Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 220965 |
| ensemblid | ENSG00000148541.13 |
| hgncid | 19371 |
| symbol | FAM13C |
| name | family with sequence similarity 13 member C |
| refseq_nuc | NM_198215.4 |
| refseq_prot | NP_937858.2 |
| ensembl_nuc | ENST00000618804.5 |
| ensembl_prot | ENSP00000481854.1 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 59246133 |
| end | 59362549 |
| strand | - |
| ver | v1.2 |
| region | chr10:59246133-59362549 |
| region5000 | chr10:59241133-59367549 |
| regionname0 | FAM13C_chr10_59246133_59362549 |
| regionname5000 | FAM13C_chr10_59241133_59367549 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 585 | 189 | 74 | 29 | 60 | 2 | 22 | 48 | FAM13C_chr10_59241133_59367549 | FAM13C | MFSCF others(580): Show |
chr10 | 59241133 | 59367549 |
| a0002 | 0/0 | 585 | 6 | 4 | 2 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | MFSCF others(580): Show |
chr10 | 59241133 | 59367549 |
| a0003 | 0/0 | 585 | 4 | 2 | 2 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | MFSCF others(580): Show |
chr10 | 59241133 | 59367549 |
| a0004 | 0/0 | 585 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | MFSCF others(580): Show |
chr10 | 59241133 | 59367549 |
| a0005 | 0/0 | 585 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | MFSCF others(580): Show |
chr10 | 59241133 | 59367549 |
| a0006 | 0/0 | 585 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | MFSCF others(580): Show |
chr10 | 59241133 | 59367549 |
| a0007 | 0/0 | 585 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | MFSCF others(580): Show |
chr10 | 59241133 | 59367549 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1755 | 184 | 70 | 29 | 59 | 2 | 22 | FAM13C_chr10_59241133_59367549 | FAM13C | ATGTT others(1750): Show |
chr10 | 59241133 | 59367549 | ||
| a0001c0004 | 0/0 | 1755 | 3 | 3 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | ATGTT others(1750): Show |
chr10 | 59241133 | 59367549 | ||
| a0001c0006 | 0/0 | 1755 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | ATGTT others(1750): Show |
chr10 | 59241133 | 59367549 | ||
| a0001c0007 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | ATGTT others(1750): Show |
chr10 | 59241133 | 59367549 | ||
| a0002c0002 | 0/0 | 1755 | 6 | 4 | 2 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | ATGTT others(1750): Show |
chr10 | 59241133 | 59367549 | ||
| a0003c0003 | 0/0 | 1755 | 4 | 2 | 2 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | ATGTT others(1750): Show |
chr10 | 59241133 | 59367549 | ||
| a0004c0005 | 0/0 | 1755 | 2 | 2 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | ATGTT others(1750): Show |
chr10 | 59241133 | 59367549 | ||
| a0005c0009 | 0/0 | 1755 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | ATGTT others(1750): Show |
chr10 | 59241133 | 59367549 | ||
| a0006c0008 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | ATGTT others(1750): Show |
chr10 | 59241133 | 59367549 | ||
| a0007c0010 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | ATGTT others(1750): Show |
chr10 | 59241133 | 59367549 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3329 | 154 | 64 | 28 | 43 | 2 | 16 | FAM13C_chr10_59241133_59367549 | FAM13C | GGAGA others(3324): Show |
chr10 | 59241133 | 59367549 |
| a0001c0001t0002 | 0/0 | 3329 | 22 | 1 | 0 | 15 | 0 | 6 | FAM13C_chr10_59241133_59367549 | FAM13C | GGAGA others(3324): Show |
chr10 | 59241133 | 59367549 |
| a0001c0001t0003 | 1/0 | 3328 | 4 | 3 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | GGAGA others(3323): Show |
chr10 | 59241133 | 59367549 |
| a0001c0001t0004 | 0/0 | 3329 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | AGAGA others(3324): Show |
chr10 | 59241133 | 59367549 |
| a0001c0001t0005 | 0/0 | 3329 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | GGAGA others(3324): Show |
chr10 | 59241133 | 59367549 |
| a0001c0001t0007 | 0/0 | 3329 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | GGAGA others(3324): Show |
chr10 | 59241133 | 59367549 |
| a0001c0001t0008 | 0/0 | 3329 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | GGAGA others(3324): Show |
chr10 | 59241133 | 59367549 |
| a0001c0004t0001 | 0/0 | 3329 | 3 | 3 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | GGAGA others(3324): Show |
chr10 | 59241133 | 59367549 |
| a0001c0006t0001 | 0/0 | 3329 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | GGAGA others(3324): Show |
chr10 | 59241133 | 59367549 |
| a0001c0007t0001 | 0/0 | 3329 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | GGAGA others(3324): Show |
chr10 | 59241133 | 59367549 |
| a0002c0002t0001 | 0/0 | 3329 | 5 | 4 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | GGAGA others(3324): Show |
chr10 | 59241133 | 59367549 |
| a0002c0002t0006 | 0/0 | 3329 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | GGAGA others(3324): Show |
chr10 | 59241133 | 59367549 |
| a0003c0003t0001 | 0/0 | 3329 | 4 | 2 | 2 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | GGAGA others(3324): Show |
chr10 | 59241133 | 59367549 |
| a0004c0005t0001 | 0/0 | 3329 | 2 | 2 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | GGAGA others(3324): Show |
chr10 | 59241133 | 59367549 |
| a0005c0009t0001 | 0/0 | 3329 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | GGAGA others(3324): Show |
chr10 | 59241133 | 59367549 |
| a0006c0008t0001 | 0/0 | 3329 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | GGAGA others(3324): Show |
chr10 | 59241133 | 59367549 |
| a0007c0010t0001 | 0/0 | 3329 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | GGAGA others(3324): Show |
chr10 | 59241133 | 59367549 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0073 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0003g0140 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0007g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0001t0008g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0004t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0004t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0004t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0006t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0001c0007t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0002c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0002c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0002c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0002c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0002c0002t0006g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0003c0003t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0003c0003t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0003c0003t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0003c0003t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0004c0005t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0004c0005t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0005c0009t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0006c0008t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| a0007c0010t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0069 | EUR | FIN | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | CHS | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | CHS | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG00639 | hp1 | a0003 | c0003 | t0001 | g0194 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | CHS | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01243 | hp1 | a0003 | c0003 | t0001 | g0195 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0095 | AMR | PUR | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01261 | hp2 | a0005 | c0009 | t0001 | g0142 | AMR | CLM | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01891 | hp2 | a0001 | c0004 | t0001 | g0100 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0171 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02145 | hp2 | a0001 | c0004 | t0001 | g0026 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0131 | AMR | PEL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02451 | hp1 | a0006 | c0008 | t0001 | g0160 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0029 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02630 | hp1 | a0001 | c0004 | t0001 | g0048 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02647 | hp1 | a0001 | c0001 | t0007 | g0185 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0170 | SAS | PJL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02886 | hp1 | a0007 | c0010 | t0001 | g0148 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | ESN | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02976 | hp1 | a0003 | c0003 | t0001 | g0192 | AFR | ESN | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03225 | hp1 | a0001 | c0007 | t0001 | g0059 | AFR | MSL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03453 | hp1 | a0004 | c0005 | t0001 | g0027 | AFR | MSL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0064 | SAS | PJL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03516 | hp1 | a0003 | c0003 | t0001 | g0193 | AFR | ESN | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0074 | SAS | BEB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | BEB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | STU | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | STU | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | STU | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | STU | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | YRI | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | YRI | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | YRI | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18995 | hp1 | a0001 | c0001 | t0005 | g0120 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | LWK | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | LWK | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19043 | hp1 | a0004 | c0005 | t0001 | g0149 | AFR | LWK | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19057 | hp1 | a0001 | c0006 | t0001 | g0109 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | YRI | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0036 | AFR | YRI | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ASW | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ASW | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | GIH | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | GIH | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01123 | hp1 | a0002 | c0002 | t0006 | g0198 | AMR | CLM | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0037 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0035 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0034 | AFR | USA | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | USA | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | USA | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | USA | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0073 | REF | REF | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0140 | REF | REF | FAM13C_chr10_59241133_59367549 | FAM13C | chr10 | 59241133 | 59367549 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:59262463 | C | G | 1 | a0003 | 4 | HG00639.hp1 HG01243.hp1 HG02976.hp1 others(1): Show |
missense_variant | MODERATE | c.1207G>C | p.Glu403Gln | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/14 | 1296/3328 | 1207/1758 | 403/585 | chr10 | 59262463 | |||
| chr10:59262543 | G | A | 1 | a0006 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.1127C>T | p.Pro376Leu | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/14 | 1216/3328 | 1127/1758 | 376/585 | chr10 | 59262543 | |||
| chr10:59268611 | C | T | 1 | a0004 | 2 | HG03453.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.884G>A | p.Ser295Asn | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/14 | 973/3328 | 884/1758 | 295/585 | chr10 | 59268611 | |||
| chr10:59323992 | G | A | 1 | a0002 | 6 | HG01123.hp1 HG01243.hp2 HG02486.hp1 others(3): Show |
missense_variant | MODERATE | c.439C>T | p.Pro147Ser | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/14 | 528/3328 | 439/1758 | 147/585 | chr10 | 59323992 | |||
| chr10:59352401 | G | A | 1 | a0005 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.193C>T | p.Pro65Ser | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/14 | 282/3328 | 193/1758 | 65/585 | chr10 | 59352401 | |||
| chr10:59352418 | G | A | 1 | a0007 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.176C>T | p.Ala59Val | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/14 | 265/3328 | 176/1758 | 59/585 | chr10 | 59352418 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:59262533 | C | T | 1 | a0001c0007 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.1137G>A | p.Ala379Ala | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/14 | 1226/3328 | 1137/1758 | 379/585 | chr10 | 59262533 | |||
| chr10:59268688 | C | T | 1 | a0001c0006 | 1 | NA19057.hp1 | synonymous_variant | LOW | c.807G>A | p.Pro269Pro | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/14 | 896/3328 | 807/1758 | 269/585 | chr10 | 59268688 | |||
| chr10:59302840 | C | T | 1 | a0001c0004 | 3 | HG01891.hp2 HG02145.hp2 HG02630.hp1 |
synonymous_variant | LOW | c.468G>A | p.Ser156Ser | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/14 | 557/3328 | 468/1758 | 156/585 | chr10 | 59302840 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:59246501 | C | T | 1 | a0001c0001t0008 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1113G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 14/14 | 1113 | chr10 | 59246501 | ||||||
| chr10:59246650 | G | A | 1 | a0001c0001t0002 | 22 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*964C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 14/14 | 964 | chr10 | 59246650 | ||||||
| chr10:59246776 | A | G | 1 | a0001c0001t0007 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*838T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 14/14 | 838 | chr10 | 59246776 | ||||||
| chr10:59247009 | C | T | 1 | a0002c0002t0006 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*605G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 14/14 | 605 | chr10 | 59247009 | ||||||
| chr10:59247042 | G | GA | 16 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(13): Show |
199 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*571dupT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 14/14 | 571 | chr10 | 59247042 | ||||||
| chr10:59247214 | A | G | 1 | a0001c0001t0005 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*400T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 14/14 | 400 | chr10 | 59247214 | ||||||
| chr10:59362549 | C | T | 1 | a0001c0001t0004 | 1 | HG02300.hp1 | 5_prime_UTR_variant | MODIFIER | c.-89G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/14 | 89 | chr10 | 59362549 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:59247774 | A | G | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(103): Show |
106 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.1635-37T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59247774 | |||||||
| chr10:59247832 | G | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
199 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(196): Show |
intron_variant | MODIFIER | c.1635-95C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59247832 | |||||||
| chr10:59248029 | C | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1635-292G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59248029 | |||||||
| chr10:59248085 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1635-348C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59248085 | |||||||
| chr10:59248126 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1635-389T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59248126 | |||||||
| chr10:59248289 | C | T | 7 | a0001c0001t0001g0045 a0001c0001t0001g0054 a0001c0001t0001g0150 others(4): Show |
7 | HG01070.hp1 HG01106.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1635-552G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59248289 | |||||||
| chr10:59248609 | AAGGGGTA others(1): Show |
A | 2 | a0004c0005t0001g0027 a0004c0005t0001g0149 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1635-880_1635-873d others(10): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59248609 | |||||||
| chr10:59249032 | T | C | 7 | a0001c0001t0001g0067 a0001c0001t0001g0089 a0001c0001t0001g0112 others(4): Show |
7 | HG01123.hp1 HG01433.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1635-1295A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249032 | |||||||
| chr10:59249040 | T | C | 2 | a0001c0001t0001g0077 a0001c0001t0001g0079 |
2 | NA18941.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1635-1303A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249040 | |||||||
| chr10:59249066 | A | G | 1 | a0001c0001t0001g0010 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1635-1329T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249066 | |||||||
| chr10:59249212 | G | T | 2 | a0004c0005t0001g0027 a0004c0005t0001g0149 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1635-1475C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249212 | |||||||
| chr10:59249265 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0154 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1635-1528C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249265 | |||||||
| chr10:59249274 | T | G | 2 | a0004c0005t0001g0027 a0004c0005t0001g0149 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1635-1537A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249274 | |||||||
| chr10:59249319 | G | GCGTGAAC | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(103): Show |
106 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.1635-1589_1635-158 others(11): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249319 | |||||||
| chr10:59249320 | C | T | 2 | a0004c0005t0001g0027 a0004c0005t0001g0149 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1635-1583G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249320 | |||||||
| chr10:59249321 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1635-1584C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249321 | |||||||
| chr10:59249372 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1635-1635G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249372 | |||||||
| chr10:59249389 | G | A | 9 | a0001c0001t0001g0178 a0001c0001t0001g0200 a0001c0001t0001g0202 others(6): Show |
9 | HG00639.hp1 HG01167.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1635-1652C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249389 | |||||||
| chr10:59249408 | G | GA | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
105 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.1635-1672dupT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249408 | |||||||
| chr10:59249408 | GA | G | 8 | a0001c0001t0001g0091 a0001c0001t0001g0151 a0001c0001t0001g0165 others(5): Show |
8 | HG01433.hp2 HG02486.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1635-1672delT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249408 | |||||||
| chr10:59249408 | GAA | G | 23 | a0001c0001t0001g0187 a0001c0001t0002g0008 a0001c0001t0002g0014 others(20): Show |
23 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.1635-1673_1635-167 others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249408 | |||||||
| chr10:59249726 | CTGTT | C | 29 | a0001c0001t0001g0091 a0001c0001t0001g0165 a0001c0001t0001g0186 others(26): Show |
29 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.1634+1845_1634+184 others(8): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249726 | |||||||
| chr10:59249936 | C | G | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(98): Show |
101 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.1634+1639G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59249936 | |||||||
| chr10:59250633 | C | T | 1 | a0001c0001t0007g0185 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1634+942G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59250633 | |||||||
| chr10:59250637 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1634+938T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59250637 | |||||||
| chr10:59250783 | G | A | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1634+792C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59250783 | |||||||
| chr10:59250874 | A | G | 46 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(43): Show |
47 | HG00639.hp2 HG01070.hp1 HG01106.hp1 others(44): Show |
intron_variant | MODIFIER | c.1634+701T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59250874 | |||||||
| chr10:59250883 | C | T | 4 | a0001c0001t0001g0165 a0001c0001t0001g0186 a0001c0001t0001g0197 others(1): Show |
4 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1634+692G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59250883 | |||||||
| chr10:59251073 | A | G | 2 | a0004c0005t0001g0027 a0004c0005t0001g0149 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1634+502T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59251073 | |||||||
| chr10:59251115 | G | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
199 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(196): Show |
intron_variant | MODIFIER | c.1634+460C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59251115 | |||||||
| chr10:59251314 | T | C | 1 | a0001c0006t0001g0109 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1634+261A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59251314 | |||||||
| chr10:59251336 | G | A | 2 | a0004c0005t0001g0027 a0004c0005t0001g0149 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1634+239C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59251336 | |||||||
| chr10:59251465 | A | T | 2 | a0004c0005t0001g0027 a0004c0005t0001g0149 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1634+110T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59251465 | |||||||
| chr10:59251565 | C | T | 43 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(40): Show |
44 | HG00639.hp2 HG01070.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.1634+10G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59251565 | |||||||
| chr10:59251566 | G | A | 1 | a0001c0001t0003g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1634+9C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 13/13 | chr10 | 59251566 | |||||||
| chr10:59251821 | A | T | 1 | a0001c0001t0002g0014 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1533-145T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 12/13 | chr10 | 59251821 | |||||||
| chr10:59252014 | C | G | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(193): Show |
197 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(194): Show |
intron_variant | MODIFIER | c.1533-338G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 12/13 | chr10 | 59252014 | |||||||
| chr10:59252112 | A | T | 1 | a0001c0001t0001g0053 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1533-436T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 12/13 | chr10 | 59252112 | |||||||
| chr10:59252214 | G | A | 11 | a0001c0001t0001g0178 a0001c0001t0001g0200 a0001c0001t0001g0202 others(8): Show |
11 | HG00639.hp1 HG01167.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1533-538C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 12/13 | chr10 | 59252214 | |||||||
| chr10:59252327 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
104 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.1532+472C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 12/13 | chr10 | 59252327 | |||||||
| chr10:59253159 | C | T | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
102 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1333-161G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 11/13 | chr10 | 59253159 | |||||||
| chr10:59253457 | C | T | 5 | a0001c0001t0001g0174 a0001c0001t0001g0191 a0002c0002t0001g0017 others(2): Show |
5 | HG00639.hp2 HG02559.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1333-459G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 11/13 | chr10 | 59253457 | |||||||
| chr10:59253688 | AG | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0147 |
3 | NA18970.hp2 NA18988.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1332+659delC | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 11/13 | chr10 | 59253688 | |||||||
| chr10:59253689 | G | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
194 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(191): Show |
intron_variant | MODIFIER | c.1332+659C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 11/13 | chr10 | 59253689 | |||||||
| chr10:59253791 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1332+557C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 11/13 | chr10 | 59253791 | |||||||
| chr10:59254004 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0087 |
2 | NA18947.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1332+344G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 11/13 | chr10 | 59254004 | |||||||
| chr10:59254020 | T | C | 5 | a0001c0001t0001g0174 a0001c0001t0001g0191 a0002c0002t0001g0017 others(2): Show |
5 | HG00639.hp2 HG02559.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1332+328A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 11/13 | chr10 | 59254020 | |||||||
| chr10:59254296 | C | A | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
102 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1332+52G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 11/13 | chr10 | 59254296 | |||||||
| chr10:59254576 | C | CATTT | 17 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(14): Show |
17 | HG01099.hp1 HG01099.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1237-137_1237-134d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59254576 | |||||||
| chr10:59254576 | CATTT | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(110): Show |
114 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(111): Show |
intron_variant | MODIFIER | c.1237-137_1237-134d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59254576 | |||||||
| chr10:59254576 | CATTTATT others(1): Show |
C | 20 | a0001c0001t0001g0033 a0001c0001t0001g0061 a0001c0001t0001g0165 others(17): Show |
20 | HG00639.hp1 HG01167.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1237-141_1237-134d others(10): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59254576 | |||||||
| chr10:59254576 | CATTTATT others(5): Show |
C | 23 | a0001c0001t0001g0091 a0001c0001t0001g0183 a0001c0001t0001g0184 others(20): Show |
23 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.1237-145_1237-134d others(14): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59254576 | |||||||
| chr10:59254650 | C | T | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
102 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1237-207G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59254650 | |||||||
| chr10:59254658 | A | C | 4 | a0003c0003t0001g0192 a0003c0003t0001g0193 a0003c0003t0001g0194 others(1): Show |
4 | HG00639.hp1 HG01243.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1237-215T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59254658 | |||||||
| chr10:59254817 | T | C | 7 | a0001c0001t0001g0067 a0001c0001t0001g0089 a0001c0001t0001g0112 others(4): Show |
7 | HG01123.hp1 HG01433.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1237-374A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59254817 | |||||||
| chr10:59254857 | G | A | 5 | a0001c0001t0001g0067 a0001c0001t0001g0089 a0001c0001t0001g0112 others(2): Show |
5 | HG01123.hp1 HG01433.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.1237-414C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59254857 | |||||||
| chr10:59254859 | C | G | 1 | a0001c0001t0002g0119 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1237-416G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59254859 | |||||||
| chr10:59254883 | C | T | 1 | a0001c0001t0002g0074 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1237-440G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59254883 | |||||||
| chr10:59255010 | G | C | 2 | a0001c0001t0001g0111 a0001c0001t0001g0137 |
2 | HG01123.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1237-567C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59255010 | |||||||
| chr10:59255186 | C | T | 11 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0054 others(8): Show |
11 | HG01070.hp1 HG01106.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1237-743G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59255186 | |||||||
| chr10:59255212 | T | C | 7 | a0001c0001t0001g0067 a0001c0001t0001g0089 a0001c0001t0001g0112 others(4): Show |
7 | HG01123.hp1 HG01433.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1237-769A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59255212 | |||||||
| chr10:59255427 | TTGTC | T | 9 | a0001c0001t0001g0178 a0001c0001t0001g0200 a0001c0001t0001g0202 others(6): Show |
9 | HG00639.hp1 HG01167.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1237-988_1237-985d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59255427 | |||||||
| chr10:59255554 | T | C | 3 | a0001c0001t0001g0058 a0001c0001t0001g0129 a0001c0001t0001g0145 |
3 | NA18939.hp2 NA18942.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1237-1111A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59255554 | |||||||
| chr10:59256256 | G | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
199 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(196): Show |
intron_variant | MODIFIER | c.1237-1813C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59256256 | |||||||
| chr10:59256415 | A | G | 5 | a0001c0001t0001g0067 a0001c0001t0001g0089 a0001c0001t0001g0112 others(2): Show |
5 | HG01123.hp1 HG01433.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.1237-1972T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59256415 | |||||||
| chr10:59256502 | A | G | 2 | a0004c0005t0001g0027 a0004c0005t0001g0149 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1237-2059T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59256502 | |||||||
| chr10:59256548 | T | C | 12 | a0001c0001t0001g0178 a0001c0001t0001g0180 a0001c0001t0001g0200 others(9): Show |
12 | HG00639.hp1 HG01167.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1237-2105A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59256548 | |||||||
| chr10:59256584 | C | A | 1 | a0001c0001t0001g0132 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1237-2141G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59256584 | |||||||
| chr10:59256873 | T | C | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(103): Show |
106 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.1237-2430A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59256873 | |||||||
| chr10:59256884 | A | G | 1 | a0005c0009t0001g0142 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1237-2441T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59256884 | |||||||
| chr10:59256907 | A | T | 6 | a0002c0002t0001g0037 a0002c0002t0001g0095 a0003c0003t0001g0192 others(3): Show |
6 | HG00639.hp1 HG01243.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.1237-2464T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59256907 | |||||||
| chr10:59256992 | A | G | 2 | a0004c0005t0001g0027 a0004c0005t0001g0149 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1237-2549T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59256992 | |||||||
| chr10:59257018 | C | T | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(98): Show |
101 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.1237-2575G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59257018 | |||||||
| chr10:59257079 | T | C | 5 | a0001c0001t0001g0174 a0001c0001t0001g0191 a0002c0002t0001g0017 others(2): Show |
5 | HG00639.hp2 HG02559.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1237-2636A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59257079 | |||||||
| chr10:59257480 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1237-3037A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59257480 | |||||||
| chr10:59257858 | A | G | 1 | a0001c0001t0002g0074 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1237-3415T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59257858 | |||||||
| chr10:59257868 | A | T | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
102 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1237-3425T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59257868 | |||||||
| chr10:59258345 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1237-3902A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59258345 | |||||||
| chr10:59258353 | C | T | 1 | a0006c0008t0001g0160 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1237-3910G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59258353 | |||||||
| chr10:59258367 | C | T | 5 | a0001c0001t0001g0067 a0001c0001t0001g0089 a0001c0001t0001g0112 others(2): Show |
5 | HG01123.hp1 HG01433.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.1237-3924G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59258367 | |||||||
| chr10:59258490 | T | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(104): Show |
107 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.1236+3944A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59258490 | |||||||
| chr10:59258631 | G | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
104 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.1236+3803C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59258631 | |||||||
| chr10:59258726 | G | A | 1 | a0002c0002t0006g0198 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1236+3708C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59258726 | |||||||
| chr10:59259058 | T | A | 4 | a0001c0001t0001g0122 a0001c0001t0001g0181 a0001c0001t0001g0182 others(1): Show |
4 | HG02451.hp2 HG03130.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1236+3376A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59259058 | |||||||
| chr10:59259924 | G | A | 43 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(40): Show |
44 | HG00639.hp2 HG01070.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.1236+2510C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59259924 | |||||||
| chr10:59260066 | C | T | 1 | a0001c0001t0002g0064 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1236+2368G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59260066 | |||||||
| chr10:59260069 | A | AT | 9 | a0001c0001t0001g0045 a0001c0001t0001g0054 a0001c0001t0001g0150 others(6): Show |
9 | HG01070.hp1 HG01106.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.1236+2364dupA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59260069 | |||||||
| chr10:59260091 | C | T | 4 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0004c0005t0001g0027 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1236+2343G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59260091 | |||||||
| chr10:59260112 | A | G | 2 | a0004c0005t0001g0027 a0004c0005t0001g0149 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1236+2322T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59260112 | |||||||
| chr10:59260150 | A | G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
199 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(196): Show |
