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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr3
111316886
C
CTTATG
intron_variant
MODIFIER
CD96
c.856-81_856-80insTTATG
chr3
111298104
C
G
intron_variant
MODIFIER
CD96
c.799+23C>G
chr3
111286375
G
C
missense_variant
MODERATE
CD96
c.424G>C
chr3
111261242
G
GCTGCTGAAATTGATCACCA
intron_variant
MODIFIER
CD96
c.61+86_61+87insCTGCTGAAATTGATCACCA
chr3
111260975
C
T
5_prime_UTR_variant
MODIFIER
CD96
c.-121C>T
chr3
69058783
C
T
splice_region_variant&intron_variant
LOW
EOGT
c.210+5G>A
chr3
69054341
T
C
synonymous_variant
LOW
EOGT
c.465A>G
chr3
69054266
A
AT
intron_variant
MODIFIER
EOGT
c.515+24_515+25insA
chr3
69054212
CA
C
intron_variant
MODIFIER
EOGT
c.515+78delT
chr3
69047141
G
A
intron_variant
MODIFIER
EOGT
c.831+21C>T
chr3
69038088
A
G
synonymous_variant
LOW
EOGT
c.912T>C
chr3
69036782
G
T
intron_variant
MODIFIER
EOGT
c.1084-118C>A
chr3
69036683
G
A
intron_variant
MODIFIER
EOGT
c.1084-19C>T
chr3
69036524
GA
G
intron_variant
MODIFIER
EOGT
c.1152+71delT
chr3
69025792
C
CGTGTGTGTGTGTGTGT
3_prime_UTR_variant
MODIFIER
EOGT
c.*961_*976dupACACACACACACACAC
chr3
58156176
G
A
intron_variant
MODIFIER
FLNB
c.7715-126G>A
chr3
58154327
C
T
synonymous_variant
LOW
FLNB
c.7452C>T
chr3
58145263
G
A
intron_variant
MODIFIER
FLNB
c.6982-18G>A
chr3
58121626
T
A
intron_variant
MODIFIER
FLNB
c.4765-80T>A
chr3
58118700
A
G
intron_variant
MODIFIER
FLNB
c.4607+42A>G