Varaico: Literature-Extracted Genetic Variants

Gene:BCR
Variant:p.R368_P383delFs

BCR

1,586 papers

RefSeq Summary

A reciprocal translocation between chromosomes 22 and 9 produces the Philadelphia chromosome, which is often found in patients with chronic myelogenous leukemia. The chromosome 22 breakpoint for this ...

Pfam Domains

Bcr-Abl_Oligoaa 3–75UCSCBcr-Abl oncoprotein oligomerisation domain
RhoGEFaa 502–689UCSCRhoGEF domain
PH_19aa 697–823UCSCPH domain
C2aa 911–1018UCSCC2 domain
RhoGAPaa 1068–1216UCSCRhoGAP domain

Gene Aliases

HGNC Name

BCR activator of RhoGEF and GTPase

HGNC Previous Symbols

D22S11; BCR1

Papers
RefSeq ID
Protein change
DNA change
Selected Variant
1 paper
NM_004327.4
p.R368_P383delFs
c.1103_1148del46
Surrounding Variants
1 paper
NM_004327.4
p.S367_F378Fs
c.1100_1134delinsAFs
1 paper
NM_004327.4
p.S367_F378delFs
c.1101_1134del34
1 paper
NM_004327.4
p.S367R
c.1099A>C
1 paper
NM_004327.4
p.S367Fs
c.1099_1101delinsACFs
1 paper
NM_004327.4
p.S367_F378delFs
c.1100_1133del34
1 paper
NM_004327.4
p.S367_S382delFs
c.1100_1145del46
1 paper
NM_004327.4
p.S367_D379Fs
c.1100_1136delinsGGAGGTFs
1 paper
NM_004327.4
p.S367_F378delFs
c.1099_1132del34
1 paper
NM_004327.4
p.S367_D379delFs
c.1099_1135del37
2 papers
NM_004327.4
p.R368_D379delFs
c.1103_1136del34
1 paper
NM_004327.4
p.R368_D379Fs
c.1102_1137delinsGAFs
1 paper
NM_004327.4
p.R368_S380delFs
c.1103_1139del37
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."