5711231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 5 prime UTR variant
orthologous variants: 37494188-A-G

5711231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 5 prime UTR variant
orthologous variants: 37494188-A-T

http://identifiers.org/hco/4/GRCh38#5711283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37494181-C-A

5711283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 5 prime UTR variant
orthologous variants: 37494181-C-G

5711283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 5 prime UTR variant
orthologous variants: 37494181-C-T

5711352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 5 prime UTR variant
orthologous variants: 37494162-G-A

5711352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 5 prime UTR variant
orthologous variants: 37494162-G-T

5711358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 5 prime UTR variant
orthologous variants: 37494156-G-A

5711358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 5 prime UTR variant
orthologous variants: 37494156-G-T

http://identifiers.org/hco/4/GRCh38#5711361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37494153-C-A

5711361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 5 prime UTR variant
orthologous variants: 37494153-C-T

5711414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: missense variant
orthologous variants: 37494117-G-A

5711414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: missense variant
orthologous variants: 37494117-G-C

5711414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: missense variant
orthologous variants: 37494117-G-T

5711541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: missense variant
orthologous variants: 37493990-G-A

5711541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: missense variant
orthologous variants: 37493990-G-T

5711556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: splice donor variant
orthologous variants: 37493975-T-C

5711556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: splice donor variant
orthologous variants: 37493975-T-G

http://identifiers.org/hco/4/GRCh38#5711584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37493960-C-A

5711584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37493960-C-G

5711584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37493960-C-T

5711603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37493942-G-A

5711603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37493942-G-T

5711610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37493935-G-A

5711610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37493935-G-T

5711750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37493774-C-T

5718118-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37491514-A-T

5718122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37491510-T-C

5718417-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37491243-T-A

5718417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37491243-T-C

5718526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37491157-G-A

5718615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37491052-C-T

5718616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37491051-A-G

5718815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37490945-A-G

5719067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37490507-C-T

5719134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37490461-G-T

http://identifiers.org/hco/4/GRCh38#5719144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37490451-C-A

5719144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37490451-C-G

http://identifiers.org/hco/4/GRCh38#5719186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37490410-A-C

5719186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37490410-A-G

5719241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 37490366-G-T

http://identifiers.org/hco/4/GRCh38#5719257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37490350-A-C

5719257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: missense variant
orthologous variants: 37490350-A-G

5719288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: missense variant
orthologous variants: 37490319-A-G

5719301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: synonymous variant
orthologous variants: 37490306-C-G

5719354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: missense variant
orthologous variants: 37490253-A-T

5719795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37489865-T-C

5719923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37489740-A-G

5720079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37489599-A-G

5720079-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37489599-A-T

5720346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37489412-G-A

5720347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37489411-A-G

http://identifiers.org/hco/4/GRCh38#5720507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37489253-C-A

5720562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37489208-G-A

5722141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37488913-C-G

5722238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37488843-C-T

5722256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37488823-G-A

http://identifiers.org/hco/4/GRCh38#5722474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37488683-C-A

5722540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, undefined
orthologous variants: 37488624-C-T

5722692-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37488479-T-A

5722719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37488450-C-T

5722893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37488271-C-T

5728783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37487189-T-A

5728783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37487189-T-C

5728784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37487188-C-T

5728833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37487125-T-C

5728993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37486212-C-T

5729055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37486150-T-G

5729204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37485987-G-A

5729204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37485987-G-T

5729263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37485928-T-G

5729270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37485921-G-A

http://identifiers.org/hco/4/GRCh38#5729431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37485762-C-A

5729431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37485762-C-T

5729484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37485708-G-A

5729484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37485708-G-T

http://identifiers.org/hco/4/GRCh38#5729507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37485681-C-A

5729507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37485681-C-G

5729507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37485681-C-T

5729653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37485547-C-G

5729735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37485476-C-T

5729787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37485439-A-G

5730000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37485246-G-C

5730065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37485183-T-C

5730168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37485086-G-A

5730186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37485064-A-G

http://identifiers.org/hco/4/GRCh38#5730452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37484723-C-A

