Item | Value |
---|---|
geneid | 51314 |
ensemblid | ENSG00000086288.12 |
hgncid | 16473 |
symbol | NME8 |
name | NME/NM23 family member 8 |
refseq_nuc | NM_016616.5 |
refseq_prot | NP_057700.3 |
ensembl_nuc | ENST00000199447.9 |
ensembl_prot | ENSP00000199447.4 |
mane_status | MANE Select |
chr | chr7 |
start | 37848597 |
end | 37900397 |
strand | + |
ver | v1.2 |
region | chr7:37848597-37900397 |
region5000 | chr7:37843597-37905397 |
regionname0 | NME8_chr7_37848597_37900397 |
regionname5000 | NME8_chr7_37843597_37905397 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 588 | 158 | 34 | 28 | 68 | 7 | 21 | 52 | NME8_chr7_37843597_37905397 | NME8 | MASKK others(583): Show |
chr7 | 37843597 | 37905397 |
a0002 | 0/0 | 588 | 74 | 5 | 5 | 54 | 1 | 9 | 44 | NME8_chr7_37843597_37905397 | NME8 | MASKK others(583): Show |
chr7 | 37843597 | 37905397 |
a0003 | 0/0 | 588 | 51 | 38 | 3 | 8 | 1 | 1 | 5 | NME8_chr7_37843597_37905397 | NME8 | MASKK others(583): Show |
chr7 | 37843597 | 37905397 |
a0004 | 0/0 | 588 | 32 | 1 | 11 | 15 | 1 | 4 | 13 | NME8_chr7_37843597_37905397 | NME8 | MASKK others(583): Show |
chr7 | 37843597 | 37905397 |
a0005 | 0/0 | 588 | 30 | 0 | 8 | 18 | 3 | 1 | 13 | NME8_chr7_37843597_37905397 | NME8 | MASKK others(583): Show |
chr7 | 37843597 | 37905397 |
a0006 | 0/0 | 588 | 12 | 0 | 4 | 5 | 1 | 2 | 5 | NME8_chr7_37843597_37905397 | NME8 | MASKK others(583): Show |
chr7 | 37843597 | 37905397 |
a0007 | 0/0 | 588 | 8 | 1 | 1 | 6 | 0 | 0 | 5 | NME8_chr7_37843597_37905397 | NME8 | MASKK others(583): Show |
chr7 | 37843597 | 37905397 |
a0008 | 0/0 | 588 | 6 | 0 | 2 | 0 | 2 | 2 | 0 | NME8_chr7_37843597_37905397 | NME8 | MASKK others(583): Show |
chr7 | 37843597 | 37905397 |
a0009 | 0/0 | 588 | 3 | 1 | 0 | 1 | 0 | 1 | 1 | NME8_chr7_37843597_37905397 | NME8 | MASKK others(583): Show |
chr7 | 37843597 | 37905397 |
a0010 | 0/0 | 588 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | MASKK others(583): Show |
chr7 | 37843597 | 37905397 |
a0011 | 0/0 | 588 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | MASKK others(583): Show |
chr7 | 37843597 | 37905397 |
a0012 | 0/0 | 588 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | MASKK others(583): Show |
chr7 | 37843597 | 37905397 |
a0013 | 0/0 | 588 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | MASKK others(583): Show |
chr7 | 37843597 | 37905397 |
a0014 | 0/0 | 545 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | MASKK others(540): Show |
chr7 | 37843597 | 37905397 |
a0015 | 0/0 | 588 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | MASKK others(583): Show |
chr7 | 37843597 | 37905397 |
a0016 | 0/0 | 151 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | MASKK others(146): Show |
chr7 | 37843597 | 37905397 |
a0017 | 0/0 | 588 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | MASKK others(583): Show |
chr7 | 37843597 | 37905397 |
a0018 | 0/0 | 588 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | MASKK others(583): Show |
chr7 | 37843597 | 37905397 |
a0019 | 0/0 | 264 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | MASKK others(259): Show |
chr7 | 37843597 | 37905397 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1764 | 109 | 25 | 23 | 48 | 3 | 10 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0001c0004 | 0/0 | 1764 | 30 | 4 | 4 | 13 | 4 | 5 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0001c0007 | 0/0 | 1764 | 17 | 5 | 1 | 6 | 0 | 5 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0001c0028 | 0/0 | 1764 | 2 | 0 | 0 | 1 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0002c0002 | 0/0 | 1764 | 37 | 5 | 2 | 26 | 0 | 4 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0002c0008 | 0/0 | 1764 | 17 | 0 | 1 | 14 | 0 | 2 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0002c0009 | 0/0 | 1764 | 17 | 0 | 1 | 12 | 1 | 3 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0002c0020 | 0/0 | 1764 | 3 | 0 | 1 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0003c0003 | 0/0 | 1764 | 31 | 22 | 3 | 4 | 1 | 1 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0003c0010 | 0/0 | 1764 | 14 | 10 | 0 | 4 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0003c0015 | 0/0 | 1764 | 4 | 4 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0003c0023 | 0/0 | 1764 | 2 | 2 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0004c0005 | 0/0 | 1764 | 25 | 1 | 11 | 8 | 1 | 4 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0004c0012 | 0/0 | 1764 | 7 | 0 | 0 | 7 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0005c0006 | 0/0 | 1764 | 18 | 0 | 4 | 12 | 2 | 0 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0005c0014 | 0/0 | 1764 | 5 | 0 | 0 | 4 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0005c0019 | 0/0 | 1764 | 3 | 0 | 3 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0005c0024 | 0/0 | 1764 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0005c0025 | 0/0 | 1764 | 2 | 0 | 1 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0006c0011 | 0/0 | 1764 | 8 | 0 | 2 | 4 | 1 | 1 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0006c0016 | 0/0 | 1764 | 4 | 0 | 2 | 1 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0007c0017 | 0/0 | 1764 | 4 | 1 | 1 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0007c0018 | 0/0 | 1764 | 4 | 0 | 0 | 4 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0008c0013 | 0/0 | 1764 | 6 | 0 | 2 | 0 | 2 | 2 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0009c0022 | 0/0 | 1764 | 2 | 1 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0009c0031 | 0/0 | 1764 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0010c0026 | 0/0 | 1764 | 2 | 0 | 2 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0011c0029 | 0/0 | 1764 | 2 | 1 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0012c0021 | 0/0 | 1764 | 2 | 1 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0013c0027 | 0/0 | 1764 | 2 | 2 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0014c0032 | 0/0 | 1764 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0015c0033 | 0/0 | 1764 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0016c0036 | 0/0 | 1764 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0017c0034 | 0/0 | 1764 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0018c0035 | 0/0 | 1764 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 | ||
a0019c0030 | 0/0 | 1764 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | ATGGC others(1759): Show |
chr7 | 37843597 | 37905397 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2308 | 55 | 20 | 10 | 18 | 2 | 5 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0001c0001t0003 | 0/0 | 2308 | 28 | 1 | 7 | 16 | 1 | 3 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0001c0001t0004 | 0/0 | 2308 | 22 | 0 | 6 | 14 | 0 | 2 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0001c0001t0005 | 0/0 | 2308 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0001c0001t0006 | 0/0 | 2308 | 2 | 2 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0001c0001t0007 | 0/0 | 2308 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0001c0004t0001 | 0/0 | 2308 | 14 | 2 | 1 | 7 | 1 | 3 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0001c0004t0003 | 0/0 | 2308 | 12 | 0 | 2 | 6 | 2 | 2 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0001c0004t0004 | 0/0 | 2308 | 2 | 0 | 1 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0001c0004t0005 | 0/0 | 2308 | 2 | 2 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0001c0007t0001 | 0/0 | 2308 | 14 | 4 | 1 | 6 | 0 | 3 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0001c0007t0003 | 0/0 | 2308 | 2 | 0 | 0 | 0 | 0 | 2 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0001c0007t0007 | 0/0 | 2308 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0001c0028t0001 | 0/0 | 2308 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0001c0028t0003 | 0/0 | 2308 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0002c0002t0001 | 0/0 | 2308 | 37 | 5 | 2 | 26 | 0 | 4 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0002c0008t0001 | 0/0 | 2308 | 17 | 0 | 1 | 14 | 0 | 2 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0002c0009t0001 | 0/0 | 2308 | 17 | 0 | 1 | 12 | 1 | 3 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0002c0020t0001 | 0/0 | 2308 | 3 | 0 | 1 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0003c0003t0001 | 0/0 | 2308 | 7 | 2 | 0 | 4 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0003c0003t0002 | 0/0 | 2308 | 23 | 19 | 3 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0003c0003t0008 | 0/0 | 2308 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0003c0010t0001 | 0/0 | 2308 | 5 | 1 | 0 | 4 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0003c0010t0002 | 0/0 | 2308 | 9 | 9 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0003c0015t0001 | 0/0 | 2308 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0003c0015t0002 | 0/0 | 2308 | 3 | 3 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0003c0023t0001 | 0/0 | 2308 | 2 | 2 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0004c0005t0001 | 0/0 | 2308 | 17 | 0 | 9 | 3 | 1 | 4 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0004c0005t0003 | 0/0 | 2308 | 7 | 1 | 2 | 4 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0004c0005t0004 | 0/0 | 2308 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0004c0012t0001 | 0/0 | 2308 | 5 | 0 | 0 | 5 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0004c0012t0004 | 0/0 | 2308 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0005c0006t0002 | 0/0 | 2308 | 18 | 0 | 4 | 12 | 2 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0005c0014t0002 | 0/0 | 2308 | 5 | 0 | 0 | 4 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0005c0019t0002 | 0/0 | 2308 | 3 | 0 | 3 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0005c0024t0002 | 0/0 | 2308 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0005c0025t0002 | 0/0 | 2308 | 2 | 0 | 1 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0006c0011t0002 | 0/0 | 2308 | 8 | 0 | 2 | 4 | 1 | 1 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0006c0016t0002 | 0/0 | 2308 | 4 | 0 | 2 | 1 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0007c0017t0001 | 0/0 | 2308 | 4 | 1 | 1 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0007c0018t0001 | 0/0 | 2308 | 4 | 0 | 0 | 4 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0008c0013t0002 | 0/0 | 2308 | 6 | 0 | 2 | 0 | 2 | 2 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0009c0022t0002 | 0/0 | 2308 | 2 | 1 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0009c0031t0001 | 0/0 | 2308 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0010c0026t0003 | 0/0 | 2308 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0010c0026t0004 | 0/0 | 2308 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0011c0029t0001 | 0/0 | 2308 | 2 | 1 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0012c0021t0002 | 0/0 | 2308 | 2 | 1 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0013c0027t0001 | 0/0 | 2308 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0013c0027t0005 | 0/0 | 2308 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0014c0032t0001 | 0/0 | 2308 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0015c0033t0002 | 0/0 | 2308 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0016c0036t0001 | 0/0 | 2308 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0017c0034t0001 | 0/0 | 2308 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0018c0035t0001 | 0/0 | 2308 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
a0019c0030t0001 | 0/0 | 2308 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | GGAGT others(2303): Show |
chr7 | 37843597 | 37905397 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0007 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0004g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0004g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0004g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0004g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0004g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0004g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0001t0007g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0003g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0004g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0004g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0005g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0004t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0007t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0007t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0007t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0007t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0007t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0007t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0007t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0007t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0007t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0007t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0007t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0007t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0007t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0007t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0007t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0007t0007g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0028t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0001c0028t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0008t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0008t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0008t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0008t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0008t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0008t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0008t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0008t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0008t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0008t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0008t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0008t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0008t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0008t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0008t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0009t0001g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0009t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0009t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0009t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0009t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0009t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0009t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0009t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0009t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0009t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0009t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0009t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0020t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0020t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0002c0020t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0003t0008g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0010t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0010t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0010t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0010t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0010t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0010t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0010t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0010t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0010t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0010t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0010t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0010t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0010t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0010t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0015t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0015t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0015t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0015t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0023t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0003c0023t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0005t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0012t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0012t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0012t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0004c0012t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0006t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0014t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0014t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0014t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0014t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0019t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0019t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0019t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0024t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0024t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0025t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0005c0025t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0006c0011t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0006c0011t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0006c0011t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0006c0011t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0006c0011t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0006c0011t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0006c0011t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0006c0016t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0006c0016t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0006c0016t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0006c0016t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0007c0017t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0007c0017t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0007c0017t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0007c0017t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0007c0018t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0007c0018t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0007c0018t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0007c0018t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0008c0013t0002g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0008c0013t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0008c0013t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0008c0013t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0009c0022t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0009c0022t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0009c0031t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0010c0026t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0010c0026t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0011c0029t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0012c0021t0002g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0013c0027t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0013c0027t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0014c0032t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0015c0033t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0016c0036t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0017c0034t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0018c0035t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
a0019c0030t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0005 | c0006 | t0002 | g0275 | EUR | GBR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00099 | hp2 | a0004 | c0005 | t0001 | g0199 | EUR | GBR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00140 | hp1 | a0005 | c0006 | t0002 | g0263 | EUR | GBR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | GBR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00280 | hp1 | a0002 | c0009 | t0001 | g0244 | EUR | FIN | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00280 | hp2 | a0001 | c0004 | t0004 | g0185 | EUR | FIN | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00323 | hp1 | a0001 | c0004 | t0003 | g0101 | EUR | FIN | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | FIN | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00423 | hp1 | a0001 | c0004 | t0003 | g0105 | EAS | CHS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00423 | hp2 | a0004 | c0012 | t0004 | g0180 | EAS | CHS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00544 | hp1 | a0007 | c0018 | t0001 | g0214 | EAS | CHS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | CHS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00558 | hp1 | a0001 | c0004 | t0003 | g0064 | EAS | CHS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00558 | hp2 | a0005 | c0014 | t0002 | g0034 | EAS | CHS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00597 | hp1 | a0005 | c0006 | t0002 | g0281 | EAS | CHS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | CHS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00609 | hp2 | a0001 | c0007 | t0001 | g0080 | EAS | CHS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00621 | hp1 | a0005 | c0024 | t0002 | g0283 | EAS | CHS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00639 | hp1 | a0001 | c0001 | t0004 | g0186 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00639 | hp2 | a0010 | c0026 | t0004 | g0178 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00673 | hp1 | a0014 | c0032 | t0001 | g0136 | EAS | CHS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00673 | hp2 | a0001 | c0004 | t0001 | g0003 | EAS | CHS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00733 | hp2 | a0003 | c0003 | t0002 | g0308 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0221 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00735 | hp2 | a0001 | c0004 | t0003 | g0099 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00738 | hp1 | a0003 | c0003 | t0002 | g0039 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00738 | hp2 | a0006 | c0011 | t0002 | g0294 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG00741 | hp2 | a0008 | c0013 | t0002 | g0033 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0076 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01069 | hp2 | a0005 | c0006 | t0002 | g0324 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01070 | hp1 | a0001 | c0001 | t0004 | g0182 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0126 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01071 | hp1 | a0005 | c0006 | t0002 | g0325 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01074 | hp1 | a0001 | c0007 | t0001 | g0075 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01074 | hp2 | a0010 | c0026 | t0003 | g0087 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01081 | hp1 | a0006 | c0011 | t0002 | g0286 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01106 | hp1 | a0004 | c0005 | t0001 | g0013 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0074 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01109 | hp1 | a0002 | c0020 | t0001 | g0205 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01169 | hp2 | a0004 | c0005 | t0001 | g0013 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01175 | hp1 | a0005 | c0006 | t0002 | g0293 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01192 | hp1 | a0004 | c0005 | t0001 | g0073 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01192 | hp2 | a0005 | c0019 | t0002 | g0288 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01243 | hp1 | a0004 | c0005 | t0001 | g0169 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01243 | hp2 | a0002 | c0002 | t0001 | g0032 | AMR | PUR | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01256 | hp1 | a0005 | c0006 | t0002 | g0323 | AMR | CLM | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01256 | hp2 | a0001 | c0004 | t0003 | g0003 | AMR | CLM | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01261 | hp1 | a0002 | c0009 | t0001 | g0239 | AMR | CLM | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01261 | hp2 | a0007 | c0017 | t0001 | g0207 | AMR | CLM | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01346 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | CLM | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0088 | AMR | CLM | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01358 | hp1 | a0011 | c0029 | t0001 | g0027 | AMR | CLM | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01358 | hp2 | a0005 | c0025 | t0002 | g0296 | AMR | CLM | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01433 | hp1 | a0012 | c0021 | t0002 | g0041 | AMR | CLM | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0050 | AMR | CLM | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01496 | hp1 | a0003 | c0003 | t0002 | g0039 | AMR | CLM | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01496 | hp2 | a0004 | c0005 | t0003 | g0046 | AMR | CLM | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01515 | hp1 | a0008 | c0013 | t0002 | g0011 | EUR | IBS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01515 | hp2 | a0001 | c0004 | t0003 | g0113 | EUR | IBS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01517 | hp1 | a0005 | c0025 | t0002 | g0292 | EUR | IBS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01517 | hp2 | a0008 | c0013 | t0002 | g0011 | EUR | IBS | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01884 | hp1 | a0003 | c0003 | t0002 | g0321 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01884 | hp2 | a0012 | c0021 | t0002 | g0041 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01928 | hp1 | a0005 | c0019 | t0002 | g0289 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01928 | hp2 | a0001 | c0004 | t0001 | g0097 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01934 | hp2 | a0004 | c0005 | t0001 | g0081 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01943 | hp1 | a0006 | c0016 | t0002 | g0271 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01943 | hp2 | a0004 | c0005 | t0001 | g0014 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01975 | hp1 | a0004 | c0005 | t0001 | g0107 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01975 | hp2 | a0001 | c0001 | t0004 | g0193 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01981 | hp1 | a0008 | c0013 | t0002 | g0033 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02040 | hp1 | a0002 | c0009 | t0001 | g0223 | EAS | KHV | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02055 | hp1 | a0003 | c0003 | t0002 | g0322 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02056 | hp1 | a0001 | c0004 | t0001 | g0003 | EAS | KHV | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02056 | hp2 | a0001 | c0001 | t0004 | g0025 | EAS | KHV | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02071 | hp1 | a0002 | c0008 | t0001 | g0260 | EAS | KHV | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | KHV | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02080 | hp1 | a0001 | c0001 | t0004 | g0025 | EAS | KHV | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02080 | hp2 | a0005 | c0006 | t0002 | g0273 | EAS | KHV | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02083 | hp2 | a0004 | c0012 | t0004 | g0179 | EAS | KHV | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02135 | hp1 | a0002 | c0009 | t0001 | g0202 | EAS | KHV | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02135 | hp2 | a0005 | c0006 | t0002 | g0277 | EAS | KHV | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02145 | hp1 | a0001 | c0001 | t0006 | g0153 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02148 | hp1 | a0004 | c0005 | t0001 | g0014 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02148 | hp2 | a0001 | c0001 | t0004 | g0009 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02155 | hp1 | a0002 | c0008 | t0001 | g0261 | EAS | CDX | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | CDX | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02165 | hp1 | a0002 | c0008 | t0001 | g0203 | EAS | CDX | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02165 | hp2 | a0003 | c0010 | t0001 | g0134 | EAS | CDX | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0031 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02258 | hp2 | a0003 | c0010 | t0002 | g0298 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02273 | hp1 | a0004 | c0005 | t0001 | g0057 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02273 | hp2 | a0005 | c0019 | t0002 | g0264 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02280 | hp1 | a0003 | c0010 | t0001 | g0256 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02280 | hp2 | a0001 | c0001 | t0007 | g0144 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02293 | hp1 | a0006 | c0016 | t0002 | g0291 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02293 | hp2 | a0001 | c0001 | t0004 | g0009 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02300 | hp1 | a0004 | c0005 | t0003 | g0104 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02300 | hp2 | a0002 | c0008 | t0001 | g0241 | AMR | PEL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02451 | hp1 | a0003 | c0003 | t0002 | g0316 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02451 | hp2 | a0003 | c0003 | t0002 | g0037 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02523 | hp1 | a0003 | c0010 | t0001 | g0127 | EAS | KHV | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02523 | hp2 | a0003 | c0003 | t0001 | g0133 | EAS | KHV | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02572 | hp1 | a0001 | c0004 | t0001 | g0124 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02615 | hp1 | a0013 | c0027 | t0001 | g0149 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02615 | hp2 | a0001 | c0007 | t0001 | g0249 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02622 | hp1 | a0015 | c0033 | t0002 | g0038 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02622 | hp2 | a0001 | c0004 | t0001 | g0151 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0031 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02647 | hp1 | a0002 | c0002 | t0001 | g0251 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02647 | hp2 | a0004 | c0005 | t0003 | g0008 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02683 | hp1 | a0003 | c0003 | t0001 | g0132 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02683 | hp2 | a0001 | c0004 | t0003 | g0003 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02717 | hp1 | a0003 | c0003 | t0001 | g0258 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02717 | hp2 | a0001 | c0007 | t0007 | g0090 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02723 | hp1 | a0003 | c0010 | t0002 | g0300 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02723 | hp2 | a0003 | c0023 | t0001 | g0255 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02735 | hp1 | a0016 | c0036 | t0001 | g0226 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02735 | hp2 | a0001 | c0001 | t0004 | g0190 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0206 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02809 | hp1 | a0003 | c0010 | t0002 | g0314 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02809 | hp2 | a0003 | c0003 | t0002 | g0303 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02818 | hp1 | a0003 | c0003 | t0002 | g0320 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02818 | hp2 | a0009 | c0022 | t0002 | g0262 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02886 | hp1 | a0003 | c0003 | t0002 | g0040 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02886 | hp2 | a0001 | c0004 | t0005 | g0197 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02895 | hp1 | a0013 | c0027 | t0005 | g0198 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02895 | hp2 | a0003 | c0010 | t0002 | g0312 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02896 | hp1 | a0003 | c0003 | t0002 | g0301 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02896 | hp2 | a0003 | c0003 | t0002 | g0042 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02897 | hp1 | a0003 | c0003 | t0002 | g0042 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02897 | hp2 | a0003 | c0010 | t0002 | g0313 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02965 | hp1 | a0003 | c0003 | t0002 | g0304 | AFR | ESN | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02970 | hp1 | a0003 | c0003 | t0002 | g0319 | AFR | ESN | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02970 | hp2 | a0003 | c0010 | t0002 | g0311 | AFR | ESN | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02976 | hp1 | a0003 | c0015 | t0002 | g0327 | AFR | ESN | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02976 | hp2 | a0001 | c0007 | t0001 | g0245 | AFR | ESN | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03017 | hp1 | a0002 | c0009 | t0001 | g0140 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0196 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03041 | hp2 | a0003 | c0015 | t0001 | g0259 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0154 | AFR | ESN | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03130 | hp2 | a0003 | c0010 | t0002 | g0307 | AFR | ESN | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03195 | hp1 | a0001 | c0007 | t0001 | g0248 | AFR | ESN | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03195 | hp2 | a0003 | c0003 | t0002 | g0318 | AFR | ESN | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03209 | hp1 | a0017 | c0034 | t0001 | g0117 | AFR | MSL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03225 | hp2 | a0003 | c0003 | t0002 | g0305 | AFR | MSL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03239 | hp1 | a0005 | c0014 | t0002 | g0287 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03239 | hp2 | a0001 | c0001 | t0004 | g0191 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03453 | hp1 | a0003 | c0003 | t0001 | g0257 | AFR | MSL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03453 | hp2 | a0003 | c0003 | t0002 | g0269 | AFR | MSL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03486 | hp1 | a0001 | c0004 | t0005 | g0195 | AFR | MSL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03486 | hp2 | a0003 | c0023 | t0001 | g0254 | AFR | MSL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03490 | hp1 | a0004 | c0005 | t0001 | g0016 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03490 | hp2 | a0008 | c0013 | t0002 | g0268 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03491 | hp1 | a0001 | c0007 | t0001 | g0021 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03491 | hp2 | a0001 | c0004 | t0003 | g0108 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03492 | hp1 | a0001 | c0007 | t0001 | g0021 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03492 | hp2 | a0004 | c0005 | t0001 | g0016 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03654 | hp1 | a0006 | c0016 | t0002 | g0290 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03654 | hp2 | a0001 | c0007 | t0003 | g0102 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03669 | hp1 | a0001 | c0004 | t0001 | g0155 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03688 | hp1 | a0006 | c0011 | t0002 | g0272 | SAS | STU | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0007 | SAS | STU | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03710 | hp1 | a0001 | c0004 | t0001 | g0171 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03710 | hp2 | a0001 | c0004 | t0001 | g0110 | SAS | PJL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03831 | hp1 | a0001 | c0007 | t0001 | g0049 | SAS | BEB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03831 | hp2 | a0002 | c0009 | t0001 | g0204 | SAS | BEB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03834 | hp1 | a0004 | c0005 | t0001 | g0158 | SAS | BEB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03834 | hp2 | a0002 | c0008 | t0001 | g0061 | SAS | BEB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03927 | hp2 | a0009 | c0022 | t0002 | g0310 | SAS | BEB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0139 | SAS | BEB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03942 | hp2 | a0001 | c0028 | t0003 | g0106 | SAS | BEB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG04115 | hp1 | a0008 | c0013 | t0002 | g0297 | SAS | STU | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG04115 | hp2 | a0002 | c0008 | t0001 | g0222 | SAS | STU | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG04184 | hp1 | a0001 | c0007 | t0003 | g0111 | SAS | BEB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG04199 | hp1 | a0002 | c0009 | t0001 | g0233 | SAS | STU | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0243 | SAS | STU | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0098 | SAS | STU | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG04204 | hp2 | a0004 | c0005 | t0001 | g0170 | SAS | STU | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18522 | hp1 | a0002 | c0002 | t0001 | g0032 | AFR | YRI | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18522 | hp2 | a0003 | c0003 | t0008 | g0299 | AFR | YRI | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18612 | hp1 | a0001 | c0007 | t0001 | g0163 | EAS | CHB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18612 | hp2 | a0002 | c0009 | t0001 | g0213 | EAS | CHB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18747 | hp1 | a0002 | c0008 | t0001 | g0028 | EAS | CHB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18747 | hp2 | a0002 | c0008 | t0001 | g0250 | EAS | CHB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | YRI | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18906 | hp2 | a0003 | c0003 | t0002 | g0315 | AFR | YRI | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18940 | hp1 | a0003 | c0003 | t0001 | g0128 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18940 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18942 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18942 | hp2 | a0007 | c0017 | t0001 | g0142 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18944 | hp1 | a0005 | c0006 | t0002 | g0267 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18944 | hp2 | a0004 | c0005 | t0003 | g0015 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18945 | hp1 | a0007 | c0018 | t0001 | g0200 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18945 | hp2 | a0005 | c0006 | t0002 | g0278 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18947 | hp1 | a0007 | c0018 | t0001 | g0052 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18949 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18949 | hp2 | a0005 | c0006 | t0002 | g0011 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18950 | hp2 | a0001 | c0004 | t0003 | g0063 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18951 | hp1 | a0004 | c0005 | t0001 | g0053 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18951 | hp2 | a0002 | c0020 | t0001 | g0212 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18952 | hp1 | a0003 | c0003 | t0001 | g0131 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18952 | hp2 | a0005 | c0006 | t0002 | g0280 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18953 | hp1 | a0006 | c0016 | t0002 | g0282 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18953 | hp2 | a0002 | c0008 | t0001 | g0059 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18954 | hp1 | a0002 | c0009 | t0001 | g0001 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18954 | hp2 | a0003 | c0010 | t0001 | g0129 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18956 | hp1 | a0002 | c0008 | t0001 | g0217 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18956 | hp2 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18957 | hp2 | a0001 | c0004 | t0003 | g0086 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18960 | hp1 | a0003 | c0010 | t0001 | g0135 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18960 | hp2 | a0001 | c0004 | t0001 | g0115 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18962 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18963 | hp2 | a0004 | c0005 | t0004 | g0187 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18966 | hp2 | a0005 | c0024 | t0002 | g0265 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18969 | hp1 | a0007 | c0018 | t0001 | g0201 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18969 | hp2 | a0002 | c0009 | t0001 | g0001 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18970 | hp1 | a0018 | c0035 | t0001 | g0235 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18970 | hp2 | a0004 | c0012 | t0001 | g0006 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18971 | hp2 | a0002 | c0008 | t0001 | g0220 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18973 | hp1 | a0019 | c0030 | t0001 | g0138 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18974 | hp1 | a0001 | c0004 | t0001 | g0167 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18974 | hp2 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18975 | hp2 | a0005 | c0014 | t0002 | g0270 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18977 | hp1 | a0001 | c0001 | t0004 | g0192 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18977 | hp2 | a0004 | c0005 | t0001 | g0008 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18978 | hp2 | a0001 | c0004 | t0001 | g0234 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18980 | hp2 | a0003 | c0003 | t0001 | g0137 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18983 | hp2 | a0002 | c0008 | t0001 | g0012 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18984 | hp1 | a0002 | c0008 | t0001 | g0028 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18984 | hp2 | a0006 | c0011 | t0002 | g0284 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18985 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18985 | hp2 | a0005 | c0006 | t0002 | g0036 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18986 | hp1 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18986 | hp2 | a0002 | c0008 | t0001 | g0252 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18988 | hp1 | a0005 | c0014 | t0002 | g0276 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18988 | hp2 | a0002 | c0009 | t0001 | g0001 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18990 | hp1 | a0005 | c0014 | t0002 | g0034 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18990 | hp2 | a0004 | c0005 | t0001 | g0103 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18991 | hp1 | a0006 | c0011 | t0002 | g0035 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18991 | hp2 | a0004 | c0012 | t0001 | g0006 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18994 | hp1 | a0009 | c0031 | t0001 | g0130 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18994 | hp2 | a0002 | c0008 | t0001 | g0219 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18995 | hp1 | a0001 | c0001 | t0004 | g0188 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18998 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19000 | hp1 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19001 | hp1 | a0002 | c0008 | t0001 | g0120 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19001 | hp2 | a0001 | c0007 | t0001 | g0055 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19003 | hp2 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19004 | hp2 | a0002 | c0009 | t0001 | g0001 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19005 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19005 | hp2 | a0001 | c0007 | t0001 | g0172 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19010 | hp1 | a0004 | c0005 | t0003 | g0015 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19010 | hp2 | a0002 | c0009 | t0001 | g0001 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0141 | AFR | LWK | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19030 | hp2 | a0003 | c0010 | t0002 | g0306 | AFR | LWK | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19054 | hp2 | a0006 | c0011 | t0002 | g0035 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19056 | hp2 | a0005 | c0006 | t0002 | g0279 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19057 | hp1 | a0001 | c0004 | t0001 | g0123 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19057 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19058 | hp1 | a0004 | c0012 | t0001 | g0006 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19060 | hp1 | a0005 | c0006 | t0002 | g0036 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19065 | hp1 | a0007 | c0017 | t0001 | g0237 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19065 | hp2 | a0001 | c0028 | t0001 | g0054 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19068 | hp1 | a0001 | c0004 | t0003 | g0094 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19070 | hp1 | a0001 | c0007 | t0001 | g0125 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19070 | hp2 | a0002 | c0008 | t0001 | g0012 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19072 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19072 | hp2 | a0002 | c0020 | t0001 | g0211 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19076 | hp1 | a0004 | c0005 | t0003 | g0109 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19076 | hp2 | a0002 | c0009 | t0001 | g0001 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19078 | hp1 | a0004 | c0012 | t0001 | g0017 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19079 | hp1 | a0001 | c0004 | t0003 | g0122 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19079 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19080 | hp1 | a0006 | c0011 | t0002 | g0266 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19081 | hp1 | a0001 | c0004 | t0001 | g0231 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19082 | hp1 | a0004 | c0012 | t0001 | g0017 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19082 | hp2 | a0005 | c0006 | t0002 | g0295 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19084 | hp1 | a0002 | c0009 | t0001 | g0238 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19084 | hp2 | a0005 | c0006 | t0002 | g0274 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19085 | hp1 | a0001 | c0001 | t0004 | g0183 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19085 | hp2 | a0002 | c0009 | t0001 | g0224 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19086 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19087 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19088 | hp2 | a0001 | c0007 | t0001 | g0079 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19091 | hp1 | a0002 | c0009 | t0001 | g0242 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19240 | hp1 | a0011 | c0029 | t0001 | g0027 | AFR | YRI | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | YRI | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0007 | EUR | TSI | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA20752 | hp2 | a0003 | c0003 | t0002 | g0309 | EUR | TSI | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA20805 | hp1 | a0006 | c0011 | t0002 | g0285 | EUR | TSI | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA20805 | hp2 | a0001 | c0004 | t0001 | g0160 | EUR | TSI | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0228 | SAS | GIH | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0093 | SAS | GIH | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0114 | AMR | CLM | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG01123 | hp2 | a0001 | c0004 | t0004 | g0194 | AMR | CLM | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02109 | hp2 | a0003 | c0003 | t0002 | g0317 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02486 | hp1 | a0003 | c0003 | t0002 | g0037 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02559 | hp1 | a0003 | c0010 | t0002 | g0038 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03471 | hp1 | a0001 | c0007 | t0001 | g0246 | AFR | MSL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG03471 | hp2 | a0003 | c0015 | t0002 | g0326 | AFR | MSL | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG06807 | hp1 | a0003 | c0015 | t0002 | g0302 | AFR | USA | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | USA | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18955 | hp1 | a0004 | c0005 | t0003 | g0095 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA18955 | hp2 | a0001 | c0001 | t0004 | g0189 | EAS | JPT | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA20300 | hp1 | a0007 | c0017 | t0001 | g0240 | AFR | USA | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | USA | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA21309 | hp1 | a0003 | c0003 | t0002 | g0040 | AFR | LWK | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | LWK | NME8_chr7_37843597_37905397 | NME8 | chr7 | 37843597 | 37905397 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:37850665 | G | A | 9 | a0003 a0005 a0006 others(6): Show |
107 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(104): Show |
missense_variant | MODERATE | c.128G>A | p.Arg43Lys | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/18 | 500/2308 | 128/1767 | 43/588 | chr7 | 37850665 | |||
chr7:37863462 | C | T | 1 | a0016 | 1 | HG02735.hp1 | stop_gained&splice_region_variant | HIGH | c.454C>T | p.Gln152* | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 8/18 | 826/2308 | 454/1767 | 152/588 | chr7 | 37863462 | |||
chr7:37865528 | A | G | 1 | a0015 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.532A>G | p.Thr178Ala | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/18 | 904/2308 | 532/1767 | 178/588 | chr7 | 37865528 | |||
chr7:37867702 | T | C | 11 | a0001 a0003 a0004 others(8): Show |
254 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(251): Show |
missense_variant&splice_region_variant | MODERATE | c.622T>C | p.Cys208Arg | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/18 | 994/2308 | 622/1767 | 208/588 | chr7 | 37867702 | |||
chr7:37867730 | T | C | 1 | a0019 | 1 | NA18973.hp1 | missense_variant | MODERATE | c.650T>C | p.Met217Thr | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/18 | 1022/2308 | 650/1767 | 217/588 | chr7 | 37867730 | |||
chr7:37867819 | G | A | 1 | a0012 | 2 | HG01433.hp1 HG01884.hp2 |
missense_variant | MODERATE | c.739G>A | p.Glu247Lys | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/18 | 1111/2308 | 739/1767 | 247/588 | chr7 | 37867819 | |||
chr7:37867873 | G | T | 1 | a0019 | 1 | NA18973.hp1 | stop_gained | HIGH | c.793G>T | p.Gly265* | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/18 | 1165/2308 | 793/1767 | 265/588 | chr7 | 37867873 | |||
chr7:37884315 | G | A | 2 | a0011 a0013 |
4 | HG01358.hp1 HG02615.hp1 HG02895.hp1 others(1): Show |
missense_variant | MODERATE | c.1007G>A | p.Arg336His | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 13/18 | 1379/2308 | 1007/1767 | 336/588 | chr7 | 37884315 | |||
chr7:37884321 | T | C | 2 | a0008 a0010 |
8 | HG00639.hp2 HG00741.hp2 HG01074.hp2 others(5): Show |
missense_variant | MODERATE | c.1013T>C | p.Ile338Thr | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 13/18 | 1385/2308 | 1013/1767 | 338/588 | chr7 | 37884321 | |||
chr7:37894471 | A | C | 1 | a0017 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.1405A>C | p.Ile469Leu | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/18 | 1777/2308 | 1405/1767 | 469/588 | chr7 | 37894471 | |||
chr7:37894544 | T | C | 4 | a0004 a0006 a0007 others(1): Show |
55 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(52): Show |
missense_variant | MODERATE | c.1478T>C | p.Ile493Thr | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/18 | 1850/2308 | 1478/1767 | 493/588 | chr7 | 37894544 | |||
chr7:37896962 | T | A | 1 | a0014 | 1 | HG00673.hp1 | stop_gained | HIGH | c.1637T>A | p.Leu546* | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/18 | 2009/2308 | 1637/1767 | 546/588 | chr7 | 37896962 | |||
chr7:37897079 | C | T | 1 | a0018 | 1 | NA18970.hp1 | missense_variant | MODERATE | c.1754C>T | p.Pro585Leu | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/18 | 2126/2308 | 1754/1767 | 585/588 | chr7 | 37897079 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:37850714 | C | T | 18 | a0003c0003 a0003c0010 a0003c0015 others(15): Show |
107 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(104): Show |
synonymous_variant | LOW | c.177C>T | p.Asp59Asp | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/18 | 549/2308 | 177/1767 | 59/588 | chr7 | 37850714 | |||
chr7:37857294 | G | A | 5 | a0005c0006 a0005c0014 a0005c0019 others(2): Show |
40 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(37): Show |
synonymous_variant | LOW | c.219G>A | p.Val73Val | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/18 | 591/2308 | 219/1767 | 73/588 | chr7 | 37857294 | |||
chr7:37876853 | A | G | 13 | a0001c0007 a0001c0028 a0002c0009 others(10): Show |
74 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(71): Show |
synonymous_variant | LOW | c.840A>G | p.Arg280Arg | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/18 | 1212/2308 | 840/1767 | 280/588 | chr7 | 37876853 | |||
chr7:37894545 | A | T | 8 | a0004c0005 a0004c0012 a0006c0011 others(5): Show |
55 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(52): Show |
synonymous_variant | LOW | c.1479A>T | p.Ile493Ile | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/18 | 1851/2308 | 1479/1767 | 493/588 | chr7 | 37894545 | |||
chr7:37896928 | T | C | 9 | a0001c0004 a0001c0028 a0002c0008 others(6): Show |
67 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(64): Show |
synonymous_variant | LOW | c.1603T>C | p.Leu535Leu | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/18 | 1975/2308 | 1603/1767 | 535/588 | chr7 | 37896928 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:37848880 | G | A | 3 | a0001c0001t0005 a0001c0004t0005 a0013c0027t0005 |
4 | HG02886.hp2 HG02895.hp1 HG03041.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-184G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/18 | 1387 | chr7 | 37848880 | ||||||
chr7:37848884 | G | A | 1 | a0001c0001t0006 | 2 | HG02145.hp1 HG03130.hp1 |
5_prime_UTR_variant | MODIFIER | c.-180G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/18 | 1383 | chr7 | 37848884 | ||||||
chr7:37848886 | G | T | 15 | a0003c0003t0002 a0003c0003t0008 a0003c0010t0002 others(12): Show |
89 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(86): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-178G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/18 | chr7 | 37848886 | |||||||
chr7:37848972 | C | T | 8 | a0001c0001t0004 a0001c0001t0005 a0001c0004t0004 others(5): Show |
32 | HG00280.hp2 HG00423.hp2 HG00639.hp1 others(29): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-92C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/18 | chr7 | 37848972 | |||||||
chr7:37849025 | C | T | 6 | a0001c0001t0003 a0001c0004t0003 a0001c0007t0003 others(3): Show |
51 | HG00323.hp1 HG00423.hp1 HG00544.hp2 others(48): Show |
5_prime_UTR_variant | MODIFIER | c.-39C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/18 | 1242 | chr7 | 37849025 | ||||||
chr7:37900382 | A | G | 3 | a0001c0001t0007 a0001c0007t0007 a0003c0003t0008 |
3 | HG02280.hp2 HG02717.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*154A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 18/18 | 3290 | chr7 | 37900382 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:37848752 | G | A | 97 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0051 others(94): Show |
109 | HG00323.hp1 HG00423.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-241+24G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 1/17 | chr7 | 37848752 | |||||||
chr7:37848758 | G | A | 12 | a0003c0003t0001g0128 a0003c0003t0001g0131 a0003c0003t0001g0132 others(9): Show |
12 | HG00673.hp1 HG02165.hp2 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.-241+30G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 1/17 | chr7 | 37848758 | |||||||
chr7:37849181 | T | C | 2 | a0002c0002t0001g0139 a0002c0009t0001g0140 |
2 | HG03017.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-8+125T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37849181 | |||||||
chr7:37849205 | A | G | 79 | a0003c0003t0002g0037 a0003c0003t0002g0039 a0003c0003t0002g0040 others(76): Show |
89 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.-8+149A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37849205 | |||||||
chr7:37849215 | G | A | 1 | a0002c0002t0001g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-8+159G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37849215 | |||||||
chr7:37849232 | A | C | 2 | a0003c0003t0002g0042 a0003c0015t0002g0327 |
3 | HG02896.hp2 HG02897.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-8+176A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37849232 | |||||||
chr7:37849252 | G | T | 1 | a0003c0015t0002g0326 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-8+196G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37849252 | |||||||
chr7:37849318 | T | A | 79 | a0003c0003t0002g0037 a0003c0003t0002g0039 a0003c0003t0002g0040 others(76): Show |
89 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.-8+262T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37849318 | |||||||
chr7:37849410 | C | T | 2 | a0002c0008t0001g0260 a0002c0008t0001g0261 |
2 | HG02071.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.-8+354C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37849410 | |||||||
chr7:37849482 | A | G | 3 | a0005c0006t0002g0323 a0005c0006t0002g0324 a0005c0006t0002g0325 |
3 | HG01069.hp2 HG01071.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.-8+426A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37849482 | |||||||
chr7:37849652 | C | T | 91 | a0003c0003t0001g0128 a0003c0003t0001g0131 a0003c0003t0001g0132 others(88): Show |
101 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.-8+596C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37849652 | |||||||
chr7:37849786 | G | A | 1 | a0007c0017t0001g0142 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-7-474G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37849786 | |||||||
chr7:37849833 | T | C | 12 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0143 others(9): Show |
16 | HG00741.hp1 HG02055.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-7-427T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37849833 | |||||||
chr7:37849868 | TC | T | 5 | a0001c0001t0001g0044 a0001c0001t0003g0043 a0001c0001t0003g0045 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-391delC | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37849868 | |||||||
