Item | Value |
---|---|
geneid | 57697 |
ensemblid | ENSG00000187790.12 |
hgncid | 23168 |
symbol | FANCM |
name | FA complementation group M |
refseq_nuc | NM_020937.4 |
refseq_prot | NP_065988.1 |
ensembl_nuc | ENST00000267430.10 |
ensembl_prot | ENSP00000267430.5 |
mane_status | MANE Select |
chr | chr14 |
start | 45135930 |
end | 45200890 |
strand | + |
ver | v1.2 |
region | chr14:45135930-45200890 |
region5000 | chr14:45130930-45205890 |
regionname0 | FANCM_chr14_45135930_45200890 |
regionname5000 | FANCM_chr14_45130930_45205890 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 2048 | 113 | 24 | 22 | 42 | 5 | 19 | 31 | FANCM_chr14_45130930_45205890 | FANCM | MSGRQ others(2043): Show |
chr14 | 45130930 | 45205890 |
a0002 | 0/0 | 2048 | 37 | 35 | 2 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | MSGRQ others(2043): Show |
chr14 | 45130930 | 45205890 |
a0003 | 0/0 | 2048 | 29 | 0 | 1 | 23 | 3 | 2 | 18 | FANCM_chr14_45130930_45205890 | FANCM | MSGRQ others(2043): Show |
chr14 | 45130930 | 45205890 |
a0004 | 0/0 | 2048 | 10 | 1 | 6 | 2 | 0 | 1 | 2 | FANCM_chr14_45130930_45205890 | FANCM | MSGRQ others(2043): Show |
chr14 | 45130930 | 45205890 |
a0005 | 0/0 | 2048 | 10 | 9 | 0 | 1 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | MSGRQ others(2043): Show |
chr14 | 45130930 | 45205890 |
a0006 | 0/0 | 2048 | 5 | 2 | 1 | 0 | 1 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | MSGRQ others(2043): Show |
chr14 | 45130930 | 45205890 |
a0007 | 0/0 | 2048 | 5 | 0 | 1 | 4 | 0 | 0 | 4 | FANCM_chr14_45130930_45205890 | FANCM | MSGRQ others(2043): Show |
chr14 | 45130930 | 45205890 |
a0008 | 0/0 | 2048 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | MSGRQ others(2043): Show |
chr14 | 45130930 | 45205890 |
a0009 | 0/0 | 2048 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | MSGRQ others(2043): Show |
chr14 | 45130930 | 45205890 |
a0010 | 0/0 | 2048 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | MSGRQ others(2043): Show |
chr14 | 45130930 | 45205890 |
a0011 | 0/0 | 2048 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | MSGRQ others(2043): Show |
chr14 | 45130930 | 45205890 |
a0012 | 0/0 | 2048 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | MSGRQ others(2043): Show |
chr14 | 45130930 | 45205890 |
a0013 | 0/0 | 2048 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FANCM_chr14_45130930_45205890 | FANCM | MSGRQ others(2043): Show |
chr14 | 45130930 | 45205890 |
a0014 | 0/0 | 2048 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | MSGRQ others(2043): Show |
chr14 | 45130930 | 45205890 |
a0015 | 0/0 | 2048 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | MSGRQ others(2043): Show |
chr14 | 45130930 | 45205890 |
a0016 | 0/0 | 2048 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | MSGRQ others(2043): Show |
chr14 | 45130930 | 45205890 |
a0017 | 0/0 | 2048 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | MSGRQ others(2043): Show |
chr14 | 45130930 | 45205890 |
a0018 | 0/0 | 2048 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | MSGRQ others(2043): Show |
chr14 | 45130930 | 45205890 |
a0019 | 0/0 | 2048 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | MSGRQ others(2043): Show |
chr14 | 45130930 | 45205890 |
a0020 | 0/0 | 2048 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | MSGRQ others(2043): Show |
chr14 | 45130930 | 45205890 |
a0021 | 0/0 | 2048 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | MSGRQ others(2043): Show |
chr14 | 45130930 | 45205890 |
a0022 | 0/0 | 2048 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | MSGRQ others(2043): Show |
chr14 | 45130930 | 45205890 |
a0023 | 0/0 | 2048 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | MSGRQ others(2043): Show |
chr14 | 45130930 | 45205890 |
a0024 | 0/0 | 2048 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | MSGRQ others(2043): Show |
chr14 | 45130930 | 45205890 |
a0025 | 0/0 | 2048 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | MSGRQ others(2043): Show |
chr14 | 45130930 | 45205890 |
a0026 | 0/0 | 2048 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | MSGRQ others(2043): Show |
chr14 | 45130930 | 45205890 |
a0027 | 0/0 | 2048 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | MSGRQ others(2043): Show |
chr14 | 45130930 | 45205890 |
a0028 | 0/1 | 2048 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | MSGRQ others(2043): Show |
chr14 | 45130930 | 45205890 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 6144 | 113 | 24 | 22 | 42 | 5 | 19 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0002c0003 | 0/0 | 6144 | 14 | 12 | 2 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0002c0006 | 0/0 | 6144 | 9 | 9 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0002c0007 | 0/0 | 6144 | 6 | 6 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0002c0008 | 0/0 | 6144 | 6 | 6 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0002c0031 | 0/0 | 6144 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0002c0032 | 0/0 | 6144 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0003c0002 | 0/0 | 6144 | 29 | 0 | 1 | 23 | 3 | 2 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0004c0004 | 0/0 | 6144 | 10 | 1 | 6 | 2 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0005c0005 | 0/0 | 6144 | 10 | 9 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0006c0010 | 0/0 | 6144 | 5 | 2 | 1 | 0 | 1 | 1 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0007c0009 | 0/0 | 6144 | 5 | 0 | 1 | 4 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0008c0011 | 0/0 | 6144 | 3 | 3 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0008c0025 | 0/0 | 6144 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0009c0016 | 0/0 | 6144 | 2 | 2 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0010c0014 | 0/0 | 6144 | 2 | 2 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0011c0015 | 0/0 | 6144 | 2 | 2 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0012c0012 | 0/0 | 6144 | 2 | 2 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0013c0013 | 0/0 | 6144 | 2 | 0 | 0 | 2 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0014c0018 | 0/0 | 6144 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0015c0028 | 0/0 | 6144 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0016c0017 | 0/0 | 6144 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0017c0027 | 0/0 | 6144 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0018c0022 | 0/0 | 6144 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0019c0029 | 0/0 | 6144 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0020c0034 | 0/0 | 6144 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0021c0026 | 0/0 | 6144 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0022c0030 | 0/0 | 6144 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0023c0023 | 0/0 | 6144 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0024c0024 | 0/0 | 6144 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0025c0033 | 0/0 | 6144 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0026c0019 | 0/0 | 6144 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0027c0020 | 0/0 | 6144 | 1 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 | ||
a0028c0021 | 0/1 | 6144 | 1 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | ATGAG others(6139): Show |
chr14 | 45130930 | 45205890 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 7131 | 113 | 24 | 22 | 42 | 5 | 19 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7126): Show |
chr14 | 45130930 | 45205890 |
a0002c0003t0001 | 0/0 | 7131 | 4 | 3 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7126): Show |
chr14 | 45130930 | 45205890 |
a0002c0003t0002 | 0/0 | 7131 | 10 | 9 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7126): Show |
chr14 | 45130930 | 45205890 |
a0002c0006t0002 | 0/0 | 7131 | 9 | 9 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7126): Show |
chr14 | 45130930 | 45205890 |
a0002c0007t0003 | 0/0 | 7132 | 6 | 6 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7127): Show |
chr14 | 45130930 | 45205890 |
a0002c0008t0004 | 0/0 | 7133 | 5 | 5 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7128): Show |
chr14 | 45130930 | 45205890 |
a0002c0008t0007 | 0/0 | 7133 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7128): Show |
chr14 | 45130930 | 45205890 |
a0002c0031t0006 | 0/0 | 7115 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7110): Show |
chr14 | 45130930 | 45205890 |
a0002c0032t0001 | 0/0 | 7131 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7126): Show |
chr14 | 45130930 | 45205890 |
a0003c0002t0001 | 0/0 | 7131 | 29 | 0 | 1 | 23 | 3 | 2 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7126): Show |
chr14 | 45130930 | 45205890 |
a0004c0004t0001 | 0/0 | 7131 | 10 | 1 | 6 | 2 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7126): Show |
chr14 | 45130930 | 45205890 |
a0005c0005t0001 | 0/0 | 7131 | 10 | 9 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7126): Show |
chr14 | 45130930 | 45205890 |
a0006c0010t0001 | 0/0 | 7131 | 5 | 2 | 1 | 0 | 1 | 1 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7126): Show |
chr14 | 45130930 | 45205890 |
a0007c0009t0001 | 0/0 | 7131 | 5 | 0 | 1 | 4 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7126): Show |
chr14 | 45130930 | 45205890 |
a0008c0011t0002 | 0/0 | 7131 | 3 | 3 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7126): Show |
chr14 | 45130930 | 45205890 |
a0008c0025t0002 | 0/0 | 7131 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7126): Show |
chr14 | 45130930 | 45205890 |
a0009c0016t0005 | 0/0 | 7131 | 2 | 2 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7126): Show |
chr14 | 45130930 | 45205890 |
a0010c0014t0001 | 0/0 | 7131 | 2 | 2 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7126): Show |
chr14 | 45130930 | 45205890 |
a0011c0015t0001 | 0/0 | 7131 | 2 | 2 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7126): Show |
chr14 | 45130930 | 45205890 |
a0012c0012t0002 | 0/0 | 7131 | 2 | 2 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7126): Show |
chr14 | 45130930 | 45205890 |
a0013c0013t0001 | 0/0 | 7131 | 2 | 0 | 0 | 2 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7126): Show |
chr14 | 45130930 | 45205890 |
a0014c0018t0001 | 0/0 | 7131 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7126): Show |
chr14 | 45130930 | 45205890 |
a0015c0028t0001 | 0/0 | 7131 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7126): Show |
chr14 | 45130930 | 45205890 |
a0016c0017t0001 | 0/0 | 7131 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7126): Show |
chr14 | 45130930 | 45205890 |
a0017c0027t0001 | 0/0 | 7131 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7126): Show |
chr14 | 45130930 | 45205890 |
a0018c0022t0001 | 0/0 | 7131 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7126): Show |
chr14 | 45130930 | 45205890 |
a0019c0029t0001 | 0/0 | 7131 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7126): Show |
chr14 | 45130930 | 45205890 |
a0020c0034t0002 | 0/0 | 7131 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7126): Show |
chr14 | 45130930 | 45205890 |
a0021c0026t0008 | 0/0 | 7131 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7126): Show |
chr14 | 45130930 | 45205890 |
a0022c0030t0001 | 0/0 | 7131 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7126): Show |
chr14 | 45130930 | 45205890 |
a0023c0023t0001 | 0/0 | 7131 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7126): Show |
chr14 | 45130930 | 45205890 |
a0024c0024t0001 | 0/0 | 7131 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7126): Show |
chr14 | 45130930 | 45205890 |
a0025c0033t0001 | 0/0 | 7131 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7126): Show |
chr14 | 45130930 | 45205890 |
a0026c0019t0001 | 0/0 | 7131 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7126): Show |
chr14 | 45130930 | 45205890 |
a0027c0020t0001 | 0/0 | 7131 | 1 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7126): Show |
chr14 | 45130930 | 45205890 |
a0028c0021t0001 | 0/1 | 7131 | 1 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | CCAGA others(7126): Show |
chr14 | 45130930 | 45205890 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0118 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0003t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0003t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0003t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0003t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0003t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0003t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0003t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0003t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0003t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0003t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0003t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0003t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0003t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0003t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0006t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0006t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0006t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0006t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0006t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0006t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0006t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0006t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0006t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0007t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0007t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0007t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0007t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0007t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0007t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0008t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0008t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0008t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0008t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0008t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0008t0007g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0031t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0032t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0004c0004t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0004c0004t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0004c0004t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0004c0004t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0004c0004t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0004c0004t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0004c0004t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0004c0004t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0004c0004t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0005c0005t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0005c0005t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0005c0005t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0005c0005t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0005c0005t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0005c0005t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0005c0005t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0005c0005t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0005c0005t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0005c0005t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0006c0010t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0006c0010t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0006c0010t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0006c0010t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0006c0010t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0007c0009t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0007c0009t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0007c0009t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0007c0009t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0007c0009t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0008c0011t0002g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0008c0011t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0008c0011t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0008c0025t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0009c0016t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0009c0016t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0010c0014t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0010c0014t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0011c0015t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0011c0015t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0012c0012t0002g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0013c0013t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0013c0013t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0014c0018t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0015c0028t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0016c0017t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0017c0027t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0018c0022t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0019c0029t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0020c0034t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0021c0026t0008g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0022c0030t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0023c0023t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0024c0024t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0025c0033t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0026c0019t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0027c0020t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0028c0021t0001g0116 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0003 | c0002 | t0001 | g0185 | EUR | FIN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | FIN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG00323 | hp1 | a0003 | c0002 | t0001 | g0183 | EUR | FIN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | FIN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG00438 | hp1 | a0014 | c0018 | t0001 | g0029 | EAS | CHS | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG00558 | hp1 | a0003 | c0002 | t0001 | g0003 | EAS | CHS | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG00597 | hp1 | a0003 | c0002 | t0001 | g0188 | EAS | CHS | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG00609 | hp2 | a0003 | c0002 | t0001 | g0186 | EAS | CHS | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG00673 | hp2 | a0003 | c0002 | t0001 | g0182 | EAS | CHS | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01099 | hp1 | a0015 | c0028 | t0001 | g0086 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01106 | hp1 | a0006 | c0010 | t0001 | g0199 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01109 | hp1 | a0002 | c0003 | t0002 | g0153 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01167 | hp1 | a0004 | c0004 | t0001 | g0123 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01169 | hp2 | a0004 | c0004 | t0001 | g0122 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01192 | hp1 | a0004 | c0004 | t0001 | g0026 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01243 | hp1 | a0004 | c0004 | t0001 | g0013 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01243 | hp2 | a0016 | c0017 | t0001 | g0050 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01255 | hp1 | a0017 | c0027 | t0001 | g0120 | AMR | CLM | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01358 | hp1 | a0002 | c0003 | t0001 | g0165 | AMR | CLM | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01358 | hp2 | a0003 | c0002 | t0001 | g0175 | AMR | CLM | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01516 | hp1 | a0006 | c0010 | t0001 | g0200 | EUR | IBS | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0075 | EUR | IBS | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01884 | hp1 | a0002 | c0003 | t0001 | g0166 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01884 | hp2 | a0009 | c0016 | t0005 | g0203 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01891 | hp1 | a0010 | c0014 | t0001 | g0138 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01952 | hp2 | a0004 | c0004 | t0001 | g0013 | AMR | PEL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01993 | hp1 | a0004 | c0004 | t0001 | g0119 | AMR | PEL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02055 | hp1 | a0002 | c0003 | t0002 | g0139 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02055 | hp2 | a0018 | c0022 | t0001 | g0022 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02056 | hp2 | a0003 | c0002 | t0001 | g0196 | EAS | KHV | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02132 | hp1 | a0019 | c0029 | t0001 | g0221 | EAS | KHV | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02145 | hp2 | a0002 | c0032 | t0001 | g0204 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02257 | hp1 | a0002 | c0007 | t0003 | g0143 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02257 | hp2 | a0002 | c0003 | t0001 | g0167 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02258 | hp1 | a0002 | c0008 | t0004 | g0168 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02258 | hp2 | a0008 | c0011 | t0002 | g0048 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02280 | hp2 | a0002 | c0006 | t0002 | g0208 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02293 | hp2 | a0007 | c0009 | t0001 | g0019 | AMR | PEL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02451 | hp1 | a0020 | c0034 | t0002 | g0136 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02615 | hp1 | a0021 | c0026 | t0008 | g0142 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02622 | hp1 | a0002 | c0006 | t0002 | g0210 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02630 | hp1 | a0002 | c0006 | t0002 | g0211 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02647 | hp1 | a0005 | c0005 | t0001 | g0160 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02717 | hp1 | a0005 | c0005 | t0001 | g0205 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02717 | hp2 | a0002 | c0003 | t0002 | g0220 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02723 | hp1 | a0005 | c0005 | t0001 | g0217 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02723 | hp2 | a0002 | c0007 | t0003 | g0146 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02809 | hp1 | a0005 | c0005 | t0001 | g0206 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02818 | hp1 | a0002 | c0031 | t0006 | g0159 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02818 | hp2 | a0002 | c0008 | t0004 | g0149 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02886 | hp1 | a0002 | c0008 | t0004 | g0148 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02886 | hp2 | a0002 | c0007 | t0003 | g0164 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02895 | hp1 | a0006 | c0010 | t0001 | g0135 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02895 | hp2 | a0012 | c0012 | t0002 | g0001 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02896 | hp2 | a0002 | c0003 | t0002 | g0150 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02897 | hp1 | a0012 | c0012 | t0002 | g0001 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02897 | hp2 | a0002 | c0003 | t0002 | g0162 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02922 | hp2 | a0002 | c0003 | t0002 | g0218 | AFR | ESN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02965 | hp1 | a0002 | c0008 | t0007 | g0161 | AFR | ESN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02965 | hp2 | a0002 | c0003 | t0002 | g0216 | AFR | ESN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02976 | hp1 | a0008 | c0011 | t0002 | g0001 | AFR | ESN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02976 | hp2 | a0010 | c0014 | t0001 | g0137 | AFR | ESN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03017 | hp1 | a0003 | c0002 | t0001 | g0172 | SAS | PJL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03041 | hp1 | a0002 | c0006 | t0002 | g0214 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03098 | hp1 | a0005 | c0005 | t0001 | g0152 | AFR | MSL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03098 | hp2 | a0002 | c0006 | t0002 | g0213 | AFR | MSL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03139 | hp1 | a0022 | c0030 | t0001 | g0014 | AFR | ESN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03139 | hp2 | a0011 | c0015 | t0001 | g0192 | AFR | ESN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03195 | hp1 | a0002 | c0006 | t0002 | g0209 | AFR | ESN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03225 | hp2 | a0002 | c0006 | t0002 | g0207 | AFR | MSL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03239 | hp1 | a0003 | c0002 | t0001 | g0190 | SAS | PJL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03239 | hp2 | a0023 | c0023 | t0001 | g0084 | SAS | PJL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03453 | hp1 | a0002 | c0007 | t0003 | g0163 | AFR | MSL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03453 | hp2 | a0024 | c0024 | t0001 | g0141 | AFR | MSL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03486 | hp1 | a0002 | c0008 | t0004 | g0147 | AFR | MSL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03486 | hp2 | a0005 | c0005 | t0001 | g0156 | AFR | MSL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03516 | hp2 | a0002 | c0006 | t0002 | g0212 | AFR | ESN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03540 | hp1 | a0002 | c0006 | t0002 | g0215 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03579 | hp2 | a0008 | c0025 | t0002 | g0133 | AFR | MSL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03831 | hp2 | a0004 | c0004 | t0001 | g0027 | SAS | BEB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03927 | hp2 | a0025 | c0033 | t0001 | g0187 | SAS | BEB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | STU | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG04199 | hp2 | a0006 | c0010 | t0001 | g0198 | SAS | STU | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG04228 | hp1 | a0026 | c0019 | t0001 | g0023 | SAS | STU | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | STU | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18522 | hp1 | a0005 | c0005 | t0001 | g0157 | AFR | YRI | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18522 | hp2 | a0002 | c0003 | t0002 | g0154 | AFR | YRI | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18906 | hp1 | a0006 | c0010 | t0001 | g0134 | AFR | YRI | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18906 | hp2 | a0002 | c0007 | t0003 | g0145 | AFR | YRI | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18939 | hp1 | a0013 | c0013 | t0001 | g0051 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18939 | hp2 | a0007 | c0009 | t0001 | g0018 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18940 | hp1 | a0003 | c0002 | t0001 | g0171 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18946 | hp2 | a0003 | c0002 | t0001 | g0003 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18952 | hp2 | a0003 | c0002 | t0001 | g0170 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18954 | hp2 | a0003 | c0002 | t0001 | g0180 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18964 | hp2 | a0003 | c0002 | t0001 | g0178 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18966 | hp1 | a0003 | c0002 | t0001 | g0003 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18966 | hp2 | a0007 | c0009 | t0001 | g0017 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18970 | hp1 | a0003 | c0002 | t0001 | g0177 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18974 | hp2 | a0007 | c0009 | t0001 | g0016 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18982 | hp2 | a0003 | c0002 | t0001 | g0181 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18984 | hp1 | a0003 | c0002 | t0001 | g0176 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18988 | hp1 | a0003 | c0002 | t0001 | g0201 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18991 | hp1 | a0003 | c0002 | t0001 | g0174 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18998 | hp1 | a0007 | c0009 | t0001 | g0020 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18999 | hp1 | a0003 | c0002 | t0001 | g0184 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18999 | hp2 | a0013 | c0013 | t0001 | g0081 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19011 | hp1 | a0003 | c0002 | t0001 | g0189 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19030 | hp1 | a0009 | c0016 | t0005 | g0202 | AFR | LWK | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | LWK | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19043 | hp1 | a0002 | c0008 | t0004 | g0140 | AFR | LWK | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19043 | hp2 | a0004 | c0004 | t0001 | g0030 | AFR | LWK | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19063 | hp1 | a0003 | c0002 | t0001 | g0195 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19066 | hp1 | a0005 | c0005 | t0001 | g0173 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19067 | hp1 | a0003 | c0002 | t0001 | g0169 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19068 | hp2 | a0004 | c0004 | t0001 | g0109 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19072 | hp1 | a0003 | c0002 | t0001 | g0193 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19074 | hp2 | a0004 | c0004 | t0001 | g0121 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19078 | hp1 | a0003 | c0002 | t0001 | g0194 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19091 | hp1 | a0003 | c0002 | t0001 | g0197 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19240 | hp1 | a0002 | c0003 | t0002 | g0219 | AFR | YRI | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19240 | hp2 | a0002 | c0003 | t0002 | g0155 | AFR | YRI | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA20752 | hp1 | a0027 | c0020 | t0001 | g0117 | EUR | TSI | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA20805 | hp1 | a0003 | c0002 | t0001 | g0179 | EUR | TSI | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0095 | EUR | TSI | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02109 | hp2 | a0005 | c0005 | t0001 | g0151 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02486 | hp1 | a0011 | c0015 | t0001 | g0191 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02559 | hp2 | a0005 | c0005 | t0001 | g0158 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03471 | hp1 | a0008 | c0011 | t0002 | g0049 | AFR | MSL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03471 | hp2 | a0002 | c0003 | t0001 | g0014 | AFR | MSL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG06807 | hp1 | a0002 | c0007 | t0003 | g0144 | AFR | USA | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | USA | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
homoSapiens | chm13v2 | a0028 | c0021 | t0001 | g0116 | REF | REF | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0118 | REF | REF | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:45136260 | A | G | 1 | a0006 | 5 | HG01106.hp1 HG01516.hp1 HG02895.hp1 others(2): Show |
missense_variant | MODERATE | c.229A>G | p.Thr77Ala | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 1/23 | 331/7131 | 229/6147 | 77/2048 | chr14 | 45136260 | |||
chr14:45137084 | C | T | 11 | a0002 a0003 a0005 others(8): Show |
91 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(88): Show |
missense_variant | MODERATE | c.524C>T | p.Ser175Phe | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/23 | 626/7131 | 524/6147 | 175/2048 | chr14 | 45137084 | |||
chr14:45137184 | A | G | 1 | a0015 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.624A>G | p.Ile208Met | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/23 | 726/7131 | 624/6147 | 208/2048 | chr14 | 45137184 | |||
chr14:45148951 | C | G | 1 | a0009 | 2 | HG01884.hp2 NA19030.hp1 |
missense_variant | MODERATE | c.874C>G | p.Pro292Ala | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/23 | 976/7131 | 874/6147 | 292/2048 | chr14 | 45148951 | |||
chr14:45151518 | C | T | 1 | a0020 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.1040C>T | p.Pro347Leu | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/23 | 1142/7131 | 1040/6147 | 347/2048 | chr14 | 45151518 | |||
chr14:45155391 | T | G | 1 | a0012 | 2 | HG02895.hp2 HG02897.hp1 |
missense_variant | MODERATE | c.1328T>G | p.Phe443Cys | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/23 | 1430/7131 | 1328/6147 | 443/2048 | chr14 | 45155391 | |||
chr14:45167125 | A | G | 1 | a0017 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.1964A>G | p.Asn655Ser | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/23 | 2066/7131 | 1964/6147 | 655/2048 | chr14 | 45167125 | |||
chr14:45173134 | A | G | 1 | a0013 | 2 | NA18939.hp1 NA18999.hp2 |
missense_variant | MODERATE | c.2240A>G | p.His747Arg | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/23 | 2342/7131 | 2240/6147 | 747/2048 | chr14 | 45173134 | |||
chr14:45173155 | G | A | 1 | a0022 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.2261G>A | p.Arg754Gln | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/23 | 2363/7131 | 2261/6147 | 754/2048 | chr14 | 45173155 | |||
chr14:45173187 | A | G | 1 | a0025 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.2293A>G | p.Ile765Val | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/23 | 2395/7131 | 2293/6147 | 765/2048 | chr14 | 45173187 | |||
chr14:45175386 | G | T | 17 | a0002 a0003 a0004 others(14): Show |
105 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(102): Show |
missense_variant | MODERATE | c.2632G>T | p.Val878Leu | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/23 | 2734/7131 | 2632/6147 | 878/2048 | chr14 | 45175386 | |||
chr14:45175503 | A | G | 2 | a0007 a0019 |
6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
missense_variant | MODERATE | c.2749A>G | p.Ile917Val | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/23 | 2851/7131 | 2749/6147 | 917/2048 | chr14 | 45175503 | |||
chr14:45175669 | C | T | 1 | a0023 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.2915C>T | p.Thr972Ile | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/23 | 3017/7131 | 2915/6147 | 972/2048 | chr14 | 45175669 | |||
chr14:45175794 | G | T | 1 | a0011 | 2 | HG02486.hp1 HG03139.hp2 |
missense_variant | MODERATE | c.3040G>T | p.Gly1014Cys | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/23 | 3142/7131 | 3040/6147 | 1014/2048 | chr14 | 45175794 | |||
chr14:45176050 | G | A | 1 | a0024 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.3296G>A | p.Arg1099His | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/23 | 3398/7131 | 3296/6147 | 1099/2048 | chr14 | 45176050 | |||
chr14:45176512 | A | G | 1 | a0018 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.3758A>G | p.Asn1253Ser | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/23 | 3860/7131 | 3758/6147 | 1253/2048 | chr14 | 45176512 | |||
chr14:45176617 | A | G | 1 | a0021 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.3863A>G | p.Asn1288Ser | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/23 | 3965/7131 | 3863/6147 | 1288/2048 | chr14 | 45176617 | |||
chr14:45176674 | A | G | 1 | a0010 | 2 | HG01891.hp1 HG02976.hp2 |
missense_variant | MODERATE | c.3920A>G | p.Tyr1307Cys | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/23 | 4022/7131 | 3920/6147 | 1307/2048 | chr14 | 45176674 | |||
chr14:45181697 | A | G | 4 | a0003 a0004 a0017 others(1): Show |
41 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(38): Show |
missense_variant | MODERATE | c.4378A>G | p.Ile1460Val | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 16/23 | 4480/7131 | 4378/6147 | 1460/2048 | chr14 | 45181697 | |||
chr14:45185264 | A | C | 1 | a0011 | 2 | HG02486.hp1 HG03139.hp2 |
missense_variant | MODERATE | c.4563A>C | p.Glu1521Asp | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/23 | 4665/7131 | 4563/6147 | 1521/2048 | chr14 | 45185264 | |||
chr14:45189246 | A | G | 1 | a0027 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.5224A>G | p.Ile1742Val | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/23 | 5326/7131 | 5224/6147 | 1742/2048 | chr14 | 45189246 | |||
chr14:45196265 | C | G | 5 | a0003 a0004 a0017 others(2): Show |
42 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(39): Show |
missense_variant | MODERATE | c.5434C>G | p.Pro1812Ala | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/23 | 5536/7131 | 5434/6147 | 1812/2048 | chr14 | 45196265 | |||
chr14:45196266 | C | T | 1 | a0014 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.5435C>T | p.Pro1812Leu | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/23 | 5537/7131 | 5435/6147 | 1812/2048 | chr14 | 45196266 | |||
chr14:45196458 | A | G | 2 | a0016 a0018 |
2 | HG01243.hp2 HG02055.hp2 |
missense_variant | MODERATE | c.5627A>G | p.Asn1876Ser | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/23 | 5729/7131 | 5627/6147 | 1876/2048 | chr14 | 45196458 | |||
chr14:45196487 | C | T | 1 | a0021 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.5656C>T | p.His1886Tyr | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/23 | 5758/7131 | 5656/6147 | 1886/2048 | chr14 | 45196487 | |||
chr14:45196515 | G | A | 1 | a0026 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.5684G>A | p.Cys1895Tyr | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/23 | 5786/7131 | 5684/6147 | 1895/2048 | chr14 | 45196515 | |||
chr14:45198775 | T | G | 1 | a0009 | 2 | HG01884.hp2 NA19030.hp1 |
missense_variant | MODERATE | c.5848T>G | p.Leu1950Val | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 22/23 | 5950/7131 | 5848/6147 | 1950/2048 | chr14 | 45198775 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:45151519 | G | A | 2 | a0007c0009 a0019c0029 |
6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
synonymous_variant | LOW | c.1041G>A | p.Pro347Pro | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/23 | 1143/7131 | 1041/6147 | 347/2048 | chr14 | 45151519 | |||
chr14:45175199 | G | A | 2 | a0002c0007 a0002c0008 |
12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
synonymous_variant | LOW | c.2445G>A | p.Ser815Ser | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/23 | 2547/7131 | 2445/6147 | 815/2048 | chr14 | 45175199 | |||
chr14:45175424 | T | C | 3 | a0002c0006 a0008c0011 a0012c0012 |
14 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(11): Show |
synonymous_variant | LOW | c.2670T>C | p.Phe890Phe | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/23 | 2772/7131 | 2670/6147 | 890/2048 | chr14 | 45175424 | |||
chr14:45176301 | T | C | 1 | a0002c0031 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.3547T>C | p.Leu1183Leu | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/23 | 3649/7131 | 3547/6147 | 1183/2048 | chr14 | 45176301 | |||
chr14:45181467 | C | T | 1 | a0002c0008 | 6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
synonymous_variant | LOW | c.4260C>T | p.Asp1420Asp | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 15/23 | 4362/7131 | 4260/6147 | 1420/2048 | chr14 | 45181467 | |||
chr14:45189164 | G | A | 2 | a0002c0007 a0011c0015 |
8 | HG02257.hp1 HG02486.hp1 HG02723.hp2 others(5): Show |
synonymous_variant | LOW | c.5142G>A | p.Ala1714Ala | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/23 | 5244/7131 | 5142/6147 | 1714/2048 | chr14 | 45189164 | |||
chr14:45189212 | G | A | 1 | a0021c0026 | 1 | HG02615.hp1 | synonymous_variant | LOW | c.5190G>A | p.Gln1730Gln | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/23 | 5292/7131 | 5190/6147 | 1730/2048 | chr14 | 45189212 | |||
chr14:45196408 | T | C | 1 | a0002c0008 | 6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
synonymous_variant | LOW | c.5577T>C | p.Asn1859Asn | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/23 | 5679/7131 | 5577/6147 | 1859/2048 | chr14 | 45196408 | |||
chr14:45200002 | T | C | 3 | a0002c0032 a0006c0010 a0021c0026 |
7 | HG01106.hp1 HG01516.hp1 HG02145.hp2 others(4): Show |
synonymous_variant | LOW | c.6141T>C | p.Asp2047Asp | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 23/23 | 6243/7131 | 6141/6147 | 2047/2048 | chr14 | 45200002 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:45200151 | TATAGAAA others(9): Show |
T | 1 | a0002c0031t0006 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*145_*160delTAGAAA others(10): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 23/23 | 145 | INFO_REALIGN_3_PRIME | chr14 | 45200151 | |||||
chr14:45200240 | G | A | 7 | a0002c0003t0002 a0002c0006t0002 a0008c0011t0002 others(4): Show |
28 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*232G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 23/23 | 232 | chr14 | 45200240 | ||||||
chr14:45200254 | T | C | 1 | a0002c0008t0007 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*246T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 23/23 | 246 | chr14 | 45200254 | ||||||
chr14:45200260 | A | AG | 3 | a0002c0007t0003 a0002c0008t0004 a0002c0008t0007 |
12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*254dupG | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 23/23 | 255 | INFO_REALIGN_3_PRIME | chr14 | 45200260 | |||||
chr14:45200646 | T | C | 1 | a0021c0026t0008 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*638T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 23/23 | 638 | chr14 | 45200646 | ||||||
chr14:45200647 | T | TG | 2 | a0002c0008t0004 a0002c0008t0007 |
6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*643dupG | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 23/23 | 644 | INFO_REALIGN_3_PRIME | chr14 | 45200647 | |||||
chr14:45200652 | A | G | 2 | a0002c0008t0004 a0002c0008t0007 |
6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*644A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 23/23 | 644 | chr14 | 45200652 | ||||||
chr14:45200872 | A | C | 1 | a0009c0016t0005 | 2 | HG01884.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*864A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 23/23 | 864 | chr14 | 45200872 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:45136615 | C | T | 91 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(88): Show |
93 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.508+76C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 1/22 | chr14 | 45136615 | |||||||
chr14:45136772 | A | T | 1 | a0008c0025t0002g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.508+233A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 1/22 | chr14 | 45136772 | |||||||
chr14:45137313 | A | C | 1 | a0019c0029t0001g0221 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.681+72A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45137313 | |||||||
chr14:45137941 | G | A | 2 | a0006c0010t0001g0134 a0006c0010t0001g0135 |
2 | HG02895.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.681+700G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45137941 | |||||||
chr14:45137959 | TA | T | 19 | a0002c0003t0002g0216 a0002c0003t0002g0218 a0002c0003t0002g0219 others(16): Show |
19 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.681+720delA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr14 | 45137959 | ||||||
chr14:45138183 | C | T | 64 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(61): Show |
66 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.681+942C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45138183 | |||||||
chr14:45138262 | G | C | 4 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(1): Show |
4 | HG02257.hp1 HG02723.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.681+1021G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45138262 | |||||||
chr14:45138321 | T | A | 89 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(86): Show |
