16226740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44384198-G-A

16226742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44384200-G-A

16226822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44384234-G-A

16226822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44384234-G-C

16226822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44384234-G-T

16226830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44384242-G-A

16227040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44384381-C-T

16227073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44384414-C-G

16227073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44384414-C-T

http://identifiers.org/hco/4/GRCh38#16227218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#44384521-A-C

16227218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44384521-A-T

16227351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44384663-G-A

16227351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44384663-G-T

http://identifiers.org/hco/4/GRCh38#16227368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#44384676-C-A

16227368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44384676-C-G

16227424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44384732-G-A

16227424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44384732-G-C

16227424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44384732-G-T

16227438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44384738-G-T

16227461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44384762-G-C

16227479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44384780-G-A

16227479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44384780-G-T

16227621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44384912-G-C

16227662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44384962-T-C

16227688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44384989-C-T

16227758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44385045-G-C

16228034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44385233-T-G

16228051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44385248-C-T

http://identifiers.org/hco/4/GRCh38#16230409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#44385780-C-A

16230409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44385780-C-G

16230769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44386158-C-G

16231243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44386960-C-G

16231243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44386960-C-T

16231333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44387056-A-G

16231913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44387782-A-G

16232089-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44388120-A-T

16232118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44388149-C-T

16232214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44388244-A-G

16232215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44388245-T-C

16232221-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44388251-A-T

16232313-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44388339-T-A

http://identifiers.org/hco/4/GRCh38#16232692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#44388789-C-A

16232694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44388791-A-G

16232720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44388811-T-C

16232819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44388891-G-C

16233437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44389518-A-G

16233621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44389676-G-A

http://identifiers.org/hco/4/GRCh38#16233709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#44389784-A-C

16234209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44390288-C-T

16234571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44390732-T-C

16234971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44391070-A-G

16235225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44391314-G-A

16235899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44392318-A-G

16236158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44392604-G-A

16236314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44392755-C-T

16236445-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44392873-T-G

16236465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44392893-A-G

16236580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44393002-A-G

16236683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44393099-G-A

16236830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44393226-G-A

16237200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44394746-A-G

16237415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44395000-C-G

16237631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44395453-A-G

16237874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44395751-A-G

16237960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44395827-A-G

16238048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44395888-G-C

16238159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44395984-A-G

16238331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44396132-C-T

16238536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44396466-C-G

16238647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44396535-G-A

16238647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44396535-G-T

16238707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44396594-T-G

16238709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44396596-C-T

16238799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: non coding transcript exon variant
orthologous variants: 44396661-A-G

16238827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: non coding transcript exon variant
orthologous variants: 44396690-T-C

16238850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: non coding transcript exon variant
orthologous variants: 44396713-T-C

http://identifiers.org/hco/4/GRCh38#16238981-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#44396920-A-C

16238981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44396920-A-G

http://identifiers.org/hco/4/GRCh38#16239295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#44397210-C-A

16239299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44397214-C-T

16239560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44397500-A-G

16239582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44397523-G-T

16239812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44397661-C-T

16239939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44397806-C-T

http://identifiers.org/hco/4/GRCh38#16239960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#44397824-C-A

16240456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44398220-T-C

16240510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44398263-T-C

16240574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44398325-C-T

16242036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44398688-G-A

16242090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44398746-T-C

16242098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44398760-C-T

16242147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44398810-C-T

16242453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44399729-T-C

16242680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44399958-A-T

16242922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44400143-A-G

16243026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44400202-C-T

http://identifiers.org/hco/4/GRCh38#16243113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#44400267-C-A

16243244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44400372-C-T

16243276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44400406-G-A

16243440-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44400558-G-C

16243488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44400600-C-T

16244557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44401016-T-A

16244640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44401099-A-G

16244746-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44401230-T-A

16245944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44402151-C-T

http://identifiers.org/hco/4/GRCh38#16246114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#44402306-C-A