chr7:37849868 | TCA | T | 122 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(119): Show |
140 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.-7-391_-7-390delCA | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37849868 | |||||||
chr7:37849869 | CA | C | 59 | a0001c0001t0001g0232 a0001c0004t0001g0231 a0001c0004t0001g0234 others(56): Show |
70 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.-7-370delA | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 37849869 | ||||||
chr7:37849869 | CAA | C | 22 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0143 others(19): Show |
26 | HG00423.hp2 HG00741.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-7-371_-7-370delAA | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 37849869 | ||||||
chr7:37849869 | CAAA | C | 23 | a0001c0001t0004g0005 a0001c0001t0004g0009 a0001c0001t0004g0025 others(20): Show |
28 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.-7-372_-7-370delAA others(1): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 37849869 | ||||||
chr7:37849880 | A | AC | 90 | a0003c0003t0001g0128 a0003c0003t0001g0131 a0003c0003t0001g0132 others(87): Show |
100 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.-7-380_-7-379insC | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37849880 | |||||||
chr7:37849886 | A | C | 91 | a0003c0003t0001g0128 a0003c0003t0001g0131 a0003c0003t0001g0132 others(88): Show |
101 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.-7-374A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37849886 | |||||||
chr7:37849994 | T | C | 2 | a0001c0001t0006g0153 a0001c0001t0006g0154 |
2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-7-266T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37849994 | |||||||
chr7:37850011 | A | G | 1 | a0001c0007t0001g0125 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-7-249A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37850011 | |||||||
chr7:37850184 | A | G | 97 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0051 others(94): Show |
109 | HG00323.hp1 HG00423.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-7-76A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | chr7 | 37850184 | |||||||
chr7:37850236 | TTTTC | T | 97 | a0003c0003t0001g0128 a0003c0003t0001g0131 a0003c0003t0001g0132 others(94): Show |
107 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.-7-16_-7-13delCTTT | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 37850236 | ||||||
chr7:37850450 | C | T | 1 | a0002c0002t0001g0253 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.91+15C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 4/17 | chr7 | 37850450 | |||||||
chr7:37850479 | G | A | 97 | a0003c0003t0001g0128 a0003c0003t0001g0131 a0003c0003t0001g0132 others(94): Show |
107 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.91+44G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 4/17 | chr7 | 37850479 | |||||||
chr7:37850580 | A | G | 1 | a0002c0002t0001g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.92-49A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 4/17 | chr7 | 37850580 | |||||||
chr7:37850599 | T | A | 1 | a0001c0004t0001g0155 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.92-30T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 4/17 | chr7 | 37850599 | |||||||
chr7:37850846 | AATAG | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0152 |
5 | HG02257.hp2 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+116_198+119del others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 37850846 | ||||||
chr7:37850922 | C | G | 6 | a0003c0003t0001g0257 a0003c0003t0001g0258 a0003c0010t0001g0256 others(3): Show |
6 | HG02280.hp1 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+187C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37850922 | |||||||
chr7:37850979 | A | G | 97 | a0003c0003t0001g0128 a0003c0003t0001g0131 a0003c0003t0001g0132 others(94): Show |
107 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.198+244A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37850979 | |||||||
chr7:37850987 | A | G | 97 | a0003c0003t0001g0128 a0003c0003t0001g0131 a0003c0003t0001g0132 others(94): Show |
107 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.198+252A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37850987 | |||||||
chr7:37851005 | T | C | 25 | a0001c0001t0004g0005 a0001c0001t0004g0009 a0001c0001t0004g0025 others(22): Show |
32 | HG00280.hp2 HG00423.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.198+270T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37851005 | |||||||
chr7:37851263 | T | C | 81 | a0003c0003t0001g0128 a0003c0003t0001g0131 a0003c0003t0001g0132 others(78): Show |
88 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.198+528T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37851263 | |||||||
chr7:37851481 | A | G | 1 | a0019c0030t0001g0138 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.198+746A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37851481 | |||||||
chr7:37851483 | TA | T | 97 | a0003c0003t0001g0128 a0003c0003t0001g0131 a0003c0003t0001g0132 others(94): Show |
107 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.198+750delA | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 37851483 | ||||||
chr7:37851492 | G | A | 97 | a0003c0003t0001g0128 a0003c0003t0001g0131 a0003c0003t0001g0132 others(94): Show |
107 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.198+757G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37851492 | |||||||
chr7:37851508 | A | G | 97 | a0003c0003t0001g0128 a0003c0003t0001g0131 a0003c0003t0001g0132 others(94): Show |
107 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.198+773A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37851508 | |||||||
chr7:37851513 | C | CTT | 97 | a0003c0003t0001g0128 a0003c0003t0001g0131 a0003c0003t0001g0132 others(94): Show |
107 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.198+778_198+779ins others(2): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37851513 | |||||||
chr7:37851654 | A | G | 2 | a0003c0003t0002g0315 a0003c0003t0002g0316 |
2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.198+919A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37851654 | |||||||
chr7:37851723 | A | G | 1 | a0002c0008t0001g0252 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.198+988A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37851723 | |||||||
chr7:37851755 | C | A | 1 | a0001c0001t0001g0156 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.198+1020C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37851755 | |||||||
chr7:37851835 | A | G | 6 | a0003c0003t0001g0257 a0003c0003t0001g0258 a0003c0010t0001g0256 others(3): Show |
6 | HG02280.hp1 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+1100A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37851835 | |||||||
chr7:37851839 | A | G | 1 | a0001c0004t0001g0124 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.198+1104A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37851839 | |||||||
chr7:37851932 | T | A | 1 | a0004c0005t0003g0046 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.198+1197T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37851932 | |||||||
chr7:37851963 | A | G | 1 | a0001c0004t0001g0123 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.198+1228A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37851963 | |||||||
chr7:37852055 | G | C | 127 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(124): Show |
145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.198+1320G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37852055 | |||||||
chr7:37852109 | C | CT | 9 | a0001c0001t0001g0177 a0001c0004t0003g0122 a0002c0002t0001g0251 others(6): Show |
9 | HG00323.hp2 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.198+1385dupT | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 37852109 | ||||||
chr7:37852109 | CT | C | 53 | a0003c0003t0002g0040 a0003c0003t0002g0042 a0003c0003t0002g0269 others(50): Show |
60 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.198+1385delT | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 37852109 | ||||||
chr7:37852188 | A | T | 1 | a0002c0008t0001g0250 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.198+1453A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37852188 | |||||||
chr7:37852190 | G | T | 82 | a0003c0003t0001g0128 a0003c0003t0001g0131 a0003c0003t0001g0132 others(79): Show |
90 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.198+1455G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37852190 | |||||||
chr7:37852318 | G | A | 1 | a0005c0006t0002g0263 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.198+1583G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37852318 | |||||||
chr7:37852325 | C | T | 4 | a0003c0010t0002g0311 a0003c0010t0002g0312 a0003c0010t0002g0313 others(1): Show |
4 | HG02809.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+1590C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37852325 | |||||||
chr7:37852359 | A | G | 1 | a0008c0013t0002g0297 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.198+1624A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37852359 | |||||||
chr7:37852365 | C | T | 12 | a0003c0003t0001g0128 a0003c0003t0001g0131 a0003c0003t0001g0132 others(9): Show |
12 | HG00673.hp1 HG02165.hp2 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.198+1630C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37852365 | |||||||
chr7:37852415 | A | C | 6 | a0003c0003t0001g0257 a0003c0003t0001g0258 a0003c0010t0001g0256 others(3): Show |
6 | HG02280.hp1 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+1680A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37852415 | |||||||
chr7:37852470 | C | A | 1 | a0005c0019t0002g0264 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.198+1735C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37852470 | |||||||
chr7:37852507 | C | T | 1 | a0002c0002t0001g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.198+1772C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37852507 | |||||||
chr7:37852531 | CACCAATC others(8): Show |
C | 1 | a0001c0001t0001g0121 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.198+1800_198+1814d others(17): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 37852531 | ||||||
chr7:37852627 | A | C | 4 | a0001c0001t0005g0196 a0001c0004t0005g0195 a0001c0004t0005g0197 others(1): Show |
4 | HG02886.hp2 HG02895.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+1892A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37852627 | |||||||
chr7:37852640 | C | T | 91 | a0003c0003t0001g0128 a0003c0003t0001g0131 a0003c0003t0001g0132 others(88): Show |
101 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.198+1905C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37852640 | |||||||
chr7:37852653 | A | G | 1 | a0001c0004t0004g0194 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.198+1918A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37852653 | |||||||
chr7:37852777 | G | A | 16 | a0001c0001t0004g0005 a0001c0001t0004g0025 a0001c0001t0004g0026 others(13): Show |
21 | HG00280.hp2 HG00423.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.198+2042G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37852777 | |||||||
chr7:37852964 | G | A | 2 | a0007c0018t0001g0200 a0007c0018t0001g0201 |
2 | NA18945.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.198+2229G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37852964 | |||||||
chr7:37853217 | G | A | 58 | a0001c0001t0001g0232 a0001c0004t0001g0231 a0001c0004t0001g0234 others(55): Show |
73 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.198+2482G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37853217 | |||||||
chr7:37853276 | G | C | 82 | a0003c0003t0001g0128 a0003c0003t0001g0131 a0003c0003t0001g0132 others(79): Show |
90 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.198+2541G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37853276 | |||||||
chr7:37853281 | T | C | 1 | a0001c0001t0003g0047 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.198+2546T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37853281 | |||||||
chr7:37853315 | G | A | 263 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(260): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.198+2580G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37853315 | |||||||
chr7:37853508 | A | T | 1 | a0012c0021t0002g0041 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.198+2773A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37853508 | |||||||
chr7:37853617 | A | G | 91 | a0003c0003t0001g0128 a0003c0003t0001g0131 a0003c0003t0001g0132 others(88): Show |
101 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.198+2882A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37853617 | |||||||
chr7:37853673 | T | A | 25 | a0001c0001t0004g0005 a0001c0001t0004g0009 a0001c0001t0004g0025 others(22): Show |
32 | HG00280.hp2 HG00423.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.198+2938T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37853673 | |||||||
chr7:37853730 | A | G | 1 | a0008c0013t0002g0268 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.198+2995A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37853730 | |||||||
chr7:37853876 | G | T | 249 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(246): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.198+3141G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37853876 | |||||||
chr7:37853878 | G | T | 91 | a0003c0003t0001g0128 a0003c0003t0001g0131 a0003c0003t0001g0132 others(88): Show |
101 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.198+3143G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37853878 | |||||||
chr7:37853995 | C | A | 91 | a0003c0003t0001g0128 a0003c0003t0001g0131 a0003c0003t0001g0132 others(88): Show |
101 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.198+3260C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37853995 | |||||||
chr7:37854098 | AG | A | 325 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(322): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.199-3175delG | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37854098 | |||||||
chr7:37854138 | T | C | 2 | a0001c0001t0006g0153 a0001c0001t0006g0154 |
2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.199-3136T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37854138 | |||||||
chr7:37854288 | T | G | 91 | a0003c0003t0001g0128 a0003c0003t0001g0131 a0003c0003t0001g0132 others(88): Show |
101 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.199-2986T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37854288 | |||||||
chr7:37854348 | C | A | 265 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(262): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.199-2926C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37854348 | |||||||
chr7:37854536 | C | T | 3 | a0001c0001t0004g0009 a0001c0001t0004g0192 a0001c0001t0004g0193 |
5 | HG01346.hp1 HG01975.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-2738C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37854536 | |||||||
chr7:37854690 | G | A | 3 | a0001c0001t0001g0157 a0003c0023t0001g0254 a0003c0023t0001g0255 |
3 | HG02723.hp2 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.199-2584G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37854690 | |||||||
chr7:37854722 | C | T | 268 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(265): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.199-2552C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37854722 | |||||||
chr7:37854804 | A | AC | 162 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(159): Show |
187 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.199-2464dupC | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 37854804 | ||||||
chr7:37854896 | A | G | 162 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(159): Show |
187 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.199-2378A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37854896 | |||||||
chr7:37855089 | C | T | 1 | a0001c0004t0001g0151 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.199-2185C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37855089 | |||||||
chr7:37855303 | A | G | 1 | a0005c0025t0002g0296 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.199-1971A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37855303 | |||||||
chr7:37855311 | T | C | 4 | a0001c0001t0005g0196 a0001c0004t0005g0195 a0001c0004t0005g0197 others(1): Show |
4 | HG02886.hp2 HG02895.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-1963T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37855311 | |||||||
chr7:37855362 | G | A | 12 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0143 others(9): Show |
16 | HG00741.hp1 HG02055.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.199-1912G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37855362 | |||||||
chr7:37855372 | A | G | 30 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(27): Show |
36 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(33): Show |
intron_variant | MODIFIER | c.199-1902A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37855372 | |||||||
chr7:37855443 | T | C | 1 | a0001c0001t0003g0050 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.199-1831T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37855443 | |||||||
chr7:37855455 | A | G | 1 | a0003c0010t0002g0314 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.199-1819A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37855455 | |||||||
chr7:37855499 | C | T | 269 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(266): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.199-1775C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37855499 | |||||||
chr7:37855529 | G | GT | 269 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(266): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.199-1743dupT | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 37855529 | ||||||
chr7:37855551 | T | C | 1 | a0001c0004t0001g0124 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.199-1723T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37855551 | |||||||
chr7:37855555 | A | G | 84 | a0001c0001t0004g0190 a0001c0001t0004g0191 a0003c0003t0001g0128 others(81): Show |
92 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.199-1719A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37855555 | |||||||
chr7:37855638 | C | T | 3 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0017c0034t0001g0117 |
3 | HG02145.hp2 HG02559.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.199-1636C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37855638 | |||||||
chr7:37855665 | T | C | 22 | a0001c0001t0004g0005 a0001c0001t0004g0025 a0001c0001t0004g0026 others(19): Show |
27 | HG00280.hp2 HG00423.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.199-1609T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37855665 | |||||||
chr7:37855845 | T | A | 1 | a0001c0001t0001g0121 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.199-1429T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37855845 | |||||||
chr7:37855889 | C | G | 2 | a0001c0007t0001g0248 a0001c0007t0001g0249 |
2 | HG02615.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.199-1385C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37855889 | |||||||
chr7:37855937 | TA | T | 12 | a0003c0003t0002g0039 a0003c0003t0002g0301 a0003c0003t0002g0303 others(9): Show |
13 | HG00733.hp2 HG00738.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.199-1326delA | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 37855937 | ||||||
chr7:37856082 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.199-1192G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37856082 | |||||||
chr7:37856092 | C | T | 2 | a0001c0001t0006g0153 a0001c0001t0006g0154 |
2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.199-1182C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37856092 | |||||||
chr7:37856128 | T | C | 2 | a0002c0008t0001g0012 a0007c0018t0001g0052 |
3 | NA18947.hp1 NA18983.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.199-1146T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37856128 | |||||||
chr7:37856243 | C | T | 84 | a0001c0001t0004g0190 a0001c0001t0004g0191 a0003c0003t0001g0128 others(81): Show |
92 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.199-1031C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37856243 | |||||||
chr7:37856407 | G | A | 132 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(129): Show |
150 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.199-867G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37856407 | |||||||
chr7:37856510 | C | G | 2 | a0001c0001t0001g0116 a0001c0004t0001g0115 |
2 | NA18960.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.199-764C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37856510 | |||||||
chr7:37856544 | C | A | 185 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(182): Show |
216 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.199-730C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37856544 | |||||||
chr7:37856549 | C | T | 1 | a0001c0001t0003g0114 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.199-725C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37856549 | |||||||
chr7:37856656 | A | G | 185 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(182): Show |
216 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.199-618A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37856656 | |||||||
chr7:37856688 | A | C | 1 | a0005c0006t0002g0036 | 2 | NA18985.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.199-586A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37856688 | |||||||
chr7:37856841 | G | C | 67 | a0003c0003t0002g0037 a0003c0003t0002g0039 a0003c0003t0002g0269 others(64): Show |
74 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.199-433G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37856841 | |||||||
chr7:37856997 | A | C | 84 | a0001c0001t0004g0190 a0001c0001t0004g0191 a0003c0003t0001g0128 others(81): Show |
92 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.199-277A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37856997 | |||||||
chr7:37857075 | G | A | 1 | a0017c0034t0001g0117 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.199-199G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37857075 | |||||||
chr7:37857099 | G | A | 12 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0143 others(9): Show |
16 | HG00741.hp1 HG02055.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.199-175G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37857099 | |||||||
chr7:37857192 | C | A | 1 | a0001c0004t0001g0115 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.199-82C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 5/17 | chr7 | 37857192 | |||||||
chr7:37857502 | G | A | 1 | a0001c0001t0004g0192 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.270+157G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37857502 | |||||||
chr7:37857510 | G | C | 1 | a0002c0009t0001g0202 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.270+165G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37857510 | |||||||
chr7:37857581 | C | T | 84 | a0001c0001t0004g0190 a0001c0001t0004g0191 a0003c0003t0001g0128 others(81): Show |
92 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.270+236C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37857581 | |||||||
chr7:37857594 | T | C | 84 | a0001c0001t0004g0190 a0001c0001t0004g0191 a0003c0003t0001g0128 others(81): Show |
92 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.270+249T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37857594 | |||||||
chr7:37857596 | A | C | 185 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(182): Show |
216 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.270+251A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37857596 | |||||||
chr7:37857607 | G | A | 67 | a0003c0003t0002g0037 a0003c0003t0002g0039 a0003c0003t0002g0269 others(64): Show |
74 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.270+262G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37857607 | |||||||
chr7:37857626 | T | G | 1 | a0005c0024t0002g0265 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.270+281T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37857626 | |||||||
chr7:37857706 | A | G | 3 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0017c0034t0001g0117 |
3 | HG02145.hp2 HG02559.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.270+361A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37857706 | |||||||
chr7:37857781 | A | T | 1 | a0001c0001t0001g0121 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.270+436A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37857781 | |||||||
chr7:37857850 | A | C | 1 | a0001c0001t0001g0121 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.270+505A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37857850 | |||||||
chr7:37857853 | C | A | 1 | a0001c0001t0001g0121 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.270+508C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37857853 | |||||||
chr7:37857854 | A | C | 1 | a0001c0001t0001g0121 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.270+509A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37857854 | |||||||
chr7:37857920 | G | A | 15 | a0001c0001t0004g0190 a0001c0001t0004g0191 a0003c0003t0001g0128 others(12): Show |
16 | HG00673.hp1 HG01433.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.270+575G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37857920 | |||||||
chr7:37857988 | G | C | 22 | a0003c0003t0002g0037 a0003c0003t0002g0039 a0003c0003t0002g0301 others(19): Show |
24 | HG00733.hp2 HG00738.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.270+643G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37857988 | |||||||
chr7:37858021 | A | C | 1 | a0002c0002t0001g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.270+676A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858021 | |||||||
chr7:37858117 | A | T | 1 | a0005c0006t0002g0295 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.270+772A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858117 | |||||||
chr7:37858260 | A | T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0152 |
5 | HG02257.hp2 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.270+915A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858260 | |||||||
chr7:37858274 | T | C | 14 | a0001c0001t0004g0190 a0001c0001t0004g0191 a0003c0003t0001g0128 others(11): Show |
14 | HG00673.hp1 HG02165.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.270+929T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858274 | |||||||
chr7:37858300 | T | A | 4 | a0001c0007t0001g0055 a0001c0007t0001g0125 a0001c0028t0001g0054 others(1): Show |
4 | NA18951.hp1 NA19001.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+955T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858300 | |||||||
chr7:37858348 | C | T | 269 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(266): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.270+1003C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858348 | |||||||
chr7:37858362 | T | A | 1 | a0003c0003t0002g0317 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.270+1017T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858362 | |||||||
chr7:37858400 | T | A | 1 | a0006c0011t0002g0266 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.270+1055T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858400 | |||||||
chr7:37858430 | C | T | 14 | a0002c0002t0001g0002 a0002c0002t0001g0030 a0002c0002t0001g0236 others(11): Show |
24 | HG00408.hp2 HG00621.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.270+1085C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858430 | |||||||
chr7:37858500 | G | A | 15 | a0001c0001t0004g0190 a0001c0001t0004g0191 a0003c0003t0001g0128 others(12): Show |
16 | HG00673.hp1 HG01433.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.270+1155G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858500 | |||||||
chr7:37858650 | AC | A | 15 | a0001c0001t0004g0190 a0001c0001t0004g0191 a0003c0003t0001g0128 others(12): Show |
16 | HG00673.hp1 HG01433.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.270+1306delC | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858650 | |||||||
chr7:37858673 | C | A | 12 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0143 others(9): Show |
16 | HG00741.hp1 HG02055.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.270+1328C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858673 | |||||||
chr7:37858674 | G | A | 1 | a0002c0008t0001g0203 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.270+1329G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858674 | |||||||
chr7:37858677 | G | A | 29 | a0001c0001t0004g0005 a0001c0001t0004g0009 a0001c0001t0004g0025 others(26): Show |
36 | HG00280.hp2 HG00423.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.270+1332G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858677 | |||||||
chr7:37858740 | G | A | 1 | a0001c0007t0001g0125 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.270+1395G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858740 | |||||||
