(4): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65060870 | ||||||
| chr14:65060870 | CAAA | C | 13 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0058 others(10): Show |
13 | HG00408.hp2 HG00609.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.1183-288_1183-286d others(5): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65060870 | ||||||
| chr14:65060870 | CAAAA | C | 91 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(88): Show |
93 | HG00140.hp1 HG00642.hp1 HG01074.hp1 others(90): Show |
intron_variant | MODIFIER | c.1183-289_1183-286d others(6): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65060870 | ||||||
| chr14:65060870 | CAAAAA | C | 47 | a0001c0001t0001g0156 a0001c0001t0001g0297 a0001c0001t0002g0001 others(44): Show |
49 | HG00438.hp1 HG00733.hp2 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.1183-290_1183-286d others(7): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65060870 | ||||||
| chr14:65060870 | CAAAAAAA | C | 25 | a0001c0001t0002g0010 a0001c0001t0002g0047 a0001c0001t0002g0059 others(22): Show |
25 | HG01175.hp2 HG02109.hp2 HG02129.hp2 others(22): Show |
intron_variant | MODIFIER | c.1183-292_1183-286d others(9): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65060870 | ||||||
| chr14:65060870 | CAAAAAAA others(1): Show |
C | 15 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0014 others(12): Show |
15 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.1183-293_1183-286d others(10): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65060870 | ||||||
| chr14:65060870 | CAAAAAAA others(2): Show |
C | 7 | a0001c0001t0002g0078 a0001c0001t0002g0099 a0001c0001t0002g0106 others(4): Show |
7 | HG01109.hp1 HG02280.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1183-294_1183-286d others(11): Show |
FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 65060870 | ||||||
| chr14:65060889 | A | C | 3 | a0001c0001t0001g0301 a0001c0001t0001g0315 a0001c0001t0001g0343 |
3 | NA18969.hp2 NA19004.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1183-292A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060889 | |||||||
| chr14:65060891 | A | C | 66 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0040 others(63): Show |
67 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.1183-290A>C | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060891 | |||||||
| chr14:65060942 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0090 |
4 | HG02145.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1183-239G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060942 | |||||||
| chr14:65060956 | G | A | 1 | a0001c0001t0002g0047 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1183-225G>A | FNTB | ENSG00000257365.8 | transcript | ENST00000246166.3 | protein_coding | 11/11 | chr14 | 65060956 |