Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 25940 |
| ensemblid | ENSG00000119812.20 |
| hgncid | 24520 |
| symbol | FAM98A |
| name | family with sequence similarity 98 member A |
| refseq_nuc | NM_015475.5 |
| refseq_prot | NP_056290.3 |
| ensembl_nuc | ENST00000238823.13 |
| ensembl_prot | ENSP00000238823.8 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 33583660 |
| end | 33599299 |
| strand | - |
| ver | v1.2 |
| region | chr2:33583660-33599299 |
| region5000 | chr2:33578660-33604299 |
| regionname0 | FAM98A_chr2_33583660_33599299 |
| regionname5000 | FAM98A_chr2_33578660_33604299 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 518 | 399 | 91 | 75 | 173 | 14 | 44 | 142 | FAM98A_chr2_33578660_33604299 | FAM98A | MECDL others(513): Show |
chr2 | 33578660 | 33604299 |
| a0002 | 0/0 | 518 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | MECDL others(513): Show |
chr2 | 33578660 | 33604299 |
| a0003 | 0/0 | 518 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | MECDL others(513): Show |
chr2 | 33578660 | 33604299 |
| a0004 | 0/0 | 518 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | MECDL others(513): Show |
chr2 | 33578660 | 33604299 |
| a0005 | 0/0 | 518 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | MECDL others(513): Show |
chr2 | 33578660 | 33604299 |
| a0006 | 0/0 | 518 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | MECDL others(513): Show |
chr2 | 33578660 | 33604299 |
| a0007 | 0/0 | 518 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | MECDL others(513): Show |
chr2 | 33578660 | 33604299 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1554 | 385 | 79 | 75 | 172 | 13 | 44 | FAM98A_chr2_33578660_33604299 | FAM98A | ATGGA others(1549): Show |
chr2 | 33578660 | 33604299 | ||
| a0001c0002 | 0/0 | 1554 | 10 | 10 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | ATGGA others(1549): Show |
chr2 | 33578660 | 33604299 | ||
| a0001c0003 | 0/0 | 1554 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | ATGGA others(1549): Show |
chr2 | 33578660 | 33604299 | ||
| a0001c0005 | 0/0 | 1554 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | ATGGA others(1549): Show |
chr2 | 33578660 | 33604299 | ||
| a0001c0006 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | ATGGA others(1549): Show |
chr2 | 33578660 | 33604299 | ||
| a0002c0004 | 0/0 | 1554 | 2 | 0 | 1 | 0 | 1 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | ATGGA others(1549): Show |
chr2 | 33578660 | 33604299 | ||
| a0003c0008 | 0/0 | 1554 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | ATGGA others(1549): Show |
chr2 | 33578660 | 33604299 | ||
| a0004c0010 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | ATGGA others(1549): Show |
chr2 | 33578660 | 33604299 | ||
| a0005c0007 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | ATGGA others(1549): Show |
chr2 | 33578660 | 33604299 | ||
| a0006c0009 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | ATGGA others(1549): Show |
chr2 | 33578660 | 33604299 | ||
| a0007c0011 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | ATGGA others(1549): Show |
chr2 | 33578660 | 33604299 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2751 | 223 | 46 | 53 | 87 | 4 | 32 | FAM98A_chr2_33578660_33604299 | FAM98A | AGTCG others(2746): Show |
chr2 | 33578660 | 33604299 |
| a0001c0001t0002 | 1/0 | 2751 | 121 | 8 | 17 | 78 | 6 | 11 | FAM98A_chr2_33578660_33604299 | FAM98A | AGTCG others(2746): Show |
chr2 | 33578660 | 33604299 |
| a0001c0001t0003 | 0/0 | 2751 | 22 | 16 | 2 | 0 | 3 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | AGTCG others(2746): Show |
chr2 | 33578660 | 33604299 |
| a0001c0001t0004 | 0/0 | 2751 | 5 | 5 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | AGTCG others(2746): Show |
chr2 | 33578660 | 33604299 |
| a0001c0001t0005 | 0/0 | 2751 | 3 | 3 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | AGTCG others(2746): Show |
chr2 | 33578660 | 33604299 |
| a0001c0001t0006 | 0/0 | 2751 | 3 | 0 | 0 | 3 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | AGTCG others(2746): Show |
chr2 | 33578660 | 33604299 |
| a0001c0001t0007 | 0/0 | 2751 | 2 | 0 | 2 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | AGTCG others(2746): Show |
chr2 | 33578660 | 33604299 |
| a0001c0001t0008 | 0/0 | 2751 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | AGTCG others(2746): Show |
chr2 | 33578660 | 33604299 |
| a0001c0001t0009 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | AGTCG others(2746): Show |
chr2 | 33578660 | 33604299 |
| a0001c0001t0010 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | AGTCG others(2746): Show |
chr2 | 33578660 | 33604299 |
| a0001c0001t0011 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | AGTCG others(2746): Show |
chr2 | 33578660 | 33604299 |
| a0001c0001t0012 | 0/0 | 2751 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | AGTCG others(2746): Show |
chr2 | 33578660 | 33604299 |
| a0001c0001t0013 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | AGTCG others(2746): Show |
chr2 | 33578660 | 33604299 |
| a0001c0002t0004 | 0/0 | 2751 | 10 | 10 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | AGTCG others(2746): Show |
chr2 | 33578660 | 33604299 |
| a0001c0003t0001 | 0/0 | 2751 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | AGTCG others(2746): Show |
chr2 | 33578660 | 33604299 |
| a0001c0005t0001 | 0/0 | 2751 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | AGTCG others(2746): Show |
chr2 | 33578660 | 33604299 |
| a0001c0006t0002 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | AGTCG others(2746): Show |
chr2 | 33578660 | 33604299 |
| a0002c0004t0001 | 0/0 | 2751 | 2 | 0 | 1 | 0 | 1 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | AGTCG others(2746): Show |
chr2 | 33578660 | 33604299 |
| a0003c0008t0001 | 0/0 | 2751 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | AGTCG others(2746): Show |
chr2 | 33578660 | 33604299 |
| a0004c0010t0001 | 0/0 | 2751 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | AGTCG others(2746): Show |
chr2 | 33578660 | 33604299 |
| a0005c0007t0002 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | AGTCG others(2746): Show |
chr2 | 33578660 | 33604299 |
| a0006c0009t0001 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | AGTCG others(2746): Show |
chr2 | 33578660 | 33604299 |
| a0007c0011t0001 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | AGTCG others(2746): Show |
chr2 | 33578660 | 33604299 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 54 | 3 | 15 | 28 | 2 | 6 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0003 | 0/0 | 19 | 8 | 4 | 5 | 0 | 2 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0004 | 0/0 | 17 | 0 | 7 | 9 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0005 | 0/0 | 13 | 0 | 0 | 13 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0006 | 0/0 | 12 | 0 | 10 | 0 | 0 | 2 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0007 | 0/0 | 10 | 2 | 3 | 3 | 0 | 2 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0010 | 0/0 | 8 | 0 | 2 | 3 | 0 | 3 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0012 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0014 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0018 | 0/0 | 4 | 1 | 0 | 0 | 2 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0068 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0002g0001 | 1/0 | 65 | 4 | 10 | 42 | 3 | 5 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0002g0009 | 0/0 | 9 | 1 | 0 | 8 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0002g0011 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0002g0020 | 0/0 | 4 | 0 | 0 | 0 | 1 | 3 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0002g0021 