5730452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37484723-C-T

5730466-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37484709-T-G

5730513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37484670-C-T

5730966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37484304-T-G

5730979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37484287-G-A

5731002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37484256-G-A

5731056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37484200-G-C

5731056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37484200-G-T

5731304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37483983-A-G

5731642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: missense variant
orthologous variants: 37483695-T-C

http://identifiers.org/hco/4/GRCh38#5731672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37483660-C-A

5731672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37483660-C-T

5731858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37483571-G-T

5731864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37483565-G-A

5731923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37483507-G-A

http://identifiers.org/hco/4/GRCh38#5732002-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37483409-A-C

5732120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37483330-C-T

5732159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37483300-T-C

5733352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 37482262-G-A

5733487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37482123-G-A

5733487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37482123-G-T

http://identifiers.org/hco/4/GRCh38#5733531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37482085-C-A

http://identifiers.org/hco/4/GRCh38#5741065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37481729-C-A

5741336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37481481-C-G

5741336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37481481-C-T

5741529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37481252-C-T

5741574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37481199-A-G

5741811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: synonymous variant
orthologous variants: 37481044-A-G

5741834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37481021-T-C

5741960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37480896-G-A

5741960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37480896-G-C

5741960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37480896-G-T

5744646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37480368-G-A

5744753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37480266-C-T

5744794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37480209-A-G

5744863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37480138-G-A

5745027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37479983-C-T

5745169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37479558-G-T

5745180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37479551-T-G

5745187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37479544-T-G

5745255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant
orthologous variants: 37479478-A-G

5745264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant
orthologous variants: 37479469-G-A

5745264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant
orthologous variants: 37479469-G-T

5745315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant
orthologous variants: 37479418-G-A

http://identifiers.org/hco/4/GRCh38#5745389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37479347-C-A

5745389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37479347-C-T

5745396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37479340-A-G

5745396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37479340-A-T

5745397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37479339-T-C

5745856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37478989-G-T

5747614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37478249-T-C

5747773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37478086-G-A

5747919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37477947-C-T

http://identifiers.org/hco/4/GRCh38#5747958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37477912-C-A

5747958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37477912-C-T

5747960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37477910-G-A

5747960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37477910-G-T

5747964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37477906-A-G

5747986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37477881-T-C

5748011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37477856-A-G

5748061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37477819-G-T

5748066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37477814-T-A

http://identifiers.org/hco/4/GRCh38#5748082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37477798-C-A

5748082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37477798-C-G

5748082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron variant
orthologous variants: 37477798-C-T

5748190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37477694-C-G

5748190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37477694-C-T

5748191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37477693-T-C

5748323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37477558-C-T

5748353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37477539-A-G

5748383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37477531-A-G

5748411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37477505-T-C

5748523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37477421-T-C

5748563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37477387-T-A

5752861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37476422-G-A

5752861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37476422-G-T

5753010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 37476273-C-T

5753066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37476216-A-G

5753067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37476215-T-G

5753095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37476212-T-C

5753207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37476129-T-C

5753464-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37475912-A-T

5753554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37475831-C-G

http://identifiers.org/hco/4/GRCh38#5753713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37475725-A-C

5753713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37475725-A-G

5753757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37475681-C-T

5753789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37475649-T-A

5753793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 37475645-C-T

5753884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 37475554-G-C

5753910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 37475528-G-A

5753910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 37475528-G-C

5753960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37475474-A-G

5753960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37475474-A-T

http://identifiers.org/hco/4/GRCh38#5754048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37475407-C-A

5754048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37475407-C-G

5754048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37475407-C-T

5754157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37475333-T-C

5754205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37475290-C-T

5754206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37475289-G-A

5754206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37475289-G-T

5755368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37474664-G-T

5755392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37474640-G-A

5755445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37474578-G-C

5755462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37474564-C-T

5755463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37474563-G-A

5755529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37474496-A-T

5755562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37474463-G-C

5755792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37474244-T-G

5756137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37473886-T-C

5756177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37473851-A-G

5756177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37473851-A-T

5756189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37473838-G-A

5756189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37473838-G-T

5756193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37473831-G-A

5756193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37473831-G-C

5756193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37473831-G-T

http://identifiers.org/hco/4/GRCh38#5756237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37473793-C-A