chr7:37858913 | A | G | 1 | a0009c0022t0002g0262 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.270+1568A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858913 | |||||||
chr7:37858972 | C | G | 1 | a0002c0002t0001g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.270+1627C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37858972 | |||||||
chr7:37859092 | G | A | 1 | a0005c0006t0002g0267 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.270+1747G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37859092 | |||||||
chr7:37859128 | G | A | 269 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(266): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.270+1783G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37859128 | |||||||
chr7:37859535 | A | G | 1 | a0002c0002t0001g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.270+2190A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37859535 | |||||||
chr7:37859693 | C | T | 1 | a0001c0004t0001g0234 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.271-2335C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37859693 | |||||||
chr7:37859812 | A | G | 1 | a0002c0009t0001g0242 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.271-2216A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37859812 | |||||||
chr7:37859825 | T | G | 3 | a0002c0002t0001g0031 a0002c0002t0001g0032 a0002c0002t0001g0251 |
5 | HG01243.hp2 HG02258.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.271-2203T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37859825 | |||||||
chr7:37859916 | G | T | 1 | a0003c0003t0001g0137 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.271-2112G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37859916 | |||||||
chr7:37859966 | C | T | 15 | a0001c0001t0004g0190 a0001c0001t0004g0191 a0003c0003t0001g0128 others(12): Show |
16 | HG00673.hp1 HG01433.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.271-2062C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37859966 | |||||||
chr7:37859992 | C | T | 4 | a0001c0001t0005g0196 a0001c0004t0005g0195 a0001c0004t0005g0197 others(1): Show |
4 | HG02886.hp2 HG02895.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-2036C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37859992 | |||||||
chr7:37860023 | T | C | 22 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0143 others(19): Show |
28 | HG00741.hp1 HG01884.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.271-2005T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37860023 | |||||||
chr7:37860260 | A | G | 2 | a0005c0006t0002g0293 a0006c0011t0002g0294 |
2 | HG00738.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.271-1768A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37860260 | |||||||
chr7:37860269 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.271-1759G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37860269 | |||||||
chr7:37860453 | T | G | 2 | a0001c0001t0006g0153 a0001c0001t0006g0154 |
2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.271-1575T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37860453 | |||||||
chr7:37860612 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.271-1416C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37860612 | |||||||
chr7:37860649 | A | G | 69 | a0003c0003t0002g0037 a0003c0003t0002g0039 a0003c0003t0002g0269 others(66): Show |
76 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.271-1379A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37860649 | |||||||
chr7:37860788 | A | G | 1 | a0002c0009t0001g0233 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.271-1240A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37860788 | |||||||
chr7:37860889 | A | G | 9 | a0003c0003t0002g0040 a0003c0003t0002g0042 a0003c0003t0002g0317 others(6): Show |
11 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.271-1139A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37860889 | |||||||
chr7:37860981 | A | C | 1 | a0013c0027t0005g0198 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.271-1047A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37860981 | |||||||
chr7:37861040 | T | A | 132 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(129): Show |
150 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.271-988T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37861040 | |||||||
chr7:37861134 | T | A | 163 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(160): Show |
188 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.271-894T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37861134 | |||||||
chr7:37861379 | G | A | 15 | a0001c0001t0004g0190 a0001c0001t0004g0191 a0003c0003t0001g0128 others(12): Show |
16 | HG00673.hp1 HG01433.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.271-649G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37861379 | |||||||
chr7:37861400 | G | A | 30 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(27): Show |
36 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(33): Show |
intron_variant | MODIFIER | c.271-628G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37861400 | |||||||
chr7:37861586 | T | G | 247 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(244): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.271-442T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37861586 | |||||||
chr7:37861616 | T | C | 1 | a0002c0009t0001g0204 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.271-412T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37861616 | |||||||
chr7:37861783 | T | C | 29 | a0001c0001t0004g0005 a0001c0001t0004g0009 a0001c0001t0004g0025 others(26): Show |
36 | HG00280.hp2 HG00423.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.271-245T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37861783 | |||||||
chr7:37861848 | A | G | 1 | a0001c0001t0004g0189 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.271-180A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37861848 | |||||||
chr7:37861888 | C | T | 29 | a0001c0001t0004g0005 a0001c0001t0004g0009 a0001c0001t0004g0025 others(26): Show |
36 | HG00280.hp2 HG00423.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.271-140C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37861888 | |||||||
chr7:37861899 | A | G | 1 | a0002c0002t0001g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.271-129A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37861899 | |||||||
chr7:37861979 | G | A | 269 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(266): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.271-49G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37861979 | |||||||
chr7:37862014 | C | T | 6 | a0003c0003t0001g0257 a0003c0003t0001g0258 a0003c0010t0001g0256 others(3): Show |
6 | HG02280.hp1 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.271-14C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37862014 | |||||||
chr7:37862025 | T | C | 1 | a0001c0001t0001g0056 | 1 | NA19006.hp2 | splice_region_variant&intron_variant | LOW | c.271-3T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 6/17 | chr7 | 37862025 | |||||||
chr7:37862348 | C | T | 1 | a0005c0025t0002g0292 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.387+204C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | chr7 | 37862348 | |||||||
chr7:37862430 | G | A | 102 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0051 others(99): Show |
114 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.387+286G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | chr7 | 37862430 | |||||||
chr7:37862567 | A | G | 163 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(160): Show |
188 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.387+423A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | chr7 | 37862567 | |||||||
chr7:37862583 | G | A | 1 | a0010c0026t0004g0178 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.387+439G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | chr7 | 37862583 | |||||||
chr7:37862609 | C | G | 1 | a0001c0004t0001g0124 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.387+465C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | chr7 | 37862609 | |||||||
chr7:37862640 | G | A | 12 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0143 others(9): Show |
16 | HG00741.hp1 HG02055.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.387+496G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | chr7 | 37862640 | |||||||
chr7:37862645 | A | AT | 257 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(254): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.387+511dupT | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 37862645 | ||||||
chr7:37862645 | A | T | 14 | a0001c0001t0004g0190 a0001c0001t0004g0191 a0003c0003t0001g0128 others(11): Show |
14 | HG00673.hp1 HG02165.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.387+501A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | chr7 | 37862645 | |||||||
chr7:37862887 | A | G | 210 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(207): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.388-509A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | chr7 | 37862887 | |||||||
chr7:37863131 | A | T | 53 | a0001c0001t0001g0232 a0001c0004t0001g0231 a0001c0004t0001g0234 others(50): Show |
67 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.388-265A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | chr7 | 37863131 | |||||||
chr7:37863153 | G | A | 1 | a0004c0005t0001g0013 | 2 | HG01106.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.388-243G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | chr7 | 37863153 | |||||||
chr7:37863181 | T | C | 2 | a0004c0005t0001g0014 a0004c0005t0001g0057 |
3 | HG01943.hp2 HG02148.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.388-215T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | chr7 | 37863181 | |||||||
chr7:37863218 | T | G | 8 | a0003c0003t0002g0040 a0003c0003t0002g0042 a0003c0003t0002g0318 others(5): Show |
10 | HG01884.hp1 HG02055.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.388-178T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | chr7 | 37863218 | |||||||
chr7:37863257 | A | G | 1 | a0001c0001t0004g0188 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.388-139A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | chr7 | 37863257 | |||||||
chr7:37863316 | A | T | 1 | a0001c0004t0003g0113 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.388-80A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | chr7 | 37863316 | |||||||
chr7:37863340 | C | T | 14 | a0001c0001t0004g0190 a0001c0001t0004g0191 a0003c0003t0001g0128 others(11): Show |
14 | HG00673.hp1 HG02165.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.388-56C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | chr7 | 37863340 | |||||||
chr7:37863393 | T | C | 3 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0017c0034t0001g0117 |
3 | HG02145.hp2 HG02559.hp2 HG03209.hp1 |
splice_region_variant&intron_variant | LOW | c.388-3T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 7/17 | chr7 | 37863393 | |||||||
chr7:37863500 | T | C | 1 | a0004c0005t0003g0015 | 2 | NA18944.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.454+38T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 8/17 | chr7 | 37863500 | |||||||
chr7:37863773 | T | A | 1 | a0012c0021t0002g0041 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.454+311T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 8/17 | chr7 | 37863773 | |||||||
chr7:37863831 | C | T | 1 | a0003c0015t0002g0326 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.454+369C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 8/17 | chr7 | 37863831 | |||||||
chr7:37863867 | T | C | 1 | a0002c0002t0001g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.454+405T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 8/17 | chr7 | 37863867 | |||||||
chr7:37863955 | G | A | 1 | a0003c0010t0001g0127 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.455-393G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 8/17 | chr7 | 37863955 | |||||||
chr7:37864244 | T | C | 27 | a0003c0003t0002g0037 a0003c0003t0002g0039 a0003c0003t0002g0269 others(24): Show |
29 | HG00733.hp2 HG00738.hp1 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.455-104T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 8/17 | chr7 | 37864244 | |||||||
chr7:37864251 | A | T | 116 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(113): Show |
133 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.455-97A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 8/17 | chr7 | 37864251 | |||||||
chr7:37864302 | C | T | 224 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(221): Show |
257 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.455-46C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 8/17 | chr7 | 37864302 | |||||||
chr7:37864303 | G | A | 1 | a0002c0002t0001g0206 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.455-45G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 8/17 | chr7 | 37864303 | |||||||
chr7:37864432 | T | C | 1 | a0007c0017t0001g0207 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.528+11T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37864432 | |||||||
chr7:37864463 | TAAC | T | 116 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(113): Show |
133 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.528+46_528+48delAA others(1): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 37864463 | ||||||
chr7:37864464 | A | T | 1 | a0003c0003t0008g0299 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.528+43A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37864464 | |||||||
chr7:37864497 | G | A | 116 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(113): Show |
133 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.528+76G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37864497 | |||||||
chr7:37864615 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.528+194C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37864615 | |||||||
chr7:37864659 | C | T | 1 | a0007c0018t0001g0201 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.528+238C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37864659 | |||||||
chr7:37864665 | C | A | 53 | a0002c0002t0001g0058 a0002c0002t0001g0060 a0002c0008t0001g0012 others(50): Show |
59 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.528+244C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37864665 | |||||||
chr7:37864711 | C | G | 1 | a0002c0002t0001g0228 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.528+290C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37864711 | |||||||
chr7:37864718 | T | C | 1 | a0003c0003t0002g0037 | 2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.528+297T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37864718 | |||||||
chr7:37864772 | G | A | 12 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0143 others(9): Show |
16 | HG00741.hp1 HG02055.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.528+351G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37864772 | |||||||
chr7:37864945 | A | G | 6 | a0003c0003t0001g0257 a0003c0003t0001g0258 a0003c0010t0001g0256 others(3): Show |
6 | HG02280.hp1 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.528+524A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37864945 | |||||||
chr7:37865016 | A | T | 53 | a0002c0002t0001g0058 a0002c0002t0001g0060 a0002c0008t0001g0012 others(50): Show |
59 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.529-509A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37865016 | |||||||
chr7:37865079 | T | C | 1 | a0005c0014t0002g0270 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.529-446T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37865079 | |||||||
chr7:37865082 | C | G | 1 | a0002c0002t0001g0227 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.529-443C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37865082 | |||||||
chr7:37865094 | A | G | 1 | a0002c0002t0001g0228 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.529-431A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37865094 | |||||||
chr7:37865291 | G | A | 1 | a0001c0004t0001g0124 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.529-234G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37865291 | |||||||
chr7:37865374 | C | A | 4 | a0001c0001t0005g0196 a0001c0004t0005g0195 a0001c0004t0005g0197 others(1): Show |
4 | HG02886.hp2 HG02895.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.529-151C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37865374 | |||||||
chr7:37865491 | G | A | 1 | a0009c0022t0002g0262 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.529-34G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 9/17 | chr7 | 37865491 | |||||||
chr7:37865665 | G | T | 1 | a0001c0001t0001g0024 | 2 | HG00140.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.621+48G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37865665 | |||||||
chr7:37865681 | A | C | 1 | a0005c0006t0002g0263 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.621+64A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37865681 | |||||||
chr7:37865683 | T | A | 2 | a0001c0001t0006g0153 a0001c0001t0006g0154 |
2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.621+66T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37865683 | |||||||
chr7:37865818 | G | A | 222 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(219): Show |
255 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.621+201G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37865818 | |||||||
chr7:37865856 | G | A | 1 | a0002c0002t0001g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.621+239G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37865856 | |||||||
chr7:37865912 | A | C | 4 | a0003c0003t0008g0299 a0003c0010t0002g0038 a0003c0010t0002g0298 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+295A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37865912 | |||||||
chr7:37866025 | G | C | 222 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(219): Show |
255 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.621+408G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37866025 | |||||||
chr7:37866061 | C | A | 29 | a0001c0001t0004g0005 a0001c0001t0004g0009 a0001c0001t0004g0025 others(26): Show |
36 | HG00280.hp2 HG00423.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.621+444C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37866061 | |||||||
chr7:37866373 | C | T | 3 | a0003c0003t0002g0039 a0003c0003t0002g0309 a0009c0022t0002g0310 |
4 | HG00738.hp1 HG01496.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+756C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37866373 | |||||||
chr7:37866395 | T | C | 330 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(327): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.621+778T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37866395 | |||||||
chr7:37866551 | C | T | 1 | a0002c0002t0001g0227 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.621+934C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37866551 | |||||||
chr7:37866552 | G | A | 1 | a0006c0016t0002g0271 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.621+935G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37866552 | |||||||
chr7:37866602 | T | TAAGATAA others(377): Show |
1 | a0001c0007t0003g0111 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.621+998_621+999ins others(384): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 37866602 | ||||||
chr7:37866693 | T | C | 40 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0143 others(37): Show |
44 | HG00558.hp1 HG00597.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.622-1009T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37866693 | |||||||
chr7:37866762 | C | T | 2 | a0001c0007t0001g0049 a0003c0010t0001g0135 |
2 | HG03831.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.622-940C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37866762 | |||||||
chr7:37866813 | G | A | 2 | a0001c0001t0001g0019 a0004c0005t0001g0158 |
3 | HG01109.hp2 HG01175.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.622-889G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37866813 | |||||||
chr7:37866875 | C | T | 275 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(272): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.622-827C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37866875 | |||||||
chr7:37866987 | T | C | 221 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(218): Show |
254 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.622-715T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37866987 | |||||||
chr7:37867127 | G | T | 221 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(218): Show |
254 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.622-575G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37867127 | |||||||
chr7:37867237 | G | T | 1 | a0001c0001t0001g0150 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.622-465G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37867237 | |||||||
chr7:37867293 | C | CT | 10 | a0001c0001t0006g0153 a0001c0001t0006g0154 a0003c0003t0002g0040 others(7): Show |
11 | HG00733.hp2 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.622-397dupT | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 37867293 | ||||||
chr7:37867416 | A | G | 29 | a0001c0001t0004g0005 a0001c0001t0004g0009 a0001c0001t0004g0025 others(26): Show |
36 | HG00280.hp2 HG00423.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.622-286A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37867416 | |||||||
chr7:37867445 | T | G | 24 | a0003c0003t0002g0037 a0003c0003t0002g0039 a0003c0003t0002g0301 others(21): Show |
26 | HG00733.hp2 HG00738.hp1 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.622-257T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37867445 | |||||||
chr7:37867631 | G | T | 1 | a0002c0002t0001g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.622-71G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 10/17 | chr7 | 37867631 | |||||||
chr7:37867925 | T | C | 12 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0143 others(9): Show |
16 | HG00741.hp1 HG02055.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.818+27T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37867925 | |||||||
chr7:37867954 | C | T | 26 | a0001c0001t0003g0047 a0001c0001t0003g0062 a0001c0001t0003g0065 others(23): Show |
26 | HG00558.hp1 HG00597.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.818+56C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37867954 | |||||||
chr7:37868085 | T | C | 1 | a0004c0005t0001g0073 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.818+187T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37868085 | |||||||
chr7:37868198 | G | A | 1 | a0001c0001t0003g0074 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.818+300G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37868198 | |||||||
chr7:37868215 | G | C | 1 | a0001c0001t0003g0062 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.818+317G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37868215 | |||||||
chr7:37868244 | G | A | 1 | a0001c0007t0001g0075 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.818+346G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37868244 | |||||||
chr7:37868388 | C | T | 2 | a0002c0008t0001g0241 a0007c0017t0001g0240 |
2 | HG02300.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.818+490C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37868388 | |||||||
chr7:37868429 | CT | C | 220 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(217): Show |
253 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.818+540delT | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37868429 | ||||||
chr7:37868481 | A | C | 2 | a0001c0001t0006g0153 a0001c0001t0006g0154 |
2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.818+583A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37868481 | |||||||
chr7:37868776 | G | A | 1 | a0004c0005t0001g0016 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.818+878G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37868776 | |||||||
chr7:37868821 | A | C | 1 | a0003c0010t0002g0306 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.818+923A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37868821 | |||||||
chr7:37868852 | T | TA | 6 | a0003c0003t0001g0257 a0003c0003t0001g0258 a0003c0010t0001g0256 others(3): Show |
6 | HG02280.hp1 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.818+958dupA | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37868852 | ||||||
chr7:37868903 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.818+1005G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37868903 | |||||||
chr7:37868971 | G | A | 2 | a0001c0001t0006g0153 a0001c0001t0006g0154 |
2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.818+1073G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37868971 | |||||||
chr7:37868993 | G | A | 1 | a0002c0002t0001g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.818+1095G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37868993 | |||||||
chr7:37869042 | G | A | 11 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0143 others(8): Show |
15 | HG00741.hp1 HG02055.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.818+1144G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37869042 | |||||||
chr7:37869145 | G | A | 1 | a0001c0004t0004g0194 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.818+1247G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37869145 | |||||||
chr7:37869177 | T | C | 111 | a0001c0001t0001g0020 a0001c0001t0001g0044 a0001c0001t0001g0048 others(108): Show |
125 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.818+1279T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37869177 | |||||||
chr7:37869185 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.818+1287C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37869185 | |||||||
chr7:37869204 | G | T | 1 | a0001c0007t0003g0111 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.818+1306G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37869204 | |||||||
chr7:37869235 | C | T | 29 | a0001c0001t0004g0005 a0001c0001t0004g0009 a0001c0001t0004g0025 others(26): Show |
36 | HG00280.hp2 HG00423.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.818+1337C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37869235 | |||||||
chr7:37869294 | C | G | 1 | a0003c0003t0002g0305 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.818+1396C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37869294 | |||||||
chr7:37869434 | T | C | 223 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(220): Show |
258 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.818+1536T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37869434 | |||||||
chr7:37869728 | G | A | 1 | a0004c0012t0004g0179 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.818+1830G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37869728 | |||||||
chr7:37869957 | C | A | 1 | a0002c0008t0001g0120 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.818+2059C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37869957 | |||||||
chr7:37869957 | C | T | 1 | a0006c0016t0002g0291 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.818+2059C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37869957 | |||||||
chr7:37870069 | C | T | 1 | a0001c0004t0005g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.818+2171C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37870069 | |||||||
chr7:37870099 | C | T | 1 | a0001c0004t0001g0155 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.818+2201C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37870099 | |||||||
chr7:37870245 | T | TA | 270 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(267): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.818+2360dupA | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37870245 | ||||||
chr7:37870245 | T | TAA | 4 | a0001c0001t0004g0009 a0001c0001t0004g0192 a0001c0001t0004g0193 others(1): Show |
6 | HG01346.hp1 HG01975.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.818+2359_818+2360d others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37870245 | ||||||
chr7:37870386 | C | A | 2 | a0001c0001t0001g0161 a0001c0004t0001g0160 |
2 | HG01934.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.818+2488C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37870386 | |||||||
chr7:37870386 | C | T | 1 | a0004c0005t0001g0057 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.818+2488C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37870386 | |||||||
chr7:37870400 | T | C | 55 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(52): Show |
64 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.818+2502T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37870400 | |||||||
chr7:37870485 | A | G | 1 | a0002c0002t0001g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.818+2587A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37870485 | |||||||
chr7:37870504 | G | A | 111 | a0001c0001t0001g0020 a0001c0001t0001g0044 a0001c0001t0001g0048 others(108): Show |
124 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.818+2606G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37870504 | |||||||
