Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10447 |
| ensemblid | ENSG00000196937.11 |
| hgncid | 18664 |
| symbol | FAM3C |
| name | FAM3 metabolism regulating signaling molecule C |
| refseq_nuc | NM_014888.3 |
| refseq_prot | NP_055703.1 |
| ensembl_nuc | ENST00000359943.8 |
| ensembl_prot | ENSP00000353025.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 121348878 |
| end | 121396308 |
| strand | - |
| ver | v1.2 |
| region | chr7:121348878-121396308 |
| region5000 | chr7:121343878-121401308 |
| regionname0 | FAM3C_chr7_121348878_121396308 |
| regionname5000 | FAM3C_chr7_121343878_121401308 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 681 | 270 | 82 | 64 | 82 | 14 | 26 | FAM3C_chr7_121343878_121401308 | FAM3C | ATGAG others(676): Show |
chr7 | 121343878 | 121401308 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2455 | 186 | 39 | 45 | 73 | 10 | 18 | FAM3C_chr7_121343878_121401308 | FAM3C | ACTTG others(2450): Show |
chr7 | 121343878 | 121401308 |
| a0001c0001t0002 | 0/0 | 2455 | 22 | 19 | 2 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | ACTTG others(2450): Show |
chr7 | 121343878 | 121401308 |
| a0001c0001t0003 | 0/0 | 2455 | 20 | 12 | 0 | 4 | 0 | 4 | FAM3C_chr7_121343878_121401308 | FAM3C | ACTTG others(2450): Show |
chr7 | 121343878 | 121401308 |
| a0001c0001t0004 | 0/0 | 2455 | 18 | 1 | 13 | 0 | 3 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | ACTTG others(2450): Show |
chr7 | 121343878 | 121401308 |
| a0001c0001t0005 | 0/0 | 2455 | 7 | 7 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | ACTTG others(2450): Show |
chr7 | 121343878 | 121401308 |
| a0001c0001t0006 | 0/0 | 2455 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | ACTTG others(2450): Show |
chr7 | 121343878 | 121401308 |
| a0001c0001t0007 | 0/0 | 2455 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | ACTTG others(2450): Show |
chr7 | 121343878 | 121401308 |
| a0001c0001t0008 | 0/0 | 2455 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | ACTTG others(2450): Show |
chr7 | 121343878 | 121401308 |
| a0001c0001t0009 | 0/0 | 2455 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | ACTTG others(2450): Show |
chr7 | 121343878 | 121401308 |
| a0001c0001t0010 | 0/0 | 2455 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | ACTTG others(2450): Show |
chr7 | 121343878 | 121401308 |
| a0001c0001t0011 | 0/0 | 2455 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | ACTTG others(2450): Show |
chr7 | 121343878 | 121401308 |
| a0001c0001t0012 | 0/0 | 2455 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | ACTTG others(2450): Show |
chr7 | 121343878 | 121401308 |
| a0001c0001t0013 | 0/0 | 2455 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | ACTTG others(2450): Show |
chr7 | 121343878 | 121401308 |
| a0001c0001t0014 | 0/0 | 2455 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | ACTTG others(2450): Show |
chr7 | 121343878 | 121401308 |
| a0001c0001t0015 | 0/0 | 2455 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | ACTTG others(2450): Show |
chr7 | 121343878 | 121401308 |
| a0001c0001t0016 | 0/0 | 2455 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | ACTTG others(2450): Show |
chr7 | 121343878 | 121401308 |
| a0001c0001t0017 | 0/0 | 2455 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | ACTTG others(2450): Show |
chr7 | 121343878 | 121401308 |
| a0001c0001t0018 | 1/0 | 2455 | 1 | 0 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | ACTTG others(2450): Show |
chr7 | 121343878 | 121401308 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 21 | 0 | 3 | 17 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0002 | 0/0 | 12 | 1 | 2 | 7 | 1 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0003 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0023 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0114 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0002g0004 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0002g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0003g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0003g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0004g0007 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0004g0008 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0004g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0004g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0005g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0005g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0005g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0006g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0006g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0007g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0007g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0008g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0008g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0009g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0010g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0011g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0012g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0013g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0014g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0015g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0016g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0017g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| a0001c0001t0018g0192 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0007 | EUR | GBR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG00140 | hp2 | a0001 | c0001 | t0009 | g0143 | EUR | GBR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0093 | EUR | FIN | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0169 | EUR | FIN | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | FIN | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | FIN | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | CHS | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | CHS | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG00558 | hp2 | a0001 | c0001 | t0013 | g0047 | EAS | CHS | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0034 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG00673 | hp2 | a0001 | c0001 | t0006 | g0148 | EAS | CHS | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0017 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01099 | hp1 | a0001 | c0001 | t0014 | g0131 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0183 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0017 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01255 | hp1 | a0001 | c0001 | t0007 | g0188 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0038 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0007 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01433 | hp1 | a0001 | c0001 | t0017 | g0054 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0189 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01928 | hp2 | a0001 | c0001 | t0007 | g0187 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0016 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0037 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02145 | hp2 | a0001 | c0001 | t0015 | g0115 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CDX | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0016 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0008 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02300 | hp2 | a0001 | c0001 | t0004 | g0036 | AMR | PEL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02602 | hp2 | a0001 | c0001 | t0012 | g0175 | SAS | PJL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0068 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02723 | hp2 | a0001 | c0001 | t0016 | g0166 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02895 | hp2 | a0001 | c0001 | t0008 | g0190 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | ESN | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | ESN | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0067 | AFR | ESN | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | ESN | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ESN | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | ESN | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | ESN | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | ESN | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | ESN | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | ESN | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0194 | AFR | MSL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | MSL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | MSL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | MSL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0191 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0173 | AFR | MSL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | MSL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0177 | SAS | PJL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | STU | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0180 | SAS | STU | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0181 | SAS | PJL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0174 | SAS | PJL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03834 | hp1 | a0001 | c0001 | t0011 | g0137 | SAS | BEB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0035 | SAS | BEB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | STU | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | STU | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0178 | SAS | STU | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | YRI | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | YRI | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | YRI | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | YRI | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | LWK | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | LWK | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | LWK | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | LWK | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19065 | hp1 | a0001 | c0001 | t0006 | g0058 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19068 | hp2 | a0001 | c0001 | t0010 | g0149 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19082 | hp1 | a0001 | c0001 | t0006 | g0160 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | YRI | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | YRI | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ASW | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0066 | AFR | ASW | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0033 | EUR | TSI | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | TSI | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | TSI | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0092 | EUR | TSI | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0065 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0193 | AFR | MSL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0114 | REF | REF | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0018 | g0192 | REF | REF | FAM3C_chr7_121343878_121401308 | FAM3C | chr7 | 121343878 | 121401308 |
| 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 |
|---|
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:121349108 | G | C | 4 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(1): Show |
32 | HG01074.hp2 HG01192.hp1 HG01433.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1353C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 1353 | chr7 | 121349108 | ||||||
| chr7:121349144 | G | A | 2 | a0001c0001t0003 a0001c0001t0012 |
21 | HG00438.hp2 HG00544.hp2 HG02258.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1317C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 1317 | chr7 | 121349144 | ||||||
| chr7:121349384 | T | C | 1 | a0001c0001t0011 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1077A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 1077 | chr7 | 121349384 | ||||||
| chr7:121349463 | T | C | 2 | a0001c0001t0006 a0001c0001t0010 |
4 | HG00673.hp2 NA19065.hp1 NA19068.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*998A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 998 | chr7 | 121349463 | ||||||
| chr7:121349477 | A | G | 4 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(1): Show |
32 | HG01074.hp2 HG01192.hp1 HG01433.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*984T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 984 | chr7 | 121349477 | ||||||
| chr7:121349484 | T | C | 1 | a0001c0001t0012 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*977A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 977 | chr7 | 121349484 | ||||||
| chr7:121349625 | A | T | 3 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0016 |
21 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*836T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 836 | chr7 | 121349625 | ||||||
| chr7:121349644 | T | C | 1 | a0001c0001t0013 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*817A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 817 | chr7 | 121349644 | ||||||
| chr7:121349664 | T | C | 1 | a0001c0001t0014 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*797A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 797 | chr7 | 121349664 | ||||||
| chr7:121349694 | T | A | 1 | a0001c0001t0015 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*767A>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 767 | chr7 | 121349694 | ||||||
| chr7:121349883 | C | T | 3 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0016 |
21 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*578G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 578 | chr7 | 121349883 | ||||||
| chr7:121349888 | C | T | 3 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0016 |
21 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*573G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 573 | chr7 | 121349888 | ||||||
| chr7:121349932 | T | C | 1 | a0001c0001t0016 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*529A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 529 | chr7 | 121349932 | ||||||
