Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55640 |
| ensemblid | ENSG00000119686.10 |
| hgncid | 20105 |
| symbol | FLVCR2 |
| name | FLVCR heme transporter 2 |
| refseq_nuc | NM_017791.3 |
| refseq_prot | NP_060261.2 |
| ensembl_nuc | ENST00000238667.9 |
| ensembl_prot | ENSP00000238667.4 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 75578620 |
| end | 75648167 |
| strand | + |
| ver | v1.2 |
| region | chr14:75578620-75648167 |
| region5000 | chr14:75573620-75653167 |
| regionname0 | FLVCR2_chr14_75578620_75648167 |
| regionname5000 | FLVCR2_chr14_75573620_75653167 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 526 | 176 | 56 | 29 | 66 | 6 | 19 | 52 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | MVNEG others(521): Show |
chr14 | 75573620 | 75653167 |
| a0002 | 1/1 | 526 | 149 | 20 | 34 | 67 | 9 | 17 | 49 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | MVNEG others(521): Show |
chr14 | 75573620 | 75653167 |
| a0003 | 0/0 | 526 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | MVNEG others(521): Show |
chr14 | 75573620 | 75653167 |
| a0004 | 0/0 | 526 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | MVNEG others(521): Show |
chr14 | 75573620 | 75653167 |
| a0005 | 0/0 | 526 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | MVNEG others(521): Show |
chr14 | 75573620 | 75653167 |
| a0006 | 0/0 | 520 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | MVNEG others(515): Show |
chr14 | 75573620 | 75653167 |
| a0007 | 0/0 | 526 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | MVNEG others(521): Show |
chr14 | 75573620 | 75653167 |
| a0008 | 0/0 | 526 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | MVNEG others(521): Show |
chr14 | 75573620 | 75653167 |
| a0009 | 0/0 | 526 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | MVNEG others(521): Show |
chr14 | 75573620 | 75653167 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1578 | 175 | 56 | 29 | 65 | 6 | 19 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | ATGGT others(1573): Show |
chr14 | 75573620 | 75653167 | ||
| a0001c0007 | 0/0 | 1578 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | ATGGT others(1573): Show |
chr14 | 75573620 | 75653167 | ||
| a0002c0002 | 1/1 | 1578 | 98 | 3 | 24 | 52 | 4 | 13 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | ATGGT others(1573): Show |
chr14 | 75573620 | 75653167 | ||
| a0002c0003 | 0/0 | 1578 | 51 | 17 | 10 | 15 | 5 | 4 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | ATGGT others(1573): Show |
chr14 | 75573620 | 75653167 | ||
| a0003c0004 | 0/0 | 1578 | 3 | 3 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | ATGGT others(1573): Show |
chr14 | 75573620 | 75653167 | ||
| a0004c0005 | 0/0 | 1578 | 3 | 3 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | ATGGT others(1573): Show |
chr14 | 75573620 | 75653167 | ||
| a0005c0010 | 0/0 | 1578 | 1 | 0 | 0 | 0 | 1 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | ATGGT others(1573): Show |
chr14 | 75573620 | 75653167 | ||
| a0006c0009 | 0/0 | 1560 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | ATGGT others(1555): Show |
chr14 | 75573620 | 75653167 | ||
| a0007c0008 | 0/0 | 1578 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | ATGGT others(1573): Show |
chr14 | 75573620 | 75653167 | ||
| a0008c0006 | 0/0 | 1578 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | ATGGT others(1573): Show |
chr14 | 75573620 | 75653167 | ||
| a0009c0011 | 0/0 | 1578 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | ATGGT others(1573): Show |
chr14 | 75573620 | 75653167 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3629 | 107 | 35 | 17 | 42 | 5 | 8 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3624): Show |
chr14 | 75573620 | 75653167 |
| a0001c0001t0002 | 0/0 | 3629 | 8 | 0 | 1 | 0 | 1 | 6 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3624): Show |
chr14 | 75573620 | 75653167 |
| a0001c0001t0004 | 0/0 | 3629 | 43 | 14 | 7 | 21 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3624): Show |
chr14 | 75573620 | 75653167 |
| a0001c0001t0007 | 0/0 | 3629 | 2 | 0 | 1 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3624): Show |
chr14 | 75573620 | 75653167 |
| a0001c0001t0008 | 0/0 | 3629 | 2 | 1 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3624): Show |
chr14 | 75573620 | 75653167 |
| a0001c0001t0009 | 0/0 | 3629 | 2 | 0 | 2 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3624): Show |
chr14 | 75573620 | 75653167 |
| a0001c0001t0010 | 0/0 | 3627 | 2 | 2 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3622): Show |
chr14 | 75573620 | 75653167 |
| a0001c0001t0012 | 0/0 | 3629 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3624): Show |
chr14 | 75573620 | 75653167 |
| a0001c0001t0013 | 0/0 | 3629 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3624): Show |
chr14 | 75573620 | 75653167 |
| a0001c0001t0014 | 0/0 | 3629 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3624): Show |
chr14 | 75573620 | 75653167 |
| a0001c0001t0015 | 0/0 | 3629 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3624): Show |
chr14 | 75573620 | 75653167 |
| a0001c0001t0016 | 0/0 | 3629 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3624): Show |
chr14 | 75573620 | 75653167 |
| a0001c0001t0017 | 0/0 | 3629 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3624): Show |
chr14 | 75573620 | 75653167 |
| a0001c0001t0018 | 0/0 | 3629 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3624): Show |
chr14 | 75573620 | 75653167 |
| a0001c0001t0019 | 0/0 | 3629 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3624): Show |
chr14 | 75573620 | 75653167 |
| a0001c0001t0020 | 0/0 | 3629 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3624): Show |
chr14 | 75573620 | 75653167 |
| a0001c0007t0004 | 0/0 | 3629 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3624): Show |
chr14 | 75573620 | 75653167 |
| a0002c0002t0002 | 1/1 | 3629 | 95 | 3 | 22 | 51 | 4 | 13 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3624): Show |
chr14 | 75573620 | 75653167 |
| a0002c0002t0011 | 0/0 | 3629 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3624): Show |
chr14 | 75573620 | 75653167 |
| a0002c0002t0021 | 0/0 | 3629 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3624): Show |
chr14 | 75573620 | 75653167 |
| a0002c0002t0026 | 0/0 | 3629 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3624): Show |
chr14 | 75573620 | 75653167 |
| a0002c0003t0003 | 0/0 | 3627 | 47 | 15 | 9 | 15 | 5 | 3 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3622): Show |
chr14 | 75573620 | 75653167 |
| a0002c0003t0022 | 0/0 | 3627 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3622): Show |
chr14 | 75573620 | 75653167 |
| a0002c0003t0023 | 0/0 | 3627 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3622): Show |
chr14 | 75573620 | 75653167 |
| a0002c0003t0024 | 0/0 | 3627 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3622): Show |
chr14 | 75573620 | 75653167 |
| a0002c0003t0025 | 0/0 | 3627 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3622): Show |
chr14 | 75573620 | 75653167 |
| a0003c0004t0005 | 0/0 | 3629 | 3 | 3 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3624): Show |
chr14 | 75573620 | 75653167 |
| a0004c0005t0006 | 0/0 | 3627 | 3 | 3 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3622): Show |
chr14 | 75573620 | 75653167 |
| a0005c0010t0002 | 0/0 | 3629 | 1 | 0 | 0 | 0 | 1 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3624): Show |
chr14 | 75573620 | 75653167 |
| a0006c0009t0002 | 0/0 | 3611 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3606): Show |
chr14 | 75573620 | 75653167 |
| a0007c0008t0001 | 0/0 | 3629 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3624): Show |
chr14 | 75573620 | 75653167 |
| a0008c0006t0001 | 0/0 | 3629 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3624): Show |
chr14 | 75573620 | 75653167 |
| a0009c0011t0003 | 0/0 | 3627 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | AGAGG others(3622): Show |
chr14 | 75573620 | 75653167 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0007g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0007g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0008g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0008g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0009g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0009g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0010g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0010g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0012g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0013g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0014g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0015g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0016g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0017g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0018g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0019g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0001t0020g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0001c0007t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0056 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0103 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0011g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0021g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0002t0026g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0022g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0023g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0024g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0002c0003t0025g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0003c0004t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0003c0004t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0003c0004t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0004c0005t0006g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0004c0005t0006g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0004c0005t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0005c0010t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0006c0009t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0007c0008t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0008c0006t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| a0009c0011t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0078 | EUR | GBR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG00099 | hp2 | a0005 | c0010 | t0002 | g0058 | EUR | GBR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG00140 | hp1 | a0002 | c0003 | t0003 | g0116 | EUR | GBR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0260 | EUR | GBR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG00323 | hp1 | a0002 | c0003 | t0003 | g0009 | EUR | FIN | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0212 | EUR | FIN | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG00408 | hp1 | a0002 | c0003 | t0003 | g0129 | EAS | CHS | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG00408 | hp2 | a0001 | c0001 | t0013 | g0291 | EAS | CHS | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG00438 | hp2 | a0001 | c0001 | t0016 | g0263 | EAS | CHS | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0026 | EAS | CHS | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0072 | EAS | CHS | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0043 | EAS | CHS | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0208 | EAS | CHS | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0084 | EAS | CHS | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG00639 | hp1 | a0002 | c0003 | t0003 | g0118 | AMR | PUR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0075 | AMR | PUR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0037 | EAS | CHS | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG00741 | hp2 | a0002 | c0003 | t0003 | g0119 | AMR | PUR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01070 | hp1 | a0001 | c0001 | t0008 | g0296 | AMR | PUR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01071 | hp1 | a0002 | c0003 | t0003 | g0117 | AMR | PUR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01071 | hp2 | a0001 | c0001 | t0009 | g0210 | AMR | PUR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01074 | hp1 | a0002 | c0002 | t0002 | g0087 | AMR | PUR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0080 | AMR | PUR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0167 | AMR | PUR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01106 | hp1 | a0002 | c0002 | t0021 | g0020 | AMR | PUR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0172 | AMR | PUR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01109 | hp2 | a0002 | c0002 | t0002 | g0086 | AMR | PUR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01167 | hp1 | a0006 | c0009 | t0002 | g0093 | AMR | PUR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0023 | AMR | PUR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0024 | AMR | PUR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0198 | AMR | PUR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01192 | hp1 | a0001 | c0001 | t0009 | g0213 | AMR | PUR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0102 | AMR | PUR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0221 | AMR | PUR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0031 | AMR | CLM | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0185 | AMR | CLM | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0010 | AMR | CLM | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0074 | AMR | CLM | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01257 | hp2 | a0002 | c0003 | t0003 | g0130 | AMR | CLM | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0081 | AMR | CLM | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0089 | AMR | CLM | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | CLM | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01433 | hp1 | a0002 | c0003 | t0003 | g0115 | AMR | CLM | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01433 | hp2 | a0001 | c0001 | t0007 | g0325 | AMR | CLM | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01496 | hp1 | a0002 | c0002 | t0002 | g0012 | AMR | CLM | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | CLM | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0273 | EUR | IBS | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0271 | EUR | IBS | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0266 | EUR | IBS | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0021 | EUR | IBS | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0018 | EUR | IBS | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0256 | EUR | IBS | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0223 | AFR | ACB | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01943 | hp1 | a0002 | c0003 | t0022 | g0133 | AMR | PEL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01943 | hp2 | a0002 | c0002 | t0002 | g0061 | AMR | PEL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01952 | hp2 | a0002 | c0003 | t0003 | g0152 | AMR | PEL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0054 | AMR | PEL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0042 | AMR | PEL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0076 | AMR | PEL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01993 | hp1 | a0002 | c0003 | t0003 | g0128 | AMR | PEL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01993 | hp2 | a0002 | c0002 | t0011 | g0060 | AMR | PEL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0038 | AMR | PEL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0107 | EAS | KHV | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02015 | hp2 | a0002 | c0003 | t0003 | g0139 | EAS | KHV | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02040 | hp1 | a0002 | c0003 | t0003 | g0141 | EAS | KHV | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0094 | EAS | KHV | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0203 | AFR | ACB | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0274 | AFR | ACB | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02071 | hp1 | a0002 | c0003 | t0003 | g0143 | EAS | KHV | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | KHV | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0029 | EAS | KHV | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02080 | hp1 | a0002 | c0002 | t0026 | g0030 | EAS | KHV | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0085 | EAS | KHV | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0049 | EAS | KHV | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | ACB | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0164 | AFR | ACB | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0019 | AMR | PEL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0189 | AMR | PEL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | CDX | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02165 | hp2 | a0002 | c0003 | t0003 | g0126 | EAS | CDX | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0098 | AFR | ACB | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02257 | hp2 | a0002 | c0003 | t0003 | g0122 | AFR | ACB | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0205 | AFR | ACB | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02258 | hp2 | a0001 | c0001 | t0012 | g0327 | AFR | ACB | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PEL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0195 | AMR | PEL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02280 | hp1 | a0002 | c0002 | t0002 | g0059 | AFR | ACB | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02293 | hp1 | a0002 | c0003 | t0003 | g0113 | AMR | PEL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0050 | AMR | PEL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | ACB | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0079 | EAS | KHV | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | GWD | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0039 | SAS | PJL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02602 | hp2 | a0001 | c0001 | t0007 | g0326 | SAS | PJL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | GWD | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02615 | hp2 | a0003 | c0004 | t0005 | g0204 | AFR | GWD | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0201 | AFR | GWD | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0207 | AFR | GWD | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | GWD | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02683 | hp1 | a0001 | c0001 | t0020 | g0214 | SAS | PJL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02683 | hp2 | a0002 | c0003 | t0003 | g0109 | SAS | PJL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02717 | hp1 | a0002 | c0003 | t0003 | g0137 | AFR | GWD | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02717 | hp2 | a0002 | c0003 | t0003 | g0161 | AFR | GWD | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02723 | hp2 | a0002 | c0003 | t0003 | g0108 | AFR | GWD | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0104 | SAS | PJL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0092 | SAS | PJL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02738 | hp1 | a0002 | c0002 | t0002 | g0048 | SAS | PJL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02738 | hp2 | a0001 | c0001 | t0014 | g0276 | SAS | PJL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02809 | hp1 | a0002 | c0003 | t0003 | g0134 | AFR | GWD | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02809 | hp2 | a0001 | c0001 | t0015 | g0307 | AFR | GWD | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02886 | hp2 | a0002 | c0003 | t0023 | g0157 | AFR | GWD | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02895 | hp1 | a0004 | c0005 | t0006 | g0153 | AFR | GWD | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0222 | AFR | GWD | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02897 | hp2 | a0004 | c0005 | t0006 | g0136 | AFR | GWD | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02922 | hp1 | a0001 | c0001 | t0017 | g0170 | AFR | ESN | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | ESN | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02965 | hp2 | a0002 | c0003 | t0003 | g0144 | AFR | ESN | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02976 | hp1 | a0002 | c0003 | t0003 | g0121 | AFR | ESN | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02976 | hp2 | a0003 | c0004 | t0005 | g0206 | AFR | ESN | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0105 | SAS | PJL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0091 | SAS | PJL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0202 | AFR | GWD | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | MSL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03098 | hp2 | a0002 | c0003 | t0003 | g0123 | AFR | MSL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03130 | hp1 | a0004 | c0005 | t0006 | g0135 | AFR | ESN | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03130 | hp2 | a0002 | c0003 | t0003 | g0112 | AFR | ESN | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ESN | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ESN | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03209 | hp1 | a0002 | c0003 | t0025 | g0151 | AFR | MSL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0169 | AFR | MSL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03453 | hp1 | a0002 | c0003 | t0003 | g0140 | AFR | MSL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | MSL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03491 | hp1 | a0002 | c0003 | t0003 | g0158 | SAS | PJL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0216 | SAS | PJL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | PJL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03492 | hp2 | a0002 | c0002 | t0002 | g0083 | SAS | PJL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | GWD | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | MSL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | MSL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03669 | hp1 | a0002 | c0002 | t0002 | g0088 | SAS | PJL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0220 | SAS | PJL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0065 | SAS | PJL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0016 | SAS | PJL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | BEB | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0184 | SAS | BEB | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03834 | hp1 | a0002 | c0003 | t0024 | g0159 | SAS | BEB | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | BEB | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | BEB | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | BEB | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | BEB | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0217 | SAS | STU | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0090 | SAS | STU | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0011 | SAS | BEB | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG04184 | hp2 | a0002 | c0003 | t0003 | g0114 | SAS | BEB | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG04199 | hp1 | a0001 | c0001 | t0018 | g0209 | SAS | STU | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0219 | SAS | STU | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0082 | SAS | STU | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0218 | SAS | STU | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | YRI | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0224 | AFR | YRI | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18943 | hp1 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18943 | hp2 | a0002 | c0003 | t0003 | g0147 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0176 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0178 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0055 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0187 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18952 | hp1 | a0007 | c0008 | t0001 | g0269 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18953 | hp2 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18954 | hp1 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18963 | hp2 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0191 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18966 | hp2 | a0002 | c0003 | t0003 | g0146 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18967 | hp1 | a0001 | c0001 | t0004 | g0182 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18968 | hp2 | a0001 | c0007 | t0004 | g0197 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18969 | hp1 | a0002 | c0003 | t0003 | g0110 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0188 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18972 | hp1 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18972 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18978 | hp2 | a0002 | c0003 | t0003 | g0149 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18982 | hp2 | a0001 | c0001 | t0004 | g0175 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0177 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18987 | hp1 | a0008 | c0006 | t0001 | g0294 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18987 | hp2 | a0001 | c0001 | t0004 | g0193 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18988 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18992 | hp2 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18993 | hp1 | a0001 | c0001 | t0004 | g0183 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18993 | hp2 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18994 | hp2 | a0002 | c0002 | t0002 | g0067 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0192 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18995 | hp2 | a0002 | c0003 | t0003 | g0148 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0068 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19004 | hp1 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19004 | hp2 | a0002 | c0003 | t0003 | g0127 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0052 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0180 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0186 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19012 | hp1 | a0009 | c0011 | t0003 | g0111 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | LWK | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | LWK | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0163 | AFR | LWK | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | LWK | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19055 | hp1 | a0002 | c0003 | t0003 | g0155 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19056 | hp1 | a0002 | c0003 | t0003 | g0154 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0062 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0196 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0200 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0051 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19067 | hp1 | a0001 | c0001 | t0004 | g0199 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19067 | hp2 | a0002 | c0003 | t0003 | g0142 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0179 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19074 | hp2 | a0002 | c0003 | t0003 | g0145 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19081 | hp1 | a0002 | c0002 | t0002 | g0040 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19082 | hp1 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19083 | hp1 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0160 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19088 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19088 | hp2 | a0001 | c0001 | t0004 | g0194 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19089 | hp1 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19089 | hp2 | a0002 | c0002 | t0002 | g0057 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19240 | hp1 | a0001 | c0001 | t0010 | g0319 | AFR | YRI | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA19240 | hp2 | a0002 | c0003 | t0003 | g0124 | AFR | YRI | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0096 | AFR | ASW | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA20129 | hp2 | a0002 | c0003 | t0003 | g0156 | AFR | ASW | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0097 | EUR | TSI | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA20752 | hp2 | a0002 | c0003 | t0003 | g0138 | EUR | TSI | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA20805 | hp1 | a0002 | c0003 | t0003 | g0120 | EUR | TSI | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA20805 | hp2 | a0002 | c0003 | t0003 | g0162 | EUR | TSI | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01123 | hp1 | a0002 | c0003 | t0003 | g0132 | AMR | CLM | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0077 | AMR | CLM | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0171 | AFR | ACB | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0168 | AFR | ACB | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG02559 | hp2 | a0002 | c0003 | t0003 | g0125 | AFR | ACB | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG03471 | hp2 | a0001 | c0001 | t0010 | g0318 | AFR | MSL | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0166 | AFR | USA | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| HG06807 | hp2 | a0003 | c0004 | t0005 | g0165 | AFR | USA | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0044 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA20300 | hp1 | a0002 | c0003 | t0003 | g0131 | AFR | USA | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | USA | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA21309 | hp1 | a0002 | c0003 | t0003 | g0150 | AFR | LWK | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| NA21309 | hp2 | a0001 | c0001 | t0019 | g0324 | AFR | LWK | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0103 | REF | REF | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0056 | REF | REF | FLVCR2_chr14_75573620_75653167 | FLVCR2 | chr14 | 75573620 | 75653167 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:75579019 | T | C | 4 | a0001 a0003 a0007 others(1): Show |
181 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(178): Show |
missense_variant | MODERATE | c.47T>C | p.Val16Ala | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/10 | 400/3629 | 47/1581 | 16/526 | chr14 | 75579019 | |||
| chr14:75579044 | CCCCAGCG others(11): Show |
C | 1 | a0006 | 1 | HG01167.hp1 | disruptive_inframe_deletion | MODERATE | c.102_119delGGTCCATC others(10): Show |
p.Val35_Ser40del | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/10 | 455/3629 | 102/1581 | 34/526 | INFO_REALIGN_3_PRIME | chr14 | 75579044 | ||
| chr14:75579445 | C | T | 1 | a0007 | 1 | NA18952.hp1 | missense_variant | MODERATE | c.473C>T | p.Ser158Leu | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/10 | 826/3629 | 473/1581 | 158/526 | chr14 | 75579445 | |||
| chr14:75622136 | C | T | 1 | a0009 | 1 | NA19012.hp1 | missense_variant | MODERATE | c.727C>T | p.Arg243Trp | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 2/10 | 1080/3629 | 727/1581 | 243/526 | chr14 | 75622136 | |||
| chr14:75624635 | C | T | 1 | a0005 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.835C>T | p.Pro279Ser | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/10 | 1188/3629 | 835/1581 | 279/526 | chr14 | 75624635 | |||
| chr14:75624705 | C | A | 1 | a0008 | 1 | NA18987.hp1 | missense_variant | MODERATE | c.905C>A | p.Ala302Asp | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/10 | 1258/3629 | 905/1581 | 302/526 | chr14 | 75624705 | |||
| chr14:75641281 | G | A | 2 | a0003 a0004 |
6 | HG02615.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
missense_variant | MODERATE | c.1441G>A | p.Ala481Thr | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 8/10 | 1794/3629 | 1441/1581 | 481/526 | chr14 | 75641281 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:75579348 | C | T | 3 | a0002c0003 a0004c0005 a0009c0011 |
55 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(52): Show |
synonymous_variant | LOW | c.376C>T | p.Leu126Leu | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/10 | 729/3629 | 376/1581 | 126/526 | chr14 | 75579348 | |||
| chr14:75579515 | G | A | 5 | a0001c0001 a0001c0007 a0003c0004 others(2): Show |
181 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(178): Show |
synonymous_variant | LOW | c.543G>A | p.Val181Val | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/10 | 896/3629 | 543/1581 | 181/526 | chr14 | 75579515 | |||
| chr14:75579620 | C | G | 5 | a0001c0001 a0001c0007 a0003c0004 others(2): Show |
181 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(178): Show |
synonymous_variant | LOW | c.648C>G | p.Ser216Ser | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/10 | 1001/3629 | 648/1581 | 216/526 | chr14 | 75579620 | |||
| chr14:75624709 | G | C | 1 | a0001c0007 | 1 | NA18968.hp2 | synonymous_variant | LOW | c.909G>C | p.Arg303Arg | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/10 | 1262/3629 | 909/1581 | 303/526 | chr14 | 75624709 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:75578733 | G | A | 1 | a0002c0002t0011 | 1 | HG01993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-240G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/10 | 240 | chr14 | 75578733 | ||||||
| chr14:75578742 | G | T | 1 | a0002c0002t0026 | 1 | HG02080.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-231G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/10 | chr14 | 75578742 | |||||||
| chr14:75578850 | GTC | G | 8 | a0001c0001t0010 a0002c0003t0003 a0002c0003t0022 others(5): Show |
57 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(54): Show |
5_prime_UTR_variant | MODIFIER | c.-119_-118delCT | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/10 | 118 | INFO_REALIGN_3_PRIME | chr14 | 75578850 | |||||
| chr14:75578862 | T | C | 2 | a0001c0001t0007 a0001c0001t0012 |
3 | HG01433.hp2 HG02258.hp2 HG02602.hp2 |
5_prime_UTR_variant | MODIFIER | c.-111T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/10 | 111 | chr14 | 75578862 | ||||||
| chr14:75578877 | T | C | 15 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 others(12): Show |
168 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(165): Show |
5_prime_UTR_variant | MODIFIER | c.-96T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/10 | 96 | chr14 | 75578877 | ||||||
| chr14:75578902 | C | T | 5 | a0001c0001t0004 a0001c0001t0012 a0001c0001t0017 others(2): Show |
49 | HG00609.hp1 HG01081.hp2 HG01106.hp2 others(46): Show |
5_prime_UTR_variant | MODIFIER | c.-71C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/10 | 71 | chr14 | 75578902 | ||||||
| chr14:75646659 | T | C | 2 | a0001c0001t0008 a0001c0001t0009 |
4 | HG01070.hp1 HG01071.hp2 HG01192.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*187T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 10/10 | 187 | chr14 | 75646659 | ||||||
| chr14:75646726 | T | C | 1 | a0001c0001t0017 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*254T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 10/10 | 254 | chr14 | 75646726 | ||||||
| chr14:75646932 | C | T | 1 | a0001c0001t0016 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*460C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 10/10 | 460 | chr14 | 75646932 | ||||||
| chr14:75646944 | C | T | 1 | a0002c0002t0021 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*472C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 10/10 | 472 | chr14 | 75646944 | ||||||
| chr14:75646989 | C | G | 1 | a0002c0003t0025 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*517C>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 10/10 | 517 | chr14 | 75646989 | ||||||
| chr14:75647050 | C | A | 1 | a0002c0003t0022 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*578C>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 10/10 | 578 | chr14 | 75647050 | ||||||
| chr14:75647068 | T | C | 1 | a0001c0001t0018 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*596T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 10/10 | 596 | chr14 | 75647068 | ||||||
| chr14:75647172 | T | C | 1 | a0001c0001t0013 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*700T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 10/10 | 700 | chr14 | 75647172 | ||||||
| chr14:75647463 | T | C | 1 | a0001c0001t0014 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*991T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 10/10 | 991 | chr14 | 75647463 | ||||||
| chr14:75647512 | C | T | 2 | a0003c0004t0005 a0004c0005t0006 |
6 | HG02615.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1040C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 10/10 | 1040 | chr14 | 75647512 | ||||||
| chr14:75647570 | C | A | 2 | a0003c0004t0005 a0004c0005t0006 |
6 | HG02615.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1098C>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 10/10 | 1098 | chr14 | 75647570 | ||||||
| chr14:75647791 | C | T | 2 | a0001c0001t0020 a0002c0003t0024 |
2 | HG02683.hp1 HG03834.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1319C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 10/10 | 1319 | chr14 | 75647791 | ||||||
| chr14:75647961 | C | T | 1 | a0002c0003t0023 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1489C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 10/10 | 1489 | chr14 | 75647961 | ||||||
| chr14:75647989 | T | C | 1 | a0001c0001t0015 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1517T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 10/10 | 1517 | chr14 | 75647989 | ||||||
| chr14:75648091 | G | T | 1 | a0001c0001t0019 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1619G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 10/10 | 1619 | chr14 | 75648091 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:75579661 | A | G | 3 | a0001c0001t0007g0325 a0001c0001t0007g0326 a0001c0001t0012g0327 |
3 | HG01433.hp2 HG02258.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.669+20A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75579661 | |||||||
| chr14:75579761 | A | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(169): Show |
181 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.669+120A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75579761 | |||||||
| chr14:75579773 | C | T | 1 | a0001c0001t0019g0324 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.669+132C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75579773 | |||||||
| chr14:75579801 | G | A | 10 | a0001c0001t0004g0163 a0001c0001t0004g0164 a0001c0001t0004g0166 others(7): Show |
10 | HG01081.hp2 HG01106.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.669+160G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75579801 | |||||||
| chr14:75579887 | C | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(93): Show |
104 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.669+246C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75579887 | |||||||
| chr14:75580343 | G | A | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | HG02630.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.669+702G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75580343 | |||||||
| chr14:75580456 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.669+815C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75580456 | |||||||
| chr14:75580459 | A | G | 8 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(5): Show |
8 | HG01168.hp1 HG01496.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.669+818A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75580459 | |||||||
| chr14:75580503 | C | T | 1 | a0002c0003t0003g0162 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.669+862C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75580503 | |||||||
| chr14:75580582 | C | T | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | HG02630.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.669+941C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75580582 | |||||||
| chr14:75580627 | G | A | 1 | a0002c0002t0002g0008 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.669+986G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75580627 | |||||||
| chr14:75580679 | C | CAG | 68 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0225 others(65): Show |
68 | HG00323.hp2 HG00609.hp1 HG01070.hp2 others(65): Show |
intron_variant | MODIFIER | c.669+1039_669+1040d others(4): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75580679 | ||||||
| chr14:75580719 | T | C | 1 | a0002c0003t0003g0009 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.669+1078T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75580719 | |||||||
| chr14:75580777 | G | A | 2 | a0001c0001t0004g0163 a0001c0001t0004g0164 |
2 | HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.669+1136G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75580777 | |||||||
| chr14:75580863 | T | C | 9 | a0001c0001t0004g0175 a0001c0001t0004g0176 a0001c0001t0004g0177 others(6): Show |
9 | NA18947.hp2 NA18950.hp1 NA18967.hp1 others(6): Show |
intron_variant | MODIFIER | c.669+1222T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75580863 | |||||||
| chr14:75580876 | G | A | 33 | a0001c0001t0004g0175 a0001c0001t0004g0176 a0001c0001t0004g0177 others(30): Show |
33 | HG01175.hp1 HG01256.hp1 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.669+1235G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75580876 | |||||||
| chr14:75581054 | TA | T | 6 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.669+1414delA | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75581054 | |||||||
| chr14:75581055 | A | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(94): Show |
105 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.669+1414A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75581055 | |||||||
| chr14:75581061 | A | C | 6 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.669+1420A>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75581061 | |||||||
| chr14:75581144 | C | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
129 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.669+1503C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75581144 | |||||||
| chr14:75581178 | A | G | 1 | a0002c0002t0002g0160 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.669+1537A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75581178 | |||||||
| chr14:75581228 | A | T | 207 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(204): Show |
215 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.669+1587A>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75581228 | |||||||
| chr14:75581387 | G | A | 1 | a0001c0001t0004g0221 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.669+1746G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75581387 | |||||||
| chr14:75581419 | A | C | 46 | a0001c0001t0001g0314 a0001c0001t0004g0163 a0001c0001t0004g0164 others(43): Show |
46 | HG00609.hp1 HG01081.hp2 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.669+1778A>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75581419 | |||||||
| chr14:75581482 | T | C | 40 | a0001c0001t0001g0002 a0001c0001t0001g0231 a0001c0001t0001g0232 others(37): Show |
41 | HG01175.hp1 HG01256.hp1 HG01433.hp2 others(38): Show |
intron_variant | MODIFIER | c.669+1841T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75581482 | |||||||
| chr14:75581597 | G | A | 58 | a0001c0001t0004g0221 a0001c0001t0004g0222 a0001c0001t0004g0223 others(55): Show |
58 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.669+1956G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75581597 | |||||||
| chr14:75581679 | G | T | 1 | a0002c0002t0002g0106 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.669+2038G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75581679 | |||||||
| chr14:75581701 | C | T | 4 | a0001c0001t0004g0169 a0001c0001t0004g0171 a0001c0001t0004g0172 others(1): Show |
4 | HG01106.hp2 HG02486.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.669+2060C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75581701 | |||||||
| chr14:75581761 | T | A | 1 | a0001c0001t0018g0209 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.669+2120T>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75581761 | |||||||
| chr14:75581814 | A | G | 54 | a0002c0003t0003g0009 a0002c0003t0003g0108 a0002c0003t0003g0109 others(51): Show |
54 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.669+2173A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75581814 | |||||||
| chr14:75581888 | G | A | 4 | a0001c0001t0002g0211 a0001c0001t0002g0212 a0001c0001t0009g0210 others(1): Show |
4 | HG00323.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+2247G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75581888 | |||||||
| chr14:75582066 | G | A | 26 | a0001c0001t0004g0175 a0001c0001t0004g0176 a0001c0001t0004g0177 others(23): Show |
26 | HG01175.hp1 HG01256.hp1 HG02148.hp2 others(23): Show |
intron_variant | MODIFIER | c.669+2425G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75582066 | |||||||
| chr14:75582067 | T | A | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | HG02630.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.669+2426T>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75582067 | |||||||
| chr14:75582189 | T | C | 1 | a0002c0002t0002g0010 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.669+2548T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75582189 | |||||||
| chr14:75582280 | A | T | 4 | a0001c0001t0001g0002 a0001c0001t0001g0231 a0001c0001t0001g0232 others(1): Show |
5 | HG02109.hp2 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.669+2639A>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75582280 | |||||||
| chr14:75582368 | G | T | 2 | a0002c0002t0002g0104 a0002c0002t0002g0105 |
2 | HG02735.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.669+2727G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75582368 | |||||||
| chr14:75582400 | G | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(107): Show |
118 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.669+2759G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75582400 | |||||||
| chr14:75582413 | G | T | 7 | a0001c0001t0004g0201 a0001c0001t0004g0202 a0001c0001t0004g0203 others(4): Show |
7 | HG02055.hp1 HG02258.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.669+2772G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75582413 | |||||||
| chr14:75582423 | T | C | 4 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0236 others(1): Show |
4 | HG02280.hp2 HG02630.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.669+2782T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75582423 | |||||||
| chr14:75582425 | T | C | 1 | a0002c0003t0003g0108 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.669+2784T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75582425 | |||||||
| chr14:75582430 | C | G | 1 | a0001c0001t0001g0174 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.669+2789C>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75582430 | |||||||
| chr14:75582546 | G | A | 4 | a0001c0001t0004g0221 a0001c0001t0004g0222 a0001c0001t0004g0223 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+2905G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75582546 | |||||||
| chr14:75582626 | G | A | 2 | a0001c0001t0019g0324 a0002c0003t0003g0161 |
2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.669+2985G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75582626 | |||||||
| chr14:75582646 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.669+3005G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75582646 | |||||||
| chr14:75582771 | T | C | 1 | a0002c0003t0003g0109 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.669+3130T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75582771 | |||||||
| chr14:75582922 | A | AC | 3 | a0001c0001t0007g0325 a0001c0001t0007g0326 a0001c0001t0012g0327 |
3 | HG01433.hp2 HG02258.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.669+3282dupC | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75582922 | ||||||
| chr14:75582924 | G | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(91): Show |
102 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.669+3283G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75582924 | |||||||
| chr14:75582943 | T | C | 7 | a0001c0001t0004g0201 a0001c0001t0004g0202 a0001c0001t0004g0203 others(4): Show |
7 | HG02055.hp1 HG02258.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.669+3302T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75582943 | |||||||
| chr14:75582988 | G | A | 4 | a0001c0001t0004g0221 a0001c0001t0004g0222 a0001c0001t0004g0223 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+3347G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75582988 | |||||||
