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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr7
55266417
T
C
synonymous_variant
LOW
EGFR
c.2709T>C
chr7
55249063
G
A
synonymous_variant
LOW
EGFR
c.2361G>A
chr7
55242609
A
G
intron_variant
MODIFIER
EGFR
c.2283+96A>G
chr7
55240461
G
C
intron_variant
MODIFIER
EGFR
c.1920-215G>C
chr7
55238874
T
A
synonymous_variant
LOW
EGFR
c.1887T>A
chr7
55238268
G
A
3_prime_UTR_variant
MODIFIER
EGFR
c.*31G>A
chr7
55229255
G
A
missense_variant
MODERATE
EGFR
c.1562G>A
chr7
55228053
A
T
intron_variant
MODIFIER
EGFR
c.1498+22A>T
chr7
55221655
G
A
intron_variant
MODIFIER
EGFR
c.748-49G>A
chr7
42187734
G
GCACA
intron_variant
MODIFIER
GLI3
c.367+90_367+91insTGTG
chr7
42088470
A
C
intron_variant
MODIFIER
GLI3
c.474-175T>G
chr7
42088222
T
C
missense_variant
MODERATE
GLI3
c.547A>G
chr7
42087966
A
G
intron_variant
MODIFIER
GLI3
c.679+124T>C
chr7
42064852
C
G
intron_variant
MODIFIER
GLI3
c.1356+11G>C
chr7
42005678
G
A
missense_variant
MODERATE
GLI3
c.2993C>T
chr7
35293193
A
G
synonymous_variant
LOW
TBX20
c.39T>C
chr7
35289889
C
CA
intron_variant
MODIFIER
TBX20
c.128-75_128-74insT
chr7
27135314
C
T
missense_variant
MODERATE
HOXA1
c.218G>A
chr7
19157054
C
A
5_prime_UTR_variant
MODIFIER
TWIST1
c.-110G>T
chr7
5569327
G
A
intron_variant
MODIFIER
ACTB
c.-6-33C>T