| chr7:121349989 | A | T | 1 | a0001c0001t0010 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*472T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 472 | chr7 | 121349989 | ||||||
| chr7:121350066 | C | T | 7 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(4): Show |
53 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*395G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 395 | chr7 | 121350066 | ||||||
| chr7:121350122 | T | C | 6 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(3): Show |
51 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*339A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 339 | chr7 | 121350122 | ||||||
| chr7:121350172 | C | T | 1 | a0001c0001t0009 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*289G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 289 | chr7 | 121350172 | ||||||
| chr7:121350279 | T | C | 1 | a0001c0001t0017 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*182A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 10/10 | 182 | chr7 | 121350279 | ||||||
| chr7:121396185 | C | A | 1 | a0001c0001t0007 | 2 | HG01255.hp1 HG01928.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-65G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/10 | chr7 | 121396185 | |||||||
| chr7:121396187 | C | T | 15 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(12): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
5_prime_UTR_variant | MODIFIER | c.-67G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/10 | 13218 | chr7 | 121396187 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:121350673 | C | A | 1 | a0001c0001t0001g0139 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.595-123G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 9/9 | chr7 | 121350673 | |||||||
| chr7:121350783 | C | G | 101 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(98): Show |
138 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.595-233G>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 9/9 | chr7 | 121350783 | |||||||
| chr7:121350836 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.595-286G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 9/9 | chr7 | 121350836 | |||||||
| chr7:121350843 | T | G | 1 | a0001c0001t0004g0038 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.595-293A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 9/9 | chr7 | 121350843 | |||||||
| chr7:121350901 | T | C | 1 | a0001c0001t0002g0163 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.594+242A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 9/9 | chr7 | 121350901 | |||||||
| chr7:121350931 | T | C | 3 | a0001c0001t0002g0040 a0001c0001t0002g0050 a0001c0001t0002g0051 |
3 | HG02809.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.594+212A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 9/9 | chr7 | 121350931 | |||||||
| chr7:121351047 | C | T | 1 | a0001c0001t0001g0045 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.594+96G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 9/9 | chr7 | 121351047 | |||||||
| chr7:121351435 | T | C | 32 | a0001c0001t0002g0181 a0001c0001t0003g0005 a0001c0001t0003g0031 others(29): Show |
42 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.468-166A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121351435 | |||||||
| chr7:121351857 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.468-588C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121351857 | |||||||
| chr7:121352020 | AAAG | A | 4 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0162 others(1): Show |
4 | HG02055.hp2 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.468-754_468-752del others(3): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121352020 | |||||||
| chr7:121352319 | G | GT | 46 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(43): Show |
57 | HG00438.hp2 HG00544.hp2 HG01074.hp2 others(54): Show |
intron_variant | MODIFIER | c.468-1051dupA | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121352319 | |||||||
| chr7:121352319 | G | GTT | 13 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0016 others(10): Show |
19 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.468-1052_468-1051d others(4): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121352319 | |||||||
| chr7:121352427 | GC | G | 17 | a0001c0001t0003g0005 a0001c0001t0003g0031 a0001c0001t0003g0065 others(14): Show |
21 | HG00438.hp2 HG00544.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.468-1159delG | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121352427 | |||||||
| chr7:121352517 | G | A | 1 | a0001c0001t0006g0148 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.468-1248C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121352517 | |||||||
| chr7:121352654 | C | T | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.468-1385G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121352654 | |||||||
| chr7:121352677 | G | A | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.468-1408C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121352677 | |||||||
| chr7:121352724 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.468-1455A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121352724 | |||||||
| chr7:121352952 | T | C | 33 | a0001c0001t0002g0181 a0001c0001t0003g0005 a0001c0001t0003g0031 others(30): Show |
43 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.468-1683A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121352952 | |||||||
| chr7:121353135 | T | A | 1 | a0001c0001t0001g0130 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.468-1866A>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121353135 | |||||||
| chr7:121353191 | G | A | 2 | a0001c0001t0002g0162 a0001c0001t0002g0163 |
2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.468-1922C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121353191 | |||||||
| chr7:121353272 | C | T | 17 | a0001c0001t0001g0084 a0001c0001t0002g0040 a0001c0001t0002g0050 others(14): Show |
20 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.468-2003G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121353272 | |||||||
| chr7:121353505 | C | T | 1 | a0001c0001t0001g0010 | 3 | NA18955.hp1 NA18956.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.468-2236G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121353505 | |||||||
| chr7:121353560 | A | G | 3 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0117 |
3 | HG02055.hp2 HG02970.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.468-2291T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121353560 | |||||||
| chr7:121353681 | C | A | 10 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(7): Show |
14 | HG01074.hp2 HG01192.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.468-2412G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121353681 | |||||||
| chr7:121353788 | G | GT | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0153 |
3 | NA18988.hp2 NA19065.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.468-2520dupA | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121353788 | |||||||
| chr7:121353917 | T | C | 1 | a0001c0001t0002g0156 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.468-2648A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121353917 | |||||||
| chr7:121353968 | A | C | 5 | a0001c0001t0003g0005 a0001c0001t0003g0065 a0001c0001t0003g0066 others(2): Show |
8 | HG02486.hp1 HG02559.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.468-2699T>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121353968 | |||||||
| chr7:121354046 | T | G | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.468-2777A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121354046 | |||||||
| chr7:121354115 | G | T | 60 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(57): Show |
84 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.468-2846C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121354115 | |||||||
| chr7:121354193 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.468-2924C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121354193 | |||||||
| chr7:121354557 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.468-3288T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121354557 | |||||||
| chr7:121354619 | T | C | 117 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(114): Show |
158 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.468-3350A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121354619 | |||||||
| chr7:121354697 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.468-3428G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121354697 | |||||||
| chr7:121354772 | T | C | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.468-3503A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121354772 | |||||||
| chr7:121354781 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.468-3512G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121354781 | |||||||
| chr7:121354782 | G | A | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.468-3513C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121354782 | |||||||
| chr7:121354818 | C | A | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.468-3549G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121354818 | |||||||
| chr7:121355280 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.468-4011A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121355280 | |||||||
| chr7:121355342 | A | G | 2 | a0001c0001t0002g0162 a0001c0001t0002g0163 |
2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.468-4073T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121355342 | |||||||
| chr7:121355373 | C | T | 6 | a0001c0001t0005g0006 a0001c0001t0005g0189 a0001c0001t0005g0193 others(3): Show |
9 | HG01891.hp2 HG02615.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.468-4104G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121355373 | |||||||
| chr7:121355392 | C | G | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.468-4123G>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121355392 | |||||||
| chr7:121355409 | T | C | 1 | a0001c0001t0002g0040 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.468-4140A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121355409 | |||||||
| chr7:121355717 | G | C | 1 | a0001c0001t0002g0156 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.467+4326C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121355717 | |||||||
| chr7:121355741 | G | C | 1 | a0001c0001t0002g0181 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.467+4302C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121355741 | |||||||
| chr7:121355864 | G | C | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.467+4179C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121355864 | |||||||
| chr7:121356039 | GA | G | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.467+4003delT | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121356039 | |||||||
| chr7:121356120 | T | C | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.467+3923A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121356120 | |||||||
| chr7:121356186 | G | A | 119 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(116): Show |
160 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.467+3857C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121356186 | |||||||
| chr7:121356196 | A | AG | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.467+3846dupC | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121356196 | |||||||
| chr7:121356405 | A | T | 1 | a0001c0001t0013g0047 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.467+3638T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121356405 | |||||||
| chr7:121356420 | A | G | 2 | a0001c0001t0001g0003 a0001c0001t0001g0182 |
6 | HG02055.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.467+3623T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121356420 | |||||||
| chr7:121356453 | C | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0055 others(2): Show |
8 | HG02083.hp2 NA18948.hp1 NA18980.hp1 others(5): Show |
intron_variant | MODIFIER | c.467+3590G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121356453 | |||||||
| chr7:121356483 | A | T | 1 | a0001c0001t0002g0181 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.467+3560T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121356483 | |||||||
| chr7:121356489 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.467+3554T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121356489 | |||||||
| chr7:121356541 | C | T | 119 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(116): Show |
160 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.467+3502G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121356541 | |||||||
| chr7:121356873 | A | G | 1 | a0001c0001t0001g0045 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.467+3170T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121356873 | |||||||
| chr7:121356910 | G | C | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.467+3133C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121356910 | |||||||
| chr7:121356985 | T | C | 58 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(55): Show |
75 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.467+3058A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121356985 | |||||||
| chr7:121357298 | G | A | 1 | a0001c0001t0017g0054 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.467+2745C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121357298 | |||||||
| chr7:121357315 | G | T | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.467+2728C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121357315 | |||||||
| chr7:121357464 | C | T | 1 | a0001c0001t0002g0111 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.467+2579G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121357464 | |||||||
| chr7:121357506 | T | A | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(120): Show |
168 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.467+2537A>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121357506 | |||||||