| chr14:75582991 | G | A | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
237 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.669+3350G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75582991 | |||||||
| chr14:75583468 | T | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0239 a0001c0001t0001g0240 others(2): Show |
6 | HG01074.hp2 HG01243.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.669+3827T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75583468 | |||||||
| chr14:75583601 | C | T | 4 | a0001c0001t0004g0221 a0001c0001t0004g0222 a0001c0001t0004g0223 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+3960C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75583601 | |||||||
| chr14:75583802 | G | A | 57 | a0001c0001t0001g0002 a0001c0001t0001g0231 a0001c0001t0001g0232 others(54): Show |
58 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.669+4161G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75583802 | |||||||
| chr14:75583955 | C | T | 2 | a0001c0001t0001g0308 a0001c0001t0001g0309 |
2 | NA18994.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.669+4314C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75583955 | |||||||
| chr14:75583993 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(88): Show |
99 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.669+4352G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75583993 | |||||||
| chr14:75584145 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.669+4504G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75584145 | |||||||
| chr14:75584192 | G | A | 1 | a0002c0003t0003g0161 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.669+4551G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75584192 | |||||||
| chr14:75584312 | C | T | 5 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(2): Show |
5 | HG02109.hp1 HG02451.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.669+4671C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75584312 | |||||||
| chr14:75584429 | C | T | 1 | a0001c0001t0004g0164 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.669+4788C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75584429 | |||||||
| chr14:75584449 | C | T | 1 | a0002c0002t0002g0102 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.669+4808C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75584449 | |||||||
| chr14:75584450 | G | A | 28 | a0001c0001t0001g0238 a0001c0001t0004g0175 a0001c0001t0004g0176 others(25): Show |
28 | HG00597.hp2 HG01175.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.669+4809G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75584450 | |||||||
| chr14:75584457 | C | T | 1 | a0002c0002t0002g0101 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.669+4816C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75584457 | |||||||
| chr14:75584503 | C | T | 11 | a0001c0001t0001g0305 a0001c0001t0002g0215 a0001c0001t0002g0216 others(8): Show |
11 | HG02683.hp1 HG02717.hp2 HG03491.hp2 others(8): Show |
intron_variant | MODIFIER | c.669+4862C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75584503 | |||||||
| chr14:75584504 | G | A | 2 | a0002c0002t0002g0014 a0002c0002t0002g0015 |
2 | NA18945.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.669+4863G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75584504 | |||||||
| chr14:75584538 | T | C | 4 | a0001c0001t0004g0221 a0001c0001t0004g0222 a0001c0001t0004g0223 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+4897T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75584538 | |||||||
| chr14:75584645 | G | A | 1 | a0002c0003t0003g0161 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.669+5004G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75584645 | |||||||
| chr14:75584716 | T | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(94): Show |
103 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.669+5075T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75584716 | |||||||
| chr14:75584732 | ACT | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0277 a0001c0001t0001g0278 others(21): Show |
27 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.669+5094_669+5095d others(4): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75584732 | ||||||
| chr14:75584742 | G | C | 1 | a0002c0002t0002g0025 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.669+5101G>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75584742 | |||||||
| chr14:75584946 | A | G | 2 | a0002c0002t0002g0099 a0002c0002t0002g0100 |
2 | NA18968.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.669+5305A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75584946 | |||||||
| chr14:75584961 | G | C | 57 | a0001c0001t0001g0002 a0001c0001t0001g0231 a0001c0001t0001g0232 others(54): Show |
58 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.669+5320G>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75584961 | |||||||
| chr14:75585118 | G | A | 1 | a0002c0003t0003g0112 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.669+5477G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75585118 | |||||||
| chr14:75585309 | T | C | 1 | a0001c0001t0001g0308 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.669+5668T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75585309 | |||||||
| chr14:75585344 | A | G | 4 | a0001c0001t0001g0321 a0001c0001t0007g0325 a0001c0001t0007g0326 others(1): Show |
4 | HG01433.hp2 HG02258.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+5703A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75585344 | |||||||
| chr14:75585629 | C | G | 1 | a0001c0001t0001g0174 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.669+5988C>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75585629 | |||||||
| chr14:75585645 | G | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(113): Show |
122 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.669+6004G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75585645 | |||||||
| chr14:75585651 | C | A | 1 | a0001c0001t0001g0174 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.669+6010C>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75585651 | |||||||
| chr14:75585672 | T | G | 5 | a0001c0001t0004g0203 a0001c0001t0004g0205 a0001c0001t0004g0207 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.669+6031T>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75585672 | |||||||
| chr14:75585685 | A | G | 64 | a0001c0001t0001g0002 a0001c0001t0001g0173 a0001c0001t0001g0225 others(61): Show |
65 | HG00408.hp1 HG01123.hp1 HG01243.hp1 others(62): Show |
intron_variant | MODIFIER | c.669+6044A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75585685 | |||||||
| chr14:75585715 | T | C | 9 | a0001c0001t0001g0243 a0001c0001t0001g0247 a0001c0001t0001g0248 others(6): Show |
9 | HG00639.hp2 HG00741.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.669+6074T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75585715 | |||||||
| chr14:75585719 | C | T | 1 | a0001c0001t0019g0324 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.669+6078C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75585719 | |||||||
| chr14:75585772 | C | T | 1 | a0002c0002t0002g0022 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.669+6131C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75585772 | |||||||
| chr14:75585784 | T | A | 10 | a0001c0001t0001g0305 a0001c0001t0002g0215 a0001c0001t0002g0216 others(7): Show |
10 | HG02683.hp1 HG03491.hp2 HG03492.hp1 others(7): Show |
intron_variant | MODIFIER | c.669+6143T>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75585784 | |||||||
| chr14:75585846 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.669+6205G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75585846 | |||||||
| chr14:75585860 | T | C | 31 | a0001c0001t0001g0174 a0001c0001t0001g0305 a0001c0001t0001g0321 others(28): Show |
31 | HG00323.hp2 HG01070.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.669+6219T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75585860 | |||||||
| chr14:75585874 | G | T | 4 | a0001c0001t0002g0211 a0001c0001t0002g0212 a0001c0001t0009g0210 others(1): Show |
4 | HG00323.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+6233G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75585874 | |||||||
| chr14:75585992 | A | C | 2 | a0001c0001t0001g0303 a0001c0001t0001g0304 |
2 | NA18967.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.669+6351A>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75585992 | |||||||
| chr14:75586079 | G | C | 1 | a0002c0002t0002g0026 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.669+6438G>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75586079 | |||||||
| chr14:75586148 | A | T | 2 | a0001c0001t0001g0301 a0002c0002t0002g0096 |
2 | HG01175.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.669+6507A>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75586148 | |||||||
| chr14:75586149 | G | A | 2 | a0001c0001t0001g0301 a0002c0002t0002g0096 |
2 | HG01175.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.669+6508G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75586149 | |||||||
| chr14:75586151 | C | T | 2 | a0001c0001t0001g0301 a0002c0002t0002g0096 |
2 | HG01175.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.669+6510C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75586151 | |||||||
| chr14:75586152 | A | G | 2 | a0001c0001t0001g0301 a0002c0002t0002g0096 |
2 | HG01175.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.669+6511A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75586152 | |||||||
| chr14:75586162 | C | T | 1 | a0002c0002t0002g0095 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.669+6521C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75586162 | |||||||
| chr14:75586254 | G | GGGT | 6 | a0001c0001t0004g0203 a0001c0001t0004g0205 a0001c0001t0004g0207 others(3): Show |
6 | HG02055.hp1 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.669+6616_669+6618d others(5): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75586254 | ||||||
| chr14:75586447 | G | T | 1 | a0001c0001t0015g0307 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.669+6806G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75586447 | |||||||
| chr14:75586449 | G | C | 4 | a0001c0001t0001g0002 a0001c0001t0001g0231 a0001c0001t0001g0232 others(1): Show |
5 | HG02109.hp2 HG02572.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.669+6808G>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75586449 | |||||||
| chr14:75586560 | C | A | 1 | a0001c0001t0001g0253 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.669+6919C>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75586560 | |||||||
| chr14:75586861 | C | T | 1 | a0002c0002t0002g0094 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.669+7220C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75586861 | |||||||
| chr14:75586877 | C | T | 1 | a0001c0001t0019g0324 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.669+7236C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75586877 | |||||||
| chr14:75586890 | A | C | 6 | a0001c0001t0004g0203 a0001c0001t0004g0205 a0001c0001t0004g0207 others(3): Show |
6 | HG02055.hp1 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.669+7249A>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75586890 | |||||||
| chr14:75587369 | C | T | 1 | a0002c0003t0003g0161 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.669+7728C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75587369 | |||||||
| chr14:75587416 | T | A | 2 | a0001c0001t0001g0173 a0001c0001t0001g0322 |
2 | HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.669+7775T>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75587416 | |||||||
| chr14:75587617 | A | G | 1 | a0002c0003t0003g0156 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.669+7976A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75587617 | |||||||
| chr14:75587715 | A | T | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.669+8074A>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75587715 | |||||||
| chr14:75587771 | A | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(199): Show |
209 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.669+8130A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75587771 | |||||||
| chr14:75587888 | C | G | 2 | a0002c0002t0002g0090 a0002c0002t0002g0091 |
2 | HG03017.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.669+8247C>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75587888 | |||||||
| chr14:75588077 | T | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0174 a0001c0001t0001g0231 others(52): Show |
56 | HG00408.hp1 HG01106.hp2 HG01123.hp1 others(53): Show |
intron_variant | MODIFIER | c.669+8436T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75588077 | |||||||
| chr14:75588091 | T | C | 2 | a0002c0002t0002g0072 a0002c0002t0002g0073 |
2 | HG00558.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.669+8450T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75588091 | |||||||
| chr14:75588159 | A | T | 1 | a0003c0004t0005g0165 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.669+8518A>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75588159 | |||||||
| chr14:75588313 | G | A | 1 | a0003c0004t0005g0165 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.669+8672G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75588313 | |||||||
| chr14:75588381 | C | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0231 a0001c0001t0001g0232 others(58): Show |
62 | HG00408.hp1 HG01106.hp2 HG01123.hp1 others(59): Show |
intron_variant | MODIFIER | c.669+8740C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75588381 | |||||||
| chr14:75588394 | C | A | 1 | a0001c0001t0004g0185 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.669+8753C>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75588394 | |||||||
| chr14:75588503 | A | G | 3 | a0002c0002t0002g0100 a0002c0003t0003g0154 a0002c0003t0003g0155 |
3 | NA18968.hp1 NA19055.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.669+8862A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75588503 | |||||||
| chr14:75588721 | C | T | 11 | a0001c0001t0001g0305 a0001c0001t0002g0215 a0001c0001t0002g0216 others(8): Show |
11 | HG02683.hp1 HG02717.hp2 HG03491.hp2 others(8): Show |
intron_variant | MODIFIER | c.669+9080C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75588721 | |||||||
| chr14:75588758 | C | T | 1 | a0001c0001t0004g0198 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.669+9117C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75588758 | |||||||
| chr14:75588759 | G | T | 10 | a0001c0001t0001g0305 a0001c0001t0002g0215 a0001c0001t0002g0216 others(7): Show |
10 | HG02683.hp1 HG03491.hp2 HG03492.hp1 others(7): Show |
intron_variant | MODIFIER | c.669+9118G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75588759 | |||||||
| chr14:75589048 | A | AT | 8 | a0001c0001t0001g0174 a0001c0001t0001g0306 a0001c0001t0002g0211 others(5): Show |
8 | HG00323.hp2 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.669+9418dupT | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75589048 | ||||||
| chr14:75589048 | AT | A | 6 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(3): Show |
6 | HG02109.hp1 HG02451.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.669+9418delT | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75589048 | ||||||
| chr14:75589059 | T | A | 54 | a0001c0001t0001g0002 a0001c0001t0001g0231 a0001c0001t0001g0232 others(51): Show |
55 | HG00408.hp1 HG01106.hp2 HG01123.hp1 others(52): Show |
intron_variant | MODIFIER | c.669+9418T>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75589059 | |||||||
| chr14:75589060 | A | T | 11 | a0001c0001t0001g0305 a0001c0001t0002g0215 a0001c0001t0002g0216 others(8): Show |
11 | HG02683.hp1 HG02717.hp2 HG03491.hp2 others(8): Show |
intron_variant | MODIFIER | c.669+9419A>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75589060 | |||||||
| chr14:75589080 | G | A | 11 | a0001c0001t0001g0305 a0001c0001t0002g0215 a0001c0001t0002g0216 others(8): Show |
11 | HG02683.hp1 HG02717.hp2 HG03491.hp2 others(8): Show |
intron_variant | MODIFIER | c.669+9439G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75589080 | |||||||
| chr14:75589122 | A | G | 3 | a0001c0001t0004g0171 a0001c0001t0004g0172 a0001c0001t0017g0170 |
3 | HG01106.hp2 HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.669+9481A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75589122 | |||||||
| chr14:75589168 | T | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
202 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.669+9527T>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75589168 | |||||||
| chr14:75589269 | G | A | 7 | a0001c0001t0001g0277 a0002c0002t0002g0016 a0002c0002t0002g0074 others(4): Show |
7 | HG00099.hp1 HG00642.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.669+9628G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75589269 | |||||||
| chr14:75589362 | C | T | 1 | a0002c0002t0002g0099 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.669+9721C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75589362 | |||||||
| chr14:75589656 | C | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
125 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.669+10015C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75589656 | |||||||
| chr14:75589712 | T | C | 1 | a0001c0001t0019g0324 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.669+10071T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75589712 | |||||||
| chr14:75589754 | C | T | 4 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0219 others(1): Show |
4 | HG03669.hp2 HG04115.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+10113C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75589754 | |||||||
| chr14:75589805 | T | C | 3 | a0001c0001t0001g0321 a0001c0001t0007g0325 a0001c0001t0007g0326 |
3 | HG01433.hp2 HG02602.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.669+10164T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75589805 | |||||||
| chr14:75589952 | C | T | 1 | a0002c0003t0003g0152 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.669+10311C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75589952 | |||||||
| chr14:75589992 | C | T | 11 | a0001c0001t0001g0305 a0001c0001t0002g0215 a0001c0001t0002g0216 others(8): Show |
11 | HG02683.hp1 HG02717.hp2 HG03491.hp2 others(8): Show |
intron_variant | MODIFIER | c.669+10351C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75589992 | |||||||
| chr14:75590129 | G | A | 1 | a0003c0004t0005g0165 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.669+10488G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75590129 | |||||||
| chr14:75590485 | C | T | 1 | a0002c0002t0002g0160 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.669+10844C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75590485 | |||||||
| chr14:75590711 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.669+11070T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75590711 | |||||||
| chr14:75591039 | G | C | 1 | a0002c0002t0002g0027 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.669+11398G>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75591039 | |||||||
| chr14:75591076 | C | T | 2 | a0001c0001t0004g0224 a0001c0001t0012g0327 |
2 | HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.669+11435C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75591076 | |||||||
| chr14:75591179 | A | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(188): Show |
198 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.669+11538A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75591179 | |||||||
| chr14:75591242 | C | T | 2 | a0001c0001t0004g0221 a0001c0001t0004g0223 |
2 | HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.669+11601C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75591242 | |||||||
| chr14:75591297 | C | A | 1 | a0002c0003t0003g0156 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.669+11656C>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75591297 | |||||||
| chr14:75591457 | C | CCATGGCT others(44): Show |
1 | a0002c0002t0002g0071 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.669+11868_669+1191 others(55): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75591457 | ||||||
| chr14:75591457 | CCATGGCT others(44): Show |
C | 1 | a0001c0001t0004g0164 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.669+11868_669+1191 others(55): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75591457 | ||||||
| chr14:75591489 | G | A | 1 | a0001c0001t0004g0186 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.669+11848G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75591489 | |||||||
| chr14:75591627 | G | A | 1 | a0002c0002t0002g0028 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.669+11986G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75591627 | |||||||
| chr14:75591675 | C | A | 1 | a0001c0001t0004g0164 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.669+12034C>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75591675 | |||||||
| chr14:75591718 | G | A | 5 | a0002c0003t0003g0108 a0002c0003t0003g0122 a0002c0003t0003g0123 others(2): Show |
5 | HG02257.hp2 HG02559.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.669+12077G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75591718 | |||||||
| chr14:75591778 | C | T | 1 | a0002c0002t0002g0070 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.669+12137C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75591778 | |||||||
| chr14:75591806 | C | CT | 30 | a0001c0001t0001g0275 a0001c0001t0001g0295 a0001c0001t0001g0300 others(27): Show |
30 | HG00639.hp1 HG00741.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.669+12190dupT | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75591806 | ||||||
| chr14:75591806 | CT | C | 20 | a0001c0001t0001g0244 a0001c0001t0001g0255 a0001c0001t0001g0256 others(17): Show |
20 | HG01255.hp2 HG01256.hp1 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.669+12190delT | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75591806 | ||||||
| chr14:75591806 | CTTTTT | C | 6 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(3): Show |
6 | HG02109.hp1 HG02451.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.669+12186_669+1219 others(9): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75591806 | ||||||
| chr14:75591832 | G | T | 1 | a0001c0001t0001g0236 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.669+12191G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75591832 | |||||||
| chr14:75591838 | G | T | 1 | a0001c0001t0004g0164 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.669+12197G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75591838 | |||||||
| chr14:75591841 | T | A | 6 | a0001c0001t0001g0244 a0002c0002t0002g0032 a0002c0002t0002g0033 others(3): Show |
6 | NA18949.hp1 NA18972.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.669+12200T>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75591841 | |||||||
| chr14:75591874 | T | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
201 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.669+12233T>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75591874 | |||||||
| chr14:75591947 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.669+12306G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75591947 | |||||||
| chr14:75592036 | G | T | 1 | a0002c0003t0003g0112 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.669+12395G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75592036 | |||||||
| chr14:75592223 | A | T | 1 | a0002c0002t0002g0027 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.669+12582A>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75592223 | |||||||
| chr14:75592297 | T | C | 2 | a0001c0001t0001g0173 a0001c0001t0001g0322 |
2 | HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.669+12656T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75592297 | |||||||
| chr14:75592333 | A | G | 1 | a0001c0001t0004g0222 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.669+12692A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75592333 | |||||||
| chr14:75592386 | G | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
131 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.669+12745G>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75592386 | |||||||
| chr14:75592448 | T | C | 1 | a0001c0001t0004g0201 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.669+12807T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75592448 | |||||||
