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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr16
89845194
A
G
intron_variant
MODIFIER
FANCA
c.1826+15T>C
chr16
89845178
T
TAC
intron_variant
MODIFIER
FANCA
c.1826+30_1826+31insGT
chr16
89845110
A
T
intron_variant
MODIFIER
FANCA
c.1826+99T>A
chr16
89842029
C
G
intron_variant
MODIFIER
FANCA
c.1900+121G>C
chr16
89839976
T
C
intron_variant
MODIFIER
FANCA
c.1901-184A>G
chr16
89839854
T
C
intron_variant
MODIFIER
FANCA
c.1901-62A>G
chr16
89839766
G
C
missense_variant
MODERATE
FANCA
c.1927C>G
chr16
89839637
C
A
intron_variant
MODIFIER
FANCA
c.2014+42G>T
chr16
89838078
A
G
splice_region_variant&intron_variant
LOW
FANCA
c.2151+8T>C
chr16
89837951
T
C
intron_variant
MODIFIER
FANCA
c.2151+135A>G
chr16
89836872
T
C
intron_variant
MODIFIER
FANCA
c.2222+100A>G
chr16
89836865
A
G
intron_variant
MODIFIER
FANCA
c.2222+107T>C
chr16
89836781
G
A
intron_variant
MODIFIER
FANCA
c.2223-114C>T
chr16
89836507
T
C
intron_variant
MODIFIER
FANCA
c.2316+67A>G
chr16
89836323
C
T
missense_variant
MODERATE
FANCA
c.2426G>A
chr16
89833774
C
G
intron_variant
MODIFIER
FANCA
c.2505-129G>C
chr16
89831558
C
T
intron_variant
MODIFIER
FANCA
c.2602-84G>A
chr16
89831520
A
T
intron_variant
MODIFIER
FANCA
c.2602-46T>A
chr16
89831243
C
A
intron_variant
MODIFIER
FANCA
c.2778+55G>T
chr16
89829201
G
C
intron_variant
MODIFIER
FANCA
c.2779-771C>G