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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr16
89866160
A
G
intron_variant
MODIFIER
FANCA
c.793-114T>C
chr16
89866043
T
C
missense_variant
MODERATE
FANCA
c.796A>G
chr16
89862434
T
C
splice_region_variant&intron_variant
LOW
FANCA
c.894-8A>G
chr16
89859035
G
A
intron_variant
MODIFIER
FANCA
c.1007-80C>T
chr16
89859015
GT
G
intron_variant
MODIFIER
FANCA
c.1007-61delA
chr16
89859008
G
A
intron_variant
MODIFIER
FANCA
c.1007-53C>T
chr16
89858525
C
G
intron_variant
MODIFIER
FANCA
c.1084-49G>C
chr16
89858505
T
C
intron_variant
MODIFIER
FANCA
c.1084-29A>G
chr16
89858417
C
A
synonymous_variant
LOW
FANCA
c.1143G>T
chr16
89858024
A
G
intron_variant
MODIFIER
FANCA
c.1226-80T>C
chr16
89857964
T
C
intron_variant
MODIFIER
FANCA
c.1226-20A>G
chr16
89857935
G
A
missense_variant
MODERATE
FANCA
c.1235C>T
chr16
89857700
A
G
intron_variant
MODIFIER
FANCA
c.1359+111T>C
chr16
89857622
T
C
intron_variant
MODIFIER
FANCA
c.1359+189A>G
chr16
89851179
C
T
intron_variant
MODIFIER
FANCA
c.1470+83G>A
chr16
89851116
TGGGGAAGGGGAA
T
intron_variant
MODIFIER
FANCA
c.1470+134_1470+145delTTCCCCTTCCCC
chr16
89849583
C
T
intron_variant
MODIFIER
FANCA
c.1471-73G>A
chr16
89849480
C
T
missense_variant
MODERATE
FANCA
c.1501G>A
chr16
89846195
A
G
intron_variant
MODIFIER
FANCA
c.1715+82T>C
chr16
89845287
A
G
intron_variant
MODIFIER
FANCA
c.1777-29T>C