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0002g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0002g0025 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0002g0026 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0003g0008 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0003g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0003g0019 | 0/0 | 4 | 1 | 1 | 0 | 1 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0003g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0004g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0005g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0005g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0006g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0007g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0007g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0008g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0009g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0010g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0011g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0012g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0001t0013g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0002t0004g0013 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0002t0004g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0002t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0002t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0003t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0005t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0001c0006t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0002c0004t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0003c0008t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0004c0010t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0005c0007t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0006c0009t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| a0007c0011t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG00140 | hp2 | a0002 | c0004 | t0001 | g0038 | EUR | GBR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG00323 | hp1 | a0001 | c0005 | t0001 | g0049 | EUR | FIN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG00323 | hp2 | a0003 | c0008 | t0001 | g0078 | EUR | FIN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | CHS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | CHS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | CHS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | CHS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG00735 | hp2 | a0001 | c0001 | t0007 | g0122 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG00738 | hp2 | a0001 | c0001 | t0012 | g0067 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01106 | hp2 | a0002 | c0004 | t0001 | g0038 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0115 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01192 | hp2 | a0001 | c0001 | t0007 | g0119 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0039 | EUR | IBS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0028 | EUR | IBS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0020 | EUR | IBS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0028 | EUR | IBS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0123 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | KHV | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | KHV | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02055 | hp1 | a0004 | c0010 | t0001 | g0076 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02132 | hp2 | a0001 | c0001 | t0009 | g0112 | EAS | KHV | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CDX | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CDX | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02257 | hp2 | a0001 | c0003 | t0001 | g0031 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02523 | hp1 | a0005 | c0007 | t0002 | g0111 | EAS | KHV | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02622 | hp1 | a0001 | c0002 | t0004 | g0055 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02630 | hp1 | a0001 | c0002 | t0004 | g0013 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0070 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0019 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02717 | hp2 | a0001 | c0002 | t0004 | g0013 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0054 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02818 | hp1 | a0001 | c0002 | t0004 | g0029 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0031 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02886 | hp2 | a0001 | c0002 | t0004 | g0066 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02896 | hp1 | a0001 | c0002 | t0004 | g0013 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02922 | hp1 | a0001 | c0002 | t0004 | g0013 | AFR | ESN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0051 | AFR | ESN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ESN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | ESN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03139 | hp2 | a0001 | c0001 | t0008 | g0074 | AFR | ESN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | MSL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | MSL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | MSL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0105 | AFR | MSL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | STU | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0071 | SAS | BEB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | STU | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | STU | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | STU | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0110 | SAS | STU | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | YRI | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | CHB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | YRI | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18952 | hp1 | a0001 | c0001 | t0013 | g0131 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18957 | hp2 | a0001 | c0001 | t0010 | g0088 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18968 | hp2 | a0001 | c0001 | t0006 | g0023 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18969 | hp1 | a0006 | c0009 | t0001 | g0089 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18998 | hp2 | a0007 | c0011 | t0001 | g0098 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | LWK | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | LWK | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19059 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19068 | hp2 | a0001 | c0001 | t0011 | g0130 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19078 | hp2 | a0001 | c0001 | t0006 | g0023 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19083 | hp2 | a0001 | c0006 | t0002 | g0107 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19087 | hp2 | a0001 | c0001 | t0006 | g0023 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0025 | EUR | TSI | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0019 | EUR | TSI | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0020 | SAS | GIH | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | GIH | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02109 | hp2 | a0001 | c0002 | t0004 | g0013 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02559 | hp1 | a0001 | c0002 | t0004 | g0029 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0106 | AFR | MSL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | MSL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | USA | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| HG06807 | hp2 | a0001 | c0002 | t0004 | g0013 | AFR | USA | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | USA | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | USA | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | LWK | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | LWK | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0068 | REF | REF | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0001 | REF | REF | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:33584927 | C | A | 1 | a0003 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.1406G>T | p.Gly469Val | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 8/8 | 1484/2751 | 1406/1557 | 469/518 | chr2 | 33584927 | |||