16246128-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44402323-C-G

16246144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44402339-C-T

16247214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44404467-C-T

16247931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44404538-G-A

16248320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44405079-A-T

16248341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44405315-T-C

16248425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44405400-T-C

16248495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44405471-C-G

16248577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44405506-A-G

16248840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44405725-C-T

http://identifiers.org/hco/4/GRCh38#16249085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#44405959-C-A

16249085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44405959-C-T

16249495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44407052-A-G

16249544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44407101-G-A

16249853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44407348-G-C

16249880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44407375-T-A

16249941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44407429-A-T

16250675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44408178-T-A

http://identifiers.org/hco/4/GRCh38#16250724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#44408220-C-A

16250724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44408220-C-T

16250786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44408282-T-G

16250973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44408506-T-C

16253660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44411846-G-A

http://identifiers.org/hco/4/GRCh38#16253833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#44412030-A-C

16253833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44412030-A-G

16253938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44412131-C-T

16254001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44412189-G-A

16254131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44412315-G-A

16254217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44412408-C-G

16254348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44412533-G-A

http://identifiers.org/hco/4/GRCh38#16254475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#44412754-C-A

16254475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44412754-C-T

16254695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44412973-T-G

16257989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44413354-G-T

16258000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44413367-G-A

http://identifiers.org/hco/4/GRCh38#16258083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#44413420-C-A

16258083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44413420-C-T

16258143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44413469-G-T

16258149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44413475-C-G

16258149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44413475-C-T

16258182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44413492-T-G

16258201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44413511-G-T

16258236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44413546-G-A

16258260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44413569-T-C

16258292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44413594-G-T

16258312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44413614-T-C

16258496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44414613-G-A

16258562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44414677-C-G

16258562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44414677-C-T

16258578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44414710-A-G

http://identifiers.org/hco/4/GRCh38#16258746-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#44414863-A-C

16258867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44414970-C-T

http://identifiers.org/hco/4/GRCh38#16258916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#44415018-A-C

16258929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44415032-C-T

16258932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44415035-T-C

16258932-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44415035-T-G

16258995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44415091-C-T

http://identifiers.org/hco/4/GRCh38#16258997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#44415093-A-C

16259108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44415186-T-C

16259943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44417138-T-G

16259944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44417139-G-A

16260051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44417248-T-C

16260557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44417979-C-G

16260631-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44418053-T-A

16260839-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44418577-T-A

16260850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44418588-T-C

16260953-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44418689-C-G

16260958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44418694-G-A

16260958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44418694-G-T

16261002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44418733-T-C

16261123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44418832-C-T

16261697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44419269-T-C

16262170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44419734-T-C

16262228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44419768-T-C

16262259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44419797-C-G

16262483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44420426-A-G

http://identifiers.org/hco/4/GRCh38#16262584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#44420473-A-C

16262597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44420486-G-A

http://identifiers.org/hco/4/GRCh38#16262738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#44420615-A-C

16263251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44420888-G-A

16263291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44420928-A-G

16263510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44421146-C-T

16263515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44421151-G-T

16263611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44421228-C-T

16264122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44422768-C-G

16264163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44422800-G-A

16264163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44422800-G-C

16264167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44422804-C-T

16264346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44423132-G-C

16264478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44423263-G-T

http://identifiers.org/hco/4/GRCh38#16265011-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#44426073-A-C

16265011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44426073-A-G

16265273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44426277-G-A

16265350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44426365-T-G

16265483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44426462-G-A

http://identifiers.org/hco/4/GRCh38#16265628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#44426598-C-A

16265702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44426882-A-G

16265702-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44426882-A-T

16265707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44426887-A-G

16265761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44426942-C-G

16265810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44426981-G-A

16265810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44426981-G-C

16265844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44427015-A-G

16265934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44427091-T-C

16266013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44427179-C-T

16266126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44427285-C-T

16266468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44427688-T-C

http://identifiers.org/hco/4/GRCh38#16266478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#44427698-C-A

16266575-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44427802-T-G

16266891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44428233-T-C

http://identifiers.org/hco/4/GRCh38#16266978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#44428314-C-A