| chr7:121357528 | T | C | 1 | a0001c0001t0004g0183 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.467+2515A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121357528 | |||||||
| chr7:121358031 | G | GC | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.467+2011dupG | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121358031 | |||||||
| chr7:121358223 | T | G | 60 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(57): Show |
84 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.467+1820A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121358223 | |||||||
| chr7:121358582 | TG | T | 13 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0016 others(10): Show |
19 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.467+1460delC | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121358582 | |||||||
| chr7:121358730 | C | T | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.467+1313G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121358730 | |||||||
| chr7:121358912 | C | T | 26 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(23): Show |
33 | HG01074.hp2 HG01192.hp1 HG01433.hp1 others(30): Show |
intron_variant | MODIFIER | c.467+1131G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121358912 | |||||||
| chr7:121359031 | A | G | 7 | a0001c0001t0002g0156 a0001c0001t0005g0006 a0001c0001t0005g0189 others(4): Show |
10 | HG01891.hp2 HG02109.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.467+1012T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121359031 | |||||||
| chr7:121359099 | G | A | 1 | a0001c0001t0005g0193 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.467+944C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121359099 | |||||||
| chr7:121359127 | T | TA | 33 | a0001c0001t0002g0181 a0001c0001t0003g0005 a0001c0001t0003g0031 others(30): Show |
43 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.467+915dupT | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121359127 | |||||||
| chr7:121359283 | T | C | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.467+760A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121359283 | |||||||
| chr7:121359407 | CGTAAGTG others(5): Show |
C | 1 | a0001c0001t0002g0040 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.467+624_467+635del others(12): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121359407 | |||||||
| chr7:121359546 | T | C | 1 | a0001c0001t0002g0165 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.467+497A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121359546 | |||||||
| chr7:121359967 | A | AT | 117 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(114): Show |
158 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.467+75dupA | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121359967 | |||||||
| chr7:121360030 | A | AAAGTTTT | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.467+12_467+13insAA others(5): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 8/9 | chr7 | 121360030 | |||||||
| chr7:121360585 | C | A | 16 | a0001c0001t0002g0040 a0001c0001t0002g0050 a0001c0001t0002g0051 others(13): Show |
19 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.383-458G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121360585 | |||||||
| chr7:121360664 | C | T | 60 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(57): Show |
84 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.383-537G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121360664 | |||||||
| chr7:121360690 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.383-563G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121360690 | |||||||
| chr7:121360708 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.383-581G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121360708 | |||||||
| chr7:121360729 | G | A | 1 | a0001c0001t0014g0131 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.383-602C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121360729 | |||||||
| chr7:121360733 | T | C | 4 | a0001c0001t0001g0029 a0001c0001t0001g0151 a0001c0001t0001g0154 others(1): Show |
5 | HG01261.hp1 HG01346.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.383-606A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121360733 | |||||||
| chr7:121360877 | A | G | 61 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(58): Show |
85 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.383-750T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121360877 | |||||||
| chr7:121360914 | A | G | 16 | a0001c0001t0002g0040 a0001c0001t0002g0050 a0001c0001t0002g0051 others(13): Show |
19 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.383-787T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121360914 | |||||||
| chr7:121361104 | A | T | 16 | a0001c0001t0002g0040 a0001c0001t0002g0050 a0001c0001t0002g0051 others(13): Show |
19 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.383-977T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121361104 | |||||||
| chr7:121361132 | A | C | 1 | a0001c0001t0002g0163 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.383-1005T>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121361132 | |||||||
| chr7:121361186 | A | C | 58 | a0001c0001t0001g0052 a0001c0001t0002g0004 a0001c0001t0002g0018 others(55): Show |
75 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.383-1059T>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121361186 | |||||||
| chr7:121361510 | A | G | 1 | a0001c0001t0002g0156 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.383-1383T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121361510 | |||||||
| chr7:121361541 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.382+1356A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121361541 | |||||||
| chr7:121361676 | G | A | 1 | a0001c0001t0002g0064 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.382+1221C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121361676 | |||||||
| chr7:121361922 | C | G | 1 | a0001c0001t0002g0040 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.382+975G>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121361922 | |||||||
| chr7:121361929 | G | A | 1 | a0001c0001t0002g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.382+968C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121361929 | |||||||
| chr7:121362134 | C | T | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.382+763G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121362134 | |||||||
| chr7:121362212 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.382+685G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121362212 | |||||||
| chr7:121362247 | G | A | 1 | a0001c0001t0016g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.382+650C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121362247 | |||||||
| chr7:121362274 | T | A | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.382+623A>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121362274 | |||||||
| chr7:121362403 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.382+494T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121362403 | |||||||
| chr7:121362428 | G | A | 2 | a0001c0001t0001g0132 a0001c0001t0001g0142 |
2 | HG02074.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.382+469C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121362428 | |||||||
| chr7:121362463 | T | G | 1 | a0001c0001t0002g0181 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.382+434A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121362463 | |||||||
| chr7:121362539 | T | C | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.382+358A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121362539 | |||||||
| chr7:121362648 | T | A | 19 | a0001c0001t0001g0122 a0001c0001t0002g0040 a0001c0001t0003g0005 others(16): Show |
23 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.382+249A>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121362648 | |||||||
| chr7:121362822 | A | G | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.382+75T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121362822 | |||||||
| chr7:121362856 | C | T | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.382+41G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 7/9 | chr7 | 121362856 | |||||||
| chr7:121363001 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.332-54C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 6/9 | chr7 | 121363001 | |||||||
| chr7:121363239 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.332-292G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 6/9 | chr7 | 121363239 | |||||||
| chr7:121363258 | G | C | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.332-311C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 6/9 | chr7 | 121363258 | |||||||
| chr7:121363520 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.332-573A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 6/9 | chr7 | 121363520 | |||||||
| chr7:121363564 | T | G | 17 | a0001c0001t0003g0005 a0001c0001t0003g0031 a0001c0001t0003g0065 others(14): Show |
21 | HG00438.hp2 HG00544.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.331+566A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 6/9 | chr7 | 121363564 | |||||||
| chr7:121364036 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.331+94C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 6/9 | chr7 | 121364036 | |||||||
| chr7:121364270 | G | T | 26 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(23): Show |
33 | HG01074.hp2 HG01192.hp1 HG01433.hp1 others(30): Show |
intron_variant | MODIFIER | c.273-82C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121364270 | |||||||
| chr7:121364380 | C | T | 6 | a0001c0001t0005g0006 a0001c0001t0005g0189 a0001c0001t0005g0193 others(3): Show |
9 | HG01891.hp2 HG02615.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.273-192G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121364380 | |||||||
| chr7:121364503 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.273-315C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121364503 | |||||||
| chr7:121364530 | G | C | 6 | a0001c0001t0005g0006 a0001c0001t0005g0189 a0001c0001t0005g0193 others(3): Show |
9 | HG01891.hp2 HG02615.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.273-342C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121364530 | |||||||
| chr7:121364656 | T | C | 1 | a0001c0001t0002g0040 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.273-468A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121364656 | |||||||
| chr7:121364694 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.273-506C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121364694 | |||||||
| chr7:121364749 | T | C | 33 | a0001c0001t0002g0181 a0001c0001t0003g0005 a0001c0001t0003g0031 others(30): Show |
43 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.273-561A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121364749 | |||||||
| chr7:121364876 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.273-688A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121364876 | |||||||
| chr7:121364935 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0046 a0001c0001t0011g0137 |
5 | HG00741.hp2 HG01081.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.273-747C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121364935 | |||||||
| chr7:121365102 | G | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0182 |
6 | HG02055.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.273-914C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121365102 | |||||||
| chr7:121365357 | A | C | 1 | a0001c0001t0002g0156 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.273-1169T>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121365357 | |||||||
| chr7:121365368 | T | C | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.273-1180A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121365368 | |||||||
| chr7:121365582 | T | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(57): Show |
84 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.273-1394A>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121365582 | |||||||
| chr7:121365672 | T | C | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.273-1484A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121365672 | |||||||
| chr7:121365967 | C | A | 1 | a0001c0001t0002g0156 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.273-1779G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121365967 | |||||||
| chr7:121366073 | T | C | 2 | a0001c0001t0002g0064 a0001c0001t0017g0054 |
2 | HG01433.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.273-1885A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121366073 | |||||||
| chr7:121366302 | TAATG | T | 2 | a0001c0001t0004g0183 a0001c0001t0016g0166 |
2 | HG01106.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.273-2118_273-2115d others(6): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121366302 | |||||||
| chr7:121366345 | TATCGTTC others(45): Show |
T | 1 | a0001c0001t0001g0135 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.273-2209_273-2158d others(54): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121366345 | |||||||
| chr7:121366687 | A | G | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.273-2499T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121366687 | |||||||
| chr7:121366749 | C | A | 26 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(23): Show |
33 | HG01074.hp2 HG01192.hp1 HG01433.hp1 others(30): Show |
intron_variant | MODIFIER | c.273-2561G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121366749 | |||||||
| chr7:121367195 | T | C | 119 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(116): Show |
160 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.273-3007A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121367195 | |||||||
| chr7:121367208 | T | C | 1 | a0001c0001t0001g0059 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.273-3020A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121367208 | |||||||
