NM_014727.3(KMT2B):c.6628C>T (p.Pro2210Ser) AND not provided

Germline classification:: Likely benign (2 submissions)
Last evaluated:: Dec 15, 2023
Review status:: 2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts

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:: RCV002020939.20

Allele description [Variation Report for NM_014727.3(KMT2B):c.6628C>T (p.Pro2210Ser)]

NM_014727.3(KMT2B):c.6628C>T (p.Pro2210Ser)

Gene:

KMT2B:lysine methyltransferase 2B [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

19q13.12

Genomic location:

Preferred name:

NM_014727.3(KMT2B):c.6628C>T (p.Pro2210Ser)

HGVS:

NC_000019.10:g.35733177C>T
NG_052906.1:g.20159C>T
NM_014727.1:c.6628C>T
NM_014727.3:c.6628C>TMANE SELECT
NP_055542.1:p.Pro2210Ser
NC_000019.9:g.36224078C>T

Protein change:

P2210S

Links:

dbSNP: rs373926591

NCBI 1000 Genomes Browser:

rs373926591

Molecular consequence:

NM_014727.3:c.6628C>T - missense variant - [Sequence Ontology: SO:0001583]

Observations:

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

Recent activity

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Nitella hyalina mitochondrion, complete genome
gi|385153400|ref|NC_017598.1|

Nucleotide
Nitella hyalina strain KGK0190 plastid, complete genome
Nitella hyalina strain KGK0190 plastid, complete genome
gi|2577867190|ref|NC_082075.1|

Nucleotide
nitella_74953_c21698_c Nitella hyalina EST library Nitella hyalina cDNA 5', mRNA...
nitella_74953_c21698_c Nitella hyalina EST library Nitella hyalina cDNA 5', mRNA sequence
gi|372861361|gnl|dbEST|70984765|gb| 985.1|

Nucleotide
Homo sapiens chromosome 1 open reading frame 61, mRNA (cDNA clone IMAGE:4154919)...
Homo sapiens chromosome 1 open reading frame 61, mRNA (cDNA clone IMAGE:4154919), with apparent retained intron
gi|14714816|gb|BC010558.1|

Nucleotide
Ink
Ink
Pigmented or colored fluid used for writing, staining, painting, drawing, printing, or copying images.<br/>

MeSH

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002298231	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Likely benign (Dec 15, 2023)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]
SCV002563525	CeGaT Center for Human Genetics Tuebingen	criteria provided, single submitter (CeGaT Center For Human Genetics Tuebingen Variant Classification Criteria Version 2)	Likely benign (Aug 1, 2023)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002298231

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Likely benign
(Dec 15, 2023)

germline

clinical testing

PubMed (1)
[See all records that cite this PMID]

SCV002563525

CeGaT Center for Human Genetics Tuebingen

criteria provided, single submitter

(CeGaT Center For Human Genetics Tuebingen Variant Classification Criteria Version 2)

Likely benign
(Aug 1, 2023)

germline

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	yes	3	not provided	not provided	not provided	not provided	clinical testing
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]

PMID:: 28492532
PMCID:: PMC5632818

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV002298231.3

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (1)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

From CeGaT Center for Human Genetics Tuebingen, SCV002563525.16

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	3	not provided	not provided	clinical testing	not provided

Description

KMT2B: BS1

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	yes	not provided	not provided	not provided		3	not provided	not provided	not provided

Last Updated: Oct 20, 2024

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