intron_variant | MODIFIER | c.1236+2284T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59260150 | |||||||
| chr10:59260160 | C | G | 1 | a0001c0001t0001g0041 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1236+2274G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59260160 | |||||||
| chr10:59260180 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1236+2254G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59260180 | |||||||
| chr10:59260986 | A | G | 1 | a0001c0007t0001g0059 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1236+1448T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59260986 | |||||||
| chr10:59261201 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1236+1233A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59261201 | |||||||
| chr10:59261396 | T | C | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(103): Show |
106 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.1236+1038A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59261396 | |||||||
| chr10:59261518 | C | T | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
102 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1236+916G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59261518 | |||||||
| chr10:59261649 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1236+785T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59261649 | |||||||
| chr10:59261805 | C | T | 1 | a0001c0001t0002g0119 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1236+629G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59261805 | |||||||
| chr10:59261816 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1236+618G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59261816 | |||||||
| chr10:59262280 | G | A | 1 | a0001c0001t0005g0120 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1236+154C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59262280 | |||||||
| chr10:59262294 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
104 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.1236+140C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 10/13 | chr10 | 59262294 | |||||||
| chr10:59262704 | A | G | 2 | a0004c0005t0001g0027 a0004c0005t0001g0149 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1025-59T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 9/13 | chr10 | 59262704 | |||||||
| chr10:59263224 | A | C | 11 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0054 others(8): Show |
11 | HG01070.hp1 HG01106.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1025-579T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 9/13 | chr10 | 59263224 | |||||||
| chr10:59263335 | T | G | 5 | a0001c0001t0001g0067 a0001c0001t0001g0089 a0001c0001t0001g0112 others(2): Show |
5 | HG01123.hp1 HG01433.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.1025-690A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 9/13 | chr10 | 59263335 | |||||||
| chr10:59263463 | T | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
199 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(196): Show |
intron_variant | MODIFIER | c.1024+622A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 9/13 | chr10 | 59263463 | |||||||
| chr10:59263785 | C | A | 1 | a0001c0001t0002g0135 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1024+300G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 9/13 | chr10 | 59263785 | |||||||
| chr10:59263892 | A | G | 1 | a0001c0001t0007g0185 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1024+193T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 9/13 | chr10 | 59263892 | |||||||
| chr10:59263934 | G | C | 1 | a0001c0001t0001g0110 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1024+151C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 9/13 | chr10 | 59263934 | |||||||
| chr10:59264201 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.943-35T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59264201 | |||||||
| chr10:59264313 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.943-147C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59264313 | |||||||
| chr10:59264598 | G | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.943-432C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59264598 | |||||||
| chr10:59264629 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.943-463G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59264629 | |||||||
| chr10:59264695 | G | A | 5 | a0001c0001t0001g0067 a0001c0001t0001g0089 a0001c0001t0001g0112 others(2): Show |
5 | HG01123.hp1 HG01433.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.943-529C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59264695 | |||||||
| chr10:59264703 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.943-537G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59264703 | |||||||
| chr10:59264758 | A | G | 130 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(127): Show |
130 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.943-592T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59264758 | |||||||
| chr10:59264903 | A | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
104 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.943-737T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59264903 | |||||||
| chr10:59264929 | G | A | 21 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0022 others(18): Show |
21 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.943-763C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59264929 | |||||||
| chr10:59264986 | C | A | 4 | a0001c0001t0001g0174 a0002c0002t0001g0017 a0002c0002t0001g0035 others(1): Show |
4 | HG02559.hp1 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.943-820G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59264986 | |||||||
| chr10:59265273 | C | G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
199 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(196): Show |
intron_variant | MODIFIER | c.943-1107G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265273 | |||||||
| chr10:59265286 | C | T | 1 | a0002c0002t0006g0198 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.943-1120G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265286 | |||||||
| chr10:59265306 | A | G | 7 | a0001c0001t0001g0172 a0001c0001t0001g0174 a0001c0001t0001g0187 others(4): Show |
7 | HG00639.hp2 HG02559.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.943-1140T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265306 | |||||||
| chr10:59265310 | A | G | 6 | a0001c0001t0001g0174 a0001c0001t0001g0187 a0001c0001t0001g0191 others(3): Show |
6 | HG00639.hp2 HG02559.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.943-1144T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265310 | |||||||
| chr10:59265311 | A | AGGGG | 8 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0044 others(5): Show |
8 | HG01891.hp1 HG02135.hp1 HG03654.hp2 others(5): Show |
intron_variant | MODIFIER | c.943-1149_943-1146d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265311 | |||||||
| chr10:59265311 | A | G | 6 | a0001c0001t0001g0174 a0001c0001t0001g0187 a0001c0001t0001g0191 others(3): Show |
6 | HG00639.hp2 HG02559.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.943-1145T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265311 | |||||||
| chr10:59265315 | GT | G | 4 | a0001c0001t0001g0091 a0001c0001t0002g0062 a0001c0001t0002g0076 others(1): Show |
4 | HG02698.hp2 HG03579.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.943-1150delA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265315 | |||||||
| chr10:59265315 | GTT | G | 19 | a0001c0001t0002g0008 a0001c0001t0002g0014 a0001c0001t0002g0020 others(16): Show |
19 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.943-1151_943-1150d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265315 | |||||||
| chr10:59265316 | T | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(62): Show |
66 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(63): Show |
intron_variant | MODIFIER | c.943-1150A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265316 | |||||||
| chr10:59265317 | T | A | 1 | a0001c0001t0001g0188 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.943-1151A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265317 | |||||||
| chr10:59265317 | T | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(64): Show |
68 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(65): Show |
intron_variant | MODIFIER | c.943-1151A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265317 | |||||||
| chr10:59265318 | T | A | 1 | a0001c0001t0001g0091 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.943-1152A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265318 | |||||||
| chr10:59265318 | T | G | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(67): Show |
71 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(68): Show |
intron_variant | MODIFIER | c.943-1152A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265318 | |||||||
| chr10:59265319 | T | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(88): Show |
92 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.943-1153A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265319 | |||||||
| chr10:59265322 | C | G | 71 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(68): Show |
71 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.943-1156G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265322 | |||||||
| chr10:59265323 | G | T | 3 | a0001c0001t0002g0062 a0001c0001t0002g0076 a0001c0001t0002g0125 |
3 | HG02698.hp2 NA18956.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.943-1157C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265323 | |||||||
| chr10:59265324 | G | T | 19 | a0001c0001t0002g0008 a0001c0001t0002g0014 a0001c0001t0002g0020 others(16): Show |
19 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.943-1158C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265324 | |||||||
| chr10:59265325 | G | T | 1 | a0001c0001t0001g0187 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.943-1159C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265325 | |||||||
| chr10:59265327 | G | A | 4 | a0001c0001t0001g0055 a0001c0001t0001g0110 a0001c0001t0001g0132 others(1): Show |
4 | HG02698.hp1 NA18994.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.943-1161C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265327 | |||||||
| chr10:59265327 | G | C | 16 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(13): Show |
17 | HG01106.hp1 HG01891.hp1 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.943-1161C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265327 | |||||||
| chr10:59265327 | G | GAGC | 5 | a0001c0001t0001g0165 a0001c0001t0001g0186 a0001c0001t0001g0197 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.943-1162_943-1161i others(5): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265327 | |||||||
| chr10:59265331 | G | C | 7 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0051 others(4): Show |
7 | HG01884.hp1 HG02258.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.943-1165C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265331 | |||||||
| chr10:59265332 | G | C | 39 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(36): Show |
40 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.943-1166C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265332 | |||||||
| chr10:59265332 | G | GCGGGGC | 8 | a0001c0001t0001g0070 a0001c0001t0001g0089 a0001c0001t0001g0112 others(5): Show |
8 | HG02145.hp2 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.943-1167_943-1166i others(8): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265332 | |||||||
| chr10:59265335 | G | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(84): Show |
88 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.943-1169C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265335 | |||||||
| chr10:59265335 | G | GCGGA | 7 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0051 others(4): Show |
7 | HG01884.hp1 HG02258.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.943-1170_943-1169i others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265335 | |||||||
| chr10:59265335 | G | GGCGGGGC others(3): Show |
2 | a0001c0001t0001g0141 a0001c0001t0001g0143 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.943-1170_943-1169i others(12): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265335 | |||||||
| chr10:59265335 | G | GGGGGGA | 14 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(11): Show |
14 | HG00609.hp2 HG01081.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.943-1170_943-1169i others(8): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265335 | |||||||
| chr10:59265335 | G | GGGGGGGA | 30 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(27): Show |
30 | HG00558.hp1 HG00673.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.943-1170_943-1169i others(9): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265335 | |||||||
| chr10:59265335 | G | GGGGGGGG others(2): Show |
17 | a0001c0001t0001g0023 a0001c0001t0001g0032 a0001c0001t0001g0039 others(14): Show |
17 | HG00597.hp1 HG00609.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.943-1170_943-1169i others(11): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265335 | |||||||
| chr10:59265335 | G | GGGGGGGG others(3): Show |
5 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0033 others(2): Show |
5 | HG01070.hp2 HG02622.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.943-1170_943-1169i others(12): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265335 | |||||||
| chr10:59265335 | G | GGGGGGGG others(4): Show |
2 | a0001c0001t0001g0028 a0001c0001t0001g0030 |
2 | HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.943-1170_943-1169i others(13): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265335 | |||||||
| chr10:59265335 | G | GGGGGGGG others(5): Show |
1 | a0001c0001t0001g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.943-1170_943-1169i others(14): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265335 | |||||||
| chr10:59265335 | G | GGGGGGGG others(6): Show |
1 | a0001c0001t0001g0049 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.943-1170_943-1169i others(15): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265335 | |||||||
| chr10:59265380 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.943-1214G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265380 | |||||||
| chr10:59265398 | G | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(65): Show |
69 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(66): Show |
intron_variant | MODIFIER | c.943-1232C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265398 | |||||||
| chr10:59265459 | T | A | 1 | a0001c0001t0001g0191 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.943-1293A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265459 | |||||||
| chr10:59265632 | A | G | 2 | a0001c0001t0001g0061 a0001c0001t0001g0096 |
2 | HG03831.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.943-1466T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265632 | |||||||
| chr10:59265775 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.943-1609A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265775 | |||||||
| chr10:59265796 | G | C | 2 | a0004c0005t0001g0027 a0004c0005t0001g0149 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.943-1630C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59265796 | |||||||
| chr10:59266060 | A | T | 1 | a0002c0002t0006g0198 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.943-1894T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59266060 | |||||||
| chr10:59266182 | T | C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0172 |
2 | HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.943-2016A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59266182 | |||||||
| chr10:59266218 | G | A | 3 | a0001c0001t0001g0067 a0001c0001t0001g0089 a0001c0001t0001g0112 |
3 | HG03704.hp1 HG03927.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.943-2052C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59266218 | |||||||
| chr10:59266221 | G | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
199 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(196): Show |
intron_variant | MODIFIER | c.943-2055C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59266221 | |||||||
| chr10:59266407 | A | G | 24 | a0001c0001t0002g0008 a0001c0001t0002g0014 a0001c0001t0002g0020 others(21): Show |
24 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.942+2146T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59266407 | |||||||
| chr10:59266490 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(88): Show |
92 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.942+2063G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59266490 | |||||||
| chr10:59266538 | A | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(92): Show |
96 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.942+2015T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59266538 | |||||||
| chr10:59266570 | A | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(88): Show |
92 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.942+1983T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59266570 | |||||||
| chr10:59266886 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.942+1667T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59266886 | |||||||
| chr10:59266901 | A | C | 3 | a0001c0001t0001g0045 a0001c0001t0001g0153 a0001c0001t0001g0201 |
3 | HG01891.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.942+1652T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59266901 | |||||||
| chr10:59267033 | T | C | 1 | a0001c0001t0001g0012 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.942+1520A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59267033 | |||||||
| chr10:59267145 | G | T | 1 | a0001c0001t0002g0064 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.942+1408C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59267145 | |||||||
| chr10:59267199 | G | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0079 |
2 | NA18941.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.942+1354C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59267199 | |||||||
| chr10:59267351 | C | T | 5 | a0001c0001t0001g0067 a0001c0001t0001g0089 a0001c0001t0001g0112 others(2): Show |
5 | HG01123.hp1 HG01433.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.942+1202G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59267351 | |||||||
| chr10:59267366 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.942+1187G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59267366 | |||||||
| chr10:59267494 | C | G | 46 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(43): Show |
47 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.942+1059G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59267494 | |||||||
| chr10:59267652 | G | A | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.942+901C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59267652 | |||||||
| chr10:59267801 | C | A | 1 | a0001c0001t0001g0098 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.942+752G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59267801 | |||||||
| chr10:59268008 | C | T | 1 | a0001c0001t0005g0120 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.942+545G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59268008 | |||||||
| chr10:59268226 | A | AAAG | 4 | a0001c0001t0001g0021 a0001c0001t0001g0096 a0004c0005t0001g0027 others(1): Show |
4 | HG03453.hp1 HG03831.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.942+324_942+326dup others(3): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59268226 | |||||||
| chr10:59268226 | AAAGAAG | A | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(87): Show |
91 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.942+321_942+326del others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59268226 | |||||||
| chr10:59268294 | A | G | 2 | a0001c0001t0001g0097 a0001c0001t0001g0146 |
2 | NA18947.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.942+259T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59268294 | |||||||
| chr10:59268430 | T | G | 2 | a0004c0005t0001g0027 a0004c0005t0001g0149 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.942+123A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59268430 | |||||||
| chr10:59268466 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0147 |
2 | NA18970.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.942+87C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59268466 | |||||||
| chr10:59268518 | C | A | 1 | a0001c0001t0001g0003 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.942+35G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 8/13 | chr10 | 59268518 | |||||||
| chr10:59268717 | G | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(65): Show |
69 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(66): Show |
intron_variant | MODIFIER | c.804-26C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | 59268717 | |||||||
| chr10:59269109 | G | A | 9 | a0001c0001t0001g0178 a0001c0001t0001g0200 a0001c0001t0001g0202 others(6): Show |
9 | HG00639.hp1 HG01167.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.804-418C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | 59269109 | |||||||
| chr10:59269417 | T | TACACAC | 5 | a0001c0001t0001g0054 a0001c0001t0001g0150 a0001c0001t0001g0153 others(2): Show |
5 | HG01106.hp1 HG01891.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.803+476_803+481dup others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | 59269417 | |||||||
| chr10:59269417 | T | TACACACA others(1): Show |
17 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0067 others(14): Show |
17 | HG00639.hp1 HG00639.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.803+474_803+481dup others(8): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | 59269417 | |||||||
| chr10:59269417 | T | TACACACA others(3): Show |
21 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0047 others(18): Show |
21 | HG01167.hp1 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.803+472_803+481dup others(10): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | 59269417 | |||||||
| chr10:59269417 | T | TACACACA others(5): Show |
12 | a0001c0001t0001g0001 a0001c0001t0001g0044 a0001c0001t0001g0046 others(9): Show |
13 | HG02486.hp2 HG02723.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.803+470_803+481dup others(12): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | 59269417 | |||||||
| chr10:59269417 | T | TACACACA others(7): Show |
12 | a0001c0001t0001g0002 a0001c0001t0001g0051 a0001c0001t0001g0089 others(9): Show |
12 | HG01243.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.803+468_803+481dup others(14): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | 59269417 | |||||||
| chr10:59269417 | T | TACACACA others(11): Show |
1 | a0001c0001t0001g0104 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.803+464_803+481dup others(18): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | 59269417 | |||||||
| chr10:59269417 | TAC | T | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
97 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.803+480_803+481del others(2): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | 59269417 | |||||||
| chr10:59269417 | TACAC | T | 3 | a0001c0001t0004g0131 a0004c0005t0001g0027 a0004c0005t0001g0149 |
3 | HG02300.hp1 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.803+478_803+481del others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | 59269417 | |||||||
| chr10:59269445 | C | A | 7 | a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0065 others(4): Show |
7 | NA18950.hp2 NA18956.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.803+454G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | 59269445 | |||||||
| chr10:59269591 | G | C | 1 | a0001c0001t0001g0184 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.803+308C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | 59269591 | |||||||
| chr10:59269616 | T | C | 26 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0002g0008 others(23): Show |
26 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.803+283A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | 59269616 | |||||||
| chr10:59269725 | G | GCAATGGC others(2): Show |
22 | a0001c0001t0002g0008 a0001c0001t0002g0014 a0001c0001t0002g0020 others(19): Show |
22 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.803+165_803+173dup others(9): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | 59269725 | |||||||
| chr10:59269778 | G | A | 4 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0004c0005t0001g0027 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.803+121C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | 59269778 | |||||||
| chr10:59269814 | C | T | 4 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0004c0005t0001g0027 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.803+85G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | 59269814 | |||||||
| chr10:59270217 | G | T | 1 | a0001c0001t0001g0122 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.593-108C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59270217 | |||||||
| chr10:59270405 | A | G | 26 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0002g0008 others(23): Show |
26 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.593-296T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59270405 | |||||||
| chr10:59270471 | C | A | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.593-362G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59270471 | |||||||
| chr10:59270519 | GA | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(62): Show |
66 | HG00639.hp1 HG00639.hp2 HG01106.hp1 others(63): Show |
intron_variant | MODIFIER | c.593-411delT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59270519 | |||||||
| chr10:59270643 | T | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(88): Show |
92 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.593-534A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59270643 | |||||||
| chr10:59270666 | T | C | 1 | a0001c0001t0002g0076 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.593-557A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59270666 | |||||||
| chr10:59270704 | T | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
199 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(196): Show |
intron_variant | MODIFIER | c.593-595A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59270704 | |||||||
| chr10:59270816 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.593-707A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59270816 | |||||||
| chr10:59270890 | C | T | 6 | a0001c0001t0001g0045 a0001c0001t0001g0054 a0001c0001t0001g0150 others(3): Show |
6 | HG01106.hp1 HG01891.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.593-781G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59270890 | |||||||
| chr10:59270953 | C | A | 4 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0004c0005t0001g0027 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.593-844G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59270953 | |||||||
| chr10:59270982 | A | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(88): Show |
92 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.593-873T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59270982 | |||||||
| chr10:59271006 | C | A | 1 | a0007c0010t0001g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.593-897G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59271006 | |||||||
| chr10:59271112 | G | C | 1 | a0001c0007t0001g0059 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.593-1003C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59271112 | |||||||
| chr10:59271328 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.593-1219A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59271328 | |||||||
| chr10:59271536 | G | A | 1 | a0001c0001t0002g0126 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.593-1427C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59271536 | |||||||
| chr10:59271873 | T | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(86): Show |
90 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.593-1764A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59271873 | |||||||
| chr10:59271949 | G | A | 1 | a0005c0009t0001g0142 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.593-1840C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59271949 | |||||||
| chr10:59272023 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.593-1914A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59272023 | |||||||
| chr10:59272458 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.593-2349T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59272458 | |||||||
| chr10:59272494 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.593-2385G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59272494 | |||||||
| chr10:59272506 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(89): Show |
93 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.593-2397C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59272506 | |||||||
| chr10:59272515 | T | C | 1 | a0001c0001t0002g0078 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.593-2406A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59272515 | |||||||
| chr10:59272659 | G | C | 1 | a0001c0001t0001g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.593-2550C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59272659 | |||||||
| chr10:59272747 | C | T | 5 | a0001c0001t0001g0174 a0001c0001t0001g0191 a0002c0002t0001g0017 others(2): Show |
5 | HG00639.hp2 HG02559.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.593-2638G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59272747 | |||||||
| chr10:59272791 | T | C | 4 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0004c0005t0001g0027 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.593-2682A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59272791 | |||||||
| chr10:59272865 | G | C | 9 | a0001c0001t0001g0002 a0001c0001t0001g0141 a0001c0001t0001g0143 others(6): Show |
9 | HG01243.hp2 HG01891.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.593-2756C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59272865 | |||||||
| chr10:59273074 | G | A | 22 | a0001c0001t0002g0008 a0001c0001t0002g0014 a0001c0001t0002g0020 others(19): Show |
22 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.593-2965C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59273074 | |||||||
| chr10:59273134 | C | T | 5 | a0001c0001t0001g0067 a0001c0001t0001g0089 a0001c0001t0001g0112 others(2): Show |
5 | HG01123.hp1 HG01433.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.593-3025G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59273134 | |||||||
| chr10:59273192 | T | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(92): Show |
96 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.593-3083A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59273192 | |||||||
| chr10:59273355 | A | C | 1 | a0001c0001t0002g0119 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.593-3246T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59273355 | |||||||
| chr10:59273366 | T | C | 1 | a0001c0001t0007g0185 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.593-3257A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59273366 | |||||||
| chr10:59273861 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.593-3752A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59273861 | |||||||
| chr10:59274218 | C | CATCTG | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(92): Show |
96 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.593-4110_593-4109i others(7): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59274218 | |||||||
| chr10:59274259 | G | C | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
102 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.593-4150C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59274259 | |||||||
| chr10:59274393 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.593-4284G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59274393 | |||||||
| chr10:59274443 | A | G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
199 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(196): Show |
intron_variant | MODIFIER | c.593-4334T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59274443 | |||||||
| chr10:59274612 | T | C | 2 | a0001c0001t0001g0081 a0001c0001t0001g0133 |
2 | HG01168.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.593-4503A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59274612 | |||||||
| chr10:59274645 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.593-4536G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59274645 | |||||||
| chr10:59274702 | T | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(89): Show |
93 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.593-4593A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59274702 | |||||||
| chr10:59275093 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.593-4984C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59275093 | |||||||
| chr10:59275148 | T | C | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
102 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.593-5039A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59275148 | |||||||
| chr10:59275384 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.593-5275G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59275384 | |||||||
| chr10:59275749 | G | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG00735.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.593-5640C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59275749 | |||||||
| chr10:59275810 | C | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(87): Show |
91 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.593-5701G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59275810 | |||||||
| chr10:59276229 | G | T | 1 | a0001c0001t0001g0022 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.593-6120C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59276229 | |||||||
| chr10:59276271 | T | A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0117 |
2 | HG03654.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.593-6162A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59276271 | |||||||
| chr10:59276423 | CA | C | 2 | a0001c0001t0001g0003 a0001c0001t0001g0013 |
2 | HG00609.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.593-6315delT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59276423 | |||||||
| chr10:59276453 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(89): Show |
93 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.593-6344C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59276453 | |||||||
| chr10:59276544 | G | C | 1 | a0001c0001t0002g0076 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.593-6435C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59276544 | |||||||
| chr10:59276635 | G | T | 12 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0031 others(9): Show |
