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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr16
354287
C
T
intron_variant
MODIFIER
AXIN1
c.1254+17G>A
chr16
343905
T
C
intron_variant
MODIFIER
AXIN1
c.1956-187A>G
chr16
341079
G
A
intron_variant
MODIFIER
AXIN1
c.2294+111C>T
chr16
339672
T
C
intron_variant
MODIFIER
AXIN1
c.2295-65A>G
chr16
338332
A
AC
intron_variant
MODIFIER
AXIN1
c.2463-85_2463-84insG
chr16
336916
C
T
missense_variant
MODERATE
PDIA2
c.1504C>T
chr16
336660
G
A
synonymous_variant
LOW
PDIA2
c.1347G>A
chr16
334732
C
T
synonymous_variant
LOW
PDIA2
c.480C>T
chr16
334580
G
C
synonymous_variant
LOW
PDIA2
c.393G>C
chr16
333138
T
C
5_prime_UTR_variant
MODIFIER
PDIA2
c.-32T>C
chr15
96880510
ATTC
A
intron_variant
MODIFIER
NR2F2
c.971-66_971-64delTTC
chr15
91030640
GTGC
G
intron_variant
MODIFIER
IQGAP1
c.4161-86_4161-84delTGC
chr15
91026477
T
C
intron_variant
MODIFIER
IQGAP1
c.3556-116T>C
chr15
91026459
G
A
intron_variant
MODIFIER
IQGAP1
c.3556-134G>A
chr15
91025891
C
CT
intron_variant
MODIFIER
IQGAP1
c.3555+378_3555+379insT
chr15
91025830
G
A
intron_variant
MODIFIER
IQGAP1
c.3555+317G>A
chr15
91017718
C
T
splice_region_variant&synonymous_variant
LOW
IQGAP1
c.2577C>T
chr15
91017651
A
G
intron_variant
MODIFIER
IQGAP1
c.2576-66A>G
chr15
91017274
T
TTTC
intron_variant
MODIFIER
IQGAP1
c.2506-22_2506-21insTTC
chr15
91017232
G
A
intron_variant
MODIFIER
IQGAP1
c.2505+33G>A