| chr14:75592635 | T | G | 1 | a0002c0002t0002g0027 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.669+12994T>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75592635 | |||||||
| chr14:75592661 | C | A | 4 | a0001c0001t0002g0211 a0001c0001t0002g0212 a0001c0001t0009g0210 others(1): Show |
4 | HG00323.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+13020C>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75592661 | |||||||
| chr14:75592726 | T | C | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(197): Show |
207 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.669+13085T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75592726 | |||||||
| chr14:75592763 | C | T | 8 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(5): Show |
8 | HG01884.hp2 HG02109.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.669+13122C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75592763 | |||||||
| chr14:75592764 | G | A | 47 | a0001c0001t0001g0002 a0001c0001t0001g0231 a0001c0001t0001g0232 others(44): Show |
48 | HG00408.hp1 HG01123.hp1 HG01257.hp2 others(45): Show |
intron_variant | MODIFIER | c.669+13123G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75592764 | |||||||
| chr14:75592821 | T | A | 1 | a0001c0001t0001g0279 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.669+13180T>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75592821 | |||||||
| chr14:75592864 | T | A | 1 | a0002c0002t0002g0027 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.669+13223T>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75592864 | |||||||
| chr14:75592993 | A | G | 1 | a0002c0002t0002g0027 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.669+13352A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75592993 | |||||||
| chr14:75593072 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.669+13431C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75593072 | |||||||
| chr14:75593113 | A | G | 1 | a0001c0001t0004g0164 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.669+13472A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75593113 | |||||||
| chr14:75593139 | A | C | 1 | a0002c0002t0002g0027 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.669+13498A>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75593139 | |||||||
| chr14:75593188 | C | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
125 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.669+13547C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75593188 | |||||||
| chr14:75593451 | G | A | 3 | a0001c0001t0001g0321 a0001c0001t0007g0325 a0001c0001t0007g0326 |
3 | HG01433.hp2 HG02602.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.669+13810G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75593451 | |||||||
| chr14:75593594 | C | A | 1 | a0001c0001t0001g0258 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.669+13953C>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75593594 | |||||||
| chr14:75593755 | A | C | 1 | a0001c0001t0001g0174 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.669+14114A>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75593755 | |||||||
| chr14:75593838 | G | A | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(205): Show |
215 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.669+14197G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75593838 | |||||||
| chr14:75594041 | C | T | 56 | a0001c0001t0001g0002 a0001c0001t0001g0231 a0001c0001t0001g0232 others(53): Show |
57 | HG00408.hp1 HG01106.hp2 HG01123.hp1 others(54): Show |
intron_variant | MODIFIER | c.669+14400C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75594041 | |||||||
| chr14:75594206 | T | TAACTGTC others(317): Show |
4 | a0001c0001t0002g0211 a0001c0001t0002g0212 a0001c0001t0009g0210 others(1): Show |
4 | HG00323.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+14581_669+1458 others(328): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75594206 | ||||||
| chr14:75594425 | A | G | 1 | a0003c0004t0005g0165 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.669+14784A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75594425 | |||||||
| chr14:75594538 | TG | T | 3 | a0001c0001t0001g0174 a0001c0001t0015g0307 a0002c0003t0003g0161 |
3 | HG02630.hp1 HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.669+14899delG | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75594538 | ||||||
| chr14:75594721 | C | CT | 44 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(41): Show |
47 | HG01106.hp2 HG01109.hp1 HG02015.hp2 others(44): Show |
intron_variant | MODIFIER | c.669+15095dupT | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75594721 | ||||||
| chr14:75594721 | CT | C | 17 | a0001c0001t0001g0305 a0001c0001t0001g0310 a0001c0001t0002g0211 others(14): Show |
17 | HG00323.hp2 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.669+15095delT | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75594721 | ||||||
| chr14:75594819 | G | A | 2 | a0001c0001t0004g0163 a0001c0001t0004g0222 |
2 | HG02895.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.669+15178G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75594819 | |||||||
| chr14:75594964 | C | T | 18 | a0001c0001t0001g0225 a0001c0001t0001g0234 a0001c0001t0001g0235 others(15): Show |
18 | HG00323.hp2 HG01070.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.669+15323C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75594964 | |||||||
| chr14:75595040 | T | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
225 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.669+15399T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75595040 | |||||||
| chr14:75595068 | T | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(107): Show |
116 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.669+15427T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75595068 | |||||||
| chr14:75595232 | C | G | 2 | a0001c0001t0001g0321 a0001c0001t0007g0326 |
2 | HG02602.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.669+15591C>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75595232 | |||||||
| chr14:75595345 | A | C | 1 | a0002c0002t0002g0091 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.669+15704A>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75595345 | |||||||
| chr14:75595392 | G | T | 1 | a0001c0001t0001g0306 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.669+15751G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75595392 | |||||||
| chr14:75595461 | A | G | 1 | a0002c0002t0002g0065 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.669+15820A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75595461 | |||||||
| chr14:75595581 | G | A | 1 | a0001c0001t0004g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.669+15940G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75595581 | |||||||
| chr14:75595797 | C | T | 1 | a0002c0002t0002g0064 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.669+16156C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75595797 | |||||||
| chr14:75596231 | C | T | 1 | a0002c0003t0003g0161 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.669+16590C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75596231 | |||||||
| chr14:75596248 | A | C | 2 | a0001c0001t0004g0164 a0001c0001t0010g0318 |
2 | HG02145.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.669+16607A>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75596248 | |||||||
| chr14:75596255 | G | A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
222 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.669+16614G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75596255 | |||||||
| chr14:75596306 | C | A | 6 | a0001c0001t0001g0225 a0001c0001t0001g0234 a0001c0001t0001g0235 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.669+16665C>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75596306 | |||||||
| chr14:75596310 | A | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
222 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.669+16669A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75596310 | |||||||
| chr14:75596339 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.669+16698C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75596339 | |||||||
| chr14:75596463 | T | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
225 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.669+16822T>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75596463 | |||||||
| chr14:75596502 | A | G | 52 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(49): Show |
55 | HG01106.hp2 HG01109.hp1 HG02015.hp2 others(52): Show |
intron_variant | MODIFIER | c.669+16861A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75596502 | |||||||
| chr14:75596572 | G | A | 4 | a0001c0001t0002g0211 a0001c0001t0002g0212 a0001c0001t0009g0210 others(1): Show |
4 | HG00323.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+16931G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75596572 | |||||||
| chr14:75596748 | A | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
226 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.669+17107A>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75596748 | |||||||
| chr14:75596778 | T | C | 1 | a0002c0002t0002g0036 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.669+17137T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75596778 | |||||||
| chr14:75596779 | T | TGC | 3 | a0001c0001t0001g0247 a0002c0002t0002g0023 a0002c0002t0002g0024 |
3 | HG01168.hp2 HG01169.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.669+17139_669+1714 others(6): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75596779 | ||||||
| chr14:75596780 | G | GC | 119 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0174 others(116): Show |
121 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.669+17151dupC | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75596780 | ||||||
| chr14:75596780 | GC | G | 18 | a0001c0001t0001g0233 a0001c0001t0001g0272 a0001c0001t0002g0215 others(15): Show |
18 | HG01074.hp1 HG01106.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.669+17151delC | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75596780 | ||||||
| chr14:75596781 | C | CG | 13 | a0001c0001t0001g0243 a0001c0001t0001g0248 a0001c0001t0001g0249 others(10): Show |
13 | HG00408.hp1 HG00639.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.669+17140_669+1714 others(5): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75596781 | |||||||
| chr14:75596782 | C | G | 7 | a0001c0001t0004g0168 a0001c0001t0004g0221 a0002c0003t0003g0130 others(4): Show |
7 | HG01123.hp1 HG01243.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.669+17141C>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75596782 | |||||||
| chr14:75596783 | C | G | 2 | a0001c0001t0004g0201 a0001c0001t0010g0318 |
2 | HG02622.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.669+17142C>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75596783 | |||||||
| chr14:75596792 | C | G | 1 | a0002c0003t0003g0162 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.669+17151C>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75596792 | |||||||
| chr14:75596829 | T | C | 11 | a0001c0001t0001g0248 a0001c0001t0002g0218 a0002c0003t0003g0128 others(8): Show |
11 | HG00408.hp1 HG01123.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.669+17188T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75596829 | |||||||
| chr14:75597000 | C | T | 1 | a0003c0004t0005g0165 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.669+17359C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75597000 | |||||||
| chr14:75597001 | A | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
226 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.669+17360A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75597001 | |||||||
| chr14:75597252 | A | G | 45 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(42): Show |
48 | HG01106.hp2 HG01109.hp1 HG02015.hp2 others(45): Show |
intron_variant | MODIFIER | c.669+17611A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75597252 | |||||||
| chr14:75597291 | AAAG | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
179 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.669+17669_669+1767 others(7): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75597291 | ||||||
| chr14:75597376 | C | T | 11 | a0001c0001t0001g0308 a0002c0002t0002g0035 a0002c0002t0002g0066 others(8): Show |
11 | HG02040.hp1 HG02071.hp1 NA18941.hp1 others(8): Show |
intron_variant | MODIFIER | c.669+17735C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75597376 | |||||||
| chr14:75597395 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.669+17754G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75597395 | |||||||
| chr14:75597516 | G | A | 13 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0002g0211 others(10): Show |
13 | HG00323.hp2 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.669+17875G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75597516 | |||||||
| chr14:75597531 | G | C | 1 | a0001c0001t0001g0265 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.669+17890G>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75597531 | |||||||
| chr14:75597577 | C | CT | 53 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(50): Show |
56 | HG01106.hp2 HG01109.hp1 HG02015.hp2 others(53): Show |
intron_variant | MODIFIER | c.669+17946dupT | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75597577 | ||||||
| chr14:75597771 | T | C | 15 | a0001c0001t0001g0174 a0001c0001t0001g0225 a0001c0001t0001g0234 others(12): Show |
15 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.669+18130T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75597771 | |||||||
| chr14:75597775 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.669+18134G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75597775 | |||||||
| chr14:75597812 | C | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(106): Show |
115 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.669+18171C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75597812 | |||||||
| chr14:75597995 | G | C | 1 | a0001c0001t0002g0219 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.669+18354G>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75597995 | |||||||
| chr14:75598267 | G | A | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
224 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.669+18626G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75598267 | |||||||
| chr14:75598281 | G | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(105): Show |
114 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.669+18640G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75598281 | |||||||
| chr14:75598580 | C | T | 5 | a0001c0001t0004g0203 a0001c0001t0004g0205 a0001c0001t0004g0207 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.669+18939C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75598580 | |||||||
| chr14:75598713 | C | T | 53 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(50): Show |
56 | HG01106.hp2 HG01109.hp1 HG02015.hp2 others(53): Show |
intron_variant | MODIFIER | c.669+19072C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75598713 | |||||||
| chr14:75598752 | A | C | 25 | a0001c0001t0001g0243 a0001c0001t0001g0247 a0001c0001t0001g0248 others(22): Show |
25 | HG00408.hp1 HG00639.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.669+19111A>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75598752 | |||||||
| chr14:75598772 | C | T | 2 | a0002c0002t0002g0100 a0002c0003t0003g0110 |
2 | NA18968.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.669+19131C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75598772 | |||||||
| chr14:75598833 | A | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
191 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.669+19192A>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75598833 | |||||||
| chr14:75599090 | C | T | 5 | a0001c0001t0004g0203 a0001c0001t0004g0205 a0001c0001t0004g0207 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.669+19449C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75599090 | |||||||
| chr14:75599169 | A | G | 2 | a0001c0001t0002g0215 a0001c0001t0002g0216 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.669+19528A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75599169 | |||||||
| chr14:75599220 | T | C | 5 | a0002c0002t0002g0012 a0002c0002t0002g0018 a0002c0002t0002g0021 others(2): Show |
5 | HG01106.hp1 HG01109.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.669+19579T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75599220 | |||||||
| chr14:75599326 | A | AC | 104 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(101): Show |
110 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.669+19694dupC | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75599326 | ||||||
| chr14:75599333 | C | CA | 4 | a0001c0001t0001g0260 a0001c0001t0001g0266 a0002c0003t0003g0113 others(1): Show |
4 | HG00140.hp2 HG01516.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.669+19692_669+1969 others(5): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75599333 | |||||||
| chr14:75599335 | C | A | 7 | a0001c0001t0001g0225 a0001c0001t0001g0234 a0001c0001t0001g0235 others(4): Show |
7 | HG01884.hp2 HG02280.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.669+19694C>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75599335 | |||||||
| chr14:75599336 | A | C | 1 | a0001c0001t0001g0252 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.669+19695A>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75599336 | |||||||
| chr14:75599492 | C | T | 1 | a0001c0001t0002g0212 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.669+19851C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75599492 | |||||||
| chr14:75599493 | G | A | 25 | a0001c0001t0001g0243 a0001c0001t0001g0247 a0001c0001t0001g0248 others(22): Show |
25 | HG00408.hp1 HG00639.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.669+19852G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75599493 | |||||||
| chr14:75599687 | C | T | 5 | a0001c0001t0004g0203 a0001c0001t0004g0205 a0001c0001t0004g0207 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.669+20046C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75599687 | |||||||
| chr14:75599811 | G | A | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
225 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.669+20170G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75599811 | |||||||
| chr14:75599948 | C | T | 3 | a0001c0001t0001g0173 a0001c0001t0001g0247 a0001c0001t0001g0322 |
3 | HG02004.hp1 HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.669+20307C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75599948 | |||||||
| chr14:75599982 | G | A | 2 | a0001c0001t0004g0164 a0001c0001t0010g0318 |
2 | HG02145.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.669+20341G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75599982 | |||||||
| chr14:75600040 | G | A | 13 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0002g0211 others(10): Show |
13 | HG00323.hp2 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.669+20399G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75600040 | |||||||
| chr14:75600237 | T | C | 3 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 |
3 | HG01168.hp1 HG01496.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.669+20596T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75600237 | |||||||
| chr14:75600263 | T | G | 2 | a0002c0002t0002g0087 a0002c0002t0002g0089 |
2 | HG01074.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.669+20622T>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75600263 | |||||||
| chr14:75600283 | G | T | 2 | a0002c0002t0002g0087 a0002c0002t0002g0089 |
2 | HG01074.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.669+20642G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75600283 | |||||||
| chr14:75600312 | C | T | 6 | a0001c0001t0001g0225 a0001c0001t0001g0234 a0001c0001t0001g0235 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.669+20671C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75600312 | |||||||
| chr14:75600334 | T | A | 1 | a0001c0001t0004g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.669+20693T>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75600334 | |||||||
| chr14:75600641 | G | A | 25 | a0001c0001t0001g0243 a0001c0001t0001g0247 a0001c0001t0001g0248 others(22): Show |
25 | HG00408.hp1 HG00639.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.669+21000G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75600641 | |||||||
| chr14:75600769 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.669+21128A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75600769 | |||||||
| chr14:75600796 | G | A | 2 | a0001c0001t0002g0217 a0001c0001t0002g0220 |
2 | HG03669.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.669+21155G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75600796 | |||||||
| chr14:75600874 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.670-21205C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75600874 | |||||||
| chr14:75600876 | CA | C | 37 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(34): Show |
37 | HG00408.hp1 HG00639.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.670-21192delA | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75600876 | ||||||
| chr14:75600884 | A | C | 3 | a0001c0001t0001g0314 a0001c0001t0004g0196 a0002c0002t0002g0013 |
3 | HG02071.hp2 NA18963.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.670-21195A>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75600884 | |||||||
| chr14:75600946 | G | A | 1 | a0001c0001t0004g0180 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.670-21133G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75600946 | |||||||
| chr14:75600978 | C | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
225 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.670-21101C>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75600978 | |||||||
| chr14:75601030 | G | A | 1 | a0002c0002t0002g0029 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.670-21049G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75601030 | |||||||
| chr14:75601258 | G | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(22): Show |
28 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.670-20821G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75601258 | |||||||
| chr14:75601283 | T | G | 1 | a0001c0001t0004g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.670-20796T>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75601283 | |||||||
| chr14:75601302 | C | G | 1 | a0001c0001t0001g0305 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.670-20777C>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75601302 | |||||||
| chr14:75601351 | T | A | 1 | a0001c0001t0019g0324 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.670-20728T>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75601351 | |||||||
| chr14:75601453 | C | T | 2 | a0002c0002t0002g0087 a0002c0002t0002g0089 |
2 | HG01074.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.670-20626C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75601453 | |||||||
| chr14:75601806 | G | A | 1 | a0002c0003t0003g0161 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.670-20273G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75601806 | |||||||
| chr14:75601961 | A | G | 5 | a0001c0001t0004g0203 a0001c0001t0004g0205 a0001c0001t0004g0207 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-20118A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75601961 | |||||||
| chr14:75602040 | T | A | 1 | a0002c0002t0002g0094 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.670-20039T>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75602040 | |||||||
| chr14:75602167 | A | G | 1 | a0001c0001t0012g0327 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.670-19912A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75602167 | |||||||
| chr14:75602200 | T | C | 1 | a0001c0001t0004g0192 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.670-19879T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75602200 | |||||||
| chr14:75602225 | C | T | 3 | a0002c0002t0002g0065 a0002c0002t0002g0090 a0002c0002t0002g0091 |
