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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr7
73922613
T
C
intron_variant
MODIFIER
GTF2IRD1
c.123+80T>C
chr7
73922331
T
C
intron_variant
MODIFIER
GTF2IRD1
c.-6-74T>C
chr7
73814749
G
C
missense_variant
MODERATE
CLIP2
c.2930G>C
chr7
73803644
T
A
intron_variant
MODIFIER
CLIP2
c.2720+55T>A
chr7
73801019
A
G
intron_variant
MODIFIER
CLIP2
c.2563+85A>G
chr7
73753250
T
C
synonymous_variant
LOW
CLIP2
c.594T>C
chr7
73752699
C
T
intron_variant
MODIFIER
CLIP2
c.122-79C>T
chr7
73752647
G
C
intron_variant
MODIFIER
CLIP2
c.122-131G>C
chr7
73530046
A
G
intron_variant
MODIFIER
LIMK1
c.1411-86A>G
chr7
73479946
GA
G
intron_variant
MODIFIER
ELN
c.2180-77delA
chr7
73472050
C
T
intron_variant
MODIFIER
ELN
c.1501+24C>T
chr7
73470782
C
T
intron_variant
MODIFIER
ELN
c.1315+17C>T
chr7
73467650
CTGTG
CTGTGTG
intron_variant
MODIFIER
ELN
c.1096+15_1096+16insTG
chr7
73467650
CTGTG
C
intron_variant
MODIFIER
ELN
c.1096+12_1096+15delTGTG
chr7
73456850
G
A
intron_variant
MODIFIER
ELN
c.233-94G>A
chr7
73455384
G
A
intron_variant
MODIFIER
ELN
c.197-162G>A
chr7
73452140
G
A
intron_variant
MODIFIER
ELN
c.196+71G>A
chr7
73449846
G
A
intron_variant
MODIFIER
ELN
c.133+102G>A
chr7
55272826
G
A
intron_variant
MODIFIER
EGFR
c.3272-123G>A
chr7
55268916
C
T
synonymous_variant
LOW
EGFR
c.2982C>T