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NM_002019.4(FLT1):c.2654_2655insA (p.Gly886fs) AND Carcinoma of colon

Germline classification:
not provided (1 submission)
Review status:
no classification provided
Somatic classification
of clinical impact:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Record status:
current
Accession:
RCV000149495.1

Allele description [Variation Report for NM_002019.4(FLT1):c.2654_2655insA (p.Gly886fs)]

NM_002019.4(FLT1):c.2654_2655insA (p.Gly886fs)

Gene:
FLT1:fms related receptor tyrosine kinase 1 [Gene - OMIM - HGNC]
Variant type:
Insertion
Cytogenetic location:
13q12.3
Genomic location:
Preferred name:
NM_002019.4(FLT1):c.2654_2655insA (p.Gly886fs)
HGVS:
  • NC_000013.11:g.28329667_28329668insT
  • NG_012003.1:g.170461_170462insA
  • NM_002019.4:c.2654_2655insAMANE SELECT
  • NP_002010.2:p.Gly886fs
  • LRG_425t1:c.2654_2655insA
  • LRG_425:g.170461_170462insA
  • LRG_425p1:p.Gly886fs
  • NC_000013.10:g.28903804_28903805insT
Protein change:
G886fs
Links:
dbSNP: rs555490448
NCBI 1000 Genomes Browser:
rs555490448
Molecular consequence:
  • NM_002019.4:c.2654_2655insA - frameshift variant - [Sequence Ontology: SO:0001589]

Condition(s)

Name:
Carcinoma of colon (CRC)
Synonyms:
Colonic carcinoma; Colon carcinoma
Identifiers:
MONDO: MONDO:0002032; MedGen: C0699790

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000196135Immunobiology Lab; University of Kashmir
no classification provided
untestedsomaticnot provided

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedsomaticnot providednot providednot providednot provided11not providednot provided

Details of each submission

From Immunobiology Lab; University of Kashmir, SCV000196135.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providednot providednot provided

Description

Converted during submission to not provided.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1somaticnot provided11not providednot providednot providednot providednot providednot provided

Last Updated: Apr 23, 2022