3 | HG03017.hp2 HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.670-19854C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75602225 | |||||||
| chr14:75602683 | G | A | 1 | a0003c0004t0005g0165 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.670-19396G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75602683 | |||||||
| chr14:75602684 | G | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
179 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.670-19395G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75602684 | |||||||
| chr14:75602787 | C | T | 13 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0002g0211 others(10): Show |
13 | HG00323.hp2 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.670-19292C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75602787 | |||||||
| chr14:75602829 | A | G | 1 | a0001c0001t0004g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.670-19250A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75602829 | |||||||
| chr14:75602859 | C | T | 1 | a0001c0001t0004g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.670-19220C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75602859 | |||||||
| chr14:75603155 | G | A | 1 | a0002c0002t0002g0092 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.670-18924G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75603155 | |||||||
| chr14:75603190 | C | T | 2 | a0001c0001t0004g0164 a0001c0001t0010g0318 |
2 | HG02145.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.670-18889C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75603190 | |||||||
| chr14:75603367 | G | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
173 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.670-18712G>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75603367 | |||||||
| chr14:75603384 | G | A | 1 | a0001c0001t0001g0312 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.670-18695G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75603384 | |||||||
| chr14:75603463 | G | A | 24 | a0001c0001t0001g0225 a0001c0001t0001g0234 a0001c0001t0001g0235 others(21): Show |
24 | HG00323.hp2 HG01070.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.670-18616G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75603463 | |||||||
| chr14:75603516 | C | CTTTTATT others(3): Show |
1 | a0002c0002t0002g0085 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.670-18562_670-1856 others(14): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75603516 | ||||||
| chr14:75603518 | G | T | 1 | a0002c0002t0002g0085 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.670-18561G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75603518 | |||||||
| chr14:75603519 | C | T | 1 | a0002c0002t0002g0085 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.670-18560C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75603519 | |||||||
| chr14:75603601 | T | A | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
225 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.670-18478T>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75603601 | |||||||
| chr14:75604081 | T | C | 18 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0002g0211 others(15): Show |
18 | HG00323.hp2 HG01070.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.670-17998T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75604081 | |||||||
| chr14:75604323 | G | A | 2 | a0002c0003t0023g0157 a0003c0004t0005g0165 |
2 | HG02886.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.670-17756G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75604323 | |||||||
| chr14:75604562 | TA | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
172 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.670-17505delA | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75604562 | ||||||
| chr14:75604758 | G | A | 25 | a0001c0001t0001g0243 a0001c0001t0001g0247 a0001c0001t0001g0248 others(22): Show |
25 | HG00408.hp1 HG00639.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.670-17321G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75604758 | |||||||
| chr14:75604766 | C | T | 25 | a0001c0001t0001g0243 a0001c0001t0001g0247 a0001c0001t0001g0248 others(22): Show |
25 | HG00408.hp1 HG00639.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.670-17313C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75604766 | |||||||
| chr14:75604887 | T | C | 5 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(2): Show |
5 | HG02109.hp1 HG02451.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-17192T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75604887 | |||||||
| chr14:75604896 | G | A | 2 | a0001c0001t0008g0296 a0002c0002t0002g0050 |
2 | HG01070.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.670-17183G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75604896 | |||||||
| chr14:75604938 | G | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(106): Show |
115 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.670-17141G>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75604938 | |||||||
| chr14:75604975 | C | T | 1 | a0002c0002t0002g0099 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.670-17104C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75604975 | |||||||
| chr14:75605006 | A | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
172 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.670-17073A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75605006 | |||||||
| chr14:75605351 | C | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(105): Show |
114 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.670-16728C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75605351 | |||||||
| chr14:75605572 | T | C | 3 | a0001c0001t0004g0166 a0001c0001t0004g0167 a0001c0001t0004g0168 |
3 | HG01081.hp2 HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.670-16507T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75605572 | |||||||
| chr14:75605613 | G | A | 1 | a0001c0001t0001g0302 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.670-16466G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75605613 | |||||||
| chr14:75605685 | T | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
225 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.670-16394T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75605685 | |||||||
| chr14:75605738 | A | T | 1 | a0001c0001t0004g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.670-16341A>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75605738 | |||||||
| chr14:75605872 | G | T | 7 | a0001c0001t0001g0225 a0001c0001t0001g0234 a0001c0001t0001g0235 others(4): Show |
7 | HG01884.hp2 HG02280.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.670-16207G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75605872 | |||||||
| chr14:75605936 | G | A | 2 | a0001c0001t0001g0288 a0001c0001t0004g0179 |
2 | NA19068.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.670-16143G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75605936 | |||||||
| chr14:75606031 | G | A | 1 | a0002c0002t0002g0011 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.670-16048G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75606031 | |||||||
| chr14:75606075 | G | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
223 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.670-16004G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75606075 | |||||||
| chr14:75606229 | G | A | 5 | a0001c0001t0004g0203 a0001c0001t0004g0205 a0001c0001t0004g0207 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-15850G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75606229 | |||||||
| chr14:75606367 | G | C | 1 | a0001c0001t0015g0307 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.670-15712G>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75606367 | |||||||
| chr14:75606373 | G | A | 12 | a0001c0001t0001g0225 a0001c0001t0001g0234 a0001c0001t0001g0235 others(9): Show |
12 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.670-15706G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75606373 | |||||||
| chr14:75606471 | AC | A | 7 | a0001c0001t0001g0244 a0002c0002t0002g0014 a0002c0002t0002g0015 others(4): Show |
7 | NA18945.hp1 NA18988.hp2 NA19005.hp1 others(4): Show |
intron_variant | MODIFIER | c.670-15607delC | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75606471 | |||||||
| chr14:75606541 | T | C | 1 | a0001c0001t0010g0318 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.670-15538T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75606541 | |||||||
| chr14:75606542 | A | C | 1 | a0001c0001t0010g0318 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.670-15537A>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75606542 | |||||||
| chr14:75606575 | C | A | 12 | a0001c0001t0001g0225 a0001c0001t0001g0234 a0001c0001t0001g0235 others(9): Show |
12 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.670-15504C>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75606575 | |||||||
| chr14:75606688 | A | G | 1 | a0001c0001t0004g0164 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.670-15391A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75606688 | |||||||
| chr14:75606850 | T | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
223 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.670-15229T>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75606850 | |||||||
| chr14:75607128 | C | T | 1 | a0001c0001t0010g0318 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.670-14951C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75607128 | |||||||
| chr14:75607281 | T | C | 25 | a0001c0001t0001g0243 a0001c0001t0001g0247 a0001c0001t0001g0248 others(22): Show |
25 | HG00408.hp1 HG00639.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.670-14798T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75607281 | |||||||
| chr14:75607409 | G | T | 1 | a0002c0003t0003g0117 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.670-14670G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75607409 | |||||||
| chr14:75607538 | C | T | 1 | a0002c0002t0002g0097 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.670-14541C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75607538 | |||||||
| chr14:75607595 | T | C | 1 | a0002c0003t0003g0117 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.670-14484T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75607595 | |||||||
| chr14:75607779 | A | G | 6 | a0001c0001t0001g0314 a0001c0001t0004g0177 a0001c0001t0004g0178 others(3): Show |
6 | HG02071.hp2 NA18950.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.670-14300A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75607779 | |||||||
| chr14:75607796 | G | A | 5 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0289 others(2): Show |
5 | NA18979.hp1 NA19011.hp1 NA19082.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-14283G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75607796 | |||||||
| chr14:75608140 | T | C | 2 | a0001c0001t0004g0164 a0001c0001t0010g0318 |
2 | HG02145.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.670-13939T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75608140 | |||||||
| chr14:75608153 | T | C | 1 | a0002c0003t0003g0117 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.670-13926T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75608153 | |||||||
| chr14:75608209 | A | G | 1 | a0002c0002t0002g0048 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.670-13870A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75608209 | |||||||
| chr14:75608312 | C | T | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
184 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.670-13767C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75608312 | |||||||
| chr14:75608344 | C | T | 1 | a0001c0001t0010g0319 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.670-13735C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75608344 | |||||||
| chr14:75608555 | G | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
222 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.670-13524G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75608555 | |||||||
| chr14:75608808 | G | A | 1 | a0001c0001t0010g0318 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.670-13271G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75608808 | |||||||
| chr14:75609100 | T | C | 7 | a0002c0003t0003g0009 a0002c0003t0003g0115 a0002c0003t0003g0116 others(4): Show |
7 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(4): Show |
intron_variant | MODIFIER | c.670-12979T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75609100 | |||||||
| chr14:75609285 | G | A | 3 | a0001c0001t0004g0171 a0001c0001t0004g0172 a0002c0003t0003g0137 |
3 | HG01106.hp2 HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.670-12794G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75609285 | |||||||
| chr14:75609315 | G | A | 1 | a0001c0001t0015g0307 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.670-12764G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75609315 | |||||||
| chr14:75609753 | A | C | 1 | a0001c0001t0001g0279 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.670-12326A>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75609753 | |||||||
| chr14:75609789 | GCATCCCT others(8): Show |
G | 1 | a0001c0001t0004g0190 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.670-12289_670-1227 others(19): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75609789 | |||||||
| chr14:75609877 | G | A | 1 | a0001c0001t0015g0307 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.670-12202G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75609877 | |||||||
| chr14:75609897 | G | A | 1 | a0002c0002t0002g0097 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.670-12182G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75609897 | |||||||
| chr14:75609898 | G | C | 1 | a0003c0004t0005g0165 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.670-12181G>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75609898 | |||||||
| chr14:75610147 | G | A | 1 | a0002c0002t0002g0037 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.670-11932G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75610147 | |||||||
| chr14:75610230 | T | A | 2 | a0002c0002t0002g0038 a0002c0002t0002g0054 |
2 | HG01975.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.670-11849T>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75610230 | |||||||
| chr14:75610385 | A | G | 1 | a0001c0001t0004g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.670-11694A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75610385 | |||||||
| chr14:75610410 | G | A | 45 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(42): Show |
48 | HG01106.hp2 HG01109.hp1 HG02015.hp2 others(45): Show |
intron_variant | MODIFIER | c.670-11669G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75610410 | |||||||
| chr14:75610434 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.670-11645C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75610434 | |||||||
| chr14:75610452 | C | CT | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(217): Show |
229 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.670-11618dupT | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75610452 | ||||||
| chr14:75610520 | C | T | 1 | a0001c0001t0019g0324 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.670-11559C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75610520 | |||||||
| chr14:75610761 | A | G | 1 | a0002c0002t0002g0008 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.670-11318A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75610761 | |||||||
| chr14:75610888 | A | G | 28 | a0001c0001t0001g0243 a0001c0001t0001g0247 a0001c0001t0001g0248 others(25): Show |
28 | HG00408.hp1 HG00639.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.670-11191A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75610888 | |||||||
| chr14:75611035 | G | A | 5 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(2): Show |
5 | HG02109.hp1 HG02451.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-11044G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75611035 | |||||||
| chr14:75611057 | C | G | 1 | a0001c0001t0001g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.670-11022C>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75611057 | |||||||
| chr14:75611245 | T | C | 1 | a0002c0002t0002g0072 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.670-10834T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75611245 | |||||||
| chr14:75611338 | G | A | 1 | a0002c0002t0002g0088 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.670-10741G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75611338 | |||||||
| chr14:75611489 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.670-10590G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75611489 | |||||||
| chr14:75611614 | TG | T | 18 | a0001c0001t0001g0225 a0001c0001t0001g0234 a0001c0001t0001g0235 others(15): Show |
18 | HG00323.hp2 HG01070.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.670-10464delG | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75611614 | |||||||
| chr14:75611620 | C | T | 1 | a0002c0002t0002g0063 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.670-10459C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75611620 | |||||||
| chr14:75611621 | G | A | 1 | a0001c0001t0004g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.670-10458G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75611621 | |||||||
| chr14:75611693 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.670-10386G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75611693 | |||||||
| chr14:75611850 | G | A | 5 | a0001c0001t0001g0225 a0001c0001t0001g0234 a0001c0001t0001g0235 others(2): Show |
5 | HG01884.hp2 HG02280.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.670-10229G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75611850 | |||||||
| chr14:75611859 | A | G | 12 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(9): Show |
12 | HG02055.hp1 HG02109.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.670-10220A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75611859 | |||||||
| chr14:75611999 | C | T | 1 | a0004c0005t0006g0135 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.670-10080C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75611999 | |||||||
| chr14:75612484 | T | A | 6 | a0002c0003t0003g0128 a0002c0003t0003g0130 a0002c0003t0003g0131 others(3): Show |
6 | HG01123.hp1 HG01257.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.670-9595T>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75612484 | |||||||
| chr14:75612636 | G | A | 1 | a0001c0001t0004g0191 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.670-9443G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75612636 | |||||||
| chr14:75612651 | G | T | 5 | a0001c0001t0001g0225 a0001c0001t0001g0234 a0001c0001t0001g0235 others(2): Show |
5 | HG01884.hp2 HG02280.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.670-9428G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75612651 | |||||||
| chr14:75612728 | T | G | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(184): Show |
196 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.670-9351T>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75612728 | |||||||
| chr14:75612822 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.670-9257C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75612822 | |||||||
| chr14:75613157 | T | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(97): Show |
105 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.670-8922T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75613157 | |||||||
| chr14:75613248 | A | C | 12 | a0001c0001t0001g0305 a0001c0001t0002g0211 a0001c0001t0002g0212 others(9): Show |
12 | HG00323.hp2 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.670-8831A>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75613248 | |||||||
| chr14:75613377 | C | T | 7 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.670-8702C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75613377 | |||||||
| chr14:75613432 | AG | A | 4 | a0001c0001t0002g0211 a0001c0001t0002g0212 a0001c0001t0009g0210 others(1): Show |
4 | HG00323.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.670-8644delG | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75613432 | ||||||
| chr14:75613510 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.670-8569C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75613510 | |||||||
| chr14:75613562 | C | G | 1 | a0001c0001t0019g0324 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.670-8517C>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75613562 | |||||||
| chr14:75613612 | C | A | 1 | a0002c0002t0002g0010 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.670-8467C>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75613612 | |||||||
| chr14:75613643 | C | T | 1 | a0001c0001t0001g0302 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.670-8436C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75613643 | |||||||
| chr14:75613676 | G | A | 31 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(28): Show |
34 | HG01106.hp2 HG01109.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.670-8403G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75613676 | |||||||
| chr14:75613691 | C | T | 1 | a0002c0003t0023g0157 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.670-8388C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75613691 | |||||||
| chr14:75613731 | A | C | 1 | a0001c0001t0004g0164 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.670-8348A>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75613731 | |||||||
| chr14:75613843 | A | T | 1 | a0002c0002t0002g0012 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.670-8236A>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75613843 | |||||||
| chr14:75613863 | T | A | 7 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.670-8216T>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75613863 | |||||||
| chr14:75614076 | A | G | 1 | a0001c0001t0015g0307 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.670-8003A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75614076 | |||||||
| chr14:75614454 | C | T | 3 | a0001c0001t0004g0201 a0001c0001t0004g0222 a0003c0004t0005g0165 |
3 | HG02622.hp1 HG02895.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.670-7625C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75614454 | |||||||
| chr14:75614686 | G | A | 44 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(41): Show |
48 | HG00438.hp1 HG01074.hp2 HG01106.hp2 others(45): Show |
intron_variant | MODIFIER | c.670-7393G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75614686 | |||||||
| chr14:75614708 | A | G | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
237 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.670-7371A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75614708 | |||||||
| chr14:75614786 | A | G | 1 | a0001c0001t0010g0318 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.670-7293A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75614786 | |||||||
| chr14:75614853 | C | T | 1 | a0002c0003t0003g0158 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.670-7226C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75614853 | |||||||
| chr14:75614933 | C | G | 1 | a0001c0001t0019g0324 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.670-7146C>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75614933 | |||||||
| chr14:75614999 | A | G | 4 | a0001c0001t0002g0211 a0001c0001t0002g0212 a0001c0001t0009g0210 others(1): Show |
4 | HG00323.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.670-7080A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75614999 | |||||||
| chr14:75615183 | A | C | 1 | a0002c0003t0003g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.670-6896A>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75615183 | |||||||
| chr14:75615221 | G | A | 4 | a0001c0001t0001g0232 a0001c0001t0004g0202 a0002c0003t0003g0108 others(1): Show |
4 | HG02723.hp2 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.670-6858G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75615221 | |||||||
| chr14:75615235 | C | A | 4 | a0001c0001t0004g0181 a0002c0002t0002g0066 a0002c0002t0002g0071 others(1): Show |
4 | NA18941.hp1 NA18972.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.670-6844C>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75615235 | |||||||
