Item | Value |
---|---|
geneid | 441327 |
ensemblid | ENSG00000285607.1 |
hgncid | 32257 |
symbol | FAM90A9 |
name | family with sequence similarity 90 member A9 |
refseq_nuc | NM_001164448.1 |
refseq_prot | NP_001157920.1 |
ensembl_nuc | ENST00000648344.1 |
ensembl_prot | ENSP00000497259.1 |
mane_status | MANE Select |
chr | chr8 |
start | 7761330 |
end | 7764340 |
strand | + |
ver | v1.2 |
region | chr8:7761330-7764340 |
region5000 | chr8:7756330-7769340 |
regionname0 | FAM90A9_chr8_7761330_7764340 |
regionname5000 | FAM90A9_chr8_7756330_7769340 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 464 | 21 | 3 | 5 | 11 | 2 | 0 | 10 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0002 | 0/0 | 464 | 12 | 1 | 6 | 1 | 1 | 3 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0003 | 0/0 | 464 | 5 | 1 | 1 | 1 | 0 | 2 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0004 | 0/0 | 464 | 5 | 0 | 2 | 3 | 0 | 0 | 3 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0005 | 0/0 | 464 | 5 | 0 | 0 | 2 | 0 | 3 | 2 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0006 | 0/0 | 464 | 4 | 0 | 1 | 2 | 1 | 0 | 2 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0007 | 0/0 | 464 | 4 | 0 | 0 | 3 | 1 | 0 | 2 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0008 | 0/0 | 464 | 3 | 0 | 0 | 2 | 0 | 1 | 1 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0009 | 0/0 | 464 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0010 | 0/0 | 464 | 2 | 0 | 1 | 1 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0011 | 0/0 | 464 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0012 | 0/0 | 464 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0013 | 0/0 | 464 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0014 | 0/0 | 464 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0015 | 0/0 | 464 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0016 | 0/0 | 464 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0017 | 0/0 | 464 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0018 | 0/0 | 464 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0019 | 0/0 | 464 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0020 | 0/0 | 464 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0021 | 0/0 | 464 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0022 | 0/0 | 464 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0023 | 0/0 | 464 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0024 | 0/0 | 464 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0025 | 0/0 | 464 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0026 | 0/0 | 464 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0027 | 0/0 | 464 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0028 | 0/0 | 464 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0029 | 0/0 | 464 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0030 | 0/0 | 464 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0031 | 0/0 | 464 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0032 | 0/0 | 464 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0033 | 0/0 | 464 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
a0034 | 0/0 | 464 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | MMARR others(459): Show |
chr8 | 7756330 | 7769340 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1392 | 20 | 2 | 5 | 11 | 2 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0001c0018 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0002c0002 | 0/0 | 1392 | 12 | 1 | 6 | 1 | 1 | 3 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0003c0003 | 0/0 | 1392 | 5 | 1 | 1 | 1 | 0 | 2 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0004c0004 | 0/0 | 1392 | 5 | 0 | 2 | 3 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0005c0005 | 0/0 | 1392 | 5 | 0 | 0 | 2 | 0 | 3 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0006c0007 | 0/0 | 1392 | 4 | 0 | 1 | 2 | 1 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0007c0006 | 0/0 | 1392 | 4 | 0 | 0 | 3 | 1 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0008c0008 | 0/0 | 1392 | 3 | 0 | 0 | 2 | 0 | 1 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0009c0009 | 0/0 | 1392 | 3 | 0 | 2 | 0 | 0 | 1 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0010c0011 | 0/0 | 1392 | 2 | 0 | 1 | 1 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0011c0033 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0011c0035 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0012c0012 | 0/0 | 1392 | 2 | 2 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0013c0010 | 0/0 | 1392 | 2 | 0 | 0 | 2 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0014c0013 | 0/0 | 1392 | 2 | 0 | 0 | 2 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0015c0032 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0016c0031 | 0/0 | 1392 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0017c0022 | 0/0 | 1392 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0018c0028 | 0/0 | 1392 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0019c0014 | 0/0 | 1392 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0020c0027 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0021c0024 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0022c0026 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0023c0036 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0024c0023 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0025c0021 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0026c0017 | 0/0 | 1392 | 1 | 0 | 0 | 0 | 0 | 1 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0027c0020 | 0/0 | 1392 | 1 | 0 | 0 | 0 | 0 | 1 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0028c0015 | 0/0 | 1392 | 1 | 0 | 0 | 0 | 0 | 1 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0029c0019 | 0/0 | 1392 | 1 | 0 | 0 | 0 | 0 | 1 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0030c0025 | 0/0 | 1392 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0031c0016 | 0/0 | 1392 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0032c0029 | 0/0 | 1392 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0033c0030 | 0/0 | 1392 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 | ||
a0034c0034 | 0/0 | 1392 | 1 | 0 | 0 | 0 | 1 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1387): Show |