91 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.681+1080T>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45138321 | |||||||
chr14:45138474 | G | T | 19 | a0002c0003t0002g0216 a0002c0003t0002g0218 a0002c0003t0002g0219 others(16): Show |
19 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.681+1233G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45138474 | |||||||
chr14:45138904 | G | C | 89 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(86): Show |
91 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.681+1663G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45138904 | |||||||
chr14:45139400 | T | C | 28 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(25): Show |
28 | HG01109.hp1 HG01358.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.682-1232T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45139400 | |||||||
chr14:45139468 | T | G | 1 | a0001c0001t0001g0015 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.682-1164T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45139468 | |||||||
chr14:45139620 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.682-1012A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45139620 | |||||||
chr14:45139932 | C | T | 1 | a0003c0002t0001g0201 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.682-700C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45139932 | |||||||
chr14:45139987 | T | C | 89 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(86): Show |
91 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.682-645T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45139987 | |||||||
chr14:45139999 | A | T | 17 | a0002c0003t0002g0216 a0002c0003t0002g0218 a0002c0003t0002g0219 others(14): Show |
17 | HG02145.hp2 HG02280.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.682-633A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45139999 | |||||||
chr14:45140194 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.682-438C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45140194 | |||||||
chr14:45140227 | G | GT | 9 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(6): Show |
9 | HG01106.hp1 HG01516.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.682-394dupT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr14 | 45140227 | ||||||
chr14:45140392 | G | A | 5 | a0007c0009t0001g0016 a0007c0009t0001g0017 a0007c0009t0001g0018 others(2): Show |
5 | HG02293.hp2 NA18939.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.682-240G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45140392 | |||||||
chr14:45140466 | A | G | 89 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(86): Show |
91 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.682-166A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45140466 | |||||||
chr14:45140551 | C | T | 1 | a0002c0008t0004g0168 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.682-81C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45140551 | |||||||
chr14:45140801 | G | A | 1 | a0003c0002t0001g0169 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.759+92G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45140801 | |||||||
chr14:45141113 | C | A | 4 | a0002c0008t0004g0147 a0002c0008t0004g0148 a0002c0008t0004g0149 others(1): Show |
4 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.759+404C>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45141113 | |||||||
chr14:45141230 | A | G | 2 | a0002c0003t0002g0139 a0002c0008t0004g0140 |
2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.759+521A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45141230 | |||||||
chr14:45141287 | C | CA | 40 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0025 others(37): Show |
40 | HG00438.hp1 HG00438.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.759+599dupA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45141287 | ||||||
chr14:45141287 | C | CAA | 25 | a0002c0003t0002g0150 a0003c0002t0001g0003 a0003c0002t0001g0169 others(22): Show |
27 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.759+598_759+599dup others(2): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45141287 | ||||||
chr14:45141287 | CAAAAAAA others(2): Show |
C | 11 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(8): Show |
11 | HG01358.hp1 HG01884.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.759+591_759+599del others(9): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45141287 | ||||||
chr14:45141504 | T | TCCTCCC | 84 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(81): Show |
86 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.759+803_759+808dup others(6): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45141504 | ||||||
chr14:45141555 | C | T | 1 | a0003c0002t0001g0190 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.759+846C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45141555 | |||||||
chr14:45141594 | C | CT | 6 | a0001c0001t0001g0015 a0001c0001t0001g0028 a0001c0001t0001g0126 others(3): Show |
6 | HG00438.hp1 HG00438.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.759+899dupT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45141594 | ||||||
chr14:45141774 | G | C | 12 | a0002c0003t0002g0216 a0002c0006t0002g0207 a0002c0006t0002g0208 others(9): Show |
12 | HG02145.hp2 HG02280.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.759+1065G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45141774 | |||||||
chr14:45141806 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.759+1097C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45141806 | |||||||
chr14:45141834 | C | T | 1 | a0019c0029t0001g0221 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.759+1125C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45141834 | |||||||
chr14:45141836 | GCCTCAGC others(2096): Show |
G | 2 | a0010c0014t0001g0137 a0010c0014t0001g0138 |
2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.759+1154_759+3256d others(2): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45141836 | ||||||
chr14:45141880 | T | C | 87 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(84): Show |
89 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.759+1171T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45141880 | |||||||
chr14:45141883 | C | A | 29 | a0003c0002t0001g0003 a0003c0002t0001g0169 a0003c0002t0001g0170 others(26): Show |
31 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.759+1174C>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45141883 | |||||||
chr14:45142057 | T | C | 2 | a0005c0005t0001g0205 a0005c0005t0001g0206 |
2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.759+1348T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45142057 | |||||||
chr14:45142154 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.759+1445C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45142154 | |||||||
chr14:45142278 | C | T | 1 | a0019c0029t0001g0221 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.759+1569C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45142278 | |||||||
chr14:45142308 | C | CT | 7 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0037 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.759+1615dupT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45142308 | ||||||
chr14:45142308 | CT | C | 5 | a0001c0001t0001g0012 a0001c0001t0001g0076 a0004c0004t0001g0027 others(2): Show |
5 | HG01256.hp1 HG02132.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.759+1615delT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45142308 | ||||||
chr14:45142316 | T | G | 1 | a0001c0001t0001g0077 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.759+1607T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45142316 | |||||||
chr14:45142489 | G | A | 11 | a0002c0003t0002g0150 a0002c0003t0002g0153 a0002c0003t0002g0154 others(8): Show |
11 | HG01109.hp1 HG02559.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.759+1780G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45142489 | |||||||
chr14:45142651 | T | C | 1 | a0020c0034t0002g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.759+1942T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45142651 | |||||||
chr14:45143025 | T | C | 87 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(84): Show |
89 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.759+2316T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45143025 | |||||||
chr14:45143058 | T | G | 86 | a0002c0003t0001g0014 a0002c0003t0001g0166 a0002c0003t0001g0167 others(83): Show |
88 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.759+2349T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45143058 | |||||||
chr14:45143072 | G | A | 87 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(84): Show |
89 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.759+2363G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45143072 | |||||||
chr14:45143166 | A | G | 1 | a0002c0032t0001g0204 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.759+2457A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45143166 | |||||||
chr14:45143171 | CT | C | 83 | a0001c0001t0001g0009 a0001c0001t0001g0060 a0001c0001t0001g0079 others(80): Show |
85 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.759+2479delT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45143171 | ||||||
chr14:45143171 | CTT | C | 5 | a0002c0003t0002g0150 a0002c0003t0002g0162 a0002c0006t0002g0207 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.759+2478_759+2479d others(4): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45143171 | ||||||
chr14:45143175 | T | C | 1 | a0020c0034t0002g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.759+2466T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45143175 | |||||||
chr14:45143244 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.759+2535T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45143244 | |||||||
chr14:45143267 | G | C | 2 | a0001c0001t0001g0053 a0016c0017t0001g0050 |
2 | HG00323.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.759+2558G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45143267 | |||||||
chr14:45143461 | A | T | 5 | a0006c0010t0001g0134 a0006c0010t0001g0135 a0006c0010t0001g0198 others(2): Show |
5 | HG01106.hp1 HG01516.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.759+2752A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45143461 | |||||||
chr14:45143505 | A | G | 1 | a0002c0007t0003g0163 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.759+2796A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45143505 | |||||||
chr14:45143690 | A | AT | 63 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0054 others(60): Show |
63 | HG00673.hp2 HG01106.hp1 HG01192.hp1 others(60): Show |
intron_variant | MODIFIER | c.759+3002dupT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45143690 | ||||||
chr14:45143690 | A | ATT | 9 | a0001c0001t0001g0088 a0002c0003t0001g0014 a0002c0003t0001g0166 others(6): Show |
9 | HG01109.hp1 HG01346.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.759+3001_759+3002d others(4): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45143690 | ||||||
chr14:45143754 | C | T | 2 | a0005c0005t0001g0205 a0005c0005t0001g0206 |
2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.759+3045C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45143754 | |||||||
chr14:45143817 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0059 |
2 | NA18952.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.759+3108C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45143817 | |||||||
chr14:45143890 | C | T | 5 | a0006c0010t0001g0134 a0006c0010t0001g0135 a0006c0010t0001g0198 others(2): Show |
5 | HG01106.hp1 HG01516.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.759+3181C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45143890 | |||||||
chr14:45143971 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.759+3262C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45143971 | |||||||
chr14:45143972 | G | A | 12 | a0002c0003t0002g0150 a0002c0003t0002g0153 a0002c0003t0002g0154 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.759+3263G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45143972 | |||||||
chr14:45144037 | CT | C | 15 | a0002c0003t0002g0216 a0002c0003t0002g0218 a0002c0003t0002g0219 others(12): Show |
15 | HG02145.hp2 HG02280.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.759+3339delT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45144037 | ||||||
chr14:45144192 | T | C | 1 | a0020c0034t0002g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.759+3483T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45144192 | |||||||
chr14:45144261 | T | G | 19 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0031 others(16): Show |
21 | HG01099.hp2 HG01261.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.759+3552T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45144261 | |||||||
chr14:45144304 | T | TC | 15 | a0002c0003t0002g0150 a0002c0003t0002g0153 a0002c0003t0002g0154 others(12): Show |
15 | HG01109.hp1 HG02109.hp2 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.759+3599dupC | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45144304 | ||||||
chr14:45144309 | T | C | 184 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(181): Show |
196 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.759+3600T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45144309 | |||||||
chr14:45144312 | A | C | 1 | a0001c0001t0001g0114 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.759+3603A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45144312 | |||||||
chr14:45144349 | C | T | 5 | a0001c0001t0001g0113 a0005c0005t0001g0205 a0005c0005t0001g0206 others(2): Show |
5 | HG02132.hp1 HG02615.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.759+3640C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45144349 | |||||||
chr14:45144352 | CCTT | C | 40 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0031 others(37): Show |
42 | HG01109.hp1 HG01261.hp2 HG02055.hp1 others(39): Show |
intron_variant | MODIFIER | c.759+3646_759+3648d others(5): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45144352 | ||||||
chr14:45144391 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.759+3682T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45144391 | |||||||
chr14:45144741 | G | T | 6 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(3): Show |
6 | HG02257.hp1 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.759+4032G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45144741 | |||||||
chr14:45144844 | GCTGGTAC | G | 2 | a0011c0015t0001g0191 a0011c0015t0001g0192 |
2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.760-3989_760-3983d others(9): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45144844 | ||||||
chr14:45144894 | A | G | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.760-3943A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45144894 | |||||||
chr14:45144955 | G | A | 1 | a0020c0034t0002g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.760-3882G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45144955 | |||||||
chr14:45145229 | T | C | 1 | a0024c0024t0001g0141 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.760-3608T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45145229 | |||||||
chr14:45145230 | C | CT | 5 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(2): Show |
5 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.760-3601dupT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45145230 | ||||||
chr14:45145329 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.760-3508C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45145329 | |||||||
chr14:45145357 | C | G | 2 | a0011c0015t0001g0191 a0011c0015t0001g0192 |
2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.760-3480C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45145357 | |||||||
chr14:45145361 | A | C | 15 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(12): Show |
15 | HG01358.hp1 HG01884.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.760-3476A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45145361 | |||||||
chr14:45145699 | C | T | 39 | a0003c0002t0001g0003 a0003c0002t0001g0169 a0003c0002t0001g0170 others(36): Show |
42 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.760-3138C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45145699 | |||||||
chr14:45145744 | G | GA | 6 | a0007c0009t0001g0016 a0007c0009t0001g0017 a0007c0009t0001g0018 others(3): Show |
6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.760-3090dupA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45145744 | ||||||
chr14:45145828 | G | A | 4 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(1): Show |
4 | NA18954.hp1 NA18968.hp2 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.760-3009G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45145828 | |||||||
chr14:45145959 | TGAGGCAG others(19): Show |
T | 6 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(3): Show |
6 | HG02257.hp1 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.760-2872_760-2847d others(28): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45145959 | ||||||
chr14:45145983 | C | T | 6 | a0002c0008t0004g0140 a0002c0008t0004g0147 a0002c0008t0004g0148 others(3): Show |
6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.760-2854C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45145983 | |||||||
chr14:45145988 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.760-2849G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45145988 | |||||||
chr14:45146007 | C | T | 6 | a0007c0009t0001g0016 a0007c0009t0001g0017 a0007c0009t0001g0018 others(3): Show |
6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.760-2830C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45146007 | |||||||
chr14:45146054 | G | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0045 others(2): Show |
7 | HG00639.hp2 HG01071.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.760-2783G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45146054 | |||||||
chr14:45146072 | G | A | 1 | a0007c0009t0001g0016 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.760-2765G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45146072 | |||||||
chr14:45146129 | T | TAC | 26 | a0002c0003t0002g0139 a0002c0003t0002g0150 a0002c0003t0002g0153 others(23): Show |
27 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.760-2707_760-2706d others(4): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45146129 | ||||||
chr14:45146144 | G | GGCA | 39 | a0003c0002t0001g0003 a0003c0002t0001g0169 a0003c0002t0001g0170 others(36): Show |
42 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.760-2691_760-2689d others(5): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45146144 | ||||||
chr14:45146227 | T | C | 6 | a0002c0008t0004g0140 a0002c0008t0004g0147 a0002c0008t0004g0148 others(3): Show |
6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.760-2610T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45146227 | |||||||
chr14:45146238 | C | G | 26 | a0002c0003t0002g0139 a0002c0003t0002g0150 a0002c0003t0002g0153 others(23): Show |
27 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.760-2599C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45146238 | |||||||
chr14:45146240 | G | GA | 134 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(131): Show |
145 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(142): Show |
intron_variant | MODIFIER | c.760-2578dupA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45146240 | ||||||
chr14:45146240 | G | GAA | 45 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0045 others(42): Show |
47 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.760-2579_760-2578d others(4): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45146240 | ||||||
chr14:45146240 | G | GAAA | 8 | a0003c0002t0001g0169 a0003c0002t0001g0174 a0003c0002t0001g0194 others(5): Show |
9 | HG01192.hp1 HG01243.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.760-2580_760-2578d others(5): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45146240 | ||||||
chr14:45146280 | A | C | 1 | a0001c0001t0001g0107 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.760-2557A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45146280 | |||||||
chr14:45146331 | C | G | 5 | a0001c0001t0001g0025 a0001c0001t0001g0038 a0001c0001t0001g0104 others(2): Show |
5 | HG02809.hp2 HG02922.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.760-2506C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45146331 | |||||||
chr14:45146428 | A | G | 3 | a0002c0003t0001g0014 a0002c0003t0001g0167 a0022c0030t0001g0014 |
3 | HG02257.hp2 HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.760-2409A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45146428 | |||||||
chr14:45146433 | T | G | 39 | a0003c0002t0001g0003 a0003c0002t0001g0169 a0003c0002t0001g0170 others(36): Show |
42 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.760-2404T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45146433 | |||||||
chr14:45146498 | G | T | 1 | a0008c0025t0002g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.760-2339G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45146498 | |||||||
chr14:45146574 | A | G | 5 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(2): Show |
5 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.760-2263A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45146574 | |||||||
chr14:45146832 | C | CA | 33 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0040 others(30): Show |
33 | HG00323.hp2 HG01106.hp2 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.760-1979dupA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45146832 | ||||||
chr14:45146832 | C | CAAA | 5 | a0006c0010t0001g0134 a0006c0010t0001g0198 a0006c0010t0001g0199 others(2): Show |
