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NM_001354604.2(MITF):c.1476C>T (p.Pro492=) AND multiple conditions

Germline classification:
Likely benign (1 submission)
Last evaluated:
Jan 31, 2024
Review status:
1 star out of maximum of 4 stars
criteria provided, single submitter
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:
RCV003767744.2

Allele description [Variation Report for NM_001354604.2(MITF):c.1476C>T (p.Pro492=)]

NM_001354604.2(MITF):c.1476C>T (p.Pro492=)

Gene:
MITF:melanocyte inducing transcription factor [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
3p13
Genomic location:
Preferred name:
NM_001354604.2(MITF):c.1476C>T (p.Pro492=)
HGVS:
  • NC_000003.12:g.69965143C>T
  • NG_011631.1:g.230662C>T
  • NM_000248.4:c.1155C>T
  • NM_001184967.2:c.1302C>T
  • NM_001354604.2:c.1476C>TMANE SELECT
  • NM_001354605.2:c.1473C>T
  • NM_001354606.2:c.1455C>T
  • NM_001354607.2:c.1407C>T
  • NM_001354608.2:c.1302C>T
  • NM_006722.3:c.1455C>T
  • NM_198158.3:c.1137C>T
  • NM_198159.3:c.1458C>T
  • NM_198177.3:c.1410C>T
  • NM_198178.3:c.969C>T
  • NP_000239.1:p.Pro385=
  • NP_001171896.1:p.Pro434=
  • NP_001341533.1:p.Pro492=
  • NP_001341534.1:p.Pro491=
  • NP_001341535.1:p.Pro485=
  • NP_001341536.1:p.Pro469=
  • NP_001341537.1:p.Pro434=
  • NP_006713.1:p.Pro485=
  • NP_937801.1:p.Pro379=
  • NP_937802.1:p.Pro486=
  • NP_937820.1:p.Pro470=
  • NP_937821.2:p.Pro323=
  • LRG_776:g.230662C>T
  • NC_000003.11:g.70014294C>T
  • NM_198159.2:c.1458C>T
  • p.Pro486Pro
Links:
dbSNP: rs745749254
NCBI 1000 Genomes Browser:
rs745749254
Molecular consequence:
  • NM_000248.4:c.1155C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001184967.2:c.1302C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001354604.2:c.1476C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001354605.2:c.1473C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001354606.2:c.1455C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001354607.2:c.1407C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001354608.2:c.1302C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_006722.3:c.1455C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_198158.3:c.1137C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_198159.3:c.1458C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_198177.3:c.1410C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_198178.3:c.969C>T - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Name:
Tietz syndrome (TADS)
Synonyms:
Albinism-deafness of Tietz; Hypopigmentation/deafness of Tietz; Tietz albinism-deafness syndrome
Identifiers:
MONDO: MONDO:0007077; MedGen: C0391816; Orphanet: 42665; OMIM: 103500
Name:
Waardenburg syndrome type 2A (WS2A)
Synonyms:
WAARDENBURG SYNDROME WITHOUT DYSTOPIA CANTHORUM
Identifiers:
MONDO: MONDO:0008671; MedGen: C1860339; Orphanet: 3440; OMIM: 193510
Name:
Melanoma, cutaneous malignant, susceptibility to, 8
Synonyms:
MELANOMA AND RENAL CELL CARCINOMA, SUSCEPTIBILITY TO; Cutaneous malignant melanoma 8
Identifiers:
MONDO: MONDO:0013759; MedGen: C3152204; Orphanet: 293822; OMIM: 614456

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV004585349Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Likely benign
(Jan 31, 2024) 		germlineclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical 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, SCV004585349.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 29, 2024