| chr2:33584933 | C | T | 1 | a0005 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.1400G>A | p.Arg467His | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 8/8 | 1478/2751 | 1400/1557 | 467/518 | chr2 | 33584933 | |||
| chr2:33585113 | C | A | 1 | a0006 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.1220G>T | p.Gly407Val | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 8/8 | 1298/2751 | 1220/1557 | 407/518 | chr2 | 33585113 | |||
| chr2:33585571 | T | C | 1 | a0002 | 2 | HG00140.hp2 HG01106.hp2 |
missense_variant | MODERATE | c.847A>G | p.Ser283Gly | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 7/8 | 925/2751 | 847/1557 | 283/518 | chr2 | 33585571 | |||
| chr2:33586638 | T | A | 1 | a0004 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.644A>T | p.Tyr215Phe | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 6/8 | 722/2751 | 644/1557 | 215/518 | chr2 | 33586638 | |||
| chr2:33588412 | T | C | 1 | a0007 | 1 | NA18998.hp2 | missense_variant | MODERATE | c.445A>G | p.Ile149Val | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 4/8 | 523/2751 | 445/1557 | 149/518 | chr2 | 33588412 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:33584917 | A | G | 1 | a0001c0002 | 10 | HG02109.hp2 HG02559.hp1 HG02622.hp1 others(7): Show |
synonymous_variant | LOW | c.1416T>C | p.Gly472Gly | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 8/8 | 1494/2751 | 1416/1557 | 472/518 | chr2 | 33584917 | |||
| chr2:33592150 | C | T | 1 | a0001c0006 | 1 | NA19083.hp2 | synonymous_variant | LOW | c.267G>A | p.Pro89Pro | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/8 | 345/2751 | 267/1557 | 89/518 | chr2 | 33592150 | |||
| chr2:33595568 | C | T | 1 | a0001c0005 | 1 | HG00323.hp1 | synonymous_variant | LOW | c.123G>A | p.Glu41Glu | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/8 | 201/2751 | 123/1557 | 41/518 | chr2 | 33595568 | |||
| chr2:33595622 | C | T | 1 | a0001c0003 | 2 | HG02257.hp2 HG02886.hp1 |
synonymous_variant | LOW | c.69G>A | p.Leu23Leu | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/8 | 147/2751 | 69/1557 | 23/518 | chr2 | 33595622 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:33583745 | T | C | 1 | a0001c0001t0011 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1031A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 8/8 | 1031 | chr2 | 33583745 | ||||||
| chr2:33584204 | G | A | 1 | a0001c0001t0010 | 1 | NA18957.hp2 | 3_prime_UTR_variant | MODIFIER | c.*572C>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 8/8 | 572 | chr2 | 33584204 | ||||||
| chr2:33584227 | A | G | 16 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(13): Show |
277 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*549T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 8/8 | 549 | chr2 | 33584227 | ||||||
| chr2:33584297 | G | C | 1 | a0001c0001t0012 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*479C>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 8/8 | 479 | chr2 | 33584297 | ||||||
| chr2:33584323 | G | C | 1 | a0001c0001t0007 | 2 | HG00735.hp2 HG01192.hp2 |
3_prime_UTR_variant | MODIFIER | c.*453C>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 8/8 | 453 | chr2 | 33584323 | ||||||
| chr2:33584381 | C | G | 1 | a0001c0001t0009 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*395G>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 8/8 | 395 | chr2 | 33584381 | ||||||
| chr2:33584385 | G | T | 1 | a0001c0001t0006 | 3 | NA18968.hp2 NA19078.hp2 NA19087.hp2 |
3_prime_UTR_variant | MODIFIER | c.*391C>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 8/8 | 391 | chr2 | 33584385 | ||||||
| chr2:33584404 | C | G | 1 | a0001c0001t0003 | 22 | HG01074.hp1 HG01109.hp1 HG01515.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*372G>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 8/8 | 372 | chr2 | 33584404 | ||||||
| chr2:33584548 | A | C | 1 | a0001c0001t0008 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*228T>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 8/8 | 228 | chr2 | 33584548 | ||||||
| chr2:33584627 | A | G | 1 | a0001c0001t0005 | 3 | HG02630.hp2 HG03471.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*149T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 8/8 | 149 | chr2 | 33584627 | ||||||
| chr2:33584759 | T | G | 2 | a0001c0001t0004 a0001c0002t0004 |
15 | HG02109.hp2 HG02280.hp1 HG02559.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*17A>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 8/8 | 17 | chr2 | 33584759 | ||||||
| chr2:33599247 | G | C | 1 | a0001c0001t0013 | 1 | NA18952.hp1 | 5_prime_UTR_variant | MODIFIER | c.-26C>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/8 | 26 | chr2 | 33599247 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:33585460 | G | T | 1 | a0001c0001t0001g0103 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.889-16C>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 7/7 | chr2 | 33585460 | |||||||
| chr2:33585890 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.721-193A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 6/7 | chr2 | 33585890 | |||||||
| chr2:33585946 | G | C | 1 | a0001c0001t0002g0040 | 2 | HG02015.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.721-249C>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 6/7 | chr2 | 33585946 | |||||||
| chr2:33585989 | C | T | 1 | a0007c0011t0001g0098 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.721-292G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 6/7 | chr2 | 33585989 | |||||||
| chr2:33586405 | A | G | 1 | a0001c0001t0001g0036 | 2 | NA19000.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.720+157T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 6/7 | chr2 | 33586405 | |||||||
| chr2:33586409 | T | C | 1 | a0001c0001t0005g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.720+153A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 6/7 | chr2 | 33586409 | |||||||
| chr2:33586428 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.720+134T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 6/7 | chr2 | 33586428 | |||||||
| chr2:33586449 | C | G | 46 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(43): Show |
152 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.720+113G>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 6/7 | chr2 | 33586449 | |||||||
| chr2:33586740 | G | T | 1 | a0001c0001t0001g0092 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.604-62C>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 5/7 | chr2 | 33586740 | |||||||
| chr2:33586770 | T | G | 1 | a0001c0001t0001g0128 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.604-92A>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 5/7 | chr2 | 33586770 | |||||||
| chr2:33586869 | A | T | 32 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0014 others(29): Show |