5 | HG01106.hp1 HG01891.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.760-1981_760-1979d others(5): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45146832 | ||||||
chr14:45146832 | CA | C | 36 | a0001c0001t0001g0044 a0001c0001t0001g0102 a0001c0001t0001g0103 others(33): Show |
38 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.760-1979delA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45146832 | ||||||
chr14:45146832 | CAAAA | C | 9 | a0002c0003t0002g0139 a0002c0003t0002g0150 a0002c0003t0002g0154 others(6): Show |
9 | HG02055.hp1 HG02717.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.760-1982_760-1979d others(6): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45146832 | ||||||
chr14:45146832 | CAAAAA | C | 16 | a0002c0003t0002g0216 a0002c0006t0002g0208 a0002c0006t0002g0209 others(13): Show |
17 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.760-1983_760-1979d others(7): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45146832 | ||||||
chr14:45147148 | T | C | 108 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(105): Show |
112 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.760-1689T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147148 | |||||||
chr14:45147265 | C | G | 2 | a0004c0004t0001g0122 a0004c0004t0001g0123 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.760-1572C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147265 | |||||||
chr14:45147467 | G | T | 12 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(9): Show |
12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.760-1370G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147467 | |||||||
chr14:45147482 | T | G | 1 | a0020c0034t0002g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.760-1355T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147482 | |||||||
chr14:45147529 | C | T | 3 | a0006c0010t0001g0198 a0006c0010t0001g0199 a0006c0010t0001g0200 |
3 | HG01106.hp1 HG01516.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.760-1308C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147529 | |||||||
chr14:45147538 | C | G | 1 | a0003c0002t0001g0175 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.760-1299C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147538 | |||||||
chr14:45147551 | G | A | 5 | a0003c0002t0001g0176 a0003c0002t0001g0177 a0003c0002t0001g0178 others(2): Show |
5 | NA18964.hp2 NA18970.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.760-1286G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147551 | |||||||
chr14:45147582 | C | G | 1 | a0001c0001t0001g0063 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.760-1255C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147582 | |||||||
chr14:45147582 | C | T | 1 | a0003c0002t0001g0175 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.760-1255C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147582 | |||||||
chr14:45147791 | G | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0064 |
2 | HG02109.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.760-1046G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147791 | |||||||
chr14:45147865 | G | C | 1 | a0021c0026t0008g0142 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.760-972G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147865 | |||||||
chr14:45147887 | G | T | 37 | a0003c0002t0001g0003 a0003c0002t0001g0169 a0003c0002t0001g0170 others(34): Show |
40 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.760-950G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147887 | |||||||
chr14:45147897 | G | GC | 14 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0044 others(11): Show |
15 | HG00639.hp1 HG01106.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.760-930dupC | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45147897 | ||||||
chr14:45147897 | G | GCC | 17 | a0002c0003t0002g0216 a0002c0006t0002g0207 a0002c0006t0002g0208 others(14): Show |
18 | HG02258.hp1 HG02258.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.760-931_760-930dup others(2): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45147897 | ||||||
chr14:45147905 | C | A | 10 | a0002c0031t0006g0159 a0005c0005t0001g0151 a0005c0005t0001g0152 others(7): Show |
10 | HG02109.hp2 HG02559.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.760-932C>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147905 | |||||||
chr14:45147905 | C | G | 6 | a0002c0032t0001g0204 a0006c0010t0001g0134 a0006c0010t0001g0135 others(3): Show |
6 | HG01106.hp1 HG01516.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.760-932C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147905 | |||||||
chr14:45147906 | C | A | 11 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(8): Show |
11 | HG01358.hp1 HG01884.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.760-931C>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147906 | |||||||
chr14:45147907 | C | A | 33 | a0003c0002t0001g0003 a0003c0002t0001g0169 a0003c0002t0001g0170 others(30): Show |
36 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.760-930C>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147907 | |||||||
chr14:45147907 | C | CA | 14 | a0001c0001t0001g0053 a0001c0001t0001g0065 a0001c0001t0001g0066 others(11): Show |
14 | HG00323.hp2 HG00597.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.760-921dupA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45147907 | ||||||
chr14:45147907 | C | G | 4 | a0001c0001t0001g0015 a0001c0001t0001g0062 a0001c0001t0001g0100 others(1): Show |
4 | HG02015.hp2 NA18994.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.760-930C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147907 | |||||||
chr14:45147908 | A | C | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.760-929A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147908 | |||||||
chr14:45147977 | C | A | 1 | a0008c0025t0002g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.760-860C>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147977 | |||||||
chr14:45148049 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.760-788T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45148049 | |||||||
chr14:45148151 | C | T | 2 | a0011c0015t0001g0191 a0011c0015t0001g0192 |
2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.760-686C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45148151 | |||||||
chr14:45148198 | A | AACAC | 5 | a0002c0007t0003g0163 a0002c0007t0003g0164 a0003c0002t0001g0180 others(2): Show |
5 | HG02886.hp2 HG03453.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.760-638_760-637ins others(4): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45148198 | ||||||
chr14:45148198 | A | AACACAC | 3 | a0003c0002t0001g0194 a0003c0002t0001g0195 a0021c0026t0008g0142 |
3 | HG02615.hp1 NA19063.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.760-638_760-637ins others(6): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45148198 | ||||||
chr14:45148198 | A | AACACACA others(1): Show |
22 | a0003c0002t0001g0003 a0003c0002t0001g0169 a0003c0002t0001g0170 others(19): Show |
24 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.760-638_760-637ins others(8): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45148198 | ||||||
chr14:45148198 | A | AACACACA others(3): Show |
5 | a0003c0002t0001g0175 a0003c0002t0001g0186 a0004c0004t0001g0013 others(2): Show |
6 | HG00609.hp2 HG01192.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.760-638_760-637ins others(10): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45148198 | ||||||
chr14:45148198 | A | AACACACA others(5): Show |
1 | a0004c0004t0001g0027 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.760-638_760-637ins others(12): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45148198 | ||||||
chr14:45148198 | A | AACACACA others(7): Show |
1 | a0025c0033t0001g0187 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.760-638_760-637ins others(14): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45148198 | ||||||
chr14:45148200 | A | AAC | 13 | a0001c0001t0001g0021 a0001c0001t0001g0041 a0001c0001t0001g0042 others(10): Show |
13 | HG01109.hp2 HG02055.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.760-603_760-602dup others(2): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45148200 | ||||||
chr14:45148200 | A | AACAC | 12 | a0001c0001t0001g0105 a0001c0001t0001g0108 a0002c0003t0001g0014 others(9): Show |
12 | HG01106.hp1 HG01358.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.760-605_760-602dup others(4): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45148200 | ||||||
chr14:45148200 | A | AACACAC | 10 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(7): Show |
10 | HG02109.hp2 HG02257.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.760-607_760-602dup others(6): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45148200 | ||||||
chr14:45148200 | A | AACACACA others(1): Show |
3 | a0005c0005t0001g0205 a0005c0005t0001g0206 a0024c0024t0001g0141 |
3 | HG02717.hp1 HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.760-609_760-602dup others(8): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45148200 | ||||||
chr14:45148200 | A | AACACACA others(3): Show |
5 | a0002c0003t0002g0139 a0002c0003t0002g0150 a0002c0003t0002g0154 others(2): Show |
5 | HG02055.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.760-611_760-602dup others(10): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45148200 | ||||||
chr14:45148200 | A | AACACACA others(5): Show |
14 | a0002c0006t0002g0207 a0002c0006t0002g0208 a0002c0006t0002g0209 others(11): Show |
14 | HG02132.hp1 HG02280.hp2 HG02293.hp2 others(11): Show |
intron_variant | MODIFIER | c.760-613_760-602dup others(12): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45148200 | ||||||
chr14:45148200 | A | AACACACA others(7): Show |
9 | a0002c0003t0002g0153 a0002c0003t0002g0218 a0002c0003t0002g0219 others(6): Show |
10 | HG01109.hp1 HG01884.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.760-615_760-602dup others(14): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45148200 | ||||||
chr14:45148200 | A | AACACACA others(9): Show |
4 | a0002c0003t0002g0216 a0002c0003t0002g0220 a0008c0011t0002g0049 others(1): Show |
4 | HG02717.hp2 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.760-617_760-602dup others(16): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45148200 | ||||||
chr14:45148200 | A | C | 40 | a0002c0007t0003g0163 a0002c0007t0003g0164 a0003c0002t0001g0003 others(37): Show |
43 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.760-637A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45148200 | |||||||
chr14:45148200 | AACAC | A | 4 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0031 others(1): Show |
5 | HG01261.hp2 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.760-605_760-602del others(4): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45148200 | ||||||
chr14:45148514 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.760-323G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45148514 | |||||||
chr14:45148561 | T | C | 3 | a0004c0004t0001g0122 a0004c0004t0001g0123 a0017c0027t0001g0120 |
3 | HG01167.hp1 HG01169.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.760-276T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45148561 | |||||||
chr14:45148731 | T | G | 1 | a0001c0001t0001g0061 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.760-106T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45148731 | |||||||
chr14:45149107 | A | G | 1 | a0027c0020t0001g0117 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.918+112A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45149107 | |||||||
chr14:45149142 | G | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0106 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.918+147G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45149142 | |||||||
chr14:45149157 | T | C | 1 | a0003c0002t0001g0169 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.918+162T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45149157 | |||||||
chr14:45149285 | G | GCA | 14 | a0001c0001t0001g0069 a0001c0001t0001g0095 a0001c0001t0001g0111 others(11): Show |
14 | HG01169.hp1 HG01891.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.918+313_918+314dup others(2): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr14 | 45149285 | ||||||
chr14:45149285 | G | GCACA | 5 | a0006c0010t0001g0134 a0006c0010t0001g0135 a0006c0010t0001g0198 others(2): Show |
5 | HG01106.hp1 HG01516.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+311_918+314dup others(4): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr14 | 45149285 | ||||||
chr14:45149285 | GCA | G | 37 | a0003c0002t0001g0003 a0003c0002t0001g0169 a0003c0002t0001g0170 others(34): Show |
40 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.918+313_918+314del others(2): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr14 | 45149285 | ||||||
chr14:45149285 | GCACACA | G | 6 | a0007c0009t0001g0016 a0007c0009t0001g0017 a0007c0009t0001g0018 others(3): Show |
6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.918+309_918+314del others(6): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr14 | 45149285 | ||||||
chr14:45149331 | A | C | 1 | a0021c0026t0008g0142 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.918+336A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45149331 | |||||||
chr14:45149484 | A | G | 5 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0045 others(2): Show |
7 | HG00639.hp2 HG01071.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.918+489A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45149484 | |||||||
chr14:45149512 | A | G | 1 | a0010c0014t0001g0138 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.918+517A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45149512 | |||||||
chr14:45149541 | A | G | 1 | a0008c0025t0002g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.918+546A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45149541 | |||||||
chr14:45149717 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.918+722T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45149717 | |||||||
chr14:45149804 | T | TACA | 37 | a0003c0002t0001g0003 a0003c0002t0001g0169 a0003c0002t0001g0170 others(34): Show |
40 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.918+829_918+831dup others(3): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr14 | 45149804 | ||||||
chr14:45150014 | A | G | 5 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0097 others(2): Show |
5 | HG00280.hp2 HG00639.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.918+1019A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45150014 | |||||||
chr14:45150036 | A | C | 2 | a0010c0014t0001g0137 a0010c0014t0001g0138 |
2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.918+1041A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45150036 | |||||||
chr14:45150574 | T | C | 1 | a0001c0001t0001g0041 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.919-823T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45150574 | |||||||
chr14:45150586 | C | T | 39 | a0003c0002t0001g0003 a0003c0002t0001g0169 a0003c0002t0001g0170 others(36): Show |
42 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.919-811C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45150586 | |||||||
chr14:45150637 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.919-760A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45150637 | |||||||
chr14:45150727 | A | G | 39 | a0003c0002t0001g0003 a0003c0002t0001g0169 a0003c0002t0001g0170 others(36): Show |
42 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.919-670A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45150727 | |||||||
chr14:45150814 | C | T | 6 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(3): Show |
6 | HG02257.hp1 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.919-583C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45150814 | |||||||
chr14:45150926 | G | A | 2 | a0002c0006t0002g0212 a0002c0006t0002g0213 |
2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.919-471G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45150926 | |||||||
chr14:45151055 | T | A | 1 | a0002c0006t0002g0208 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.919-342T>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45151055 | |||||||
chr14:45151104 | A | G | 7 | a0002c0032t0001g0204 a0006c0010t0001g0134 a0006c0010t0001g0135 others(4): Show |
7 | HG01106.hp1 HG01516.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.919-293A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45151104 | |||||||
chr14:45151116 | G | A | 9 | a0002c0031t0006g0159 a0005c0005t0001g0151 a0005c0005t0001g0152 others(6): Show |
9 | HG02109.hp2 HG02559.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.919-281G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45151116 | |||||||
chr14:45151840 | G | T | 39 | a0003c0002t0001g0003 a0003c0002t0001g0169 a0003c0002t0001g0170 others(36): Show |
42 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1050+312G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | chr14 | 45151840 | |||||||
chr14:45151912 | T | TA | 15 | a0001c0001t0001g0021 a0001c0001t0001g0032 a0001c0001t0001g0054 others(12): Show |
15 | HG01261.hp1 HG02056.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1050+406dupA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr14 | 45151912 | ||||||
chr14:45151912 | TA | T | 33 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0037 others(30): Show |
33 | HG01109.hp1 HG01256.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.1050+406delA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr14 | 45151912 | ||||||
chr14:45151912 | TAA | T | 12 | a0002c0003t0002g0216 a0002c0006t0002g0207 a0002c0006t0002g0208 others(9): Show |
13 | HG02258.hp2 HG02280.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1050+405_1050+406d others(4): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr14 | 45151912 | ||||||
chr14:45151930 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1050+402A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | chr14 | 45151930 | |||||||
chr14:45151991 | T | C | 39 | a0003c0002t0001g0003 a0003c0002t0001g0169 a0003c0002t0001g0170 others(36): Show |
42 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1050+463T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | chr14 | 45151991 | |||||||
chr14:45152009 | T | A | 1 | a0001c0001t0001g0042 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1050+481T>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | chr14 | 45152009 | |||||||
chr14:45152032 | C | CT | 5 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(2): Show |
5 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1050+518dupT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr14 | 45152032 | ||||||
chr14:45152032 | CT | C | 39 | a0003c0002t0001g0003 a0003c0002t0001g0169 a0003c0002t0001g0170 others(36): Show |
42 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1050+518delT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr14 | 45152032 | ||||||
chr14:45152065 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1050+537A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | chr14 | 45152065 | |||||||
chr14:45152315 | T | C | 108 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(105): Show |
112 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.1050+787T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | chr14 | 45152315 | |||||||
chr14:45152475 | G | A | 1 | a0004c0004t0001g0109 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1050+947G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | chr14 | 45152475 | |||||||
chr14:45152557 | G | A | 1 | a0001c0001t0001g0008 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1050+1029G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | chr14 | 45152557 | |||||||
chr14:45153062 | T | C | 35 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(32): Show |
35 | HG01106.hp1 HG01358.hp1 HG01516.hp1 others(32): Show |
intron_variant | MODIFIER | c.1051-858T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | chr14 | 45153062 | |||||||
chr14:45153354 | A | C | 26 | a0002c0003t0002g0139 a0002c0003t0002g0150 a0002c0003t0002g0153 others(23): Show |
27 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1051-566A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | chr14 | 45153354 | |||||||
chr14:45153355 | A | G | 108 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(105): Show |
112 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.1051-565A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | chr14 | 45153355 | |||||||
chr14:45153616 | A | G | 37 | a0003c0002t0001g0003 a0003c0002t0001g0169 a0003c0002t0001g0170 others(34): Show |
40 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1051-304A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | chr14 | 45153616 | |||||||
chr14:45154084 | T | C | 1 | a0020c0034t0002g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1183+32T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 6/22 | chr14 | 45154084 | |||||||
chr14:45154211 | G | A | 6 | a0007c0009t0001g0016 a0007c0009t0001g0017 a0007c0009t0001g0018 others(3): Show |
6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.1183+159G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 6/22 | chr14 | 45154211 | |||||||
chr14:45154257 | T | C | 40 | a0003c0002t0001g0003 a0003c0002t0001g0169 a0003c0002t0001g0170 others(37): Show |
43 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.1183+205T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 6/22 | chr14 | 45154257 | |||||||
chr14:45154270 | G | C | 1 | a0002c0008t0007g0161 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1183+218G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 6/22 | chr14 | 45154270 | |||||||
chr14:45154273 | C | T | 2 | a0005c0005t0001g0205 a0005c0005t0001g0206 |
2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1183+221C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 6/22 | chr14 | 45154273 | |||||||