12 | HG00673.hp2 HG01099.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.593-6526C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59276635 | |||||||
| chr10:59276679 | G | T | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
105 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.593-6570C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59276679 | |||||||
| chr10:59276802 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.592+6561C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59276802 | |||||||
| chr10:59276911 | T | A | 1 | a0001c0001t0001g0187 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.592+6452A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59276911 | |||||||
| chr10:59276969 | G | A | 2 | a0004c0005t0001g0027 a0004c0005t0001g0149 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.592+6394C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59276969 | |||||||
| chr10:59277094 | G | A | 1 | a0001c0001t0002g0062 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.592+6269C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59277094 | |||||||
| chr10:59277224 | C | T | 4 | a0001c0001t0001g0165 a0001c0001t0001g0186 a0001c0001t0001g0197 others(1): Show |
4 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.592+6139G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59277224 | |||||||
| chr10:59277312 | T | A | 1 | a0005c0009t0001g0142 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.592+6051A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59277312 | |||||||
| chr10:59277613 | G | A | 1 | a0001c0001t0002g0090 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.592+5750C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59277613 | |||||||
| chr10:59277735 | T | C | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(1): Show |
4 | HG02055.hp2 HG02451.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.592+5628A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59277735 | |||||||
| chr10:59277895 | C | A | 1 | a0001c0001t0001g0122 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.592+5468G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59277895 | |||||||
| chr10:59278462 | G | T | 1 | a0001c0001t0001g0025 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.592+4901C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59278462 | |||||||
| chr10:59278506 | C | A | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.592+4857G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59278506 | |||||||
| chr10:59278656 | C | T | 26 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(23): Show |
27 | HG01884.hp1 HG01891.hp2 HG02135.hp1 others(24): Show |
intron_variant | MODIFIER | c.592+4707G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59278656 | |||||||
| chr10:59278833 | T | TAC | 4 | a0001c0001t0001g0019 a0001c0001t0001g0169 a0001c0001t0001g0188 others(1): Show |
4 | HG00323.hp2 HG01070.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.592+4528_592+4529d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59278833 | |||||||
| chr10:59278833 | TAC | T | 14 | a0001c0001t0001g0151 a0001c0001t0001g0178 a0001c0001t0001g0200 others(11): Show |
14 | HG00639.hp1 HG01167.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.592+4528_592+4529d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59278833 | |||||||
| chr10:59278833 | TACAC | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(73): Show |
77 | HG00558.hp2 HG00597.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.592+4526_592+4529d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59278833 | |||||||
| chr10:59278862 | T | C | 1 | a0002c0002t0006g0198 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.592+4501A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59278862 | |||||||
| chr10:59278957 | G | A | 10 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0050 others(7): Show |
10 | HG02004.hp2 HG02698.hp1 NA18941.hp1 others(7): Show |
intron_variant | MODIFIER | c.592+4406C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59278957 | |||||||
| chr10:59278979 | T | A | 1 | a0001c0001t0001g0053 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.592+4384A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59278979 | |||||||
| chr10:59279091 | C | G | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.592+4272G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59279091 | |||||||
| chr10:59279183 | C | T | 13 | a0001c0001t0001g0178 a0001c0001t0001g0200 a0001c0001t0001g0202 others(10): Show |
13 | HG00639.hp1 HG01167.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.592+4180G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59279183 | |||||||
| chr10:59279395 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.592+3968A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59279395 | |||||||
| chr10:59279483 | A | G | 1 | a0001c0001t0001g0043 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.592+3880T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59279483 | |||||||
| chr10:59279713 | A | C | 4 | a0001c0001t0001g0165 a0001c0001t0001g0186 a0001c0001t0001g0197 others(1): Show |
4 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.592+3650T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59279713 | |||||||
| chr10:59279866 | T | C | 4 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0032 others(1): Show |
4 | HG02622.hp1 HG02922.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.592+3497A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59279866 | |||||||
| chr10:59280166 | C | A | 1 | a0001c0004t0001g0026 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.592+3197G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59280166 | |||||||
| chr10:59280811 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.592+2552G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59280811 | |||||||
| chr10:59280967 | C | G | 5 | a0001c0001t0001g0067 a0001c0001t0001g0089 a0001c0001t0001g0112 others(2): Show |
5 | HG01123.hp1 HG01433.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.592+2396G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59280967 | |||||||
| chr10:59280972 | G | A | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
102 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.592+2391C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59280972 | |||||||
| chr10:59280982 | G | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(77): Show |
81 | HG00558.hp2 HG00597.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.592+2381C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59280982 | |||||||
| chr10:59281003 | G | C | 1 | a0001c0001t0001g0187 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.592+2360C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59281003 | |||||||
| chr10:59281387 | G | A | 5 | a0001c0001t0001g0067 a0001c0001t0001g0089 a0001c0001t0001g0112 others(2): Show |
5 | HG01123.hp1 HG01433.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.592+1976C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59281387 | |||||||
| chr10:59281422 | C | G | 27 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(24): Show |
28 | HG01884.hp1 HG01891.hp2 HG02135.hp1 others(25): Show |
intron_variant | MODIFIER | c.592+1941G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59281422 | |||||||
| chr10:59281572 | T | C | 5 | a0001c0001t0001g0067 a0001c0001t0001g0089 a0001c0001t0001g0112 others(2): Show |
5 | HG01123.hp1 HG01433.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.592+1791A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59281572 | |||||||
| chr10:59281854 | A | T | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(81): Show |
85 | HG00558.hp2 HG00597.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.592+1509T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59281854 | |||||||
| chr10:59281951 | G | T | 1 | a0002c0002t0006g0198 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.592+1412C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59281951 | |||||||
| chr10:59281962 | T | G | 1 | a0001c0001t0002g0126 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.592+1401A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59281962 | |||||||
| chr10:59282245 | C | A | 11 | a0001c0001t0001g0178 a0001c0001t0001g0200 a0001c0001t0001g0202 others(8): Show |
11 | HG00639.hp1 HG01167.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.592+1118G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59282245 | |||||||
| chr10:59282343 | T | C | 4 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0004c0005t0001g0027 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.592+1020A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59282343 | |||||||
| chr10:59282474 | T | G | 1 | a0007c0010t0001g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.592+889A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59282474 | |||||||
| chr10:59282560 | A | G | 5 | a0001c0001t0001g0067 a0001c0001t0001g0089 a0001c0001t0001g0112 others(2): Show |
5 | HG01123.hp1 HG01433.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.592+803T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59282560 | |||||||
| chr10:59282764 | C | T | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
102 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.592+599G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59282764 | |||||||
| chr10:59282832 | GA | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(80): Show |
84 | HG00558.hp2 HG00597.hp2 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.592+530delT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59282832 | |||||||
| chr10:59282921 | G | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(73): Show |
77 | HG00558.hp2 HG00597.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.592+442C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59282921 | |||||||
| chr10:59283156 | C | A | 5 | a0001c0001t0001g0174 a0001c0001t0001g0191 a0002c0002t0001g0017 others(2): Show |
5 | HG00639.hp2 HG02559.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.592+207G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59283156 | |||||||
| chr10:59283158 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.592+205C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59283158 | |||||||
| chr10:59283222 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.592+141C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59283222 | |||||||
| chr10:59283291 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(45): Show |
49 | HG00639.hp2 HG01106.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.592+72C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 6/13 | chr10 | 59283291 | |||||||
| chr10:59283484 | G | A | 5 | a0001c0001t0001g0019 a0001c0001t0001g0086 a0001c0001t0001g0136 others(2): Show |
5 | HG00323.hp2 HG00735.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-37C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59283484 | |||||||
| chr10:59283678 | C | G | 5 | a0001c0001t0001g0067 a0001c0001t0001g0089 a0001c0001t0001g0112 others(2): Show |
5 | HG01123.hp1 HG01433.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-231G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59283678 | |||||||
| chr10:59283691 | G | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
199 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(196): Show |
intron_variant | MODIFIER | c.508-244C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59283691 | |||||||
| chr10:59283826 | T | C | 3 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0164 |
3 | HG02572.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.508-379A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59283826 | |||||||
| chr10:59284031 | A | ATG | 2 | a0001c0001t0001g0115 a0001c0001t0001g0187 |
2 | HG00597.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.508-586_508-585dup others(2): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59284031 | |||||||
| chr10:59284031 | A | ATGTGTG | 26 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(23): Show |
26 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.508-590_508-585dup others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59284031 | |||||||
| chr10:59284031 | A | ATGTGTGT others(1): Show |
35 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(32): Show |
36 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.508-592_508-585dup others(8): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59284031 | |||||||
| chr10:59284031 | A | ATGTGTGT others(3): Show |
7 | a0001c0001t0001g0045 a0001c0001t0001g0054 a0001c0001t0001g0091 others(4): Show |
7 | HG01106.hp1 HG01891.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.508-594_508-585dup others(10): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59284031 | |||||||
| chr10:59284031 | A | ATGTGTGT others(5): Show |
5 | a0001c0001t0001g0165 a0001c0001t0001g0186 a0001c0001t0001g0197 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.508-596_508-585dup others(12): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59284031 | |||||||
| chr10:59284031 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.508-584T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59284031 | |||||||
| chr10:59284031 | ATGTG | A | 7 | a0001c0001t0001g0002 a0001c0001t0001g0141 a0001c0001t0001g0143 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.508-588_508-585del others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59284031 | |||||||
| chr10:59284154 | C | T | 2 | a0004c0005t0001g0027 a0004c0005t0001g0149 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.508-707G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59284154 | |||||||
| chr10:59284276 | T | C | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
102 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.508-829A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59284276 | |||||||
| chr10:59284421 | C | T | 2 | a0004c0005t0001g0027 a0004c0005t0001g0149 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.508-974G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59284421 | |||||||
| chr10:59284423 | G | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(81): Show |
85 | HG00558.hp2 HG00597.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.508-976C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59284423 | |||||||
| chr10:59284741 | C | CCA | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(81): Show |
85 | HG00558.hp2 HG00597.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.508-1296_508-1295d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59284741 | |||||||
| chr10:59284816 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.508-1369T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59284816 | |||||||
| chr10:59284839 | T | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(91): Show |
95 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.508-1392A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59284839 | |||||||
| chr10:59285105 | C | A | 2 | a0004c0005t0001g0027 a0004c0005t0001g0149 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.508-1658G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59285105 | |||||||
| chr10:59285311 | G | C | 1 | a0002c0002t0001g0035 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.508-1864C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59285311 | |||||||
| chr10:59285398 | C | CAG | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(91): Show |
95 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.508-1952_508-1951i others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59285398 | |||||||
| chr10:59285742 | G | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.508-2295C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59285742 | |||||||
| chr10:59285804 | C | G | 1 | a0001c0001t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.508-2357G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59285804 | |||||||
| chr10:59285885 | T | C | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.508-2438A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59285885 | |||||||
| chr10:59285961 | C | CTG | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(91): Show |
95 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.508-2516_508-2515d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59285961 | |||||||
| chr10:59286026 | C | T | 2 | a0004c0005t0001g0027 a0004c0005t0001g0149 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.508-2579G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286026 | |||||||
| chr10:59286091 | G | A | 1 | a0001c0001t0002g0126 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.508-2644C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286091 | |||||||
| chr10:59286289 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.508-2842G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286289 | |||||||
| chr10:59286470 | G | A | 9 | a0001c0001t0001g0178 a0001c0001t0001g0200 a0001c0001t0001g0202 others(6): Show |
9 | HG00639.hp1 HG01167.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.508-3023C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286470 | |||||||
| chr10:59286516 | A | AAT | 4 | a0001c0001t0001g0174 a0001c0001t0001g0191 a0002c0002t0001g0017 others(1): Show |
4 | HG00639.hp2 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-3071_508-3070d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | |||||||
| chr10:59286516 | A | AATAT | 71 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(68): Show |
71 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.508-3073_508-3070d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | |||||||
| chr10:59286516 | A | AATATAT | 39 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(36): Show |
40 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.508-3075_508-3070d others(8): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | |||||||
| chr10:59286516 | A | AATATATA others(1): Show |
11 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0101 others(8): Show |
11 | HG01243.hp2 HG01891.hp2 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.508-3077_508-3070d others(10): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | |||||||
| chr10:59286516 | A | AATATATA others(3): Show |
1 | a0001c0007t0001g0059 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.508-3079_508-3070d others(12): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | |||||||
| chr10:59286516 | A | AATATATA others(5): Show |
5 | a0001c0001t0001g0002 a0001c0001t0001g0112 a0001c0001t0001g0143 others(2): Show |
5 | HG02572.hp2 HG02886.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-3081_508-3070d others(14): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | |||||||
| chr10:59286516 | A | AATATATA others(7): Show |
3 | a0001c0001t0001g0051 a0001c0001t0001g0196 a0001c0001t0002g0135 |
3 | HG02257.hp2 HG03471.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.508-3083_508-3070d others(16): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | |||||||
| chr10:59286516 | A | AATATATA others(9): Show |
3 | a0001c0001t0001g0025 a0001c0001t0001g0108 a0001c0004t0001g0026 |
3 | HG00735.hp2 HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.508-3085_508-3070d others(18): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | |||||||
| chr10:59286516 | A | AATATATA others(11): Show |
4 | a0001c0001t0001g0070 a0001c0001t0001g0107 a0001c0001t0001g0153 others(1): Show |
4 | HG02258.hp2 HG02280.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-3087_508-3070d others(20): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | |||||||
| chr10:59286516 | A | AATATATA others(13): Show |
3 | a0001c0001t0001g0054 a0001c0001t0001g0091 a0001c0001t0001g0151 |
3 | HG01433.hp2 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.508-3089_508-3070d others(22): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | |||||||
| chr10:59286516 | A | AATATATA others(17): Show |
4 | a0001c0001t0001g0045 a0001c0001t0001g0067 a0001c0001t0001g0172 others(1): Show |
4 | HG01891.hp1 HG02647.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.508-3093_508-3070d others(26): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | |||||||
| chr10:59286516 | A | AATATATA others(21): Show |
1 | a0001c0001t0001g0150 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.508-3070_508-3069i others(30): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | |||||||
| chr10:59286516 | A | AATATATA others(31): Show |
1 | a0001c0001t0002g0066 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.508-3070_508-3069i others(40): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | |||||||
| chr10:59286516 | A | AATATATA others(23): Show |
2 | a0001c0001t0001g0089 a0001c0001t0002g0014 |
2 | NA18959.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.508-3070_508-3069i others(32): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | |||||||
| chr10:59286516 | A | AATATATA others(25): Show |
2 | a0001c0001t0002g0071 a0001c0001t0002g0170 |
2 | HG00673.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.508-3070_508-3069i others(34): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | |||||||
| chr10:59286516 | A | AATATATA others(27): Show |
1 | a0001c0001t0002g0020 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.508-3070_508-3069i others(36): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | |||||||
| chr10:59286516 | A | AATATATA others(29): Show |
2 | a0001c0001t0002g0064 a0001c0001t0002g0078 |
2 | HG00558.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.508-3070_508-3069i others(38): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | |||||||
| chr10:59286516 | A | AATATATA others(31): Show |
2 | a0001c0001t0002g0074 a0001c0001t0002g0119 |
2 | HG02683.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.508-3070_508-3069i others(40): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | |||||||
| chr10:59286516 | A | AATATATA others(33): Show |
5 | a0001c0001t0002g0008 a0001c0001t0002g0068 a0001c0001t0002g0076 others(2): Show |
5 | HG02698.hp2 HG03540.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-3070_508-3069i others(42): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | |||||||
| chr10:59286516 | A | AATATATA others(37): Show |
2 | a0001c0001t0002g0062 a0001c0001t0002g0126 |
2 | NA18994.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.508-3070_508-3069i others(46): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | |||||||
| chr10:59286516 | A | AATATATA others(41): Show |
2 | a0001c0001t0002g0063 a0001c0001t0002g0065 |
2 | NA18988.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.508-3070_508-3069i others(50): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | |||||||
| chr10:59286516 | A | AATATATA others(45): Show |
1 | a0001c0001t0002g0125 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.508-3070_508-3069i others(54): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | |||||||
| chr10:59286516 | A | ATATATAT | 2 | a0001c0001t0001g0077 a0001c0001t0001g0123 |
2 | HG02132.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.508-3070_508-3069i others(9): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | |||||||
| chr10:59286516 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0179 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.508-3070_508-3069i others(15): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | |||||||
| chr10:59286516 | A | ATATATAT others(24): Show |
1 | a0002c0002t0006g0198 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.508-3070_508-3069i others(33): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | |||||||
| chr10:59286516 | AAT | A | 6 | a0001c0001t0001g0187 a0003c0003t0001g0192 a0003c0003t0001g0193 others(3): Show |
6 | HG00639.hp1 HG01243.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.508-3071_508-3070d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | |||||||
| chr10:59286516 | AATAT | A | 14 | a0001c0001t0001g0165 a0001c0001t0001g0178 a0001c0001t0001g0180 others(11): Show |
14 | HG01167.hp1 HG02055.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.508-3073_508-3070d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | |||||||
| chr10:59286516 | AATATAT | A | 3 | a0001c0001t0007g0185 a0004c0005t0001g0027 a0004c0005t0001g0149 |
3 | HG02647.hp1 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.508-3075_508-3070d others(8): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | |||||||
| chr10:59286516 | AATATATA others(3): Show |
A | 1 | a0001c0001t0002g0082 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.508-3079_508-3070d others(12): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286516 | |||||||
| chr10:59286786 | C | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(71): Show |
75 | HG00558.hp2 HG00597.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.508-3339G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286786 | |||||||
| chr10:59286791 | T | C | 5 | a0001c0001t0001g0067 a0001c0001t0001g0089 a0001c0001t0001g0112 others(2): Show |
5 | HG01123.hp1 HG01433.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-3344A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286791 | |||||||
| chr10:59286804 | C | T | 1 | a0001c0001t0007g0185 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.508-3357G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286804 | |||||||
| chr10:59286890 | C | T | 2 | a0004c0005t0001g0027 a0004c0005t0001g0149 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.508-3443G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286890 | |||||||
| chr10:59286905 | G | C | 2 | a0004c0005t0001g0027 a0004c0005t0001g0149 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.508-3458C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286905 | |||||||
| chr10:59286972 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.508-3525A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286972 | |||||||
| chr10:59286988 | C | G | 1 | a0001c0001t0001g0042 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.508-3541G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59286988 | |||||||
| chr10:59287010 | G | A | 5 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0032 others(2): Show |
5 | HG02622.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.508-3563C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287010 | |||||||
| chr10:59287021 | G | A | 10 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0054 others(7): Show |
10 | HG01106.hp1 HG01891.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.508-3574C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287021 | |||||||
| chr10:59287033 | C | CA | 18 | a0001c0001t0001g0053 a0001c0001t0001g0101 a0001c0001t0001g0164 others(15): Show |
18 | HG00639.hp1 HG01167.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.508-3587dupT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287033 | |||||||
| chr10:59287033 | CA | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(38): Show |
42 | HG00323.hp1 HG00639.hp2 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.508-3587delT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287033 | |||||||
| chr10:59287105 | G | A | 1 | a0001c0001t0007g0185 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.508-3658C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287105 | |||||||
| chr10:59287200 | G | T | 1 | a0001c0001t0001g0041 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.508-3753C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287200 | |||||||
| chr10:59287284 | T | A | 1 | a0001c0001t0001g0083 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.508-3837A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287284 | |||||||
| chr10:59287295 | C | A | 2 | a0004c0005t0001g0027 a0004c0005t0001g0149 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.508-3848G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287295 | |||||||
| chr10:59287331 | T | A | 12 | a0001c0001t0001g0178 a0001c0001t0001g0180 a0001c0001t0001g0200 others(9): Show |
12 | HG00639.hp1 HG01167.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.508-3884A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287331 | |||||||
| chr10:59287336 | CAA | C | 24 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0025 others(21): Show |
24 | HG00597.hp1 HG01243.hp1 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.508-3891_508-3890d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287336 | |||||||
| chr10:59287336 | CAAA | C | 70 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(67): Show |
70 | HG00323.hp1 HG00609.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.508-3892_508-3890d others(5): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287336 | |||||||
| chr10:59287336 | CAAAA | C | 16 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0055 others(13): Show |
16 | HG00558.hp1 HG01070.hp2 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.508-3893_508-3890d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287336 | |||||||
| chr10:59287336 | CAAAAA | C | 17 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0054 others(14): Show |
17 | HG01106.hp1 HG01123.hp1 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.508-3894_508-3890d others(7): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287336 | |||||||
| chr10:59287336 | CAAAAAA | C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(42): Show |
46 | HG00558.hp2 HG00597.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.508-3895_508-3890d others(8): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287336 | |||||||
| chr10:59287336 | CAAAAAAA | C | 16 | a0001c0001t0001g0051 a0001c0001t0001g0143 a0001c0001t0001g0155 others(13): Show |
16 | HG02109.hp1 HG02572.hp2 HG02683.hp1 others(13): Show |
intron_variant | MODIFIER | c.508-3896_508-3890d others(9): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287336 | |||||||
| chr10:59287367 | G | T | 5 | a0001c0001t0001g0019 a0001c0001t0001g0086 a0001c0001t0001g0136 others(2): Show |
5 | HG00323.hp2 HG00735.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-3920C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287367 | |||||||
| chr10:59287579 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.508-4132C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287579 | |||||||
| chr10:59287740 | A | G | 1 | a0001c0001t0002g0119 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.508-4293T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287740 | |||||||
| chr10:59287757 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.508-4310A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287757 | |||||||
| chr10:59287808 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.508-4361A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59287808 | |||||||
| chr10:59288218 | G | T | 1 | a0001c0001t0001g0188 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.508-4771C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59288218 | |||||||
| chr10:59288337 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.508-4890A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59288337 | |||||||
| chr10:59288363 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.508-4916G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59288363 | |||||||
| chr10:59288483 | A | AAAG | 11 | a0001c0001t0001g0091 a0001c0001t0001g0122 a0001c0001t0001g0165 others(8): Show |
11 | HG02055.hp2 HG02451.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.508-5039_508-5037d others(5): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59288483 | |||||||
| chr10:59288483 | AAAG | A | 23 | a0001c0001t0001g0046 a0001c0001t0002g0008 a0001c0001t0002g0014 others(20): Show |
23 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.508-5039_508-5037d others(5): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59288483 | |||||||
| chr10:59289076 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.508-5629G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59289076 | |||||||
| chr10:59289165 | C | T | 1 | a0001c0001t0007g0185 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.508-5718G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59289165 | |||||||
| chr10:59289275 | C | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.508-5828G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59289275 | |||||||
| chr10:59289287 | G | A | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 |
3 | HG02055.hp1 HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.508-5840C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59289287 | |||||||
| chr10:59289300 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.508-5853T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59289300 | |||||||
| chr10:59289502 | C | T | 1 | a0001c0004t0001g0026 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.508-6055G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59289502 | |||||||
| chr10:59289644 | C | G | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.508-6197G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59289644 | |||||||
| chr10:59289785 | G | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
199 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(196): Show |
intron_variant | MODIFIER | c.508-6338C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59289785 | |||||||
| chr10:59289801 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.508-6354C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59289801 | |||||||
| chr10:59290081 | T | A | 5 | a0001c0001t0001g0067 a0001c0001t0001g0089 a0001c0001t0001g0112 others(2): Show |
5 | HG01123.hp1 HG01433.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-6634A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59290081 | |||||||
| chr10:59290554 | C | A | 1 | a0001c0001t0001g0021 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.508-7107G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59290554 | |||||||
| chr10:59290579 | T | C | 26 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(23): Show |
27 | HG01884.hp1 HG01891.hp2 HG02135.hp1 others(24): Show |
intron_variant | MODIFIER | c.508-7132A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59290579 | |||||||
| chr10:59290867 | G | T | 44 | a0001c0001t0001g0067 a0001c0001t0001g0089 a0001c0001t0001g0091 others(41): Show |
44 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.508-7420C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59290867 | |||||||
| chr10:59290893 | A | G | 34 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0033 others(31): Show |
34 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.508-7446T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59290893 | |||||||
| chr10:59290966 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.508-7519G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59290966 | |||||||
| chr10:59291024 | G | T | 5 | a0001c0001t0001g0122 a0001c0001t0001g0165 a0001c0001t0001g0186 others(2): Show |
5 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-7577C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291024 | |||||||
| chr10:59291115 | A | G | 55 | a0001c0001t0001g0067 a0001c0001t0001g0089 a0001c0001t0001g0091 others(52): Show |
55 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.508-7668T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291115 | |||||||
| chr10:59291203 | A | G | 12 | a0001c0001t0001g0045 a0001c0001t0001g0150 a0001c0001t0001g0153 others(9): Show |