83 | HG00323.hp1 HG00423.hp1 HG00738.hp2 others(80): Show |
intron_variant | MODIFIER | c.604-191T>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 5/7 | chr2 | 33586869 | |||||||
| chr2:33586929 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.604-251G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 5/7 | chr2 | 33586929 | |||||||
| chr2:33587046 | A | G | 5 | a0001c0001t0001g0010 a0001c0001t0001g0041 a0001c0001t0001g0125 others(2): Show |
13 | HG01070.hp2 HG01361.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.603+194T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 5/7 | chr2 | 33587046 | |||||||
| chr2:33587138 | A | T | 1 | a0001c0001t0001g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.603+102T>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 5/7 | chr2 | 33587138 | |||||||
| chr2:33587161 | C | A | 1 | a0001c0001t0001g0128 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.603+79G>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 5/7 | chr2 | 33587161 | |||||||
| chr2:33587624 | C | T | 1 | a0001c0001t0002g0118 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.523-304G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 4/7 | chr2 | 33587624 | |||||||
| chr2:33587675 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.523-355T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 4/7 | chr2 | 33587675 | |||||||
| chr2:33587735 | T | A | 83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(80): Show |
254 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.523-415A>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 4/7 | chr2 | 33587735 | |||||||
| chr2:33587735 | T | G | 1 | a0001c0001t0001g0042 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.523-415A>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 4/7 | chr2 | 33587735 | |||||||
| chr2:33587746 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.523-426G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 4/7 | chr2 | 33587746 | |||||||
| chr2:33587747 | G | A | 8 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0032 others(5): Show |
17 | HG00738.hp2 HG01255.hp1 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.523-427C>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 4/7 | chr2 | 33587747 | |||||||
| chr2:33587804 | T | C | 3 | a0001c0001t0001g0072 a0001c0001t0001g0102 a0001c0001t0001g0103 |
3 | HG01243.hp1 HG03209.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.523-484A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 4/7 | chr2 | 33587804 | |||||||
| chr2:33587901 | T | C | 2 | a0001c0001t0001g0034 a0004c0010t0001g0076 |
3 | HG01884.hp1 HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.522+434A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 4/7 | chr2 | 33587901 | |||||||
| chr2:33587960 | A | G | 1 | a0001c0001t0002g0110 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.522+375T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 4/7 | chr2 | 33587960 | |||||||
| chr2:33587964 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.522+371C>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 4/7 | chr2 | 33587964 | |||||||
| chr2:33588051 | T | C | 4 | a0001c0001t0001g0104 a0001c0001t0005g0070 a0001c0001t0005g0105 others(1): Show |
4 | HG02630.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.522+284A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 4/7 | chr2 | 33588051 | |||||||
| chr2:33588071 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.522+264A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 4/7 | chr2 | 33588071 | |||||||
| chr2:33588196 | C | A | 1 | a0001c0001t0001g0125 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.522+139G>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 4/7 | chr2 | 33588196 | |||||||
| chr2:33588900 | A | AT | 54 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(51): Show |
169 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.338-382dupA | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33588900 | |||||||
| chr2:33588941 | A | C | 1 | a0001c0001t0001g0087 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.338-422T>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33588941 | |||||||
| chr2:33589116 | C | G | 1 | a0001c0001t0001g0086 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.338-597G>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33589116 | |||||||
| chr2:33589180 | A | C | 1 | a0001c0001t0001g0042 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.338-661T>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33589180 | |||||||
| chr2:33589264 | G | C | 38 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0014 others(35): Show |
106 | HG00323.hp1 HG00423.hp1 HG00738.hp2 others(103): Show |
intron_variant | MODIFIER | c.338-745C>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33589264 | |||||||
| chr2:33589415 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.338-896A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33589415 | |||||||
| chr2:33589523 | A | G | 46 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(43): Show |
152 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.338-1004T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33589523 | |||||||
| chr2:33589525 | A | G | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | NA18954.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.338-1006T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33589525 | |||||||
| chr2:33589622 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.338-1103C>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33589622 | |||||||
| chr2:33589823 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.338-1304A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33589823 | |||||||
| chr2:33590104 | G | A | 1 | a0001c0001t0001g0042 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.338-1585C>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33590104 | |||||||
| chr2:33590222 | C | T | 1 | a0002c0004t0001g0038 | 2 | HG00140.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.338-1703G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33590222 | |||||||
| chr2:33590317 | T | G | 95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(92): Show |
278 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(275): Show |
intron_variant | MODIFIER | c.337+1763A>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33590317 | |||||||
| chr2:33590348 | C | T | 1 | a0001c0001t0011g0130 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.337+1732G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33590348 | |||||||
| chr2:33590404 | A | G | 39 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(36): Show |
144 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.337+1676T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33590404 | |||||||
| chr2:33590584 | G | A | 4 | a0001c0001t0001g0104 a0001c0001t0005g0070 a0001c0001t0005g0105 others(1): Show |
4 | HG02630.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.337+1496C>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33590584 | |||||||
| chr2:33590746 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.337+1334A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33590746 | |||||||
| chr2:33590881 | T | C | 37 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0014 others(34): Show |
104 | HG00323.hp1 HG00423.hp1 HG00738.hp2 others(101): Show |
intron_variant | MODIFIER | c.337+1199A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33590881 | |||||||
| chr2:33591133 | A | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0085 |