| chr7:121367289 | C | T | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.273-3101G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121367289 | |||||||
| chr7:121367291 | T | C | 1 | a0001c0001t0012g0175 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.273-3103A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121367291 | |||||||
| chr7:121367509 | T | C | 2 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.273-3321A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121367509 | |||||||
| chr7:121367579 | C | A | 1 | a0001c0001t0017g0054 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.273-3391G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121367579 | |||||||
| chr7:121367807 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.272+3493T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121367807 | |||||||
| chr7:121367947 | C | G | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.272+3353G>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121367947 | |||||||
| chr7:121368066 | T | C | 1 | a0001c0001t0001g0161 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.272+3234A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368066 | |||||||
| chr7:121368149 | T | C | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.272+3151A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368149 | |||||||
| chr7:121368228 | T | C | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.272+3072A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368228 | |||||||
| chr7:121368264 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.272+3036T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368264 | |||||||
| chr7:121368486 | C | T | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.272+2814G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368486 | |||||||
| chr7:121368677 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.272+2623A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368677 | |||||||
| chr7:121368755 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.272+2545G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368755 | |||||||
| chr7:121368861 | A | G | 1 | a0001c0001t0004g0183 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.272+2439T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368861 | |||||||
| chr7:121368863 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.272+2437G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368863 | |||||||
| chr7:121368871 | T | C | 1 | a0001c0001t0001g0015 | 2 | HG01346.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.272+2429A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368871 | |||||||
| chr7:121368953 | A | G | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.272+2347T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368953 | |||||||
| chr7:121368969 | GTTGT | G | 12 | a0001c0001t0003g0031 a0001c0001t0003g0069 a0001c0001t0003g0171 others(9): Show |
13 | HG00438.hp2 HG00544.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.272+2327_272+2330d others(6): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368969 | |||||||
| chr7:121368972 | GT | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(83): Show |
127 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.272+2327delA | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368972 | |||||||
| chr7:121368972 | GTT | G | 6 | a0001c0001t0001g0009 a0001c0001t0001g0074 a0001c0001t0001g0081 others(3): Show |
6 | HG00639.hp1 HG01243.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.272+2326_272+2327d others(4): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368972 | |||||||
| chr7:121368972 | GTTT | G | 8 | a0001c0001t0002g0040 a0001c0001t0004g0007 a0001c0001t0004g0008 others(5): Show |
10 | HG00140.hp1 HG01255.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.272+2325_272+2327d others(5): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368972 | |||||||
| chr7:121368972 | GTTTT | G | 34 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(31): Show |
43 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.272+2324_272+2327d others(6): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368972 | |||||||
| chr7:121368972 | GTTTTT | G | 6 | a0001c0001t0005g0006 a0001c0001t0005g0189 a0001c0001t0005g0193 others(3): Show |
9 | HG01891.hp2 HG02615.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.272+2323_272+2327d others(7): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368972 | |||||||
| chr7:121368974 | T | G | 1 | a0001c0001t0001g0117 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.272+2326A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368974 | |||||||
| chr7:121368975 | T | G | 1 | a0001c0001t0001g0055 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.272+2325A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368975 | |||||||
| chr7:121368976 | T | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0085 others(1): Show |
7 | HG02083.hp2 NA18948.hp1 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.272+2324A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121368976 | |||||||
| chr7:121369033 | G | A | 1 | a0001c0001t0002g0181 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.272+2267C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121369033 | |||||||
| chr7:121369052 | C | T | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.272+2248G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121369052 | |||||||
| chr7:121369234 | A | G | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.272+2066T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121369234 | |||||||
| chr7:121369271 | A | G | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.272+2029T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121369271 | |||||||
| chr7:121369316 | G | A | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.272+1984C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121369316 | |||||||
| chr7:121369899 | G | C | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.272+1401C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121369899 | |||||||
| chr7:121369939 | T | TAA | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.272+1359_272+1360d others(4): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121369939 | |||||||
| chr7:121369945 | G | A | 6 | a0001c0001t0005g0006 a0001c0001t0005g0189 a0001c0001t0005g0193 others(3): Show |
9 | HG01891.hp2 HG02615.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.272+1355C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121369945 | |||||||
| chr7:121370112 | T | C | 1 | a0001c0001t0010g0149 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.272+1188A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121370112 | |||||||
| chr7:121370155 | T | C | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.272+1145A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121370155 | |||||||
| chr7:121370358 | G | C | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.272+942C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121370358 | |||||||
| chr7:121370361 | T | C | 33 | a0001c0001t0002g0181 a0001c0001t0003g0005 a0001c0001t0003g0031 others(30): Show |
43 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.272+939A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121370361 | |||||||
| chr7:121370462 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.272+838A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121370462 | |||||||
| chr7:121370469 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.272+831G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121370469 | |||||||
| chr7:121370844 | C | T | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.272+456G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121370844 | |||||||
| chr7:121371157 | G | GA | 6 | a0001c0001t0005g0006 a0001c0001t0005g0189 a0001c0001t0005g0193 others(3): Show |
9 | HG01891.hp2 HG02615.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.272+142dupT | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 5/9 | chr7 | 121371157 | |||||||
| chr7:121371561 | G | T | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.149-138C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 4/9 | chr7 | 121371561 | |||||||
| chr7:121371593 | A | T | 1 | a0001c0001t0002g0156 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.149-170T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 4/9 | chr7 | 121371593 | |||||||
| chr7:121371600 | T | A | 1 | a0001c0001t0017g0054 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.149-177A>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 4/9 | chr7 | 121371600 | |||||||
| chr7:121371614 | A | C | 1 | a0001c0001t0001g0128 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.149-191T>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 4/9 | chr7 | 121371614 | |||||||
| chr7:121371789 | T | C | 1 | a0001c0001t0001g0023 | 2 | HG01517.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.148+321A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 4/9 | chr7 | 121371789 | |||||||
| chr7:121372010 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.148+100G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 4/9 | chr7 | 121372010 | |||||||
| chr7:121372022 | A | T | 1 | a0001c0001t0001g0074 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.148+88T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 4/9 | chr7 | 121372022 | |||||||
| chr7:121372142 | GA | G | 11 | a0001c0001t0002g0004 a0001c0001t0002g0018 a0001c0001t0002g0041 others(8): Show |
18 | HG01074.hp2 HG01192.hp1 HG01891.hp2 others(15): Show |
splice_region_variant&intron_variant | LOW | c.119-4delT | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121372142 | |||||||
| chr7:121372181 | T | C | 1 | a0001c0001t0002g0181 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.119-42A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121372181 | |||||||
| chr7:121372215 | C | T | 1 | a0001c0001t0015g0115 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.119-76G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121372215 | |||||||
| chr7:121372241 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.119-102T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121372241 | |||||||
| chr7:121372337 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.119-198C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121372337 | |||||||
| chr7:121372527 | C | T | 2 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.119-388G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121372527 | |||||||
| chr7:121372639 | A | T | 1 | a0001c0001t0001g0028 | 2 | HG02523.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.119-500T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121372639 | |||||||
| chr7:121372718 | T | G | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.119-579A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121372718 | |||||||
| chr7:121372821 | T | C | 17 | a0001c0001t0003g0005 a0001c0001t0003g0031 a0001c0001t0003g0065 others(14): Show |
21 | HG00438.hp2 HG00544.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.119-682A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121372821 | |||||||
| chr7:121372861 | A | G | 1 | a0001c0001t0002g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.119-722T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121372861 | |||||||
| chr7:121373176 | G | GTCAGGAT others(15): Show |
5 | a0001c0001t0001g0009 a0001c0001t0001g0044 a0001c0001t0001g0082 others(2): Show |
7 | HG01891.hp1 HG02258.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.119-1059_119-1038d others(24): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121373176 | |||||||
| chr7:121373176 | GTCAGGAT others(15): Show |
G | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.119-1059_119-1038d others(24): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121373176 | |||||||
| chr7:121373353 | T | G | 1 | a0001c0001t0001g0093 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.119-1214A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121373353 | |||||||
| chr7:121373747 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.119-1608C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121373747 | |||||||
| chr7:121373818 | C | T | 1 | a0001c0001t0002g0040 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.119-1679G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121373818 | |||||||
| chr7:121373831 | G | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0078 a0001c0001t0001g0079 |
4 | NA18969.hp2 NA18994.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.119-1692C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121373831 | |||||||
| chr7:121373866 | C | CA | 10 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(7): Show |
14 | HG01074.hp2 HG01192.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.119-1728dupT | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121373866 | |||||||
| chr7:121373888 | C | T | 1 | a0001c0001t0003g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.119-1749G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121373888 | |||||||
| chr7:121373922 | C | G | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.119-1783G>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121373922 | |||||||
| chr7:121373995 | CA | C | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.119-1857delT | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121373995 | |||||||
| chr7:121374121 | C | T | 1 | a0001c0001t0002g0181 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.119-1982G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121374121 | |||||||
| chr7:121374144 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.119-2005C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121374144 | |||||||
| chr7:121374338 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.119-2199C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121374338 | |||||||
| chr7:121374351 | C | G | 1 | a0001c0001t0001g0106 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.119-2212G>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121374351 | |||||||