chr8 | 7756330 | 7769340 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1395 | 20 | 2 | 5 | 11 | 2 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0001c0018t0001 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0002c0002t0001 | 0/0 | 1395 | 12 | 1 | 6 | 1 | 1 | 3 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0003c0003t0001 | 0/0 | 1395 | 5 | 1 | 1 | 1 | 0 | 2 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0004c0004t0001 | 0/0 | 1395 | 5 | 0 | 2 | 3 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0005c0005t0001 | 0/0 | 1395 | 5 | 0 | 0 | 2 | 0 | 3 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0006c0007t0001 | 0/0 | 1395 | 4 | 0 | 1 | 2 | 1 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0007c0006t0001 | 0/0 | 1395 | 4 | 0 | 0 | 3 | 1 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0008c0008t0001 | 0/0 | 1395 | 3 | 0 | 0 | 2 | 0 | 1 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0009c0009t0001 | 0/0 | 1395 | 3 | 0 | 2 | 0 | 0 | 1 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0010c0011t0001 | 0/0 | 1395 | 2 | 0 | 1 | 1 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0011c0033t0001 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0011c0035t0001 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0012c0012t0001 | 0/0 | 1395 | 2 | 2 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0013c0010t0001 | 0/0 | 1395 | 2 | 0 | 0 | 2 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0014c0013t0001 | 0/0 | 1395 | 2 | 0 | 0 | 2 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0015c0032t0001 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0016c0031t0001 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0017c0022t0001 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0018c0028t0001 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0019c0014t0001 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0020c0027t0001 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0021c0024t0001 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0022c0026t0001 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0023c0036t0001 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0024c0023t0001 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0025c0021t0001 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0026c0017t0001 | 0/0 | 1395 | 1 | 0 | 0 | 0 | 0 | 1 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0027c0020t0001 | 0/0 | 1395 | 1 | 0 | 0 | 0 | 0 | 1 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0028c0015t0001 | 0/0 | 1395 | 1 | 0 | 0 | 0 | 0 | 1 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0029c0019t0001 | 0/0 | 1395 | 1 | 0 | 0 | 0 | 0 | 1 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0030c0025t0001 | 0/0 | 1395 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0031c0016t0001 | 0/0 | 1395 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0032c0029t0001 | 0/0 | 1395 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0033c0030t0001 | 0/0 | 1395 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
a0034c0034t0001 | 0/0 | 1395 | 1 | 0 | 0 | 0 | 1 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | ATGAT others(1390): Show |
chr8 | 7756330 | 7769340 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 10 | 0 | 3 | 5 | 2 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0001c0018t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0002c0002t0001g0005 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0002c0002t0001g0008 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0002c0002t0001g0009 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0002c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0003c0003t0001g0002 | 0/0 | 4 | 1 | 0 | 1 | 0 | 2 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0003c0003t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0004c0004t0001g0003 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0005c0005t0001g0004 | 0/0 | 5 | 0 | 0 | 2 | 0 | 3 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0006c0007t0001g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0006c0007t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0007c0006t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0007c0006t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0008c0008t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0008c0008t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0008c0008t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0009c0009t0001g0002 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0010c0011t0001g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0011c0033t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0011c0035t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0012c0012t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0012c0012t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0013c0010t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0014c0013t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0014c0013t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0015c0032t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0016c0031t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0017c0022t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0018c0028t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0019c0014t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0020c0027t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0021c0024t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0022c0026t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0023c0036t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0024c0023t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0025c0021t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0026c0017t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0027c0020t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0028c0015t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0029c0019t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0030c0025t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0031c0016t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0032c0029t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0033c0030t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
