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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr15
22929906
A
G
intron_variant
MODIFIER
CYFIP1
c.569+11A>G
chr15
22929905
C
G
intron_variant
MODIFIER
CYFIP1
c.569+10C>G
chr15
22928537
G
C
intron_variant
MODIFIER
CYFIP1
c.387+27G>C
chr15
22926307
A
G
intron_variant
MODIFIER
CYFIP1
c.207+242A>G
chr15
22926229
G
A
intron_variant
MODIFIER
CYFIP1
c.207+164G>A
chr15
22925624
G
A
intron_variant
MODIFIER
CYFIP1
c.-6-153G>A
chr15
22925605
C
T
intron_variant
MODIFIER
CYFIP1
c.-6-172C>T
chr14
102568367
T
A
missense_variant
MODERATE
HSP90AA1
c.211A>T
chr14
102568296
G
A
synonymous_variant
LOW
HSP90AA1
c.282C>T
chr14
102552775
T
G
intron_variant
MODIFIER
HSP90AA1
c.367-60A>C
chr14
102552773
A
G
intron_variant
MODIFIER
HSP90AA1
c.367-58T>C
chr14
102551795
T
TTAA
intron_variant
MODIFIER
HSP90AA1
c.896-28_896-27insTTA
chr14
102550803
G
A
synonymous_variant
LOW
HSP90AA1
c.1446C>T
chr14
102550569
G
A
intron_variant
MODIFIER
HSP90AA1
c.1513+167C>T
chr14
102550069
TA
T
intron_variant
MODIFIER
HSP90AA1
c.1705-40delT
chr14
102549839
A
G
intron_variant
MODIFIER
HSP90AA1
c.1852+44T>C
chr14
102549262
A
G
intron_variant
MODIFIER
HSP90AA1
c.2121+109T>C
chr14
102548384
C
T
intron_variant
MODIFIER
HSP90AA1
c.2455+64G>A
chr14
102548224
T
C
intron_variant
MODIFIER
HSP90AA1
c.2456-66A>G
chr14
96949747
G
GT
intron_variant
MODIFIER
AK7
c.1974+191_1974+192insT