chr7:37870519 | G | A | 1 | a0012c0021t0002g0041 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.818+2621G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37870519 | |||||||
chr7:37870588 | CA | C | 215 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0020 others(212): Show |
257 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.818+2710delA | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37870588 | ||||||
chr7:37870588 | CAA | C | 19 | a0001c0001t0001g0147 a0001c0001t0001g0157 a0001c0001t0001g0174 others(16): Show |
20 | HG01975.hp1 HG02055.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.818+2709_818+2710d others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37870588 | ||||||
chr7:37870699 | T | C | 4 | a0003c0003t0001g0257 a0003c0010t0001g0256 a0003c0023t0001g0254 others(1): Show |
4 | HG02280.hp1 HG02723.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.818+2801T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37870699 | |||||||
chr7:37870826 | A | G | 1 | a0003c0010t0002g0300 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.818+2928A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37870826 | |||||||
chr7:37870923 | T | C | 1 | a0001c0004t0003g0063 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.818+3025T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37870923 | |||||||
chr7:37870938 | A | G | 27 | a0001c0007t0001g0055 a0001c0007t0001g0075 a0001c0007t0001g0125 others(24): Show |
34 | HG01074.hp1 HG01192.hp2 HG01261.hp1 others(31): Show |
intron_variant | MODIFIER | c.818+3040A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37870938 | |||||||
chr7:37871122 | T | C | 1 | a0005c0006t0002g0273 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.818+3224T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37871122 | |||||||
chr7:37871131 | G | T | 4 | a0003c0003t0002g0315 a0003c0003t0002g0316 a0012c0021t0002g0041 others(1): Show |
5 | HG01433.hp1 HG01884.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.818+3233G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37871131 | |||||||
chr7:37871153 | G | C | 2 | a0003c0003t0002g0269 a0013c0027t0001g0149 |
2 | HG02615.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.818+3255G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37871153 | |||||||
chr7:37871255 | G | A | 1 | a0018c0035t0001g0235 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.818+3357G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37871255 | |||||||
chr7:37871344 | C | T | 1 | a0004c0005t0004g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.818+3446C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37871344 | |||||||
chr7:37871426 | G | A | 1 | a0004c0005t0004g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.818+3528G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37871426 | |||||||
chr7:37871439 | T | A | 1 | a0001c0001t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.818+3541T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37871439 | |||||||
chr7:37871562 | T | G | 1 | a0002c0002t0001g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.818+3664T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37871562 | |||||||
chr7:37871574 | C | G | 75 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0077 others(72): Show |
86 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.818+3676C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37871574 | |||||||
chr7:37871666 | T | G | 1 | a0002c0008t0001g0252 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.818+3768T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37871666 | |||||||
chr7:37871701 | A | G | 55 | a0001c0001t0001g0044 a0001c0001t0001g0091 a0001c0001t0001g0096 others(52): Show |
61 | HG00323.hp1 HG00558.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.818+3803A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37871701 | |||||||
chr7:37871766 | C | T | 7 | a0003c0010t0002g0038 a0003c0010t0002g0298 a0003c0010t0002g0311 others(4): Show |
7 | HG02258.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.818+3868C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37871766 | |||||||
chr7:37871939 | C | G | 2 | a0001c0007t0007g0090 a0003c0010t0002g0300 |
2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.818+4041C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37871939 | |||||||
chr7:37871949 | C | T | 1 | a0001c0007t0001g0049 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.818+4051C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37871949 | |||||||
chr7:37872002 | A | G | 1 | a0002c0008t0001g0241 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.818+4104A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37872002 | |||||||
chr7:37872385 | C | A | 1 | a0003c0003t0001g0137 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.819-4447C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37872385 | |||||||
chr7:37872419 | C | A | 33 | a0001c0001t0006g0153 a0001c0001t0006g0154 a0001c0007t0001g0021 others(30): Show |
37 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.819-4413C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37872419 | |||||||
chr7:37872592 | A | G | 212 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(209): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.819-4240A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37872592 | |||||||
chr7:37872623 | A | G | 3 | a0002c0002t0001g0031 a0002c0002t0001g0032 a0002c0002t0001g0251 |
5 | HG01243.hp2 HG02258.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.819-4209A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37872623 | |||||||
chr7:37872656 | T | G | 245 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(242): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.819-4176T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37872656 | |||||||
chr7:37872684 | G | A | 3 | a0002c0002t0001g0031 a0002c0002t0001g0032 a0002c0002t0001g0251 |
5 | HG01243.hp2 HG02258.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.819-4148G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37872684 | |||||||
chr7:37872695 | G | A | 211 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(208): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.819-4137G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37872695 | |||||||
chr7:37872745 | ACT | A | 211 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(208): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.819-4084_819-4083d others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37872745 | ||||||
chr7:37872752 | A | T | 33 | a0001c0001t0006g0153 a0001c0001t0006g0154 a0001c0007t0001g0021 others(30): Show |
37 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.819-4080A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37872752 | |||||||
chr7:37872778 | AACTC | A | 211 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(208): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.819-4052_819-4049d others(6): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37872778 | ||||||
chr7:37872884 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.819-3948C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37872884 | |||||||
chr7:37872901 | G | A | 1 | a0008c0013t0002g0297 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.819-3931G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37872901 | |||||||
chr7:37872921 | A | T | 5 | a0001c0001t0006g0153 a0001c0001t0006g0154 a0002c0009t0001g0244 others(2): Show |
5 | HG00280.hp1 HG02145.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.819-3911A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37872921 | |||||||
chr7:37872925 | C | A | 1 | a0003c0010t0002g0298 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.819-3907C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37872925 | |||||||
chr7:37872933 | G | T | 211 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(208): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.819-3899G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37872933 | |||||||
chr7:37872958 | G | T | 3 | a0001c0001t0006g0153 a0001c0001t0006g0154 a0002c0009t0001g0244 |
3 | HG00280.hp1 HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.819-3874G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37872958 | |||||||
chr7:37873027 | T | A | 33 | a0001c0001t0006g0153 a0001c0001t0006g0154 a0001c0007t0001g0021 others(30): Show |
37 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.819-3805T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873027 | |||||||
chr7:37873075 | A | G | 211 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(208): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.819-3757A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873075 | |||||||
chr7:37873116 | G | A | 1 | a0002c0002t0001g0228 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.819-3716G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873116 | |||||||
chr7:37873129 | G | A | 21 | a0001c0007t0001g0021 a0001c0007t0001g0079 a0001c0007t0001g0080 others(18): Show |
25 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.819-3703G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873129 | |||||||
chr7:37873146 | A | G | 244 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(241): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.819-3686A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873146 | |||||||
chr7:37873154 | G | T | 211 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(208): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.819-3678G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873154 | |||||||
chr7:37873175 | C | T | 2 | a0001c0001t0006g0153 a0001c0001t0006g0154 |
2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.819-3657C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873175 | |||||||
chr7:37873317 | G | A | 108 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(105): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.819-3515G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873317 | |||||||
chr7:37873359 | C | CAAA | 44 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0077 others(41): Show |
49 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.819-3460_819-3458d others(5): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37873359 | ||||||
chr7:37873359 | C | CAAAA | 99 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(96): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.819-3461_819-3458d others(6): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37873359 | ||||||
chr7:37873359 | C | CAAAAA | 9 | a0001c0001t0001g0173 a0001c0001t0001g0176 a0001c0001t0004g0181 others(6): Show |
9 | HG01981.hp2 HG02738.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.819-3462_819-3458d others(7): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37873359 | ||||||
chr7:37873359 | CA | C | 6 | a0001c0001t0001g0112 a0001c0004t0003g0101 a0003c0003t0002g0042 others(3): Show |
7 | HG00323.hp1 HG02572.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.819-3458delA | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37873359 | ||||||
chr7:37873370 | A | AAAAAAAA others(3): Show |
3 | a0003c0010t0001g0256 a0003c0023t0001g0254 a0003c0023t0001g0255 |
3 | HG02280.hp1 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.819-3458_819-3457i others(12): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37873370 | ||||||
chr7:37873370 | A | AAAAAAAA others(2): Show |
55 | a0001c0001t0001g0232 a0001c0001t0003g0047 a0001c0001t0003g0062 others(52): Show |
64 | HG00544.hp2 HG00597.hp2 HG01074.hp1 others(61): Show |
intron_variant | MODIFIER | c.819-3458_819-3457i others(11): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37873370 | ||||||
chr7:37873395 | G | A | 213 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(210): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.819-3437G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873395 | |||||||
chr7:37873491 | T | TAAACAAT others(40): Show |
4 | a0003c0003t0002g0269 a0011c0029t0001g0027 a0012c0021t0002g0041 others(1): Show |
6 | HG01358.hp1 HG01433.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.819-3341_819-3340i others(49): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873491 | |||||||
chr7:37873492 | T | A | 4 | a0003c0003t0002g0269 a0011c0029t0001g0027 a0012c0021t0002g0041 others(1): Show |
6 | HG01358.hp1 HG01433.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.819-3340T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873492 | |||||||
chr7:37873509 | T | A | 1 | a0001c0001t0003g0065 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.819-3323T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873509 | |||||||
chr7:37873591 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.819-3241A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873591 | |||||||
chr7:37873604 | A | G | 1 | a0005c0006t0002g0295 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.819-3228A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873604 | |||||||
chr7:37873729 | T | G | 2 | a0002c0008t0001g0059 a0006c0016t0002g0282 |
2 | NA18953.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.819-3103T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873729 | |||||||
chr7:37873848 | A | G | 1 | a0013c0027t0001g0149 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.819-2984A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873848 | |||||||
chr7:37873887 | C | G | 1 | a0003c0010t0002g0300 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.819-2945C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873887 | |||||||
chr7:37873901 | G | T | 211 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(208): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.819-2931G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873901 | |||||||
chr7:37873949 | T | C | 213 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(210): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.819-2883T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873949 | |||||||
chr7:37873995 | A | G | 211 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(208): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.819-2837A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37873995 | |||||||
chr7:37874012 | G | A | 247 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(244): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.819-2820G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37874012 | |||||||
chr7:37874125 | A | T | 211 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(208): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.819-2707A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37874125 | |||||||
chr7:37874158 | G | A | 1 | a0005c0024t0002g0283 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.819-2674G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37874158 | |||||||
chr7:37874183 | T | G | 150 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(147): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.819-2649T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37874183 | |||||||
chr7:37874328 | G | A | 212 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(209): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.819-2504G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37874328 | |||||||
chr7:37874333 | G | C | 211 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(208): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.819-2499G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37874333 | |||||||
chr7:37874354 | G | A | 33 | a0001c0001t0006g0153 a0001c0001t0006g0154 a0001c0007t0001g0021 others(30): Show |
37 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.819-2478G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37874354 | |||||||
chr7:37874481 | G | A | 1 | a0002c0009t0001g0244 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.819-2351G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37874481 | |||||||
chr7:37874511 | G | A | 211 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(208): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.819-2321G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37874511 | |||||||
chr7:37874567 | A | G | 4 | a0003c0003t0002g0269 a0011c0029t0001g0027 a0012c0021t0002g0041 others(1): Show |
6 | HG01358.hp1 HG01433.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.819-2265A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37874567 | |||||||
chr7:37874625 | C | A | 2 | a0001c0004t0001g0231 a0007c0017t0001g0142 |
2 | NA18942.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.819-2207C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37874625 | |||||||
chr7:37874719 | C | T | 1 | a0016c0036t0001g0226 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.819-2113C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37874719 | |||||||
chr7:37874834 | T | C | 3 | a0005c0006t0002g0275 a0005c0006t0002g0293 a0006c0011t0002g0294 |
3 | HG00099.hp1 HG00738.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.819-1998T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37874834 | |||||||
chr7:37874862 | A | G | 36 | a0001c0001t0006g0153 a0001c0001t0006g0154 a0001c0007t0001g0021 others(33): Show |
40 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.819-1970A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37874862 | |||||||
chr7:37874972 | C | T | 6 | a0001c0001t0001g0020 a0001c0001t0003g0007 a0001c0001t0003g0043 others(3): Show |
9 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.819-1860C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37874972 | |||||||
chr7:37875015 | A | G | 1 | a0001c0004t0001g0171 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.819-1817A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875015 | |||||||
chr7:37875065 | G | C | 244 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(241): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.819-1767G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875065 | |||||||
chr7:37875092 | C | T | 1 | a0007c0017t0001g0142 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.819-1740C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875092 | |||||||
chr7:37875114 | A | G | 28 | a0001c0001t0001g0232 a0001c0001t0003g0047 a0001c0001t0003g0062 others(25): Show |
30 | HG00544.hp2 HG00597.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.819-1718A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875114 | |||||||
chr7:37875134 | A | C | 244 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(241): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.819-1698A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875134 | |||||||
chr7:37875147 | A | G | 43 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0077 others(40): Show |
47 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.819-1685A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875147 | |||||||
chr7:37875176 | G | A | 33 | a0001c0001t0006g0153 a0001c0001t0006g0154 a0001c0007t0001g0021 others(30): Show |
37 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.819-1656G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875176 | |||||||
chr7:37875223 | A | G | 39 | a0001c0001t0001g0020 a0001c0001t0001g0162 a0001c0001t0001g0176 others(36): Show |
46 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.819-1609A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875223 | |||||||
chr7:37875358 | T | A | 243 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(240): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.819-1474T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875358 | |||||||
chr7:37875401 | G | GAC | 35 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0159 others(32): Show |
41 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.819-1414_819-1413d others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37875401 | ||||||
chr7:37875420 | C | A | 2 | a0001c0001t0001g0174 a0001c0004t0001g0123 |
2 | NA19057.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.819-1412C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875420 | |||||||
chr7:37875471 | CAGAG | C | 140 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(137): Show |
167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.819-1357_819-1354d others(6): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37875471 | ||||||
chr7:37875506 | G | T | 1 | a0001c0007t0001g0049 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.819-1326G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875506 | |||||||
chr7:37875535 | G | A | 3 | a0003c0003t0002g0042 a0003c0003t0002g0318 a0003c0015t0002g0327 |
4 | HG02896.hp2 HG02897.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.819-1297G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875535 | |||||||
chr7:37875573 | AT | A | 14 | a0001c0001t0001g0232 a0001c0001t0003g0047 a0001c0001t0003g0062 others(11): Show |
14 | HG00597.hp2 HG02040.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.819-1252delT | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37875573 | ||||||
chr7:37875613 | T | G | 1 | a0001c0001t0001g0168 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.819-1219T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875613 | |||||||
chr7:37875663 | A | T | 2 | a0001c0001t0006g0153 a0001c0001t0006g0154 |
2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.819-1169A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875663 | |||||||
chr7:37875669 | A | C | 2 | a0013c0027t0001g0149 a0013c0027t0005g0198 |
2 | HG02615.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.819-1163A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875669 | |||||||
chr7:37875671 | G | A | 10 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0143 others(7): Show |
14 | HG00741.hp1 HG02055.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.819-1161G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875671 | |||||||
chr7:37875872 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.819-960G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875872 | |||||||
chr7:37875973 | C | T | 3 | a0003c0003t0002g0042 a0003c0003t0002g0318 a0003c0015t0002g0327 |
4 | HG02896.hp2 HG02897.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.819-859C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875973 | |||||||
chr7:37875978 | C | T | 140 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(137): Show |
167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.819-854C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875978 | |||||||
chr7:37875993 | G | A | 1 | a0003c0010t0002g0300 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.819-839G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37875993 | |||||||
chr7:37876042 | C | T | 67 | a0001c0001t0006g0153 a0001c0001t0006g0154 a0001c0007t0001g0021 others(64): Show |
76 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.819-790C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37876042 | |||||||
chr7:37876074 | G | T | 207 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(204): Show |
243 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.819-758G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37876074 | |||||||
chr7:37876108 | C | CT | 207 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(204): Show |
243 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.819-724_819-723ins others(1): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37876108 | |||||||
chr7:37876124 | C | T | 1 | a0005c0025t0002g0296 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.819-708C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37876124 | |||||||
chr7:37876214 | C | A | 67 | a0001c0001t0006g0153 a0001c0001t0006g0154 a0001c0007t0001g0021 others(64): Show |
76 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.819-618C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37876214 | |||||||
chr7:37876215 | A | C | 1 | a0002c0009t0001g0244 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.819-617A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37876215 | |||||||
chr7:37876216 | C | CTATA | 4 | a0001c0001t0004g0009 a0001c0001t0004g0193 a0002c0002t0001g0206 others(1): Show |
6 | HG01346.hp1 HG01975.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.819-603_819-600dup others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37876216 | ||||||
chr7:37876216 | CTATA | C | 3 | a0001c0007t0001g0245 a0003c0010t0002g0038 a0015c0033t0002g0038 |
3 | HG02559.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.819-603_819-600del others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37876216 | ||||||
chr7:37876225 | TATATATA others(5): Show |
T | 1 | a0001c0001t0001g0024 | 2 | HG00140.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.819-603_819-592del others(12): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37876225 | ||||||
chr7:37876229 | T | G | 43 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0143 others(40): Show |
51 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.819-603T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37876229 | |||||||
chr7:37876229 | T | TATAG | 8 | a0001c0001t0001g0145 a0001c0001t0001g0157 a0001c0001t0001g0174 others(5): Show |
8 | HG00735.hp2 HG02809.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.819-575_819-572dup others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37876229 | ||||||
chr7:37876229 | T | TATAGATA others(5): Show |
2 | a0001c0001t0001g0112 a0003c0015t0002g0327 |
2 | HG02572.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.819-583_819-572dup others(12): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37876229 | ||||||
chr7:37876229 | T | TATATATA others(1): Show |
23 | a0001c0001t0001g0232 a0001c0001t0003g0047 a0001c0001t0003g0062 others(20): Show |
23 | HG00544.hp2 HG00597.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.819-600_819-599ins others(8): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37876229 | ||||||
chr7:37876229 | T | TATATATA others(5): Show |
1 | a0003c0003t0002g0318 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.819-600_819-599ins others(12): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37876229 | ||||||
chr7:37876229 | T | TATATATA others(9): Show |
1 | a0003c0003t0002g0042 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.819-600_819-599ins others(16): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37876229 | ||||||
chr7:37876229 | TATAG | T | 30 | a0001c0001t0001g0022 a0001c0001t0006g0153 a0001c0001t0006g0154 others(27): Show |
35 | HG00280.hp1 HG01074.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.819-575_819-572del others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37876229 | ||||||
chr7:37876229 | TATAGATA others(1): Show |
T | 48 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0159 others(45): Show |
64 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.819-579_819-572del others(8): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37876229 | ||||||
chr7:37876229 | TATAGATA others(5): Show |
T | 38 | a0001c0001t0001g0019 a0001c0001t0001g0077 a0001c0001t0001g0078 others(35): Show |
41 | HG00099.hp2 HG00423.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.819-583_819-572del others(12): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37876229 | ||||||
chr7:37876231 | TAG | T | 5 | a0002c0020t0001g0205 a0003c0010t0001g0256 a0003c0010t0002g0306 others(2): Show |
5 | HG01109.hp1 HG02280.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.819-599_819-598del others(2): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37876231 | ||||||
chr7:37876231 | TAGATAG | T | 24 | a0001c0001t0001g0048 a0001c0001t0001g0051 a0001c0001t0001g0056 others(21): Show |
28 | HG00323.hp2 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.819-599_819-594del others(6): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37876231 | ||||||
chr7:37876231 | TAGATAGA others(3): Show |
T | 1 | a0001c0001t0001g0168 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.819-599_819-590del others(10): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37876231 | ||||||
chr7:37876233 | G | T | 4 | a0001c0001t0004g0192 a0003c0003t0002g0269 a0012c0021t0002g0041 others(1): Show |
5 | HG01433.hp1 HG01884.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.819-599G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37876233 | |||||||
chr7:37876235 | T | A | 23 | a0001c0001t0001g0232 a0001c0001t0003g0047 a0001c0001t0003g0062 others(20): Show |
23 | HG00544.hp2 HG00597.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.819-597T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37876235 | |||||||
chr7:37876237 | G | T | 4 | a0001c0001t0006g0153 a0001c0001t0006g0154 a0013c0027t0001g0149 others(1): Show |
4 | HG02145.hp1 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.819-595G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37876237 | |||||||
chr7:37876372 | C | T | 28 | a0001c0001t0001g0232 a0001c0001t0003g0047 a0001c0001t0003g0062 others(25): Show |
30 | HG00544.hp2 HG00597.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.819-460C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37876372 | |||||||
chr7:37876386 | C | A | 31 | a0001c0007t0001g0021 a0001c0007t0001g0079 a0001c0007t0001g0080 others(28): Show |
35 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.819-446C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37876386 | |||||||