a0034c0034t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG00099 | hp2 | a0006 | c0007 | t0001 | g0033 | EUR | GBR | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG00609 | hp1 | a0008 | c0008 | t0001 | g0020 | EAS | CHS | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG00609 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | CHS | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | CHS | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG00621 | hp2 | a0007 | c0006 | t0001 | g0006 | EAS | CHS | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG00639 | hp1 | a0016 | c0031 | t0001 | g0024 | AMR | PUR | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG00639 | hp2 | a0009 | c0009 | t0001 | g0002 | AMR | PUR | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG00642 | hp2 | a0003 | c0003 | t0001 | g0021 | AMR | PUR | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG00733 | hp1 | a0017 | c0022 | t0001 | g0019 | AMR | PUR | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0038 | AMR | PUR | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG01106 | hp2 | a0006 | c0007 | t0001 | g0007 | AMR | PUR | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG01261 | hp2 | a0018 | c0028 | t0001 | g0005 | AMR | CLM | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0008 | EUR | IBS | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG01943 | hp1 | a0004 | c0004 | t0001 | g0003 | AMR | PEL | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG01943 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG01981 | hp1 | a0019 | c0014 | t0001 | g0040 | AMR | PEL | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG01981 | hp2 | a0009 | c0009 | t0001 | g0002 | AMR | PEL | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG02080 | hp2 | a0010 | c0011 | t0001 | g0010 | EAS | KHV | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG02300 | hp1 | a0004 | c0004 | t0001 | g0003 | AMR | PEL | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG02300 | hp2 | a0010 | c0011 | t0001 | g0010 | AMR | PEL | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG02615 | hp1 | a0011 | c0035 | t0001 | g0016 | AFR | GWD | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG02615 | hp2 | a0012 | c0012 | t0001 | g0015 | AFR | GWD | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG02723 | hp1 | a0020 | c0027 | t0001 | g0018 | AFR | GWD | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG02723 | hp2 | a0021 | c0024 | t0001 | g0036 | AFR | GWD | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG02895 | hp1 | a0001 | c0018 | t0001 | g0034 | AFR | GWD | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG02895 | hp2 | a0022 | c0026 | t0001 | g0028 | AFR | GWD | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG02896 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG02897 | hp1 | a0023 | c0036 | t0001 | g0003 | AFR | GWD | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG02897 | hp2 | a0024 | c0023 | t0001 | g0027 | AFR | GWD | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG03098 | hp1 | a0012 | c0012 | t0001 | g0007 | AFR | MSL | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG03130 | hp1 | a0025 | c0021 | t0001 | g0026 | AFR | ESN | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG03130 | hp2 | a0003 | c0003 | t0001 | g0002 | AFR | ESN | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG03239 | hp1 | a0005 | c0005 | t0001 | g0004 | SAS | PJL | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG03239 | hp2 | a0026 | c0017 | t0001 | g0012 | SAS | PJL | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG03490 | hp1 | a0005 | c0005 | t0001 | g0004 | SAS | PJL | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG03490 | hp2 | a0008 | c0008 | t0001 | g0012 | SAS | PJL | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG03669 | hp1 | a0027 | c0020 | t0001 | g0011 | SAS | PJL | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG03669 | hp2 | a0009 | c0009 | t0001 | g0002 | SAS | PJL | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG03710 | hp1 | a0005 | c0005 | t0001 | g0004 | SAS | PJL | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG03710 | hp2 | a0028 | c0015 | t0001 | g0001 | SAS | PJL | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG03927 | hp1 | a0029 | c0019 | t0001 | g0011 | SAS | BEB | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG03927 | hp2 | a0003 | c0003 | t0001 | g0002 | SAS | BEB | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0009 | SAS | BEB | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG04184 | hp2 | a0002 | c0002 | t0001 | g0009 | SAS | BEB | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0008 | SAS | STU | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
HG04204 | hp2 | a0003 | c0003 | t0001 | g0002 | SAS | STU | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
NA18939 | hp1 | a0005 | c0005 | t0001 | g0004 | EAS | JPT | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
NA18939 | hp2 | a0007 | c0006 | t0001 | g0006 | EAS | JPT | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
NA18957 | hp2 | a0004 | c0004 | t0001 | g0003 | EAS | JPT | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
NA18962 | hp1 | a0030 | c0025 | t0001 | g0025 | EAS | JPT | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
NA18962 | hp2 | a0007 | c0006 | t0001 | g0006 | EAS | JPT | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
NA18973 | hp2 | a0005 | c0005 | t0001 | g0004 | EAS | JPT | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
NA18974 | hp1 | a0004 | c0004 | t0001 | g0003 | EAS | JPT | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
NA18974 | hp2 | a0031 | c0016 | t0001 | g0006 | EAS | JPT | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
NA19004 | hp1 | a0013 | c0010 | t0001 | g0014 | EAS | JPT | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
NA19005 | hp1 | a0014 | c0013 | t0001 | g0037 | EAS | JPT | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
NA19005 | hp2 | a0008 | c0008 | t0001 | g0029 | EAS | JPT | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
NA19007 | hp1 | a0006 | c0007 | t0001 | g0007 | EAS | JPT | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
NA19007 | hp2 | a0014 | c0013 | t0001 | g0015 | EAS | JPT | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
NA19043 | hp1 | a0015 | c0032 | t0001 | g0023 | AFR | LWK | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
NA19043 | hp2 | a0011 | c0033 | t0001 | g0017 | AFR | LWK | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
NA19063 | hp2 | a0032 | c0029 | t0001 | g0041 | EAS | JPT | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
NA19067 | hp1 | a0013 | c0010 | t0001 | g0014 | EAS | JPT | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
NA19081 | hp2 | a0006 | c0007 | t0001 | g0007 | EAS | JPT | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
NA19087 | hp1 | a0033 | c0030 | t0001 | g0039 | EAS | JPT | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
NA19087 | hp2 | a0004 | c0004 | t0001 | g0003 | EAS | JPT | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