12 | HG00639.hp2 HG01106.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.508-7756T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291203 | |||||||
| chr10:59291291 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.508-7844C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291291 | |||||||
| chr10:59291411 | T | G | 1 | a0001c0001t0002g0076 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.508-7964A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291411 | |||||||
| chr10:59291439 | C | T | 1 | a0001c0001t0001g0012 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.508-7992G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291439 | |||||||
| chr10:59291516 | G | A | 33 | a0001c0001t0001g0045 a0001c0001t0001g0067 a0001c0001t0001g0089 others(30): Show |
33 | HG00639.hp1 HG01106.hp1 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.508-8069C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291516 | |||||||
| chr10:59291523 | A | G | 1 | a0001c0001t0001g0054 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.508-8076T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291523 | |||||||
| chr10:59291579 | T | C | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.508-8132A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291579 | |||||||
| chr10:59291670 | A | AG | 160 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(157): Show |
160 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.508-8224dupC | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291670 | |||||||
| chr10:59291770 | C | A | 1 | a0001c0001t0001g0112 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.508-8323G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291770 | |||||||
| chr10:59291785 | C | CT | 21 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(18): Show |
22 | HG01167.hp1 HG01884.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.508-8339dupA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291785 | |||||||
| chr10:59291785 | CT | C | 22 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0025 others(19): Show |
22 | HG00323.hp2 HG01891.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.508-8339delA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291785 | |||||||
| chr10:59291785 | CTT | C | 147 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(144): Show |
147 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(144): Show |
intron_variant | MODIFIER | c.508-8340_508-8339d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291785 | |||||||
| chr10:59291785 | CTTT | C | 5 | a0001c0001t0001g0067 a0001c0001t0001g0089 a0001c0001t0001g0112 others(2): Show |
5 | HG03704.hp1 HG03927.hp2 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.508-8341_508-8339d others(5): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291785 | |||||||
| chr10:59291870 | G | C | 1 | a0001c0001t0001g0187 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.508-8423C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291870 | |||||||
| chr10:59291902 | C | T | 1 | a0001c0001t0002g0008 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.508-8455G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291902 | |||||||
| chr10:59291953 | G | T | 12 | a0001c0001t0001g0067 a0001c0001t0001g0089 a0001c0001t0001g0112 others(9): Show |
12 | HG00639.hp1 HG01243.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.508-8506C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291953 | |||||||
| chr10:59291972 | T | C | 4 | a0001c0001t0001g0174 a0002c0002t0001g0017 a0002c0002t0001g0035 others(1): Show |
4 | HG02559.hp1 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-8525A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291972 | |||||||
| chr10:59291977 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0201 |
2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.508-8530C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291977 | |||||||
| chr10:59291979 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.508-8532T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291979 | |||||||
| chr10:59291989 | C | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0137 |
2 | HG01123.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.508-8542G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291989 | |||||||
| chr10:59291990 | A | G | 2 | a0001c0001t0001g0111 a0001c0001t0001g0137 |
2 | HG01123.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.508-8543T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291990 | |||||||
| chr10:59291992 | A | G | 2 | a0001c0001t0001g0111 a0001c0001t0001g0137 |
2 | HG01123.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.508-8545T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59291992 | |||||||
| chr10:59292004 | G | T | 1 | a0001c0001t0001g0141 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.508-8557C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59292004 | |||||||
| chr10:59292010 | T | C | 5 | a0001c0001t0001g0067 a0001c0001t0001g0089 a0001c0001t0001g0112 others(2): Show |
5 | HG01433.hp2 HG03704.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.508-8563A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59292010 | |||||||
| chr10:59292010 | T | G | 1 | a0001c0001t0001g0088 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.508-8563A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59292010 | |||||||
| chr10:59292027 | G | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
199 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(196): Show |
intron_variant | MODIFIER | c.508-8580C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59292027 | |||||||
| chr10:59292077 | T | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(7): Show |
10 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(7): Show |
intron_variant | MODIFIER | c.508-8630A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59292077 | |||||||
| chr10:59292079 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.508-8632G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59292079 | |||||||
| chr10:59292172 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.508-8725G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59292172 | |||||||
| chr10:59292209 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.508-8762C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59292209 | |||||||
| chr10:59292241 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.508-8794C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59292241 | |||||||
| chr10:59292278 | C | G | 31 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0061 others(28): Show |
31 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.508-8831G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59292278 | |||||||
| chr10:59292309 | C | G | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
200 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(197): Show |
intron_variant | MODIFIER | c.508-8862G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59292309 | |||||||
| chr10:59292363 | T | G | 1 | a0001c0001t0001g0188 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.508-8916A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59292363 | |||||||
| chr10:59292575 | T | C | 18 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0042 others(15): Show |
18 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.508-9128A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59292575 | |||||||
| chr10:59292947 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.508-9500A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59292947 | |||||||
| chr10:59293069 | C | CT | 24 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0032 others(21): Show |
24 | HG00639.hp2 HG01106.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.508-9623dupA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59293069 | |||||||
| chr10:59293069 | C | CTT | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(93): Show |
97 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.508-9624_508-9623d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59293069 | |||||||
| chr10:59293069 | C | CTTT | 21 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0044 others(18): Show |
21 | HG00735.hp2 HG01123.hp1 HG02300.hp1 others(18): Show |
intron_variant | MODIFIER | c.508-9625_508-9623d others(5): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59293069 | |||||||
| chr10:59293069 | CTTTTTTT others(3): Show |
C | 56 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0025 others(53): Show |
56 | HG00558.hp2 HG00609.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.508-9632_508-9623d others(12): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59293069 | |||||||
| chr10:59293106 | T | G | 4 | a0001c0001t0001g0092 a0001c0001t0001g0155 a0001c0001t0001g0158 others(1): Show |
4 | HG02970.hp1 HG03098.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-9659A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59293106 | |||||||
| chr10:59293198 | T | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
200 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(197): Show |
intron_variant | MODIFIER | c.507+9603A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59293198 | |||||||
| chr10:59293240 | A | AT | 56 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0025 others(53): Show |
56 | HG00558.hp2 HG00609.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.507+9560dupA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59293240 | |||||||
| chr10:59293266 | C | T | 1 | a0001c0001t0002g0126 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.507+9535G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59293266 | |||||||
| chr10:59293296 | T | C | 8 | a0001c0001t0001g0051 a0001c0001t0001g0054 a0001c0001t0001g0070 others(5): Show |
8 | HG01106.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.507+9505A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59293296 | |||||||
| chr10:59293371 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.507+9430G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59293371 | |||||||
| chr10:59293588 | T | A | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): Show |
85 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.507+9213A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59293588 | |||||||
| chr10:59293661 | C | A | 4 | a0001c0001t0001g0174 a0002c0002t0001g0017 a0002c0002t0001g0035 others(1): Show |
4 | HG02559.hp1 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+9140G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59293661 | |||||||
| chr10:59293676 | A | G | 1 | a0002c0002t0001g0036 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.507+9125T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59293676 | |||||||
| chr10:59293770 | G | A | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
200 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(197): Show |
intron_variant | MODIFIER | c.507+9031C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59293770 | |||||||
| chr10:59293820 | C | A | 55 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0025 others(52): Show |
55 | HG00558.hp2 HG00609.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.507+8981G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59293820 | |||||||
| chr10:59293879 | T | C | 20 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0042 others(17): Show |
20 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.507+8922A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59293879 | |||||||
| chr10:59294095 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.507+8706G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59294095 | |||||||
| chr10:59294123 | TA | T | 3 | a0001c0001t0001g0153 a0001c0001t0001g0187 a0001c0001t0001g0201 |
3 | HG01891.hp1 HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.507+8677delT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59294123 | |||||||
| chr10:59294124 | A | T | 1 | a0001c0001t0001g0173 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.507+8677T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59294124 | |||||||
| chr10:59294496 | T | C | 3 | a0001c0001t0001g0067 a0001c0001t0001g0112 a0001c0001t0001g0151 |
3 | HG01433.hp2 HG03704.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.507+8305A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59294496 | |||||||
| chr10:59294931 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.507+7870T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59294931 | |||||||
| chr10:59295083 | C | T | 1 | a0001c0001t0001g0007 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.507+7718G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59295083 | |||||||
| chr10:59295171 | C | A | 20 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0042 others(17): Show |
20 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.507+7630G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59295171 | |||||||
| chr10:59295250 | A | G | 14 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(11): Show |
14 | HG00609.hp1 HG00673.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.507+7551T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59295250 | |||||||
| chr10:59295336 | G | A | 27 | a0001c0001t0001g0025 a0001c0001t0001g0061 a0001c0001t0001g0152 others(24): Show |
27 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.507+7465C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59295336 | |||||||
| chr10:59295377 | C | T | 106 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(103): Show |
106 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.507+7424G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59295377 | |||||||
| chr10:59295384 | G | C | 8 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0046 others(5): Show |
8 | HG01123.hp1 HG02647.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.507+7417C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59295384 | |||||||
| chr10:59295494 | C | CTA | 2 | a0004c0005t0001g0027 a0004c0005t0001g0149 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.507+7306_507+7307i others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59295494 | |||||||
| chr10:59295554 | C | G | 2 | a0002c0002t0001g0037 a0002c0002t0001g0095 |
2 | HG01243.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.507+7247G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59295554 | |||||||
| chr10:59295709 | C | A | 2 | a0004c0005t0001g0027 a0004c0005t0001g0149 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.507+7092G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59295709 | |||||||
| chr10:59295817 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.507+6984A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59295817 | |||||||
| chr10:59296123 | T | A | 20 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0042 others(17): Show |
20 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.507+6678A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59296123 | |||||||
| chr10:59296371 | A | G | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): Show |
85 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.507+6430T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59296371 | |||||||
| chr10:59296390 | C | A | 61 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0025 others(58): Show |
61 | HG00558.hp2 HG00609.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.507+6411G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59296390 | |||||||
| chr10:59296624 | T | A | 4 | a0001c0001t0001g0174 a0002c0002t0001g0017 a0002c0002t0001g0035 others(1): Show |
4 | HG02559.hp1 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+6177A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59296624 | |||||||
| chr10:59296707 | T | G | 1 | a0001c0001t0002g0119 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.507+6094A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59296707 | |||||||
| chr10:59296743 | C | A | 1 | a0001c0001t0001g0025 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.507+6058G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59296743 | |||||||
| chr10:59297082 | C | T | 51 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0025 others(48): Show |
51 | HG00558.hp2 HG00609.hp2 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.507+5719G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59297082 | |||||||
| chr10:59297083 | G | A | 1 | a0002c0002t0006g0198 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.507+5718C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59297083 | |||||||
| chr10:59297212 | C | T | 2 | a0004c0005t0001g0027 a0004c0005t0001g0149 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.507+5589G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59297212 | |||||||
| chr10:59297536 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.507+5265A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59297536 | |||||||
| chr10:59297551 | C | T | 2 | a0004c0005t0001g0027 a0004c0005t0001g0149 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.507+5250G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59297551 | |||||||
| chr10:59297580 | G | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(194): Show |
198 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(195): Show |
intron_variant | MODIFIER | c.507+5221C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59297580 | |||||||
| chr10:59297676 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.507+5125C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59297676 | |||||||
| chr10:59297744 | A | C | 8 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0046 others(5): Show |
8 | HG01123.hp1 HG02647.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.507+5057T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59297744 | |||||||
| chr10:59297873 | C | T | 4 | a0001c0001t0001g0091 a0001c0001t0001g0153 a0001c0001t0001g0187 others(1): Show |
4 | HG01891.hp1 HG02723.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.507+4928G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59297873 | |||||||
| chr10:59297900 | C | CA | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(90): Show |
93 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.507+4900dupT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59297900 | |||||||
| chr10:59297943 | T | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(194): Show |
198 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(195): Show |
intron_variant | MODIFIER | c.507+4858A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59297943 | |||||||
| chr10:59297949 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.507+4852G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59297949 | |||||||
| chr10:59297953 | A | C | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.507+4848T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59297953 | |||||||
| chr10:59297976 | C | T | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(107): Show |
110 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.507+4825G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59297976 | |||||||
| chr10:59297992 | A | G | 4 | a0001c0001t0001g0165 a0001c0001t0001g0186 a0001c0001t0001g0197 others(1): Show |
4 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+4809T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59297992 | |||||||
| chr10:59298265 | G | A | 4 | a0001c0001t0001g0174 a0002c0002t0001g0017 a0002c0002t0001g0035 others(1): Show |
4 | HG02559.hp1 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+4536C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59298265 | |||||||
| chr10:59298273 | T | C | 2 | a0001c0001t0001g0188 a0001c0007t0001g0059 |
2 | HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.507+4528A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59298273 | |||||||
| chr10:59298277 | A | G | 27 | a0001c0001t0001g0025 a0001c0001t0001g0061 a0001c0001t0001g0152 others(24): Show |
27 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.507+4524T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59298277 | |||||||
| chr10:59298409 | G | T | 4 | a0001c0001t0001g0165 a0001c0001t0001g0186 a0001c0001t0001g0197 others(1): Show |
4 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+4392C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59298409 | |||||||
| chr10:59298642 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(194): Show |
198 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(195): Show |
intron_variant | MODIFIER | c.507+4159T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59298642 | |||||||
| chr10:59299038 | C | T | 90 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(87): Show |
90 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.507+3763G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59299038 | |||||||
| chr10:59299272 | T | TA | 4 | a0001c0001t0001g0004 a0001c0001t0001g0058 a0001c0001t0001g0084 others(1): Show |
4 | NA18942.hp1 NA18942.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.507+3528dupT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59299272 | |||||||
| chr10:59299344 | GC | G | 27 | a0001c0001t0001g0025 a0001c0001t0001g0061 a0001c0001t0001g0152 others(24): Show |
27 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.507+3456delG | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59299344 | |||||||
| chr10:59299385 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.507+3416T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59299385 | |||||||
| chr10:59299445 | G | C | 2 | a0004c0005t0001g0027 a0004c0005t0001g0149 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.507+3356C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59299445 | |||||||
| chr10:59299474 | T | C | 2 | a0001c0001t0002g0090 a0001c0001t0004g0131 |
2 | HG02300.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.507+3327A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59299474 | |||||||
| chr10:59299511 | C | CT | 6 | a0001c0001t0001g0067 a0001c0001t0001g0091 a0001c0001t0001g0112 others(3): Show |
6 | HG01433.hp2 HG03453.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.507+3289dupA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59299511 | |||||||
| chr10:59299511 | CT | C | 26 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0028 others(23): Show |
26 | HG01106.hp1 HG01123.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.507+3289delA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59299511 | |||||||
| chr10:59299511 | CTT | C | 20 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0042 others(17): Show |
20 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.507+3288_507+3289d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59299511 | |||||||
| chr10:59299545 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.507+3256G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59299545 | |||||||
| chr10:59299610 | A | C | 1 | a0001c0001t0001g0184 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.507+3191T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59299610 | |||||||
| chr10:59299696 | G | T | 8 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0046 others(5): Show |
8 | HG01123.hp1 HG02647.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.507+3105C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59299696 | |||||||
| chr10:59299904 | A | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
149 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(146): Show |
intron_variant | MODIFIER | c.507+2897T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59299904 | |||||||
| chr10:59299987 | A | C | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.507+2814T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59299987 | |||||||
| chr10:59300052 | G | A | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(86): Show |
89 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.507+2749C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59300052 | |||||||
| chr10:59300077 | A | G | 6 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(3): Show |
6 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.507+2724T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59300077 | |||||||
| chr10:59300313 | T | G | 8 | a0001c0001t0001g0051 a0001c0001t0001g0054 a0001c0001t0001g0070 others(5): Show |
8 | HG01106.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.507+2488A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59300313 | |||||||
| chr10:59300324 | C | T | 2 | a0004c0005t0001g0027 a0004c0005t0001g0149 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.507+2477G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59300324 | |||||||
| chr10:59300349 | C | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0116 |
2 | HG00609.hp1 HG00673.hp2 |
intron_variant | MODIFIER | c.507+2452G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59300349 | |||||||
| chr10:59300536 | G | A | 4 | a0001c0001t0001g0165 a0001c0001t0001g0186 a0001c0001t0001g0197 others(1): Show |
4 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+2265C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59300536 | |||||||
| chr10:59300635 | C | G | 8 | a0001c0001t0001g0051 a0001c0001t0001g0054 a0001c0001t0001g0070 others(5): Show |
8 | HG01106.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.507+2166G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59300635 | |||||||
| chr10:59300655 | G | C | 1 | a0001c0001t0001g0173 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.507+2146C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59300655 | |||||||
| chr10:59300683 | C | G | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.507+2118G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59300683 | |||||||
| chr10:59300808 | C | A | 8 | a0001c0001t0001g0051 a0001c0001t0001g0054 a0001c0001t0001g0070 others(5): Show |
8 | HG01106.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.507+1993G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59300808 | |||||||
| chr10:59300812 | T | C | 2 | a0004c0005t0001g0027 a0004c0005t0001g0149 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.507+1989A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59300812 | |||||||
| chr10:59300919 | C | T | 27 | a0001c0001t0001g0025 a0001c0001t0001g0061 a0001c0001t0001g0152 others(24): Show |
27 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.507+1882G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59300919 | |||||||
| chr10:59300922 | T | C | 12 | a0001c0001t0001g0122 a0001c0001t0001g0178 a0001c0001t0001g0180 others(9): Show |
12 | HG00639.hp1 HG01167.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.507+1879A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59300922 | |||||||
| chr10:59301032 | A | G | 43 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(40): Show |
43 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.507+1769T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59301032 | |||||||
| chr10:59301068 | T | C | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): Show |
85 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.507+1733A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59301068 | |||||||
| chr10:59301269 | T | C | 1 | a0001c0001t0001g0033 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.507+1532A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59301269 | |||||||
| chr10:59301324 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(194): Show |
198 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(195): Show |
intron_variant | MODIFIER | c.507+1477T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59301324 | |||||||
| chr10:59301595 | T | TA | 12 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0046 others(9): Show |
12 | HG01123.hp1 HG02486.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.507+1205dupT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59301595 | |||||||
| chr10:59301613 | C | G | 1 | a0001c0001t0001g0091 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.507+1188G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59301613 | |||||||
| chr10:59301690 | C | G | 1 | a0001c0001t0001g0091 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.507+1111G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59301690 | |||||||
| chr10:59301727 | A | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(149): Show |
153 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.507+1074T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59301727 | |||||||
| chr10:59301747 | A | G | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(88): Show |
91 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.507+1054T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59301747 | |||||||
| chr10:59301829 | T | A | 5 | a0001c0001t0001g0067 a0001c0001t0001g0112 a0001c0001t0001g0151 others(2): Show |
5 | HG01433.hp2 HG03453.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+972A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59301829 | |||||||
| chr10:59301983 | G | A | 8 | a0001c0001t0001g0051 a0001c0001t0001g0054 a0001c0001t0001g0070 others(5): Show |
8 | HG01106.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.507+818C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59301983 | |||||||
| chr10:59302008 | G | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(117): Show |
120 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.507+793C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59302008 | |||||||
| chr10:59302625 | C | T | 4 | a0003c0003t0001g0192 a0003c0003t0001g0193 a0003c0003t0001g0194 others(1): Show |
4 | HG00639.hp1 HG01243.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+176G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59302625 | |||||||
| chr10:59302778 | T | C | 20 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0042 others(17): Show |
20 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.507+23A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | 59302778 | |||||||
| chr10:59303134 | A | G | 12 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0046 others(9): Show |
12 | HG01123.hp1 HG02486.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.444-270T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59303134 | |||||||
| chr10:59303214 | A | G | 1 | a0001c0001t0002g0076 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.444-350T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59303214 | |||||||
| chr10:59303254 | G | A | 28 | a0001c0001t0001g0025 a0001c0001t0001g0061 a0001c0001t0001g0152 others(25): Show |
28 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.444-390C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59303254 | |||||||
| chr10:59303397 | A | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(150): Show |
154 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.444-533T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59303397 | |||||||
| chr10:59303515 | A | C | 1 | a0001c0001t0001g0104 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.444-651T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59303515 | |||||||
| chr10:59303568 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.444-704G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59303568 | |||||||
| chr10:59303860 | G | T | 3 | a0001c0001t0001g0121 a0001c0001t0001g0130 a0001c0001t0001g0133 |
3 | HG00738.hp2 HG01081.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.444-996C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59303860 | |||||||
| chr10:59303934 | G | T | 3 | a0001c0001t0001g0083 a0001c0001t0001g0102 a0001c0001t0001g0167 |
3 | HG01081.hp1 HG01106.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.444-1070C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59303934 | |||||||
| chr10:59304009 | G | A | 1 | a0002c0002t0006g0198 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.444-1145C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304009 | |||||||
| chr10:59304105 | G | A | 3 | a0001c0001t0001g0067 a0001c0001t0001g0112 a0001c0001t0001g0151 |
3 | HG01433.hp2 HG03704.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.444-1241C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304105 | |||||||
| chr10:59304129 | C | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(194): Show |
198 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(195): Show |
intron_variant | MODIFIER | c.444-1265G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304129 | |||||||
| chr10:59304547 | C | T | 20 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0042 others(17): Show |
20 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.444-1683G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304547 | |||||||
| chr10:59304761 | G | GAGGGA | 44 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(41): Show |
44 | HG00558.hp1 HG00597.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.444-1902_444-1898d others(7): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304761 | |||||||
| chr10:59304761 | G | GAGGGAAG others(3): Show |
33 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(30): Show |
33 | HG00323.hp1 HG00323.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.444-1907_444-1898d others(12): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304761 | |||||||
| chr10:59304761 | G | GAGGGAAG others(8): Show |
13 | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0001g0039 others(10): Show |
13 | HG01099.hp1 HG01099.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.444-1912_444-1898d others(17): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304761 | |||||||
| chr10:59304761 | G | GAGGGAAG others(13): Show |
10 | a0001c0001t0001g0025 a0001c0001t0001g0152 a0001c0001t0001g0175 others(7): Show |
10 | HG00738.hp1 HG02630.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.444-1917_444-1898d others(22): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304761 | |||||||
| chr10:59304761 | G | GAGGGAAG others(18): Show |
22 | a0001c0001t0001g0047 a0001c0001t0001g0061 a0001c0001t0001g0070 others(19): Show |
22 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.444-1922_444-1898d others(27): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304761 | |||||||
| chr10:59304761 | G | GAGGGAAG others(23): Show |
19 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0042 others(16): Show |
19 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.444-1898_444-1897i others(32): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304761 | |||||||
| chr10:59304761 | G | GAGGGAAG others(23): Show |
18 | a0001c0001t0001g0001 a0001c0001t0001g0044 a0001c0001t0001g0054 others(15): Show |
19 | HG00558.hp2 HG01106.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.444-1927_444-1898d others(32): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304761 | |||||||
| chr10:59304761 | G | GAGGGAAG others(28): Show |
11 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0092 others(8): Show |
11 | HG00639.hp1 HG00673.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.444-1932_444-1898d others(37): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304761 | |||||||
| chr10:59304761 | G | GAGGGAAG others(33): Show |
4 | a0001c0001t0001g0051 a0003c0003t0001g0192 a0003c0003t0001g0193 others(1): Show |
4 | HG01243.hp1 HG02976.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.444-1937_444-1898d others(42): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304761 | |||||||