| chr7:121374498 | A | G | 1 | a0001c0001t0017g0054 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.119-2359T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121374498 | |||||||
| chr7:121374572 | A | G | 1 | a0001c0001t0003g0174 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.119-2433T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121374572 | |||||||
| chr7:121374661 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.119-2522G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121374661 | |||||||
| chr7:121374759 | G | A | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.119-2620C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121374759 | |||||||
| chr7:121374906 | A | C | 1 | a0001c0001t0016g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.119-2767T>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121374906 | |||||||
| chr7:121374960 | C | T | 6 | a0001c0001t0005g0006 a0001c0001t0005g0189 a0001c0001t0005g0193 others(3): Show |
9 | HG01891.hp2 HG02615.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.119-2821G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121374960 | |||||||
| chr7:121375013 | G | C | 1 | a0001c0001t0001g0014 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.119-2874C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121375013 | |||||||
| chr7:121375193 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.119-3054C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121375193 | |||||||
| chr7:121375274 | G | C | 4 | a0001c0001t0002g0004 a0001c0001t0002g0018 a0001c0001t0002g0041 others(1): Show |
8 | HG01074.hp2 HG01192.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.119-3135C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121375274 | |||||||
| chr7:121375404 | C | A | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0004 others(56): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.119-3265G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121375404 | |||||||
| chr7:121375474 | T | A | 1 | a0001c0001t0001g0081 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.119-3335A>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121375474 | |||||||
| chr7:121375554 | A | C | 1 | a0001c0001t0012g0175 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.118+3356T>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121375554 | |||||||
| chr7:121375833 | T | G | 2 | a0001c0001t0003g0031 a0001c0001t0003g0069 |
3 | HG02258.hp1 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.118+3077A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121375833 | |||||||
| chr7:121376049 | T | A | 1 | a0001c0001t0001g0098 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.118+2861A>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121376049 | |||||||
| chr7:121376157 | T | C | 1 | a0001c0001t0007g0187 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.118+2753A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121376157 | |||||||
| chr7:121376342 | G | C | 1 | a0001c0001t0001g0124 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.118+2568C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121376342 | |||||||
| chr7:121376368 | A | T | 6 | a0001c0001t0005g0006 a0001c0001t0005g0189 a0001c0001t0005g0193 others(3): Show |
9 | HG01891.hp2 HG02615.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.118+2542T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121376368 | |||||||
| chr7:121376750 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.118+2160A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121376750 | |||||||
| chr7:121376830 | A | G | 2 | a0001c0001t0003g0065 a0001c0001t0003g0067 |
2 | HG02486.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.118+2080T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121376830 | |||||||
| chr7:121377077 | A | T | 1 | a0001c0001t0001g0127 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.118+1833T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121377077 | |||||||
| chr7:121377089 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.118+1821C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121377089 | |||||||
| chr7:121377106 | G | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0161 others(1): Show |
8 | HG02055.hp1 HG02647.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.118+1804C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121377106 | |||||||
| chr7:121377407 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.118+1503G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121377407 | |||||||
| chr7:121377420 | C | A | 64 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(61): Show |
92 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.118+1490G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121377420 | |||||||
| chr7:121377758 | T | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.118+1152A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121377758 | |||||||
| chr7:121378525 | C | T | 66 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(63): Show |
94 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.118+385G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121378525 | |||||||
| chr7:121378605 | T | G | 17 | a0001c0001t0003g0005 a0001c0001t0003g0031 a0001c0001t0003g0065 others(14): Show |
21 | HG00438.hp2 HG00544.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.118+305A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121378605 | |||||||
| chr7:121378713 | T | TAGAA | 99 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(96): Show |
137 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.118+193_118+196dup others(4): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121378713 | |||||||
| chr7:121378786 | A | G | 3 | a0001c0001t0001g0039 a0001c0001t0001g0106 a0001c0001t0001g0107 |
3 | HG01099.hp2 HG01261.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.118+124T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121378786 | |||||||
| chr7:121378803 | A | T | 64 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(61): Show |
92 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.118+107T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121378803 | |||||||
| chr7:121378810 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.118+100G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 3/9 | chr7 | 121378810 | |||||||
| chr7:121379065 | A | G | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.14-51T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121379065 | |||||||
| chr7:121379199 | T | C | 4 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0161 others(1): Show |
8 | HG02055.hp1 HG02647.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.14-185A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121379199 | |||||||
| chr7:121379408 | G | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0161 others(1): Show |
8 | HG02055.hp1 HG02647.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.14-394C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121379408 | |||||||
| chr7:121379425 | T | C | 1 | a0001c0001t0008g0191 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.14-411A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121379425 | |||||||
| chr7:121379466 | A | G | 3 | a0001c0001t0001g0039 a0001c0001t0001g0106 a0001c0001t0001g0107 |
3 | HG01099.hp2 HG01261.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.14-452T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121379466 | |||||||
| chr7:121379517 | A | G | 1 | a0001c0001t0003g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.14-503T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121379517 | |||||||
| chr7:121379550 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.14-536A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121379550 | |||||||
| chr7:121379751 | G | A | 1 | a0001c0001t0002g0165 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.14-737C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121379751 | |||||||
| chr7:121379908 | T | C | 4 | a0001c0001t0002g0004 a0001c0001t0002g0018 a0001c0001t0002g0041 others(1): Show |
8 | HG01074.hp2 HG01192.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.14-894A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121379908 | |||||||
| chr7:121380596 | G | T | 1 | a0001c0001t0004g0183 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.14-1582C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380596 | |||||||
| chr7:121380604 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.14-1590G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380604 | |||||||
| chr7:121380733 | T | TTA | 13 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0046 others(10): Show |
16 | HG00642.hp1 HG00741.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.14-1721_14-1720dup others(2): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380733 | |||||||
| chr7:121380733 | T | TTATA | 4 | a0001c0001t0001g0059 a0001c0001t0001g0140 a0001c0001t0001g0161 others(1): Show |
4 | HG01884.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.14-1723_14-1720dup others(4): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380733 | |||||||
| chr7:121380733 | T | TTATATA | 7 | a0001c0001t0001g0003 a0001c0001t0001g0182 a0001c0001t0002g0181 others(4): Show |
14 | HG02055.hp1 HG02486.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.14-1725_14-1720dup others(6): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380733 | |||||||
| chr7:121380733 | T | TTATATAT others(1): Show |
4 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0003g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.14-1727_14-1720dup others(8): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380733 | |||||||
| chr7:121380733 | T | TTATATAT others(3): Show |
9 | a0001c0001t0002g0004 a0001c0001t0002g0018 a0001c0001t0002g0163 others(6): Show |
13 | HG00544.hp2 HG01074.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.14-1729_14-1720dup others(10): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380733 | |||||||
| chr7:121380733 | T | TTATATAT others(5): Show |
7 | a0001c0001t0002g0041 a0001c0001t0002g0063 a0001c0001t0002g0165 others(4): Show |
8 | HG00438.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.14-1731_14-1720dup others(12): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380733 | |||||||
| chr7:121380733 | T | TTATATAT others(7): Show |
3 | a0001c0001t0002g0162 a0001c0001t0003g0178 a0001c0001t0004g0017 |
4 | HG00738.hp1 HG01106.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.14-1733_14-1720dup others(14): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380733 | |||||||
| chr7:121380733 | T | TTATATAT others(9): Show |
1 | a0001c0001t0004g0036 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.14-1735_14-1720dup others(16): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380733 | |||||||
| chr7:121380733 | T | TTATATAT others(13): Show |
4 | a0001c0001t0002g0051 a0001c0001t0004g0007 a0001c0001t0004g0183 others(1): Show |
6 | HG00140.hp1 HG01106.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.14-1739_14-1720dup others(20): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380733 | |||||||
| chr7:121380733 | T | TTATATAT others(15): Show |
4 | a0001c0001t0004g0035 a0001c0001t0004g0037 a0001c0001t0004g0169 others(1): Show |
4 | HG00280.hp2 HG01978.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.14-1741_14-1720dup others(22): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380733 | |||||||
| chr7:121380733 | T | TTATATAT others(17): Show |
4 | a0001c0001t0002g0050 a0001c0001t0004g0008 a0001c0001t0004g0033 others(1): Show |
6 | HG01255.hp1 HG01358.hp2 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.14-1720_14-1719ins others(24): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380733 | |||||||
| chr7:121380733 | T | TTATATAT others(19): Show |
3 | a0001c0001t0002g0040 a0001c0001t0004g0016 a0001c0001t0004g0034 |
4 | HG00639.hp2 HG01975.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.14-1720_14-1719ins others(26): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380733 | |||||||
| chr7:121380733 | T | TTATATAT others(21): Show |
1 | a0001c0001t0004g0038 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.14-1720_14-1719ins others(28): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380733 | |||||||
| chr7:121380757 | G | A | 2 | a0001c0001t0002g0060 a0001c0001t0002g0061 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.14-1743C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380757 | |||||||
| chr7:121380758 | A | T | 2 | a0001c0001t0002g0060 a0001c0001t0002g0061 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.14-1744T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380758 | |||||||
| chr7:121380759 | C | A | 2 | a0001c0001t0002g0060 a0001c0001t0002g0061 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.14-1745G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380759 | |||||||
| chr7:121380760 | A | T | 2 | a0001c0001t0002g0060 a0001c0001t0002g0061 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.14-1746T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380760 | |||||||
| chr7:121380761 | C | A | 2 | a0001c0001t0002g0060 a0001c0001t0002g0061 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.14-1747G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380761 | |||||||
| chr7:121380762 | T | TATATATA others(9): Show |
1 | a0001c0001t0002g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.14-1749_14-1748ins others(16): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380762 | |||||||
| chr7:121380762 | T | TATATATA others(5): Show |
1 | a0001c0001t0002g0060 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.14-1749_14-1748ins others(12): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380762 | |||||||
| chr7:121380995 | C | G | 1 | a0001c0001t0002g0060 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.13+1962G>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121380995 | |||||||
| chr7:121381316 | T | A | 1 | a0001c0001t0001g0138 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.13+1641A>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121381316 | |||||||