NA20805 | hp1 | a0034 | c0034 | t0001 | g0004 | EUR | TSI | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
NA20805 | hp2 | a0007 | c0006 | t0001 | g0022 | EUR | TSI | FAM90A9_chr8_7756330_7769340 | FAM90A9 | chr8 | 7756330 | 7769340 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:7761400 | G | A | 1 | a0013 | 2 | NA19004.hp1 NA19067.hp1 |
missense_variant | MODERATE | c.71G>A | p.Arg24Gln | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 1/4 | 71/1395 | 71/1395 | 24/464 | chr8 | 7761400 | |||
chr8:7761418 | C | G | 2 | a0013 a0023 |
3 | HG02897.hp1 NA19004.hp1 NA19067.hp1 |
missense_variant | MODERATE | c.89C>G | p.Pro30Arg | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 1/4 | 89/1395 | 89/1395 | 30/464 | chr8 | 7761418 | |||
chr8:7761422 | G | C | 1 | a0019 | 1 | HG01981.hp1 | missense_variant | MODERATE | c.93G>C | p.Arg31Ser | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 1/4 | 93/1395 | 93/1395 | 31/464 | chr8 | 7761422 | |||
chr8:7761996 | G | C | 1 | a0028 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.173G>C | p.Arg58Thr | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 2/4 | 173/1395 | 173/1395 | 58/464 | chr8 | 7761996 | |||
chr8:7762076 | T | C | 3 | a0008 a0026 a0031 |
5 | HG00609.hp1 HG03239.hp2 HG03490.hp2 others(2): Show |
missense_variant | MODERATE | c.253T>C | p.Trp85Arg | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 2/4 | 253/1395 | 253/1395 | 85/464 | chr8 | 7762076 | |||
chr8:7762089 | T | C | 5 | a0003 a0007 a0009 others(2): Show |
15 | HG00609.hp2 HG00621.hp2 HG00639.hp2 others(12): Show |
missense_variant | MODERATE | c.266T>C | p.Val89Ala | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 2/4 | 266/1395 | 266/1395 | 89/464 | chr8 | 7762089 | |||
chr8:7762089 | T | G | 18 | a0001 a0004 a0006 others(15): Show |
50 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(47): Show |
missense_variant | MODERATE | c.266T>G | p.Val89Gly | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 2/4 | 266/1395 | 266/1395 | 89/464 | chr8 | 7762089 | |||
chr8:7762705 | C | T | 21 | a0001 a0003 a0004 others(18): Show |
63 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(60): Show |
missense_variant | MODERATE | c.424C>T | p.His142Tyr | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 3/4 | 424/1395 | 424/1395 | 142/464 | chr8 | 7762705 | |||
chr8:7762712 | G | C | 1 | a0025 | 1 | HG03130.hp1 | missense_variant&splice_region_variant | MODERATE | c.431G>C | p.Arg144Thr | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 3/4 | 431/1395 | 431/1395 | 144/464 | chr8 | 7762712 | |||
chr8:7763409 | C | G | 1 | a0022 | 1 | HG02895.hp2 | missense_variant | MODERATE | c.464C>G | p.Thr155Ser | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 464/1395 | 464/1395 | 155/464 | chr8 | 7763409 | |||
chr8:7763426 | G | T | 21 | a0001 a0003 a0004 others(18): Show |
63 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(60): Show |
missense_variant | MODERATE | c.481G>T | p.Val161Leu | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 481/1395 | 481/1395 | 161/464 | chr8 | 7763426 | |||
chr8:7763435 | G | A | 2 | a0017 a0022 |
2 | HG00733.hp1 HG02895.hp2 |
missense_variant | MODERATE | c.490G>A | p.Val164Ile | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 490/1395 | 490/1395 | 164/464 | chr8 | 7763435 | |||
chr8:7763441 | G | A | 2 | a0022 a0024 |
2 | HG02895.hp2 HG02897.hp2 |
missense_variant | MODERATE | c.496G>A | p.Ala166Thr | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 496/1395 | 496/1395 | 166/464 | chr8 | 7763441 | |||
chr8:7763456 | G | A | 21 | a0001 a0003 a0004 others(18): Show |
63 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(60): Show |
missense_variant | MODERATE | c.511G>A | p.Ala171Thr | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 511/1395 | 511/1395 | 171/464 | chr8 | 7763456 | |||
chr8:7763460 | A | C | 14 | a0001 a0004 a0006 others(11): Show |
44 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(41): Show |
missense_variant | MODERATE | c.515A>C | p.Glu172Ala | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 515/1395 | 515/1395 | 172/464 | chr8 | 7763460 | |||
chr8:7763477 | T | A | 2 | a0013 a0023 |
3 | HG02897.hp1 NA19004.hp1 NA19067.hp1 |
missense_variant | MODERATE | c.532T>A | p.Ser178Thr | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 532/1395 | 532/1395 | 178/464 | chr8 | 7763477 | |||
chr8:7763540 | C | T | 1 | a0025 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.595C>T | p.Pro199Ser | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 595/1395 | 595/1395 | 199/464 | chr8 | 7763540 | |||
chr8:7763564 | G | T | 1 | a0034 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.619G>T | p.Ala207Ser | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 619/1395 | 619/1395 | 207/464 | chr8 | 7763564 | |||
chr8:7763575 | G | C | 8 | a0002 a0005 a0016 others(5): Show |
23 | HG00621.hp1 HG00639.hp1 HG01074.hp1 others(20): Show |
missense_variant | MODERATE | c.630G>C | p.Met210Ile | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 630/1395 | 630/1395 | 210/464 | chr8 | 7763575 | |||
chr8:7763637 | G | T | 1 | a0014 | 2 | NA19005.hp1 NA19007.hp2 |
missense_variant | MODERATE | c.692G>T | p.Ser231Ile | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 692/1395 | 692/1395 | 231/464 | chr8 | 7763637 | |||
chr8:7763638 | C | G | 1 | a0025 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.693C>G | p.Ser231Arg | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 693/1395 | 693/1395 | 231/464 | chr8 | 7763638 | |||
chr8:7763639 | A | C | 27 | a0001 a0002 a0003 others(24): Show |
81 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(78): Show |
missense_variant | MODERATE | c.694A>C | p.Ser232Arg | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 694/1395 | 694/1395 | 232/464 | chr8 | 7763639 | |||
chr8:7763639 | A | G | 1 | a0025 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.694A>G | p.Ser232Gly | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 694/1395 | 694/1395 | 232/464 | chr8 | 7763639 | |||
chr8:7763652 | G | A | 4 | a0002 a0018 a0032 others(1): Show |
15 | HG00621.hp1 HG01074.hp1 HG01074.hp2 others(12): Show |
missense_variant | MODERATE | c.707G>A | p.Gly236Asp | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 707/1395 | 707/1395 | 236/464 | chr8 | 7763652 | |||
chr8:7763697 | T | C | 3 | a0017 a0022 a0025 |
3 | HG00733.hp1 HG02895.hp2 HG03130.hp1 |
missense_variant | MODERATE | c.752T>C | p.Leu251Pro | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 752/1395 | 752/1395 | 251/464 | chr8 | 7763697 | |||