| chr14:75615263 | T | C | 1 | a0002c0002t0002g0083 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.670-6816T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75615263 | |||||||
| chr14:75615281 | G | A | 3 | a0002c0002t0002g0066 a0002c0002t0002g0071 a0002c0003t0003g0142 |
3 | NA18941.hp1 NA18983.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.670-6798G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75615281 | |||||||
| chr14:75615321 | A | T | 159 | a0001c0001t0001g0005 a0001c0001t0001g0229 a0001c0001t0001g0235 others(156): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.670-6758A>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75615321 | |||||||
| chr14:75615467 | G | A | 1 | a0002c0003t0003g0154 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.670-6612G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75615467 | |||||||
| chr14:75615517 | G | A | 5 | a0002c0003t0003g0009 a0002c0003t0003g0115 a0002c0003t0003g0116 others(2): Show |
5 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(2): Show |
intron_variant | MODIFIER | c.670-6562G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75615517 | |||||||
| chr14:75615522 | G | A | 1 | a0001c0001t0004g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.670-6557G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75615522 | |||||||
| chr14:75615746 | G | A | 1 | a0002c0003t0003g0114 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.670-6333G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75615746 | |||||||
| chr14:75615784 | CCGAGGCG others(2): Show |
C | 3 | a0001c0001t0001g0233 a0001c0001t0001g0315 a0001c0001t0015g0307 |
3 | HG02723.hp1 HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.670-6292_670-6284d others(11): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75615784 | ||||||
| chr14:75615862 | C | CA | 22 | a0001c0001t0001g0228 a0001c0001t0001g0237 a0001c0001t0001g0246 others(19): Show |
22 | HG00597.hp1 HG01167.hp1 HG01515.hp1 others(19): Show |
intron_variant | MODIFIER | c.670-6202dupA | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75615862 | ||||||
| chr14:75615862 | C | CAA | 137 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0229 others(134): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.670-6203_670-6202d others(4): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75615862 | ||||||
| chr14:75615862 | C | CAAA | 6 | a0001c0001t0001g0308 a0001c0001t0004g0190 a0002c0002t0002g0087 others(3): Show |
6 | HG01074.hp1 HG01192.hp2 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.670-6204_670-6202d others(5): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75615862 | ||||||
| chr14:75615894 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.670-6185G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75615894 | |||||||
| chr14:75615899 | A | G | 4 | a0001c0001t0001g0311 a0001c0001t0001g0312 a0001c0001t0016g0263 others(1): Show |
4 | HG00438.hp2 HG01361.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.670-6180A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75615899 | |||||||
| chr14:75615949 | C | A | 1 | a0002c0003t0003g0138 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.670-6130C>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75615949 | |||||||
| chr14:75615951 | C | T | 17 | a0001c0001t0001g0228 a0001c0001t0001g0245 a0001c0001t0001g0246 others(14): Show |
17 | HG01167.hp1 HG01515.hp1 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.670-6128C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75615951 | |||||||
| chr14:75615982 | G | A | 1 | a0001c0001t0004g0222 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.670-6097G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75615982 | |||||||
| chr14:75616026 | C | CA | 7 | a0001c0001t0001g0286 a0001c0001t0004g0182 a0002c0002t0002g0055 others(4): Show |
7 | HG02615.hp2 HG02897.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.670-6031dupA | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75616026 | ||||||
| chr14:75616026 | C | CAA | 24 | a0001c0001t0001g0005 a0001c0001t0001g0251 a0001c0001t0001g0255 others(21): Show |
25 | HG00609.hp2 HG01123.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.670-6032_670-6031d others(4): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75616026 | ||||||
| chr14:75616026 | C | CAAA | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0173 others(44): Show |
51 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.670-6033_670-6031d others(5): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75616026 | ||||||
| chr14:75616026 | C | CAAAA | 28 | a0001c0001t0001g0228 a0001c0001t0001g0245 a0001c0001t0001g0256 others(25): Show |
28 | HG00408.hp1 HG00438.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.670-6034_670-6031d others(6): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75616026 | ||||||
| chr14:75616026 | C | CAAAAAAA others(2): Show |
9 | a0001c0001t0001g0317 a0001c0001t0004g0192 a0001c0001t0004g0205 others(6): Show |
9 | HG01168.hp1 HG01243.hp1 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.670-6039_670-6031d others(11): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75616026 | ||||||
| chr14:75616026 | C | CAAAAAAA others(3): Show |
98 | a0001c0001t0001g0002 a0001c0001t0001g0225 a0001c0001t0001g0227 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.670-6040_670-6031d others(12): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75616026 | ||||||
| chr14:75616026 | C | CAAAAAAA others(4): Show |
42 | a0001c0001t0001g0226 a0001c0001t0001g0238 a0001c0001t0001g0243 others(39): Show |
42 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.670-6041_670-6031d others(13): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75616026 | ||||||
| chr14:75616026 | C | CAAAAAAA others(5): Show |
5 | a0001c0001t0001g0253 a0001c0001t0001g0260 a0001c0001t0010g0318 others(2): Show |
5 | HG00140.hp2 HG03209.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-6042_670-6031d others(14): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75616026 | ||||||
| chr14:75616026 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0004g0190 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.670-6043_670-6031d others(15): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75616026 | ||||||
| chr14:75616048 | A | AAAAAAAA others(4): Show |
1 | a0002c0002t0002g0094 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.670-6031_670-6030i others(13): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75616048 | |||||||
| chr14:75616058 | T | G | 157 | a0001c0001t0001g0002 a0001c0001t0001g0225 a0001c0001t0001g0226 others(154): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.670-6021T>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75616058 | |||||||
| chr14:75616065 | A | T | 1 | a0001c0001t0001g0007 | 2 | HG01109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.670-6014A>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75616065 | |||||||
| chr14:75616086 | C | G | 3 | a0002c0002t0002g0025 a0002c0002t0002g0052 a0002c0002t0002g0053 |
3 | NA19005.hp2 NA19074.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.670-5993C>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75616086 | |||||||
| chr14:75616191 | G | T | 1 | a0001c0001t0004g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.670-5888G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75616191 | |||||||
| chr14:75616266 | G | T | 5 | a0003c0004t0005g0165 a0003c0004t0005g0204 a0003c0004t0005g0206 others(2): Show |
5 | HG02615.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-5813G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75616266 | |||||||
| chr14:75616337 | A | T | 3 | a0001c0001t0001g0272 a0001c0001t0001g0315 a0001c0001t0015g0307 |
3 | HG02809.hp2 HG02965.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.670-5742A>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75616337 | |||||||
| chr14:75616338 | T | A | 22 | a0001c0001t0001g0228 a0001c0001t0001g0246 a0001c0001t0001g0256 others(19): Show |
22 | HG00323.hp2 HG01515.hp1 HG01517.hp2 others(19): Show |
intron_variant | MODIFIER | c.670-5741T>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75616338 | |||||||
| chr14:75616461 | A | T | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(254): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.670-5618A>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75616461 | |||||||
| chr14:75616497 | T | A | 2 | a0001c0001t0001g0275 a0002c0002t0002g0059 |
2 | HG02280.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.670-5582T>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75616497 | |||||||
| chr14:75616559 | A | G | 1 | a0001c0001t0004g0180 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.670-5520A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75616559 | |||||||
| chr14:75616602 | C | G | 1 | a0001c0001t0004g0222 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.670-5477C>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75616602 | |||||||
| chr14:75616781 | G | C | 3 | a0001c0001t0002g0211 a0001c0001t0009g0210 a0001c0001t0009g0213 |
3 | HG01070.hp2 HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.670-5298G>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75616781 | |||||||
| chr14:75616918 | G | A | 5 | a0003c0004t0005g0165 a0003c0004t0005g0204 a0003c0004t0005g0206 others(2): Show |
5 | HG02615.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-5161G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75616918 | |||||||
| chr14:75616925 | G | A | 1 | a0002c0003t0003g0150 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.670-5154G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75616925 | |||||||
| chr14:75617182 | G | A | 1 | a0001c0001t0002g0212 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.670-4897G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75617182 | |||||||
| chr14:75617239 | A | C | 157 | a0001c0001t0001g0002 a0001c0001t0001g0225 a0001c0001t0001g0226 others(154): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.670-4840A>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75617239 | |||||||
| chr14:75617767 | A | C | 1 | a0001c0001t0001g0236 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.670-4312A>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75617767 | |||||||
| chr14:75617840 | C | T | 3 | a0001c0001t0001g0278 a0001c0001t0001g0314 a0001c0001t0004g0196 |
3 | NA18963.hp1 NA19062.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.670-4239C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75617840 | |||||||
| chr14:75618148 | C | T | 1 | a0001c0001t0002g0217 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.670-3931C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75618148 | |||||||
| chr14:75618218 | C | T | 1 | a0001c0001t0004g0203 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.670-3861C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75618218 | |||||||
| chr14:75618263 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.670-3816G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75618263 | |||||||
| chr14:75618325 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.670-3754G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75618325 | |||||||
| chr14:75618471 | T | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(68): Show |
76 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.670-3608T>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75618471 | |||||||
| chr14:75618544 | C | G | 1 | a0001c0001t0001g0236 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.670-3535C>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75618544 | |||||||
| chr14:75618745 | C | T | 4 | a0002c0002t0002g0037 a0002c0002t0002g0073 a0002c0003t0003g0129 others(1): Show |
4 | HG00408.hp1 HG00673.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.670-3334C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75618745 | |||||||
| chr14:75618885 | G | GT | 57 | a0001c0001t0001g0225 a0001c0001t0001g0228 a0001c0001t0001g0230 others(54): Show |
57 | HG00323.hp2 HG00438.hp1 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.670-3178dupT | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75618885 | ||||||
| chr14:75618930 | T | G | 158 | a0001c0001t0001g0002 a0001c0001t0001g0225 a0001c0001t0001g0226 others(155): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.670-3149T>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75618930 | |||||||
| chr14:75618961 | C | T | 1 | a0002c0003t0003g0130 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.670-3118C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75618961 | |||||||
| chr14:75618976 | C | T | 1 | a0001c0001t0017g0170 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.670-3103C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75618976 | |||||||
| chr14:75619076 | T | C | 93 | a0001c0001t0001g0243 a0001c0001t0001g0261 a0001c0001t0001g0267 others(90): Show |
93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.670-3003T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75619076 | |||||||
| chr14:75619109 | A | G | 1 | a0001c0001t0002g0217 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.670-2970A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75619109 | |||||||
| chr14:75619129 | T | G | 2 | a0001c0001t0004g0201 a0001c0001t0004g0203 |
2 | HG02055.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.670-2950T>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75619129 | |||||||
| chr14:75619176 | G | C | 1 | a0001c0001t0001g0233 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.670-2903G>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75619176 | |||||||
| chr14:75619220 | C | T | 1 | a0002c0002t0002g0022 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.670-2859C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75619220 | |||||||
| chr14:75619263 | A | G | 1 | a0001c0001t0007g0326 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.670-2816A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75619263 | |||||||
| chr14:75619333 | G | T | 1 | a0001c0001t0004g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.670-2746G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75619333 | |||||||
| chr14:75619477 | T | TCATC | 12 | a0001c0001t0001g0279 a0001c0001t0001g0306 a0001c0001t0001g0315 others(9): Show |
12 | HG00099.hp2 HG01081.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.670-2561_670-2558d others(6): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75619477 | ||||||
| chr14:75619477 | TCATC | T | 12 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0235 others(9): Show |
12 | HG02145.hp2 HG02280.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.670-2561_670-2558d others(6): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75619477 | ||||||
| chr14:75619477 | TCATCCAT others(1): Show |
T | 9 | a0001c0001t0001g0305 a0001c0001t0002g0212 a0001c0001t0004g0163 others(6): Show |
9 | HG00323.hp2 HG02683.hp1 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.670-2565_670-2558d others(10): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75619477 | ||||||
| chr14:75619477 | TCATCCAT others(5): Show |
T | 16 | a0001c0001t0001g0228 a0001c0001t0001g0245 a0001c0001t0001g0246 others(13): Show |
16 | HG01167.hp1 HG01515.hp1 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.670-2569_670-2558d others(14): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75619477 | ||||||
| chr14:75619742 | G | T | 3 | a0001c0001t0004g0166 a0001c0001t0004g0167 a0001c0001t0004g0168 |
3 | HG01081.hp2 HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.670-2337G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75619742 | |||||||
| chr14:75619769 | C | T | 1 | a0002c0002t0021g0020 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.670-2310C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75619769 | |||||||
| chr14:75619784 | G | A | 7 | a0001c0001t0001g0244 a0001c0001t0001g0262 a0001c0001t0001g0286 others(4): Show |
7 | NA18947.hp1 NA18949.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.670-2295G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75619784 | |||||||
| chr14:75619873 | G | T | 4 | a0001c0001t0001g0232 a0001c0001t0004g0202 a0002c0003t0003g0108 others(1): Show |
4 | HG02723.hp2 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.670-2206G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75619873 | |||||||
| chr14:75619905 | C | A | 1 | a0001c0001t0001g0233 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.670-2174C>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75619905 | |||||||
| chr14:75620117 | A | G | 1 | a0001c0001t0004g0222 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.670-1962A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75620117 | |||||||
| chr14:75620516 | T | C | 158 | a0001c0001t0001g0002 a0001c0001t0001g0225 a0001c0001t0001g0226 others(155): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.670-1563T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75620516 | |||||||
| chr14:75620671 | C | T | 1 | a0001c0001t0002g0212 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.670-1408C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75620671 | |||||||
| chr14:75620672 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.670-1407G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75620672 | |||||||
| chr14:75620728 | G | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0299 |
3 | HG01109.hp1 HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.670-1351G>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75620728 | |||||||
| chr14:75620809 | A | T | 169 | a0001c0001t0001g0002 a0001c0001t0001g0225 a0001c0001t0001g0226 others(166): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.670-1270A>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75620809 | |||||||
| chr14:75620863 | G | A | 1 | a0002c0002t0002g0022 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.670-1216G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75620863 | |||||||
| chr14:75621008 | T | A | 2 | a0002c0002t0002g0023 a0002c0002t0002g0024 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.670-1071T>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75621008 | |||||||
| chr14:75621013 | G | A | 2 | a0001c0001t0001g0315 a0001c0001t0015g0307 |
2 | HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.670-1066G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75621013 | |||||||
| chr14:75621014 | C | T | 1 | a0001c0001t0004g0222 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.670-1065C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75621014 | |||||||
| chr14:75621015 | C | T | 1 | a0001c0001t0001g0286 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.670-1064C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75621015 | |||||||
| chr14:75621203 | A | G | 1 | a0001c0001t0001g0236 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.670-876A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75621203 | |||||||
| chr14:75621207 | A | T | 1 | a0001c0001t0001g0236 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.670-872A>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75621207 | |||||||
| chr14:75621209 | G | T | 1 | a0001c0001t0001g0236 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.670-870G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75621209 | |||||||
| chr14:75621277 | G | A | 156 | a0001c0001t0001g0002 a0001c0001t0001g0225 a0001c0001t0001g0226 others(153): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.670-802G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75621277 | |||||||
| chr14:75621280 | C | T | 2 | a0002c0002t0002g0104 a0002c0002t0002g0105 |
2 | HG02735.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.670-799C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75621280 | |||||||
| chr14:75621434 | A | G | 156 | a0001c0001t0001g0002 a0001c0001t0001g0225 a0001c0001t0001g0226 others(153): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.670-645A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75621434 | |||||||
| chr14:75621486 | C | T | 2 | a0001c0001t0001g0306 a0001c0001t0004g0164 |
2 | HG02145.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.670-593C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75621486 | |||||||
| chr14:75621487 | G | A | 1 | a0001c0001t0002g0212 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.670-592G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75621487 | |||||||
| chr14:75621507 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.670-572T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75621507 | |||||||
| chr14:75621827 | C | T | 3 | a0001c0001t0004g0201 a0001c0001t0004g0203 a0001c0001t0004g0222 |
3 | HG02055.hp1 HG02622.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.670-252C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75621827 | |||||||
| chr14:75621888 | G | A | 5 | a0003c0004t0005g0165 a0003c0004t0005g0204 a0003c0004t0005g0206 others(2): Show |
5 | HG02615.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-191G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75621888 | |||||||
| chr14:75621914 | GA | G | 3 | a0002c0002t0002g0040 a0002c0002t0002g0055 a0002c0002t0002g0057 |
3 | NA18950.hp2 NA19081.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.670-163delA | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 75621914 | ||||||
| chr14:75622012 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.670-67C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75622012 | |||||||
| chr14:75622017 | C | T | 6 | a0001c0001t0001g0238 a0001c0001t0001g0250 a0001c0001t0001g0258 others(3): Show |
6 | HG00597.hp2 HG01175.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.670-62C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 1/9 | chr14 | 75622017 | |||||||
| chr14:75622338 | G | C | 1 | a0001c0001t0004g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.811+118G>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 2/9 | chr14 | 75622338 | |||||||
| chr14:75622494 | G | T | 8 | a0001c0001t0001g0248 a0001c0001t0001g0309 a0001c0001t0002g0220 others(5): Show |
8 | HG03669.hp2 HG03831.hp2 HG03942.hp1 others(5): Show |
intron_variant | MODIFIER | c.811+274G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 2/9 | chr14 | 75622494 | |||||||
| chr14:75622514 | A | G | 3 | a0001c0001t0004g0201 a0001c0001t0004g0203 a0001c0001t0004g0222 |
3 | HG02055.hp1 HG02622.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.811+294A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 2/9 | chr14 | 75622514 | |||||||
| chr14:75622711 | G | A | 156 | a0001c0001t0001g0002 a0001c0001t0001g0225 a0001c0001t0001g0226 others(153): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.811+491G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 2/9 | chr14 | 75622711 | |||||||
| chr14:75622746 | A | C | 1 | a0002c0002t0002g0106 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.811+526A>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 2/9 | chr14 | 75622746 | |||||||
| chr14:75622756 | G | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0254 others(46): Show |
53 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.811+536G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 2/9 | chr14 | 75622756 | |||||||
| chr14:75622827 | A | T | 2 | a0001c0001t0004g0222 a0002c0002t0002g0035 |
2 | HG02895.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.811+607A>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 2/9 | chr14 | 75622827 | |||||||
| chr14:75622835 | T | C | 1 | a0001c0001t0001g0236 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.811+615T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 2/9 | chr14 | 75622835 | |||||||
| chr14:75622965 | TTTTATTT others(1): Show |
T | 13 | a0001c0001t0001g0228 a0001c0001t0001g0245 a0001c0001t0001g0246 others(10): Show |
13 | HG01167.hp1 HG01515.hp1 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.811+761_811+768del others(8): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 75622965 | ||||||
| chr14:75623107 | G | A | 3 | a0001c0001t0001g0264 a0001c0001t0001g0271 a0001c0001t0001g0321 |
3 | HG01261.hp2 HG01515.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.811+887G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 2/9 | chr14 | 75623107 | |||||||
| chr14:75623143 | G | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0254 others(46): Show |
53 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.811+923G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 2/9 | chr14 | 75623143 | |||||||