3 | HG01123.hp1 HG01358.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.337+947T>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33591133 | |||||||
| chr2:33591195 | C | CT | 42 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(39): Show |
149 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.337+884dupA | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33591195 | |||||||
| chr2:33591482 | G | A | 1 | a0001c0001t0002g0113 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.337+598C>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33591482 | |||||||
| chr2:33591518 | C | T | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): Show |
260 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.337+562G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33591518 | |||||||
| chr2:33591674 | G | A | 4 | a0001c0001t0001g0104 a0001c0001t0005g0070 a0001c0001t0005g0105 others(1): Show |
4 | HG02630.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.337+406C>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33591674 | |||||||
| chr2:33591714 | C | T | 6 | a0001c0001t0001g0061 a0001c0001t0003g0008 a0001c0001t0003g0015 others(3): Show |
22 | HG01074.hp1 HG01109.hp1 HG01515.hp2 others(19): Show |
intron_variant | MODIFIER | c.337+366G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33591714 | |||||||
| chr2:33591739 | A | G | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(86): Show |
264 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.337+341T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33591739 | |||||||
| chr2:33591827 | A | C | 1 | a0001c0001t0008g0074 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.337+253T>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33591827 | |||||||
| chr2:33591841 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.337+239C>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33591841 | |||||||
| chr2:33591848 | G | A | 1 | a0001c0001t0004g0054 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.337+232C>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33591848 | |||||||
| chr2:33591877 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.337+203A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33591877 | |||||||
| chr2:33591950 | G | A | 6 | a0001c0001t0001g0056 a0001c0001t0004g0017 a0001c0001t0004g0054 others(3): Show |
15 | HG02109.hp2 HG02280.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.337+130C>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33591950 | |||||||
| chr2:33592071 | T | G | 1 | a0001c0001t0002g0114 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.337+9A>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33592071 | |||||||
| chr2:33592302 | T | C | 17 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0032 others(14): Show |
35 | HG00738.hp2 HG01255.hp1 HG01516.hp1 others(32): Show |
intron_variant | MODIFIER | c.203-88A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33592302 | |||||||
| chr2:33592442 | T | G | 1 | a0001c0001t0001g0042 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.203-228A>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33592442 | |||||||
| chr2:33592492 | A | G | 39 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(36): Show |
144 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.203-278T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33592492 | |||||||
| chr2:33592509 | G | C | 1 | a0001c0001t0001g0042 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.203-295C>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33592509 | |||||||
| chr2:33592558 | C | T | 3 | a0001c0001t0002g0025 a0001c0001t0002g0109 a0001c0001t0002g0115 |
5 | HG01167.hp1 HG01169.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.203-344G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33592558 | |||||||
| chr2:33592814 | T | C | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): Show |
260 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.203-600A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33592814 | |||||||
| chr2:33592835 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.203-621G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33592835 | |||||||
| chr2:33592843 | C | T | 4 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0081 others(1): Show |
11 | HG01167.hp2 HG01993.hp1 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.203-629G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33592843 | |||||||
| chr2:33593060 | G | C | 3 | a0001c0002t0004g0013 a0001c0002t0004g0029 a0001c0002t0004g0055 |
9 | HG02109.hp2 HG02559.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.203-846C>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33593060 | |||||||
| chr2:33593131 | C | T | 43 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(40): Show |
148 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.203-917G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33593131 | |||||||
| chr2:33593254 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.203-1040T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33593254 | |||||||
| chr2:33593694 | C | T | 1 | a0001c0001t0008g0074 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.203-1480G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33593694 | |||||||
| chr2:33594000 | C | A | 7 | a0001c0001t0002g0020 a0001c0001t0002g0118 a0001c0001t0002g0121 others(4): Show |
13 | HG00735.hp2 HG01074.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.202+1489G>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594000 | |||||||
| chr2:33594326 | C | T | 37 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0014 others(34): Show |
102 | HG00323.hp1 HG00423.hp1 HG00738.hp2 others(99): Show |
intron_variant | MODIFIER | c.202+1163G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594326 | |||||||
| chr2:33594385 | G | A | 37 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0014 others(34): Show |
102 | HG00323.hp1 HG00423.hp1 HG00738.hp2 others(99): Show |
intron_variant | MODIFIER | c.202+1104C>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594385 | |||||||
| chr2:33594412 | G | A | 6 | a0001c0001t0001g0061 a0001c0001t0003g0008 a0001c0001t0003g0015 others(3): Show |
19 | HG01109.hp1 HG01515.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.202+1077C>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594412 | |||||||
| chr2:33594535 | T | TA | 5 | a0001c0001t0002g0009 a0001c0001t0002g0045 a0001c0001t0002g0115 others(2): Show |
13 | HG01175.hp2 HG02056.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.202+953dupT | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594535 | |||||||
| chr2:33594535 | TA | T | 9 | a0001c0001t0001g0007 a0001c0001t0001g0030 a0001c0001t0001g0057 others(6): Show |
20 | HG00323.hp1 HG01081.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.202+953delT | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594535 | |||||||
| chr2:33594555 | AAAAAATT others(2): Show |
A | 9 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0034 others(6): Show |
9 | HG01257.hp2 HG01358.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.202+925_202+933del others(9): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594555 | |||||||
| chr2:33594556 | AAAAATTA others(1): Show |
A | 32 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(29): Show |
132 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.202+925_202+932del others(8): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594556 | |||||||
| chr2:33594557 | AAAATTAT | A | 6 | a0001c0001t0001g0002 a0001c0001t0001g0072 a0001c0001t0001g0087 others(3): Show |
9 | HG01243.hp1 HG02280.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.202+925_202+931del others(7): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594557 | |||||||