chr8:7763705 | G | T | 4 | a0007 a0008 a0010 others(1): Show |
10 | HG00609.hp1 HG00621.hp2 HG02080.hp2 others(7): Show |
missense_variant | MODERATE | c.760G>T | p.Ala254Ser | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 760/1395 | 760/1395 | 254/464 | chr8 | 7763705 | |||
chr8:7763717 | G | A | 2 | a0004 a0019 |
6 | HG01943.hp1 HG01981.hp1 HG02300.hp1 others(3): Show |
missense_variant | MODERATE | c.772G>A | p.Ala258Thr | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 772/1395 | 772/1395 | 258/464 | chr8 | 7763717 | |||
chr8:7763741 | A | T | 2 | a0024 a0030 |
2 | HG02897.hp2 NA18962.hp1 |
missense_variant | MODERATE | c.796A>T | p.Thr266Ser | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 796/1395 | 796/1395 | 266/464 | chr8 | 7763741 | |||
chr8:7763744 | T | C | 4 | a0007 a0008 a0010 others(1): Show |
10 | HG00609.hp1 HG00621.hp2 HG02080.hp2 others(7): Show |
missense_variant | MODERATE | c.799T>C | p.Ser267Pro | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 799/1395 | 799/1395 | 267/464 | chr8 | 7763744 | |||
chr8:7763748 | A | T | 2 | a0017 a0022 |
2 | HG00733.hp1 HG02895.hp2 |
missense_variant | MODERATE | c.803A>T | p.Gln268Leu | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 803/1395 | 803/1395 | 268/464 | chr8 | 7763748 | |||
chr8:7763834 | C | A | 1 | a0030 | 1 | NA18962.hp1 | missense_variant | MODERATE | c.889C>A | p.Pro297Thr | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 889/1395 | 889/1395 | 297/464 | chr8 | 7763834 | |||
chr8:7763888 | A | G | 1 | a0025 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.943A>G | p.Ile315Val | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 943/1395 | 943/1395 | 315/464 | chr8 | 7763888 | |||
chr8:7763924 | G | A | 1 | a0026 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.979G>A | p.Ala327Thr | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 979/1395 | 979/1395 | 327/464 | chr8 | 7763924 | |||
chr8:7763928 | C | T | 2 | a0027 a0029 |
2 | HG03669.hp1 HG03927.hp1 |
missense_variant | MODERATE | c.983C>T | p.Pro328Leu | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 983/1395 | 983/1395 | 328/464 | chr8 | 7763928 | |||
chr8:7763952 | C | A | 2 | a0003 a0009 |
8 | HG00609.hp2 HG00639.hp2 HG00642.hp2 others(5): Show |
missense_variant | MODERATE | c.1007C>A | p.Ala336Asp | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 1007/1395 | 1007/1395 | 336/464 | chr8 | 7763952 | |||
chr8:7763969 | C | A | 2 | a0027 a0029 |
2 | HG03669.hp1 HG03927.hp1 |
missense_variant | MODERATE | c.1024C>A | p.Pro342Thr | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 1024/1395 | 1024/1395 | 342/464 | chr8 | 7763969 | |||
chr8:7764023 | G | A | 1 | a0010 | 2 | HG02080.hp2 HG02300.hp2 |
missense_variant | MODERATE | c.1078G>A | p.Asp360Asn | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 1078/1395 | 1078/1395 | 360/464 | chr8 | 7764023 | |||
chr8:7764025 | C | A | 1 | a0029 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.1080C>A | p.Asp360Glu | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 1080/1395 | 1080/1395 | 360/464 | chr8 | 7764025 | |||
chr8:7764045 | C | G | 17 | a0001 a0003 a0004 others(14): Show |
58 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(55): Show |
missense_variant | MODERATE | c.1100C>G | p.Thr367Arg | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 1100/1395 | 1100/1395 | 367/464 | chr8 | 7764045 | |||
chr8:7764056 | C | A | 1 | a0009 | 3 | HG00639.hp2 HG01981.hp2 HG03669.hp2 |
missense_variant | MODERATE | c.1111C>A | p.Pro371Thr | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 1111/1395 | 1111/1395 | 371/464 | chr8 | 7764056 | |||
chr8:7764089 | T | C | 2 | a0003 a0009 |
8 | HG00609.hp2 HG00639.hp2 HG00642.hp2 others(5): Show |
missense_variant | MODERATE | c.1144T>C | p.Ser382Pro | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 1144/1395 | 1144/1395 | 382/464 | chr8 | 7764089 | |||
chr8:7764092 | G | A | 1 | a0004 | 5 | HG01943.hp1 HG02300.hp1 NA18957.hp2 others(2): Show |
missense_variant | MODERATE | c.1147G>A | p.Ala383Thr | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 1147/1395 | 1147/1395 | 383/464 | chr8 | 7764092 | |||
chr8:7764098 | A | G | 7 | a0007 a0008 a0010 others(4): Show |
13 | HG00609.hp1 HG00621.hp2 HG01261.hp2 others(10): Show |
missense_variant | MODERATE | c.1153A>G | p.Ser385Gly | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 1153/1395 | 1153/1395 | 385/464 | chr8 | 7764098 | |||
chr8:7764128 | C | T | 1 | a0025 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.1183C>T | p.Leu395Phe | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 1183/1395 | 1183/1395 | 395/464 | chr8 | 7764128 | |||
chr8:7764174 | C | A | 2 | a0003 a0009 |
8 | HG00609.hp2 HG00639.hp2 HG00642.hp2 others(5): Show |
missense_variant | MODERATE | c.1229C>A | p.Ala410Glu | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 1229/1395 | 1229/1395 | 410/464 | chr8 | 7764174 | |||
chr8:7764228 | C | G | 1 | a0012 | 2 | HG02615.hp2 HG03098.hp1 |
missense_variant | MODERATE | c.1283C>G | p.Pro428Arg | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 1283/1395 | 1283/1395 | 428/464 | chr8 | 7764228 | |||
chr8:7764316 | G | C | 1 | a0010 | 2 | HG02080.hp2 HG02300.hp2 |
missense_variant | MODERATE | c.1371G>C | p.Glu457Asp | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 1371/1395 | 1371/1395 | 457/464 | chr8 | 7764316 | |||
chr8:7764319 | C | G | 1 | a0008 | 3 | HG00609.hp1 HG03490.hp2 NA19005.hp2 |
missense_variant | MODERATE | c.1374C>G | p.Asp458Glu | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 1374/1395 | 1374/1395 | 458/464 | chr8 | 7764319 | |||
chr8:7764327 | C | T | 4 | a0006 a0012 a0013 others(1): Show |
9 | HG00099.hp2 HG01106.hp2 HG02615.hp2 others(6): Show |
missense_variant | MODERATE | c.1382C>T | p.Ser461Phe | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 1382/1395 | 1382/1395 | 461/464 | chr8 | 7764327 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:7761434 | C | T | 1 | a0011c0035 | 1 | HG02615.hp1 | synonymous_variant | LOW | c.105C>T | p.Pro35Pro | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 1/4 | 105/1395 | 105/1395 | 35/464 | chr8 | 7761434 | |||
chr8:7762084 | C | T | 1 | a0011c0035 | 1 | HG02615.hp1 | synonymous_variant | LOW | c.261C>T | p.Pro87Pro | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 2/4 | 261/1395 | 261/1395 | 87/464 | chr8 | 7762084 | |||