| chr10:59304761 | G | GAGGGAAG others(43): Show |
1 | a0001c0001t0001g0173 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.444-1947_444-1898d others(52): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304761 | |||||||
| chr10:59304761 | GAGGGA | G | 2 | a0001c0001t0001g0189 a0001c0001t0007g0185 |
2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.444-1902_444-1898d others(7): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304761 | |||||||
| chr10:59304786 | A | AAAGGAAG others(23): Show |
1 | a0001c0001t0001g0075 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.444-1923_444-1922i others(32): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304786 | |||||||
| chr10:59304798 | G | GGGAAGGG others(2): Show |
4 | a0001c0001t0001g0011 a0001c0001t0001g0072 a0001c0001t0001g0116 others(1): Show |
4 | HG00609.hp1 HG00673.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.444-1943_444-1935d others(11): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304798 | |||||||
| chr10:59304810 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.444-1946C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304810 | |||||||
| chr10:59304815 | A | G | 2 | a0001c0001t0001g0049 a0001c0001t0001g0139 |
2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.444-1951T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304815 | |||||||
| chr10:59304823 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.444-1959T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304823 | |||||||
| chr10:59304828 | A | C | 1 | a0001c0001t0001g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.444-1964T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304828 | |||||||
| chr10:59304834 | C | A | 2 | a0001c0001t0001g0139 a0001c0001t0001g0173 |
2 | HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.444-1970G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304834 | |||||||
| chr10:59304834 | C | CGGGGGA | 77 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
77 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.444-1976_444-1971d others(8): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304834 | |||||||
| chr10:59304847 | G | A | 4 | a0001c0001t0001g0165 a0001c0001t0001g0186 a0001c0001t0001g0197 others(1): Show |
4 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.444-1983C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304847 | |||||||
| chr10:59304852 | A | C | 1 | a0001c0001t0001g0043 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.444-1988T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304852 | |||||||
| chr10:59304857 | A | G | 1 | a0001c0001t0001g0043 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.444-1993T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304857 | |||||||
| chr10:59304862 | A | G | 1 | a0001c0001t0001g0043 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.444-1998T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304862 | |||||||
| chr10:59304863 | A | G | 1 | a0001c0001t0001g0043 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.444-1999T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304863 | |||||||
| chr10:59304869 | G | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(72): Show |
76 | HG00609.hp2 HG00639.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.444-2005C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304869 | |||||||
| chr10:59304895 | T | C | 30 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(27): Show |
31 | HG00639.hp1 HG01167.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.444-2031A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304895 | |||||||
| chr10:59304906 | G | T | 14 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(11): Show |
14 | HG00609.hp1 HG00673.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.444-2042C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59304906 | |||||||
| chr10:59305123 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.444-2259G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59305123 | |||||||
| chr10:59305202 | A | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.444-2338T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59305202 | |||||||
| chr10:59305226 | G | T | 20 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0042 others(17): Show |
20 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.444-2362C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59305226 | |||||||
| chr10:59305408 | G | A | 28 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(25): Show |
29 | HG00639.hp1 HG01167.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.444-2544C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59305408 | |||||||
| chr10:59305438 | T | C | 2 | a0001c0001t0001g0067 a0001c0001t0001g0112 |
2 | HG03704.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.444-2574A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59305438 | |||||||
| chr10:59305520 | A | G | 1 | a0001c0001t0002g0071 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.444-2656T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59305520 | |||||||
| chr10:59305628 | AT | A | 20 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0042 others(17): Show |
20 | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.444-2765delA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59305628 | |||||||
| chr10:59305682 | A | C | 6 | a0001c0001t0001g0091 a0001c0001t0001g0153 a0001c0001t0001g0187 others(3): Show |
6 | HG01891.hp1 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.444-2818T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59305682 | |||||||
| chr10:59306012 | A | G | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
200 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(197): Show |
intron_variant | MODIFIER | c.444-3148T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59306012 | |||||||
| chr10:59306175 | G | C | 3 | a0001c0001t0001g0147 a0001c0001t0002g0008 a0005c0009t0001g0142 |
3 | HG01261.hp2 HG03540.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.444-3311C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59306175 | |||||||
| chr10:59306255 | G | T | 95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(92): Show |
95 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.444-3391C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59306255 | |||||||
| chr10:59306437 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.444-3573C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59306437 | |||||||
| chr10:59306544 | A | C | 1 | a0001c0001t0001g0005 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.444-3680T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59306544 | |||||||
| chr10:59306554 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0099 others(1): Show |
4 | HG01071.hp2 HG02135.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.444-3690C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59306554 | |||||||
| chr10:59306559 | A | G | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.444-3695T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59306559 | |||||||
| chr10:59306573 | G | C | 1 | a0001c0001t0001g0042 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.444-3709C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59306573 | |||||||
| chr10:59306676 | G | C | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(86): Show |
89 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.444-3812C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59306676 | |||||||
| chr10:59306684 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.444-3820A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59306684 | |||||||
| chr10:59306903 | G | T | 95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(92): Show |
95 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.444-4039C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59306903 | |||||||
| chr10:59306974 | G | C | 66 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(63): Show |
66 | HG00558.hp2 HG00609.hp2 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.444-4110C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59306974 | |||||||
| chr10:59307105 | G | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(194): Show |
198 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(195): Show |
intron_variant | MODIFIER | c.444-4241C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59307105 | |||||||
| chr10:59307328 | C | A | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(112): Show |
115 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.444-4464G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59307328 | |||||||
| chr10:59307468 | T | C | 6 | a0001c0001t0001g0091 a0001c0001t0001g0153 a0001c0001t0001g0187 others(3): Show |
6 | HG01891.hp1 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.444-4604A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59307468 | |||||||
| chr10:59307483 | C | T | 4 | a0001c0001t0001g0165 a0001c0001t0001g0186 a0001c0001t0001g0197 others(1): Show |
4 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.444-4619G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59307483 | |||||||
| chr10:59307585 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.444-4721C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59307585 | |||||||
| chr10:59307641 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.444-4777A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59307641 | |||||||
| chr10:59307667 | G | A | 4 | a0001c0001t0001g0091 a0001c0001t0001g0153 a0001c0001t0001g0187 others(1): Show |
4 | HG01891.hp1 HG02723.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.444-4803C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59307667 | |||||||
| chr10:59307674 | T | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(194): Show |
198 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(195): Show |
intron_variant | MODIFIER | c.444-4810A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59307674 | |||||||
| chr10:59307793 | C | A | 1 | a0007c0010t0001g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.444-4929G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59307793 | |||||||
| chr10:59307820 | T | A | 1 | a0001c0001t0001g0042 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.444-4956A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59307820 | |||||||
| chr10:59308198 | G | A | 113 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(110): Show |
113 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.444-5334C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59308198 | |||||||
| chr10:59308198 | G | C | 4 | a0001c0001t0001g0191 a0001c0001t0003g0018 a0001c0001t0003g0171 others(1): Show |
4 | HG00639.hp2 HG02145.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.444-5334C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59308198 | |||||||
| chr10:59308344 | A | T | 5 | a0001c0001t0001g0165 a0001c0001t0001g0172 a0001c0001t0001g0186 others(2): Show |
5 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.444-5480T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59308344 | |||||||
| chr10:59308365 | A | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0044 a0001c0001t0001g0097 others(1): Show |
5 | NA18941.hp2 NA18947.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.444-5501T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59308365 | |||||||
| chr10:59308372 | C | T | 5 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0003g0018 others(2): Show |
5 | HG00639.hp2 HG02145.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.444-5508G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59308372 | |||||||
| chr10:59308566 | C | CCACCATC others(27): Show |
103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
104 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.444-5736_444-5703d others(36): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59308566 | |||||||
| chr10:59308606 | T | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0050 a0001c0001t0001g0106 |
3 | HG02004.hp2 NA18965.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.444-5742A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59308606 | |||||||
| chr10:59308762 | C | A | 22 | a0001c0001t0001g0025 a0001c0001t0001g0061 a0001c0001t0001g0152 others(19): Show |
22 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.444-5898G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59308762 | |||||||
| chr10:59308886 | G | A | 1 | a0002c0002t0006g0198 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.444-6022C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59308886 | |||||||
| chr10:59309063 | A | G | 5 | a0001c0001t0001g0165 a0001c0001t0001g0172 a0001c0001t0001g0186 others(2): Show |
5 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.444-6199T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59309063 | |||||||
| chr10:59309114 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.444-6250C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59309114 | |||||||
| chr10:59309123 | G | T | 11 | a0001c0001t0001g0165 a0001c0001t0001g0172 a0001c0001t0001g0174 others(8): Show |
11 | HG02486.hp2 HG02559.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.444-6259C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59309123 | |||||||
| chr10:59309137 | C | T | 15 | a0001c0001t0001g0085 a0001c0001t0001g0165 a0001c0001t0001g0172 others(12): Show |
15 | HG00639.hp2 HG02257.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.444-6273G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59309137 | |||||||
| chr10:59309343 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.444-6479G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59309343 | |||||||
| chr10:59309418 | T | C | 3 | a0001c0001t0001g0173 a0001c0001t0001g0183 a0001c0001t0001g0184 |
3 | HG02965.hp2 HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.444-6554A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59309418 | |||||||
| chr10:59309451 | C | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(107): Show |
111 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.444-6587G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59309451 | |||||||
| chr10:59309649 | T | C | 2 | a0001c0001t0001g0070 a0002c0002t0006g0198 |
2 | HG01123.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.444-6785A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59309649 | |||||||
| chr10:59309822 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.444-6958G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59309822 | |||||||
| chr10:59309846 | T | C | 1 | a0001c0004t0001g0048 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.444-6982A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59309846 | |||||||
| chr10:59309885 | A | T | 1 | a0001c0001t0001g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.444-7021T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59309885 | |||||||
| chr10:59309927 | TA | T | 4 | a0001c0001t0001g0174 a0002c0002t0001g0017 a0002c0002t0001g0035 others(1): Show |
4 | HG02559.hp1 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.444-7064delT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59309927 | |||||||
| chr10:59309950 | T | C | 3 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0007c0010t0001g0148 |
3 | HG00639.hp2 HG02257.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.444-7086A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59309950 | |||||||
| chr10:59310148 | G | A | 2 | a0001c0001t0001g0070 a0002c0002t0006g0198 |
2 | HG01123.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.444-7284C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59310148 | |||||||
| chr10:59310160 | C | G | 1 | a0001c0001t0002g0080 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.444-7296G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59310160 | |||||||
| chr10:59310317 | A | G | 4 | a0001c0001t0001g0174 a0002c0002t0001g0017 a0002c0002t0001g0035 others(1): Show |
4 | HG02559.hp1 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.444-7453T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59310317 | |||||||
| chr10:59310807 | T | G | 37 | a0001c0001t0001g0025 a0001c0001t0001g0061 a0001c0001t0001g0070 others(34): Show |
37 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.444-7943A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59310807 | |||||||
| chr10:59310840 | C | T | 4 | a0001c0001t0001g0092 a0001c0001t0001g0155 a0001c0001t0001g0158 others(1): Show |
4 | HG02970.hp1 HG03098.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.444-7976G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59310840 | |||||||
| chr10:59311067 | A | G | 37 | a0001c0001t0001g0025 a0001c0001t0001g0061 a0001c0001t0001g0070 others(34): Show |
37 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.444-8203T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59311067 | |||||||
| chr10:59311237 | C | A | 1 | a0001c0001t0001g0070 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.444-8373G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59311237 | |||||||
| chr10:59311928 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.444-9064G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59311928 | |||||||
| chr10:59311991 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0070 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.444-9127G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59311991 | |||||||
| chr10:59312139 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(104): Show |
108 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.444-9275G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59312139 | |||||||
| chr10:59312146 | T | G | 4 | a0001c0001t0001g0174 a0002c0002t0001g0017 a0002c0002t0001g0035 others(1): Show |
4 | HG02559.hp1 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.444-9282A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59312146 | |||||||
| chr10:59312173 | C | T | 7 | a0001c0001t0001g0009 a0001c0001t0001g0046 a0001c0001t0001g0049 others(4): Show |
7 | HG00639.hp2 HG02257.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.444-9309G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59312173 | |||||||
| chr10:59312297 | G | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0046 a0001c0001t0001g0049 others(1): Show |
4 | HG02897.hp2 HG03486.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.444-9433C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59312297 | |||||||
| chr10:59312326 | G | T | 1 | a0001c0001t0001g0091 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.444-9462C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59312326 | |||||||
| chr10:59312373 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.444-9509T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59312373 | |||||||
| chr10:59312422 | T | C | 1 | a0001c0001t0001g0092 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.444-9558A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59312422 | |||||||
| chr10:59312423 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.444-9559G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59312423 | |||||||
| chr10:59312489 | A | G | 4 | a0001c0001t0001g0178 a0001c0001t0001g0200 a0001c0001t0001g0202 others(1): Show |
4 | HG01167.hp1 HG02622.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.444-9625T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59312489 | |||||||
| chr10:59312596 | C | A | 34 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0061 others(31): Show |
34 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.444-9732G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59312596 | |||||||
| chr10:59312886 | A | C | 1 | a0001c0001t0002g0090 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.444-10022T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59312886 | |||||||
| chr10:59312929 | T | A | 35 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0061 others(32): Show |
35 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.444-10065A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59312929 | |||||||
| chr10:59312994 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.444-10130G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59312994 | |||||||
| chr10:59313108 | G | C | 33 | a0001c0001t0001g0025 a0001c0001t0001g0061 a0001c0001t0001g0152 others(30): Show |
33 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.444-10244C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59313108 | |||||||
| chr10:59313134 | G | A | 11 | a0001c0001t0001g0174 a0001c0001t0001g0178 a0001c0001t0001g0200 others(8): Show |
11 | HG01123.hp1 HG01167.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.444-10270C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59313134 | |||||||
| chr10:59313213 | T | C | 7 | a0001c0001t0001g0165 a0001c0001t0001g0186 a0001c0001t0001g0189 others(4): Show |
7 | HG00639.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.444-10349A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59313213 | |||||||
| chr10:59313281 | G | T | 4 | a0001c0001t0001g0165 a0001c0001t0001g0186 a0001c0001t0001g0197 others(1): Show |
4 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.444-10417C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59313281 | |||||||
| chr10:59313497 | G | A | 168 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(165): Show |
168 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(165): Show |
intron_variant | MODIFIER | c.443+10491C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59313497 | |||||||
| chr10:59313570 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.443+10418G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59313570 | |||||||
| chr10:59313573 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.443+10415C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59313573 | |||||||
| chr10:59313622 | G | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0075 |
2 | HG00609.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.443+10366C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59313622 | |||||||
| chr10:59313685 | T | C | 2 | a0001c0001t0001g0155 a0001c0001t0001g0159 |
2 | HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.443+10303A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59313685 | |||||||
| chr10:59313726 | G | T | 1 | a0001c0001t0001g0156 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.443+10262C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59313726 | |||||||
| chr10:59313841 | G | A | 4 | a0001c0001t0001g0165 a0001c0001t0001g0186 a0001c0001t0001g0197 others(1): Show |
4 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.443+10147C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59313841 | |||||||
| chr10:59313854 | A | G | 33 | a0001c0001t0001g0025 a0001c0001t0001g0061 a0001c0001t0001g0152 others(30): Show |
33 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.443+10134T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59313854 | |||||||
| chr10:59314217 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.443+9771T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59314217 | |||||||
| chr10:59314249 | G | A | 4 | a0001c0001t0001g0174 a0002c0002t0001g0017 a0002c0002t0001g0035 others(1): Show |
4 | HG02559.hp1 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.443+9739C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59314249 | |||||||
| chr10:59314260 | C | A | 1 | a0001c0001t0001g0150 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.443+9728G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59314260 | |||||||
| chr10:59314284 | A | G | 1 | a0001c0001t0001g0043 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.443+9704T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59314284 | |||||||
| chr10:59314296 | C | G | 33 | a0001c0001t0001g0025 a0001c0001t0001g0061 a0001c0001t0001g0152 others(30): Show |
33 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.443+9692G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59314296 | |||||||
| chr10:59314351 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.443+9637G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59314351 | |||||||
| chr10:59314887 | A | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0118 |
2 | HG02735.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.443+9101T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59314887 | |||||||
| chr10:59315203 | G | C | 3 | a0001c0001t0001g0084 a0001c0001t0001g0106 a0001c0001t0002g0082 |
3 | HG00597.hp2 NA18942.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.443+8785C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59315203 | |||||||
| chr10:59315419 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.443+8569T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59315419 | |||||||
| chr10:59315445 | G | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0196 |
2 | HG02257.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.443+8543C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59315445 | |||||||
| chr10:59315446 | G | T | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(193): Show |
197 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(194): Show |
intron_variant | MODIFIER | c.443+8542C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59315446 | |||||||
| chr10:59315453 | T | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(136): Show |
139 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.443+8535A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59315453 | |||||||
| chr10:59315483 | T | C | 5 | a0001c0001t0001g0092 a0003c0003t0001g0192 a0003c0003t0001g0193 others(2): Show |
5 | HG00639.hp1 HG01243.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.443+8505A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59315483 | |||||||
| chr10:59315499 | T | G | 1 | a0001c0001t0002g0065 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.443+8489A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59315499 | |||||||
| chr10:59315515 | G | T | 15 | a0001c0001t0001g0043 a0001c0001t0001g0152 a0001c0001t0001g0158 others(12): Show |
15 | HG00738.hp1 HG02257.hp1 HG02683.hp1 others(12): Show |
intron_variant | MODIFIER | c.443+8473C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59315515 | |||||||
| chr10:59315689 | C | T | 3 | a0001c0001t0001g0051 a0001c0001t0001g0169 a0001c0001t0001g0179 |
3 | HG01070.hp1 HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.443+8299G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59315689 | |||||||
| chr10:59315849 | T | G | 1 | a0001c0001t0001g0060 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.443+8139A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59315849 | |||||||
| chr10:59315898 | A | G | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.443+8090T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59315898 | |||||||
| chr10:59315913 | C | T | 3 | a0001c0001t0001g0054 a0001c0001t0001g0165 a0001c0001t0001g0196 |
3 | HG02257.hp2 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.443+8075G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59315913 | |||||||
| chr10:59315997 | T | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(34): Show |
38 | HG00323.hp2 HG00609.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.443+7991A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59315997 | |||||||
| chr10:59316040 | ATG | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(94): Show |
98 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.443+7946_443+7947d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59316040 | |||||||
| chr10:59316077 | G | A | 27 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0025 others(24): Show |
27 | HG00639.hp2 HG01123.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.443+7911C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59316077 | |||||||
| chr10:59316235 | G | T | 1 | a0001c0001t0002g0076 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.443+7753C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59316235 | |||||||
| chr10:59316415 | A | G | 9 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0093 others(6): Show |
9 | HG02486.hp2 HG02572.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.443+7573T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59316415 | |||||||
| chr10:59316513 | T | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0129 |
2 | NA18942.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.443+7475A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59316513 | |||||||
| chr10:59316599 | G | A | 23 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0025 others(20): Show |
23 | HG00639.hp2 HG01123.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.443+7389C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59316599 | |||||||
| chr10:59316712 | G | T | 1 | a0001c0001t0001g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.443+7276C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59316712 | |||||||
| chr10:59316718 | C | T | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(188): Show |
192 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(189): Show |
intron_variant | MODIFIER | c.443+7270G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59316718 | |||||||
| chr10:59316819 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.443+7169C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59316819 | |||||||
| chr10:59316864 | A | G | 3 | a0001c0001t0001g0054 a0001c0001t0001g0165 a0001c0001t0001g0196 |
3 | HG02257.hp2 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.443+7124T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59316864 | |||||||
| chr10:59316976 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.443+7012A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59316976 | |||||||
| chr10:59317126 | A | ATG | 19 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(16): Show |
19 | HG00735.hp1 HG01071.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.443+6860_443+6861d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59317126 | |||||||
| chr10:59317126 | A | ATGTG | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(71): Show |
75 | HG00323.hp2 HG00558.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.443+6858_443+6861d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59317126 | |||||||
| chr10:59317126 | A | ATGTGTG | 5 | a0001c0001t0001g0012 a0001c0001t0001g0084 a0001c0001t0001g0106 others(2): Show |
5 | HG00597.hp2 HG03225.hp2 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.443+6856_443+6861d others(8): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59317126 | |||||||
| chr10:59317126 | ATG | A | 73 | a0001c0001t0001g0009 a0001c0001t0001g0028 a0001c0001t0001g0030 others(70): Show |
73 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.443+6860_443+6861d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59317126 | |||||||
| chr10:59317126 | ATGTG | A | 5 | a0001c0001t0001g0025 a0001c0001t0001g0070 a0001c0001t0001g0139 others(2): Show |
5 | HG02280.hp1 HG02280.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.443+6858_443+6861d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59317126 | |||||||
| chr10:59317228 | C | T | 1 | a0001c0001t0002g0008 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.443+6760G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59317228 | |||||||
| chr10:59317558 | A | G | 23 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0025 others(20): Show |
23 | HG00639.hp2 HG01123.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.443+6430T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59317558 | |||||||
| chr10:59317589 | C | A | 1 | a0001c0004t0001g0026 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.443+6399G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59317589 | |||||||
| chr10:59317653 | C | T | 1 | a0001c0001t0002g0062 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.443+6335G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59317653 | |||||||
| chr10:59317781 | A | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(90): Show |
94 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.443+6207T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59317781 | |||||||
| chr10:59317837 | G | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(90): Show |
94 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.443+6151C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59317837 | |||||||
| chr10:59317861 | G | A | 23 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0025 others(20): Show |
23 | HG00639.hp2 HG01123.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.443+6127C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59317861 | |||||||
| chr10:59318005 | C | T | 5 | a0001c0001t0001g0178 a0001c0001t0001g0200 a0001c0001t0001g0201 others(2): Show |
5 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.443+5983G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59318005 | |||||||
| chr10:59318076 | G | A | 6 | a0002c0002t0001g0017 a0002c0002t0001g0035 a0002c0002t0001g0036 others(3): Show |
6 | HG01123.hp1 HG01243.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.443+5912C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59318076 | |||||||
| chr10:59318192 | T | TCTAAGTT others(327): Show |
3 | a0001c0001t0001g0178 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | HG01167.hp1 HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.443+5795_443+5796i others(336): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59318192 | |||||||
| chr10:59318192 | T | TCTAAGTT others(328): Show |
2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.443+5795_443+5796i others(337): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59318192 | |||||||
| chr10:59318193 | C | T | 6 | a0002c0002t0001g0017 a0002c0002t0001g0035 a0002c0002t0001g0036 others(3): Show |
6 | HG01123.hp1 HG01243.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.443+5795G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59318193 | |||||||
| chr10:59318273 | TA | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
134 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(131): Show |
intron_variant | MODIFIER | c.443+5714delT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59318273 | |||||||
| chr10:59318284 | C | T | 23 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0025 others(20): Show |
23 | HG00639.hp2 HG01123.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.443+5704G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59318284 | |||||||
| chr10:59318346 | C | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
134 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(131): Show |
intron_variant | MODIFIER | c.443+5642G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59318346 | |||||||
| chr10:59318349 | G | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(90): Show |
94 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.443+5639C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59318349 | |||||||
| chr10:59318685 | TGAA | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(90): Show |
94 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.443+5300_443+5302d others(5): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59318685 | |||||||