| chr7:121381360 | T | C | 2 | a0001c0001t0007g0187 a0001c0001t0007g0188 |
2 | HG01255.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.13+1597A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121381360 | |||||||
| chr7:121381425 | AAACACAA others(3): Show |
A | 1 | a0001c0001t0001g0120 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.13+1522_13+1531del others(10): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121381425 | |||||||
| chr7:121381556 | CTTACT | C | 2 | a0001c0001t0002g0162 a0001c0001t0002g0163 |
2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.13+1396_13+1400del others(5): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121381556 | |||||||
| chr7:121381656 | C | CCA | 20 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0019 others(17): Show |
25 | HG00609.hp2 HG00621.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.13+1299_13+1300dup others(2): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121381656 | |||||||
| chr7:121381656 | C | CCACACAC others(1): Show |
13 | a0001c0001t0002g0181 a0001c0001t0003g0005 a0001c0001t0003g0065 others(10): Show |
16 | HG00438.hp2 HG00544.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.13+1293_13+1300dup others(8): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121381656 | |||||||
| chr7:121381656 | C | CCACACAC others(3): Show |
15 | a0001c0001t0003g0172 a0001c0001t0003g0173 a0001c0001t0004g0007 others(12): Show |
20 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.13+1291_13+1300dup others(10): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121381656 | |||||||
| chr7:121381656 | C | CCACACAC others(5): Show |
2 | a0001c0001t0004g0008 a0001c0001t0016g0166 |
2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.13+1289_13+1300dup others(12): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121381656 | |||||||
| chr7:121381656 | CCA | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0048 others(9): Show |
12 | HG00558.hp2 HG01069.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.13+1299_13+1300del others(2): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121381656 | |||||||
| chr7:121381656 | CCACACAC others(3): Show |
C | 2 | a0001c0001t0003g0031 a0001c0001t0003g0069 |
3 | HG02258.hp1 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.13+1291_13+1300del others(10): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121381656 | |||||||
| chr7:121381656 | CCACACAC others(11): Show |
C | 2 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.13+1283_13+1300del others(18): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121381656 | |||||||
| chr7:121381742 | GTTC | G | 17 | a0001c0001t0003g0005 a0001c0001t0003g0031 a0001c0001t0003g0065 others(14): Show |
21 | HG00438.hp2 HG00544.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.13+1212_13+1214del others(3): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121381742 | |||||||
| chr7:121382133 | G | A | 2 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.13+824C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121382133 | |||||||
| chr7:121382214 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.13+743G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121382214 | |||||||
| chr7:121382301 | T | C | 1 | a0001c0001t0002g0163 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.13+656A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121382301 | |||||||
| chr7:121382350 | T | G | 4 | a0001c0001t0002g0040 a0001c0001t0002g0060 a0001c0001t0002g0061 others(1): Show |
4 | HG02280.hp1 HG02922.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.13+607A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121382350 | |||||||
| chr7:121382365 | C | G | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0072 others(8): Show |
13 | HG01243.hp2 HG01496.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.13+592G>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121382365 | |||||||
| chr7:121382418 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0161 others(1): Show |
8 | HG02055.hp1 HG02647.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.13+539G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121382418 | |||||||
| chr7:121382549 | G | GT | 6 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0122 others(3): Show |
8 | HG00323.hp1 HG01169.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.13+407dupA | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121382549 | |||||||
| chr7:121382549 | GT | G | 61 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0052 others(58): Show |
82 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.13+407delA | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121382549 | |||||||
| chr7:121382549 | GTT | G | 58 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(55): Show |
82 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.13+406_13+407delAA | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121382549 | |||||||
| chr7:121382567 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.13+390A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121382567 | |||||||
| chr7:121382767 | A | C | 1 | a0001c0001t0003g0174 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.13+190T>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121382767 | |||||||
| chr7:121382889 | T | C | 3 | a0001c0001t0001g0039 a0001c0001t0001g0106 a0001c0001t0001g0107 |
3 | HG01099.hp2 HG01261.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.13+68A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 2/9 | chr7 | 121382889 | |||||||
| chr7:121383142 | TA | T | 41 | a0001c0001t0001g0074 a0001c0001t0001g0081 a0001c0001t0002g0181 others(38): Show |
54 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.-41-133delT | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121383142 | |||||||
| chr7:121383415 | C | T | 33 | a0001c0001t0002g0181 a0001c0001t0003g0005 a0001c0001t0003g0031 others(30): Show |
43 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.-41-405G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121383415 | |||||||
| chr7:121383507 | A | G | 33 | a0001c0001t0002g0181 a0001c0001t0003g0005 a0001c0001t0003g0031 others(30): Show |
43 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.-41-497T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121383507 | |||||||
| chr7:121383520 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0141 |
3 | HG01358.hp1 HG02148.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.-41-510C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121383520 | |||||||
| chr7:121383530 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-41-520G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121383530 | |||||||
| chr7:121383577 | T | C | 1 | a0001c0001t0001g0108 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-41-567A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121383577 | |||||||
| chr7:121383724 | T | C | 13 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0016 others(10): Show |
19 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.-41-714A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121383724 | |||||||
| chr7:121383904 | G | C | 1 | a0001c0001t0001g0153 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-41-894C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121383904 | |||||||
| chr7:121384166 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-41-1156T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384166 | |||||||
| chr7:121384257 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-41-1247C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384257 | |||||||
| chr7:121384473 | T | A | 35 | a0001c0001t0002g0050 a0001c0001t0002g0051 a0001c0001t0002g0181 others(32): Show |
45 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.-41-1463A>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384473 | |||||||
| chr7:121384573 | T | C | 4 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0161 others(1): Show |
8 | HG02055.hp1 HG02647.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-41-1563A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384573 | |||||||
| chr7:121384654 | G | A | 33 | a0001c0001t0002g0181 a0001c0001t0003g0005 a0001c0001t0003g0031 others(30): Show |
43 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.-41-1644C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384654 | |||||||
| chr7:121384808 | A | T | 1 | a0001c0001t0001g0120 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1798T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384808 | |||||||
| chr7:121384817 | C | G | 1 | a0001c0001t0001g0120 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1807G>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384817 | |||||||
| chr7:121384818 | C | A | 1 | a0001c0001t0001g0120 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1808G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384818 | |||||||
| chr7:121384826 | G | T | 1 | a0001c0001t0001g0120 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1816C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384826 | |||||||
| chr7:121384827 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1817G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384827 | |||||||
| chr7:121384829 | A | C | 1 | a0001c0001t0001g0120 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1819T>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384829 | |||||||
| chr7:121384835 | T | G | 1 | a0001c0001t0001g0120 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1825A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384835 | |||||||
| chr7:121384840 | C | G | 1 | a0001c0001t0001g0120 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1830G>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384840 | |||||||
| chr7:121384845 | A | T | 1 | a0001c0001t0001g0120 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1835T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384845 | |||||||
| chr7:121384846 | T | G | 2 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-41-1836A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384846 | |||||||
| chr7:121384847 | C | G | 1 | a0001c0001t0001g0120 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1837G>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384847 | |||||||
| chr7:121384849 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1839T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384849 | |||||||
| chr7:121384850 | C | A | 1 | a0001c0001t0001g0120 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1840G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384850 | |||||||
| chr7:121384853 | C | A | 1 | a0001c0001t0001g0120 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1843G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384853 | |||||||
| chr7:121384854 | A | T | 1 | a0001c0001t0001g0120 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1844T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384854 | |||||||
| chr7:121384855 | G | T | 1 | a0001c0001t0001g0120 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1845C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384855 | |||||||
| chr7:121384856 | G | T | 1 | a0001c0001t0001g0120 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1846C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384856 | |||||||
| chr7:121384857 | A | T | 1 | a0001c0001t0001g0120 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1847T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384857 | |||||||
| chr7:121384859 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1849T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384859 | |||||||
| chr7:121384860 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1850C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384860 | |||||||
| chr7:121384865 | A | T | 1 | a0001c0001t0001g0120 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1855T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384865 | |||||||
| chr7:121384866 | T | A | 1 | a0001c0001t0001g0120 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1856A>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384866 | |||||||
| chr7:121384872 | A | C | 1 | a0001c0001t0001g0120 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1862T>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384872 | |||||||
| chr7:121384884 | A | T | 1 | a0001c0001t0001g0120 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1874T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384884 | |||||||
| chr7:121384888 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1878G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384888 | |||||||
| chr7:121384891 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1881C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384891 | |||||||
| chr7:121384894 | G | T | 1 | a0001c0001t0001g0120 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1884C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384894 | |||||||
| chr7:121384895 | C | A | 1 | a0001c0001t0001g0120 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1885G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384895 | |||||||
| chr7:121384896 | A | T | 1 | a0001c0001t0001g0120 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-41-1886T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384896 | |||||||
| chr7:121384966 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-41-1956C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121384966 | |||||||
| chr7:121385032 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-41-2022G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121385032 | |||||||
| chr7:121385093 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-41-2083A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121385093 | |||||||
| chr7:121385162 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-41-2152G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121385162 | |||||||
| chr7:121385241 | A | G | 33 | a0001c0001t0002g0181 a0001c0001t0003g0005 a0001c0001t0003g0031 others(30): Show |