| chr2:33594558 | AAATT | A | 10 | a0001c0001t0001g0010 a0001c0001t0001g0041 a0001c0001t0001g0125 others(7): Show |
18 | HG01361.hp2 HG01517.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.202+927_202+930del others(4): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594558 | |||||||
| chr2:33594558 | AAATTAT | A | 3 | a0001c0001t0005g0106 a0001c0002t0004g0013 a0001c0002t0004g0029 |
9 | HG02109.hp2 HG02559.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.202+925_202+930del others(6): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594558 | |||||||
| chr2:33594559 | AATT | A | 7 | a0001c0001t0001g0064 a0001c0001t0001g0126 a0001c0001t0003g0008 others(4): Show |
14 | HG01109.hp1 HG01515.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.202+927_202+929del others(3): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594559 | |||||||
| chr2:33594561 | T | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0053 others(2): Show |
9 | HG01516.hp1 HG01517.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.202+928A>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594561 | |||||||
| chr2:33594561 | TTATA | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0056 others(3): Show |
10 | HG00738.hp2 HG01255.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.202+924_202+927del others(4): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594561 | |||||||
| chr2:33594562 | TATA | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0002t0004g0066 |
7 | HG01516.hp1 HG01517.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.202+924_202+926del others(3): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594562 | |||||||
| chr2:33594563 | A | T | 17 | a0001c0001t0001g0010 a0001c0001t0001g0041 a0001c0001t0001g0064 others(14): Show |
38 | HG01070.hp2 HG01109.hp1 HG01361.hp2 others(35): Show |
intron_variant | MODIFIER | c.202+926T>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594563 | |||||||
| chr2:33594564 | T | A | 1 | a0001c0001t0001g0063 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.202+925A>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594564 | |||||||
| chr2:33594565 | A | T | 48 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(45): Show |
162 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.202+924T>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594565 | |||||||
| chr2:33594572 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0124 |
3 | HG02896.hp2 HG02897.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.202+917A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594572 | |||||||
| chr2:33594572 | TATATAC | T | 14 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0016 others(11): Show |
46 | HG00323.hp1 HG00423.hp1 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.202+911_202+916del others(6): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594572 | |||||||
| chr2:33594572 | TATATACA others(3): Show |
T | 1 | a0001c0003t0001g0031 | 2 | HG02257.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.202+907_202+916del others(10): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594572 | |||||||
| chr2:33594572 | TATATACA others(9): Show |
T | 1 | a0001c0001t0001g0083 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.202+901_202+916del others(16): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594572 | |||||||
| chr2:33594574 | T | C | 4 | a0001c0001t0001g0042 a0001c0001t0001g0061 a0001c0001t0001g0073 others(1): Show |
5 | HG02896.hp2 HG02897.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.202+915A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594574 | |||||||
| chr2:33594574 | TATAC | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0095 |
4 | NA18948.hp2 NA18999.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.202+911_202+914del others(4): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594574 | |||||||
| chr2:33594576 | T | C | 26 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0041 others(23): Show |
54 | HG00621.hp2 HG00738.hp2 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.202+913A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594576 | |||||||
| chr2:33594576 | T | TAC | 9 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0020 others(6): Show |
16 | HG00597.hp1 HG00735.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.202+911_202+912dup others(2): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594576 | |||||||
| chr2:33594578 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0063 a0001c0002t0004g0066 |
4 | HG02615.hp2 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.202+911G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594578 | |||||||
| chr2:33594600 | CATACATA others(15): Show |
C | 1 | a0001c0001t0001g0061 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.202+867_202+888del others(22): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594600 | |||||||
| chr2:33594606 | T | A | 1 | a0001c0001t0003g0015 | 4 | HG02559.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.202+883A>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594606 | |||||||
| chr2:33594608 | C | CACACATA others(21): Show |
2 | a0001c0001t0002g0108 a0001c0006t0002g0107 |
2 | HG00544.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.202+853_202+880dup others(28): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594608 | |||||||
| chr2:33594608 | CACACATA others(21): Show |
C | 13 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0043 others(10): Show |
21 | HG00408.hp1 HG00597.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.202+853_202+880del others(28): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594608 | |||||||
| chr2:33594614 | T | C | 37 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0014 others(34): Show |
103 | HG00323.hp1 HG00423.hp1 HG00738.hp2 others(100): Show |
intron_variant | MODIFIER | c.202+875A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594614 | |||||||
| chr2:33594614 | TATATATA others(19): Show |
T | 4 | a0001c0001t0001g0012 a0001c0001t0001g0081 a0001c0001t0001g0082 others(1): Show |
12 | HG01167.hp2 HG01993.hp1 NA18957.hp1 others(9): Show |
intron_variant | MODIFIER | c.202+849_202+874del others(26): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594614 | |||||||
| chr2:33594622 | T | C | 1 | a0001c0001t0001g0002 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.202+867A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594622 | |||||||
| chr2:33594632 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.202+857A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594632 | |||||||
| chr2:33594636 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.202+853A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594636 | |||||||
| chr2:33594636 | TACACATA others(37): Show |
T | 1 | a0001c0001t0001g0018 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.202+809_202+852del others(44): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594636 | |||||||
| chr2:33594642 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.202+847A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594642 | |||||||
| chr2:33594644 | TATATATA others(5): Show |
T | 1 | a0001c0001t0001g0016 | 4 | HG01891.hp1 HG02572.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.202+833_202+844del others(12): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594644 | |||||||
| chr2:33594648 | TATAC | T | 8 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0062 others(5): Show |
15 | HG00738.hp2 HG01255.hp1 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.202+837_202+840del others(4): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594648 | |||||||