chr8:7762096 | C | A | 1 | a0001c0018 | 1 | HG02895.hp1 | synonymous_variant | LOW | c.273C>A | p.Ala91Ala | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 2/4 | 273/1395 | 273/1395 | 91/464 | chr8 | 7762096 | |||
chr8:7762695 | G | A | 24 | a0001c0001 a0001c0018 a0003c0003 others(21): Show |
65 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(62): Show |
synonymous_variant | LOW | c.414G>A | p.Glu138Glu | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 3/4 | 414/1395 | 414/1395 | 138/464 | chr8 | 7762695 | |||
chr8:7763452 | A | C | 7 | a0003c0003 a0007c0006 a0008c0008 others(4): Show |
19 | HG00609.hp1 HG00609.hp2 HG00621.hp2 others(16): Show |
synonymous_variant | LOW | c.507A>C | p.Ser169Ser | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 507/1395 | 507/1395 | 169/464 | chr8 | 7763452 | |||
chr8:7763455 | T | A | 7 | a0003c0003 a0007c0006 a0008c0008 others(4): Show |
19 | HG00609.hp1 HG00609.hp2 HG00621.hp2 others(16): Show |
synonymous_variant | LOW | c.510T>A | p.Ala170Ala | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 510/1395 | 510/1395 | 170/464 | chr8 | 7763455 | |||
chr8:7763557 | A | T | 6 | a0003c0003 a0007c0006 a0008c0008 others(3): Show |
17 | HG00609.hp1 HG00609.hp2 HG00621.hp2 others(14): Show |
synonymous_variant | LOW | c.612A>T | p.Thr204Thr | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 612/1395 | 612/1395 | 204/464 | chr8 | 7763557 | |||
chr8:7763569 | C | T | 1 | a0025c0021 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.624C>T | p.Ala208Ala | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 624/1395 | 624/1395 | 208/464 | chr8 | 7763569 | |||
chr8:7763605 | C | G | 1 | a0022c0026 | 1 | HG02895.hp2 | synonymous_variant | LOW | c.660C>G | p.Arg220Arg | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 660/1395 | 660/1395 | 220/464 | chr8 | 7763605 | |||
chr8:7763644 | C | T | 2 | a0027c0020 a0029c0019 |
2 | HG03669.hp1 HG03927.hp1 |
synonymous_variant | LOW | c.699C>T | p.Pro233Pro | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 699/1395 | 699/1395 | 233/464 | chr8 | 7763644 | |||
chr8:7763692 | C | A | 3 | a0017c0022 a0022c0026 a0025c0021 |
3 | HG00733.hp1 HG02895.hp2 HG03130.hp1 |
synonymous_variant | LOW | c.747C>A | p.Gly249Gly | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 747/1395 | 747/1395 | 249/464 | chr8 | 7763692 | |||
chr8:7763692 | C | T | 2 | a0024c0023 a0030c0025 |
2 | HG02897.hp2 NA18962.hp1 |
synonymous_variant | LOW | c.747C>T | p.Gly249Gly | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 747/1395 | 747/1395 | 249/464 | chr8 | 7763692 | |||
chr8:7763704 | C | T | 1 | a0025c0021 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.759C>T | p.Ala253Ala | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 759/1395 | 759/1395 | 253/464 | chr8 | 7763704 | |||
chr8:7763737 | G | T | 2 | a0024c0023 a0030c0025 |
2 | HG02897.hp2 NA18962.hp1 |
synonymous_variant | LOW | c.792G>T | p.Ala264Ala | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 792/1395 | 792/1395 | 264/464 | chr8 | 7763737 | |||
chr8:7763746 | G | A | 22 | a0001c0001 a0001c0018 a0003c0003 others(19): Show |
63 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(60): Show |
synonymous_variant | LOW | c.801G>A | p.Ser267Ser | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 801/1395 | 801/1395 | 267/464 | chr8 | 7763746 | |||
chr8:7763746 | G | T | 2 | a0024c0023 a0030c0025 |
2 | HG02897.hp2 NA18962.hp1 |
synonymous_variant | LOW | c.801G>T | p.Ser267Ser | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 801/1395 | 801/1395 | 267/464 | chr8 | 7763746 | |||
chr8:7763953 | C | G | 1 | a0022c0026 | 1 | HG02895.hp2 | synonymous_variant | LOW | c.1008C>G | p.Ala336Ala | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 1008/1395 | 1008/1395 | 336/464 | chr8 | 7763953 | |||
chr8:7764073 | C | T | 1 | a0033c0030 | 1 | NA19087.hp1 | synonymous_variant | LOW | c.1128C>T | p.Cys376Cys | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 1128/1395 | 1128/1395 | 376/464 | chr8 | 7764073 | |||
chr8:7764214 | C | T | 8 | a0003c0003 a0007c0006 a0008c0008 others(5): Show |
20 | HG00609.hp1 HG00609.hp2 HG00621.hp2 others(17): Show |
synonymous_variant | LOW | c.1269C>T | p.Phe423Phe | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 1269/1395 | 1269/1395 | 423/464 | chr8 | 7764214 | |||
chr8:7764226 | C | T | 2 | a0017c0022 a0024c0023 |
2 | HG00733.hp1 HG02897.hp2 |
synonymous_variant | LOW | c.1281C>T | p.Ser427Ser | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 4/4 | 1281/1395 | 1281/1395 | 427/464 | chr8 | 7764226 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:7761459 | C | G | 30 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(27): Show |
55 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(52): Show |
splice_region_variant&intron_variant | LOW | c.123+7C>G | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 1/3 | chr8 | 7761459 | |||||||
chr8:7761468 | G | C | 5 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0031 others(2): Show |
14 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.123+16G>C | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 1/3 | chr8 | 7761468 | |||||||
chr8:7761472 | T | A | 1 | a0010c0011t0001g0010 | 2 | HG02080.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.123+20T>A | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 1/3 | chr8 | 7761472 | |||||||
chr8:7761491 | G | A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0028c0015t0001g0001 |
12 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.123+39G>A | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 1/3 | chr8 | 7761491 | |||||||
chr8:7761493 | T | G | 1 | a0011c0035t0001g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.123+41T>G | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 1/3 | chr8 | 7761493 | |||||||
chr8:7761511 | G | C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0035 a0001c0018t0001g0034 others(1): Show |
5 | HG00099.hp2 HG01071.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+59G>C | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 1/3 | chr8 | 7761511 | |||||||
chr8:7761668 | A | C | 3 | a0008c0008t0001g0012 a0008c0008t0001g0029 a0026c0017t0001g0012 |
3 | HG03239.hp2 HG03490.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.123+216A>C | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 1/3 | chr8 | 7761668 | |||||||
chr8:7761696 | G | T | 1 | a0001c0001t0001g0035 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.123+244G>T | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 1/3 | chr8 | 7761696 | |||||||