43 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.-41-2231T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121385241 | |||||||
| chr7:121385304 | C | T | 2 | a0001c0001t0002g0060 a0001c0001t0002g0061 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-41-2294G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121385304 | |||||||
| chr7:121385330 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-41-2320A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121385330 | |||||||
| chr7:121385448 | T | C | 60 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(57): Show |
84 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.-41-2438A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121385448 | |||||||
| chr7:121385523 | A | C | 36 | a0001c0001t0001g0119 a0001c0001t0002g0050 a0001c0001t0002g0051 others(33): Show |
46 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.-41-2513T>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121385523 | |||||||
| chr7:121385825 | G | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0161 others(1): Show |
8 | HG02055.hp1 HG02647.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-41-2815C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121385825 | |||||||
| chr7:121385962 | G | A | 3 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0113 |
3 | HG02976.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-41-2952C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121385962 | |||||||
| chr7:121386023 | G | A | 1 | a0001c0001t0008g0190 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-41-3013C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121386023 | |||||||
| chr7:121386043 | T | C | 6 | a0001c0001t0005g0006 a0001c0001t0005g0189 a0001c0001t0005g0193 others(3): Show |
9 | HG01891.hp2 HG02615.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-41-3033A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121386043 | |||||||
| chr7:121386067 | A | G | 1 | a0001c0001t0001g0045 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-41-3057T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121386067 | |||||||
| chr7:121386435 | T | C | 2 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-41-3425A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121386435 | |||||||
| chr7:121386469 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-41-3459A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121386469 | |||||||
| chr7:121386569 | C | A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-41-3559G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121386569 | |||||||
| chr7:121386579 | C | T | 2 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-41-3569G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121386579 | |||||||
| chr7:121386664 | T | C | 1 | a0001c0001t0009g0143 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-41-3654A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121386664 | |||||||
| chr7:121386687 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-41-3677C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121386687 | |||||||
| chr7:121386687 | G | GCA | 3 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0113 |
3 | HG02976.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-41-3679_-41-3678d others(4): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121386687 | |||||||
| chr7:121386689 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-41-3679T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121386689 | |||||||
| chr7:121386692 | C | CAT | 5 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0002g0165 others(2): Show |
5 | HG02280.hp1 HG03579.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.-41-3684_-41-3683d others(4): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121386692 | |||||||
| chr7:121386692 | CAT | C | 70 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(67): Show |
98 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.-41-3684_-41-3683d others(4): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121386692 | |||||||
| chr7:121386694 | T | C | 2 | a0001c0001t0001g0003 a0001c0001t0001g0093 |
3 | HG00280.hp1 HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-41-3684A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121386694 | |||||||
| chr7:121386696 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-41-3686A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121386696 | |||||||
| chr7:121386920 | T | A | 1 | a0001c0001t0002g0165 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-41-3910A>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121386920 | |||||||
| chr7:121387026 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-41-4016G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121387026 | |||||||
| chr7:121387107 | G | A | 2 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-41-4097C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121387107 | |||||||
| chr7:121387380 | C | T | 44 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(41): Show |
65 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.-41-4370G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121387380 | |||||||
| chr7:121387388 | A | T | 2 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-41-4378T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121387388 | |||||||
| chr7:121387442 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-41-4432C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121387442 | |||||||
| chr7:121387836 | G | A | 17 | a0001c0001t0003g0005 a0001c0001t0003g0031 a0001c0001t0003g0065 others(14): Show |
21 | HG00438.hp2 HG00544.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-41-4826C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121387836 | |||||||
| chr7:121388235 | A | AAC | 75 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0025 others(72): Show |
106 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.-41-5227_-41-5226d others(4): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121388235 | |||||||
| chr7:121388235 | A | AACAC | 8 | a0001c0001t0001g0026 a0001c0001t0001g0056 a0001c0001t0001g0089 others(5): Show |
9 | HG00438.hp1 HG01496.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.-41-5229_-41-5226d others(6): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121388235 | |||||||
| chr7:121388235 | A | AACACAC | 55 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(52): Show |
81 | HG00323.hp2 HG00558.hp1 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.-41-5231_-41-5226d others(8): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121388235 | |||||||
| chr7:121388235 | A | AACACACA others(1): Show |
19 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0096 others(16): Show |
25 | HG00140.hp1 HG00280.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.-41-5233_-41-5226d others(10): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121388235 | |||||||
| chr7:121388235 | A | AACACACA others(3): Show |
7 | a0001c0001t0001g0161 a0001c0001t0004g0017 a0001c0001t0004g0033 others(4): Show |
11 | HG00639.hp2 HG00738.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.-41-5235_-41-5226d others(12): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121388235 | |||||||
| chr7:121388235 | A | AACACACA others(5): Show |
6 | a0001c0001t0001g0003 a0001c0001t0001g0182 a0001c0001t0002g0063 others(3): Show |
10 | HG01891.hp2 HG02055.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-41-5237_-41-5226d others(14): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121388235 | |||||||
| chr7:121388235 | AAC | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0154 |
2 | NA18969.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-41-5227_-41-5226d others(4): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121388235 | |||||||
| chr7:121388286 | C | T | 109 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(106): Show |
151 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.-41-5276G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121388286 | |||||||
| chr7:121388398 | G | A | 15 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0016 others(12): Show |
21 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.-41-5388C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121388398 | |||||||
| chr7:121388434 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-41-5424C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121388434 | |||||||
| chr7:121388623 | T | C | 2 | a0001c0001t0002g0156 a0001c0001t0002g0181 |
2 | HG02109.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-41-5613A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121388623 | |||||||
| chr7:121388934 | T | C | 2 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-41-5924A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121388934 | |||||||
| chr7:121389017 | T | C | 1 | a0001c0001t0004g0017 | 2 | HG00738.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.-41-6007A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121389017 | |||||||
| chr7:121389157 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-41-6147T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121389157 | |||||||
| chr7:121389504 | C | T | 1 | a0001c0001t0003g0172 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-41-6494G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121389504 | |||||||
| chr7:121389751 | C | G | 1 | a0001c0001t0004g0169 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-42+6411G>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121389751 | |||||||
| chr7:121389762 | C | CA | 14 | a0001c0001t0001g0110 a0001c0001t0001g0157 a0001c0001t0003g0031 others(11): Show |
15 | HG00438.hp2 HG00544.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-42+6399dupT | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121389762 | |||||||
| chr7:121390063 | T | C | 2 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-42+6099A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390063 | |||||||
| chr7:121390209 | T | C | 2 | a0001c0001t0002g0060 a0001c0001t0002g0061 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-42+5953A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390209 | |||||||
| chr7:121390260 | C | A | 3 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0113 |
3 | HG02976.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-42+5902G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390260 | |||||||
| chr7:121390513 | C | A | 4 | a0001c0001t0001g0042 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
4 | HG00673.hp1 NA18968.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.-42+5649G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390513 | |||||||
| chr7:121390692 | C | T | 1 | a0001c0001t0015g0115 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-42+5470G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390692 | |||||||
| chr7:121390784 | C | T | 1 | a0001c0001t0003g0172 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-42+5378G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390784 | |||||||
| chr7:121390813 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-42+5349G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390813 | |||||||
| chr7:121390848 | T | G | 1 | a0001c0001t0001g0090 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-42+5314A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390848 | |||||||
| chr7:121390850 | G | GGGT | 2 | a0001c0001t0001g0022 a0001c0001t0001g0094 |
3 | HG02647.hp1 HG02698.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-42+5311_-42+5312i others(5): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390850 | |||||||
| chr7:121390851 | G | GGT | 6 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0091 others(3): Show |
8 | HG00280.hp1 HG00323.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.-42+5310_-42+5311i others(4): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390851 | |||||||
| chr7:121390852 | G | GT | 10 | a0001c0001t0001g0039 a0001c0001t0001g0083 a0001c0001t0001g0084 others(7): Show |
10 | HG00735.hp1 HG01099.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.-42+5309_-42+5310i others(3): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390852 | |||||||
| chr7:121390852 | G | T | 1 | a0001c0001t0001g0090 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-42+5310C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390852 | |||||||
| chr7:121390852 | GC | G | 10 | a0001c0001t0001g0009 a0001c0001t0001g0070 a0001c0001t0001g0075 others(7): Show |
12 | HG00738.hp2 HG01069.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.-42+5309delG | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390852 | |||||||
| chr7:121390853 | C | CGG | 17 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(14): Show |
22 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.-42+5307_-42+5308d others(4): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390853 | |||||||
| chr7:121390853 | C | CGGG | 21 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(18): Show |
24 | HG00558.hp2 HG00738.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.-42+5306_-42+5308d others(5): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390853 | |||||||
| chr7:121390853 | C | CGGGG | 24 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0032 others(21): Show |
30 | HG00140.hp2 HG00544.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.-42+5305_-42+5308d others(6): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390853 | |||||||
| chr7:121390853 | C | CGGGGG | 18 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0015 others(15): Show |
21 | HG00323.hp1 HG00642.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.-42+5304_-42+5308d others(7): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390853 | |||||||
| chr7:121390853 | C | CGGGGGGG others(3): Show |
2 | a0001c0001t0001g0110 a0001c0001t0003g0174 |
2 | HG03710.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-42+5299_-42+5308d others(12): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390853 | |||||||
| chr7:121390853 | C | CGGGGGGG others(4): Show |
1 | a0001c0001t0002g0064 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-42+5298_-42+5308d others(13): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390853 | |||||||