| chr14:75623197 | G | A | 1 | a0001c0001t0004g0203 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.811+977G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 2/9 | chr14 | 75623197 | |||||||
| chr14:75623201 | C | T | 1 | a0002c0002t0002g0085 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.811+981C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 2/9 | chr14 | 75623201 | |||||||
| chr14:75623281 | C | T | 1 | a0002c0003t0003g0162 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.811+1061C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 2/9 | chr14 | 75623281 | |||||||
| chr14:75623567 | C | T | 3 | a0001c0001t0001g0233 a0001c0001t0001g0315 a0001c0001t0015g0307 |
3 | HG02723.hp1 HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.812-1045C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 2/9 | chr14 | 75623567 | |||||||
| chr14:75623606 | A | C | 1 | a0001c0001t0017g0170 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.812-1006A>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 2/9 | chr14 | 75623606 | |||||||
| chr14:75623944 | C | T | 3 | a0001c0001t0004g0201 a0001c0001t0004g0203 a0001c0001t0004g0222 |
3 | HG02055.hp1 HG02622.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.812-668C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 2/9 | chr14 | 75623944 | |||||||
| chr14:75624046 | C | T | 8 | a0001c0001t0001g0305 a0001c0001t0002g0212 a0001c0001t0014g0276 others(5): Show |
8 | HG00323.hp2 HG02683.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.812-566C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 2/9 | chr14 | 75624046 | |||||||
| chr14:75624348 | G | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0254 others(46): Show |
53 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.812-264G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 2/9 | chr14 | 75624348 | |||||||
| chr14:75624519 | T | C | 1 | a0001c0001t0004g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.812-93T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 2/9 | chr14 | 75624519 | |||||||
| chr14:75624587 | G | C | 1 | a0001c0007t0004g0197 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.812-25G>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 2/9 | chr14 | 75624587 | |||||||
| chr14:75624854 | T | G | 12 | a0001c0001t0001g0245 a0001c0001t0001g0256 a0001c0001t0001g0273 others(9): Show |
12 | HG01167.hp1 HG01515.hp1 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.952+102T>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75624854 | |||||||
| chr14:75624877 | A | G | 19 | a0001c0001t0001g0005 a0001c0001t0001g0255 a0001c0001t0004g0185 others(16): Show |
20 | HG00609.hp2 HG01123.hp1 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.952+125A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75624877 | |||||||
| chr14:75624882 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.952+130G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75624882 | |||||||
| chr14:75625087 | A | AT | 203 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0225 others(200): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.952+342dupT | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 75625087 | ||||||
| chr14:75625174 | G | A | 50 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0173 others(47): Show |
54 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.952+422G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75625174 | |||||||
| chr14:75625344 | T | C | 1 | a0002c0003t0003g0130 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.952+592T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75625344 | |||||||
| chr14:75625465 | A | C | 1 | a0001c0001t0004g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.952+713A>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75625465 | |||||||
| chr14:75625555 | C | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0173 others(47): Show |
54 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.952+803C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75625555 | |||||||
| chr14:75625778 | A | G | 8 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0004g0202 others(5): Show |
8 | HG02647.hp1 HG02723.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.952+1026A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75625778 | |||||||
| chr14:75625926 | A | G | 8 | a0001c0001t0001g0305 a0001c0001t0002g0212 a0001c0001t0014g0276 others(5): Show |
8 | HG00323.hp2 HG02683.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.952+1174A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75625926 | |||||||
| chr14:75626021 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.952+1269G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75626021 | |||||||
| chr14:75626062 | G | T | 1 | a0001c0001t0001g0303 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.952+1310G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75626062 | |||||||
| chr14:75626086 | G | A | 46 | a0001c0001t0001g0229 a0001c0001t0001g0238 a0001c0001t0001g0244 others(43): Show |
46 | HG00597.hp2 HG01175.hp1 HG01257.hp2 others(43): Show |
intron_variant | MODIFIER | c.952+1334G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75626086 | |||||||
| chr14:75626148 | T | C | 1 | a0001c0001t0001g0306 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.952+1396T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75626148 | |||||||
| chr14:75626153 | G | A | 1 | a0001c0001t0001g0309 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.952+1401G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75626153 | |||||||
| chr14:75626154 | G | T | 1 | a0001c0001t0004g0184 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.952+1402G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75626154 | |||||||
| chr14:75626419 | A | G | 13 | a0001c0001t0001g0260 a0001c0001t0001g0266 a0001c0001t0004g0181 others(10): Show |
13 | HG00140.hp2 HG01081.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.952+1667A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75626419 | |||||||
| chr14:75626711 | G | C | 1 | a0001c0001t0001g0236 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.952+1959G>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75626711 | |||||||
| chr14:75626937 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.952+2185T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75626937 | |||||||
| chr14:75627119 | G | A | 60 | a0001c0001t0001g0229 a0001c0001t0001g0238 a0001c0001t0001g0244 others(57): Show |
60 | HG00140.hp2 HG00597.hp2 HG01081.hp1 others(57): Show |
intron_variant | MODIFIER | c.952+2367G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75627119 | |||||||
| chr14:75627203 | T | C | 1 | a0002c0002t0002g0049 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.952+2451T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75627203 | |||||||
| chr14:75627414 | A | G | 19 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0174 others(16): Show |
21 | HG01074.hp2 HG01081.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.952+2662A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75627414 | |||||||
| chr14:75627554 | C | T | 60 | a0001c0001t0001g0229 a0001c0001t0001g0238 a0001c0001t0001g0244 others(57): Show |
60 | HG00140.hp2 HG00597.hp2 HG01081.hp1 others(57): Show |
intron_variant | MODIFIER | c.952+2802C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75627554 | |||||||
| chr14:75627555 | C | T | 60 | a0001c0001t0001g0229 a0001c0001t0001g0238 a0001c0001t0001g0244 others(57): Show |
60 | HG00140.hp2 HG00597.hp2 HG01081.hp1 others(57): Show |
intron_variant | MODIFIER | c.952+2803C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75627555 | |||||||
| chr14:75627631 | A | G | 9 | a0001c0001t0001g0173 a0001c0001t0007g0325 a0001c0001t0012g0327 others(6): Show |
9 | HG01433.hp2 HG02258.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.952+2879A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75627631 | |||||||
| chr14:75627856 | A | G | 1 | a0001c0001t0001g0280 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.952+3104A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75627856 | |||||||
| chr14:75627946 | A | C | 1 | a0001c0001t0001g0270 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.952+3194A>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75627946 | |||||||
| chr14:75627999 | G | A | 7 | a0001c0001t0001g0002 a0001c0001t0004g0163 a0001c0001t0004g0221 others(4): Show |
8 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.952+3247G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75627999 | |||||||
| chr14:75628122 | AT | A | 11 | a0001c0001t0001g0260 a0001c0001t0001g0266 a0001c0001t0004g0181 others(8): Show |
11 | HG00140.hp2 HG01081.hp1 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.952+3381delT | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 75628122 | ||||||
| chr14:75628154 | G | A | 2 | a0001c0001t0001g0230 a0001c0001t0004g0222 |
2 | HG02895.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.952+3402G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75628154 | |||||||
| chr14:75628184 | G | C | 1 | a0002c0003t0003g0117 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.952+3432G>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75628184 | |||||||
| chr14:75628264 | G | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0004g0163 others(5): Show |
9 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.952+3512G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75628264 | |||||||
| chr14:75628306 | G | C | 101 | a0001c0001t0001g0007 a0001c0001t0001g0228 a0001c0001t0001g0231 others(98): Show |
102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.952+3554G>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75628306 | |||||||
| chr14:75628334 | C | T | 13 | a0001c0001t0001g0260 a0001c0001t0001g0266 a0001c0001t0004g0181 others(10): Show |
13 | HG00140.hp2 HG01081.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.952+3582C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75628334 | |||||||
| chr14:75628442 | C | T | 1 | a0002c0003t0003g0129 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.952+3690C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75628442 | |||||||
| chr14:75628475 | T | C | 5 | a0001c0001t0004g0202 a0001c0001t0004g0224 a0001c0001t0010g0319 others(2): Show |
5 | HG03041.hp2 NA18906.hp2 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.952+3723T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75628475 | |||||||
| chr14:75628869 | A | C | 1 | a0002c0002t0002g0059 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.952+4117A>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75628869 | |||||||
| chr14:75629192 | C | T | 1 | a0002c0003t0003g0144 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.953-4437C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75629192 | |||||||
| chr14:75629360 | G | C | 27 | a0001c0001t0001g0229 a0001c0001t0001g0238 a0001c0001t0001g0250 others(24): Show |
27 | HG00597.hp2 HG01175.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.953-4269G>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75629360 | |||||||
| chr14:75629372 | G | A | 7 | a0001c0001t0001g0305 a0001c0001t0014g0276 a0001c0001t0020g0214 others(4): Show |
7 | HG02683.hp1 HG02683.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.953-4257G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75629372 | |||||||
| chr14:75629762 | G | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0004g0163 others(5): Show |
9 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.953-3867G>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75629762 | |||||||
| chr14:75629771 | T | C | 13 | a0001c0001t0001g0260 a0001c0001t0001g0266 a0001c0001t0004g0181 others(10): Show |
13 | HG00140.hp2 HG01081.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.953-3858T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75629771 | |||||||
| chr14:75629776 | T | C | 2 | a0002c0002t0002g0048 a0002c0002t0002g0065 |
2 | HG02738.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.953-3853T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75629776 | |||||||
| chr14:75629824 | T | C | 2 | a0001c0001t0001g0310 a0001c0001t0001g0313 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.953-3805T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75629824 | |||||||
| chr14:75629866 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.953-3763T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75629866 | |||||||
| chr14:75630029 | C | G | 1 | a0002c0003t0003g0134 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.953-3600C>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75630029 | |||||||
| chr14:75630287 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.953-3342C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75630287 | |||||||
| chr14:75630288 | G | C | 22 | a0001c0001t0001g0260 a0001c0001t0001g0266 a0001c0001t0001g0305 others(19): Show |
22 | HG00140.hp2 HG00323.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.953-3341G>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75630288 | |||||||
| chr14:75630434 | A | C | 11 | a0001c0001t0001g0260 a0001c0001t0001g0266 a0001c0001t0004g0181 others(8): Show |
11 | HG00140.hp2 HG01081.hp1 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.953-3195A>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75630434 | |||||||
| chr14:75631018 | G | A | 1 | a0001c0001t0001g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.953-2611G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75631018 | |||||||
| chr14:75631197 | C | T | 3 | a0001c0001t0001g0173 a0001c0001t0007g0325 a0001c0001t0012g0327 |
3 | HG01433.hp2 HG02258.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.953-2432C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75631197 | |||||||
| chr14:75631337 | C | T | 1 | a0002c0003t0003g0109 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.953-2292C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75631337 | |||||||
| chr14:75631338 | G | A | 14 | a0001c0001t0001g0260 a0001c0001t0001g0266 a0001c0001t0002g0217 others(11): Show |
14 | HG00140.hp2 HG01081.hp1 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.953-2291G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75631338 | |||||||
| chr14:75631379 | G | A | 57 | a0001c0001t0001g0225 a0001c0001t0001g0229 a0001c0001t0001g0238 others(54): Show |
57 | HG00597.hp2 HG01175.hp1 HG01257.hp2 others(54): Show |
intron_variant | MODIFIER | c.953-2250G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75631379 | |||||||
| chr14:75631426 | C | T | 1 | a0002c0003t0003g0134 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.953-2203C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75631426 | |||||||
| chr14:75631486 | A | G | 2 | a0001c0001t0001g0243 a0001c0001t0001g0317 |
2 | HG00741.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.953-2143A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75631486 | |||||||
| chr14:75631505 | T | C | 7 | a0001c0001t0001g0002 a0001c0001t0004g0163 a0001c0001t0004g0221 others(4): Show |
8 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.953-2124T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75631505 | |||||||
| chr14:75631656 | T | C | 2 | a0001c0001t0001g0245 a0002c0002t0002g0076 |
2 | HG01981.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.953-1973T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75631656 | |||||||
| chr14:75631693 | G | A | 13 | a0001c0001t0001g0260 a0001c0001t0001g0266 a0001c0001t0004g0181 others(10): Show |
13 | HG00140.hp2 HG01081.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.953-1936G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75631693 | |||||||
| chr14:75631788 | G | A | 1 | a0001c0001t0004g0178 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.953-1841G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75631788 | |||||||
| chr14:75631922 | T | C | 81 | a0001c0001t0001g0002 a0001c0001t0001g0225 a0001c0001t0001g0229 others(78): Show |
82 | HG00140.hp2 HG00323.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.953-1707T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75631922 | |||||||
| chr14:75632032 | G | A | 1 | a0002c0003t0003g0134 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.953-1597G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75632032 | |||||||
| chr14:75632053 | G | T | 1 | a0001c0001t0004g0179 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.953-1576G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75632053 | |||||||
| chr14:75632082 | G | T | 1 | a0001c0001t0001g0285 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.953-1547G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75632082 | |||||||
| chr14:75632310 | C | T | 90 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(87): Show |
94 | HG00140.hp2 HG00323.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.953-1319C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75632310 | |||||||
| chr14:75632371 | CAGAG | C | 9 | a0001c0001t0001g0305 a0001c0001t0002g0212 a0001c0001t0014g0276 others(6): Show |
9 | HG00323.hp2 HG02683.hp1 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.953-1254_953-1251d others(6): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 75632371 | ||||||
| chr14:75632443 | C | T | 7 | a0001c0001t0001g0002 a0001c0001t0004g0163 a0001c0001t0004g0221 others(4): Show |
8 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.953-1186C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75632443 | |||||||
| chr14:75632479 | G | A | 13 | a0001c0001t0001g0260 a0001c0001t0001g0266 a0001c0001t0004g0181 others(10): Show |
13 | HG00140.hp2 HG01081.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.953-1150G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75632479 | |||||||
| chr14:75632485 | G | T | 1 | a0006c0009t0002g0093 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.953-1144G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75632485 | |||||||
| chr14:75633241 | G | A | 2 | a0001c0001t0020g0214 a0002c0003t0024g0159 |
2 | HG02683.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.953-388G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75633241 | |||||||
| chr14:75633289 | C | A | 4 | a0002c0003t0003g0122 a0002c0003t0003g0123 a0002c0003t0003g0124 others(1): Show |
4 | HG02257.hp2 HG02559.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.953-340C>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75633289 | |||||||
| chr14:75633418 | T | C | 2 | a0002c0002t0002g0032 a0002c0002t0002g0033 |
2 | NA18949.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.953-211T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75633418 | |||||||
| chr14:75633560 | G | T | 1 | a0001c0001t0015g0307 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.953-69G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75633560 | |||||||
| chr14:75633615 | G | A | 2 | a0001c0001t0004g0201 a0001c0001t0004g0203 |
2 | HG02055.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.953-14G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 3/9 | chr14 | 75633615 | |||||||
| chr14:75633770 | T | C | 2 | a0001c0001t0004g0201 a0001c0001t0004g0203 |
2 | HG02055.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1020+74T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 4/9 | chr14 | 75633770 | |||||||
| chr14:75633934 | A | AT | 6 | a0001c0001t0001g0002 a0001c0001t0004g0203 a0001c0001t0004g0221 others(3): Show |
7 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1020+251dupT | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 75633934 | ||||||
| chr14:75634189 | C | T | 12 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0237 others(9): Show |
13 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1020+493C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 4/9 | chr14 | 75634189 | |||||||
| chr14:75634446 | T | C | 7 | a0001c0001t0001g0244 a0001c0001t0001g0262 a0001c0001t0001g0286 others(4): Show |
7 | NA18947.hp1 NA18949.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.1021-464T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 4/9 | chr14 | 75634446 | |||||||
| chr14:75634534 | C | T | 1 | a0001c0001t0001g0279 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1021-376C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 4/9 | chr14 | 75634534 | |||||||
| chr14:75634641 | A | C | 12 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0237 others(9): Show |
13 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1021-269A>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 4/9 | chr14 | 75634641 | |||||||
| chr14:75634723 | G | T | 1 | a0002c0002t0002g0019 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1021-187G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 4/9 | chr14 | 75634723 | |||||||
| chr14:75634779 | C | T | 1 | a0001c0001t0002g0212 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1021-131C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 4/9 | chr14 | 75634779 | |||||||
| chr14:75635043 | T | C | 39 | a0001c0001t0001g0229 a0001c0001t0001g0238 a0001c0001t0001g0250 others(36): Show |
39 | HG00140.hp2 HG00597.hp2 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.1124+30T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75635043 | |||||||
| chr14:75635049 | A | G | 12 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0237 others(9): Show |
13 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1124+36A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75635049 | |||||||
| chr14:75635083 | G | C | 1 | a0001c0001t0015g0307 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1124+70G>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75635083 | |||||||
| chr14:75635138 | G | C | 2 | a0002c0002t0002g0023 a0002c0002t0002g0024 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1124+125G>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75635138 | |||||||
| chr14:75635539 | A | C | 2 | a0001c0001t0004g0201 a0001c0001t0004g0203 |
2 | HG02055.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1124+526A>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75635539 | |||||||
| chr14:75635548 | C | T | 12 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0237 others(9): Show |
13 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1124+535C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75635548 | |||||||
| chr14:75635657 | G | A | 1 | a0001c0001t0014g0276 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1124+644G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75635657 | |||||||
| chr14:75635681 | A | G | 1 | a0002c0003t0003g0144 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1124+668A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75635681 | |||||||
| chr14:75635872 | T | C | 11 | a0001c0001t0001g0002 a0001c0001t0001g0237 a0001c0001t0004g0163 others(8): Show |
12 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1124+859T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75635872 | |||||||
| chr14:75635874 | G | A | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1124+861G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75635874 | |||||||
| chr14:75635994 | C | T | 2 | a0001c0001t0004g0201 a0001c0001t0004g0203 |
2 | HG02055.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1124+981C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75635994 | |||||||
| chr14:75636124 | G | C | 1 | a0001c0001t0002g0212 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1124+1111G>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75636124 | |||||||
| chr14:75636322 | G | C | 4 | a0001c0001t0001g0264 a0001c0001t0001g0271 a0001c0001t0001g0321 others(1): Show |
4 | HG01261.hp2 HG01515.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1124+1309G>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75636322 | |||||||
| chr14:75636328 | C | G | 8 | a0001c0001t0001g0305 a0001c0001t0002g0212 a0001c0001t0014g0276 others(5): Show |
8 | HG00323.hp2 HG02683.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.1124+1315C>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75636328 | |||||||
| chr14:75636336 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1124+1323G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75636336 | |||||||
| chr14:75636376 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1124+1363G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75636376 | |||||||