chr14:45154378 | GC | G | 12 | a0003c0002t0001g0169 a0003c0002t0001g0170 a0003c0002t0001g0174 others(9): Show |
12 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.1184-318delC | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 6/22 | chr14 | 45154378 | |||||||
chr14:45154398 | T | TA | 20 | a0001c0001t0001g0041 a0001c0001t0001g0110 a0001c0001t0001g0126 others(17): Show |
21 | HG01106.hp1 HG01106.hp2 HG01516.hp1 others(18): Show |
intron_variant | MODIFIER | c.1184-281dupA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr14 | 45154398 | ||||||
chr14:45154398 | TA | T | 45 | a0001c0001t0001g0060 a0001c0001t0001g0098 a0001c0001t0001g0103 others(42): Show |
48 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.1184-281delA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr14 | 45154398 | ||||||
chr14:45154466 | A | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0052 a0001c0001t0001g0090 |
3 | HG02056.hp1 HG02129.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.1184-231A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 6/22 | chr14 | 45154466 | |||||||
chr14:45155178 | A | C | 26 | a0002c0003t0002g0139 a0002c0003t0002g0150 a0002c0003t0002g0153 others(23): Show |
27 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1310-195A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 7/22 | chr14 | 45155178 | |||||||
chr14:45155234 | T | A | 1 | a0021c0026t0008g0142 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1310-139T>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 7/22 | chr14 | 45155234 | |||||||
chr14:45155286 | A | G | 5 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0045 others(2): Show |
7 | HG00639.hp2 HG01071.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.1310-87A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 7/22 | chr14 | 45155286 | |||||||
chr14:45155305 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1310-68A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 7/22 | chr14 | 45155305 | |||||||
chr14:45155330 | G | GA | 26 | a0002c0003t0002g0139 a0002c0003t0002g0150 a0002c0003t0002g0153 others(23): Show |
27 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1310-36dupA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr14 | 45155330 | ||||||
chr14:45155485 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1396+26G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45155485 | |||||||
chr14:45155491 | C | T | 1 | a0002c0006t0002g0215 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1396+32C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45155491 | |||||||
chr14:45155596 | CA | C | 2 | a0010c0014t0001g0137 a0010c0014t0001g0138 |
2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1396+139delA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | 45155596 | ||||||
chr14:45155738 | G | A | 35 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(32): Show |
35 | HG01106.hp1 HG01358.hp1 HG01516.hp1 others(32): Show |
intron_variant | MODIFIER | c.1396+279G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45155738 | |||||||
chr14:45155747 | C | T | 1 | a0006c0010t0001g0199 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1396+288C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45155747 | |||||||
chr14:45155888 | TA | T | 108 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(105): Show |
112 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.1396+431delA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | 45155888 | ||||||
chr14:45155980 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1396+521A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45155980 | |||||||
chr14:45155987 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1396+528A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45155987 | |||||||
chr14:45156190 | T | G | 1 | a0005c0005t0001g0151 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1396+731T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45156190 | |||||||
chr14:45156668 | C | T | 2 | a0010c0014t0001g0137 a0010c0014t0001g0138 |
2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1396+1209C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45156668 | |||||||
chr14:45156788 | T | A | 2 | a0009c0016t0005g0202 a0009c0016t0005g0203 |
2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1396+1329T>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45156788 | |||||||
chr14:45156802 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1396+1343C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45156802 | |||||||
chr14:45156872 | T | G | 1 | a0020c0034t0002g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1396+1413T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45156872 | |||||||
chr14:45156916 | C | CA | 39 | a0001c0001t0001g0024 a0001c0001t0001g0031 a0001c0001t0001g0036 others(36): Show |
39 | HG01106.hp1 HG01516.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.1396+1479dupA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | 45156916 | ||||||
chr14:45156916 | C | CAA | 22 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(19): Show |
22 | HG01109.hp1 HG01358.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1396+1478_1396+147 others(6): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | 45156916 | ||||||
chr14:45156916 | CA | C | 5 | a0001c0001t0001g0059 a0002c0006t0002g0210 a0003c0002t0001g0172 others(2): Show |
5 | HG02622.hp1 HG02976.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.1396+1479delA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | 45156916 | ||||||
chr14:45157025 | T | C | 1 | a0002c0008t0004g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1396+1566T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45157025 | |||||||
chr14:45157036 | A | G | 6 | a0002c0003t0002g0139 a0002c0003t0002g0150 a0002c0003t0002g0153 others(3): Show |
6 | HG01109.hp1 HG02055.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1396+1577A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45157036 | |||||||
chr14:45157071 | A | C | 6 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(3): Show |
6 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1396+1612A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45157071 | |||||||
chr14:45157071 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1396+1612A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45157071 | |||||||
chr14:45157535 | G | C | 1 | a0002c0003t0002g0220 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1397-1561G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45157535 | |||||||
chr14:45157764 | C | T | 3 | a0006c0010t0001g0198 a0006c0010t0001g0199 a0006c0010t0001g0200 |
3 | HG01106.hp1 HG01516.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1397-1332C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45157764 | |||||||
chr14:45157903 | A | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0132 a0014c0018t0001g0029 |
4 | HG00438.hp1 HG00609.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1397-1193A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45157903 | |||||||
chr14:45157925 | C | G | 106 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(103): Show |
110 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.1397-1171C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45157925 | |||||||
chr14:45158111 | T | G | 1 | a0001c0001t0001g0113 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1397-985T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45158111 | |||||||
chr14:45158344 | C | A | 1 | a0005c0005t0001g0151 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1397-752C>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45158344 | |||||||
chr14:45158405 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1397-691G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45158405 | |||||||
chr14:45158439 | G | A | 1 | a0010c0014t0001g0137 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1397-657G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45158439 | |||||||
chr14:45158459 | C | T | 1 | a0003c0002t0001g0003 | 3 | HG00558.hp1 NA18946.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1397-637C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45158459 | |||||||
chr14:45158607 | T | G | 1 | a0001c0001t0001g0110 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1397-489T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45158607 | |||||||
chr14:45158947 | T | C | 2 | a0010c0014t0001g0137 a0010c0014t0001g0138 |
2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1397-149T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45158947 | |||||||
chr14:45159021 | G | A | 1 | a0007c0009t0001g0019 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1397-75G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45159021 | |||||||
chr14:45159038 | T | G | 109 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(106): Show |
113 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.1397-58T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45159038 | |||||||
chr14:45159080 | TTA | T | 40 | a0003c0002t0001g0003 a0003c0002t0001g0169 a0003c0002t0001g0170 others(37): Show |
43 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(40): Show |
splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.1397-3_1397-2delTA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | 45159080 | ||||||
chr14:45159084 | A | G | 1 | a0002c0032t0001g0204 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1397-12A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45159084 | |||||||
chr14:45159346 | T | G | 1 | a0021c0026t0008g0142 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1581+66T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45159346 | |||||||
chr14:45159427 | A | C | 2 | a0005c0005t0001g0205 a0005c0005t0001g0206 |
2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1581+147A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45159427 | |||||||
chr14:45159461 | A | C | 1 | a0002c0006t0002g0213 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1581+181A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45159461 | |||||||
chr14:45159515 | G | T | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1581+235G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45159515 | |||||||
chr14:45159547 | T | G | 6 | a0007c0009t0001g0016 a0007c0009t0001g0017 a0007c0009t0001g0018 others(3): Show |
6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.1581+267T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45159547 | |||||||
chr14:45159550 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1581+270C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45159550 | |||||||
chr14:45159572 | C | T | 205 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(202): Show |
216 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.1581+292C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45159572 | |||||||
chr14:45159654 | A | G | 6 | a0007c0009t0001g0016 a0007c0009t0001g0017 a0007c0009t0001g0018 others(3): Show |
6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.1581+374A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45159654 | |||||||
chr14:45159800 | A | C | 13 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(10): Show |
13 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1581+520A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45159800 | |||||||
chr14:45159815 | T | C | 6 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(3): Show |
6 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1581+535T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45159815 | |||||||
chr14:45159819 | G | C | 1 | a0021c0026t0008g0142 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1581+539G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45159819 | |||||||
chr14:45159912 | A | G | 1 | a0005c0005t0001g0206 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1581+632A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45159912 | |||||||
chr14:45160002 | G | GT | 10 | a0001c0001t0001g0036 a0001c0001t0001g0052 a0001c0001t0001g0067 others(7): Show |
10 | HG01346.hp2 HG01993.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1581+739dupT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr14 | 45160002 | ||||||
chr14:45160002 | G | T | 1 | a0001c0001t0001g0028 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1581+722G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45160002 | |||||||
chr14:45160002 | GTT | G | 59 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(56): Show |
60 | HG00609.hp2 HG01106.hp1 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.1581+738_1581+739d others(4): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr14 | 45160002 | ||||||
chr14:45160002 | GTTT | G | 35 | a0002c0031t0006g0159 a0003c0002t0001g0003 a0003c0002t0001g0169 others(32): Show |
38 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.1581+737_1581+739d others(5): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr14 | 45160002 | ||||||
chr14:45160004 | T | G | 1 | a0002c0003t0002g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1581+724T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45160004 | |||||||
chr14:45160037 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1581+757G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45160037 | |||||||
chr14:45160096 | G | A | 6 | a0002c0008t0004g0140 a0002c0008t0004g0147 a0002c0008t0004g0148 others(3): Show |
6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1581+816G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45160096 | |||||||
chr14:45160241 | G | A | 1 | a0002c0031t0006g0159 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1581+961G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45160241 | |||||||
chr14:45160268 | A | T | 12 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(9): Show |
12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1581+988A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45160268 | |||||||
chr14:45160290 | G | A | 3 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0037 |
3 | HG02145.hp1 HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1581+1010G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45160290 | |||||||
chr14:45160305 | T | G | 1 | a0021c0026t0008g0142 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1581+1025T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45160305 | |||||||
chr14:45160318 | CT | C | 18 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0055 others(15): Show |
18 | HG00323.hp1 HG00323.hp2 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.1581+1054delT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr14 | 45160318 | ||||||
chr14:45160480 | G | A | 27 | a0002c0003t0002g0139 a0002c0003t0002g0150 a0002c0003t0002g0153 others(24): Show |
28 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1581+1200G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45160480 | |||||||
chr14:45160491 | T | A | 1 | a0002c0003t0002g0220 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1581+1211T>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45160491 | |||||||
chr14:45160567 | C | T | 2 | a0010c0014t0001g0137 a0010c0014t0001g0138 |
2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1581+1287C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45160567 | |||||||
chr14:45160623 | C | T | 6 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(3): Show |
6 | HG02257.hp1 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1581+1343C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45160623 | |||||||
chr14:45160658 | T | C | 12 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(9): Show |
12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1581+1378T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45160658 | |||||||
chr14:45160708 | A | T | 1 | a0004c0004t0001g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1581+1428A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45160708 | |||||||
chr14:45161128 | A | G | 6 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(3): Show |
6 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1581+1848A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45161128 | |||||||
chr14:45161153 | C | T | 2 | a0003c0002t0001g0169 a0003c0002t0001g0182 |
2 | HG00673.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1581+1873C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45161153 | |||||||
chr14:45161191 | C | T | 1 | a0002c0031t0006g0159 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1581+1911C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45161191 | |||||||
chr14:45161319 | T | A | 1 | a0001c0001t0001g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1581+2039T>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45161319 | |||||||
chr14:45161369 | G | T | 1 | a0001c0001t0001g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1581+2089G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45161369 | |||||||
chr14:45161378 | G | A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0108 a0001c0001t0001g0124 |
3 | HG03669.hp2 NA19005.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1581+2098G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45161378 | |||||||
chr14:45161506 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1581+2226C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45161506 | |||||||
chr14:45161595 | A | G | 6 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(3): Show |
6 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1581+2315A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45161595 | |||||||
chr14:45161768 | C | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0060 |
2 | NA18960.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1581+2488C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45161768 | |||||||
chr14:45161817 | A | G | 1 | a0021c0026t0008g0142 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1581+2537A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45161817 | |||||||
chr14:45162015 | T | A | 1 | a0003c0002t0001g0184 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1582-2344T>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45162015 | |||||||
chr14:45162124 | G | A | 1 | a0020c0034t0002g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1582-2235G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45162124 | |||||||
chr14:45162616 | A | G | 2 | a0001c0001t0001g0087 a0015c0028t0001g0086 |
2 | HG01099.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1582-1743A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45162616 | |||||||
chr14:45162752 | A | G | 6 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(3): Show |
6 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1582-1607A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45162752 | |||||||
chr14:45162828 | A | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0060 |
2 | NA18960.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1582-1531A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45162828 | |||||||
chr14:45162847 | G | A | 6 | a0002c0032t0001g0204 a0006c0010t0001g0134 a0006c0010t0001g0135 others(3): Show |
6 | HG01106.hp1 HG01516.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1582-1512G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45162847 | |||||||
chr14:45162869 | T | G | 8 | a0005c0005t0001g0151 a0005c0005t0001g0152 a0005c0005t0001g0156 others(5): Show |
8 | HG02109.hp2 HG02559.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1582-1490T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45162869 | |||||||
chr14:45162881 | C | G | 6 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(3): Show |
6 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1582-1478C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45162881 | |||||||
chr14:45163002 | CCGA | C | 38 | a0003c0002t0001g0003 a0003c0002t0001g0169 a0003c0002t0001g0170 others(35): Show |
41 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1582-1356_1582-135 others(7): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45163002 | |||||||
chr14:45163013 | C | T | 6 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(3): Show |
6 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1582-1346C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45163013 | |||||||
chr14:45163137 | G | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0045 others(2): Show |
7 | HG00639.hp2 HG01071.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.1582-1222G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45163137 | |||||||
chr14:45163238 | G | A | 1 | a0001c0001t0001g0006 | 2 | HG00639.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1582-1121G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45163238 | |||||||
chr14:45163299 | A | T | 1 | a0004c0004t0001g0119 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1582-1060A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45163299 | |||||||
chr14:45163383 | A | T | 2 | a0011c0015t0001g0191 a0011c0015t0001g0192 |
2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1582-976A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45163383 | |||||||
chr14:45163485 | T | G | 1 | a0001c0001t0001g0011 | 2 | HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1582-874T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45163485 | |||||||
chr14:45163610 | T | C | 1 | a0024c0024t0001g0141 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1582-749T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45163610 | |||||||
chr14:45164096 | C | G | 1 | a0001c0001t0001g0010 | 2 | NA18970.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1582-263C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45164096 | |||||||
chr14:45164127 | G | A | 1 | a0005c0005t0001g0156 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1582-232G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45164127 | |||||||