| chr7:121390853 | C | CGGGGGGG others(5): Show |
1 | a0001c0001t0002g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-42+5297_-42+5308d others(14): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390853 | |||||||
| chr7:121390853 | C | CGGGGGGG others(9): Show |
1 | a0001c0001t0001g0062 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-42+5293_-42+5308d others(18): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390853 | |||||||
| chr7:121390853 | C | G | 21 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(18): Show |
24 | HG00280.hp1 HG00323.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.-42+5309G>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390853 | |||||||
| chr7:121390853 | C | T | 24 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(21): Show |
41 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.-42+5309G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390853 | |||||||
| chr7:121390854 | G | T | 10 | a0001c0001t0001g0009 a0001c0001t0001g0070 a0001c0001t0001g0075 others(7): Show |
12 | HG00738.hp2 HG01069.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.-42+5308C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390854 | |||||||
| chr7:121390855 | G | T | 5 | a0001c0001t0001g0019 a0001c0001t0001g0071 a0001c0001t0001g0072 others(2): Show |
6 | HG02135.hp2 HG03225.hp1 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.-42+5307C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390855 | |||||||
| chr7:121390860 | G | C | 2 | a0001c0001t0001g0003 a0001c0001t0001g0182 |
6 | HG02055.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-42+5302C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390860 | |||||||
| chr7:121390864 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-42+5298C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390864 | |||||||
| chr7:121390865 | G | T | 14 | a0001c0001t0001g0161 a0001c0001t0002g0040 a0001c0001t0002g0060 others(11): Show |
17 | HG01891.hp2 HG02280.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.-42+5297C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390865 | |||||||
| chr7:121390866 | G | GAGC | 2 | a0001c0001t0001g0003 a0001c0001t0001g0182 |
6 | HG02055.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-42+5295_-42+5296i others(5): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390866 | |||||||
| chr7:121390880 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-42+5282C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121390880 | |||||||
| chr7:121391571 | G | A | 3 | a0001c0001t0001g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 |
3 | HG02486.hp2 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-42+4591C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121391571 | |||||||
| chr7:121391825 | C | T | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(109): Show |
154 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.-42+4337G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121391825 | |||||||
| chr7:121391895 | A | T | 3 | a0001c0001t0001g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 |
3 | HG02486.hp2 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-42+4267T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121391895 | |||||||
| chr7:121391950 | T | C | 3 | a0001c0001t0001g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 |
3 | HG02486.hp2 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-42+4212A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121391950 | |||||||
| chr7:121391958 | A | G | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | HG00639.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-42+4204T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121391958 | |||||||
| chr7:121392218 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-42+3944G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121392218 | |||||||
| chr7:121392566 | G | GT | 4 | a0001c0001t0002g0004 a0001c0001t0002g0018 a0001c0001t0002g0041 others(1): Show |
8 | HG01074.hp2 HG01192.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-42+3595dupA | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121392566 | |||||||
| chr7:121392799 | C | T | 4 | a0001c0001t0001g0049 a0001c0001t0001g0070 a0001c0001t0002g0050 others(1): Show |
4 | HG02486.hp2 HG02809.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-42+3363G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121392799 | |||||||
| chr7:121393008 | G | T | 1 | a0001c0001t0001g0062 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-42+3154C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121393008 | |||||||
| chr7:121393009 | G | C | 1 | a0001c0001t0002g0165 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-42+3153C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121393009 | |||||||
| chr7:121393067 | T | C | 60 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(57): Show |
84 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.-42+3095A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121393067 | |||||||
| chr7:121393137 | A | G | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(105): Show |
150 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.-42+3025T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121393137 | |||||||
| chr7:121393147 | T | C | 4 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0162 others(1): Show |
4 | HG02055.hp2 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-42+3015A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121393147 | |||||||
| chr7:121393362 | G | T | 1 | a0001c0001t0003g0171 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-42+2800C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121393362 | |||||||
| chr7:121393542 | C | T | 3 | a0001c0001t0001g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 |
3 | HG02486.hp2 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-42+2620G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121393542 | |||||||
| chr7:121393614 | A | T | 1 | a0001c0001t0001g0062 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-42+2548T>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121393614 | |||||||
| chr7:121393626 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-42+2536T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121393626 | |||||||
| chr7:121393709 | C | T | 2 | a0001c0001t0002g0060 a0001c0001t0002g0061 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-42+2453G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121393709 | |||||||
| chr7:121393795 | T | G | 1 | a0001c0001t0001g0164 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-42+2367A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121393795 | |||||||
| chr7:121393854 | T | C | 1 | a0001c0001t0002g0165 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-42+2308A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121393854 | |||||||
| chr7:121394114 | G | C | 1 | a0001c0001t0016g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-42+2048C>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121394114 | |||||||
| chr7:121394198 | T | C | 3 | a0001c0001t0001g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 |
3 | HG02486.hp2 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-42+1964A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121394198 | |||||||
| chr7:121394204 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0182 |
7 | HG02055.hp1 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-42+1958G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121394204 | |||||||
| chr7:121394213 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-42+1949A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121394213 | |||||||
| chr7:121394537 | T | C | 1 | a0001c0001t0005g0193 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-42+1625A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121394537 | |||||||
| chr7:121394629 | G | A | 3 | a0001c0001t0001g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 |
3 | HG02486.hp2 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-42+1533C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121394629 | |||||||
| chr7:121394740 | C | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0006g0058 |
3 | NA18988.hp2 NA19065.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-42+1422G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121394740 | |||||||
| chr7:121394975 | G | A | 2 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-42+1187C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121394975 | |||||||
| chr7:121394987 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0004g0169 |
2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.-42+1175C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121394987 | |||||||
| chr7:121395029 | T | A | 3 | a0001c0001t0001g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 |
3 | HG02486.hp2 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-42+1133A>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395029 | |||||||
| chr7:121395195 | A | G | 1 | a0001c0001t0001g0055 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-42+967T>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395195 | |||||||
| chr7:121395204 | T | G | 3 | a0001c0001t0001g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 |
3 | HG02486.hp2 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-42+958A>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395204 | |||||||
| chr7:121395210 | CGGATACA others(33): Show |
C | 1 | a0001c0001t0001g0170 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-42+912_-42+951del others(40): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395210 | |||||||
| chr7:121395225 | A | C | 1 | a0001c0001t0001g0074 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-42+937T>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395225 | |||||||
| chr7:121395234 | C | CATACATA others(29): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0108 a0001c0001t0001g0161 |
3 | NA18948.hp2 NA19002.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-42+892_-42+927dup others(36): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395234 | |||||||
| chr7:121395234 | CATACATA others(11): Show |
C | 101 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(98): Show |
139 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-42+910_-42+927del others(18): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395234 | |||||||
| chr7:121395234 | CATACATA others(29): Show |
C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0049 a0001c0001t0001g0059 others(3): Show |
10 | HG02055.hp1 HG02486.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-42+892_-42+927del others(36): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395234 | |||||||
| chr7:121395296 | C | CATATATA others(73): Show |
1 | a0001c0001t0017g0054 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-42+865_-42+866ins others(80): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395296 | |||||||
| chr7:121395300 | T | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-42+862A>G | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395300 | |||||||
| chr7:121395302 | TATGGATA others(9): Show |
T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-42+844_-42+859del others(16): Show |
FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395302 | |||||||
| chr7:121395464 | T | TA | 11 | a0001c0001t0003g0031 a0001c0001t0003g0171 a0001c0001t0003g0172 others(8): Show |
12 | HG00438.hp2 HG00544.hp2 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.-42+697dupT | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395464 | |||||||
| chr7:121395464 | TA | T | 9 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(6): Show |
9 | HG00558.hp2 HG01943.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-42+697delT | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395464 | |||||||
| chr7:121395660 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-42+502G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395660 | |||||||
| chr7:121395671 | G | A | 1 | a0001c0001t0002g0181 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-42+491C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395671 | |||||||
| chr7:121395717 | C | G | 1 | a0001c0001t0002g0041 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-42+445G>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395717 | |||||||
| chr7:121395753 | G | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0182 |
6 | HG02055.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-42+409C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395753 | |||||||
| chr7:121395821 | C | G | 1 | a0001c0001t0002g0040 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-42+341G>C | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395821 | |||||||
| chr7:121395881 | C | A | 1 | a0001c0001t0005g0194 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-42+281G>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395881 | |||||||
| chr7:121395925 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-42+237G>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121395925 | |||||||
| chr7:121396050 | G | T | 12 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0016 others(9): Show |
18 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.-42+112C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121396050 | |||||||
| chr7:121396063 | G | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 |
5 | HG00735.hp2 HG01346.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.-42+99C>A | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121396063 | |||||||
| chr7:121396082 | G | A | 1 | a0001c0001t0004g0183 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-42+80C>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121396082 | |||||||
| chr7:121396112 | T | A | 3 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 |
3 | HG01884.hp1 HG01978.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.-42+50A>T | FAM3C | ENSG00000196937.11 | transcript | ENST00000359943.8 | protein_coding | 1/9 | chr7 | 121396112 |