| chr14:75636501 | G | T | 300 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(297): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1124+1488G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75636501 | |||||||
| chr14:75636547 | G | T | 1 | a0001c0001t0001g0306 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1124+1534G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75636547 | |||||||
| chr14:75636651 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1124+1638G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75636651 | |||||||
| chr14:75636814 | GA | G | 9 | a0001c0001t0001g0305 a0001c0001t0002g0212 a0001c0001t0014g0276 others(6): Show |
9 | HG00323.hp2 HG02683.hp1 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.1124+1802delA | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75636814 | |||||||
| chr14:75636904 | G | T | 1 | a0001c0001t0001g0236 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1124+1891G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75636904 | |||||||
| chr14:75637150 | C | A | 1 | a0001c0001t0002g0212 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1124+2137C>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75637150 | |||||||
| chr14:75637239 | T | C | 1 | a0002c0003t0003g0131 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1125-2113T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75637239 | |||||||
| chr14:75637261 | G | A | 11 | a0001c0001t0001g0002 a0001c0001t0001g0237 a0001c0001t0004g0163 others(8): Show |
12 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1125-2091G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75637261 | |||||||
| chr14:75637396 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1125-1956A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75637396 | |||||||
| chr14:75637464 | C | T | 1 | a0002c0003t0003g0144 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1125-1888C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75637464 | |||||||
| chr14:75637656 | G | A | 1 | a0002c0003t0003g0108 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1125-1696G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75637656 | |||||||
| chr14:75637684 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1125-1668G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75637684 | |||||||
| chr14:75637728 | CA | C | 91 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(88): Show |
94 | HG00597.hp1 HG00609.hp2 HG01074.hp2 others(91): Show |
intron_variant | MODIFIER | c.1125-1607delA | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 75637728 | ||||||
| chr14:75637750 | G | T | 1 | a0001c0001t0001g0306 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1125-1602G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75637750 | |||||||
| chr14:75637929 | G | A | 6 | a0001c0001t0001g0280 a0001c0001t0001g0290 a0002c0002t0002g0049 others(3): Show |
6 | HG00558.hp1 HG02074.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.1125-1423G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75637929 | |||||||
| chr14:75638326 | A | G | 1 | a0002c0002t0002g0067 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1125-1026A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75638326 | |||||||
| chr14:75638352 | G | T | 5 | a0001c0001t0001g0002 a0001c0001t0004g0221 a0001c0001t0004g0223 others(2): Show |
6 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1125-1000G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75638352 | |||||||
| chr14:75638483 | G | C | 1 | a0001c0001t0001g0246 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1125-869G>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75638483 | |||||||
| chr14:75638908 | T | C | 2 | a0001c0001t0007g0325 a0001c0001t0012g0327 |
2 | HG01433.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1125-444T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75638908 | |||||||
| chr14:75638993 | G | T | 3 | a0001c0001t0001g0250 a0001c0001t0004g0198 a0002c0003t0003g0130 |
3 | HG01175.hp1 HG01257.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1125-359G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75638993 | |||||||
| chr14:75639155 | G | A | 1 | a0001c0001t0001g0234 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1125-197G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75639155 | |||||||
| chr14:75639167 | C | T | 3 | a0001c0001t0001g0173 a0001c0001t0007g0325 a0001c0001t0012g0327 |
3 | HG01433.hp2 HG02258.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1125-185C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 5/9 | chr14 | 75639167 | |||||||
| chr14:75639604 | G | A | 1 | a0002c0003t0003g0162 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1235+142G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 6/9 | chr14 | 75639604 | |||||||
| chr14:75639751 | G | A | 1 | a0001c0001t0012g0327 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1235+289G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 6/9 | chr14 | 75639751 | |||||||
| chr14:75639909 | G | A | 1 | a0002c0002t0002g0016 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1235+447G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 6/9 | chr14 | 75639909 | |||||||
| chr14:75640014 | C | T | 1 | a0002c0003t0003g0144 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1235+552C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 6/9 | chr14 | 75640014 | |||||||
| chr14:75640045 | G | A | 2 | a0001c0001t0014g0276 a0002c0003t0003g0144 |
2 | HG02738.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1235+583G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 6/9 | chr14 | 75640045 | |||||||
| chr14:75640143 | C | T | 6 | a0003c0004t0005g0165 a0003c0004t0005g0204 a0003c0004t0005g0206 others(3): Show |
6 | HG02615.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1235+681C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 6/9 | chr14 | 75640143 | |||||||
| chr14:75640190 | C | T | 2 | a0001c0001t0001g0256 a0001c0001t0001g0273 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1235+728C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 6/9 | chr14 | 75640190 | |||||||
| chr14:75640214 | G | A | 3 | a0001c0001t0004g0169 a0001c0001t0004g0171 a0002c0003t0003g0108 |
3 | HG02486.hp2 HG02723.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1236-741G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 6/9 | chr14 | 75640214 | |||||||
| chr14:75640254 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1236-701G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 6/9 | chr14 | 75640254 | |||||||
| chr14:75640258 | C | CA | 107 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0236 others(104): Show |
107 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.1236-678dupA | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr14 | 75640258 | ||||||
| chr14:75640258 | C | CAA | 6 | a0001c0001t0008g0274 a0003c0004t0005g0165 a0003c0004t0005g0204 others(3): Show |
6 | HG02055.hp2 HG02615.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1236-679_1236-678d others(4): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr14 | 75640258 | ||||||
| chr14:75640258 | CA | C | 19 | a0001c0001t0001g0002 a0001c0001t0001g0235 a0001c0001t0001g0237 others(16): Show |
20 | HG00408.hp2 HG01243.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1236-678delA | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr14 | 75640258 | ||||||
| chr14:75640405 | T | TTG | 12 | a0001c0001t0001g0002 a0001c0001t0001g0231 a0001c0001t0001g0266 others(9): Show |
13 | HG01243.hp1 HG01516.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1236-522_1236-521d others(4): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr14 | 75640405 | ||||||
| chr14:75640405 | T | TTGTG | 3 | a0001c0001t0001g0233 a0001c0001t0001g0235 a0001c0001t0004g0201 |
3 | HG02622.hp1 HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1236-524_1236-521d others(6): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr14 | 75640405 | ||||||
| chr14:75640405 | T | TTGTGTGT others(3): Show |
1 | a0001c0001t0007g0326 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1236-530_1236-521d others(12): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr14 | 75640405 | ||||||
| chr14:75640405 | TTG | T | 179 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(176): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1236-522_1236-521d others(4): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr14 | 75640405 | ||||||
| chr14:75640621 | G | A | 1 | a0001c0001t0007g0325 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1236-334G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 6/9 | chr14 | 75640621 | |||||||
| chr14:75640643 | T | C | 15 | a0001c0001t0001g0250 a0001c0001t0001g0253 a0001c0001t0001g0261 others(12): Show |
15 | HG01175.hp1 HG01257.hp2 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.1236-312T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 6/9 | chr14 | 75640643 | |||||||
| chr14:75641096 | G | T | 1 | a0002c0003t0003g0139 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1341+36G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 7/9 | chr14 | 75641096 | |||||||
| chr14:75641112 | G | A | 3 | a0001c0001t0001g0264 a0001c0001t0001g0271 a0001c0001t0017g0170 |
3 | HG01261.hp2 HG01515.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1341+52G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 7/9 | chr14 | 75641112 | |||||||
| chr14:75641171 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1342-11T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 7/9 | chr14 | 75641171 | |||||||
| chr14:75641334 | C | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0226 a0001c0001t0001g0227 others(2): Show |
6 | HG01109.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1453+41C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 8/9 | chr14 | 75641334 | |||||||
| chr14:75641585 | T | C | 1 | a0001c0001t0001g0236 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1454-258T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 8/9 | chr14 | 75641585 | |||||||
| chr14:75641741 | G | T | 1 | a0001c0001t0001g0238 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1454-102G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 8/9 | chr14 | 75641741 | |||||||
| chr14:75642079 | C | T | 43 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0254 others(40): Show |
47 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.1509+181C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75642079 | |||||||
| chr14:75642080 | G | T | 14 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0235 others(11): Show |
14 | HG02602.hp2 HG02615.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1509+182G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75642080 | |||||||
| chr14:75642188 | A | C | 4 | a0001c0001t0001g0235 a0001c0001t0001g0237 a0001c0001t0004g0201 others(1): Show |
4 | HG02602.hp2 HG02622.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1509+290A>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75642188 | |||||||
| chr14:75642215 | G | A | 1 | a0001c0001t0004g0203 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1509+317G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75642215 | |||||||
| chr14:75642369 | G | A | 1 | a0001c0001t0014g0276 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1509+471G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75642369 | |||||||
| chr14:75642370 | G | A | 83 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(80): Show |
86 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.1509+472G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75642370 | |||||||
| chr14:75642473 | T | C | 2 | a0001c0001t0004g0205 a0001c0001t0004g0207 |
2 | HG02258.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1509+575T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75642473 | |||||||
| chr14:75642612 | T | C | 6 | a0003c0004t0005g0165 a0003c0004t0005g0204 a0003c0004t0005g0206 others(3): Show |
6 | HG02615.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1509+714T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75642612 | |||||||
| chr14:75642759 | C | T | 1 | a0002c0002t0002g0084 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1509+861C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75642759 | |||||||
| chr14:75643018 | T | C | 4 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0014g0276 others(1): Show |
4 | HG02723.hp1 HG02738.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1509+1120T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75643018 | |||||||
| chr14:75643021 | C | A | 195 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(192): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1509+1123C>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75643021 | |||||||
| chr14:75643050 | C | T | 8 | a0001c0001t0001g0002 a0001c0001t0004g0169 a0001c0001t0004g0171 others(5): Show |
9 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1509+1152C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75643050 | |||||||
| chr14:75643628 | A | C | 1 | a0002c0002t0002g0084 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1509+1730A>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75643628 | |||||||
| chr14:75643962 | C | T | 2 | a0001c0001t0020g0214 a0002c0003t0024g0159 |
2 | HG02683.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1509+2064C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75643962 | |||||||
| chr14:75644038 | G | GA | 107 | a0001c0001t0001g0007 a0001c0001t0001g0173 a0001c0001t0001g0226 others(104): Show |
108 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.1509+2153dupA | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 75644038 | ||||||
| chr14:75644152 | A | AT | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1510-2246dupT | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 75644152 | ||||||
| chr14:75644289 | C | T | 298 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(295): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.1510-2112C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75644289 | |||||||
| chr14:75644355 | T | C | 1 | a0001c0001t0019g0324 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1510-2046T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75644355 | |||||||
| chr14:75644629 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1510-1772A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75644629 | |||||||
| chr14:75644647 | A | G | 1 | a0002c0002t0002g0089 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1510-1754A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75644647 | |||||||
| chr14:75644764 | C | A | 3 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0002c0003t0003g0112 |
3 | HG02922.hp2 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1510-1637C>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75644764 | |||||||
| chr14:75644802 | G | A | 1 | a0001c0001t0001g0321 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1510-1599G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75644802 | |||||||
| chr14:75644997 | T | C | 1 | a0002c0002t0002g0082 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1510-1404T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75644997 | |||||||
| chr14:75645012 | G | C | 1 | a0002c0003t0003g0144 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1510-1389G>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75645012 | |||||||
| chr14:75645026 | C | T | 12 | a0001c0001t0001g0275 a0001c0001t0002g0211 a0001c0001t0004g0189 others(9): Show |
12 | HG01070.hp2 HG01106.hp1 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.1510-1375C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75645026 | |||||||
| chr14:75645030 | C | T | 1 | a0002c0003t0003g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1510-1371C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75645030 | |||||||
| chr14:75645032 | T | TGG | 4 | a0001c0001t0001g0232 a0001c0001t0004g0201 a0001c0001t0019g0324 others(1): Show |
4 | HG01257.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1510-1368_1510-136 others(6): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 75645032 | ||||||
| chr14:75645033 | G | GGGGTGT | 8 | a0001c0001t0001g0002 a0001c0001t0001g0225 a0001c0001t0001g0235 others(5): Show |
9 | HG01884.hp2 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1510-1367_1510-136 others(10): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 75645033 | ||||||
| chr14:75645033 | G | GGT | 3 | a0002c0002t0002g0039 a0002c0002t0002g0101 a0006c0009t0002g0093 |
3 | HG01167.hp1 HG02602.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.1510-1325_1510-132 others(6): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 75645033 | ||||||
| chr14:75645033 | GGT | G | 34 | a0001c0001t0001g0005 a0001c0001t0001g0229 a0001c0001t0001g0250 others(31): Show |
35 | HG01175.hp1 HG01433.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.1510-1325_1510-132 others(6): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 75645033 | ||||||
| chr14:75645033 | GGTGT | G | 98 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0174 others(95): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.1510-1327_1510-132 others(8): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 75645033 | ||||||
| chr14:75645033 | GGTGTGT | G | 5 | a0001c0001t0001g0245 a0001c0001t0004g0194 a0002c0002t0002g0061 others(2): Show |
5 | HG01361.hp1 HG01433.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510-1329_1510-132 others(10): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 75645033 | ||||||
| chr14:75645033 | GGTGTGTG others(1): Show |
G | 83 | a0001c0001t0001g0007 a0001c0001t0001g0173 a0001c0001t0001g0226 others(80): Show |
84 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1510-1331_1510-132 others(12): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 75645033 | ||||||
| chr14:75645033 | GGTGTGTG others(3): Show |
G | 44 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0233 others(41): Show |
48 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.1510-1333_1510-132 others(14): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 75645033 | ||||||
| chr14:75645033 | GGTGTGTG others(7): Show |
G | 6 | a0003c0004t0005g0165 a0003c0004t0005g0204 a0003c0004t0005g0206 others(3): Show |
6 | HG02615.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1510-1337_1510-132 others(18): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 75645033 | ||||||
| chr14:75645033 | GGTGTGTG others(15): Show |
G | 1 | a0001c0001t0014g0276 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1510-1345_1510-132 others(26): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 75645033 | ||||||
| chr14:75645035 | T | G | 13 | a0001c0001t0001g0230 a0001c0001t0001g0236 a0001c0001t0001g0237 others(10): Show |
13 | HG00597.hp1 HG01243.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.1510-1366T>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75645035 | |||||||
| chr14:75645037 | T | G | 32 | a0001c0001t0001g0005 a0001c0001t0001g0229 a0001c0001t0001g0250 others(29): Show |
33 | HG01175.hp1 HG01433.hp2 HG01496.hp2 others(30): Show |
intron_variant | MODIFIER | c.1510-1364T>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75645037 | |||||||
| chr14:75645039 | T | G | 98 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0174 others(95): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.1510-1362T>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75645039 | |||||||
| chr14:75645041 | T | G | 5 | a0001c0001t0001g0245 a0001c0001t0004g0194 a0002c0002t0002g0061 others(2): Show |
5 | HG01361.hp1 HG01433.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510-1360T>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75645041 | |||||||
| chr14:75645043 | T | G | 83 | a0001c0001t0001g0007 a0001c0001t0001g0173 a0001c0001t0001g0226 others(80): Show |
84 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1510-1358T>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75645043 | |||||||
| chr14:75645045 | T | G | 44 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0233 others(41): Show |
48 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.1510-1356T>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75645045 | |||||||
| chr14:75645049 | T | G | 6 | a0003c0004t0005g0165 a0003c0004t0005g0204 a0003c0004t0005g0206 others(3): Show |
6 | HG02615.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1510-1352T>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75645049 | |||||||
| chr14:75645057 | T | G | 1 | a0001c0001t0014g0276 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1510-1344T>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75645057 | |||||||
| chr14:75645191 | G | A | 2 | a0001c0001t0002g0217 a0001c0001t0002g0219 |
2 | HG04115.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1510-1210G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75645191 | |||||||
| chr14:75645217 | A | G | 14 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0235 others(11): Show |
14 | HG02602.hp2 HG02615.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1510-1184A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75645217 | |||||||
| chr14:75645258 | C | T | 1 | a0001c0001t0001g0295 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1510-1143C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75645258 | |||||||
| chr14:75645301 | T | C | 8 | a0001c0001t0001g0225 a0001c0001t0001g0232 a0001c0001t0001g0315 others(5): Show |
8 | HG01884.hp2 HG02257.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1510-1100T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75645301 | |||||||
| chr14:75645318 | G | A | 3 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0002c0003t0003g0144 |
3 | HG02723.hp1 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1510-1083G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75645318 | |||||||
| chr14:75645873 | G | C | 6 | a0003c0004t0005g0165 a0003c0004t0005g0204 a0003c0004t0005g0206 others(3): Show |
6 | HG02615.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1510-528G>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75645873 | |||||||
| chr14:75645917 | CA | C | 99 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(96): Show |
102 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.1510-462delA | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 75645917 | ||||||
| chr14:75645917 | CAA | C | 109 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0173 others(106): Show |
111 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1510-463_1510-462d others(4): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 75645917 | ||||||
| chr14:75645917 | CAAAAAAA others(5): Show |
C | 1 | a0002c0003t0003g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1510-473_1510-462d others(14): Show |
FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 75645917 | ||||||
| chr14:75645939 | A | G | 1 | a0001c0001t0014g0276 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1510-462A>G | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75645939 | |||||||
| chr14:75645988 | C | T | 2 | a0001c0001t0001g0237 a0001c0001t0004g0201 |
2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1510-413C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75645988 | |||||||
| chr14:75646013 | T | A | 1 | a0001c0001t0019g0324 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1510-388T>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75646013 | |||||||
| chr14:75646069 | GA | G | 4 | a0001c0001t0001g0002 a0001c0001t0004g0221 a0001c0001t0004g0223 others(1): Show |
5 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510-328delA | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 75646069 | ||||||
| chr14:75646126 | G | A | 2 | a0001c0001t0004g0224 a0002c0003t0003g0150 |
2 | NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1510-275G>A | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75646126 | |||||||
| chr14:75646153 | G | T | 2 | a0001c0001t0001g0230 a0001c0001t0004g0222 |
2 | HG02895.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1510-248G>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75646153 | |||||||
| chr14:75646304 | T | C | 2 | a0001c0001t0001g0003 a0001c0001t0001g0241 |
3 | HG02622.hp2 HG02897.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1510-97T>C | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75646304 | |||||||
| chr14:75646308 | C | T | 1 | a0002c0003t0003g0144 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1510-93C>T | FLVCR2 | ENSG00000119686.10 | transcript | ENST00000238667.9 | protein_coding | 9/9 | chr14 | 75646308 |