chr7:37876413 | TAAAC | T | 67 | a0001c0001t0006g0153 a0001c0001t0006g0154 a0001c0007t0001g0021 others(64): Show |
76 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.819-416_819-413del others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 37876413 | ||||||
chr7:37876681 | AT | A | 67 | a0001c0001t0006g0153 a0001c0001t0006g0154 a0001c0007t0001g0021 others(64): Show |
76 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.819-150delT | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37876681 | |||||||
chr7:37876694 | G | A | 2 | a0001c0007t0001g0021 a0001c0007t0003g0111 |
3 | HG03491.hp1 HG03492.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.819-138G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37876694 | |||||||
chr7:37876709 | A | T | 140 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(137): Show |
167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.819-123A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 11/17 | chr7 | 37876709 | |||||||
chr7:37877026 | A | G | 1 | a0011c0029t0001g0027 | 2 | HG01358.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.994+19A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37877026 | |||||||
chr7:37877085 | A | G | 1 | a0005c0006t0002g0280 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.994+78A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37877085 | |||||||
chr7:37877197 | A | G | 28 | a0001c0001t0001g0232 a0001c0001t0003g0047 a0001c0001t0003g0062 others(25): Show |
30 | HG00544.hp2 HG00597.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.994+190A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37877197 | |||||||
chr7:37877354 | T | A | 1 | a0003c0003t0002g0039 | 2 | HG00738.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.994+347T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37877354 | |||||||
chr7:37877472 | A | G | 1 | a0006c0016t0002g0271 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.994+465A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37877472 | |||||||
chr7:37877490 | A | G | 140 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(137): Show |
167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.994+483A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37877490 | |||||||
chr7:37877687 | G | A | 1 | a0003c0003t0002g0037 | 2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.994+680G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37877687 | |||||||
chr7:37877794 | C | G | 2 | a0001c0001t0006g0153 a0001c0001t0006g0154 |
2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.994+787C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37877794 | |||||||
chr7:37877863 | T | C | 207 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(204): Show |
243 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.994+856T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37877863 | |||||||
chr7:37877898 | G | C | 1 | a0001c0001t0001g0247 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.994+891G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37877898 | |||||||
chr7:37878002 | A | G | 206 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(203): Show |
242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.994+995A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37878002 | |||||||
chr7:37878220 | A | G | 207 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(204): Show |
243 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.994+1213A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37878220 | |||||||
chr7:37878286 | A | G | 206 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(203): Show |
242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.994+1279A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37878286 | |||||||
chr7:37878343 | T | A | 206 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(203): Show |
242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.994+1336T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37878343 | |||||||
chr7:37878394 | G | C | 111 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0048 others(108): Show |
129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.994+1387G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37878394 | |||||||
chr7:37878478 | C | T | 1 | a0005c0025t0002g0296 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.994+1471C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37878478 | |||||||
chr7:37878499 | C | G | 30 | a0001c0007t0001g0021 a0001c0007t0001g0079 a0001c0007t0001g0080 others(27): Show |
34 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.994+1492C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37878499 | |||||||
chr7:37878563 | A | T | 203 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(200): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.994+1556A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37878563 | |||||||
chr7:37878739 | T | C | 3 | a0003c0003t0002g0042 a0003c0003t0002g0318 a0003c0015t0002g0327 |
4 | HG02896.hp2 HG02897.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.994+1732T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37878739 | |||||||
chr7:37878936 | G | C | 1 | a0013c0027t0001g0149 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.994+1929G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37878936 | |||||||
chr7:37878989 | G | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0143 others(9): Show |
16 | HG00741.hp1 HG02055.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.994+1982G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37878989 | |||||||
chr7:37879110 | G | A | 203 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(200): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.994+2103G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37879110 | |||||||
chr7:37879126 | T | TTA | 95 | a0001c0001t0001g0232 a0001c0001t0003g0047 a0001c0001t0003g0062 others(92): Show |
106 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.994+2133_994+2134d others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37879126 | ||||||
chr7:37879211 | T | C | 206 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(203): Show |
242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.994+2204T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37879211 | |||||||
chr7:37879263 | C | A | 2 | a0002c0020t0001g0211 a0002c0020t0001g0212 |
2 | NA18951.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.994+2256C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37879263 | |||||||
chr7:37879283 | T | G | 206 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(203): Show |
242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.994+2276T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37879283 | |||||||
chr7:37879559 | A | G | 4 | a0002c0002t0001g0010 a0002c0002t0001g0216 a0002c0002t0001g0229 others(1): Show |
6 | NA18962.hp1 NA18968.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.994+2552A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37879559 | |||||||
chr7:37879767 | G | C | 203 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(200): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.994+2760G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37879767 | |||||||
chr7:37879846 | C | A | 63 | a0001c0001t0006g0153 a0001c0001t0006g0154 a0001c0007t0001g0021 others(60): Show |
72 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.994+2839C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37879846 | |||||||
chr7:37879901 | A | G | 56 | a0001c0001t0001g0044 a0001c0001t0001g0091 a0001c0001t0001g0096 others(53): Show |
62 | HG00323.hp1 HG00558.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.994+2894A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37879901 | |||||||
chr7:37879943 | T | A | 61 | a0001c0007t0001g0021 a0001c0007t0001g0049 a0001c0007t0001g0055 others(58): Show |
70 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.994+2936T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37879943 | |||||||
chr7:37879952 | A | G | 1 | a0003c0010t0002g0307 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.994+2945A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37879952 | |||||||
chr7:37879990 | G | A | 172 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(169): Show |
206 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.994+2983G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37879990 | |||||||
chr7:37880085 | TTG | T | 171 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(168): Show |
203 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.994+3080_994+3081d others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37880085 | ||||||
chr7:37880086 | TG | T | 3 | a0002c0002t0001g0002 a0002c0009t0001g0238 a0006c0011t0002g0035 |
3 | NA18985.hp1 NA18991.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.994+3080delG | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37880086 | |||||||
chr7:37880087 | G | T | 29 | a0001c0001t0001g0232 a0001c0001t0003g0047 a0001c0001t0003g0062 others(26): Show |
31 | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.994+3080G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37880087 | |||||||
chr7:37880150 | T | G | 3 | a0003c0003t0002g0042 a0003c0003t0002g0318 a0003c0015t0002g0327 |
4 | HG02896.hp2 HG02897.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.994+3143T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37880150 | |||||||
chr7:37880307 | T | C | 203 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(200): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.994+3300T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37880307 | |||||||
chr7:37880355 | C | T | 1 | a0009c0031t0001g0130 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.994+3348C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37880355 | |||||||
chr7:37880392 | G | A | 2 | a0001c0001t0006g0153 a0001c0001t0006g0154 |
2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.994+3385G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37880392 | |||||||
chr7:37880403 | C | T | 203 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(200): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.994+3396C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37880403 | |||||||
chr7:37880411 | A | G | 42 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0077 others(39): Show |
46 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.994+3404A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37880411 | |||||||
chr7:37880512 | G | A | 61 | a0001c0007t0001g0021 a0001c0007t0001g0049 a0001c0007t0001g0055 others(58): Show |
70 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.994+3505G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37880512 | |||||||
chr7:37880569 | G | A | 203 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(200): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.994+3562G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37880569 | |||||||
chr7:37880718 | A | T | 2 | a0012c0021t0002g0041 a0017c0034t0001g0117 |
3 | HG01433.hp1 HG01884.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.995-3585A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37880718 | |||||||
chr7:37880757 | G | T | 1 | a0001c0001t0001g0156 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.995-3546G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37880757 | |||||||
chr7:37880784 | C | T | 203 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(200): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.995-3519C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37880784 | |||||||
chr7:37880802 | AT | A | 202 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(199): Show |
238 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.995-3493delT | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37880802 | ||||||
chr7:37880812 | G | A | 3 | a0002c0009t0001g0001 a0002c0009t0001g0238 a0002c0009t0001g0242 |
8 | NA18954.hp1 NA18969.hp2 NA18988.hp2 others(5): Show |
intron_variant | MODIFIER | c.995-3491G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37880812 | |||||||
chr7:37880868 | G | A | 203 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(200): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.995-3435G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37880868 | |||||||
chr7:37880882 | T | A | 1 | a0001c0004t0001g0124 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.995-3421T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37880882 | |||||||
chr7:37881030 | T | C | 1 | a0003c0003t0002g0318 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.995-3273T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37881030 | |||||||
chr7:37881073 | T | C | 2 | a0001c0001t0006g0153 a0001c0001t0006g0154 |
2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.995-3230T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37881073 | |||||||
chr7:37881081 | C | G | 203 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(200): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.995-3222C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37881081 | |||||||
chr7:37881265 | T | C | 203 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(200): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.995-3038T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37881265 | |||||||
chr7:37881279 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0091 |
2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.995-3024G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37881279 | |||||||
chr7:37881520 | T | C | 1 | a0003c0003t0001g0137 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.995-2783T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37881520 | |||||||
chr7:37881525 | T | C | 203 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(200): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.995-2778T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37881525 | |||||||
chr7:37881580 | C | T | 3 | a0002c0002t0001g0031 a0002c0002t0001g0032 a0002c0002t0001g0251 |
5 | HG01243.hp2 HG02258.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.995-2723C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37881580 | |||||||
chr7:37881650 | T | C | 203 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(200): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.995-2653T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37881650 | |||||||
chr7:37881755 | T | C | 203 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(200): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.995-2548T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37881755 | |||||||
chr7:37881941 | T | G | 2 | a0001c0001t0001g0078 a0009c0022t0002g0310 |
2 | HG00733.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.995-2362T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37881941 | |||||||
chr7:37881972 | C | T | 2 | a0004c0005t0001g0014 a0004c0005t0001g0057 |
3 | HG01943.hp2 HG02148.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.995-2331C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37881972 | |||||||
chr7:37882028 | G | A | 203 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(200): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.995-2275G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882028 | |||||||
chr7:37882098 | T | C | 27 | a0001c0007t0001g0021 a0001c0007t0001g0079 a0001c0007t0001g0080 others(24): Show |
31 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.995-2205T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882098 | |||||||
chr7:37882323 | C | T | 1 | a0007c0017t0001g0207 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.995-1980C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882323 | |||||||
chr7:37882487 | A | G | 2 | a0001c0001t0006g0153 a0001c0001t0006g0154 |
2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.995-1816A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882487 | |||||||
chr7:37882546 | G | GGAAAGAA others(5): Show |
1 | a0001c0004t0004g0194 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.995-1714_995-1703d others(14): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882546 | ||||||
chr7:37882546 | GGAAAGAA others(1): Show |
G | 3 | a0001c0001t0001g0145 a0003c0003t0001g0258 a0003c0015t0002g0326 |
3 | HG02717.hp1 HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.995-1710_995-1703d others(10): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882546 | ||||||
chr7:37882551 | G | C | 3 | a0002c0009t0001g0244 a0013c0027t0001g0149 a0013c0027t0005g0198 |
3 | HG00280.hp1 HG02615.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.995-1752G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882551 | |||||||
chr7:37882552 | A | G | 1 | a0002c0002t0001g0208 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.995-1751A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882552 | |||||||
chr7:37882555 | GAAAGAAA others(3): Show |
G | 1 | a0003c0003t0002g0301 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.995-1746_995-1737d others(12): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882555 | ||||||
chr7:37882581 | AAGAAAGA others(21): Show |
A | 1 | a0005c0006t0002g0279 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.995-1718_995-1691d others(30): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882581 | ||||||
chr7:37882581 | AAGAAAGA others(25): Show |
A | 2 | a0001c0001t0001g0166 a0003c0003t0002g0319 |
2 | HG02970.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.995-1702_995-1671d others(34): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882581 | ||||||
chr7:37882585 | AAGAAAGA others(17): Show |
A | 10 | a0001c0001t0004g0181 a0003c0003t0002g0039 a0003c0003t0002g0309 others(7): Show |
11 | HG00738.hp1 HG00738.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.995-1714_995-1691d others(26): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882585 | ||||||
chr7:37882585 | AAGAAAGA others(19): Show |
A | 1 | a0002c0002t0001g0206 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.995-1714_995-1689d others(28): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882585 | ||||||
chr7:37882585 | AAGAAAGA others(21): Show |
A | 9 | a0001c0001t0001g0051 a0001c0001t0001g0164 a0001c0001t0001g0165 others(6): Show |
9 | HG01070.hp1 HG02818.hp1 HG03669.hp1 others(6): Show |
intron_variant | MODIFIER | c.995-1702_995-1675d others(30): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882585 | ||||||
chr7:37882589 | AAGAAAGA others(7): Show |
A | 12 | a0001c0001t0001g0176 a0001c0001t0003g0007 a0001c0001t0003g0043 others(9): Show |
16 | HG00099.hp1 HG00639.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.995-1710_995-1697d others(16): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882589 | ||||||
chr7:37882589 | AAGAAAGA others(15): Show |
A | 6 | a0001c0001t0004g0009 a0001c0001t0004g0192 a0001c0007t0001g0163 others(3): Show |
8 | HG01346.hp1 HG02135.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.995-1710_995-1689d others(24): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882589 | ||||||
chr7:37882589 | AAGAAAGA others(17): Show |
A | 15 | a0001c0001t0001g0078 a0001c0001t0001g0082 a0001c0001t0001g0173 others(12): Show |
16 | HG00558.hp1 HG00621.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.995-1702_995-1679d others(26): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882589 | ||||||
chr7:37882593 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.995-1710A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882593 | |||||||
chr7:37882593 | AAGAAAGA others(3): Show |
A | 1 | a0001c0001t0001g0112 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.995-1706_995-1697d others(12): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882593 | ||||||
chr7:37882593 | AAGAAAGA others(7): Show |
A | 2 | a0001c0001t0006g0153 a0013c0027t0001g0149 |
2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.995-1706_995-1693d others(16): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882593 | ||||||
chr7:37882593 | AAGAAAGA others(11): Show |
A | 10 | a0001c0001t0001g0024 a0001c0007t0001g0049 a0001c0007t0001g0075 others(7): Show |
11 | HG00140.hp2 HG01074.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.995-1706_995-1689d others(20): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882593 | ||||||
chr7:37882593 | AAGAAAGA others(13): Show |
A | 1 | a0001c0004t0003g0105 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.995-1702_995-1683d others(22): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882593 | ||||||
chr7:37882597 | A | AAGAAAGA others(3): Show |
3 | a0001c0004t0003g0003 a0003c0003t0002g0316 a0016c0036t0001g0226 |
3 | HG02451.hp1 HG02683.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.995-1703_995-1702i others(12): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | ||||||
chr7:37882597 | A | AAGAAAGA others(7): Show |
4 | a0001c0001t0003g0045 a0001c0004t0003g0003 a0004c0005t0001g0008 others(1): Show |
5 | HG01256.hp2 NA18943.hp1 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.995-1703_995-1702i others(16): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | ||||||
chr7:37882597 | A | AAGAAAGA others(17): Show |
1 | a0001c0004t0001g0003 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.995-1703_995-1702i others(26): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | ||||||
chr7:37882597 | A | AAGAAAGA others(13): Show |
1 | a0001c0001t0003g0093 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.995-1703_995-1702i others(22): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | ||||||
chr7:37882597 | A | AAGAAAGA others(15): Show |
1 | a0001c0001t0003g0050 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.995-1703_995-1702i others(24): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | ||||||
chr7:37882597 | A | AAGAAAGA others(15): Show |
1 | a0001c0001t0001g0091 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.995-1703_995-1702i others(24): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | ||||||
chr7:37882597 | A | AAGAAAGA others(9): Show |
5 | a0001c0001t0001g0044 a0001c0001t0003g0114 a0003c0003t0002g0305 others(2): Show |
5 | HG01123.hp1 HG01192.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.995-1703_995-1702i others(18): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | ||||||
chr7:37882597 | A | AAGAAAGA others(11): Show |
2 | a0001c0004t0001g0115 a0001c0004t0003g0113 |
2 | HG01515.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.995-1703_995-1702i others(20): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | ||||||
chr7:37882597 | A | AAGAAAGA others(5): Show |
6 | a0001c0001t0003g0092 a0001c0004t0003g0101 a0002c0002t0001g0221 others(3): Show |
6 | HG00323.hp1 HG00735.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.995-1703_995-1702i others(14): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | ||||||
chr7:37882597 | A | AAGAAAGA others(7): Show |
3 | a0001c0001t0001g0116 a0005c0014t0002g0034 a0005c0014t0002g0287 |
3 | HG03239.hp1 NA18990.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.995-1703_995-1702i others(16): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | ||||||
chr7:37882597 | A | AAGAAAGA others(9): Show |
1 | a0001c0001t0001g0119 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.995-1703_995-1702i others(18): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | ||||||
chr7:37882597 | A | AAGAAAGA others(11): Show |
1 | a0001c0001t0001g0100 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.995-1703_995-1702i others(20): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | ||||||
chr7:37882597 | A | AAGAAAGA others(4): Show |
1 | a0004c0005t0003g0046 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.995-1703_995-1702i others(13): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | ||||||
chr7:37882597 | A | AAGAAAGA others(6): Show |
1 | a0004c0005t0001g0014 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.995-1703_995-1702i others(15): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | ||||||
chr7:37882597 | A | AAGAAAGA others(1): Show |
6 | a0001c0004t0003g0094 a0003c0003t0002g0315 a0004c0005t0003g0008 others(3): Show |
6 | HG00558.hp2 HG02647.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.995-1703_995-1702i others(10): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | ||||||
chr7:37882597 | A | AAGAAAGA others(4): Show |
1 | a0003c0003t0002g0037 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.995-1703_995-1702i others(13): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | ||||||
chr7:37882597 | A | AAGAAAGA others(3): Show |
1 | a0003c0003t0002g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.995-1703_995-1702i others(12): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | ||||||
chr7:37882597 | A | AAGAAAGA others(5): Show |
3 | a0001c0004t0001g0097 a0001c0004t0001g0123 a0003c0003t0001g0137 |
3 | HG01928.hp2 NA18980.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.995-1703_995-1702i others(14): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | ||||||
chr7:37882597 | A | AAGAAAGA others(9): Show |
1 | a0001c0004t0003g0099 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.995-1703_995-1702i others(18): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | ||||||
chr7:37882597 | A | G | 24 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0020 others(21): Show |
30 | HG00140.hp1 HG00741.hp1 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.995-1706A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882597 | |||||||
chr7:37882597 | AAG | A | 3 | a0002c0002t0001g0031 a0002c0002t0001g0251 a0002c0009t0001g0238 |
4 | HG02258.hp1 HG02630.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.995-1688_995-1687d others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | ||||||
chr7:37882597 | AAGAG | A | 3 | a0001c0001t0005g0196 a0001c0004t0005g0197 a0003c0003t0008g0299 |
3 | HG02886.hp2 HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.995-1690_995-1687d others(6): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | ||||||
chr7:37882597 | AAGAGAG | A | 3 | a0001c0007t0001g0245 a0002c0020t0001g0205 a0003c0010t0001g0256 |
3 | HG01109.hp1 HG02280.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.995-1692_995-1687d others(8): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | ||||||
chr7:37882597 | AAGAGAGA others(1): Show |
A | 15 | a0001c0001t0001g0168 a0001c0001t0001g0177 a0001c0001t0003g0083 others(12): Show |
15 | HG00323.hp2 HG01081.hp2 HG02155.hp1 others(12): Show |
intron_variant | MODIFIER | c.995-1694_995-1687d others(10): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | ||||||
chr7:37882597 | AAGAGAGA others(3): Show |
A | 11 | a0001c0001t0006g0154 a0001c0007t0003g0102 a0001c0028t0001g0054 others(8): Show |
16 | HG00280.hp1 HG02040.hp1 HG02895.hp1 others(13): Show |
intron_variant | MODIFIER | c.995-1696_995-1687d others(12): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | ||||||
chr7:37882597 | AAGAGAGA others(5): Show |
A | 14 | a0001c0001t0001g0056 a0001c0004t0001g0234 a0001c0007t0007g0090 others(11): Show |
15 | HG01081.hp1 HG02717.hp2 HG02886.hp1 others(12): Show |
intron_variant | MODIFIER | c.995-1698_995-1687d others(14): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | ||||||
chr7:37882597 | AAGAGAGA others(7): Show |
A | 5 | a0001c0001t0004g0193 a0001c0007t0001g0055 a0001c0007t0001g0248 others(2): Show |
5 | HG01928.hp1 HG01975.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.995-1700_995-1687d others(16): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | ||||||
chr7:37882597 | AAGAGAGA others(9): Show |
A | 53 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(50): Show |
67 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.995-1702_995-1687d others(18): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882597 | ||||||
chr7:37882599 | G | GAA | 22 | a0001c0001t0001g0232 a0001c0001t0003g0047 a0001c0001t0003g0062 others(19): Show |
22 | HG00597.hp2 HG00673.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.995-1703_995-1702i others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882599 | ||||||
chr7:37882599 | G | GAAAGAA | 5 | a0001c0001t0003g0089 a0001c0001t0004g0190 a0001c0028t0003g0106 others(2): Show |
5 | HG00544.hp2 HG02683.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.995-1703_995-1702i others(8): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882599 | ||||||
chr7:37882599 | GAGAGAGA others(27): Show |
G | 1 | a0002c0002t0001g0228 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.995-1700_995-1667d others(36): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882599 | ||||||
chr7:37882601 | G | A | 43 | a0001c0001t0001g0156 a0001c0001t0003g0008 a0001c0001t0003g0085 others(40): Show |
48 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.995-1702G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882601 | |||||||
chr7:37882603 | G | A | 24 | a0001c0001t0001g0232 a0001c0001t0003g0047 a0001c0001t0003g0062 others(21): Show |
25 | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.995-1700G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882603 | |||||||
chr7:37882605 | G | A | 41 | a0001c0001t0001g0156 a0001c0001t0003g0065 a0001c0001t0003g0070 others(38): Show |
45 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.995-1698G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882605 | |||||||
chr7:37882605 | GAGAGAGA others(9): Show |
G | 7 | a0001c0001t0001g0020 a0005c0006t0002g0263 a0005c0006t0002g0273 others(4): Show |