| chr10:59318850 | A | G | 12 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0025 others(9): Show |
12 | HG00639.hp2 HG02451.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.443+5138T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59318850 | |||||||
| chr10:59319072 | A | AAC | 22 | a0001c0001t0001g0011 a0001c0001t0001g0033 a0001c0001t0001g0040 others(19): Show |
22 | HG01099.hp1 HG01243.hp2 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.443+4914_443+4915d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319072 | |||||||
| chr10:59319072 | A | AACAC | 3 | a0001c0001t0001g0133 a0001c0001t0001g0190 a0001c0004t0001g0100 |
3 | HG01168.hp1 HG01891.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.443+4912_443+4915d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319072 | |||||||
| chr10:59319072 | A | AACACAC | 3 | a0001c0001t0002g0076 a0001c0004t0001g0048 a0002c0002t0006g0198 |
3 | HG01123.hp1 HG02630.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.443+4910_443+4915d others(8): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319072 | |||||||
| chr10:59319072 | AAC | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(41): Show |
45 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.443+4914_443+4915d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319072 | |||||||
| chr10:59319072 | AACAC | A | 14 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0030 others(11): Show |
14 | HG00323.hp2 HG00673.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.443+4912_443+4915d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319072 | |||||||
| chr10:59319072 | AACACAC | A | 9 | a0001c0001t0001g0052 a0001c0001t0001g0057 a0001c0001t0001g0096 others(6): Show |
9 | HG00558.hp1 HG01123.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.443+4910_443+4915d others(8): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319072 | |||||||
| chr10:59319072 | AACACACA others(1): Show |
A | 14 | a0001c0001t0001g0054 a0001c0001t0001g0070 a0001c0001t0001g0075 others(11): Show |
14 | HG00735.hp2 HG02257.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.443+4908_443+4915d others(10): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319072 | |||||||
| chr10:59319072 | AACACACA others(3): Show |
A | 25 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(22): Show |
25 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.443+4906_443+4915d others(12): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319072 | |||||||
| chr10:59319072 | AACACACA others(5): Show |
A | 2 | a0001c0001t0001g0154 a0001c0007t0001g0059 |
2 | HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.443+4904_443+4915d others(14): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319072 | |||||||
| chr10:59319072 | AACACACA others(9): Show |
A | 1 | a0001c0001t0001g0091 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.443+4900_443+4915d others(18): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319072 | |||||||
| chr10:59319103 | ACACACAC others(11): Show |
A | 5 | a0001c0001t0001g0178 a0001c0001t0001g0200 a0001c0001t0001g0201 others(2): Show |
5 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.443+4867_443+4884d others(20): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319103 | |||||||
| chr10:59319107 | ACACACAC others(7): Show |
A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0093 a0001c0001t0001g0094 others(1): Show |
4 | HG02572.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.443+4867_443+4880d others(16): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319107 | |||||||
| chr10:59319109 | ACACACAC others(5): Show |
A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0188 |
2 | HG02451.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.443+4867_443+4878d others(14): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319109 | |||||||
| chr10:59319113 | ACACACAT others(1): Show |
A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0197 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.443+4867_443+4874d others(10): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319113 | |||||||
| chr10:59319117 | ACATT | A | 2 | a0001c0001t0001g0191 a0001c0001t0001g0199 |
2 | HG00639.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.443+4867_443+4870d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319117 | |||||||
| chr10:59319120 | T | C | 7 | a0001c0001t0001g0186 a0002c0002t0001g0017 a0002c0002t0001g0035 others(4): Show |
7 | HG01123.hp1 HG01243.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.443+4868A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319120 | |||||||
| chr10:59319121 | T | A | 7 | a0001c0001t0001g0186 a0002c0002t0001g0017 a0002c0002t0001g0035 others(4): Show |
7 | HG01123.hp1 HG01243.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.443+4867A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319121 | |||||||
| chr10:59319171 | T | C | 1 | a0007c0010t0001g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.443+4817A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319171 | |||||||
| chr10:59319267 | C | T | 1 | a0001c0001t0001g0004 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.443+4721G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319267 | |||||||
| chr10:59319439 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.443+4549C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319439 | |||||||
| chr10:59319541 | C | T | 1 | a0001c0001t0002g0080 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.443+4447G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319541 | |||||||
| chr10:59319546 | A | G | 2 | a0001c0001t0001g0187 a0001c0001t0007g0185 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.443+4442T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319546 | |||||||
| chr10:59319595 | G | A | 23 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0025 others(20): Show |
23 | HG00639.hp2 HG01123.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.443+4393C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59319595 | |||||||
| chr10:59320000 | A | T | 1 | a0001c0001t0001g0191 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.443+3988T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59320000 | |||||||
| chr10:59320578 | C | T | 23 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0025 others(20): Show |
23 | HG00639.hp2 HG01123.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.443+3410G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59320578 | |||||||
| chr10:59320729 | T | C | 2 | a0001c0001t0001g0088 a0001c0001t0002g0090 |
2 | HG03927.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.443+3259A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59320729 | |||||||
| chr10:59320860 | G | T | 5 | a0001c0001t0001g0054 a0001c0001t0001g0091 a0001c0001t0001g0165 others(2): Show |
5 | HG02257.hp2 HG02922.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.443+3128C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59320860 | |||||||
| chr10:59320876 | T | C | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.443+3112A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59320876 | |||||||
| chr10:59321059 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.443+2929T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321059 | |||||||
| chr10:59321207 | AT | A | 5 | a0002c0002t0001g0017 a0002c0002t0001g0035 a0002c0002t0001g0036 others(2): Show |
5 | HG01243.hp2 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.443+2780delA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321207 | |||||||
| chr10:59321430 | AC | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0061 a0001c0001t0001g0098 others(3): Show |
6 | HG02109.hp2 HG02135.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.443+2557delG | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321430 | |||||||
| chr10:59321431 | C | CTT | 2 | a0001c0001t0001g0054 a0001c0001t0001g0172 |
2 | HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.443+2556_443+2557i others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321431 | |||||||
| chr10:59321431 | CCT | C | 28 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(25): Show |
29 | HG00323.hp2 HG00609.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.443+2555_443+2556d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321431 | |||||||
| chr10:59321431 | CCTT | C | 31 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0023 others(28): Show |
31 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.443+2554_443+2556d others(5): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321431 | |||||||
| chr10:59321431 | CCTTT | C | 16 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0049 others(13): Show |
16 | HG00639.hp1 HG01070.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.443+2553_443+2556d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321431 | |||||||
| chr10:59321431 | CCTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0091 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.443+2546_443+2556d others(13): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321431 | |||||||
| chr10:59321431 | CCTTTTTT others(6): Show |
C | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.443+2544_443+2556d others(15): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321431 | |||||||
| chr10:59321432 | C | CT | 28 | a0001c0001t0001g0028 a0001c0001t0001g0038 a0001c0001t0001g0039 others(25): Show |
28 | HG00558.hp1 HG00609.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.443+2555dupA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321432 | |||||||
| chr10:59321432 | C | T | 7 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0040 others(4): Show |
7 | HG01099.hp1 HG01099.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.443+2556G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321432 | |||||||
| chr10:59321432 | CTTTT | C | 5 | a0001c0001t0001g0178 a0001c0001t0001g0191 a0001c0001t0001g0200 others(2): Show |
5 | HG00639.hp2 HG01167.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.443+2552_443+2555d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321432 | |||||||
| chr10:59321432 | CTTTTT | C | 6 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0093 others(3): Show |
6 | HG02451.hp2 HG02572.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.443+2551_443+2555d others(7): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321432 | |||||||
| chr10:59321432 | CTTTTTTT | C | 8 | a0001c0001t0001g0153 a0001c0001t0001g0186 a0002c0002t0001g0017 others(5): Show |
8 | HG01123.hp1 HG01243.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.443+2549_443+2555d others(9): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321432 | |||||||
| chr10:59321441 | T | C | 4 | a0001c0001t0001g0143 a0001c0001t0001g0150 a0001c0001t0001g0151 others(1): Show |
4 | HG01106.hp1 HG01433.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.443+2547A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321441 | |||||||
| chr10:59321461 | G | A | 6 | a0002c0002t0001g0017 a0002c0002t0001g0035 a0002c0002t0001g0036 others(3): Show |
6 | HG01123.hp1 HG01243.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.443+2527C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321461 | |||||||
| chr10:59321664 | A | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(82): Show |
86 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.443+2324T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321664 | |||||||
| chr10:59321694 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.443+2294C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321694 | |||||||
| chr10:59321715 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.443+2273G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321715 | |||||||
| chr10:59321846 | A | G | 23 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0025 others(20): Show |
23 | HG00639.hp2 HG01123.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.443+2142T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321846 | |||||||
| chr10:59321853 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.443+2135G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321853 | |||||||
| chr10:59321953 | A | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(113): Show |
117 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.443+2035T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59321953 | |||||||
| chr10:59322014 | C | A | 1 | a0001c0001t0001g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.443+1974G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59322014 | |||||||
| chr10:59322059 | T | A | 15 | a0001c0001t0001g0070 a0001c0001t0001g0122 a0001c0001t0001g0154 others(12): Show |
15 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.443+1929A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59322059 | |||||||
| chr10:59322204 | AT | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(83): Show |
87 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.443+1783delA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59322204 | |||||||
| chr10:59322232 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.443+1756G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59322232 | |||||||
| chr10:59322303 | A | C | 23 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0025 others(20): Show |
23 | HG00639.hp2 HG01123.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.443+1685T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59322303 | |||||||
| chr10:59322308 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(90): Show |
94 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.443+1680G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59322308 | |||||||
| chr10:59322583 | C | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(91): Show |
95 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.443+1405G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59322583 | |||||||
| chr10:59322912 | C | A | 1 | a0001c0001t0007g0185 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.443+1076G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59322912 | |||||||
| chr10:59323022 | T | G | 11 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0093 others(8): Show |
11 | HG00639.hp2 HG02451.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.443+966A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59323022 | |||||||
| chr10:59323242 | C | A | 6 | a0002c0002t0001g0017 a0002c0002t0001g0035 a0002c0002t0001g0036 others(3): Show |
6 | HG01123.hp1 HG01243.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.443+746G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59323242 | |||||||
| chr10:59323457 | C | A | 5 | a0001c0001t0001g0178 a0001c0001t0001g0200 a0001c0001t0001g0201 others(2): Show |
5 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.443+531G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59323457 | |||||||
| chr10:59323522 | A | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.443+466T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59323522 | |||||||
| chr10:59323557 | G | A | 23 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0025 others(20): Show |
23 | HG00639.hp2 HG01123.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.443+431C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59323557 | |||||||
| chr10:59323619 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.443+369T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59323619 | |||||||
| chr10:59323722 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.443+266G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59323722 | |||||||
| chr10:59323906 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.443+82G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59323906 | |||||||
| chr10:59323930 | A | AGTTG | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(113): Show |
117 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.443+57_443+58insCA others(2): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | 59323930 | |||||||
| chr10:59324184 | C | G | 1 | a0001c0001t0001g0058 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.325-78G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59324184 | |||||||
| chr10:59324318 | C | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0188 |
2 | HG02451.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.325-212G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59324318 | |||||||
| chr10:59324408 | G | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(90): Show |
94 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.325-302C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59324408 | |||||||
| chr10:59324455 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.325-349T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59324455 | |||||||
| chr10:59324508 | T | TCA | 5 | a0001c0001t0001g0178 a0001c0001t0001g0200 a0001c0001t0001g0201 others(2): Show |
5 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.325-404_325-403dup others(2): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59324508 | |||||||
| chr10:59324526 | A | C | 1 | a0001c0001t0002g0124 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.325-420T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59324526 | |||||||
| chr10:59324538 | T | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(90): Show |
94 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.325-432A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59324538 | |||||||
| chr10:59324550 | A | C | 1 | a0001c0001t0001g0045 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.325-444T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59324550 | |||||||
| chr10:59324607 | T | G | 3 | a0001c0001t0001g0154 a0001c0004t0001g0100 a0001c0007t0001g0059 |
3 | HG01891.hp2 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.325-501A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59324607 | |||||||
| chr10:59324663 | A | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(113): Show |
117 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.325-557T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59324663 | |||||||
| chr10:59324902 | A | C | 5 | a0001c0001t0001g0178 a0001c0001t0001g0200 a0001c0001t0001g0201 others(2): Show |
5 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.325-796T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59324902 | |||||||
| chr10:59324906 | CAAAACT | C | 23 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0025 others(20): Show |
23 | HG00639.hp2 HG01123.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.325-806_325-801del others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59324906 | |||||||
| chr10:59324983 | G | A | 5 | a0001c0001t0001g0102 a0001c0001t0001g0133 a0001c0001t0001g0136 others(2): Show |
5 | HG01106.hp2 HG01168.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.325-877C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59324983 | |||||||
| chr10:59325064 | TAATAAAT others(15): Show |
T | 1 | a0001c0001t0001g0049 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.325-980_325-959del others(22): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59325064 | |||||||
| chr10:59325095 | G | A | 23 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0025 others(20): Show |
23 | HG00639.hp2 HG01123.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.325-989C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59325095 | |||||||
| chr10:59325125 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.325-1019A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59325125 | |||||||
| chr10:59325128 | T | A | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.325-1022A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59325128 | |||||||
| chr10:59325322 | C | T | 67 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0031 others(64): Show |
67 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.325-1216G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59325322 | |||||||
| chr10:59325371 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.325-1265C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59325371 | |||||||
| chr10:59325379 | G | A | 5 | a0001c0001t0001g0178 a0001c0001t0001g0200 a0001c0001t0001g0201 others(2): Show |
5 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.325-1273C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59325379 | |||||||
| chr10:59325474 | C | A | 5 | a0002c0002t0001g0017 a0002c0002t0001g0035 a0002c0002t0001g0036 others(2): Show |
5 | HG01243.hp2 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.325-1368G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59325474 | |||||||
| chr10:59325482 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.325-1376T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59325482 | |||||||
| chr10:59325503 | G | A | 23 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0025 others(20): Show |
23 | HG00639.hp2 HG01123.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.325-1397C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59325503 | |||||||
| chr10:59325522 | C | T | 1 | a0001c0004t0001g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.325-1416G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59325522 | |||||||
| chr10:59325569 | C | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(113): Show |
117 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.325-1463G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59325569 | |||||||
| chr10:59325645 | C | T | 5 | a0002c0002t0001g0017 a0002c0002t0001g0035 a0002c0002t0001g0036 others(2): Show |
5 | HG01243.hp2 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.325-1539G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59325645 | |||||||
| chr10:59325895 | A | G | 1 | a0001c0001t0001g0011 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.325-1789T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59325895 | |||||||
| chr10:59325944 | G | T | 10 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0093 others(7): Show |
10 | HG00639.hp2 HG02486.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.325-1838C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59325944 | |||||||
| chr10:59326450 | G | T | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
185 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(182): Show |
intron_variant | MODIFIER | c.325-2344C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59326450 | |||||||
| chr10:59326528 | C | T | 2 | a0001c0001t0001g0091 a0001c0001t0001g0196 |
2 | HG02257.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.325-2422G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59326528 | |||||||
| chr10:59326684 | G | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(114): Show |
118 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.325-2578C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59326684 | |||||||
| chr10:59326818 | T | G | 5 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0031 others(2): Show |
5 | HG02622.hp1 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.325-2712A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59326818 | |||||||
| chr10:59327349 | G | A | 1 | a0001c0001t0002g0074 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.325-3243C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59327349 | |||||||
| chr10:59327536 | G | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(118): Show |
122 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.325-3430C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59327536 | |||||||
| chr10:59327572 | CA | C | 31 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0092 others(28): Show |
31 | HG00639.hp1 HG00639.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.325-3467delT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59327572 | |||||||
| chr10:59327573 | A | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(87): Show |
91 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.325-3467T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59327573 | |||||||
| chr10:59327575 | C | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0175 a0001c0001t0001g0176 others(2): Show |
5 | HG02809.hp2 HG02886.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.325-3469G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59327575 | |||||||
| chr10:59327575 | C | CA | 58 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(55): Show |
59 | HG00323.hp2 HG00597.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.325-3470dupT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59327575 | |||||||
| chr10:59327575 | C | CCA | 11 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0055 others(8): Show |
11 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.325-3470_325-3469i others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59327575 | |||||||
| chr10:59327575 | C | CCCA | 7 | a0001c0001t0001g0023 a0001c0001t0001g0050 a0001c0001t0001g0077 others(4): Show |
7 | HG01071.hp1 HG02004.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.325-3470_325-3469i others(5): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59327575 | |||||||
| chr10:59327661 | C | T | 9 | a0001c0001t0001g0092 a0001c0001t0001g0153 a0001c0001t0001g0191 others(6): Show |
9 | HG00639.hp1 HG00639.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.325-3555G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59327661 | |||||||
| chr10:59327675 | G | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(132): Show |
136 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.325-3569C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59327675 | |||||||
| chr10:59327686 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.325-3580A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59327686 | |||||||
| chr10:59327714 | C | T | 4 | a0001c0001t0001g0143 a0001c0001t0001g0150 a0001c0001t0001g0151 others(1): Show |
4 | HG01106.hp1 HG01433.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.325-3608G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59327714 | |||||||
| chr10:59327937 | G | A | 1 | a0001c0001t0002g0066 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.325-3831C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59327937 | |||||||
| chr10:59327998 | C | T | 2 | a0001c0001t0001g0070 a0001c0001t0001g0122 |
2 | HG02280.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.325-3892G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59327998 | |||||||
| chr10:59328008 | A | G | 1 | a0007c0010t0001g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.325-3902T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59328008 | |||||||
| chr10:59328039 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.325-3933G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59328039 | |||||||
| chr10:59328152 | T | C | 9 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(6): Show |
9 | HG00735.hp1 HG01071.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.325-4046A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59328152 | |||||||
| chr10:59328154 | T | G | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(123): Show |
127 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(124): Show |
intron_variant | MODIFIER | c.325-4048A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59328154 | |||||||
| chr10:59328191 | T | A | 5 | a0001c0001t0001g0178 a0001c0001t0001g0200 a0001c0001t0001g0201 others(2): Show |
5 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.325-4085A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59328191 | |||||||
| chr10:59328487 | A | AAAAAC | 30 | a0001c0001t0001g0007 a0001c0001t0001g0092 a0001c0001t0001g0153 others(27): Show |
30 | HG00639.hp1 HG00639.hp2 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.325-4386_325-4382d others(7): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59328487 | |||||||
| chr10:59328487 | AAAAAC | A | 6 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0093 others(3): Show |
6 | HG02257.hp1 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.325-4386_325-4382d others(7): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59328487 | |||||||
| chr10:59328487 | AAAAACAA others(3): Show |
A | 1 | a0001c0001t0001g0005 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.325-4391_325-4382d others(12): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59328487 | |||||||
| chr10:59328502 | C | G | 1 | a0001c0001t0001g0150 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.325-4396G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59328502 | |||||||
| chr10:59328521 | A | T | 34 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0025 others(31): Show |
34 | HG00639.hp1 HG00639.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.325-4415T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59328521 | |||||||
| chr10:59328647 | A | C | 1 | a0001c0001t0001g0092 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.325-4541T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59328647 | |||||||
| chr10:59329165 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.325-5059T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329165 | |||||||
| chr10:59329232 | G | T | 1 | a0001c0001t0001g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.325-5126C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329232 | |||||||
| chr10:59329280 | A | G | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(78): Show |
82 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.325-5174T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329280 | |||||||
| chr10:59329342 | GTT | G | 28 | a0001c0001t0001g0028 a0001c0001t0001g0038 a0001c0001t0001g0069 others(25): Show |
28 | HG00323.hp1 HG00597.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.325-5238_325-5237d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329342 | |||||||
| chr10:59329342 | GTTT | G | 29 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(26): Show |
29 | HG00558.hp1 HG00609.hp1 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.325-5239_325-5237d others(5): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329342 | |||||||
| chr10:59329342 | GTTTTTTT others(2): Show |
G | 5 | a0001c0001t0001g0122 a0001c0001t0001g0164 a0001c0001t0001g0180 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.325-5245_325-5237d others(11): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329342 | |||||||
| chr10:59329342 | GTTTTTTT others(3): Show |
G | 9 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0070 others(6): Show |
9 | HG02280.hp1 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.325-5246_325-5237d others(12): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329342 | |||||||
| chr10:59329342 | GTTTTTTT others(4): Show |
G | 13 | a0001c0001t0001g0178 a0001c0001t0001g0200 a0001c0001t0001g0201 others(10): Show |
13 | HG01167.hp1 HG01243.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.325-5247_325-5237d others(13): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329342 | |||||||
| chr10:59329342 | GTTTTTTT others(5): Show |
G | 12 | a0001c0001t0001g0007 a0001c0001t0001g0092 a0001c0001t0001g0153 others(9): Show |
12 | HG00639.hp1 HG00639.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.325-5248_325-5237d others(14): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329342 | |||||||
| chr10:59329342 | GTTTTTTT others(6): Show |
G | 1 | a0002c0002t0006g0198 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.325-5249_325-5237d others(15): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329342 | |||||||
| chr10:59329342 | GTTTTTTT others(11): Show |
G | 1 | a0001c0001t0001g0075 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.325-5254_325-5237d others(20): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329342 | |||||||
| chr10:59329342 | GTTTTTTT others(12): Show |
G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(82): Show |
86 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.325-5255_325-5237d others(21): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329342 | |||||||
| chr10:59329342 | GTTTTTTT others(13): Show |
G | 6 | a0001c0001t0001g0024 a0001c0001t0001g0054 a0001c0001t0001g0091 others(3): Show |
6 | HG01070.hp2 HG02257.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.325-5256_325-5237d others(22): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329342 | |||||||
| chr10:59329448 | G | T | 34 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0025 others(31): Show |
34 | HG00639.hp1 HG00639.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.325-5342C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329448 | |||||||
| chr10:59329550 | A | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(89): Show |
93 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.325-5444T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329550 | |||||||
| chr10:59329582 | CTCCTGAC others(9): Show |
C | 5 | a0001c0001t0001g0178 a0001c0001t0001g0200 a0001c0001t0001g0201 others(2): Show |
5 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.325-5492_325-5477d others(18): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329582 | |||||||
| chr10:59329586 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.325-5480A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329586 | |||||||
| chr10:59329615 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.325-5509G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329615 | |||||||
| chr10:59329650 | G | A | 3 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0007g0185 |
3 | HG02647.hp1 HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.325-5544C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329650 | |||||||
| chr10:59329697 | T | C | 34 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0025 others(31): Show |
34 | HG00639.hp1 HG00639.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.325-5591A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329697 | |||||||
| chr10:59329707 | G | A | 26 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(23): Show |
26 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.325-5601C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329707 | |||||||
| chr10:59329745 | T | G | 1 | a0001c0001t0001g0137 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.325-5639A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59329745 | |||||||
| chr10:59330026 | G | A | 1 | a0001c0001t0001g0004 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.325-5920C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59330026 | |||||||
| chr10:59330101 | G | C | 1 | a0001c0001t0001g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.325-5995C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59330101 | |||||||
| chr10:59330243 | T | G | 1 | a0001c0001t0002g0014 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.325-6137A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59330243 | |||||||
| chr10:59330303 | T | C | 9 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(6): Show |
9 | HG00735.hp1 HG01071.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.325-6197A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59330303 | |||||||
| chr10:59330400 | G | A | 2 | a0001c0001t0001g0084 a0001c0001t0002g0082 |
2 | HG00597.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.325-6294C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59330400 | |||||||