| chr2:33594648 | TATACACA others(25): Show |
T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0053 a0001c0001t0001g0069 |
4 | HG01891.hp2 HG02145.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.202+809_202+840del others(32): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594648 | |||||||
| chr2:33594650 | T | C | 3 | a0001c0001t0001g0034 a0001c0001t0001g0043 a0004c0010t0001g0076 |
3 | HG02055.hp1 HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.202+839A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594650 | |||||||
| chr2:33594652 | CACACATA others(47): Show |
C | 2 | a0001c0001t0001g0034 a0004c0010t0001g0076 |
2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.202+783_202+836del others(54): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594652 | |||||||
| chr2:33594656 | C | T | 24 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0022 others(21): Show |
77 | HG00323.hp1 HG00423.hp1 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.202+833G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594656 | |||||||
| chr2:33594662 | TATACACA others(27): Show |
T | 1 | a0001c0003t0001g0031 | 2 | HG02257.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.202+793_202+826del others(34): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594662 | |||||||
| chr2:33594666 | CACATATA others(33): Show |
C | 6 | a0001c0001t0001g0056 a0001c0001t0004g0017 a0001c0001t0004g0054 others(3): Show |
15 | HG02109.hp2 HG02280.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.202+783_202+822del others(40): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594666 | |||||||
| chr2:33594668 | CATATATA others(23): Show |
C | 4 | a0001c0001t0001g0041 a0001c0001t0001g0104 a0001c0001t0001g0125 others(1): Show |
5 | HG02698.hp2 HG03195.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.202+791_202+820del others(30): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594668 | |||||||
| chr2:33594668 | CATATATA others(25): Show |
C | 1 | a0001c0001t0003g0028 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.202+789_202+820del others(32): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594668 | |||||||
| chr2:33594668 | CATATATA others(27): Show |
C | 11 | a0001c0001t0001g0014 a0001c0001t0001g0062 a0001c0001t0001g0063 others(8): Show |
28 | HG00738.hp2 HG01109.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.202+787_202+820del others(34): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594668 | |||||||
| chr2:33594668 | CATATATA others(29): Show |
C | 13 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0018 others(10): Show |
45 | HG00323.hp1 HG00423.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.202+785_202+820del others(36): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594668 | |||||||
| chr2:33594676 | TATACACA others(25): Show |
T | 1 | a0001c0001t0001g0042 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.202+781_202+812del others(32): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594676 | |||||||
| chr2:33594678 | T | C | 31 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(28): Show |
125 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.202+811A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594678 | |||||||
| chr2:33594678 | TACACACA others(23): Show |
T | 1 | a0001c0001t0001g0124 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.202+781_202+810del others(30): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594678 | |||||||
| chr2:33594680 | CACACATA others(19): Show |
C | 33 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(30): Show |
127 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.202+783_202+808del others(26): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594680 | |||||||
| chr2:33594684 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.202+805G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594684 | |||||||
| chr2:33594684 | CATATATA others(15): Show |
C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0016 |
6 | HG01891.hp1 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.202+783_202+804del others(22): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594684 | |||||||
| chr2:33594696 | CATAT | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0053 a0001c0001t0001g0069 |
4 | HG01891.hp2 HG02145.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.202+789_202+792del others(4): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594696 | |||||||
| chr2:33594702 | T | C | 5 | a0001c0001t0001g0032 a0001c0001t0001g0053 a0001c0001t0001g0069 others(2): Show |
8 | HG01515.hp2 HG01517.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.202+787A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594702 | |||||||
| chr2:33594704 | T | C | 17 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0053 others(14): Show |
37 | HG00408.hp1 HG00738.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.202+785A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594704 | |||||||
| chr2:33594704 | T | TAC | 3 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0006g0023 |
5 | HG01167.hp2 HG01993.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.202+784_202+785ins others(2): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594704 | |||||||
| chr2:33594706 | T | C | 39 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(36): Show |
107 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.202+783A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594706 | |||||||
| chr2:33594976 | T | C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0073 |
3 | HG03195.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.202+513A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594976 | |||||||
| chr2:33594986 | T | C | 1 | a0001c0001t0008g0074 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.202+503A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594986 | |||||||
| chr2:33595057 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.202+432G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33595057 | |||||||
| chr2:33595074 | T | C | 1 | a0001c0001t0006g0023 | 3 | NA18968.hp2 NA19078.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.202+415A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33595074 | |||||||
| chr2:33595085 | T | A | 1 | a0001c0001t0002g0116 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.202+404A>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33595085 | |||||||
| chr2:33595319 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.202+170G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33595319 | |||||||
| chr2:33595347 | C | T | 1 | a0001c0001t0002g0024 | 3 | NA19076.hp2 NA19078.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.202+142G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33595347 | |||||||
| chr2:33595731 | A | G | 4 | a0001c0001t0003g0008 a0001c0001t0003g0015 a0001c0001t0003g0027 others(1): Show |
16 | HG01109.hp1 HG02055.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.54-94T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33595731 | |||||||
| chr2:33595836 | G | A | 1 | a0001c0001t0002g0117 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.54-199C>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33595836 | |||||||
| chr2:33595889 | CTAAAT | C | 5 | a0001c0001t0003g0008 a0001c0001t0003g0015 a0001c0001t0003g0027 others(2): Show |
18 | HG01109.hp1 HG01515.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.54-257_54-253delAT others(3): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33595889 | |||||||