9 | HG00140.hp1 HG01074.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.995-1694_995-1679d others(18): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882605 | ||||||
chr7:37882607 | G | A | 21 | a0001c0001t0003g0047 a0001c0001t0003g0066 a0001c0001t0003g0067 others(18): Show |
22 | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.995-1696G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882607 | |||||||
chr7:37882609 | G | A | 61 | a0001c0001t0001g0156 a0001c0001t0001g0168 a0001c0001t0001g0177 others(58): Show |
66 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.995-1694G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882609 | |||||||
chr7:37882609 | GAGAGAGA others(5): Show |
G | 4 | a0002c0002t0001g0058 a0002c0008t0001g0241 a0003c0003t0002g0301 others(1): Show |
4 | HG02300.hp2 HG02896.hp1 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.995-1690_995-1679d others(14): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882609 | ||||||
chr7:37882611 | G | A | 26 | a0001c0001t0003g0066 a0001c0001t0003g0068 a0001c0001t0003g0089 others(23): Show |
32 | HG00280.hp1 HG00544.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.995-1692G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882611 | |||||||
chr7:37882611 | GAGAGAA | G | 4 | a0003c0010t0002g0312 a0003c0010t0002g0313 a0003c0010t0002g0314 others(1): Show |
4 | HG01884.hp2 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.995-1688_995-1683d others(8): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882611 | ||||||
chr7:37882611 | GAGAGAAA others(3): Show |
G | 2 | a0002c0002t0001g0209 a0002c0002t0001g0210 |
2 | NA18964.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.995-1688_995-1679d others(12): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882611 | ||||||
chr7:37882613 | G | A | 88 | a0001c0001t0001g0018 a0001c0001t0001g0056 a0001c0001t0001g0119 others(85): Show |
96 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.995-1690G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882613 | |||||||
chr7:37882613 | G | GAA | 3 | a0001c0001t0001g0018 a0001c0001t0001g0143 a0001c0001t0001g0150 |
3 | HG00741.hp1 HG02055.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.995-1689_995-1688i others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882613 | ||||||
chr7:37882613 | G | GAGAA | 6 | a0001c0001t0001g0004 a0001c0001t0001g0147 a0001c0001t0001g0148 others(3): Show |
9 | HG02257.hp2 HG02280.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.995-1662_995-1659d others(6): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882613 | ||||||
chr7:37882613 | G | GAGAGAA | 3 | a0001c0001t0001g0146 a0001c0001t0001g0152 a0003c0003t0002g0303 |
3 | HG02630.hp1 HG02809.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.995-1687_995-1686i others(8): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882613 | ||||||
chr7:37882613 | G | GAGAGAGA others(1): Show |
4 | a0001c0001t0001g0118 a0001c0001t0001g0157 a0001c0001t0001g0247 others(1): Show |
4 | HG02145.hp2 HG02258.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.995-1687_995-1686i others(10): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882613 | ||||||
chr7:37882613 | G | GAGAGAGA others(7): Show |
1 | a0003c0015t0002g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.995-1687_995-1686i others(16): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882613 | ||||||
chr7:37882613 | GAGAA | G | 5 | a0003c0003t0002g0269 a0003c0003t0002g0318 a0005c0006t0002g0036 others(2): Show |
6 | HG01433.hp1 HG03195.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.995-1662_995-1659d others(6): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882613 | ||||||
chr7:37882613 | GAGAAAGA others(1): Show |
G | 3 | a0001c0001t0001g0162 a0005c0006t0002g0274 a0006c0011t0002g0266 |
3 | HG03927.hp1 NA19080.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.995-1666_995-1659d others(10): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882613 | ||||||
chr7:37882615 | G | A | 1 | a0002c0009t0001g0244 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.995-1688G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882615 | |||||||
chr7:37882615 | GAAAGAA | G | 12 | a0001c0001t0001g0176 a0001c0001t0003g0007 a0001c0001t0003g0043 others(9): Show |
15 | HG00099.hp1 HG00639.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.995-1686_995-1681d others(8): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882615 | ||||||
chr7:37882616 | A | AG | 3 | a0001c0001t0003g0092 a0001c0004t0004g0194 a0002c0002t0001g0221 |
3 | HG00735.hp1 HG01123.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.995-1687_995-1686i others(3): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882616 | |||||||
chr7:37882617 | A | G | 20 | a0001c0001t0001g0112 a0001c0001t0003g0008 a0001c0001t0004g0181 others(17): Show |
23 | HG00738.hp1 HG00738.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.995-1686A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882617 | |||||||
chr7:37882617 | AAG | A | 5 | a0001c0007t0001g0172 a0002c0009t0001g0213 a0004c0012t0001g0006 others(2): Show |
7 | HG02083.hp2 NA18612.hp2 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.995-1684_995-1683d others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882617 | ||||||
chr7:37882621 | A | AAG | 3 | a0002c0009t0001g0140 a0003c0010t0001g0135 a0004c0005t0001g0053 |
3 | HG03017.hp1 NA18951.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.995-1680_995-1679d others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882621 | ||||||
chr7:37882621 | A | G | 12 | a0001c0001t0004g0181 a0003c0003t0002g0039 a0003c0003t0002g0309 others(9): Show |
14 | HG00738.hp1 HG00738.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.995-1682A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882621 | |||||||
chr7:37882621 | AAG | A | 9 | a0001c0007t0001g0021 a0001c0007t0001g0080 a0001c0007t0007g0090 others(6): Show |
11 | HG00423.hp2 HG00609.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.995-1680_995-1679d others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882621 | ||||||
chr7:37882623 | G | GAA | 4 | a0001c0007t0001g0079 a0002c0020t0001g0211 a0003c0010t0001g0127 others(1): Show |
4 | HG02523.hp1 NA18945.hp1 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.995-1678_995-1677d others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882623 | ||||||
chr7:37882629 | AAG | A | 4 | a0001c0001t0001g0156 a0005c0024t0002g0283 a0013c0027t0001g0149 others(1): Show |
4 | HG00621.hp1 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.995-1672_995-1671d others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882629 | ||||||
chr7:37882631 | GAA | G | 3 | a0001c0001t0004g0184 a0001c0004t0003g0105 a0002c0008t0001g0252 |
3 | HG00423.hp1 NA18986.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.995-1670_995-1669d others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882631 | ||||||
chr7:37882633 | AAG | A | 37 | a0001c0001t0001g0022 a0001c0001t0001g0077 a0001c0001t0001g0121 others(34): Show |
50 | HG00280.hp2 HG01106.hp1 HG01169.hp2 others(47): Show |
intron_variant | MODIFIER | c.995-1668_995-1667d others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882633 | ||||||
chr7:37882635 | G | A | 1 | a0002c0002t0001g0228 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.995-1668G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882635 | |||||||
chr7:37882639 | G | A | 122 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(119): Show |
143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.995-1664G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882639 | |||||||
chr7:37882641 | A | AAAAG | 5 | a0001c0028t0003g0106 a0007c0018t0001g0052 a0007c0018t0001g0214 others(2): Show |
5 | HG00544.hp1 HG03942.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.995-1661_995-1660i others(6): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882641 | ||||||
chr7:37882641 | A | G | 122 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(119): Show |
143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.995-1662A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882641 | |||||||
chr7:37882641 | AAG | A | 47 | a0001c0001t0001g0022 a0001c0001t0001g0077 a0001c0001t0001g0121 others(44): Show |
61 | HG00280.hp2 HG00423.hp1 HG01106.hp1 others(58): Show |
intron_variant | MODIFIER | c.995-1658_995-1657d others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882641 | ||||||
chr7:37882641 | AAGAGAAA others(9): Show |
A | 2 | a0002c0002t0001g0031 a0002c0002t0001g0251 |
3 | HG02258.hp1 HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.995-1658_995-1643d others(18): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882641 | ||||||
chr7:37882643 | G | A | 129 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(126): Show |
150 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.995-1660G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882643 | |||||||
chr7:37882643 | G | GAAAGAAA others(55): Show |
1 | a0001c0001t0003g0066 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.995-1659_995-1658i others(64): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882643 | ||||||
chr7:37882643 | G | GAAAGAAA others(59): Show |
1 | a0004c0005t0001g0053 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.995-1659_995-1658i others(68): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882643 | ||||||
chr7:37882643 | G | GAAAGAAA others(47): Show |
1 | a0001c0001t0001g0232 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.995-1659_995-1658i others(56): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882643 | ||||||
chr7:37882643 | G | GAAAGAAA others(51): Show |
1 | a0001c0001t0003g0047 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.995-1659_995-1658i others(60): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882643 | ||||||
chr7:37882643 | G | GAAAGAAA others(47): Show |
3 | a0001c0001t0003g0067 a0001c0001t0003g0068 a0002c0002t0001g0225 |
3 | HG02071.hp2 NA18957.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.995-1659_995-1658i others(56): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882643 | ||||||
chr7:37882643 | G | GAAAGAAA others(43): Show |
6 | a0001c0001t0003g0069 a0001c0001t0003g0071 a0001c0001t0003g0089 others(3): Show |
6 | HG00544.hp2 HG00673.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.995-1659_995-1658i others(52): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882643 | ||||||
chr7:37882643 | G | GAAAGAAA others(39): Show |
4 | a0001c0001t0003g0062 a0001c0001t0003g0072 a0001c0001t0004g0191 others(1): Show |
4 | HG02683.hp1 HG03239.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.995-1659_995-1658i others(48): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882643 | ||||||
chr7:37882643 | G | GAAAGAAA others(35): Show |
5 | a0001c0001t0003g0065 a0002c0002t0001g0139 a0002c0008t0001g0250 others(2): Show |
5 | HG02523.hp2 HG03942.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.995-1659_995-1658i others(44): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882643 | ||||||
chr7:37882643 | G | GAAAGAAA others(31): Show |
1 | a0001c0001t0003g0070 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.995-1659_995-1658i others(40): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882643 | ||||||
chr7:37882643 | G | GAAAGAGA others(27): Show |
1 | a0002c0002t0001g0243 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.995-1659_995-1658i others(36): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37882643 | ||||||
chr7:37882655 | A | G | 2 | a0013c0027t0001g0149 a0013c0027t0005g0198 |
2 | HG02615.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.995-1648A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882655 | |||||||
chr7:37882657 | G | A | 2 | a0013c0027t0001g0149 a0013c0027t0005g0198 |
2 | HG02615.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.995-1646G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882657 | |||||||
chr7:37882724 | G | T | 1 | a0001c0004t0001g0231 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.995-1579G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882724 | |||||||
chr7:37882931 | A | C | 1 | a0007c0018t0001g0214 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.995-1372A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882931 | |||||||
chr7:37882942 | G | A | 2 | a0001c0004t0001g0231 a0007c0017t0001g0142 |
2 | NA18942.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.995-1361G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882942 | |||||||
chr7:37882987 | G | A | 29 | a0001c0001t0001g0232 a0001c0001t0003g0047 a0001c0001t0003g0062 others(26): Show |
31 | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.995-1316G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37882987 | |||||||
chr7:37883085 | A | G | 3 | a0002c0002t0001g0031 a0002c0002t0001g0032 a0002c0002t0001g0251 |
5 | HG01243.hp2 HG02258.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.995-1218A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37883085 | |||||||
chr7:37883199 | G | A | 203 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(200): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.995-1104G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37883199 | |||||||
chr7:37883205 | A | G | 1 | a0002c0009t0001g0244 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.995-1098A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37883205 | |||||||
chr7:37883284 | T | G | 1 | a0001c0004t0001g0123 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.995-1019T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37883284 | |||||||
chr7:37883330 | T | A | 203 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(200): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.995-973T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37883330 | |||||||
chr7:37883376 | T | G | 1 | a0001c0001t0003g0092 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.995-927T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37883376 | |||||||
chr7:37883408 | C | A | 1 | a0001c0001t0004g0191 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.995-895C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37883408 | |||||||
chr7:37883438 | A | C | 1 | a0001c0004t0001g0110 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.995-865A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37883438 | |||||||
chr7:37883496 | C | T | 203 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(200): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.995-807C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37883496 | |||||||
chr7:37883673 | C | T | 203 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(200): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.995-630C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37883673 | |||||||
chr7:37883892 | G | A | 3 | a0001c0007t0001g0055 a0001c0007t0001g0125 a0001c0028t0001g0054 |
3 | NA19001.hp2 NA19065.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.995-411G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37883892 | |||||||
chr7:37883909 | A | T | 28 | a0001c0007t0001g0049 a0001c0007t0001g0055 a0001c0007t0001g0075 others(25): Show |
33 | HG01074.hp1 HG01109.hp1 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.995-394A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37883909 | |||||||
chr7:37883917 | C | T | 203 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(200): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.995-386C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37883917 | |||||||
chr7:37883962 | T | TAC | 74 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0077 others(71): Show |
81 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.995-318_995-317dup others(2): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37883962 | ||||||
chr7:37883962 | T | TACAC | 4 | a0001c0001t0001g0168 a0002c0002t0001g0225 a0002c0002t0001g0227 others(1): Show |
4 | HG00280.hp1 HG01081.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.995-320_995-317dup others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37883962 | ||||||
chr7:37883983 | ACACC | A | 28 | a0001c0007t0001g0021 a0001c0007t0001g0079 a0001c0007t0001g0080 others(25): Show |
34 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.995-316_995-313del others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37883983 | ||||||
chr7:37883985 | A | C | 1 | a0002c0008t0001g0222 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.995-318A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37883985 | |||||||
chr7:37883985 | ACC | A | 4 | a0003c0010t0002g0311 a0003c0010t0002g0312 a0003c0010t0002g0313 others(1): Show |
4 | HG02809.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.995-316_995-315del others(2): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 37883985 | ||||||
chr7:37883987 | C | A | 178 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(175): Show |
212 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.995-316C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37883987 | |||||||
chr7:37884247 | G | A | 201 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(198): Show |
237 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.995-56G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 12/17 | chr7 | 37884247 | |||||||
chr7:37884739 | G | A | 1 | a0003c0015t0002g0326 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1139+292G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 13/17 | chr7 | 37884739 | |||||||
chr7:37885053 | T | C | 3 | a0002c0002t0001g0031 a0002c0002t0001g0032 a0002c0002t0001g0251 |
5 | HG01243.hp2 HG02258.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1140-92T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 13/17 | chr7 | 37885053 | |||||||
chr7:37885135 | T | G | 203 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(200): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1140-10T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 13/17 | chr7 | 37885135 | |||||||
chr7:37885277 | A | G | 203 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(200): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1247+25A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37885277 | |||||||
chr7:37885286 | C | T | 30 | a0001c0007t0001g0021 a0001c0007t0001g0079 a0001c0007t0001g0080 others(27): Show |
36 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.1247+34C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37885286 | |||||||
chr7:37885339 | C | G | 1 | a0003c0003t0002g0269 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1247+87C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37885339 | |||||||
chr7:37885472 | T | A | 1 | a0014c0032t0001g0136 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1247+220T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37885472 | |||||||
chr7:37885534 | C | T | 1 | a0001c0004t0004g0194 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1247+282C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37885534 | |||||||
chr7:37885653 | C | T | 203 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(200): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1247+401C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37885653 | |||||||
chr7:37885836 | T | C | 203 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(200): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1247+584T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37885836 | |||||||
chr7:37885982 | A | G | 2 | a0003c0010t0002g0312 a0003c0010t0002g0313 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1247+730A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37885982 | |||||||
chr7:37886046 | A | G | 31 | a0001c0007t0001g0049 a0001c0007t0001g0055 a0001c0007t0001g0075 others(28): Show |
36 | HG01074.hp1 HG01109.hp1 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.1247+794A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37886046 | |||||||
chr7:37886328 | C | T | 3 | a0003c0010t0001g0256 a0003c0023t0001g0254 a0003c0023t0001g0255 |
3 | HG02280.hp1 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1247+1076C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37886328 | |||||||
chr7:37886400 | A | G | 1 | a0005c0006t0002g0277 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1247+1148A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37886400 | |||||||
chr7:37886491 | C | T | 326 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(323): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.1247+1239C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37886491 | |||||||
chr7:37886709 | G | A | 203 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(200): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1247+1457G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37886709 | |||||||
chr7:37886862 | C | CA | 114 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(111): Show |
137 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.1248-1405dupA | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 37886862 | ||||||
chr7:37886913 | T | C | 203 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(200): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1248-1364T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37886913 | |||||||
chr7:37887116 | A | G | 1 | a0001c0001t0004g0189 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1248-1161A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37887116 | |||||||
chr7:37887156 | A | C | 109 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(106): Show |
132 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1248-1121A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37887156 | |||||||
chr7:37887520 | G | T | 1 | a0005c0006t0002g0275 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1248-757G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37887520 | |||||||
chr7:37887657 | G | C | 1 | a0001c0007t0007g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1248-620G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37887657 | |||||||
chr7:37887786 | C | G | 1 | a0005c0019t0002g0289 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1248-491C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37887786 | |||||||
chr7:37887887 | A | G | 4 | a0003c0010t0002g0311 a0003c0010t0002g0312 a0003c0010t0002g0313 others(1): Show |
4 | HG02809.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1248-390A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37887887 | |||||||
chr7:37887946 | A | G | 2 | a0004c0005t0001g0199 a0006c0011t0002g0272 |
2 | HG00099.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1248-331A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37887946 | |||||||
chr7:37887948 | G | C | 48 | a0001c0001t0001g0044 a0001c0001t0001g0091 a0001c0001t0001g0096 others(45): Show |
53 | HG00323.hp1 HG00558.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.1248-329G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37887948 | |||||||
chr7:37887980 | C | T | 41 | a0001c0001t0001g0020 a0001c0001t0001g0162 a0001c0001t0001g0176 others(38): Show |
48 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.1248-297C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37887980 | |||||||
chr7:37887996 | G | A | 1 | a0001c0001t0003g0093 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1248-281G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37887996 | |||||||
chr7:37888007 | A | G | 1 | a0003c0010t0002g0307 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1248-270A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37888007 | |||||||
chr7:37888100 | G | A | 172 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(169): Show |
206 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1248-177G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37888100 | |||||||
chr7:37888138 | T | C | 1 | a0006c0016t0002g0282 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1248-139T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37888138 | |||||||
chr7:37888177 | T | G | 203 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(200): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1248-100T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37888177 | |||||||
chr7:37888249 | G | A | 1 | a0007c0017t0001g0142 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1248-28G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 14/17 | chr7 | 37888249 | |||||||
chr7:37888740 | G | A | 1 | a0008c0013t0002g0268 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1399+312G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37888740 | |||||||
chr7:37888942 | A | G | 5 | a0001c0001t0006g0153 a0001c0001t0006g0154 a0002c0009t0001g0244 others(2): Show |
5 | HG00280.hp1 HG02145.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1399+514A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37888942 | |||||||
chr7:37889102 | C | T | 1 | a0003c0003t0002g0037 | 2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1399+674C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37889102 | |||||||
chr7:37889257 | T | A | 1 | a0001c0001t0001g0152 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1399+829T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37889257 | |||||||
chr7:37889346 | C | G | 28 | a0001c0001t0001g0232 a0001c0001t0003g0062 a0001c0001t0003g0065 others(25): Show |
30 | HG00544.hp2 HG00673.hp1 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.1399+918C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37889346 | |||||||
chr7:37889371 | G | A | 1 | a0003c0015t0002g0326 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1399+943G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37889371 | |||||||
chr7:37889452 | C | A | 202 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(199): Show |
238 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.1399+1024C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37889452 | |||||||
chr7:37889685 | AG | A | 8 | a0001c0001t0001g0020 a0001c0001t0003g0007 a0001c0001t0003g0043 others(5): Show |
12 | HG00738.hp1 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1399+1258delG | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37889685 | |||||||
chr7:37889717 | G | T | 1 | a0002c0002t0001g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1399+1289G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37889717 | |||||||
chr7:37889844 | G | T | 2 | a0013c0027t0001g0149 a0013c0027t0005g0198 |
2 | HG02615.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1399+1416G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37889844 | |||||||
chr7:37889948 | AT | A | 65 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0048 others(62): Show |
82 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.1399+1524delT | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 37889948 | ||||||
chr7:37889966 | T | G | 203 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(200): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1399+1538T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37889966 | |||||||
chr7:37890087 | T | C | 1 | a0007c0018t0001g0214 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1399+1659T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37890087 | |||||||
chr7:37890092 | T | G | 23 | a0001c0001t0001g0024 a0001c0007t0001g0049 a0001c0007t0001g0055 others(20): Show |
29 | HG00140.hp2 HG01074.hp1 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.1399+1664T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37890092 | |||||||
chr7:37890250 | A | G | 2 | a0003c0023t0001g0254 a0003c0023t0001g0255 |
2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1399+1822A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37890250 | |||||||
chr7:37890298 | G | A | 1 | a0003c0015t0002g0326 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1399+1870G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37890298 | |||||||
chr7:37890491 | C | T | 3 | a0001c0007t0001g0055 a0001c0007t0001g0125 a0001c0028t0001g0054 |
3 | NA19001.hp2 NA19065.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1399+2063C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37890491 | |||||||
chr7:37890610 | C | A | 63 | a0001c0001t0001g0024 a0001c0007t0001g0021 a0001c0007t0001g0049 others(60): Show |
75 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.1399+2182C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37890610 | |||||||
chr7:37890772 | G | A | 41 | a0001c0001t0001g0020 a0001c0001t0001g0162 a0001c0001t0001g0176 others(38): Show |
48 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.1399+2344G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37890772 | |||||||
chr7:37890802 | A | G | 30 | a0001c0001t0001g0232 a0001c0001t0003g0062 a0001c0001t0003g0065 others(27): Show |
32 | HG00544.hp2 HG00673.hp1 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.1399+2374A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37890802 | |||||||
chr7:37890839 | A | G | 2 | a0001c0001t0006g0153 a0001c0001t0006g0154 |
2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1399+2411A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37890839 | |||||||
chr7:37890864 | T | C | 1 | a0002c0009t0001g0244 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1399+2436T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37890864 | |||||||
chr7:37890938 | A | G | 1 | a0002c0020t0001g0205 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1399+2510A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37890938 | |||||||