chr14:45164215 | C | G | 109 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(106): Show |
113 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.1582-144C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45164215 | |||||||
chr14:45164225 | A | G | 1 | a0002c0031t0006g0159 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1582-134A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45164225 | |||||||
chr14:45164319 | A | G | 39 | a0003c0002t0001g0003 a0003c0002t0001g0169 a0003c0002t0001g0170 others(36): Show |
42 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1582-40A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45164319 | |||||||
chr14:45164595 | CA | C | 27 | a0002c0003t0002g0139 a0002c0003t0002g0150 a0002c0003t0002g0153 others(24): Show |
28 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1788+31delA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45164595 | |||||||
chr14:45164711 | C | T | 3 | a0006c0010t0001g0198 a0006c0010t0001g0199 a0006c0010t0001g0200 |
3 | HG01106.hp1 HG01516.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1788+146C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45164711 | |||||||
chr14:45164736 | G | A | 1 | a0003c0002t0001g0196 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1788+171G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45164736 | |||||||
chr14:45164873 | G | T | 10 | a0005c0005t0001g0151 a0005c0005t0001g0152 a0005c0005t0001g0156 others(7): Show |
10 | HG02109.hp2 HG02486.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1788+308G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45164873 | |||||||
chr14:45164907 | T | A | 1 | a0004c0004t0001g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1788+342T>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45164907 | |||||||
chr14:45164960 | CTAAA | C | 6 | a0002c0008t0004g0140 a0002c0008t0004g0147 a0002c0008t0004g0148 others(3): Show |
6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1788+399_1788+402d others(6): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr14 | 45164960 | ||||||
chr14:45165296 | G | A | 2 | a0010c0014t0001g0137 a0010c0014t0001g0138 |
2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1788+731G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45165296 | |||||||
chr14:45165296 | G | T | 17 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(14): Show |
17 | HG01358.hp1 HG01884.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1788+731G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45165296 | |||||||
chr14:45165360 | A | C | 2 | a0003c0002t0001g0003 a0003c0002t0001g0196 |
4 | HG00558.hp1 HG02056.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.1788+795A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45165360 | |||||||
chr14:45165373 | C | G | 1 | a0001c0001t0001g0061 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1788+808C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45165373 | |||||||
chr14:45165415 | G | A | 1 | a0003c0002t0001g0003 | 3 | HG00558.hp1 NA18946.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1788+850G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45165415 | |||||||
chr14:45165483 | G | C | 1 | a0008c0025t0002g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1788+918G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45165483 | |||||||
chr14:45165534 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0031 others(2): Show |
7 | HG01261.hp2 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1788+969C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45165534 | |||||||
chr14:45165557 | A | G | 1 | a0001c0001t0001g0044 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1788+992A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45165557 | |||||||
chr14:45165611 | T | C | 6 | a0005c0005t0001g0151 a0005c0005t0001g0152 a0005c0005t0001g0156 others(3): Show |
6 | HG02109.hp2 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1788+1046T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45165611 | |||||||
chr14:45165947 | A | G | 23 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(20): Show |
23 | HG01358.hp1 HG01884.hp1 HG02132.hp1 others(20): Show |
intron_variant | MODIFIER | c.1789-1003A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45165947 | |||||||
chr14:45166111 | C | T | 1 | a0002c0032t0001g0204 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1789-839C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45166111 | |||||||
chr14:45166155 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1789-795G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45166155 | |||||||
chr14:45166277 | G | A | 12 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(9): Show |
12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1789-673G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45166277 | |||||||
chr14:45166534 | C | A | 1 | a0002c0003t0002g0219 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1789-416C>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45166534 | |||||||
chr14:45166669 | A | T | 2 | a0002c0006t0002g0211 a0002c0006t0002g0214 |
2 | HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1789-281A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45166669 | |||||||
chr14:45166766 | A | G | 3 | a0002c0003t0001g0014 a0002c0003t0001g0167 a0022c0030t0001g0014 |
3 | HG02257.hp2 HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1789-184A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45166766 | |||||||
chr14:45166777 | C | CA | 15 | a0001c0001t0001g0039 a0001c0001t0001g0045 a0001c0001t0001g0063 others(12): Show |
15 | HG01952.hp1 HG02055.hp1 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.1789-154dupA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr14 | 45166777 | ||||||
chr14:45166777 | C | CAA | 15 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(12): Show |
15 | HG01358.hp1 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1789-155_1789-154d others(4): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr14 | 45166777 | ||||||
chr14:45166904 | A | G | 1 | a0002c0003t0001g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1789-46A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45166904 | |||||||
chr14:45167268 | A | G | 1 | a0002c0007t0003g0164 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2002+105A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45167268 | |||||||
chr14:45167304 | G | A | 99 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(96): Show |
103 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.2002+141G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45167304 | |||||||
chr14:45167564 | A | C | 1 | a0001c0001t0001g0063 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2002+401A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45167564 | |||||||
chr14:45167580 | T | C | 7 | a0002c0031t0006g0159 a0007c0009t0001g0016 a0007c0009t0001g0017 others(4): Show |
7 | HG02132.hp1 HG02293.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.2002+417T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45167580 | |||||||
chr14:45167885 | A | G | 17 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(14): Show |
17 | HG01358.hp1 HG01884.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.2002+722A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45167885 | |||||||
chr14:45167984 | C | T | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0008c0025t0002g0133 |
3 | HG03491.hp2 HG03492.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2002+821C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45167984 | |||||||
chr14:45167997 | G | A | 7 | a0002c0031t0006g0159 a0007c0009t0001g0016 a0007c0009t0001g0017 others(4): Show |
7 | HG02132.hp1 HG02293.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.2002+834G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45167997 | |||||||
chr14:45168007 | A | T | 1 | a0003c0002t0001g0172 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2002+844A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45168007 | |||||||
chr14:45168149 | A | G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0031 others(2): Show |
7 | HG01261.hp2 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.2002+986A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45168149 | |||||||
chr14:45168771 | C | CATAGTAT others(23): Show |
2 | a0011c0015t0001g0191 a0011c0015t0001g0192 |
2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2002+1621_2002+165 others(34): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr14 | 45168771 | ||||||
chr14:45168784 | T | TTATATAT others(23): Show |
2 | a0010c0014t0001g0137 a0010c0014t0001g0138 |
2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2002+1626_2002+165 others(34): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr14 | 45168784 | ||||||
chr14:45168946 | C | CAG | 110 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(107): Show |
114 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.2003-1642_2003-164 others(6): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr14 | 45168946 | ||||||
chr14:45169026 | A | G | 1 | a0005c0005t0001g0173 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2003-1563A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45169026 | |||||||
chr14:45169057 | G | A | 11 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(8): Show |
11 | HG01358.hp1 HG01884.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2003-1532G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45169057 | |||||||
chr14:45169264 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2003-1325C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45169264 | |||||||
chr14:45169383 | G | GT | 62 | a0002c0003t0002g0139 a0002c0003t0002g0150 a0002c0003t0002g0153 others(59): Show |
66 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.2003-1194dupT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr14 | 45169383 | ||||||
chr14:45169383 | G | GTT | 5 | a0003c0002t0001g0176 a0003c0002t0001g0177 a0003c0002t0001g0184 others(2): Show |
5 | NA18970.hp1 NA18984.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.2003-1195_2003-119 others(6): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr14 | 45169383 | ||||||
chr14:45169410 | T | A | 3 | a0001c0001t0001g0132 a0002c0032t0001g0204 a0014c0018t0001g0029 |
3 | HG00438.hp1 HG02145.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.2003-1179T>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45169410 | |||||||
chr14:45169432 | C | A | 6 | a0007c0009t0001g0016 a0007c0009t0001g0017 a0007c0009t0001g0018 others(3): Show |
6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.2003-1157C>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45169432 | |||||||
chr14:45169484 | C | T | 39 | a0003c0002t0001g0003 a0003c0002t0001g0169 a0003c0002t0001g0170 others(36): Show |
42 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.2003-1105C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45169484 | |||||||
chr14:45169591 | G | C | 4 | a0002c0008t0004g0147 a0002c0008t0004g0148 a0002c0008t0004g0149 others(1): Show |
4 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2003-998G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45169591 | |||||||
chr14:45169616 | G | T | 1 | a0003c0002t0001g0184 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2003-973G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45169616 | |||||||
chr14:45170128 | A | T | 17 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(14): Show |
17 | HG01358.hp1 HG01884.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.2003-461A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45170128 | |||||||
chr14:45170170 | G | T | 1 | a0002c0032t0001g0204 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2003-419G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45170170 | |||||||
chr14:45170333 | C | G | 6 | a0005c0005t0001g0151 a0005c0005t0001g0152 a0005c0005t0001g0156 others(3): Show |
6 | HG02109.hp2 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2003-256C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45170333 | |||||||
chr14:45170777 | T | C | 2 | a0011c0015t0001g0191 a0011c0015t0001g0192 |
2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2160+31T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | chr14 | 45170777 | |||||||
chr14:45170782 | C | G | 26 | a0002c0003t0002g0139 a0002c0003t0002g0150 a0002c0003t0002g0153 others(23): Show |
27 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.2160+36C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | chr14 | 45170782 | |||||||
chr14:45170985 | CTG | C | 6 | a0007c0009t0001g0016 a0007c0009t0001g0017 a0007c0009t0001g0018 others(3): Show |
6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.2160+242_2160+243d others(4): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr14 | 45170985 | ||||||
chr14:45171090 | A | G | 9 | a0002c0006t0002g0208 a0002c0006t0002g0215 a0002c0032t0001g0204 others(6): Show |
9 | HG01106.hp1 HG01516.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2160+344A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | chr14 | 45171090 | |||||||
chr14:45171147 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2160+401T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | chr14 | 45171147 | |||||||
chr14:45171169 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2160+423G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | chr14 | 45171169 | |||||||
chr14:45171202 | A | C | 41 | a0003c0002t0001g0003 a0003c0002t0001g0169 a0003c0002t0001g0170 others(38): Show |
44 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.2160+456A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | chr14 | 45171202 | |||||||
chr14:45171294 | AATTATGC others(4): Show |
A | 1 | a0001c0001t0001g0074 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2160+551_2160+561d others(13): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr14 | 45171294 | ||||||
chr14:45171325 | A | AT | 7 | a0002c0003t0002g0153 a0007c0009t0001g0016 a0007c0009t0001g0017 others(4): Show |
7 | HG01109.hp1 HG02132.hp1 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.2160+589dupT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr14 | 45171325 | ||||||
chr14:45171354 | A | G | 110 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(107): Show |
114 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.2160+608A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | chr14 | 45171354 | |||||||
chr14:45171447 | A | G | 1 | a0002c0007t0003g0143 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2160+701A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | chr14 | 45171447 | |||||||
chr14:45171485 | C | T | 1 | a0024c0024t0001g0141 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2160+739C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | chr14 | 45171485 | |||||||
chr14:45171642 | C | T | 7 | a0002c0031t0006g0159 a0007c0009t0001g0016 a0007c0009t0001g0017 others(4): Show |
7 | HG02132.hp1 HG02293.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.2160+896C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | chr14 | 45171642 | |||||||
chr14:45171691 | T | TTG | 2 | a0001c0001t0001g0104 a0024c0024t0001g0141 |
2 | HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2160+976_2160+977d others(4): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr14 | 45171691 | ||||||
chr14:45171691 | TTG | T | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(142): Show |
156 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.2160+976_2160+977d others(4): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr14 | 45171691 | ||||||
chr14:45171691 | TTGTG | T | 4 | a0001c0001t0001g0036 a0001c0001t0001g0075 a0002c0003t0002g0216 others(1): Show |
4 | HG01516.hp2 HG02145.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2160+974_2160+977d others(6): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr14 | 45171691 | ||||||
chr14:45171691 | TTGTGTG | T | 2 | a0010c0014t0001g0137 a0010c0014t0001g0138 |
2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2160+972_2160+977d others(8): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr14 | 45171691 | ||||||
chr14:45171691 | TTGTGTGT others(7): Show |
T | 39 | a0003c0002t0001g0003 a0003c0002t0001g0169 a0003c0002t0001g0170 others(36): Show |
42 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.2160+964_2160+977d others(16): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr14 | 45171691 | ||||||
chr14:45171692 | TGTGTGTG | T | 2 | a0011c0015t0001g0191 a0011c0015t0001g0192 |
2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2160+947_2160+953d others(9): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | chr14 | 45171692 | |||||||
chr14:45171811 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2160+1065A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | chr14 | 45171811 | |||||||
chr14:45172401 | C | T | 6 | a0005c0005t0001g0151 a0005c0005t0001g0152 a0005c0005t0001g0156 others(3): Show |
6 | HG02109.hp2 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2161-654C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | chr14 | 45172401 | |||||||
chr14:45172511 | C | T | 2 | a0001c0001t0001g0058 a0001c0001t0001g0060 |
2 | NA18960.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.2161-544C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | chr14 | 45172511 | |||||||
chr14:45172653 | T | C | 17 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(14): Show |
17 | HG01358.hp1 HG01884.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.2161-402T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | chr14 | 45172653 | |||||||
chr14:45172705 | A | G | 2 | a0005c0005t0001g0205 a0005c0005t0001g0206 |
2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2161-350A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | chr14 | 45172705 | |||||||
chr14:45173303 | C | A | 1 | a0002c0008t0004g0168 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2316+93C>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | chr14 | 45173303 | |||||||
chr14:45173469 | C | G | 12 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(9): Show |
12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2316+259C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | chr14 | 45173469 | |||||||
chr14:45173535 | T | C | 1 | a0004c0004t0001g0027 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2316+325T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | chr14 | 45173535 | |||||||
chr14:45173805 | C | T | 2 | a0010c0014t0001g0137 a0010c0014t0001g0138 |
2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2316+595C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | chr14 | 45173805 | |||||||
chr14:45173806 | G | A | 7 | a0002c0003t0002g0139 a0002c0003t0002g0150 a0002c0003t0002g0153 others(4): Show |
7 | HG01109.hp1 HG02055.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.2316+596G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | chr14 | 45173806 | |||||||
chr14:45173827 | G | C | 1 | a0002c0003t0002g0220 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2316+617G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | chr14 | 45173827 | |||||||
chr14:45173852 | T | G | 1 | a0006c0010t0001g0135 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2316+642T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | chr14 | 45173852 | |||||||
chr14:45174057 | C | G | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2316+847C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | chr14 | 45174057 | |||||||
chr14:45174095 | A | G | 1 | a0001c0001t0001g0052 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2316+885A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | chr14 | 45174095 | |||||||
chr14:45174158 | AG | A | 38 | a0003c0002t0001g0003 a0003c0002t0001g0169 a0003c0002t0001g0170 others(35): Show |
41 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2317-911delG | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr14 | 45174158 | ||||||
chr14:45174168 | C | T | 2 | a0006c0010t0001g0134 a0006c0010t0001g0135 |
2 | HG02895.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2317-903C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | chr14 | 45174168 | |||||||
chr14:45174385 | T | TA | 32 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0071 others(29): Show |
32 | HG01346.hp2 HG01358.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.2317-672dupA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr14 | 45174385 | ||||||
chr14:45174400 | C | A | 1 | a0001c0001t0001g0073 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2317-671C>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | chr14 | 45174400 | |||||||
chr14:45174429 | T | C | 6 | a0005c0005t0001g0151 a0005c0005t0001g0152 a0005c0005t0001g0156 others(3): Show |
6 | HG02109.hp2 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2317-642T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | chr14 | 45174429 | |||||||
chr14:45174635 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2317-436T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | chr14 | 45174635 | |||||||
chr14:45174665 | T | TGAAAGAG others(242): Show |
1 | a0001c0001t0001g0113 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2317-392_2317-391i others(251): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr14 | 45174665 | ||||||
chr14:45174822 | A | G | 1 | a0002c0008t0004g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2317-249A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | chr14 | 45174822 | |||||||
chr14:45174926 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2317-145G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | chr14 | 45174926 | |||||||
chr14:45174977 | A | G | 1 | a0003c0002t0001g0177 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2317-94A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | chr14 | 45174977 | |||||||
chr14:45176983 | T | G | 1 | a0002c0031t0006g0159 | 1 | HG02818.hp1 | splice_region_variant&intron_variant | LOW | c.4222+7T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45176983 | |||||||