16267073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44428401-G-T

16267292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44428601-A-G

16267390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44428687-G-A

16267420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44428719-T-C

16270512-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44429092-A-T

16270572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44429213-G-A

16270620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44429258-T-C

16270627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44429265-T-C

16270869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44429464-G-C

16271093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44429726-T-C

16271249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44430011-C-T

16271416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44430176-T-C

16271534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44430296-G-A

16271660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44430440-A-G

16272292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44434815-G-A

16272601-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44435045-G-C

http://identifiers.org/hco/4/GRCh38#16272608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#44435052-A-C

16272638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44435073-C-T

16272639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44435074-T-C

16272640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44435075-C-T

16272825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44435260-A-G

16272842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44435278-T-C

16274810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44437731-C-T

16275621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44441542-C-T

16278469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44442025-C-T

16278705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44442290-G-A

16278705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44442290-G-C

16278832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44442411-G-A

16278923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44442500-T-A

16278971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44442541-G-A

http://identifiers.org/hco/4/GRCh38#16279082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#44442635-C-A

16279110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44442663-A-G

http://identifiers.org/hco/4/GRCh38#16279242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#44442789-C-A

16279296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44442841-G-A

16279296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44442841-G-C

16279352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44442895-G-A

16280601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44445119-T-A

16280676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44445170-G-C

16282399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44445794-C-G

http://identifiers.org/hco/4/GRCh38#16282641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#44446120-C-A

16282663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44446144-A-G

16282701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44446176-G-A

16282766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44446239-C-T

16282830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44446303-G-A

16287153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44460575-T-C

16287229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44460651-A-G

16287243-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44460665-A-T

16287343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44460761-T-C

16287468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44460884-A-G

16287772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44460955-T-A

16287772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44460955-T-G

16287777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44460960-T-A

16287777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44460960-T-C

16287842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44461040-C-G

16287885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44461080-A-G

16289851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44461545-A-G

16289925-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44461618-T-A

16289925-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44461618-T-G

16289951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44461644-T-C

16290057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44461694-A-G

16290138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44461777-C-T

16290545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44462173-G-A

16290582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44462251-G-A

16290648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44462307-T-C

16290751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44462410-C-T

16290810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44462454-A-G

16290833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44462477-G-T

16290981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44462615-C-T

16291287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44462887-A-G

http://identifiers.org/hco/4/GRCh38#16291522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#44463089-C-A

16291522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44463089-C-T

16291782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44464019-G-T

16291885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44464076-G-C

16292509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44464585-G-C

16292509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44464585-G-T

16292746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44464858-T-C

16293307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44465405-G-C

16293447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44465545-C-T

16313188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44468205-G-A

16313206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44468223-T-C

16313279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44468287-T-G

16314081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44476832-C-T

16314338-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44477064-C-G

16314604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44477328-A-G

http://identifiers.org/hco/4/GRCh38#16314642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#44477365-C-A

16314765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44477485-G-A

16314844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44477544-C-T

16314991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44477681-C-T

16315038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44477711-T-A

16315038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44477711-T-G

16315119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44477786-G-C

16315119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44477786-G-T

16315203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44477868-A-G

16315311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44477974-C-T

16315364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44478013-C-T

16315438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44478092-G-A

16315678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44478300-C-T

16315679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44478301-G-A

16316172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44478710-T-C

16316444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44478961-G-A

16316555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44479068-G-A

16316763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44479275-T-C

16316909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44479422-G-T

http://identifiers.org/hco/4/GRCh38#16317362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#44479691-C-A

16317362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44479691-C-T

16317396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44479724-C-T

16317452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44479780-G-C

16317576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44479909-T-C

16317716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44480049-T-C

16317722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44480054-T-C

16317768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44480091-T-G

16318170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44481567-C-T

16318177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44481574-C-T

16318361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44481758-G-A

16318370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44481767-T-C

16318683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44482115-A-G

http://identifiers.org/hco/4/GRCh38#16318720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#44482152-C-A

16318737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44482169-A-G

16318769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44482173-G-T

16318933-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44482326-T-G

http://identifiers.org/hco/4/GRCh38#16319297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26832
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#44482379-C-A