chr7:37891027 | T | G | 2 | a0001c0001t0006g0153 a0001c0001t0006g0154 |
2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1399+2599T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37891027 | |||||||
chr7:37891145 | A | G | 1 | a0002c0002t0001g0216 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1399+2717A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37891145 | |||||||
chr7:37891166 | A | G | 1 | a0005c0014t0002g0287 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1399+2738A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37891166 | |||||||
chr7:37891207 | T | C | 1 | a0002c0002t0001g0215 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1399+2779T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37891207 | |||||||
chr7:37891228 | T | C | 4 | a0002c0009t0001g0001 a0002c0009t0001g0223 a0002c0009t0001g0238 others(1): Show |
9 | HG02040.hp1 NA18954.hp1 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.1399+2800T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37891228 | |||||||
chr7:37891323 | A | T | 1 | a0001c0001t0001g0165 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1399+2895A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37891323 | |||||||
chr7:37891405 | C | T | 203 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(200): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1399+2977C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37891405 | |||||||
chr7:37891493 | C | G | 1 | a0002c0002t0001g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1400-2973C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37891493 | |||||||
chr7:37891736 | A | G | 3 | a0003c0010t0001g0256 a0003c0023t0001g0254 a0003c0023t0001g0255 |
3 | HG02280.hp1 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1400-2730A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37891736 | |||||||
chr7:37891754 | T | C | 270 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(267): Show |
315 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.1400-2712T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37891754 | |||||||
chr7:37891879 | A | G | 30 | a0001c0001t0001g0232 a0001c0001t0003g0062 a0001c0001t0003g0065 others(27): Show |
32 | HG00544.hp2 HG00673.hp1 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.1400-2587A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37891879 | |||||||
chr7:37891930 | A | G | 2 | a0001c0001t0006g0153 a0001c0001t0006g0154 |
2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1400-2536A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37891930 | |||||||
chr7:37891934 | TC | T | 32 | a0001c0001t0001g0024 a0001c0007t0001g0049 a0001c0007t0001g0055 others(29): Show |
38 | HG00140.hp2 HG01074.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.1400-2530delC | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 37891934 | ||||||
chr7:37891959 | T | A | 1 | a0005c0006t0002g0277 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1400-2507T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37891959 | |||||||
chr7:37892184 | T | G | 15 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0143 others(12): Show |
19 | HG00741.hp1 HG02055.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1400-2282T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37892184 | |||||||
chr7:37892247 | T | G | 201 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(198): Show |
237 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1400-2219T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37892247 | |||||||
chr7:37892387 | T | C | 1 | a0001c0001t0003g0114 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1400-2079T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37892387 | |||||||
chr7:37892568 | A | C | 1 | a0001c0001t0001g0121 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1400-1898A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37892568 | |||||||
chr7:37892593 | T | A | 1 | a0007c0018t0001g0214 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1400-1873T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37892593 | |||||||
chr7:37892653 | T | G | 69 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0048 others(66): Show |
86 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1400-1813T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37892653 | |||||||
chr7:37892844 | C | T | 1 | a0013c0027t0001g0149 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1400-1622C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37892844 | |||||||
chr7:37892845 | G | A | 28 | a0001c0007t0001g0021 a0001c0007t0001g0172 a0001c0007t0003g0111 others(25): Show |
34 | HG00423.hp2 HG00544.hp1 HG02083.hp2 others(31): Show |
intron_variant | MODIFIER | c.1400-1621G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37892845 | |||||||
chr7:37892856 | T | TG | 8 | a0001c0001t0001g0082 a0001c0001t0003g0047 a0001c0001t0004g0005 others(5): Show |
12 | HG00597.hp2 HG02615.hp1 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.1400-1603dupG | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 37892856 | ||||||
chr7:37892858 | G | A | 1 | a0001c0001t0006g0153 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1400-1608G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37892858 | |||||||
chr7:37892888 | G | T | 195 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(192): Show |
228 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.1400-1578G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37892888 | |||||||
chr7:37892942 | G | A | 24 | a0001c0001t0001g0232 a0001c0001t0003g0062 a0001c0001t0003g0065 others(21): Show |
26 | HG00280.hp1 HG01346.hp1 HG01975.hp2 others(23): Show |
intron_variant | MODIFIER | c.1400-1524G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37892942 | |||||||
chr7:37893097 | A | C | 40 | a0001c0001t0001g0019 a0001c0001t0001g0077 a0001c0001t0001g0078 others(37): Show |
44 | HG00099.hp2 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1400-1369A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37893097 | |||||||
chr7:37893140 | T | C | 1 | a0007c0017t0001g0207 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1400-1326T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37893140 | |||||||
chr7:37893221 | G | C | 273 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(270): Show |
317 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.1400-1245G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37893221 | |||||||
chr7:37893286 | G | A | 196 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(193): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.1400-1180G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37893286 | |||||||
chr7:37893388 | A | G | 1 | a0001c0007t0007g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1400-1078A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37893388 | |||||||
chr7:37893420 | A | G | 3 | a0003c0010t0002g0038 a0003c0010t0002g0298 a0015c0033t0002g0038 |
3 | HG02258.hp2 HG02559.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1400-1046A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37893420 | |||||||
chr7:37893457 | T | G | 109 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(106): Show |
129 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1400-1009T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37893457 | |||||||
chr7:37893551 | C | A | 249 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(246): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1400-915C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37893551 | |||||||
chr7:37893695 | T | C | 2 | a0001c0001t0004g0193 a0007c0017t0001g0240 |
2 | HG01975.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1400-771T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37893695 | |||||||
chr7:37893895 | G | A | 1 | a0003c0010t0002g0314 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1400-571G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37893895 | |||||||
chr7:37893949 | C | T | 2 | a0013c0027t0001g0149 a0017c0034t0001g0117 |
2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1400-517C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37893949 | |||||||
chr7:37894005 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1400-461A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37894005 | |||||||
chr7:37894038 | G | C | 37 | a0001c0001t0001g0077 a0001c0001t0003g0092 a0001c0001t0003g0093 others(34): Show |
41 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.1400-428G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37894038 | |||||||
chr7:37894065 | C | T | 24 | a0001c0001t0001g0116 a0001c0001t0001g0168 a0001c0001t0001g0232 others(21): Show |
24 | HG00609.hp2 HG01069.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.1400-401C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37894065 | |||||||
chr7:37894332 | G | A | 1 | a0003c0003t0002g0301 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1400-134G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37894332 | |||||||
chr7:37894381 | C | G | 228 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(225): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1400-85C>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 15/17 | chr7 | 37894381 | |||||||
chr7:37894632 | G | A | 224 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(221): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1544+22G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37894632 | |||||||
chr7:37894718 | A | C | 25 | a0001c0001t0001g0096 a0001c0001t0001g0121 a0001c0001t0003g0045 others(22): Show |
31 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.1544+108A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37894718 | |||||||
chr7:37894730 | T | G | 1 | a0009c0031t0001g0130 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1544+120T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37894730 | |||||||
chr7:37894794 | T | G | 6 | a0001c0001t0001g0020 a0001c0001t0003g0007 a0001c0001t0003g0043 others(3): Show |
9 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1544+184T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37894794 | |||||||
chr7:37894800 | A | C | 324 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(321): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1544+190A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37894800 | |||||||
chr7:37894855 | T | C | 25 | a0001c0001t0001g0116 a0001c0001t0001g0168 a0001c0001t0001g0232 others(22): Show |
26 | HG00609.hp2 HG01069.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.1544+245T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37894855 | |||||||
chr7:37894863 | T | C | 26 | a0001c0001t0001g0096 a0001c0001t0001g0121 a0001c0001t0003g0045 others(23): Show |
32 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.1544+253T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37894863 | |||||||
chr7:37894863 | TCCTTC | T | 3 | a0001c0007t0001g0245 a0001c0007t0001g0246 a0002c0009t0001g0140 |
3 | HG02976.hp2 HG03017.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1544+268_1544+272d others(7): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 37894863 | ||||||
chr7:37894950 | T | G | 1 | a0005c0006t0002g0274 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1544+340T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37894950 | |||||||
chr7:37894980 | C | T | 62 | a0001c0001t0001g0077 a0001c0004t0001g0003 a0001c0004t0001g0097 others(59): Show |
68 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.1544+370C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37894980 | |||||||
chr7:37894987 | A | G | 18 | a0001c0001t0001g0116 a0001c0001t0001g0168 a0001c0001t0001g0232 others(15): Show |
18 | HG00609.hp2 HG01069.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1544+377A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37894987 | |||||||
chr7:37895071 | A | G | 97 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0082 others(94): Show |
111 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1544+461A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895071 | |||||||
chr7:37895190 | A | G | 13 | a0004c0005t0001g0073 a0004c0005t0001g0158 a0004c0005t0001g0170 others(10): Show |
16 | HG00099.hp2 HG00423.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1544+580A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895190 | |||||||
chr7:37895212 | C | T | 1 | a0002c0002t0001g0236 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1544+602C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895212 | |||||||
chr7:37895294 | A | C | 4 | a0001c0001t0001g0174 a0001c0007t0001g0245 a0001c0007t0001g0246 others(1): Show |
5 | HG02451.hp2 HG02486.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1544+684A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895294 | |||||||
chr7:37895339 | G | A | 18 | a0001c0001t0001g0116 a0001c0001t0001g0168 a0001c0001t0001g0232 others(15): Show |
18 | HG00609.hp2 HG01069.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1544+729G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895339 | |||||||
chr7:37895366 | T | G | 63 | a0001c0001t0001g0077 a0001c0004t0001g0003 a0001c0004t0001g0097 others(60): Show |
69 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.1544+756T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895366 | |||||||
chr7:37895402 | T | C | 3 | a0002c0002t0001g0031 a0002c0002t0001g0032 a0002c0002t0001g0251 |
5 | HG01243.hp2 HG02258.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1544+792T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895402 | |||||||
chr7:37895477 | T | C | 1 | a0003c0003t0008g0299 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1544+867T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895477 | |||||||
chr7:37895504 | C | A | 61 | a0001c0004t0001g0003 a0001c0004t0001g0097 a0001c0004t0001g0110 others(58): Show |
67 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.1544+894C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895504 | |||||||
chr7:37895548 | G | A | 3 | a0001c0004t0003g0101 a0001c0004t0003g0113 a0001c0004t0004g0194 |
3 | HG00323.hp1 HG01123.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.1544+938G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895548 | |||||||
chr7:37895572 | A | G | 3 | a0002c0002t0001g0031 a0002c0002t0001g0032 a0002c0002t0001g0251 |
5 | HG01243.hp2 HG02258.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1544+962A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895572 | |||||||
chr7:37895610 | A | G | 1 | a0012c0021t0002g0041 | 2 | HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1544+1000A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895610 | |||||||
chr7:37895646 | C | T | 6 | a0001c0001t0004g0009 a0001c0007t0001g0075 a0002c0009t0001g0239 others(3): Show |
8 | HG01074.hp1 HG01192.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1544+1036C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895646 | |||||||
chr7:37895681 | C | T | 1 | a0001c0007t0001g0125 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1544+1071C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895681 | |||||||
chr7:37895875 | C | T | 295 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(292): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.1545-995C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895875 | |||||||
chr7:37895892 | A | C | 1 | a0006c0011t0002g0286 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1545-978A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895892 | |||||||
chr7:37895909 | G | C | 34 | a0001c0001t0001g0024 a0001c0001t0001g0082 a0001c0001t0001g0118 others(31): Show |
42 | HG00140.hp2 HG00639.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.1545-961G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895909 | |||||||
chr7:37895965 | A | G | 295 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(292): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.1545-905A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37895965 | |||||||
chr7:37896052 | CGT | C | 4 | a0001c0007t0001g0055 a0003c0010t0001g0129 a0003c0010t0001g0135 others(1): Show |
4 | NA18952.hp2 NA18954.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.1545-813_1545-812d others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 37896052 | ||||||
chr7:37896053 | G | A | 21 | a0001c0001t0001g0096 a0001c0001t0001g0121 a0001c0001t0003g0045 others(18): Show |
27 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.1545-817G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37896053 | |||||||
chr7:37896068 | G | A | 34 | a0001c0001t0001g0024 a0001c0001t0001g0082 a0001c0001t0001g0118 others(31): Show |
42 | HG00140.hp2 HG00639.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.1545-802G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37896068 | |||||||
chr7:37896093 | G | A | 295 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(292): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.1545-777G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37896093 | |||||||
chr7:37896095 | C | T | 1 | a0001c0004t0001g0171 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1545-775C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37896095 | |||||||
chr7:37896128 | T | G | 63 | a0001c0001t0001g0077 a0001c0004t0001g0003 a0001c0004t0001g0097 others(60): Show |
69 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.1545-742T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37896128 | |||||||
chr7:37896188 | G | T | 295 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(292): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.1545-682G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37896188 | |||||||
chr7:37896383 | G | GAA | 166 | a0001c0001t0001g0048 a0001c0001t0001g0051 a0001c0001t0001g0056 others(163): Show |
189 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.1545-486_1545-485i others(4): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 37896383 | ||||||
chr7:37896447 | G | A | 4 | a0003c0010t0002g0311 a0003c0010t0002g0312 a0003c0010t0002g0313 others(1): Show |
4 | HG02809.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1545-423G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37896447 | |||||||
chr7:37896499 | G | T | 25 | a0001c0001t0001g0096 a0001c0001t0001g0121 a0001c0001t0003g0045 others(22): Show |
31 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.1545-371G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37896499 | |||||||
chr7:37896684 | C | T | 294 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(291): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1545-186C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37896684 | |||||||
chr7:37896687 | C | T | 294 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(291): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1545-183C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37896687 | |||||||
chr7:37896782 | T | C | 294 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(291): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1545-88T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 16/17 | chr7 | 37896782 | |||||||
chr7:37897152 | A | G | 2 | a0001c0001t0005g0196 a0003c0003t0002g0317 |
2 | HG02109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.*15+45A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37897152 | |||||||
chr7:37897246 | A | G | 1 | a0001c0001t0003g0088 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.*15+139A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37897246 | |||||||
chr7:37897298 | C | T | 7 | a0001c0001t0001g0112 a0001c0001t0001g0145 a0003c0003t0001g0258 others(4): Show |
8 | HG02572.hp2 HG02717.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.*15+191C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37897298 | |||||||
chr7:37897431 | T | C | 61 | a0001c0004t0001g0003 a0001c0004t0001g0097 a0001c0004t0001g0110 others(58): Show |
67 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.*15+324T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37897431 | |||||||
chr7:37897512 | C | T | 4 | a0001c0004t0001g0124 a0001c0004t0001g0151 a0003c0015t0001g0259 others(1): Show |
4 | HG02572.hp1 HG02622.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.*15+405C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37897512 | |||||||
chr7:37897548 | C | A | 56 | a0001c0001t0001g0096 a0001c0001t0001g0112 a0001c0001t0001g0116 others(53): Show |
65 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.*15+441C>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37897548 | |||||||
chr7:37897572 | G | A | 217 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(214): Show |
253 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.*15+465G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37897572 | |||||||
chr7:37897687 | C | T | 1 | a0017c0034t0001g0117 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.*15+580C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37897687 | |||||||
chr7:37897696 | T | C | 326 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(323): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.*15+589T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37897696 | |||||||
chr7:37897706 | T | C | 217 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(214): Show |
253 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.*15+599T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37897706 | |||||||
chr7:37897781 | T | C | 27 | a0001c0001t0001g0116 a0001c0001t0001g0143 a0001c0001t0001g0168 others(24): Show |
28 | HG00609.hp2 HG01069.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.*15+674T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37897781 | |||||||
chr7:37897821 | T | C | 27 | a0001c0001t0001g0116 a0001c0001t0001g0143 a0001c0001t0001g0168 others(24): Show |
28 | HG00609.hp2 HG01069.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.*15+714T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37897821 | |||||||
chr7:37897870 | T | C | 1 | a0003c0010t0002g0300 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.*15+763T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37897870 | |||||||
chr7:37898033 | A | G | 27 | a0001c0001t0001g0116 a0001c0001t0001g0143 a0001c0001t0001g0168 others(24): Show |
28 | HG00609.hp2 HG01069.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.*15+926A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37898033 | |||||||
chr7:37898085 | C | T | 27 | a0001c0001t0001g0116 a0001c0001t0001g0143 a0001c0001t0001g0168 others(24): Show |
28 | HG00609.hp2 HG01069.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.*15+978C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37898085 | |||||||
chr7:37898409 | A | G | 45 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0044 others(42): Show |
55 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.*15+1302A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37898409 | |||||||
chr7:37898633 | A | G | 7 | a0001c0001t0003g0093 a0001c0001t0004g0192 a0001c0007t0001g0021 others(4): Show |
8 | HG02735.hp1 HG02738.hp1 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.*15+1526A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37898633 | |||||||
chr7:37898712 | GGTGAAAT others(7): Show |
G | 1 | a0002c0009t0001g0233 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.*16-1531_*16-1518d others(16): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37898712 | |||||||
chr7:37898752 | C | T | 1 | a0002c0002t0001g0227 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.*16-1492C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37898752 | |||||||
chr7:37898770 | A | T | 1 | a0002c0009t0001g0233 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.*16-1474A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37898770 | |||||||
chr7:37898820 | A | G | 50 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(47): Show |
61 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.*16-1424A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37898820 | |||||||
chr7:37898836 | T | C | 26 | a0001c0001t0001g0116 a0001c0001t0001g0168 a0001c0001t0001g0232 others(23): Show |
27 | HG00609.hp2 HG01069.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.*16-1408T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37898836 | |||||||
chr7:37898855 | G | A | 1 | a0003c0003t0001g0133 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.*16-1389G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37898855 | |||||||
chr7:37898882 | A | T | 26 | a0001c0001t0001g0116 a0001c0001t0001g0168 a0001c0001t0001g0232 others(23): Show |
27 | HG00609.hp2 HG01069.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.*16-1362A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37898882 | |||||||
chr7:37898895 | A | T | 1 | a0002c0008t0001g0260 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.*16-1349A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37898895 | |||||||
chr7:37899008 | G | A | 50 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(47): Show |
61 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.*16-1236G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37899008 | |||||||
chr7:37899035 | T | G | 26 | a0001c0001t0001g0116 a0001c0001t0001g0168 a0001c0001t0001g0232 others(23): Show |
27 | HG00609.hp2 HG01069.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.*16-1209T>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37899035 | |||||||
chr7:37899169 | A | C | 298 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(295): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.*16-1075A>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37899169 | |||||||
chr7:37899332 | C | T | 1 | a0002c0009t0001g0202 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.*16-912C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37899332 | |||||||
chr7:37899425 | G | C | 1 | a0001c0001t0007g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.*16-819G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37899425 | |||||||
chr7:37899495 | TG | T | 25 | a0001c0001t0001g0116 a0001c0001t0001g0168 a0001c0001t0001g0232 others(22): Show |
26 | HG00609.hp2 HG01069.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.*16-743delG | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 37899495 | ||||||
chr7:37899528 | G | T | 1 | a0002c0009t0001g0233 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.*16-716G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37899528 | |||||||
chr7:37899537 | G | C | 2 | a0001c0001t0001g0044 a0001c0001t0001g0091 |
2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.*16-707G>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37899537 | |||||||
chr7:37899637 | A | G | 24 | a0001c0001t0001g0096 a0001c0001t0001g0121 a0001c0001t0003g0045 others(21): Show |
30 | HG00544.hp2 HG00597.hp2 HG02083.hp1 others(27): Show |
intron_variant | MODIFIER | c.*16-607A>G | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37899637 | |||||||
chr7:37899763 | G | A | 26 | a0001c0001t0001g0116 a0001c0001t0001g0168 a0001c0001t0001g0232 others(23): Show |
27 | HG00609.hp2 HG01069.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.*16-481G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37899763 | |||||||
chr7:37899802 | A | T | 1 | a0006c0016t0002g0282 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.*16-442A>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37899802 | |||||||
chr7:37899862 | T | C | 26 | a0001c0001t0001g0116 a0001c0001t0001g0168 a0001c0001t0001g0232 others(23): Show |
27 | HG00609.hp2 HG01069.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.*16-382T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37899862 | |||||||
chr7:37899990 | G | A | 1 | a0001c0007t0001g0248 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.*16-254G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37899990 | |||||||
chr7:37900102 | G | T | 1 | a0017c0034t0001g0117 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.*16-142G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37900102 | |||||||
chr7:37900126 | C | T | 1 | a0017c0034t0001g0117 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.*16-118C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37900126 | |||||||
chr7:37900128 | C | T | 1 | a0002c0002t0001g0221 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.*16-116C>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37900128 | |||||||
chr7:37900182 | G | A | 26 | a0001c0001t0001g0116 a0001c0001t0001g0168 a0001c0001t0001g0232 others(23): Show |
27 | HG00609.hp2 HG01069.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.*16-62G>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37900182 | |||||||
chr7:37900201 | G | T | 4 | a0001c0004t0003g0064 a0002c0008t0001g0028 a0002c0008t0001g0260 others(1): Show |
5 | HG00558.hp1 HG02071.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.*16-43G>T | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37900201 | |||||||
chr7:37900212 | T | A | 1 | a0009c0022t0002g0310 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.*16-32T>A | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37900212 | |||||||
chr7:37900238 | T | C | 51 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(48): Show |
62 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(59): Show |
splice_region_variant&intron_variant | LOW | c.*16-6T>C | NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 17/17 | chr7 | 37900238 |