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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr17
38548371
TA
T
intron_variant
MODIFIER
TOP2A
c.4089-9delT
chr17
37822311
A
C
synonymous_variant
LOW
TCAP
c.453A>C
chr17
37821435
G
T
upstream_gene_variant
MODIFIER
TCAP
c.-15G>T
chr17
29705947
T
C
downstream_gene_variant
MODIFIER
NF1
c.*8903T>C
chr17
29679246
G
A
intron_variant
MODIFIER
NF1
c.7458-29G>A
chr17
29670190
C
G
intron_variant
MODIFIER
NF1
c.7189+37C>G
chr17
29663625
T
A
intron_variant
MODIFIER
NF1
c.6148-28T>A
chr17
29663624
T
A
intron_variant
MODIFIER
NF1
c.6148-29T>A
chr17
29654974
G
A
intron_variant
MODIFIER
NF1
c.5609+117G>A
chr17
29654876
T
A
intron_variant
MODIFIER
NF1
c.5609+19T>A
chr17
29653293
T
C
intron_variant
MODIFIER
NF1
c.5268+23T>C
chr17
29563085
T
TG
intron_variant
MODIFIER
NF1
c.3974+46_3974+47insG
chr17
29563076
T
TG
intron_variant
MODIFIER
NF1
c.3974+37_3974+38insG
chr17
29559932
C
A
intron_variant
MODIFIER
NF1
c.3496+33C>A
chr17
29558082
T
C
intron_variant
MODIFIER
NF1
c.3197+139T>C
chr17
29553485
G
A
synonymous_variant
LOW
NF1
c.2034G>A
chr17
29553336
G
GAC
intron_variant
MODIFIER
NF1
c.2002-117_2002-116insAC
chr17
29546175
T
C
intron_variant
MODIFIER
NF1
c.1641+39T>C
chr17
29541437
T
C
intron_variant
MODIFIER
NF1
c.1393-32T>C
chr17
29508775
G
A
synonymous_variant
LOW
NF1
c.702G>A