5756237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37473793-C-T

http://identifiers.org/hco/4/GRCh38#5756330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37473699-A-C

5756330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 37473699-A-G

5756823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37473089-G-A

5756823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37473089-G-T

5756873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37473041-G-T

5756897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37473017-G-A

5757203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37472728-T-G

5757390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37472560-A-G

5783626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 37471839-G-T

5783641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 37471824-G-A

5783641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 37471824-G-T

5783653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 37471812-C-T

5783663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 37471802-C-T

http://identifiers.org/hco/4/GRCh38#5783744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37471721-C-A

5783744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 37471721-C-T

http://identifiers.org/hco/4/GRCh38#5783811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37471655-C-A

5783848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37471624-C-G

5783861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37471611-A-G

5783861-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37471611-A-T

http://identifiers.org/hco/4/GRCh38#5793665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37470823-C-A

5793665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37470823-C-T

5793681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37470807-G-A

5793681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37470807-G-T

http://identifiers.org/hco/4/GRCh38#5793746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37470746-C-A

5793746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37470746-C-T

5793777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37470717-T-C

5793780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37470714-G-A

5793780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37470714-G-C

5793797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37470697-G-T

5794010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37470493-C-G

5794188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37470356-G-T

5794202-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37470339-T-G

5794215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37470326-A-G

5796595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37469429-G-C

5796800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37469240-G-C

http://identifiers.org/hco/4/GRCh38#5796911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37469179-C-A

5796911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37469179-C-T

5796954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37469145-G-A

5796954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37469145-G-C

5796954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37469145-G-T

http://identifiers.org/hco/4/GRCh38#5796960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37469139-C-A

5796987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37469113-G-T

5796992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37469108-G-A

5796992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37469108-G-T

http://identifiers.org/hco/4/GRCh38#5797048-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37469058-A-C

5797048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37469058-A-G

http://identifiers.org/hco/4/GRCh38#5797256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37468849-C-A

http://identifiers.org/hco/4/GRCh38#5797276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37468829-C-A

5797276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37468829-C-T

http://identifiers.org/hco/4/GRCh38#5797278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37468827-C-A

5797278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37468827-C-G

5797278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37468827-C-T

http://identifiers.org/hco/4/GRCh38#5797342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37468796-C-A

5797342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37468796-C-G

5797342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37468796-C-T

http://identifiers.org/hco/4/GRCh38#5797343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37468795-A-C

5797343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37468795-A-G

5797343-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37468795-A-T

5797388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37468743-A-G

5797397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37468736-A-G

5797397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37468736-A-T

5797404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37468729-A-G

5797406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37468727-T-C

5797406-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37468727-T-G

5797472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37468663-C-T

5797473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37468662-T-C

5797506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37468630-A-G

5797541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37468595-C-T

5797596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37468527-C-T

http://identifiers.org/hco/4/GRCh38#5797615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37468516-C-A

5797730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37468410-G-A

5797750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37468390-G-C

5797842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37468304-C-T

5797855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37468289-G-C

5797872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37468272-C-T

5797886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37468260-T-C

5797959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37468194-C-T

http://identifiers.org/hco/4/GRCh38#5797969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37468184-C-A

5797969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37468184-C-T

5798344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37467844-A-G

5798353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37467835-G-C

5798357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37467831-C-T

5798362-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37467826-T-G

http://identifiers.org/hco/4/GRCh38#5798395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37467794-A-C

5798443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37467769-C-T

http://identifiers.org/hco/4/GRCh38#5798560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37467729-C-A

5798560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37467729-C-G

5798560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37467729-C-T

http://identifiers.org/hco/4/GRCh38#5798561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37467728-C-A

5798561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37467728-C-T

http://identifiers.org/hco/4/GRCh38#5798578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37467717-C-A

5798578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 37467717-C-G

5798578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 37467717-C-T

5798628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37467667-G-A

5798666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 37467629-G-A

5798673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37467622-G-T

5798727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37467568-G-T

http://identifiers.org/hco/4/GRCh38#5801707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37466756-C-A