chr14:45177059 | T | A | 1 | a0001c0001t0001g0037 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4222+83T>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45177059 | |||||||
chr14:45177140 | TAGATTTA others(73): Show |
T | 6 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(3): Show |
6 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.4222+167_4222+246d others(82): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr14 | 45177140 | ||||||
chr14:45177310 | C | T | 6 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(3): Show |
6 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.4222+334C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45177310 | |||||||
chr14:45177456 | G | C | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.4222+480G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45177456 | |||||||
chr14:45177856 | A | G | 5 | a0006c0010t0001g0134 a0006c0010t0001g0135 a0006c0010t0001g0198 others(2): Show |
5 | HG01106.hp1 HG01516.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.4222+880A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45177856 | |||||||
chr14:45177920 | C | T | 3 | a0002c0003t0001g0014 a0002c0003t0001g0167 a0022c0030t0001g0014 |
3 | HG02257.hp2 HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.4222+944C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45177920 | |||||||
chr14:45177941 | G | A | 40 | a0003c0002t0001g0003 a0003c0002t0001g0169 a0003c0002t0001g0170 others(37): Show |
43 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.4222+965G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45177941 | |||||||
chr14:45178108 | C | A | 12 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(9): Show |
12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.4222+1132C>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45178108 | |||||||
chr14:45178150 | A | G | 12 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(9): Show |
12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.4222+1174A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45178150 | |||||||
chr14:45178245 | A | G | 1 | a0008c0025t0002g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4222+1269A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45178245 | |||||||
chr14:45178368 | G | T | 1 | a0023c0023t0001g0084 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.4222+1392G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45178368 | |||||||
chr14:45178603 | T | C | 2 | a0010c0014t0001g0137 a0010c0014t0001g0138 |
2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.4222+1627T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45178603 | |||||||
chr14:45178908 | A | G | 1 | a0001c0001t0001g0083 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.4222+1932A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45178908 | |||||||
chr14:45178928 | A | G | 110 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(107): Show |
114 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.4222+1952A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45178928 | |||||||
chr14:45179068 | A | G | 12 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(9): Show |
12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.4222+2092A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45179068 | |||||||
chr14:45179375 | T | C | 1 | a0003c0002t0001g0172 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.4223-2055T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45179375 | |||||||
chr14:45179396 | C | T | 1 | a0002c0007t0003g0164 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4223-2034C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45179396 | |||||||
chr14:45179460 | C | G | 6 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(3): Show |
6 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.4223-1970C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45179460 | |||||||
chr14:45179484 | T | C | 6 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(3): Show |
6 | HG02257.hp1 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.4223-1946T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45179484 | |||||||
chr14:45179522 | A | G | 6 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(3): Show |
6 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.4223-1908A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45179522 | |||||||
chr14:45179541 | G | T | 1 | a0002c0008t0004g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4223-1889G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45179541 | |||||||
chr14:45179561 | CT | C | 156 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(153): Show |
166 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.4223-1849delT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr14 | 45179561 | ||||||
chr14:45179561 | CTT | C | 13 | a0001c0001t0001g0077 a0001c0001t0001g0130 a0002c0006t0002g0214 others(10): Show |
13 | HG02056.hp2 HG02109.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.4223-1850_4223-184 others(6): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr14 | 45179561 | ||||||
chr14:45179561 | CTTTTTTT others(4): Show |
C | 8 | a0002c0006t0002g0208 a0002c0006t0002g0215 a0002c0032t0001g0204 others(5): Show |
8 | HG01106.hp1 HG01516.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.4223-1859_4223-184 others(15): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr14 | 45179561 | ||||||
chr14:45179565 | T | C | 2 | a0001c0001t0001g0047 a0001c0001t0001g0076 |
2 | HG01256.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.4223-1865T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45179565 | |||||||
chr14:45179604 | C | G | 12 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(9): Show |
12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.4223-1826C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45179604 | |||||||
chr14:45179710 | T | A | 1 | a0001c0001t0001g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4223-1720T>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45179710 | |||||||
chr14:45179840 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4223-1590G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45179840 | |||||||
chr14:45179935 | T | C | 6 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(3): Show |
6 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.4223-1495T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45179935 | |||||||
chr14:45180141 | A | G | 12 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(9): Show |
12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.4223-1289A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45180141 | |||||||
chr14:45180149 | A | G | 6 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(3): Show |
6 | HG02257.hp1 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.4223-1281A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45180149 | |||||||
chr14:45180300 | GCA | G | 2 | a0011c0015t0001g0191 a0011c0015t0001g0192 |
2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4223-1129_4223-112 others(6): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45180300 | |||||||
chr14:45180432 | G | GT | 8 | a0001c0001t0001g0087 a0002c0032t0001g0204 a0006c0010t0001g0134 others(5): Show |
8 | HG01099.hp1 HG01106.hp1 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.4223-987dupT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr14 | 45180432 | ||||||
chr14:45180478 | G | C | 2 | a0005c0005t0001g0205 a0005c0005t0001g0206 |
2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.4223-952G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45180478 | |||||||
chr14:45180497 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.4223-933A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45180497 | |||||||
chr14:45180749 | A | G | 2 | a0011c0015t0001g0191 a0011c0015t0001g0192 |
2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4223-681A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45180749 | |||||||
chr14:45180774 | T | G | 4 | a0007c0009t0001g0016 a0007c0009t0001g0017 a0007c0009t0001g0018 others(1): Show |
4 | NA18939.hp2 NA18966.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.4223-656T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45180774 | |||||||
chr14:45180827 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4223-603C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45180827 | |||||||
chr14:45180861 | A | G | 2 | a0011c0015t0001g0191 a0011c0015t0001g0192 |
2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4223-569A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45180861 | |||||||
chr14:45180955 | A | G | 14 | a0002c0003t0002g0216 a0002c0006t0002g0207 a0002c0006t0002g0208 others(11): Show |
15 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.4223-475A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45180955 | |||||||
chr14:45181196 | A | T | 7 | a0002c0032t0001g0204 a0006c0010t0001g0134 a0006c0010t0001g0135 others(4): Show |
7 | HG01106.hp1 HG01516.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.4223-234A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45181196 | |||||||
chr14:45181330 | C | T | 14 | a0002c0003t0002g0216 a0002c0006t0002g0207 a0002c0006t0002g0208 others(11): Show |
15 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.4223-100C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45181330 | |||||||
chr14:45181366 | G | C | 12 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(9): Show |
12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.4223-64G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45181366 | |||||||
chr14:45181601 | A | G | 2 | a0002c0006t0002g0211 a0002c0006t0002g0214 |
2 | HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4318-36A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 15/22 | chr14 | 45181601 | |||||||
chr14:45181610 | G | A | 101 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(98): Show |
105 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.4318-27G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 15/22 | chr14 | 45181610 | |||||||
chr14:45182065 | A | G | 3 | a0003c0002t0001g0181 a0003c0002t0001g0189 a0003c0002t0001g0194 |
3 | NA18982.hp2 NA19011.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.4386+360A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 16/22 | chr14 | 45182065 | |||||||
chr14:45182224 | A | G | 2 | a0010c0014t0001g0137 a0010c0014t0001g0138 |
2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.4386+519A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 16/22 | chr14 | 45182224 | |||||||
chr14:45182256 | A | AT | 5 | a0006c0010t0001g0134 a0006c0010t0001g0135 a0006c0010t0001g0198 others(2): Show |
5 | HG01106.hp1 HG01516.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.4386+552dupT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr14 | 45182256 | ||||||
chr14:45182433 | G | A | 5 | a0006c0010t0001g0134 a0006c0010t0001g0135 a0006c0010t0001g0198 others(2): Show |
5 | HG01106.hp1 HG01516.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.4386+728G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 16/22 | chr14 | 45182433 | |||||||
chr14:45182478 | G | A | 178 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(175): Show |
188 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.4386+773G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 16/22 | chr14 | 45182478 | |||||||
chr14:45182535 | T | G | 1 | a0002c0032t0001g0204 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4386+830T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 16/22 | chr14 | 45182535 | |||||||
chr14:45182629 | C | T | 1 | a0002c0032t0001g0204 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4386+924C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 16/22 | chr14 | 45182629 | |||||||
chr14:45182762 | G | A | 109 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(106): Show |
113 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.4387-1012G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 16/22 | chr14 | 45182762 | |||||||
chr14:45182783 | TTGTA | T | 6 | a0007c0009t0001g0016 a0007c0009t0001g0017 a0007c0009t0001g0018 others(3): Show |
6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.4387-987_4387-984d others(6): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr14 | 45182783 | ||||||
chr14:45182853 | C | T | 1 | a0002c0031t0006g0159 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4387-921C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 16/22 | chr14 | 45182853 | |||||||
chr14:45182885 | A | G | 1 | a0002c0031t0006g0159 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4387-889A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 16/22 | chr14 | 45182885 | |||||||
chr14:45183106 | T | C | 2 | a0010c0014t0001g0137 a0010c0014t0001g0138 |
2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.4387-668T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 16/22 | chr14 | 45183106 | |||||||
chr14:45183116 | G | C | 2 | a0010c0014t0001g0137 a0010c0014t0001g0138 |
2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.4387-658G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 16/22 | chr14 | 45183116 | |||||||
chr14:45183735 | A | T | 12 | a0003c0002t0001g0169 a0003c0002t0001g0170 a0003c0002t0001g0174 others(9): Show |
12 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.4387-39A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 16/22 | chr14 | 45183735 | |||||||
chr14:45183770 | A | T | 1 | a0004c0004t0001g0123 | 1 | HG01167.hp1 | splice_region_variant&intron_variant | LOW | c.4387-4A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 16/22 | chr14 | 45183770 | |||||||
chr14:45184529 | G | A | 6 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(3): Show |
6 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.4515+627G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 17/22 | chr14 | 45184529 | |||||||
chr14:45184660 | C | CA | 8 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0039 others(5): Show |
8 | HG01192.hp2 HG02056.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.4516-538dupA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr14 | 45184660 | ||||||
chr14:45184660 | C | CAAAAAAA | 10 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(7): Show |
10 | HG02257.hp1 HG02723.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.4516-544_4516-538d others(9): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr14 | 45184660 | ||||||
chr14:45184674 | A | AC | 27 | a0002c0003t0002g0150 a0002c0003t0002g0154 a0002c0003t0002g0155 others(24): Show |
28 | HG01884.hp2 HG02258.hp2 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.4516-543_4516-542i others(3): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 17/22 | chr14 | 45184674 | |||||||
chr14:45184674 | A | C | 52 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(49): Show |
55 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.4516-543A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 17/22 | chr14 | 45184674 | |||||||
chr14:45184776 | C | CT | 23 | a0001c0001t0001g0021 a0001c0001t0001g0132 a0002c0003t0002g0216 others(20): Show |
24 | HG02056.hp1 HG02132.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.4516-427dupT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr14 | 45184776 | ||||||
chr14:45184866 | C | T | 8 | a0005c0005t0001g0151 a0005c0005t0001g0152 a0005c0005t0001g0156 others(5): Show |
8 | HG02109.hp2 HG02559.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.4516-351C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 17/22 | chr14 | 45184866 | |||||||
chr14:45184894 | T | C | 100 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(97): Show |
104 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.4516-323T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 17/22 | chr14 | 45184894 | |||||||
chr14:45184940 | A | AT | 5 | a0001c0001t0001g0036 a0001c0001t0001g0068 a0001c0001t0001g0115 others(2): Show |
5 | HG02145.hp1 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.4516-262dupT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr14 | 45184940 | ||||||
chr14:45184940 | AT | A | 51 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(48): Show |
54 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.4516-262delT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr14 | 45184940 | ||||||
chr14:45184982 | A | G | 1 | a0002c0008t0004g0168 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4516-235A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 17/22 | chr14 | 45184982 | |||||||
chr14:45185054 | T | C | 7 | a0002c0032t0001g0204 a0006c0010t0001g0134 a0006c0010t0001g0135 others(4): Show |
7 | HG01106.hp1 HG01516.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.4516-163T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 17/22 | chr14 | 45185054 | |||||||
chr14:45185207 | TCTTA | T | 110 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(107): Show |
114 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(111): Show |
splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.4516-5_4516-2delCT others(2): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr14 | 45185207 | ||||||
chr14:45185703 | A | G | 6 | a0007c0009t0001g0016 a0007c0009t0001g0017 a0007c0009t0001g0018 others(3): Show |
6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.4672+330A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45185703 | |||||||
chr14:45185705 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4672+332A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45185705 | |||||||
chr14:45185775 | T | A | 1 | a0003c0002t0001g0184 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.4672+402T>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45185775 | |||||||
chr14:45185848 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4672+475T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45185848 | |||||||
chr14:45186164 | G | A | 1 | a0003c0002t0001g0169 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.4672+791G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45186164 | |||||||
chr14:45186190 | T | A | 3 | a0002c0003t0002g0218 a0002c0003t0002g0219 a0002c0003t0002g0220 |
3 | HG02717.hp2 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4672+817T>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45186190 | |||||||
chr14:45186343 | A | G | 41 | a0003c0002t0001g0003 a0003c0002t0001g0169 a0003c0002t0001g0170 others(38): Show |
44 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.4672+970A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45186343 | |||||||
chr14:45186689 | A | G | 1 | a0014c0018t0001g0029 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4673-1092A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45186689 | |||||||
chr14:45186866 | A | C | 1 | a0024c0024t0001g0141 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4673-915A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45186866 | |||||||
chr14:45187096 | A | G | 12 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(9): Show |
12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.4673-685A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45187096 | |||||||
chr14:45187209 | CT | C | 28 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0052 others(25): Show |
28 | HG00438.hp2 HG01106.hp1 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.4673-559delT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr14 | 45187209 | ||||||
chr14:45187243 | T | C | 27 | a0002c0003t0002g0139 a0002c0003t0002g0150 a0002c0003t0002g0153 others(24): Show |
28 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.4673-538T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45187243 | |||||||
chr14:45187314 | T | TA | 39 | a0003c0002t0001g0003 a0003c0002t0001g0169 a0003c0002t0001g0170 others(36): Show |
42 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.4673-458dupA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr14 | 45187314 | ||||||
chr14:45187341 | T | A | 1 | a0002c0003t0001g0165 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.4673-440T>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45187341 | |||||||
chr14:45187351 | C | T | 12 | a0003c0002t0001g0003 a0003c0002t0001g0171 a0003c0002t0001g0175 others(9): Show |
15 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(12): Show |
intron_variant | MODIFIER | c.4673-430C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45187351 | |||||||
chr14:45187422 | C | T | 1 | a0002c0031t0006g0159 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4673-359C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45187422 | |||||||
chr14:45187441 | T | C | 1 | a0001c0001t0001g0037 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4673-340T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45187441 | |||||||
chr14:45187447 | T | A | 1 | a0001c0001t0001g0062 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.4673-334T>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45187447 | |||||||
chr14:45187547 | G | A | 12 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(9): Show |
12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.4673-234G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45187547 | |||||||
chr14:45187596 | C | G | 5 | a0006c0010t0001g0134 a0006c0010t0001g0135 a0006c0010t0001g0198 others(2): Show |
5 | HG01106.hp1 HG01516.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.4673-185C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45187596 | |||||||
chr14:45187704 | TAGATTGA others(7): Show |
T | 6 | a0007c0009t0001g0016 a0007c0009t0001g0017 a0007c0009t0001g0018 others(3): Show |
6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.4673-76_4673-63del others(14): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45187704 | |||||||
chr14:45187719 | T | C | 6 | a0007c0009t0001g0016 a0007c0009t0001g0017 a0007c0009t0001g0018 others(3): Show |
6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.4673-62T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45187719 | |||||||