chr8:7761706 | T | A | 1 | a0001c0001t0001g0035 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.124-241T>A | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 1/3 | chr8 | 7761706 | |||||||
chr8:7761719 | C | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0031 others(5): Show |
17 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.124-228C>G | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 1/3 | chr8 | 7761719 | |||||||
chr8:7761765 | C | A | 37 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(34): Show |
66 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.124-182C>A | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 1/3 | chr8 | 7761765 | |||||||
chr8:7761768 | T | C | 4 | a0005c0005t0001g0004 a0011c0033t0001g0017 a0020c0027t0001g0018 others(1): Show |
8 | HG02723.hp1 HG03239.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.124-179T>C | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 1/3 | chr8 | 7761768 | |||||||
chr8:7761790 | T | C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0004c0004t0001g0003 others(3): Show |
12 | HG01943.hp1 HG02300.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.124-157T>C | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 1/3 | chr8 | 7761790 | |||||||
chr8:7761792 | C | T | 38 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(35): Show |
63 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.124-155C>T | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 1/3 | chr8 | 7761792 | |||||||
chr8:7761795 | G | A | 1 | a0017c0022t0001g0019 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.124-152G>A | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 1/3 | chr8 | 7761795 | |||||||
chr8:7761798 | C | G | 22 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0032 others(19): Show |
41 | HG00099.hp1 HG00609.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.124-149C>G | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 1/3 | chr8 | 7761798 | |||||||
chr8:7761801 | T | G | 1 | a0030c0025t0001g0025 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.124-146T>G | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 1/3 | chr8 | 7761801 | |||||||
chr8:7761805 | G | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(36): Show |
64 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.124-142G>A | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 1/3 | chr8 | 7761805 | |||||||
chr8:7761816 | G | A | 1 | a0001c0001t0001g0031 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.124-131G>A | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 1/3 | chr8 | 7761816 | |||||||
chr8:7761822 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.124-125A>G | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 1/3 | chr8 | 7761822 | |||||||
chr8:7761943 | A | G | 25 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(22): Show |
42 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(39): Show |
splice_region_variant&intron_variant | LOW | c.124-4A>G | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 1/3 | chr8 | 7761943 | |||||||
chr8:7762152 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA19081.hp1 | splice_region_variant&intron_variant | LOW | c.323+6C>T | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 2/3 | chr8 | 7762152 | |||||||
chr8:7762177 | T | A | 1 | a0022c0026t0001g0028 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.323+31T>A | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 2/3 | chr8 | 7762177 | |||||||
chr8:7762178 | A | G | 2 | a0017c0022t0001g0019 a0022c0026t0001g0028 |
2 | HG00733.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.323+32A>G | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 2/3 | chr8 | 7762178 | |||||||
chr8:7762181 | A | G | 40 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(37): Show |
65 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.323+35A>G | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 2/3 | chr8 | 7762181 | |||||||
chr8:7762183 | G | A | 40 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(37): Show |
65 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.323+37G>A | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 2/3 | chr8 | 7762183 | |||||||
chr8:7762185 | T | G | 29 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(26): Show |
49 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.323+39T>G | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 2/3 | chr8 | 7762185 | |||||||
chr8:7762192 | T | C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(18): Show |
38 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.323+46T>C | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 2/3 | chr8 | 7762192 | |||||||
chr8:7762205 | T | C | 4 | a0008c0008t0001g0012 a0008c0008t0001g0020 a0008c0008t0001g0029 others(1): Show |
4 | HG00609.hp1 HG03239.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.323+59T>C | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 2/3 | chr8 | 7762205 | |||||||
chr8:7762224 | T | C | 3 | a0003c0003t0001g0002 a0003c0003t0001g0021 a0009c0009t0001g0002 |
8 | HG00609.hp2 HG00639.hp2 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.323+78T>C | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 2/3 | chr8 | 7762224 | |||||||
chr8:7762255 | G | A | 38 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(35): Show |
63 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.323+109G>A | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 2/3 | chr8 | 7762255 | |||||||
chr8:7762291 | C | G | 1 | a0008c0008t0001g0029 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.323+145C>G | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 2/3 | chr8 | 7762291 | |||||||
chr8:7762294 | G | A | 1 | a0014c0013t0001g0037 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.323+148G>A | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 2/3 | chr8 | 7762294 | |||||||
chr8:7762296 | T | C | 1 | a0025c0021t0001g0026 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.323+150T>C | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 2/3 | chr8 | 7762296 | |||||||
chr8:7762348 | C | G | 1 | a0001c0001t0001g0035 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.323+202C>G | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 2/3 | chr8 | 7762348 | |||||||
chr8:7762380 | G | C | 38 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(35): Show |
66 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.324-225G>C | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 2/3 | chr8 | 7762380 | |||||||
