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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr15
22993170
A
C
intron_variant
MODIFIER
CYFIP1
c.3042+15A>C
chr15
22962184
T
A
intron_variant
MODIFIER
CYFIP1
c.2083-71T>A
chr15
22960938
C
T
intron_variant
MODIFIER
CYFIP1
c.2082+49C>T
chr15
22960868
G
C
synonymous_variant
LOW
CYFIP1
c.2061G>C
chr15
22960700
A
G
intron_variant
MODIFIER
CYFIP1
c.1986-93A>G
chr15
22958151
C
T
intron_variant
MODIFIER
CYFIP1
c.1829-35C>T
chr15
22958104
A
G
intron_variant
MODIFIER
CYFIP1
c.1829-82A>G
chr15
22955307
AC
A
intron_variant
MODIFIER
CYFIP1
c.1674+28delC
chr15
22933967
A
G
intron_variant
MODIFIER
CYFIP1
c.795+91A>G
chr15
22926307
A
G
intron_variant
MODIFIER
CYFIP1
c.207+242A>G
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
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