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|
OCUa
|
bpb
|
Lowc
|
Highd
|
Region
|
Gene
|
Mutationh
|
|---|
|
9
|
48,280,960
|
1/1
|
2/2
|
3ʹUTR
|
MC2R
|
3-bp deletioni
|
|
11
|
56,199,847
|
0/0e
|
1/1f
|
Frameshift
|
TTC23L
|
2-bp deletion
|
|
12
|
138,684,799
|
1/1
|
0/0
|
Frameshift
|
ENSOCUG00000031631
|
2-bp deletion
|
|
12
|
138,685,173
|
1/1
|
0/0
|
Frameshift
|
ENSOCUG00000031631
|
1-bp insertion
|
|
12
|
138,685,179
|
1/1
|
0/0
|
Frameshift
|
ENSOCUG00000031631
|
2-bp deletion
|
|
14
|
33,195,918
|
1/1
|
2/2g
|
3ʹUTR
|
ENSOCUG00000006264
|
25-bp deletioni
|
|
15
|
4,723,998
|
1/1
|
0/0
|
3ʹUTR
|
SLC18A1
|
4-bp deletion
|
|
19
|
40,686,575
|
0/0
|
1/1
|
5ʹUTR
|
FBXL20
|
90-bp insertion
|
|
19
|
43,006,505
|
0/0
|
1/1
|
Frameshift
|
GHDC
|
2-bp deletion
|
|
19
|
44,276,359
|
1/1
|
0/0
|
3ʹUTR
|
CD300LG
|
8-bp deletion
|
- aOryctolagus cuniculus (OCU) chromosome
- bFunctional mutation location in base pairs
- cGenotype of line with low VE of LS
- dGenotype of line with high VE of LS
- e0/0 indicates that the functional mutation is the homozygous for the reference allele
- f1/1 indicates that the functional mutation is homozygous for the alternative allele
- g2/2 indicates that the functional mutation is homozygous for a new allele not present in the reference genome
- hAll INDELs were marked according to the reference allele of OryCun v2.0.103
- iWith reference to the alternative allele of OryCun v2.0.103