| chr10:59330591 | A | T | 20 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0092 others(17): Show |
20 | HG00639.hp1 HG00639.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.325-6485T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59330591 | |||||||
| chr10:59330753 | G | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
126 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.325-6647C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59330753 | |||||||
| chr10:59330899 | C | T | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(184): Show |
188 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(185): Show |
intron_variant | MODIFIER | c.325-6793G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59330899 | |||||||
| chr10:59331108 | G | T | 1 | a0001c0001t0003g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.325-7002C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59331108 | |||||||
| chr10:59331116 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.325-7010A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59331116 | |||||||
| chr10:59331149 | G | C | 1 | a0001c0001t0001g0005 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.325-7043C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59331149 | |||||||
| chr10:59331232 | T | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
121 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.325-7126A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59331232 | |||||||
| chr10:59331243 | G | T | 1 | a0007c0010t0001g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.325-7137C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59331243 | |||||||
| chr10:59331321 | C | T | 11 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0153 others(8): Show |
11 | HG00639.hp1 HG00639.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.325-7215G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59331321 | |||||||
| chr10:59331403 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.325-7297G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59331403 | |||||||
| chr10:59331409 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.325-7303C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59331409 | |||||||
| chr10:59331542 | T | A | 1 | a0001c0001t0001g0047 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.325-7436A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59331542 | |||||||
| chr10:59331598 | C | T | 6 | a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0064 others(3): Show |
6 | HG03492.hp1 NA18965.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.325-7492G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59331598 | |||||||
| chr10:59331650 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.325-7544C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59331650 | |||||||
| chr10:59331752 | A | G | 9 | a0001c0001t0001g0092 a0001c0001t0001g0153 a0001c0001t0001g0191 others(6): Show |
9 | HG00639.hp1 HG00639.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.325-7646T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59331752 | |||||||
| chr10:59331847 | A | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(88): Show |
92 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.325-7741T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59331847 | |||||||
| chr10:59331869 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.325-7763A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59331869 | |||||||
| chr10:59332056 | G | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(119): Show |
123 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.325-7950C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59332056 | |||||||
| chr10:59332157 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.325-8051T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59332157 | |||||||
| chr10:59332240 | A | ATG | 6 | a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0064 others(3): Show |
6 | HG03492.hp1 NA18965.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.325-8136_325-8135d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59332240 | |||||||
| chr10:59332733 | C | T | 5 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0186 others(2): Show |
5 | HG02647.hp1 HG02723.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.325-8627G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59332733 | |||||||
| chr10:59333008 | T | TTTAC | 7 | a0001c0001t0001g0085 a0001c0001t0001g0183 a0001c0001t0001g0184 others(4): Show |
7 | HG02647.hp1 HG02723.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.325-8903_325-8902i others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59333008 | |||||||
| chr10:59333008 | T | TTTATTTA others(1): Show |
79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(76): Show |
80 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.325-8903_325-8902i others(10): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59333008 | |||||||
| chr10:59333008 | T | TTTATTTA others(5): Show |
3 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0174 |
3 | HG00735.hp1 HG02109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.325-8903_325-8902i others(14): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59333008 | |||||||
| chr10:59333008 | T | TTTATTTA others(9): Show |
2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG00735.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.325-8903_325-8902i others(18): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59333008 | |||||||
| chr10:59333025 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(88): Show |
92 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.325-8919C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59333025 | |||||||
| chr10:59333129 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0188 |
2 | HG02451.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.325-9023G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59333129 | |||||||
| chr10:59333131 | A | C | 3 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG02055.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.325-9025T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59333131 | |||||||
| chr10:59333252 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.325-9146G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59333252 | |||||||
| chr10:59333260 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.325-9154C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59333260 | |||||||
| chr10:59333463 | G | C | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.325-9357C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59333463 | |||||||
| chr10:59333578 | T | C | 6 | a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0064 others(3): Show |
6 | HG03492.hp1 NA18965.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.325-9472A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59333578 | |||||||
| chr10:59333716 | TTTTA | T | 28 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0153 others(25): Show |
28 | HG00639.hp1 HG00639.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.325-9614_325-9611d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59333716 | |||||||
| chr10:59333784 | T | C | 4 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(1): Show |
4 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.325-9678A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59333784 | |||||||
| chr10:59333893 | T | C | 4 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(1): Show |
4 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.325-9787A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59333893 | |||||||
| chr10:59334164 | C | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
121 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.325-10058G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59334164 | |||||||
| chr10:59334421 | G | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0061 a0001c0001t0001g0067 others(2): Show |
5 | HG03654.hp1 HG03927.hp2 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.325-10315C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59334421 | |||||||
| chr10:59334495 | C | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(88): Show |
92 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.325-10389G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59334495 | |||||||
| chr10:59334507 | C | A | 2 | a0001c0001t0001g0154 a0001c0007t0001g0059 |
2 | HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.325-10401G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59334507 | |||||||
| chr10:59334544 | G | T | 10 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0070 others(7): Show |
10 | HG01891.hp2 HG02280.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.325-10438C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59334544 | |||||||
| chr10:59334567 | A | G | 40 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(37): Show |
41 | HG00323.hp2 HG00609.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.325-10461T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59334567 | |||||||
| chr10:59334623 | C | T | 28 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0153 others(25): Show |
28 | HG00639.hp1 HG00639.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.325-10517G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59334623 | |||||||
| chr10:59334747 | C | T | 11 | a0001c0001t0001g0189 a0001c0001t0001g0200 a0001c0001t0001g0201 others(8): Show |
11 | HG01123.hp1 HG01167.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.325-10641G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59334747 | |||||||
| chr10:59335448 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0188 |
2 | HG02451.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.325-11342A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59335448 | |||||||
| chr10:59335596 | C | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0188 |
2 | HG02451.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.325-11490G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59335596 | |||||||
| chr10:59335699 | C | T | 6 | a0001c0001t0001g0143 a0002c0002t0001g0035 a0002c0002t0001g0036 others(3): Show |
6 | HG01123.hp1 HG01243.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.325-11593G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59335699 | |||||||
| chr10:59335829 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.325-11723G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59335829 | |||||||
| chr10:59335840 | A | T | 1 | a0007c0010t0001g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.325-11734T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59335840 | |||||||
| chr10:59335986 | G | C | 35 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(32): Show |
35 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.325-11880C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59335986 | |||||||
| chr10:59336492 | C | G | 3 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG02055.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.325-12386G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59336492 | |||||||
| chr10:59336625 | T | C | 1 | a0001c0001t0001g0190 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.325-12519A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59336625 | |||||||
| chr10:59336721 | G | C | 1 | a0001c0001t0001g0019 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.325-12615C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59336721 | |||||||
| chr10:59336869 | A | G | 5 | a0002c0002t0001g0035 a0002c0002t0001g0036 a0002c0002t0001g0037 others(2): Show |
5 | HG01123.hp1 HG01243.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.325-12763T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59336869 | |||||||
| chr10:59336933 | C | T | 5 | a0002c0002t0001g0035 a0002c0002t0001g0036 a0002c0002t0001g0037 others(2): Show |
5 | HG01123.hp1 HG01243.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.325-12827G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59336933 | |||||||
| chr10:59337075 | A | G | 5 | a0001c0001t0001g0178 a0001c0001t0001g0200 a0001c0001t0001g0201 others(2): Show |
5 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.325-12969T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337075 | |||||||
| chr10:59337165 | G | T | 1 | a0001c0001t0001g0007 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.325-13059C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337165 | |||||||
| chr10:59337540 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.325-13434A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337540 | |||||||
| chr10:59337655 | T | C | 46 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(43): Show |
46 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.325-13549A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337655 | |||||||
| chr10:59337667 | CT | C | 6 | a0001c0001t0001g0172 a0001c0001t0001g0178 a0001c0001t0001g0200 others(3): Show |
6 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.325-13562delA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337667 | |||||||
| chr10:59337667 | CTT | C | 18 | a0001c0001t0001g0022 a0001c0001t0001g0053 a0001c0001t0001g0057 others(15): Show |
18 | HG00558.hp1 HG00673.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.325-13563_325-1356 others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337667 | |||||||
| chr10:59337667 | CTTT | C | 102 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0023 others(99): Show |
102 | HG00323.hp1 HG00558.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.325-13564_325-1356 others(7): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337667 | |||||||
| chr10:59337667 | CTTTT | C | 9 | a0001c0001t0001g0024 a0001c0001t0001g0084 a0001c0001t0001g0113 others(6): Show |
9 | HG01070.hp2 HG01123.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.325-13565_325-1356 others(8): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337667 | |||||||
| chr10:59337667 | CTTTTT | C | 5 | a0001c0001t0001g0182 a0002c0002t0001g0035 a0002c0002t0001g0036 others(2): Show |
5 | HG01243.hp2 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.325-13566_325-1356 others(9): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337667 | |||||||
| chr10:59337667 | CTTTTTTT others(3): Show |
C | 1 | a0007c0010t0001g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.325-13571_325-1356 others(14): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337667 | |||||||
| chr10:59337667 | CTTTTTTT others(4): Show |
C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(53): Show |
57 | HG00323.hp2 HG00609.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.325-13572_325-1356 others(15): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337667 | |||||||
| chr10:59337667 | CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0001g0169 a0001c0001t0003g0171 |
2 | HG01070.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.325-13573_325-1356 others(16): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337667 | |||||||
| chr10:59337667 | CTTTTTTT others(14): Show |
C | 1 | a0001c0001t0002g0135 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.325-13582_325-1356 others(25): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337667 | |||||||
| chr10:59337681 | T | C | 5 | a0001c0001t0001g0178 a0001c0001t0001g0200 a0001c0001t0001g0201 others(2): Show |
5 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.325-13575A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337681 | |||||||
| chr10:59337773 | G | A | 46 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(43): Show |
46 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.325-13667C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337773 | |||||||
| chr10:59337805 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.325-13699C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337805 | |||||||
| chr10:59337959 | C | T | 3 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG02055.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.325-13853G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337959 | |||||||
| chr10:59337978 | C | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(51): Show |
55 | HG00323.hp2 HG00609.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.325-13872G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59337978 | |||||||
| chr10:59338001 | C | T | 46 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(43): Show |
46 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.325-13895G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59338001 | |||||||
| chr10:59338100 | T | C | 124 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(121): Show |
124 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.325-13994A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59338100 | |||||||
| chr10:59338108 | G | T | 74 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0028 others(71): Show |
74 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.325-14002C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59338108 | |||||||
| chr10:59338190 | T | C | 125 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(122): Show |
125 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.324+14080A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59338190 | |||||||
| chr10:59338460 | G | T | 7 | a0001c0001t0001g0191 a0001c0001t0001g0197 a0001c0001t0001g0199 others(4): Show |
7 | HG00639.hp1 HG00639.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.324+13810C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59338460 | |||||||
| chr10:59338532 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.324+13738C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59338532 | |||||||
| chr10:59338639 | T | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0188 |
2 | HG02451.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.324+13631A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59338639 | |||||||
| chr10:59338687 | C | A | 53 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(50): Show |
54 | HG00323.hp2 HG00609.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.324+13583G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59338687 | |||||||
| chr10:59338832 | G | A | 1 | a0001c0001t0003g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.324+13438C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59338832 | |||||||
| chr10:59338840 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.324+13430G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59338840 | |||||||
| chr10:59338916 | C | T | 46 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(43): Show |
46 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.324+13354G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59338916 | |||||||
| chr10:59338933 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.324+13337A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59338933 | |||||||
| chr10:59339165 | G | A | 11 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(8): Show |
11 | HG00639.hp1 HG00639.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.324+13105C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59339165 | |||||||
| chr10:59339409 | G | GA | 125 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(122): Show |
125 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.324+12860dupT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59339409 | |||||||
| chr10:59339795 | A | G | 75 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0028 others(72): Show |
75 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.324+12475T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59339795 | |||||||
| chr10:59339819 | A | C | 1 | a0001c0001t0001g0173 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.324+12451T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59339819 | |||||||
| chr10:59339970 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.324+12300T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59339970 | |||||||
| chr10:59340046 | C | T | 1 | a0007c0010t0001g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.324+12224G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59340046 | |||||||
| chr10:59340216 | TA | T | 46 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(43): Show |
46 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.324+12053delT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59340216 | |||||||
| chr10:59340220 | A | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.324+12050T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59340220 | |||||||
| chr10:59340233 | T | A | 3 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG02055.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.324+12037A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59340233 | |||||||
| chr10:59340283 | T | C | 1 | a0002c0002t0006g0198 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.324+11987A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59340283 | |||||||
| chr10:59340294 | G | C | 2 | a0001c0001t0001g0025 a0001c0001t0003g0034 |
2 | HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.324+11976C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59340294 | |||||||
| chr10:59340377 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
2 | NA18956.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.324+11893C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59340377 | |||||||
| chr10:59340519 | C | T | 124 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(121): Show |
124 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.324+11751G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59340519 | |||||||
| chr10:59340724 | A | T | 1 | a0001c0001t0001g0070 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.324+11546T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59340724 | |||||||
| chr10:59340740 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.324+11530T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59340740 | |||||||
| chr10:59340922 | T | C | 3 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0007g0185 |
3 | HG02647.hp1 HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.324+11348A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59340922 | |||||||
| chr10:59341112 | C | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(51): Show |
55 | HG00323.hp2 HG00609.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.324+11158G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59341112 | |||||||
| chr10:59341180 | G | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG00735.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.324+11090C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59341180 | |||||||
| chr10:59341322 | C | T | 74 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0028 others(71): Show |
74 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.324+10948G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59341322 | |||||||
| chr10:59341465 | G | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
199 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(196): Show |
intron_variant | MODIFIER | c.324+10805C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59341465 | |||||||
| chr10:59341515 | C | T | 49 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(46): Show |
49 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.324+10755G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59341515 | |||||||
| chr10:59341521 | C | G | 125 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(122): Show |
125 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.324+10749G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59341521 | |||||||
| chr10:59341546 | G | A | 3 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG02055.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.324+10724C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59341546 | |||||||
| chr10:59341590 | G | C | 1 | a0001c0001t0001g0053 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.324+10680C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59341590 | |||||||
| chr10:59341604 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.324+10666C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59341604 | |||||||
| chr10:59341630 | G | A | 75 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0028 others(72): Show |
75 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.324+10640C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59341630 | |||||||
| chr10:59341664 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.324+10606G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59341664 | |||||||
| chr10:59341685 | T | C | 124 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(121): Show |
124 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.324+10585A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59341685 | |||||||
| chr10:59341864 | C | A | 49 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(46): Show |
49 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.324+10406G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59341864 | |||||||
| chr10:59342086 | A | T | 3 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG02055.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.324+10184T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59342086 | |||||||
| chr10:59342192 | A | C | 29 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(26): Show |
29 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.324+10078T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59342192 | |||||||
| chr10:59342276 | A | G | 125 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(122): Show |
125 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.324+9994T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59342276 | |||||||
| chr10:59342332 | C | T | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
199 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(196): Show |
intron_variant | MODIFIER | c.324+9938G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59342332 | |||||||
| chr10:59342360 | TA | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
196 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(193): Show |
intron_variant | MODIFIER | c.324+9909delT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59342360 | |||||||
| chr10:59342574 | C | T | 46 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(43): Show |
46 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.324+9696G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59342574 | |||||||
| chr10:59342698 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.324+9572C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59342698 | |||||||
| chr10:59342729 | C | T | 145 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0021 others(142): Show |
145 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(142): Show |
intron_variant | MODIFIER | c.324+9541G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59342729 | |||||||
| chr10:59342889 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.324+9381A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59342889 | |||||||
| chr10:59343021 | C | T | 145 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0021 others(142): Show |
145 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(142): Show |
intron_variant | MODIFIER | c.324+9249G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59343021 | |||||||
| chr10:59343340 | T | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(50): Show |
54 | HG00323.hp2 HG00609.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.324+8930A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59343340 | |||||||
| chr10:59343421 | TA | T | 75 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0028 others(72): Show |
75 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.324+8848delT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59343421 | |||||||
| chr10:59343547 | A | C | 3 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0007g0185 |
3 | HG02647.hp1 HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.324+8723T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59343547 | |||||||
| chr10:59343567 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.324+8703C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59343567 | |||||||
| chr10:59343862 | C | T | 73 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0028 others(70): Show |
73 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.324+8408G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59343862 | |||||||
| chr10:59343872 | A | G | 14 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0031 others(11): Show |
14 | HG02145.hp2 HG02622.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.324+8398T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59343872 | |||||||
| chr10:59343875 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.324+8395A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59343875 | |||||||
| chr10:59343910 | C | A | 2 | a0001c0001t0003g0018 a0002c0002t0001g0017 |
2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.324+8360G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59343910 | |||||||
| chr10:59343949 | C | CT | 50 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(47): Show |
50 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.324+8320dupA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59343949 | |||||||
| chr10:59343964 | T | C | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG01099.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.324+8306A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59343964 | |||||||
| chr10:59343968 | C | CT | 6 | a0001c0001t0001g0172 a0001c0001t0001g0178 a0001c0001t0001g0200 others(3): Show |
6 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.324+8301dupA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59343968 | |||||||
| chr10:59343968 | CT | C | 49 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(46): Show |
49 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.324+8301delA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59343968 | |||||||
| chr10:59343993 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.324+8277C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59343993 | |||||||
| chr10:59344001 | G | A | 49 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(46): Show |
49 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.324+8269C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344001 | |||||||
| chr10:59344086 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.324+8184G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344086 | |||||||
| chr10:59344158 | T | G | 1 | a0001c0001t0002g0170 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.324+8112A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344158 | |||||||
| chr10:59344200 | G | A | 73 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0028 others(70): Show |
73 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.324+8070C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344200 | |||||||
| chr10:59344211 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.324+8059G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344211 | |||||||
| chr10:59344234 | T | C | 1 | a0001c0001t0001g0145 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.324+8036A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344234 | |||||||
| chr10:59344284 | CT | C | 41 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(38): Show |
41 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.324+7985delA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344284 | |||||||
| chr10:59344287 | T | C | 1 | a0007c0010t0001g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.324+7983A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344287 | |||||||
| chr10:59344340 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.324+7930C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344340 | |||||||
| chr10:59344427 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.324+7843G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344427 | |||||||
| chr10:59344445 | A | AT | 111 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(108): Show |
111 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.324+7824dupA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344445 | |||||||
| chr10:59344445 | A | ATT | 13 | a0001c0001t0001g0087 a0001c0001t0001g0180 a0001c0001t0001g0181 others(10): Show |
13 | HG00639.hp1 HG00639.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.324+7823_324+7824d others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344445 | |||||||
| chr10:59344528 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.324+7742G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344528 | |||||||
| chr10:59344556 | A | G | 73 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0028 others(70): Show |
73 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.324+7714T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344556 | |||||||
| chr10:59344565 | A | G | 49 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(46): Show |
49 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.324+7705T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344565 | |||||||
| chr10:59344597 | A | T | 49 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(46): Show |
49 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.324+7673T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344597 | |||||||
| chr10:59344780 | G | T | 1 | a0003c0003t0001g0192 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.324+7490C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344780 | |||||||
| chr10:59344822 | A | T | 1 | a0001c0001t0001g0049 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.324+7448T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344822 | |||||||
| chr10:59344835 | T | C | 1 | a0001c0001t0001g0005 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.324+7435A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344835 | |||||||
| chr10:59344862 | C | T | 144 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0021 others(141): Show |
144 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(141): Show |
intron_variant | MODIFIER | c.324+7408G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344862 | |||||||
| chr10:59344876 | G | A | 1 | a0007c0010t0001g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.324+7394C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344876 | |||||||
| chr10:59344944 | C | G | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0190 |
3 | HG00597.hp1 HG00609.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.324+7326G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59344944 | |||||||
| chr10:59345032 | C | T | 4 | a0002c0002t0001g0035 a0002c0002t0001g0036 a0002c0002t0001g0037 others(1): Show |
4 | HG01243.hp2 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+7238G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59345032 | |||||||
| chr10:59345033 | G | A | 5 | a0001c0001t0001g0172 a0001c0001t0001g0200 a0001c0001t0001g0201 others(2): Show |
5 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.324+7237C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59345033 | |||||||
