Variant · Deletion

CDKN2A NM_000077.5(CDKN2A):c.98_150+1488del

CI-VAR-00393446Explore in graph →NM_000077.5:c.98_150+1488delClinVar 4224771

Curated evidence

Evidence by cancer (0 items)

Grouped by cancer context first, then therapy. The same variant can be sensitizing in one cancer and irrelevant in another — contexts are never merged. 50 items per page; a cancer group may continue on the next page.

Data not yet available

No curated evidence item references this variant yet.

ClinVar

Clinical significance (1)

ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.

clinvarCurated1 interpretation · review status and star rating as assigned by ClinVar.

Variation	Clinical significance	Review status	Stars	Conditions	Origin	Submitters	Last evaluated	Source
4224771	Pathogenic	criteria provided, single submitter	1	Hereditary cancer-predisposing syndrome	germline	1	Jul 08, 2025	clinvar

Nomenclature

Record

Gene: CDKN2A
Type: Deletion
HGVS c.: NM_000077.5:c.98_150+1488del
Assembly: GRCh38
Position: chr9:21973189-21974730
Ref / Alt: CCCATATGTAAATATTTAAATCATGATAGAAATCCAAAGCAAAAAGAAAATGAATCAATTGAATTAAAATGTGTAGGATGCTTAAACCCATTTGATAATATATCCATTTGATAATATACTAATATGAATTTAGTACTTTAAAATGTTATATAAATAAATGTTCCTATATTAAACACCAATGTAGTTAGGATTCTAAGCCAACATCATTTCCCCTTTTCTACATGTTCTTCTCCCGTCTCCATTAAAAATTGTCAAAACTATCCACTTTTCTTTTTCCTTTTTGTTTTTAAACAAATAAGGTCTCTTCTAAGATATTGTAGGACTACAAAGCCAAACTCCCGGGTTCAAGCTGTTGGCAAAATTTTAGAGATGCTAAGTTACCCATGTATTAATTACTTTTAAATCCTCCCCTAACTCCCTCACAAAACAGGAGTAGGGAGAGGAGAAACACCTCTGTTCAAAAATGAGGAATTGAAAACTCTTATCACAAATAAACTATATCAAGTAAGCTAAAGATAGTAAAAGAGCAAAAATGTTAGCAGATATTCCCAAAATGGTAACTACATATTACCTCTGGAATGATCACATGAATGTGGCTCATTATTTCCTAAGTTCCTACAGCAAACATATATTTATTTGCCCTACTCAGTTAAAAATAAACACAATATGTAGTTGCTTCTGAATAATTTTTCTCTCTCTCTTTCTCTCTTTCTTTCTTTCGACAAAGTCTCACTCTGTCACCCAGGCTGGAGTGAAGTGGCTCCATCTCGCTGTTCACTACAACCTCAGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAACCTCCCGAGTAGCTGGGATTACAGGCGCCTGCCACCACCCCCGGCTACTTTTTGTATTTTTAGTAGAGGCGAGGTTTCACCTGTTGGCCAGGCTGGTCTCGAACTCCCGACCTCAGGTGATTCCCCCCGCCTTGATCTCCCAAAGTGAAGGGATTACAAGGCGTGAGGCACCGCGCCCGGCCGCTTCTGAATAATTTCGATCAAAATTTATATTCGATATTTATTCCAACATACACCACAGATTTCCACTGATAATCCCTCCTAGTAAGAAAGATAAGCTCCATCCAGGTATCTGTGAATTGGAGGCTAAGTAGTCCCAGCACATCTTACATTTCTTTAAGACTCCCTTTTTATCCCAAACGTTCGTAAATTTTGTATCTGATAAAGAGCATACTTCCATCTAATACAAATATGTTCCCCCCTTCAGATCTTCTCAGCATTCGAGAGATCTGTACGCGCGTGGCTCCTCATTCCTCTTCCTTGGCTTCCCAAGCCCCCAGGGCGTCGCCAGGAGGAGGTCTGTGATTACAAACCCCTTCTGAAAACTCCCCAGGAAGCCTCCCCTTTTTCCGGAGAATCGAAGCGCTACCTGATTCCAATTCCCCTGCAAACTTCGTCCTCCAGAGTCGCCCGCCATCCCCTGCTCCCGCTGCAGACCCTCTACCCACCTGGATCGGCCTCCGACCGTAACTATTCGGTGCGTTGGGCAGCGCCCCCGCCT → C

Per-assembly coordinates