5801707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37466756-C-T

5801710-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37466753-T-G

5801729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37466735-A-G

5801867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37466581-T-C

5801868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37466580-G-T

5801874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37466574-G-T

5801907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37466560-G-A

5801907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37466560-G-T

5801923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37466545-G-T

http://identifiers.org/hco/4/GRCh38#5802010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37466458-C-A

5802010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 37466458-C-T

http://identifiers.org/hco/4/GRCh38#5802103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37466365-C-A

5802103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37466365-C-T

http://identifiers.org/hco/4/GRCh38#5802121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37466338-C-A

5802946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37466111-T-G

http://identifiers.org/hco/4/GRCh38#5803264-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37465793-A-C

5803308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37465749-T-C

5803308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37465749-T-G

5803426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37465620-C-T

5803434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37465612-A-G

5803533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37465535-G-C

http://identifiers.org/hco/4/GRCh38#5804597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37464796-C-A

5804607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37464786-G-A

5804607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37464786-G-T

5804729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 37464667-G-A

5804779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 37464617-C-T

5804780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 37464616-C-T

http://identifiers.org/hco/4/GRCh38#5804784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/5/GRCm39#37464612-C-A

5804784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 37464612-C-T

5807259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37461552-G-A

5807381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37461429-G-C

5807389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37461421-T-C

5807479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37461351-G-A

5807498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37461330-T-C

5807590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37461240-G-T

5807625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37461179-C-G

http://identifiers.org/hco/4/GRCh38#5807638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37461166-C-A

5807649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37461156-G-T

http://identifiers.org/hco/4/GRCh38#5808081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37460802-C-A

5808081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37460802-C-T

5808095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37460788-G-A

http://identifiers.org/hco/4/GRCh38#5808113-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37460768-A-C

5808186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37460668-C-T

5808205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 37460649-C-T

5808208-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 37460646-T-A

5808208-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 37460646-T-G

5808223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 37460631-T-G

5808235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 37460619-T-C

http://identifiers.org/hco/4/GRCh38#5808390-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37460425-A-C

5808409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37460405-G-A

5808409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37460405-G-C

5808483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37460334-G-A

5808538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37460291-C-T

5808620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37460221-G-T

5808771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37460079-T-C

5809369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37459119-T-C

5809373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37459111-G-T

http://identifiers.org/hco/4/GRCh38#5809402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37459085-C-A

5809402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37459085-C-T

5809406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37459082-A-G

5809420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37459068-G-A

5809420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37459068-G-T

5809434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37459048-G-T

5809531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 37458980-A-T

5809633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37458890-T-C

5809633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37458890-T-G

5809708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37458816-A-G

http://identifiers.org/hco/4/GRCh38#5809781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37458750-C-A

5810046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37458501-A-G

5810196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37458368-G-A

5810196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37458368-G-T

http://identifiers.org/hco/4/GRCh38#5810197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37458367-C-A

5810197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37458367-C-G

5810365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 37458239-A-G

5810451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 37458153-G-A

5810528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37458093-G-T

http://identifiers.org/hco/4/GRCh38#5810583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37458050-C-A

5810583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37458050-C-T

http://identifiers.org/hco/4/GRCh38#5810592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37458045-A-C

5810592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37458045-A-G

5810611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37458026-A-T

5810668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37457953-T-C

5810670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37457951-G-A

5810880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37457845-T-G

5810930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37457826-C-T

5811021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 37457735-G-A

5811021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 37457735-G-T

5811040-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37457716-T-A

5811040-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37457716-T-G

5811439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37457133-A-G

http://identifiers.org/hco/4/GRCh38#5811553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37457041-A-C

5811553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37457041-A-G

5811561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37457033-G-A

5811561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37457033-G-T

http://identifiers.org/hco/4/GRCh38#5811571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37457023-C-A

5811571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37457023-C-T

http://identifiers.org/hco/4/GRCh38#5811582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37457012-C-A

5811582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37457012-C-T

5811620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37456974-A-G

5811622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37456972-C-T

5811627-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37456967-T-A

5811628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37456966-C-T

5811644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37456952-G-T

http://identifiers.org/hco/4/GRCh38#5811646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37456950-C-A

5811646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3497
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37456950-C-T