chr14:45188104 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4779+217C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 19/22 | chr14 | 45188104 | |||||||
chr14:45188298 | C | G | 6 | a0007c0009t0001g0016 a0007c0009t0001g0017 a0007c0009t0001g0018 others(3): Show |
6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.4779+411C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 19/22 | chr14 | 45188298 | |||||||
chr14:45188386 | A | AT | 12 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(9): Show |
12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.4780-408dupT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr14 | 45188386 | ||||||
chr14:45188754 | GTTAA | G | 6 | a0007c0009t0001g0016 a0007c0009t0001g0017 a0007c0009t0001g0018 others(3): Show |
6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.4780-45_4780-42del others(4): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr14 | 45188754 | ||||||
chr14:45189385 | A | T | 3 | a0006c0010t0001g0198 a0006c0010t0001g0199 a0006c0010t0001g0200 |
3 | HG01106.hp1 HG01516.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.5340+23A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45189385 | |||||||
chr14:45189511 | A | T | 5 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(2): Show |
5 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.5340+149A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45189511 | |||||||
chr14:45189588 | A | G | 28 | a0002c0003t0002g0139 a0002c0003t0002g0150 a0002c0003t0002g0153 others(25): Show |
29 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.5340+226A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45189588 | |||||||
chr14:45189756 | G | A | 1 | a0002c0003t0002g0218 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5340+394G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45189756 | |||||||
chr14:45189837 | G | A | 38 | a0003c0002t0001g0003 a0003c0002t0001g0169 a0003c0002t0001g0170 others(35): Show |
41 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.5340+475G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45189837 | |||||||
chr14:45190044 | G | A | 6 | a0002c0032t0001g0204 a0006c0010t0001g0134 a0006c0010t0001g0135 others(3): Show |
6 | HG01106.hp1 HG01516.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.5340+682G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45190044 | |||||||
chr14:45190194 | T | C | 12 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(9): Show |
12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.5340+832T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45190194 | |||||||
chr14:45190268 | A | G | 6 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(3): Show |
6 | HG02257.hp1 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.5340+906A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45190268 | |||||||
chr14:45190408 | C | G | 8 | a0002c0006t0002g0208 a0002c0006t0002g0215 a0002c0032t0001g0204 others(5): Show |
8 | HG01106.hp1 HG01516.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.5340+1046C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45190408 | |||||||
chr14:45190637 | T | C | 1 | a0002c0031t0006g0159 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5340+1275T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45190637 | |||||||
chr14:45191396 | A | G | 99 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(96): Show |
103 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.5340+2034A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45191396 | |||||||
chr14:45191557 | G | C | 107 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(104): Show |
111 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.5340+2195G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45191557 | |||||||
chr14:45191582 | AATAG | A | 6 | a0002c0008t0004g0140 a0002c0008t0004g0147 a0002c0008t0004g0148 others(3): Show |
6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.5340+2224_5340+222 others(8): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr14 | 45191582 | ||||||
chr14:45191636 | G | T | 12 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(9): Show |
12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.5340+2274G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45191636 | |||||||
chr14:45191832 | A | G | 3 | a0001c0001t0001g0021 a0001c0001t0001g0052 a0001c0001t0001g0090 |
3 | HG02056.hp1 HG02129.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.5340+2470A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45191832 | |||||||
chr14:45191873 | T | C | 12 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(9): Show |
12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.5340+2511T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45191873 | |||||||
chr14:45191880 | A | G | 6 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(3): Show |
6 | HG02257.hp1 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.5340+2518A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45191880 | |||||||
chr14:45191954 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.5340+2592G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45191954 | |||||||
chr14:45191955 | C | A | 1 | a0005c0005t0001g0205 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.5340+2593C>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45191955 | |||||||
chr14:45192173 | C | T | 1 | a0005c0005t0001g0217 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.5340+2811C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45192173 | |||||||
chr14:45192215 | T | C | 1 | a0023c0023t0001g0084 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5340+2853T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45192215 | |||||||
chr14:45192229 | A | C | 12 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(9): Show |
12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.5340+2867A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45192229 | |||||||
chr14:45192527 | C | T | 8 | a0002c0006t0002g0208 a0002c0006t0002g0215 a0002c0032t0001g0204 others(5): Show |
8 | HG01106.hp1 HG01516.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.5340+3165C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45192527 | |||||||
chr14:45192585 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.5340+3223G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45192585 | |||||||
chr14:45192599 | C | T | 5 | a0001c0001t0001g0025 a0001c0001t0001g0038 a0001c0001t0001g0104 others(2): Show |
5 | HG02809.hp2 HG02922.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.5340+3237C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45192599 | |||||||
chr14:45192602 | C | A | 6 | a0002c0008t0004g0140 a0002c0008t0004g0147 a0002c0008t0004g0148 others(3): Show |
6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.5340+3240C>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45192602 | |||||||
chr14:45192609 | C | G | 2 | a0005c0005t0001g0205 a0005c0005t0001g0206 |
2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.5340+3247C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45192609 | |||||||
chr14:45192629 | C | G | 6 | a0002c0008t0004g0140 a0002c0008t0004g0147 a0002c0008t0004g0148 others(3): Show |
6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.5340+3267C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45192629 | |||||||
chr14:45192638 | A | G | 100 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(97): Show |
104 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.5340+3276A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45192638 | |||||||
chr14:45192980 | G | A | 6 | a0002c0003t0002g0139 a0002c0003t0002g0150 a0002c0003t0002g0153 others(3): Show |
6 | HG01109.hp1 HG02055.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.5341-3192G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45192980 | |||||||
chr14:45193065 | A | G | 1 | a0002c0008t0007g0161 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.5341-3107A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45193065 | |||||||
chr14:45193122 | T | C | 30 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(27): Show |
34 | HG00323.hp2 HG00639.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.5341-3050T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45193122 | |||||||
chr14:45193311 | C | T | 39 | a0003c0002t0001g0003 a0003c0002t0001g0169 a0003c0002t0001g0170 others(36): Show |
42 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.5341-2861C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45193311 | |||||||
chr14:45193374 | T | C | 108 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(105): Show |
112 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.5341-2798T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45193374 | |||||||
chr14:45193384 | G | C | 1 | a0001c0001t0001g0075 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.5341-2788G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45193384 | |||||||
chr14:45193386 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.5341-2786T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45193386 | |||||||
chr14:45193388 | C | G | 1 | a0001c0001t0001g0069 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.5341-2784C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45193388 | |||||||
chr14:45193390 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.5341-2782T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45193390 | |||||||
chr14:45193436 | A | G | 3 | a0001c0001t0001g0054 a0001c0001t0001g0075 a0001c0001t0001g0078 |
3 | HG01255.hp2 HG01516.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.5341-2736A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45193436 | |||||||
chr14:45193561 | G | A | 1 | a0008c0025t0002g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5341-2611G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45193561 | |||||||
chr14:45193762 | GT | G | 6 | a0002c0008t0004g0140 a0002c0008t0004g0147 a0002c0008t0004g0148 others(3): Show |
6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.5341-2399delT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr14 | 45193762 | ||||||
chr14:45193906 | G | A | 6 | a0002c0008t0004g0140 a0002c0008t0004g0147 a0002c0008t0004g0148 others(3): Show |
6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.5341-2266G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45193906 | |||||||
chr14:45193933 | A | G | 2 | a0010c0014t0001g0137 a0010c0014t0001g0138 |
2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.5341-2239A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45193933 | |||||||
chr14:45194263 | T | C | 9 | a0002c0003t0002g0139 a0002c0003t0002g0150 a0002c0003t0002g0153 others(6): Show |
9 | HG01109.hp1 HG02055.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.5341-1909T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45194263 | |||||||
chr14:45194298 | G | A | 1 | a0003c0002t0001g0190 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.5341-1874G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45194298 | |||||||
chr14:45194316 | C | CA | 8 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0002c0003t0001g0014 others(5): Show |
8 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.5341-1847dupA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr14 | 45194316 | ||||||
chr14:45194625 | G | A | 112 | a0001c0001t0001g0025 a0001c0001t0001g0038 a0001c0001t0001g0104 others(109): Show |
116 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.5341-1547G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45194625 | |||||||
chr14:45194630 | A | G | 1 | a0018c0022t0001g0022 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.5341-1542A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45194630 | |||||||
chr14:45194631 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.5341-1541C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45194631 | |||||||
chr14:45194718 | G | A | 1 | a0014c0018t0001g0029 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.5341-1454G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45194718 | |||||||
chr14:45194812 | C | CT | 9 | a0001c0001t0001g0028 a0001c0001t0001g0103 a0002c0006t0002g0212 others(6): Show |
9 | HG00438.hp2 HG01167.hp2 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.5341-1343dupT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr14 | 45194812 | ||||||
chr14:45194812 | CT | C | 6 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(3): Show |
6 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.5341-1343delT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr14 | 45194812 | ||||||
chr14:45194839 | C | T | 6 | a0002c0008t0004g0140 a0002c0008t0004g0147 a0002c0008t0004g0148 others(3): Show |
6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.5341-1333C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45194839 | |||||||
chr14:45194842 | C | T | 5 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(2): Show |
5 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.5341-1330C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45194842 | |||||||
chr14:45194847 | C | T | 40 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(37): Show |
41 | HG01106.hp1 HG01109.hp1 HG01358.hp1 others(38): Show |
intron_variant | MODIFIER | c.5341-1325C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45194847 | |||||||
chr14:45194855 | A | G | 1 | a0002c0031t0006g0159 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5341-1317A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45194855 | |||||||
chr14:45194894 | T | C | 5 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(2): Show |
5 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.5341-1278T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45194894 | |||||||
chr14:45194896 | C | T | 4 | a0002c0008t0004g0147 a0002c0008t0004g0148 a0002c0008t0004g0149 others(1): Show |
4 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.5341-1276C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45194896 | |||||||
chr14:45194946 | A | G | 1 | a0005c0005t0001g0152 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5341-1226A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45194946 | |||||||
chr14:45195060 | T | C | 6 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(3): Show |
6 | HG02257.hp1 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.5341-1112T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45195060 | |||||||
chr14:45195128 | G | A | 6 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(3): Show |
6 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.5341-1044G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45195128 | |||||||
chr14:45195325 | A | G | 2 | a0003c0002t0001g0171 a0003c0002t0001g0201 |
2 | NA18940.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.5341-847A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45195325 | |||||||
chr14:45195431 | T | G | 1 | a0002c0006t0002g0212 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.5341-741T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45195431 | |||||||
chr14:45195518 | C | G | 108 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(105): Show |
112 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.5341-654C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45195518 | |||||||
chr14:45195598 | T | C | 1 | a0008c0025t0002g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5341-574T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45195598 | |||||||
chr14:45195626 | A | G | 1 | a0008c0025t0002g0133 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5341-546A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45195626 | |||||||
chr14:45195711 | T | C | 3 | a0001c0001t0001g0034 a0001c0001t0001g0076 a0001c0001t0001g0085 |
3 | HG01099.hp2 HG01256.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.5341-461T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45195711 | |||||||
chr14:45195861 | G | A | 1 | a0019c0029t0001g0221 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.5341-311G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45195861 | |||||||
chr14:45195953 | C | T | 1 | a0005c0005t0001g0158 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5341-219C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45195953 | |||||||
chr14:45196109 | G | A | 6 | a0005c0005t0001g0151 a0005c0005t0001g0152 a0005c0005t0001g0156 others(3): Show |
6 | HG02109.hp2 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.5341-63G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45196109 | |||||||
chr14:45196153 | G | A | 1 | a0002c0008t0004g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.5341-19G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45196153 | |||||||
chr14:45196639 | T | C | 6 | a0007c0009t0001g0016 a0007c0009t0001g0017 a0007c0009t0001g0018 others(3): Show |
6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.5716+92T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/22 | chr14 | 45196639 | |||||||
chr14:45197226 | A | G | 1 | a0016c0017t0001g0050 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.5716+679A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/22 | chr14 | 45197226 | |||||||
chr14:45197294 | G | T | 107 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(104): Show |
111 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.5716+747G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/22 | chr14 | 45197294 | |||||||
chr14:45197315 | C | T | 6 | a0002c0007t0003g0143 a0002c0007t0003g0144 a0002c0007t0003g0145 others(3): Show |
6 | HG02257.hp1 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.5716+768C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/22 | chr14 | 45197315 | |||||||
chr14:45197335 | A | G | 1 | a0010c0014t0001g0138 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5716+788A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/22 | chr14 | 45197335 | |||||||
chr14:45197396 | C | T | 1 | a0010c0014t0001g0138 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5716+849C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/22 | chr14 | 45197396 | |||||||
chr14:45197418 | C | T | 1 | a0002c0003t0002g0155 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.5716+871C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/22 | chr14 | 45197418 | |||||||
chr14:45197470 | G | GT | 6 | a0005c0005t0001g0151 a0005c0005t0001g0152 a0005c0005t0001g0156 others(3): Show |
6 | HG02109.hp2 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.5716+935dupT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr14 | 45197470 | ||||||
chr14:45197470 | GT | G | 87 | a0002c0003t0002g0139 a0002c0003t0002g0150 a0002c0003t0002g0153 others(84): Show |
91 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.5716+935delT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr14 | 45197470 | ||||||
chr14:45197767 | CT | C | 92 | a0002c0003t0002g0139 a0002c0003t0002g0150 a0002c0003t0002g0153 others(89): Show |
96 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.5717-863delT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr14 | 45197767 | ||||||
chr14:45197767 | CTT | C | 6 | a0002c0003t0001g0014 a0002c0003t0001g0165 a0002c0003t0001g0166 others(3): Show |
6 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.5717-864_5717-863d others(4): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr14 | 45197767 | ||||||
chr14:45197785 | AT | A | 1 | a0001c0001t0001g0008 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.5717-858delT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/22 | chr14 | 45197785 | |||||||
chr14:45197854 | C | T | 6 | a0002c0008t0004g0140 a0002c0008t0004g0147 a0002c0008t0004g0148 others(3): Show |
6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.5717-790C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/22 | chr14 | 45197854 | |||||||
chr14:45197898 | A | G | 6 | a0002c0008t0004g0140 a0002c0008t0004g0147 a0002c0008t0004g0148 others(3): Show |
6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.5717-746A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/22 | chr14 | 45197898 | |||||||
chr14:45198029 | AG | A | 38 | a0003c0002t0001g0003 a0003c0002t0001g0169 a0003c0002t0001g0170 others(35): Show |
41 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.5717-614delG | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/22 | chr14 | 45198029 | |||||||
chr14:45198545 | A | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0060 |
2 | NA18960.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.5717-99A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/22 | chr14 | 45198545 | |||||||
chr14:45199024 | G | A | 2 | a0010c0014t0001g0137 a0010c0014t0001g0138 |
2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.6008+89G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 22/22 | chr14 | 45199024 | |||||||
chr14:45199140 | G | C | 1 | a0002c0003t0002g0218 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6008+205G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 22/22 | chr14 | 45199140 | |||||||
chr14:45199172 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.6008+237C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 22/22 | chr14 | 45199172 | |||||||
chr14:45199385 | C | T | 8 | a0005c0005t0001g0151 a0005c0005t0001g0152 a0005c0005t0001g0156 others(5): Show |
8 | HG02109.hp2 HG02559.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.6008+450C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 22/22 | chr14 | 45199385 | |||||||
chr14:45199455 | A | C | 28 | a0002c0003t0002g0139 a0002c0003t0002g0150 a0002c0003t0002g0153 others(25): Show |
29 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.6009-415A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 22/22 | chr14 | 45199455 | |||||||
chr14:45199618 | A | C | 2 | a0002c0006t0002g0211 a0002c0006t0002g0214 |
2 | HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.6009-252A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 22/22 | chr14 | 45199618 |