| chr2:33595973 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.54-336T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33595973 | |||||||
| chr2:33596106 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0048 a0001c0001t0001g0052 |
4 | HG01981.hp2 HG03654.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.54-469G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33596106 | |||||||
| chr2:33596254 | C | T | 3 | a0001c0001t0001g0104 a0001c0001t0005g0105 a0001c0001t0005g0106 |
3 | HG03195.hp2 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.54-617G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33596254 | |||||||
| chr2:33596269 | T | G | 1 | a0001c0001t0001g0103 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.54-632A>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33596269 | |||||||
| chr2:33596331 | G | C | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(99): Show |
288 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.54-694C>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33596331 | |||||||
| chr2:33596372 | C | A | 1 | a0001c0001t0001g0082 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.54-735G>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33596372 | |||||||
| chr2:33596398 | A | G | 1 | a0001c0002t0004g0029 | 2 | HG02559.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.54-761T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33596398 | |||||||
| chr2:33596405 | T | A | 1 | a0001c0001t0002g0123 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.54-768A>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33596405 | |||||||
| chr2:33596444 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0003c0008t0001g0078 |
15 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.54-807G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33596444 | |||||||
| chr2:33596450 | T | G | 39 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0014 others(36): Show |
107 | HG00323.hp1 HG00423.hp1 HG00738.hp2 others(104): Show |
intron_variant | MODIFIER | c.54-813A>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33596450 | |||||||
| chr2:33596491 | T | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0097 others(4): Show |
19 | HG00438.hp2 HG00597.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.54-854A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33596491 | |||||||
| chr2:33596617 | C | T | 37 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0014 others(34): Show |
102 | HG00323.hp1 HG00423.hp1 HG00738.hp2 others(99): Show |
intron_variant | MODIFIER | c.54-980G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33596617 | |||||||
| chr2:33596666 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(91): Show |
274 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.54-1029A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33596666 | |||||||
| chr2:33596707 | C | G | 10 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0012 others(7): Show |
45 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.54-1070G>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33596707 | |||||||
| chr2:33596844 | A | T | 5 | a0001c0001t0003g0008 a0001c0001t0003g0015 a0001c0001t0003g0027 others(2): Show |
18 | HG01109.hp1 HG01515.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.54-1207T>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33596844 | |||||||
| chr2:33596891 | C | CA | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(86): Show |
268 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.54-1255dupT | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33596891 | |||||||
| chr2:33596963 | A | T | 39 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0014 others(36): Show |
105 | HG00323.hp1 HG00423.hp1 HG00738.hp2 others(102): Show |
intron_variant | MODIFIER | c.54-1326T>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33596963 | |||||||
| chr2:33597046 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.54-1409A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33597046 | |||||||
| chr2:33597102 | T | C | 2 | a0001c0001t0001g0034 a0004c0010t0001g0076 |
3 | HG01884.hp1 HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.54-1465A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33597102 | |||||||
| chr2:33597132 | A | G | 1 | a0001c0001t0001g0042 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.54-1495T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33597132 | |||||||
| chr2:33597139 | C | G | 3 | a0001c0001t0001g0104 a0001c0001t0005g0105 a0001c0001t0005g0106 |
3 | HG03195.hp2 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.54-1502G>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33597139 | |||||||
| chr2:33597211 | T | G | 1 | a0001c0001t0002g0127 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.54-1574A>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33597211 | |||||||
| chr2:33597253 | G | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(33): Show |
140 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.54-1616C>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33597253 | |||||||
| chr2:33597459 | T | G | 1 | a0001c0001t0006g0023 | 3 | NA18968.hp2 NA19078.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.53+1710A>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33597459 | |||||||
| chr2:33597632 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0128 |
9 | HG01070.hp2 HG01361.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.53+1537C>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33597632 | |||||||
| chr2:33597892 | C | A | 1 | a0001c0001t0002g0129 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.53+1277G>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33597892 | |||||||
| chr2:33597896 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.53+1273T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33597896 | |||||||
| chr2:33598120 | T | G | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG01243.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.53+1049A>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33598120 | |||||||
| chr2:33598224 | T | C | 2 | a0001c0001t0002g0021 a0001c0001t0011g0130 |
5 | HG02293.hp1 NA18952.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.53+945A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33598224 | |||||||
| chr2:33598227 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.53+942T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33598227 | |||||||
| chr2:33598472 | A | C | 87 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(84): Show |
262 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.53+697T>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33598472 | |||||||
| chr2:33598571 | C | G | 2 | a0001c0001t0002g0011 a0001c0001t0002g0046 |
8 | HG02132.hp1 NA18950.hp2 NA18990.hp2 others(5): Show |
intron_variant | MODIFIER | c.53+598G>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33598571 | |||||||
| chr2:33598777 | G | C | 1 | a0001c0001t0001g0042 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.53+392C>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33598777 | |||||||
| chr2:33598803 | C | T | 1 | a0001c0001t0002g0045 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.53+366G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33598803 | |||||||
| chr2:33599028 | G | T | 1 | a0001c0001t0002g0044 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.53+141C>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33599028 | |||||||
| chr2:33599052 | A | C | 1 | a0001c0001t0001g0043 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.53+117T>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33599052 |