| chr10:59345188 | CA | C | 4 | a0002c0002t0001g0035 a0002c0002t0001g0036 a0002c0002t0001g0037 others(1): Show |
4 | HG01243.hp2 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+7081delT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59345188 | |||||||
| chr10:59345190 | T | C | 29 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(26): Show |
29 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.324+7080A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59345190 | |||||||
| chr10:59345303 | T | C | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.324+6967A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59345303 | |||||||
| chr10:59345346 | A | T | 49 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(46): Show |
49 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.324+6924T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59345346 | |||||||
| chr10:59345552 | T | C | 7 | a0001c0001t0001g0191 a0001c0001t0001g0197 a0001c0001t0001g0199 others(4): Show |
7 | HG00639.hp1 HG00639.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.324+6718A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59345552 | |||||||
| chr10:59345715 | A | C | 75 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0028 others(72): Show |
75 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.324+6555T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59345715 | |||||||
| chr10:59345883 | C | G | 1 | a0001c0001t0001g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.324+6387G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59345883 | |||||||
| chr10:59346083 | G | C | 1 | a0001c0001t0001g0025 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.324+6187C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59346083 | |||||||
| chr10:59346137 | T | C | 1 | a0001c0001t0001g0033 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.324+6133A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59346137 | |||||||
| chr10:59346207 | T | TAGAAA | 124 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(121): Show |
124 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.324+6058_324+6062d others(7): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59346207 | |||||||
| chr10:59346222 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.324+6048T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59346222 | |||||||
| chr10:59346228 | T | C | 49 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(46): Show |
49 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.324+6042A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59346228 | |||||||
| chr10:59346237 | T | C | 75 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0028 others(72): Show |
75 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.324+6033A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59346237 | |||||||
| chr10:59346340 | T | C | 10 | a0001c0001t0001g0021 a0001c0001t0001g0061 a0001c0001t0001g0067 others(7): Show |
10 | HG03492.hp1 HG03927.hp2 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.324+5930A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59346340 | |||||||
| chr10:59346627 | G | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(51): Show |
55 | HG00323.hp2 HG00609.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.324+5643C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59346627 | |||||||
| chr10:59346657 | T | C | 4 | a0001c0001t0001g0054 a0001c0001t0001g0165 a0001c0001t0001g0183 others(1): Show |
4 | HG02922.hp1 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+5613A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59346657 | |||||||
| chr10:59346934 | C | G | 124 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0022 others(121): Show |
124 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.324+5336G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59346934 | |||||||
| chr10:59347044 | G | A | 74 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0028 others(71): Show |
74 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.324+5226C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59347044 | |||||||
| chr10:59347125 | A | T | 65 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0031 others(62): Show |
65 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.324+5145T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59347125 | |||||||
| chr10:59347434 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.324+4836C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59347434 | |||||||
| chr10:59347462 | C | G | 1 | a0001c0001t0001g0105 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.324+4808G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59347462 | |||||||
| chr10:59347518 | A | AT | 6 | a0001c0001t0001g0085 a0002c0002t0001g0035 a0002c0002t0001g0036 others(3): Show |
6 | HG01123.hp1 HG01243.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.324+4751dupA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59347518 | |||||||
| chr10:59347518 | AT | A | 8 | a0001c0001t0001g0019 a0001c0001t0001g0191 a0001c0001t0001g0197 others(5): Show |
8 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(5): Show |
intron_variant | MODIFIER | c.324+4751delA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59347518 | |||||||
| chr10:59347520 | T | C | 78 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0025 others(75): Show |
78 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.324+4750A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59347520 | |||||||
| chr10:59347618 | G | C | 1 | a0001c0004t0001g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.324+4652C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59347618 | |||||||
| chr10:59347644 | A | G | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG01099.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.324+4626T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59347644 | |||||||
| chr10:59347690 | G | C | 4 | a0001c0001t0001g0054 a0001c0001t0001g0165 a0001c0001t0001g0183 others(1): Show |
4 | HG02922.hp1 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+4580C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59347690 | |||||||
| chr10:59347884 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.324+4386G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59347884 | |||||||
| chr10:59348203 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.324+4067C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59348203 | |||||||
| chr10:59348406 | C | G | 1 | a0001c0001t0001g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.324+3864G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59348406 | |||||||
| chr10:59348644 | T | G | 1 | a0001c0001t0001g0009 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.324+3626A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59348644 | |||||||
| chr10:59348784 | C | T | 49 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(46): Show |
49 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.324+3486G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59348784 | |||||||
| chr10:59348785 | A | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0188 |
2 | HG02451.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.324+3485T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59348785 | |||||||
| chr10:59348914 | G | A | 5 | a0001c0001t0001g0141 a0001c0001t0001g0153 a0001c0001t0001g0154 others(2): Show |
5 | HG01891.hp2 HG02723.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.324+3356C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59348914 | |||||||
| chr10:59349212 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.324+3058T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59349212 | |||||||
| chr10:59349228 | T | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
199 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(196): Show |
intron_variant | MODIFIER | c.324+3042A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59349228 | |||||||
| chr10:59349325 | T | C | 3 | a0001c0001t0001g0155 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02970.hp1 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.324+2945A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59349325 | |||||||
| chr10:59349357 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.324+2913C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59349357 | |||||||
| chr10:59349602 | C | CAAA | 48 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(45): Show |
48 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.324+2665_324+2667d others(5): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59349602 | |||||||
| chr10:59349646 | T | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
179 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(176): Show |
intron_variant | MODIFIER | c.324+2624A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59349646 | |||||||
| chr10:59349676 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.324+2594A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59349676 | |||||||
| chr10:59349803 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.324+2467C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59349803 | |||||||
| chr10:59349970 | T | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(126): Show |
130 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.324+2300A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59349970 | |||||||
| chr10:59349994 | T | C | 1 | a0001c0001t0002g0008 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.324+2276A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59349994 | |||||||
| chr10:59350010 | A | C | 74 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0028 others(71): Show |
74 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.324+2260T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59350010 | |||||||
| chr10:59350066 | T | A | 1 | a0001c0001t0001g0102 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.324+2204A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59350066 | |||||||
| chr10:59350075 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.324+2195A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59350075 | |||||||
| chr10:59350316 | G | A | 1 | a0004c0005t0001g0149 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.324+1954C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59350316 | |||||||
| chr10:59350618 | T | C | 3 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0007g0185 |
3 | HG02647.hp1 HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.324+1652A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59350618 | |||||||
| chr10:59350845 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.324+1425T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59350845 | |||||||
| chr10:59350877 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.324+1393A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59350877 | |||||||
| chr10:59351013 | G | A | 1 | a0001c0001t0003g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.324+1257C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59351013 | |||||||
| chr10:59351195 | G | C | 1 | a0001c0001t0001g0169 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.324+1075C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59351195 | |||||||
| chr10:59351331 | C | CA | 59 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(56): Show |
60 | HG00323.hp2 HG00609.hp2 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.324+938dupT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59351331 | |||||||
| chr10:59351331 | C | CAA | 72 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0028 others(69): Show |
72 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.324+937_324+938dup others(2): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59351331 | |||||||
| chr10:59351331 | C | CAAAA | 7 | a0001c0001t0001g0191 a0001c0001t0001g0197 a0001c0001t0001g0199 others(4): Show |
7 | HG00639.hp1 HG00639.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.324+935_324+938dup others(4): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59351331 | |||||||
| chr10:59351331 | C | CAAAAA | 28 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(25): Show |
28 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.324+934_324+938dup others(5): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59351331 | |||||||
| chr10:59351331 | C | CAAAAAA | 10 | a0001c0001t0001g0056 a0001c0001t0001g0085 a0001c0001t0001g0086 others(7): Show |
10 | HG01243.hp2 HG01261.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.324+933_324+938dup others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59351331 | |||||||
| chr10:59351542 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0165 |
2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.324+728C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59351542 | |||||||
| chr10:59351588 | C | T | 46 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(43): Show |
46 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.324+682G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59351588 | |||||||
| chr10:59351797 | C | G | 1 | a0001c0001t0001g0111 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.324+473G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59351797 | |||||||
| chr10:59351986 | A | G | 59 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(56): Show |
60 | HG00323.hp2 HG00609.hp2 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.324+284T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59351986 | |||||||
| chr10:59352215 | G | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
146 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.324+55C>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | 59352215 | |||||||
| chr10:59352534 | A | G | 1 | a0001c0001t0001g0025 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.120-60T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59352534 | |||||||
| chr10:59352761 | A | G | 3 | a0001c0001t0001g0141 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG02723.hp1 HG02897.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.120-287T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59352761 | |||||||
| chr10:59352818 | A | G | 1 | a0001c0001t0003g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.120-344T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59352818 | |||||||
| chr10:59352893 | C | T | 28 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(25): Show |
28 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.120-419G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59352893 | |||||||
| chr10:59353038 | T | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
172 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(169): Show |
intron_variant | MODIFIER | c.120-564A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59353038 | |||||||
| chr10:59353106 | A | G | 1 | a0001c0001t0001g0173 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.120-632T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59353106 | |||||||
| chr10:59353363 | C | A | 28 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(25): Show |
29 | HG00323.hp2 HG00609.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.120-889G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59353363 | |||||||
| chr10:59353504 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.120-1030A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59353504 | |||||||
| chr10:59353519 | A | C | 29 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(26): Show |
29 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.120-1045T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59353519 | |||||||
| chr10:59353610 | A | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
179 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(176): Show |
intron_variant | MODIFIER | c.120-1136T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59353610 | |||||||
| chr10:59353681 | T | C | 4 | a0001c0001t0001g0054 a0001c0001t0001g0165 a0001c0001t0001g0183 others(1): Show |
4 | HG02922.hp1 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.120-1207A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59353681 | |||||||
| chr10:59353765 | A | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
184 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(181): Show |
intron_variant | MODIFIER | c.120-1291T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59353765 | |||||||
| chr10:59354067 | C | CTTTA | 13 | a0001c0001t0001g0021 a0001c0001t0001g0052 a0001c0001t0001g0053 others(10): Show |
13 | HG01884.hp2 HG03492.hp1 HG03492.hp2 others(10): Show |
intron_variant | MODIFIER | c.120-1597_120-1594d others(6): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59354067 | |||||||
| chr10:59354067 | C | T | 1 | a0001c0001t0002g0071 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.120-1593G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59354067 | |||||||
| chr10:59354075 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.120-1601A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59354075 | |||||||
| chr10:59354155 | CT | C | 5 | a0001c0001t0001g0178 a0001c0001t0001g0200 a0001c0001t0001g0201 others(2): Show |
5 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.120-1682delA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59354155 | |||||||
| chr10:59354213 | A | G | 7 | a0001c0001t0001g0166 a0001c0001t0001g0180 a0001c0001t0001g0181 others(4): Show |
7 | HG02055.hp2 HG02258.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.119+1674T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59354213 | |||||||
| chr10:59354220 | T | C | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.119+1667A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59354220 | |||||||
| chr10:59354233 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(85): Show |
89 | HG00323.hp2 HG00609.hp2 HG00673.hp2 others(86): Show |
intron_variant | MODIFIER | c.119+1654C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59354233 | |||||||
| chr10:59354474 | G | A | 1 | a0001c0004t0001g0048 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.119+1413C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59354474 | |||||||
| chr10:59354498 | C | G | 1 | a0001c0001t0001g0070 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.119+1389G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59354498 | |||||||
| chr10:59354745 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.119+1142A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59354745 | |||||||
| chr10:59354844 | T | C | 3 | a0001c0001t0001g0197 a0001c0001t0001g0199 a0002c0002t0006g0198 |
3 | HG01123.hp1 HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.119+1043A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59354844 | |||||||
| chr10:59354870 | T | C | 1 | a0001c0001t0002g0068 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.119+1017A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59354870 | |||||||
| chr10:59354995 | C | CAAT | 18 | a0001c0001t0001g0167 a0001c0001t0001g0169 a0001c0001t0001g0186 others(15): Show |
18 | HG00639.hp1 HG00639.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.119+889_119+891dup others(3): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59354995 | |||||||
| chr10:59355013 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.119+874A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59355013 | |||||||
| chr10:59355354 | C | T | 18 | a0001c0001t0001g0051 a0001c0001t0001g0163 a0001c0001t0001g0169 others(15): Show |
18 | HG01070.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.119+533G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59355354 | |||||||
| chr10:59355413 | A | G | 32 | a0001c0001t0001g0051 a0001c0001t0001g0070 a0001c0001t0001g0163 others(29): Show |
32 | HG00639.hp1 HG00639.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.119+474T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59355413 | |||||||
| chr10:59355463 | A | G | 1 | a0001c0001t0001g0054 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.119+424T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59355463 | |||||||
| chr10:59355532 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.119+355G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59355532 | |||||||
| chr10:59355566 | A | G | 14 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(11): Show |
14 | HG00323.hp2 HG00609.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.119+321T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59355566 | |||||||
| chr10:59355657 | C | A | 1 | a0006c0008t0001g0160 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.119+230G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59355657 | |||||||
| chr10:59355722 | G | A | 15 | a0001c0001t0001g0051 a0001c0001t0001g0169 a0001c0001t0001g0172 others(12): Show |
15 | HG01070.hp1 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.119+165C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59355722 | |||||||
| chr10:59355847 | T | C | 1 | a0001c0001t0001g0145 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.119+40A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 2/13 | chr10 | 59355847 | |||||||
| chr10:59355952 | G | A | 1 | a0001c0001t0002g0008 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.63-9C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59355952 | |||||||
| chr10:59356377 | T | G | 1 | a0001c0001t0001g0146 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.63-434A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59356377 | |||||||
| chr10:59356424 | G | A | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.63-481C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59356424 | |||||||
| chr10:59356424 | G | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.63-481C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59356424 | |||||||
| chr10:59356541 | C | T | 3 | a0001c0001t0001g0163 a0001c0001t0001g0183 a0001c0001t0001g0184 |
3 | HG02965.hp2 HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.63-598G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59356541 | |||||||
| chr10:59356761 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.63-818C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59356761 | |||||||
| chr10:59356819 | C | CGACTCAG others(51): Show |
1 | a0001c0001t0001g0147 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.63-877_63-876insCC others(56): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59356819 | |||||||
| chr10:59356824 | A | T | 1 | a0001c0001t0001g0147 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.63-881T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59356824 | |||||||
| chr10:59356827 | C | G | 1 | a0001c0001t0001g0147 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.63-884G>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59356827 | |||||||
| chr10:59356828 | T | A | 1 | a0001c0001t0001g0147 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.63-885A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59356828 | |||||||
| chr10:59356847 | C | T | 15 | a0001c0001t0001g0051 a0001c0001t0001g0169 a0001c0001t0001g0172 others(12): Show |
15 | HG01070.hp1 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.63-904G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59356847 | |||||||
| chr10:59356935 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.63-992G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59356935 | |||||||
| chr10:59356949 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.63-1006A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59356949 | |||||||
| chr10:59356976 | T | G | 2 | a0001c0001t0001g0051 a0001c0001t0001g0179 |
2 | HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.63-1033A>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59356976 | |||||||
| chr10:59357008 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.63-1065G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59357008 | |||||||
| chr10:59357010 | C | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.63-1067G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59357010 | |||||||
| chr10:59357020 | G | T | 1 | a0001c0001t0001g0009 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.63-1077C>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59357020 | |||||||
| chr10:59357027 | G | A | 15 | a0001c0001t0001g0051 a0001c0001t0001g0169 a0001c0001t0001g0172 others(12): Show |
15 | HG01070.hp1 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.63-1084C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59357027 | |||||||
| chr10:59357062 | C | T | 1 | a0001c0001t0002g0008 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.63-1119G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59357062 | |||||||
| chr10:59357153 | T | A | 3 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG02055.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.63-1210A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59357153 | |||||||
| chr10:59357258 | T | C | 13 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(10): Show |
13 | HG00735.hp1 HG01071.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.63-1315A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59357258 | |||||||
| chr10:59357282 | T | C | 3 | a0001c0001t0001g0152 a0001c0001t0001g0183 a0001c0001t0001g0184 |
3 | HG00738.hp1 HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.63-1339A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59357282 | |||||||
| chr10:59357341 | A | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.63-1398T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59357341 | |||||||
| chr10:59357374 | A | G | 1 | a0007c0010t0001g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.63-1431T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59357374 | |||||||
| chr10:59357455 | A | C | 3 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0007g0185 |
3 | HG02647.hp1 HG02723.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.63-1512T>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59357455 | |||||||
| chr10:59357466 | A | G | 1 | a0001c0001t0001g0002 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.63-1523T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59357466 | |||||||
| chr10:59357645 | T | C | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.63-1702A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59357645 | |||||||
| chr10:59357841 | C | T | 17 | a0001c0001t0001g0051 a0001c0001t0001g0169 a0001c0001t0001g0172 others(14): Show |
17 | HG01070.hp1 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.63-1898G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59357841 | |||||||
| chr10:59358053 | T | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(71): Show |
75 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.63-2110A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59358053 | |||||||
| chr10:59358072 | T | A | 1 | a0001c0001t0001g0163 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.63-2129A>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59358072 | |||||||
| chr10:59358225 | A | T | 1 | a0001c0001t0001g0053 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.63-2282T>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59358225 | |||||||
| chr10:59358291 | C | T | 17 | a0001c0001t0001g0051 a0001c0001t0001g0169 a0001c0001t0001g0172 others(14): Show |
17 | HG01070.hp1 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.63-2348G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59358291 | |||||||
| chr10:59358295 | T | C | 13 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(10): Show |
13 | HG00735.hp1 HG01071.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.63-2352A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59358295 | |||||||
| chr10:59358308 | G | A | 15 | a0001c0001t0001g0051 a0001c0001t0001g0169 a0001c0001t0001g0172 others(12): Show |
15 | HG01070.hp1 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.63-2365C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59358308 | |||||||
| chr10:59358479 | G | A | 3 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG02055.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.63-2536C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59358479 | |||||||
| chr10:59358532 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.63-2589T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59358532 | |||||||
| chr10:59358556 | T | C | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.63-2613A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59358556 | |||||||
| chr10:59358583 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.63-2640G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59358583 | |||||||
| chr10:59358660 | T | C | 15 | a0001c0001t0001g0051 a0001c0001t0001g0169 a0001c0001t0001g0172 others(12): Show |
15 | HG01070.hp1 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.63-2717A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59358660 | |||||||
| chr10:59358702 | TC | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.63-2760delG | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59358702 | |||||||
| chr10:59358912 | C | T | 15 | a0001c0001t0001g0051 a0001c0001t0001g0169 a0001c0001t0001g0172 others(12): Show |
15 | HG01070.hp1 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.63-2969G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59358912 | |||||||
| chr10:59359057 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0152 |
2 | HG00323.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.63-3114C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59359057 | |||||||
| chr10:59359250 | C | T | 3 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG02055.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.62+3149G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59359250 | |||||||
| chr10:59359646 | T | C | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.62+2753A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59359646 | |||||||
| chr10:59359656 | C | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG02723.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.62+2743G>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59359656 | |||||||
| chr10:59359934 | G | A | 15 | a0001c0001t0001g0051 a0001c0001t0001g0169 a0001c0001t0001g0172 others(12): Show |
15 | HG01070.hp1 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.62+2465C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59359934 | |||||||
| chr10:59360012 | T | C | 1 | a0001c0001t0001g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.62+2387A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59360012 | |||||||
| chr10:59360076 | C | T | 3 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG02055.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.62+2323G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59360076 | |||||||
| chr10:59360124 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.62+2275G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59360124 | |||||||
| chr10:59360260 | T | C | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.62+2139A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59360260 | |||||||
| chr10:59360483 | A | G | 1 | a0001c0004t0001g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.62+1916T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59360483 | |||||||
| chr10:59360490 | A | G | 15 | a0001c0001t0001g0051 a0001c0001t0001g0169 a0001c0001t0001g0172 others(12): Show |
15 | HG01070.hp1 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.62+1909T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59360490 | |||||||
| chr10:59360532 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.62+1867A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59360532 | |||||||
| chr10:59360567 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.62+1832T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59360567 | |||||||
| chr10:59360724 | C | T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(69): Show |
73 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.62+1675G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59360724 | |||||||
| chr10:59360853 | G | GA | 15 | a0001c0001t0001g0006 a0001c0001t0001g0155 a0001c0001t0001g0156 others(12): Show |
15 | HG01071.hp2 HG02055.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.62+1545dupT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59360853 | |||||||
| chr10:59360853 | GA | G | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(66): Show |
70 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.62+1545delT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59360853 | |||||||
| chr10:59360853 | GAA | G | 11 | a0001c0001t0001g0007 a0001c0001t0001g0188 a0001c0001t0001g0189 others(8): Show |
11 | HG00639.hp1 HG00639.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.62+1544_62+1545del others(2): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59360853 | |||||||
| chr10:59360853 | GAAAAAAA others(7): Show |
G | 11 | a0001c0001t0001g0169 a0001c0001t0001g0172 a0001c0001t0001g0173 others(8): Show |
11 | HG01070.hp1 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.62+1532_62+1545del others(14): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59360853 | |||||||
| chr10:59360924 | C | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(3): Show |
6 | HG00735.hp1 HG01071.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.62+1475G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59360924 | |||||||
| chr10:59360958 | A | G | 16 | a0001c0001t0001g0169 a0001c0001t0001g0172 a0001c0001t0001g0173 others(13): Show |
16 | HG01070.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.62+1441T>C | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59360958 | |||||||
| chr10:59361212 | GT | G | 15 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0191 others(12): Show |
15 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.62+1186delA | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59361212 | |||||||
| chr10:59361605 | CAT | C | 19 | a0001c0001t0001g0169 a0001c0001t0001g0172 a0001c0001t0001g0173 others(16): Show |
19 | HG01070.hp1 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.62+792_62+793delAT | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59361605 | |||||||
| chr10:59361641 | T | C | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.62+758A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59361641 | |||||||
| chr10:59361862 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.62+537C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59361862 | |||||||
| chr10:59361986 | C | T | 1 | a0001c0001t0001g0002 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.62+413G>A | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59361986 | |||||||
| chr10:59361995 | G | A | 4 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(1): Show |
4 | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.62+404C>T | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59361995 | |||||||
| chr10:59362382 | T | C | 13 | a0001c0001t0001g0191 a0001c0001t0001g0196 a0001c0001t0001g0197 others(10): Show |
13 | HG00639.hp1 HG00639.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.62+17A>G | FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | 59362382 |