chr8:7762415 | G | T | 1 | a0013c0010t0001g0014 | 2 | NA19004.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.324-190G>T | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 2/3 | chr8 | 7762415 | |||||||
chr8:7762416 | T | C | 4 | a0008c0008t0001g0012 a0008c0008t0001g0020 a0008c0008t0001g0029 others(1): Show |
4 | HG00609.hp1 HG03239.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.324-189T>C | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 2/3 | chr8 | 7762416 | |||||||
chr8:7762418 | C | G | 38 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(35): Show |
63 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.324-187C>G | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 2/3 | chr8 | 7762418 | |||||||
chr8:7762452 | G | T | 1 | a0011c0035t0001g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.324-153G>T | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 2/3 | chr8 | 7762452 | |||||||
chr8:7762523 | A | ATGGGGCT others(33): Show |
1 | a0001c0001t0001g0043 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.324-60_324-59insTT others(38): Show |
FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 7762523 | ||||||
chr8:7762536 | C | T | 3 | a0003c0003t0001g0002 a0003c0003t0001g0021 a0009c0009t0001g0002 |
8 | HG00609.hp2 HG00639.hp2 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.324-69C>T | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 2/3 | chr8 | 7762536 | |||||||
chr8:7762546 | C | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(46): Show |
84 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.324-59C>T | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 2/3 | chr8 | 7762546 | |||||||
chr8:7762580 | G | C | 6 | a0022c0026t0001g0028 a0024c0023t0001g0027 a0025c0021t0001g0026 others(3): Show |
6 | HG02895.hp2 HG02897.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.324-25G>C | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 2/3 | chr8 | 7762580 | |||||||
chr8:7762591 | T | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(38): Show |
66 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.324-14T>C | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 2/3 | chr8 | 7762591 | |||||||
chr8:7762597 | T | C | 3 | a0007c0006t0001g0006 a0010c0011t0001g0010 a0031c0016t0001g0006 |
6 | HG00621.hp2 HG02080.hp2 HG02300.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.324-8T>C | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 2/3 | chr8 | 7762597 | |||||||
chr8:7762715 | T | C | 38 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(35): Show |
63 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(60): Show |
splice_donor_variant&intron_variant | HIGH | c.432+2T>C | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 3/3 | chr8 | 7762715 | |||||||
chr8:7762740 | C | T | 38 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(35): Show |
63 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.432+27C>T | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 3/3 | chr8 | 7762740 | |||||||
chr8:7762831 | G | T | 1 | a0022c0026t0001g0028 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.432+118G>T | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 3/3 | chr8 | 7762831 | |||||||
chr8:7762839 | C | T | 2 | a0032c0029t0001g0041 a0033c0030t0001g0039 |
2 | NA19063.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.432+126C>T | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 3/3 | chr8 | 7762839 | |||||||
chr8:7762886 | A | G | 1 | a0011c0033t0001g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.432+173A>G | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 3/3 | chr8 | 7762886 | |||||||
chr8:7762887 | G | C | 38 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(35): Show |
63 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.432+174G>C | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 3/3 | chr8 | 7762887 | |||||||
chr8:7762904 | G | T | 39 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(36): Show |
64 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.432+191G>T | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 3/3 | chr8 | 7762904 | |||||||
chr8:7762918 | C | T | 1 | a0025c0021t0001g0026 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.432+205C>T | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 3/3 | chr8 | 7762918 | |||||||
chr8:7762945 | C | T | 2 | a0022c0026t0001g0028 a0025c0021t0001g0026 |
2 | HG02895.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.432+232C>T | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 3/3 | chr8 | 7762945 | |||||||
chr8:7762954 | C | A | 1 | a0007c0006t0001g0022 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.432+241C>A | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 3/3 | chr8 | 7762954 | |||||||
chr8:7762961 | A | G | 1 | a0021c0024t0001g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.432+248A>G | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 3/3 | chr8 | 7762961 | |||||||
chr8:7763010 | G | A | 1 | a0025c0021t0001g0026 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.432+297G>A | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 3/3 | chr8 | 7763010 | |||||||
chr8:7763015 | T | G | 4 | a0003c0003t0001g0002 a0003c0003t0001g0021 a0009c0009t0001g0002 others(1): Show |
10 | HG00609.hp2 HG00639.hp2 HG00642.hp2 others(7): Show |
intron_variant | MODIFIER | c.432+302T>G | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 3/3 | chr8 | 7763015 | |||||||
chr8:7763056 | G | C | 2 | a0032c0029t0001g0041 a0033c0030t0001g0039 |
2 | NA19063.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.433-322G>C | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 3/3 | chr8 | 7763056 | |||||||
chr8:7763067 | C | T | 36 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(33): Show |
59 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.433-311C>T | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 3/3 | chr8 | 7763067 | |||||||
chr8:7763161 | G | A | 1 | a0019c0014t0001g0040 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.433-217G>A | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 3/3 | chr8 | 7763161 | |||||||
chr8:7763290 | C | A | 1 | a0003c0003t0001g0021 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.433-88C>A | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 3/3 | chr8 | 7763290 | |||||||
chr8:7763297 | A | C | 2 | a0022c0026t0001g0028 a0024c0023t0001g0027 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.433-81A>C | FAM90A9 | ENSG00000285607.1 | transcript | ENST00000648344.1 | protein_coding | 3/3 | chr8 | 7763297 |